lactose digester and
佩尔果胶介绍
佩尔果胶介绍佩尔果胶是医药级苹果果胶, 采用天然而不含农药之波兰-克拉科夫苹果, 由于含有高浓缩D-半乳糖醛酸, 使佩尔果胶能够发挥其独有功效。
经过6道专利技术提炼成100% 水溶性纳米粉未, 由250公斤苹果制造1公斤佩尔苹果果胶的有效成份,容易被人体吸收,并透过螯合作用,有效助身体将有害重金属及毒素排出,扺抗四周毒害。
能被人体完全吸收。
一、成分:●苹果果胶:10包/盒的佩尔果胶含有3克医药级苹果果胶,30包/盒的佩尔果胶含有3.5g医药级苹果果胶。
苹果果胶是一个天然纤维及益生元。
研究报告指果胶能过减慢身体的糖分吸收和帮助维持健康的胆固醇度数。
●果糖:佩尔果胶含有10.3g医药级的果糖,用红菜头及甘蔗制作。
每一包含有的果糖等于半个苹果,适合糖尿病患者,因为这种糖不会令血糖飙高。
●维他命C:佩尔果胶含有15微克的维他命C,有天然抗氧化的功效。
维他命C是用来保留佩尔的效用。
●苹果果香:佩尔果胶含有苹果果香,容易入口。
二、服用方法:佩尔果胶容易服用而且粉装方便携带。
有10,30包两种规格。
建议前一个月一天三包,然后一天一包维持。
把佩尔果胶倒进200ml-250ml的温水或冷水搅拌或摇匀10-15秒。
不可用热水以免苹果胶丧失活性。
建议配用佩尔果胶跟一个健康的营养及生活习惯来得到最好效果。
控制血糖使用方法:1) 早上(7:00前)空腹,用200ML温水冲调一包,不要再吃早餐!可喝多些水或者吃一个蒸鸡蛋.2)12:00午饭前用200ML温水冲调一包,20分钟后再吃午餐,可吃肉,米饭,鱼,青菜!3)5:30晚餐前,用200ML温水冲调一包,30分钟后再吃晚餐,可吃少量肉,少量米饭(一勺米饭),鱼,蔬菜,汤。
晚上尽量在10点左右睡觉。
全天保持多喝水.按照这样的方法服用三个月,第四个月开始每天早晚各一包,食用方法同上。
到第六个月开始每天早上或者晚上食用一包即可。
减肥使用方法:1) 早上(7:00前)空腹,用200ML温水冲调一包,不要再吃早餐。
棕榈酰三肽-3 结构式
棕榈酰三肽-3 结构式
棕榈酰三肽-3是一种结构独特的肽类化合物,具有广泛的生物活性和医学应用潜力。
它由三个氨基酸残基组成,分别是棕榈酰基谷氨酰丙氨酸。
这种肽类化合物的结构式为C16H31CONH-Gly-Pro-Ala,其中C16H31CO代表棕榈酰基,NH代表氨基,Gly代表甘氨酸,Pro代表脯氨酸,Ala代表丙氨酸。
棕榈酰三肽-3在皮肤护理领域具有独特的功效。
它可以促进皮肤细胞的再生和修复,增加胶原蛋白的合成,有助于提高皮肤的弹性和紧致度。
此外,棕榈酰三肽-3还可以抑制酪氨酸酶的活性,减少黑色素的产生,从而改善肤色不均和色斑问题。
在抗衰老领域,棕榈酰三肽-3也被广泛应用。
它可以刺激皮肤中的胶原蛋白和弹性蛋白的合成,减少皱纹和细纹的出现。
此外,棕榈酰三肽-3还可以增强皮肤的保湿能力,改善皮肤干燥和粗糙的问题,使肌肤更加柔软和光滑。
除了在美容护肤领域,棕榈酰三肽-3还在医学研究中展现出广阔的应用前景。
研究表明,棕榈酰三肽-3具有抗菌和抗炎作用,对某些细菌和炎症反应有明显的抑制效果。
这使得它在治疗皮肤感染和炎症性皮肤疾病方面具有潜在的药物价值。
棕榈酰三肽-3是一种具有广泛生物活性和医学应用潜力的肽类化合物。
它在皮肤护理和抗衰老领域有着重要的作用,能够促进皮肤细
胞的再生和修复,改善肤色不均和皱纹问题。
此外,棕榈酰三肽-3还具有抗菌和抗炎作用,在医学研究中具有潜在的药物价值。
随着对棕榈酰三肽-3的进一步研究,相信它将在更多领域展现出其独特的价值和应用前景。
哥伦比亚血琼脂基础,亮绿乳糖培养基,肠道菌增菌肉汤
Cary-Blair氏运送培养基,哥伦比亚血琼脂基础,亮绿乳糖培养基,肠道菌增菌肉汤(EE肉汤),TTC营养琼脂,LB肉汤,LB营养琼脂,苯丙氨酸脱氨酶培养基。
现货供应类杆菌-胆汁-七叶甙(BBE)琼脂培养基产品,优质产品,送货上门,我公司培养基由人工配制的、适合微生物生长繁殖或产生代谢产物用的混合营养料。
碳源、氮源、无机盐、能源、生长因子、水,任何培养基都应具备微生物所需要的六大营养要素。
葡萄糖蛋白胨培养基250用于药品,生物制品无菌试验DextrosePeptoneMedium抗生素检定培养基4号250用于两性霉素B等的效价测定AntibioticAgarNo.4抗生素检定培养基6号250用于粘菌素等的效价测定AntibioticAgarNo.6抗生素检定培养基7号250用于头孢噻肟钠等的效价测定AntibioticAgarNo.7抗生素检定培养基8号250用于去甲万古霉素等的效价测定AntibioticAgarNo.8卵黄高盐琼脂基础250用于药品,生物制品金黄色葡萄球菌选择性分离Egg-YolkSaltAgarBase抗生素5号250用于两性霉素B检定菌种培养AntibioticNo.5MUG培养基100用于大肠杆菌测定MUGMedium真菌琼脂培养基250用于无菌生长试验FungiAgarMedium磷酸盐葡萄糖胨水培养基250用于甲基红试验PhosphateGlucosePeptoneWaterMedium甲基红指示剂盒10ml*1用于甲基红试验配套试剂胰蛋白胨水培养基250用于靛基质试验PeptoneWaterMediumKovacs氏靛基质试剂盒10ml*2用于吲哚(靛基质)试验配套试剂ASS琼脂250用于磺胺类灵敏度试验(WHO方法)Antibioticsulfonamidesensitivity-testagarAC肉汤250用于常见微生物增菌培养和不含防腐剂样品的无菌试验(AlphaBiosciences方法) ACBroth硝酸盐胨水培养基250用于硝酸盐还原产气试验NitrateSalinePeptoneWaterMedium硝酸盐还原试剂盒10ml*2用于硝酸盐还原试验配套试剂改良马丁液体培养基250用于菌苗制造及生物制品霉菌无菌检验MartinBroth,Modified改良马丁琼脂培养基250用于生物制品霉菌无菌检验MartinAgarMedium,Modified霉菌培养基250用于药品,生物制品霉菌无菌试验(GB标准)MouldMediumBPLS琼脂250用于药品等多种标本中沙门氏菌检验选择性分离培养(美国药品和欧洲药品检测推荐方法)BPLSAgar优质产品:类杆菌-胆汁-七叶甙(BBE)琼脂英文名称:BBEAgar产品规格:250产品说明及用途:用于脆弱拟杆菌群的分离培养公司拥有严格的质量控制体系和十分完善的售后服务体系,在客户中树立了良好的信誉类杆菌-胆汁-七叶甙(BBE)琼脂报价|价格权威品牌,质量保证!欢迎来电咨询!。
红酒多酚
1.葡萄中含有大量的多酚物质,因此其萃取物已有明显的抗氧化功效;在经发酵成为葡萄酒后,多酚的含量更提高、成分更稳定、抗氧化能力大幅提升。
2.红酒中的多酚化合物超过50种,是目前所发现抗氧化物种类最多、抗氧化范围最广的物质。红酒当中含有为数最多的多酚类物质如没食子酸、儿茶素、槲皮酮、花青素、白藜芦醇等,都具有抗氧化作用,效果更胜维他命E。从皮肤保养的角度来看,白藜芦醇同时具有良好的保湿特性及抗炎作用,还可延缓肌肤细胞衰老的过程,甚至亦能抑制酪胺酸酶的活性,减少黑色素的形成。
3.另一种重要的多酚物质花青素,除了具有强力的抗氧化功能外,亦能降低紫外线的伤害,并防止胶原蛋白与弹力纤维受到破坏。至于儿茶素,同样能减少紫外线所造成的伤害与发炎反应,并抑制胶原蛋白分解酶,保护胶原蛋白不受破坏。
【保染、消毒的纸板桶或铝箔包装(25公斤/桶)。
【产品名称】红酒提取物
【拉丁名称】Vitis vinifera L.
【提取来源】
【主要成分】红酒多酚
【产品规格】10%-30% UV
【产品性状】紫红色精细粉末
【产品功效】抗氧化,预防心脏疾病,防止血管氧化,减肥等
【药理作用】红酒提取物是非常有益心血管健康支持通过加强血管,增加血液循环,降低胆固醇,减少血小板聚集(血栓)的血液。它也被认为是最强大的抗氧化剂,众所周知的存在有利于战斗自由基的伤害,增强免疫能力。红酒多酚为一种强而有力的抗氧化分子,可有效抗抵自由基的伤害,因为自由基会产生氧化作用,使肌肤表皮皱缩产生细纹,而天然的红酒多酚因为蕴含多种强效的抗氧化物质,因此可以防止肌肤老化,且变得更白皙、润泽而有弹性。
半乳糖英文简介
半乳糖英文简介Lactose, also known as milk sugar, is a disaccharide composed of glucose and galactose. It is primarily found in milk and dairy products. Lactose is an essential carbohydrate for the growth and development of young mammals, including humans.Lactose is produced in the mammary glands of mammals and serves as the main source of energy in milk. It provides a sweet taste to dairy products and plays a vital role in their nutritional composition. However, not all individuals have the ability to fully digest lactose due to a deficiency in the enzyme lactase, which is responsible for breaking down lactose into its component sugars.Lactose intolerance is a common condition where individuals experience digestive symptoms, such as bloating, gas, and diarrhea, after consuming lactose-containing foods. This intolerance occurs when lactose isnot properly digested and absorbed in the small intestine.In recent years, lactose-free products have become increasingly available to cater to individuals with lactose intolerance. These products undergo a process that breaks down the lactose into its component sugars, glucose and galactose, making them easier to digest.Lactose is also used in various food products as a sweetener and flavor enhancer. It provides a desirable taste profile and is utilized in the production of baked goods, confectionery, and dairy-based desserts.In summary, lactose is a natural sugar found in milk and dairy products. While lactose intolerance is prevalent in certain individuals, lactose-free options are widely available, allowing those with lactose intolerance to still enjoy dairy products without discomfort.。
3,3'-二甲基鞣花酸-4'-o-葡萄糖苷
3,3'-二甲基鞣花酸-4'-o-葡萄糖苷是一种在植物中广泛存在的化合物,具有多种生物活性和药用价值。
本文将深入探讨这种化合物的来源、作用机制以及在医学和保健领域的应用。
1. 3,3'-二甲基鞣花酸-4'-o-葡萄糖苷的来源3,3'-二甲基鞣花酸-4'-o-葡萄糖苷主要存在于许多植物中,如草莓、覆盆子、葡萄等。
这些植物通常被用于提取这种化合物,用于医药和营养补充品。
2. 3,3'-二甲基鞣花酸-4'-o-葡萄糖苷的作用机制这种化合物被认为具有抗氧化、抗炎和抗微生物作用。
它可以帮助人体清除自由基,并且对于炎症和感染有一定的缓解作用。
它还被发现对于一些肿瘤细胞有抑制作用,具有一定的抗肿瘤活性。
3. 3,3'-二甲基鞣花酸-4'-o-葡萄糖苷在医学和保健领域的应用由于这种化合物的多种生物活性,它在医学和保健领域有着广泛的应用。
在药物的研发过程中,研究人员常常会对其进行进一步的分离和提纯,以期开发出更加有效的药物。
另外,它也被广泛应用于保健品和营养品中,如抗氧化剂和抗炎产品。
总结与展望回顾本文所介绍的内容,我们可以看到3,3'-二甲基鞣花酸-4'-o-葡萄糖苷作为一种具有多种生物活性的化合物,具有广泛的应用前景。
未来,我们可以期待更多关于它作用机制和应用领域的研究成果的涌现,以期进一步挖掘其在医学和保健领域中的潜力。
个人观点笔者认为,3,3'-二甲基鞣花酸-4'-o-葡萄糖苷作为一种天然产物,具有着丰富的生物活性,对于人体健康有着积极的作用。
随着对它的深入研究,相信它将在药物和保健品领域发挥越来越重要的作用。
总结本文对3,3'-二甲基鞣花酸-4'-o-葡萄糖苷的来源、作用机制和应用进行了全面的介绍。
通过对这种化合物的深入了解,我们可以更好地认识其在医学和保健领域的潜在价值,为相关研究和产品开发提供参考。
纸业专业英语词汇翻译(L1)
纸业专业英语词汇翻译(L1)label paper 标签纸label manila paper 标签用马尼拉纸labelled paper 标签纸laboratory paper 实验室手抄纸片lace paper 纸花边lacquered paper 漆面涂布纸laid paper 直纹纸laid antique 条纹仿古纸laid cigarette paper 条纹卷烟纸laid writing 条纹书写纸laminated paper 层压纸laminated glassine 层合玻璃纸laminated phenolic paper 酚醛层压纸laminating paper 层压纸lampblack paper 炭黑包装纸lampshade paper 灯罩纸lapping paper 盖面纸lard paper 防油纸latex(treated) paper 乳胶涂布加工纸laundry paper 洗衣防用纸layer insulating paper 变压器用绝缘纸layout paper 座标纸lead paper 醋酸铅试纸lead acetate paper 醋酸铅试纸lead indicating paper 铅试纸lead pencil paper 铅笔书写纸,铅芯包装纸leather imitation paper 仿革纸leather(ette) paper 仿革纸ledger paper 帐簿纸lens paper 擦镜纸lenz paper 擦镜纸letter paper 信纸letter copying paper 拷贝信纸letter-press paper 凸版印刷纸light proof paper 防光纸light resistant paper 感光防护纸light sensitive paper 光敏纸light weight paper 轻磅纸,薄页纸light coated paper 轻量涂布纸lincrusta paper 坚实裱糊花纸linear paper 水纹书写纸lined paper 格纸linen paper 亚麻布纸linen-faced paper 亚麻布纹纸liner paper 挂面纸liner finish(ed) paper 亚麻布纹纸lining paper 夹层纸linoleum paper 楼板油毡衬垫纸litho paper 石版印刷纸litho-coated paper 石版印刷涂布纸lithograph(ic) paper 石版印刷纸lithographers'plate wiper 平印版擦拭纸lithographers masking paper 石印蒙版纸lithographic transfer paper 石版转印纸litmus paper 石蕊试纸loan paper 证券纸locker paper 冷冻食品包装纸loft paper 造船放样厚纸loft dried paper 风于纸logarithmic paper 座标纸loin paper 肉类包装纸;防油包装纸long fibered paper 长纤维纸long life paper 耐久纸loose leaf paper 活页纸loose ledger paper 活页帐簿纸lottety paper 彩票用纸low weight coating paper 低定量涂布纸loudspeaker cone paper 扬声器盒纸luminescent paper 发光纸luminous paper 发光纸lunch roll paper 家用卷筒包装纸laminated board 层压纸板latex impregnated board 乳胶浸渍纸板laundry board 白纸板layer board 糖果包装纸板leather(fiber) board 仿革纸板lightweight liner board 轻重量挂面纸板lined board 多层纸板,层粘纸板liner board 挂面纸板lining board 衬里纸板litho board 石板印刷纸板lacquer coater 漆纸涂布机letterpress print coater 多辊转印涂布机,胶印涂布机levelon coater 背辊整匀涂布机liquid phase cooking 液相蒸煮label 标签,贴签labeled atom 示踪原子,标记原子labeling machine 贴签机labeller 贴签机lability 不稳定性labilized hydrogen ion 活化氢离子labor productivity 劳动生产率labor protection 劳动保护laboratory beater 实验室打浆机laboratory digester 实验室蒸煮锅laboratory jordan 实验室锥形磨浆机laboratory paper machine 实验室纸机laboratory refiner 实验室用磨浆机laboratory test 实验室试验lac(ca) 虫漆,虫胶,虫脂lacewood (platanus occidentalis) 单球悬殊铃木,美国梧桐lacquer (真)漆lactitol 乳糖酸lactone isomerism 内酯异构现象lactose 乳糖laevoisomer 左旋(同分)异构体lag 滞后lagging 滞后lagoon 曝气塘lagooning (废水)曝气laid antique 条纹仿古纸laid dandy(rcll) 条纹水印辊laid finish 条纹印痕laid line 条纹印痕laid mo(u)ld 手抄纸网laid writing 条纹水印书写纸lake(color) 色淀(染料)lake pigment 湖色;沉淀色粒lamella 湖色,薄层,薄板;胞间层lamellar micelle 层状胶束lamellar structure 层状结构lamina 薄片,薄板;层压板laminar folw 层流laminate 层压laminate mo(u)lding 层压制模lajminated material 层压物体lajminated plastics 层压塑料(制品)lajminated state 层压状态lajminated structure 层状结构,层压结构lajminated thermosetting resin 层状热固性树脂lajminated wood 层压板laminater 层压机laminating 层压,层贴laminating machine 层压机laminating press 层压压榨laminating resin 层压树脂laminating wax 层压蜡lamination 层压laminator 层压机lamort screen lamort高频振动回转筛lamp black 灯(碳)黑lampen mill lancaster 圆网洗涤机组land depot (陆上)木场land fill (废物)填注池lantsen resotronic regulator lantsen 电磁共鸣式浓度调节器lap 湿浆板;盖片;复盖lap machine 湿抄机lap wood 枝桠材lapping 纸板压榨larch (larix) 落叶松(属)larch fir(abies nobilis lindl.) 大冷杉larch pine (pinus nigra arnold;pinus laricio poir.) 南欧黑松large royal 英国纸张尺寸(27"×20")large tooth aspen (populus grandidentata michx.) 大齿白杨laser 激光laser-die cut 激光切纸laser zee meter 电势激光测定仪last cut 最后馏分last runnings 尾馏分late wood 晚材latency 潜伏状态latency chest 消潜浆池;消潜槽latent heat 潜热latent image 潜像,潜影latent solvent 惰性溶剂lateral branch 侧枝lateral chain 侧链lateral order 侧序lateral porosity 横向透气度latex 胶乳lathe 旋床,车床lathe work (钞票纸或证券纸的)彩纹latice (latex的复数)胶乳lattice coordination number 品格配位数,点阵配位数lauan(shorea sp.) 娑罗双树属laurel(laurus) 月桂(属)laurel (laurus nobilis l.) 月桂树laurel oak (quercus laurifolia michx.) 月桂叶栎树laurel willow (salix pentandra l.) 五蕊柳lava flybar 玄武岩刀辊lava roll (玄武岩)石辊lay steel 毛毯台layboy 堆纸台,码纸台layer 层laying machine 码纸机layman 选纸工,码纸工;湿抄工layout 平面布置layout sheet 转印台纸;键盘纸leach 浸析,沥滤;脱盐leaching 浸析,沥滤;脱盐leachin tank 浸析槽lead 超前;螺距;铅lead cover 铅盖;铅封lead lining 铅衬leadd over 引纸,领纸leadd roll 导纸辊leadd strips 领纸纸条leadd saw 前导圆锯leading dryer 前导烘缸leading edge 前导端,引导端;领纸纸条leading roll 导辊,导纸辊leading through tape 领纸纸条leaf 叶leaf fiber 叶部纤维leaf filter 叶片过滤器leaf sheath 叶鞘leaf valve 簧片阀leaf wood 阔叶木leaflet 活叶(纸)leak 泄漏leather-jacket (eucalyptus punctata dc.) 斑叶桉leather fiber 仿革纸板lebanon cedar (cerus libani laws.) 西南亚雪松ledger stock 帐本废纸left hand machine 左手(造纸)机left handed screw 左旋螺丝leftovers 废料,剩余物lemon grass 柠檬草lemon scented gum(eucalyptus citriodora hook.) 柠檬桉length grading 长度分级lenzites 木材腐败菌的一种leptathrix 铁细菌之一种lethal concentration 致死浓度lethal dose 致死剂量letter card 明信片纸letter press coating 辊式涂布letter press ink 凸版印刷用油墨letter press printing 凸版印刷leuce dye 无色染料;染料隐色基level 水平(面);水位,液面;平坦;级位;程度level control 液面控制,水位控制level control dam 液面控制堰,水位控制堰level controller 液面控制器,水位控制器level dying agent 染料均化剂level indicator 液面计level meter 液面计level recorder 液面记录器levelator 均平器leveling 均化;均涂,均染leveling agent 均化剂leveling index 均涂指数leveling roll 均平辊leveling serew 调平螺丝lever 杆;杠杆lever arm 杠杆臂lever drive 杠杆传动lever weighting 杠杆重锤,杠杆加重levigation analysis 淘选分析levo 左旋levulinic acid 乙酰丙酸liber 韧皮部libriform fiber 韧型纤维lick up 领纸,引纸lick-up felt 领纸毛毯,引纸毛毯licking 领纸,引纸lid 盖子liebeck disintegrater 损纸高频疏解机liebermann-storch test 纸张含松香定性检验法life (使用)寿命life test (使用)寿命试验lift 升液器;升降机;电梯;举起;扬程lifter 升降台lift of pump 泵的扬程lift truck 堤升货车lifting 举起lifting capacity of crane 吊车升举容量lifting device 提升装置lifting equipment 提升装置lifting head sheet-handling system 升端送纸系统lifting jack 升举千斤顶lifting mechanism 提升机构lifting of roll 提举辊子lifting power 提升能力lifting truck 提升小车light 光;轻light absorption 光吸收light ageing 光老化light and shade watermatk 黑白水印light and shadow watermark 黑白水印light beaten stock 轻度打浆浆料light beating 轻刀打浆light burring 轻刻石light current 弱电流;光电流light demander 阳性树,喜光树种light fastness 耐光性能light filter 滤光器light fugitive 不耐光的light resistance 耐光性light scattering 光散射light scattering coefficient 光散射系数light sensitive 光敏的light sensitive cell 光敏电池light source 光源light transmission 光传导,光透射light weight 轻量,低定量light weight chip 轻量木片lighter bar (打浆机飞刀辊)提升装置lighter stand (打浆机飞刀辊)升降架lightwood 轻木,轻质木材;易燃木lightwood oil 轻木油;汽馏松节油lignan (i-conidendrin) 立格南ligneous 木质化ligneous plant 木化植物,木本植物lignification 木化(作用)lignified fiber 木化纤维lignified tissue 木化组织lignin 木素lignin-carbohydrate complex 木素水化合物复合体lignin content 木素含量lignin sulfonate 木素磺酸盐lignin sulfonic acid 木素磺酸lignocellulose 木化纤维素lignoceric acid 甘四(烷)酸lignolite (硅化合物矿物化加工的)表面坚固的描图纸或纸板(商业名称)lignosite 木素磺酸钙(水泥塑化剂,商业名称)lignosulfonate 木素磺酸盐lignosulfonic acid 木素磺酸lignum vitae 愈疮木lilac (syringa) 紫丁香属limb 零件;部件;分度盘lime 石灰lime bleach liquor 漂液lime bucket elevator 斗式石灰提升机lime chlorite 次氯酸钙lime classifier 石灰消化分离器lime dust 石灰尘lime kiln 石灰窑lime liquor 石灰液lime makeup 补充石灰lime milk 石灰乳lime mud 白泥,石灰渣lime mud disposal 石灰渣处理lime mud folter 白泥过滤机,真空洗渣机lime mud kiln 白泥煅烧炉lime reburning 白泥煅烧。
乳酸脱氢酶冻干配方
乳酸脱氢酶冻干配方英文回答:Lactate dehydrogenase (LDH) is an enzyme that plays a crucial role in the conversion of lactate to pyruvate during anaerobic glycolysis. LDH is widely used in various fields, including clinical diagnostics, food industry, and research. To ensure the stability and long-term storage of LDH, freeze-drying or lyophilization is commonly employed. In this response, we will discuss the formulation of a freeze-dried LDH preparation.The formulation of a freeze-dried LDH preparation involves several key components and steps. These include the selection of excipients, the preparation of the LDH solution, the freezing process, and the lyophilization process.1. Excipients: Excipients are substances added to the LDH solution to enhance stability, protect the enzyme fromdenaturation, and improve the reconstitution properties of the freeze-dried product. Commonly used excipients for LDH freeze-drying include sugars (such as sucrose or trehalose), bulking agents (such as mannitol), and cryoprotectants (such as polyethylene glycol).2. LDH solution preparation: The LDH solution is prepared by dissolving LDH enzyme in a suitable buffer solution. The buffer helps maintain the pH and stability of the enzyme during the freeze-drying process. The concentration of LDH in the solution may vary depending on the desired activity of the final product.3. Freezing process: After the LDH solution is prepared, it is subjected to a controlled freezing process. Slow freezing is typically employed to minimize the formation of ice crystals, which can damage the enzyme structure. The freezing process can be achieved using specialized equipment, such as a freeze-drying machine or a controlled-rate freezer.4. Lyophilization process: Once the LDH solution isfrozen, it undergoes the lyophilization process. During lyophilization, the frozen LDH solution is subjected to reduced pressure, and the ice is sublimed directly from the solid state to the vapor state. This process removes the water content from the LDH solution, resulting in a dry and stable product.The freeze-dried LDH preparation can be reconstitutedby adding a suitable amount of water or buffer solution.The reconstituted LDH retains its enzymatic activity andcan be used for various applications, such as enzyme assays or diagnostic tests.中文回答:乳酸脱氢酶(LDH)是一种在无氧糖酵解过程中将乳酸转化为丙酮酸的关键酶。
纸业专业英语词汇翻译(L1)
纸业专业英语词汇翻译(L1)纸业专业英语词汇翻译(L1)纸业专业英语词汇翻译(L1)label paper 标签纸label manila paper 标签用马尼拉纸labelled paper 标签纸laboratory paper 实验室手抄纸片lace paper 纸花边lacquered paper 漆面涂布纸laid paper 直纹纸laid antique 条纹仿古纸laid cigarette paper 条纹卷烟纸laid writing 条纹书写纸laminated paper 层压纸laminated glassine 层合玻璃纸laminated phenolic paper 酚醛层压纸laminating paper 层压纸lampblack paper 炭黑包装纸lampshade paper 灯罩纸lapping paper 盖面纸lard paper 防油纸latex(treated) paper 乳胶涂布加工纸laundry paper 洗衣防用纸layer insulating paper 变压器用绝缘纸layout paper 座标纸lead paper 醋酸铅试纸lead acetate paper 醋酸铅试纸lead indicating paper 铅试纸lead pencil paper 铅笔书写纸,铅芯包装纸leather imitation paper 仿革纸leather(ette) paper 仿革纸ledger paper 帐簿纸lens paper 擦镜纸lenz paper 擦镜纸letter paper 信纸letter copying paper 拷贝信纸letter-press paper 凸版印刷纸light proof paper 防光纸light resistant paper 感光防护纸light sensitive paper 光敏纸light weight paper 轻磅纸,薄页纸light coated paper 轻量涂布纸lincrusta paper 坚实裱糊花纸linear paper 水纹书写纸lined paper 格纸linen paper 亚麻布纸linen-faced paper 亚麻布纹纸liner paper 挂面纸liner finish(ed) paper 亚麻布纹纸lining paper 夹层纸linoleum paper 楼板油毡衬垫纸litho paper 石版印刷纸litho-coated paper 石版印刷涂布纸lithograph(ic) paper 石版印刷纸lithographers'plate wiper 平印版擦拭纸lithographers masking paper 石印蒙版纸lithographic transfer paper 石版转印纸litmus paper 石蕊试纸loan paper 证券纸locker paper 冷冻食品包装纸loft paper 造船放样厚纸loft dried paper 风于纸logarithmic paper 座标纸loin paper 肉类包装纸;防油包装纸long fibered paper 长纤维纸long life paper 耐久纸loose leaf paper 活页纸loose ledger paper 活页帐簿纸lottety paper 彩票用纸low weight coating paper 低定量涂布纸loudspeaker cone paper 扬声器盒纸luminescent paper 发光纸luminous paper 发光纸lunch roll paper 家用卷筒包装纸laminated board 层压纸板latex impregnated board 乳胶浸渍纸板laundry board 白纸板layer board 糖果包装纸板leather(fiber) board 仿革纸板lightweight liner board 轻重量挂面纸板lined board 多层纸板,层粘纸板liner board 挂面纸板lining board 衬里纸板litho board 石板印刷纸板lacquer coater 漆纸涂布机letterpress print coater 多辊转印涂布机,胶印涂布机levelon coater 背辊整匀涂布机liquid phase cooking 液相蒸煮label 标签,贴签labeled atom 示踪原子,标记原子labeling machine 贴签机labeller 贴签机lability 不稳定性labilized hydrogen ion 活化氢离子labor productivity 劳动生产率labor protection 劳动保护laboratory beater 实验室打浆机laboratory digester 实验室蒸煮锅laboratory jordan 实验室锥形磨浆机laboratory paper machine 实验室纸机laboratory refiner 实验室用磨浆机laboratory test 实验室试验lac(ca) 虫漆,虫胶,虫脂lacewood (platanus occidentalis) 单球悬殊铃木,美国梧桐lacquer (真)漆lactitol 乳糖酸lactone isomerism 内酯异构现象lactose 乳糖laevoisomer 左旋(同分)异构体lag 滞后lagging 滞后lagoon 曝气塘lagooning (废水)曝气laid antique 条纹仿古纸laid dandy(rcll) 条纹水印辊laid finish 条纹印痕laid line 条纹印痕laid mo(u)ld 手抄纸网laid writing 条纹水印书写纸lake(color) 色淀(染料)lake pigment 湖色;沉淀色粒lamella 湖色,薄层,薄板;胞间层lamellar micelle 层状胶束lamellar structure 层状结构lamina 薄片,薄板;层压板laminar folw 层流laminate 层压laminate mo(u)lding 层压制模lajminated material 层压物体lajminated plastics 层压塑料(制品)lajminated state 层压状态lajminated structure 层状结构,层压结构lajminated thermosetting resin 层状热固性树脂lajminated wood 层压板laminater 层压机laminating 层压,层贴laminating machine 层压机laminating press 层压压榨laminating resin 层压树脂laminating wax 层压蜡lamination 层压laminator 层压机lamort screen lamort高频振动回转筛lamp black 灯(碳)黑lampen mill lancaster 圆网洗涤机组land depot (陆上)木场land fill (废物)填注池lantsen resotronic regulator lantsen 电磁共鸣式浓度调节器lap 湿浆板;盖片;复盖lap machine 湿抄机lap wood 枝桠材lapping 纸板压榨larch (larix) 落叶松(属)larch fir(abies nobilis lindl.) 大冷杉larch pine (pinus nigra arnold;pinus laricio poir.) 南欧黑松large royal 英国纸张尺寸(27"×20")large tooth aspen (populus grandidentata michx.) 大齿白杨laser 激光laser-die cut 激光切纸laser zee meter 电势激光测定仪last cut 最后馏分last runnings 尾馏分late wood 晚材latency 潜伏状态latency chest 消潜浆池;消潜槽latent heat 潜热latent image 潜像,潜影latent solvent 惰性溶剂lateral branch 侧枝lateral chain 侧链lateral order 侧序lateral porosity 横向透气度latex 胶乳lathe 旋床,车床lathe work (钞票纸或证券纸的)彩纹latice (latex的复数)胶乳lattice coordination number 品格配位数,点阵配位数lauan(shorea sp.) 娑罗双树属laurel(laurus) 月桂(属)laurel (laurus nobilis l.) 月桂树laurel oak (quercus laurifolia michx.) 月桂叶栎树laurel willow (salix pentandra l.) 五蕊柳lava flybar 玄武岩刀辊lava roll (玄武岩)石辊lay steel 毛毯台layboy 堆纸台,码纸台layer 层laying machine 码纸机layman 选纸工,码纸工;湿抄工layout 平面布置layout sheet 转印台纸;键盘纸leach 浸析,沥滤;脱盐leaching 浸析,沥滤;脱盐leachin tank 浸析槽lead 超前;螺距;铅lead cover 铅盖;铅封lead lining 铅衬leadd over 引纸,领纸leadd roll 导纸辊leadd strips 领纸纸条leadd saw 前导圆锯leading dryer 前导烘缸leading edge 前导端,引导端;领纸纸条leading roll 导辊,导纸辊leading through tape 领纸纸条leaf 叶leaf fiber 叶部纤维leaf filter 叶片过滤器leaf sheath 叶鞘leaf valve 簧片阀leaf wood 阔叶木leaflet 活叶(纸)leak 泄漏leather-jacket (eucalyptus punctata dc.) 斑叶桉leather fiber 仿革纸板lebanon cedar (cerus libani laws.) 西南亚雪松ledger stock 帐本废纸left hand machine 左手(造纸)机left handed screw 左旋螺丝leftovers 废料,剩余物lemon grass 柠檬草lemon scented gum(eucalyptus citriodora hook.) 柠檬桉length grading 长度分级lenzites 木材腐败菌的一种leptathrix 铁细菌之一种lethal concentration 致死浓度lethal dose 致死剂量letter card 明信片纸letter press coating 辊式涂布letter press ink 凸版印刷用油墨letter press printing 凸版印刷leuce dye 无色染料;染料隐色基level 水平(面);水位,液面;平坦;级位;程度level control 液面控制,水位控制level control dam 液面控制堰,水位控制堰level controller 液面控制器,水位控制器level dying agent 染料均化剂level indicator 液面计level meter 液面计level recorder 液面记录器levelator 均平器leveling 均化;均涂,均染leveling agent 均化剂leveling index 均涂指数leveling roll 均平辊leveling serew 调平螺丝lever 杆;杠杆lever arm 杠杆臂lever drive 杠杆传动lever weighting 杠杆重锤,杠杆加重levigation analysis 淘选分析levo 左旋levulinic acid 乙酰丙酸liber 韧皮部libriform fiber 韧型纤维lick up 领纸,引纸lick-up felt 领纸毛毯,引纸毛毯licking 领纸,引纸lid 盖子liebeck disintegrater 损纸高频疏解机liebermann-storch test 纸张含松香定性检验法life (使用)寿命life test (使用)寿命试验lift 升液器;升降机;电梯;举起;扬程lifter 升降台lift of pump 泵的扬程lift truck 堤升货车lifting 举起lifting capacity of crane 吊车升举容量lifting device 提升装置lifting equipment 提升装置lifting head sheet-handling system 升端送纸系统lifting jack 升举千斤顶lifting mechanism 提升机构lifting of roll 提举辊子lifting power 提升能力lifting truck 提升小车light 光;轻light absorption 光吸收light ageing 光老化light and shade watermatk 黑白水印light and shadow watermark 黑白水印light beaten stock 轻度打浆浆料light beating 轻刀打浆light burring 轻刻石light current 弱电流;光电流light demander 阳性树,喜光树种light fastness 耐光性能light filter 滤光器light fugitive 不耐光的light resistance 耐光性light scattering 光散射light scattering coefficient 光散射系数light sensitive 光敏的light sensitive cell 光敏电池light source 光源light transmission 光传导,光透射light weight 轻量,低定量light weight chip 轻量木片lighter bar (打浆机飞刀辊)提升装置lighter stand (打浆机飞刀辊)升降架lightwood 轻木,轻质木材;易燃木lightwood oil 轻木油;汽馏松节油lignan (i-conidendrin) 立格南ligneous 木质化ligneous plant 木化植物,木本植物lignification 木化(作用)lignified fiber 木化纤维lignified tissue 木化组织lignin 木素lignin-carbohydrate complex 木素水化合物复合体lignin content 木素含量lignin sulfonate 木素磺酸盐lignin sulfonic acid 木素磺酸lignocellulose 木化纤维素lignoceric acid 甘四(烷)酸lignolite (硅化合物矿物化加工的)表面坚固的描图纸或纸板(商业名称)lignosite 木素磺酸钙(水泥塑化剂,商业名称)lignosulfonate 木素磺酸盐lignosulfonic acid 木素磺酸lignum vitae 愈疮木lilac (syringa) 紫丁香属limb 零件;部件;分度盘lime 石灰lime bleach liquor 漂液lime bucket elevator 斗式石灰提升机lime chlorite 次氯酸钙lime classifier 石灰消化分离器lime dust 石灰尘lime kiln 石灰窑lime liquor 石灰液lime makeup 补充石灰lime milk 石灰乳lime mud 白泥,石灰渣lime mud disposal 石灰渣处理lime mud folter 白泥过滤机,真空洗渣机lime mud kiln 白泥煅烧炉lime reburning 白泥煅烧纸业专业英语词汇翻译(L1) 相关内容:。
代谢“废物”乳酸在肿瘤微环境中的免疫抑制作用
代谢“废物”乳酸在肿瘤微环境中的免疫抑制作用苑思羽1侯俊杰2张片红1(1.浙江大学医学院附属第二医院营养科,杭州 310009;2.吉林省人民医院肿瘤综合治疗科,长春 130021)中图分类号R730.3 文献标志码 A 文章编号1000-484X(2024)04-0832-08[摘要]近年来,肿瘤微环境(TME)备受科学家们的关注,它是由肿瘤细胞、肿瘤相关成纤维细胞(CAFs)、免疫细胞、血管、细胞外基质、周围支持组织及其所在的代谢环境等共同组成的复杂体系。
免疫逃逸和代谢改变(葡萄糖有氧代谢转至无氧代谢产生乳酸)是此体系的两个基本特征。
虽然过去一直认为乳酸是TME中的代谢废物,但现在人们普遍认为乳酸的增加和TME的酸化在肿瘤发生发展中发挥关键作用,包括免疫逃逸、组织侵袭/肿瘤转移、血管生成和肿瘤耐药等。
因此,研究TME 中乳酸代谢、免疫抑制、血管生成、肿瘤耐药等关键过程的调控机制,可为靶向TME的新治疗策略提供理论基础和实践依据。
[关键词]乳酸代谢;免疫抑制;肿瘤微环境Immunosuppressive effect of metabolic "waste" lactic acid in tumor microenvironmentYUAN Siyu1, HOU Junjie2, ZHANG Pianhong1. 1. Department of Clinical Nutrition, the Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou 310009,China;2. Department of Tumor Comprehensive Therapy, Jilin Provincial People's Hospital, Changchun 130021, China[Abstract]In recent years, the tumor microenvironment (TME) has garnered significant attention from scientists. It is a com‑plex system composed of tumor cells, cancer-associated fibroblasts (CAFs), immune cells, blood vessels, extracellular matrix, sur‑rounding supportive tissues and their metabolic environment. Two fundamental characteristics of this system are immune escape and metabolic changes (the shift from aerobic to anaerobic metabolism of glucose, leading to lactate production). Although lactate has tra‑ditionally been considered a metabolic "waste" product in the TME, it is now widely recognized that the increase in lactate and the acidification of the tumor microenvironment play key roles in tumor development and progression, including immune escape, tissue in‑vasion/tumor metastasis,angiogenesis and tumor drug resistance. Therefore,studying the regulatory mechanisms of lactate metabo‑lism, immune suppression, angiogenesis, and tumor drug resistance in the TME can provide a theoretical basis and practical evidence for new therapeutic strategies targeting the TME.[Key words]Lactic acid metabolism;Immunosuppressive;Tumor microenvironment1 乳酸的分子结构与生理功能乳酸为三碳分子的酸性物质,属于羧酸,其分子式为C3H6O3。
lactose_mono_hydrate_d-乳糖单水合物_概述说明
lactose mono hydrate d-乳糖单水合物概述说明1. 引言1.1 概述Lactose monohydrate, also known as d-lactose monohydrate, is a type of sugar commonly found in milk and dairy products. It is a crystalline substance that consists of one molecule of lactose combined with one molecule of water. As the major carbohydrate present in milk, lactose provides an important source of energy for newborns and serves as a building block for the synthesis of other essential compounds.1.2 文章结构This article aims to provide an overview and explanation of lactose monohydrate, discussing its properties, uses, and potential health implications. The content will be organized into several sections to facilitate understanding.1.3 目的The purpose of this article is to introduce readers to the topic of lactose monohydrate and enhance their understanding of its significance in various aspects. By exploring its chemical structure, physicalcharacteristics, and applications, readers will gain insights into the role this substance plays in the food industry, pharmaceutical preparations, and human health. Additionally, potential concerns related to lactose intolerance and allergenic effects will also be discussed to provide a comprehensive overview.Note: The provided response is written in plain text format as requested.2. 正文D-乳糖单水合物是一种常见的天然产物,在食品、制药和化妆品行业中得到广泛应用。
乳糖酶缺乏与乳糖不耐受症状的临床特点分析
现代消化及介入诊疗2221年第26卷第2期Mob/n Dig/tion&Bd/vexUon222/Veh26,No.2-179-.论著.乳糖酶缺乏与乳糖不耐受症状的临床特点分析张宸山,郑中文2,布小玲2,许凌丽5,胡裕荣5,宁雨露2棊佩妍7赖卓成2沙卫红22【摘要】目的探讨乳糖酶缺乏及乳糖不耐受症状的临床特点。
方法回顾性分析了84例于广东省人民医院门诊就诊的以腹痛、腹泻、腹胀、肠鸣为主要症状的患者,并接受胃肠镜、腹部CT、抽血及氢呼气试验等检查评估,根据患者的主要诊断,氢呼气试验结果及乳糖不耐受症状进行分组,比较各组的临床指标,包括年龄、性别、体质量指数、血常规、过敏原检测、血清总蛋白及白蛋白、c-反应蛋白、血沉等指标及氢呼气试验结果。
结果功能性腹泻、肠易激综合征组相较于其他功能性胃肠病组、器质性疾病组,岀现乳糖不耐受症状的比例更高(P<105)o相比乳糖不耐受症状阴性组,乳糖不耐受症状阳性组患者的体质量指数、血清总蛋白及血清白蛋白水平降低,且差异均具有统计学意义(P<2.05)。
不同乳糖酶缺乏程度各组患者在合并器质性疾病、食物不耐受、乳糖不耐受症状上无明显差别(P>2.05),白细胞计数、血红蛋白、中性粒细胞计数、血清总蛋白、血清白蛋白、C-反应蛋白及血沉等指标比较差异也无统计学意义(P>2.05)。
结论进食乳制品后是否岀现症状与乳糖酶是否缺乏或缺乏程度之间缺乏一致性。
是否存在乳糖酶缺乏似乎对患者的营养情况并无明显影响,但岀现自我报告的乳糖不耐受症状的患者相比无症状者长期营养状况趋于下降。
【关键词】乳糖酶缺乏;乳糖不耐受;临床特点;氢呼气试验;营养中图分类号:R374.7文献标志码:A DOI:12.3969/j.i/u1072-2159.222(.22.205Preliminaro discussion foo the deereec of aduih lactase deficiency and its canicai signincanccZHANG Chen12,ZHENG Zhoog-wen22,BU Xiao-Un2,XU Ling-lt3,HU Yu-rong3,NIAG Yu-lu1,QI Pei-yan,LAA Zhuo-cheng', SHA Wei-Uong111.Thn Second Schoo)of COnicai Meeiciae,Sontaem Meicai U niversita,Guaagzhon,510515,Chiaa;2.af Gastmenterolof,, Guaagdong Provinciai People's hospitai(Guangdong Academa of Medea)Sciences),Guaagzhon,511080,China;3.General Prachco, DasPt Streei Commuuita HeaH Servica Cenas f Panya Distrid,Guaagzhon,511133,China;4.General Prachco,Guaagdong Interoationai Traven HeaU Care Centre,Guaagzhon,511035,China[Abstroct I Objective The aim of this study is to investigate the clinical characteUstics of objective lactase defi/enca and sudjective lactose intolerance symptoms.Methodt89ootyaUex-s w:ith a/dominal pain;diarrUea;a/dominal distension and borUoryymus as the main symptoms were included and evaluated by endoscone,a/dominal CT,bloop samp/ng and hyprogex breath test (HBT):The padexts were divi/ed into diWerext groops accorUing to the main diagnosis,HBT results and subjective lactose intolerance symptoms.The clinical indexes of each gronx were compared including age ,sex,boby mass index,bloop rootine ,detection of aderaen,serum total protein ,aldumin,Cgeaction protein ,erythrocyte sedimedtado/rate and the results of HBT.R su O c The WiciUexco of subjective lactose intolerance symptoms was higher in padexts with i/Ua/le bowel syp/rome and fu/c/oogl diarrUea compared to padexts w:ith other functional diseases vs oryanic diseases(P<2.05).Compared w:ith paUexts withoot subjective lactose intolerance symptoms,those w:ith symptoms showed Uwes level of BMI,serum total protein and serum aldumin,the diWerexces were statistically sig/ficant(P<2.05).There was no significant diWerexco on the coexistence of oryanic diseases,the i/cibe/ce of foob intolerance and subjective lactose intolerance,wh/e bloop cell coo/t,/e/Woohil coo/t,hemogUbin;serum total protein,serum albumin ,ESR and C RP among padexts w:ith diWerext deyrecs of iactaso deficie/ca(P> 2.05).Conclasion there is a lacO of co/siste/ca between subjective lactose intolerance symptoms and objective lactase deficiency.Objective lactase deficie/ca does not seem to have a sig/ficant edect on the n/triLo/gl status of padexts,but the long-term n/Witional status of patients with sudjective lactose作者单位:510515南方医科大学第二临床医学院;512080广东省人民医院(广东省医学科学院)消化内科;3511432广州市番禺区大石街社区卫生服务中心,全科医学;4510635广州国际旅游卫生保健中心,全科医学通信作者:沙卫红E-mad:wh-sha@#共同第一作者基金项目:广东省中医药局科研项目(26271209)-173-现代消化及介入诊疗262-年第26卷第2期M o P uu DiJutWp&Utemention262-,Veb26,No.2intolerance symptoms tends to be PeclineP compareP w:ith asymptomatic patients.【Key wordst Lactase peficienca;Lactose intolerance symptoms;C/nicai chamcte/shcs;Hypmgep breath tesh Nutrition乳糖酶缺乏在世界范围内普遍存在,其发生率随种族和地区而异,在我国的发病率约为75%~120%[1]o如肠道乳糖酶缺乏,导致乳糖在小肠内无法被完全分解吸收,进入结肠后易被细菌分解并产生氢气,呼出的氢气量可以通过氢呼气试验(hyPmgep breath test,HBT)检测,是诊断乳糖酶缺乏的金标准。
这个夏天,拥抱青春亮白——法国圣蒂丝
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2016新编酪蛋白水解物
酪蛋白水解物一、中文名称:酪蛋白水解物二、拉丁文名称/或英文名称:Lactium三、主要成分:多肽四、酪蛋白水解物(Lactium)的来源酪蛋白水解物(Lactium)是以脱脂牛奶为原料,经过分离酪蛋白、水解、喷雾干燥等程序得到的一种酪蛋白水解产物。
其典型化学成分为:蛋白质75%,脂肪1%,水分5%,灰分15%,乳糖1%。
可溶解于水,无苦味,pH2-9时稳定,热稳定,可耐180℃高温50min。
酪蛋白水解后得到的αs1-Cn (f91-100),是一种含10个氨基酸的三维结构多肽,在Lactium中的典型含量为1.8%,其氨基酸序列为:Tyr-Leu-Gly-Tyr-Leu-Glu-Gln-Leu-Leu-Arg。
五、酪蛋白水解物(Lactium )生产工艺流程图和简述1.工艺流程图:脱脂牛奶酪蛋白分离碱化胰蛋白酶水解酸化热处理巴氏杀菌浓缩、喷雾干燥过筛包装2. 工艺说明1.)以脱脂牛奶为原料,沉淀分离酪蛋白2.)使用氢氧化钠将其碱化到pH为7.5-8.5之间3.)在40-55℃下用胰蛋白酶进行水解。
得到的产物中,游离10肽在干物质中的含量最低为1.8%。
4.)用盐酸进行酸处理,将pH降到3.0-5.05.)在90℃下热处理1.5分钟6.) 85℃进行巴氏杀菌、浓缩,此步骤为关键控制点7.)喷雾干燥(进风温度180-200℃),得到粉末产品。
8.)过筛得到粒度在1mm以下的均匀粉末,其中游离10肽的含量最低为1.8%。
此过3. 拟公告的生产工艺简述:以脱脂牛奶为原料,经过酪蛋白分离、水解、浓缩、喷雾干燥等工艺制成。
六、酪蛋白水解物(Lactium)对酸奶的促进作用酸奶具有促进肠道蠕动与消化和机体物质的代谢,并具有提高人体免疫力、防衰老、抗肿瘤等作用。
酸奶中的大量乳酸菌及乳酸代谢产物能调节人体肠道微生态平衡,达到补充营养、防病、治病和保健的目的。
将酪蛋白水解物(含蛋白质7.6%)以2%(w/w)添加到奶液中混合发酵,做空白样对照。
茉莉酸甲酯和水杨酸对西兰花硫代葡萄糖苷含量调控和营养品质的影响
茉莉酸甲酯和水杨酸对西兰花硫代葡萄糖苷含量调控和营养品质的影响茉莉酸甲酯和水杨酸对西兰花硫代葡萄糖苷含量调控和营养品质的影响摘要:本研究旨在探究使用茉莉酸甲酯(MeJA)和水杨酸(SA)来调控西兰花硫代葡萄糖苷(glucosinolate)含量对其营养品质的影响。
结果表明,MeJA和SA的处理均显著增加了西兰花硫代葡萄糖苷的含量,其中MeJA的处理效果更为明显。
MeJA和SA的处理均显著提高了西兰花中的总多酚和VC的含量,同时MeJA的处理显著提高了总黄酮的含量,而SA的处理对总黄酮含量影响不显著。
此外,MeJA和SA的处理增强了西兰花的抗氧化活性和总糖含量,同时降低了硝酸盐含量。
因此,该研究结果表明MeJA和SA的处理可以调控西兰花硫代葡萄糖苷的含量,并且有效地提高了其营养品质,表现出良好的应用前景。
关键词:西兰花、茉莉酸甲酯、水杨酸、硫代葡萄糖苷、营养品质引言:西兰花是一种重要的蔬菜,在国内外消费市场均占有重要地位。
其含有丰富的硫代葡萄糖苷,具有抗氧化、降脂、抗癌等多种生理活性作用。
因此,西兰花蔬菜的种植和营养研究备受关注。
茉莉酸甲酯(MeJA)和水杨酸(SA)是两种常用的植物生长调节剂,已被广泛应用于植物增产、抗病虫害和提高养分品质等方面。
但是,其对西兰花硫代葡萄糖苷含量和营养品质的影响还没有被系统地研究。
方法:本研究在大田条件下进行,以六个月龄的‘青岛六号’西兰花为试验材料,采用喷雾法处理MeJA和SA,设置3个浓度处理组,分别为0、50、100mg/L,每个处理设3个重复,共计18个试验单位。
处理后,测定硫代葡萄糖苷、总多酚、VC、总黄酮、抗氧化活性、总糖和硝酸盐含量的变化。
结果:MeJA和SA的处理均能显著提高西兰花硫代葡萄糖苷含量(P < 0.05),其中MeJA的处理效果更为明显。
MeJA和SA 的处理均显著提高了西兰花中的总多酚和VC的含量(P <0.05),这可能是由于MeJA和SA的处理能提高植物对自由基的清除能力,从而增加了抗氧化物的含量。
Lactose digestion by milk fermented
1Cátedra de SaludPública, Facultad de Medicina, Universidad de Buenos Aires, Argentina.AbstractThe aim of the present study was to determine whether a fermented milk containingLactobacillus casei and Lactobacillus acidophilus strains isolated from human subjects (CFM) and developed by CERELA (Centro de referencia para Lactobacilos) is better tolerated than regular milk (RM) by subjects with lactase deficiency (< 1 unidad) and lactose intolerance. We studied the digestion of the lactose present in the two milkpreparations which were administered to 18 healthy subjects with lactase deficiency and12 control subjects. Each subject ingested in random sequence on different days, 480 mlCFM, 480 ml RM and 240 ml CFM and 240 ml RM. Breathhydrogen (H2) test was used to measure lactose absorption and orocecal transit time (OCTT). The peak H2 ppm results after 480 ml of CFM were ingested, reached 19.5 +/- 12.1 ppm. The same reading when 480 ml of RM were ingested was 52.6 +/- 31.9 ppm (p < 0.008). The results also showed that 480 ml of CFM delayed OCTT median 111.0 +/- 6.78 min versus 54.0 +/- 5.09 min of RM (p < 0.001) and reduced the development of symptoms (p < 0.08) such as bloating (p < 0.05), borborygmi (p < 0.025) diarrhea (p < 0.05) and abdominal colics (p < 0.05). In spite of the small number of cases studied, it seems justified to conclude that CERELA fermented milk significantly influences lactose digestion and minor development ofsymptoms in lactase-deficient subjects and lengthens significantly the orocecal transit time compared with regular milk.。
Lactips公司从牛奶蛋白生产具有水溶性和热塑性的薄膜
Lactips公司从牛奶蛋白生产具有水溶性和热塑性的薄膜佚名
【期刊名称】《中国洗涤用品工业》
【年(卷),期】2017(0)6
【摘要】法国Lactips公司开发了一项新技术,即利用牛奶蛋白生产生物塑料。
该公司创始人Marie-Helelie Gramatikoff于2013年与Frederic Prochazka会面并发现了他研究方向的潜力,因而于2014年成立该公司。
Prochazka从2007年开始研究牛奶蛋白,主耍致力于利用牛奶蛋白合成可持续化学品。
他开发的新技术是利用牛奶酪蛋白生产具有水溶特性的热塑性塑料。
【总页数】2页(P89-90)
【关键词】牛奶蛋白;热塑性塑料;生产;水溶性;薄膜;生物塑料;蛋白合成;水溶特性【正文语种】中文
【中图分类】TQ325
【相关文献】
1.重要含硫香料生产技术;新型非放射性夜明材料;天然级肉味香精生产技术;新型光致变色颜料生产技术;炉内喷钙脱硫成套技术;“国荟”芦荟系列产品;TiO2光催化剂固定化及催化反应器应用技术;高氨氮废水生物脱氮技术;环境友好型水溶性塑料薄膜的开发棗聚乙烯醇吹塑新工艺等 [J],
2.法国Lactips开启牛奶蛋白制可降解塑料研究 [J], ;
3.重庆市农业局关于重庆兴维实业总公司等企业不再具有兽药生产资格的通知/重庆市农业局关于合川市牧大兽药生产有限公司等企业不再具有兽药生产资格的通知[J],
4.由丙烯酸酯橡胶和热塑性聚酰胺组成的具有极高力学强度和极好生产率的热塑性弹性体 [J],
5.静态高压处理对牛奶蛋白浓缩粉水溶性的影响 [J], Udabage P;孙鹏
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《矢车菊素-3-O-葡萄糖苷对脂多糖诱导内皮细胞的保护作用及其在急性肺损伤中治疗作用》
《矢车菊素-3-O-葡萄糖苷对脂多糖诱导内皮细胞的保护作用及其在急性肺损伤中治疗作用》一、引言急性肺损伤(ALI)是一种常见的临床疾病,其发病机制复杂,涉及多种炎症介质和细胞因子的参与。
内皮细胞损伤是ALI 发生发展的重要环节,因此,寻找有效的内皮细胞保护剂成为治疗ALI的关键。
近年来,矢车菊素-3-O-葡萄糖苷(Cyanidin-3-O-glucoside,C3G)因其良好的抗氧化、抗炎及保护细胞的作用而备受关注。
本文旨在探讨C3G对脂多糖(LPS)诱导内皮细胞的保护作用及其在急性肺损伤中的治疗作用。
二、矢车菊素-3-O-葡萄糖苷的特性与作用机制矢车菊素-3-O-葡萄糖苷是一种天然的黄酮类化合物,具有抗氧化、抗炎、抗肿瘤等多种生物活性。
其作用机制主要在于通过清除自由基、抑制氧化应激反应、调节细胞信号转导等途径,实现对细胞的保护作用。
三、C3G对LPS诱导内皮细胞的保护作用LPS是革兰氏阴性菌细胞壁的主要成分,进入机体后可通过激活免疫应答引发炎症反应。
在内皮细胞中,LPS的刺激可引发细胞损伤,导致内皮功能障碍。
而C3G可以通过抑制氧化应激反应、抑制NF-κB信号通路的激活等途径,减轻LPS对内皮细胞的损伤,保护内皮细胞的正常功能。
四、C3G在急性肺损伤中的治疗作用急性肺损伤的发病过程中,内皮细胞的损伤是关键环节。
C3G通过保护内皮细胞,减轻炎症反应,从而对急性肺损伤产生治疗作用。
实验研究表明,给予C3G治疗的小鼠模型中,肺组织炎症反应减轻,肺功能得到改善,生存率显著提高。
此外,C3G 还可以通过调节免疫应答,降低机体的炎症反应程度,进一步发挥治疗作用。
五、结论综上所述,矢车菊素-3-O-葡萄糖苷(C3G)对脂多糖(LPS)诱导的内皮细胞具有明显的保护作用,并能在急性肺损伤中发挥治疗作用。
其作用机制主要在于抑制氧化应激反应、调节细胞信号转导等途径。
实验研究表明,C3G能够减轻肺组织炎症反应,改善肺功能,提高生存率。
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ORIGINAL ARTICLEEffect of dairy and non-dairy calcium on fecal fat excretion in lactose digester and maldigester obese adultsMS Buchowski 1,2,M Aslam 1,C Dossett 4,C Dorminy 4,L Choi 3and S Acra 21Department of Medicine,Vanderbilt University Medical Center,Nashville,TN,USA;2Department of Pediatrics,Vanderbilt University Medical Center,Nashville,TN,USA;3Department of Biostatistics,Vanderbilt University Medical Center,Nashville,TN,USA and 4Department of Clinical Research Center,Vanderbilt University Medical Center,Nashville,TN,USABackground:The effect of dietary calcium (Ca)on fecal fat excretion in lactose maldigestion is not known.Objective:To investigate the effect of dairy and non-dairy dietary Ca on fecal fat excretion in lactose digesters and maldigesters during moderate energy restriction.Design:A randomized cross-over trial comparing the effect of 500mg versus 1500mg dairy and non-dairy Ca on fecal fat excretion in 34healthy adults during moderate (À30%)energy restriction induced weight loss for 12weeks.The participants were classified as lactose digester or maldigester on the basis of breath hydrogen test.Measurements:Anthropometric parameters and body composition,resting energy expenditure,energy and nutrient intake,fecal fat,physical activity,blood pressure,blood and urine sampling for pertinent measurements.Results:Fecal fat loss expressed as percent of fat intake was significantly higher with 1500mg (high Ca)as compared with 500mg (low Ca)Ca intake per day (mean:3.0%;95%CI:2.3to 3.7%;P o 0.001)independent of Ca source and lactose digestion status.Conclusions:During a moderate energy restriction induced weight loss,a high-Ca diet causes an increase in fecal fat excretion independent of Ca source.Ca intake related fecal fat loss is also independent of the ability to digest lactose and it is not diminished over time (US Clinical Trial Registration: NCT00808275)International Journal of Obesity (2010)34,127–135;doi:10.1038/ijo.2009.212;published online 13October 2009Keywords:dietary calcium;dairy;fecal fat;lactose maldigestion;body weight lossIntroductionThere is an ongoing controversy over the role of calcium (Ca)intake on body-energy regulation.Low levels of dietary Ca and dairy products have been identified as potential contributing factor to obesity,and have also been linked to increased risk of hypertension and insulin resistance.1–3Despite supportive epidemiological reports,2,4–7interven-tional and mechanistic studies,8–12the suggested anti-obesity effect of dairy and non-dairy Ca supplementation remains far from proven as not all investigations have confirmed these findings.Several studies indicate that Ca supplementation or dairy products may have no effect,13–19or even an adverse effect,20on body weight.Further,recent reviews and meta-analyses 18,21of randomized controlled trials with or without concomitant energy restriction indicate that neither Ca supplementation nor dairy products reliably facilitate weight loss.When found,such a relation-ship relates to decreased rate of weight 22or fat gain,rather than weight or fat loss.Two recent trials 23,24have reported over two-fold increase in fecal fat loss with increase in dietary Ca intake for 7days.The authors concluded that their observation might con-tribute to an explanation for why high-Ca diet might be inversely related to body weight.However,the long-term effects of Ca supplementation on fecal fat excretion are unknown.Moreover,there is no clear evidence that dairy-derived Ca would be more effective in causing fecal energy loss than non-dairy Ca.Lactose maldigestion has been linked to low dairy Ca intake and osteoporosis,25although a preponderance of evidence suggests that lactose maldigestion should not limitReceived 21June 2009;revised 28August 2009;accepted 31August 2009;published online 13October 2009Correspondence:Dr M Buchowski,Department of Medicine,Vanderbilt University Medical Center,Nashville,TN 37232,USA.E-mail:maciej.buchowski@International Journal of Obesity (2010)34,127–135&2010Macmillan Publishers Limited All rights reserved 0307-0565/10$/ijoCa intake since most of the maldigesters can tolerate several servings of dairy foods daily.26However,the effect of lactose maldigestion on fecal fat loss secondary to dairy and non-dairy Ca supplementation has not been systematically studied. The goal of the present study was to determine the effect of dietary Ca on fecal fat loss.We examined the association between lactose maldigestion,dietary Ca level and source, weight loss induced by energy restriction,and fecal fat loss for12weeks.We tested the hypothesis that dietary dairy and non-dairy Ca affects energy balance by increasing fecal loss of fat.We also examined a possibility that fecal fat excretion might be different in lactose maldigesters than in lactose digesters.Materials and methodsParticipant selectionWe studied healthy males(10)and females(24),aged21–50 years with body mass index29–35kg mÀ2.The volunteers were recruited using flyers,mass e-mails,and word of mouth. Potential participants with history of medical illness,includ-ing diabetes,hypertension,renal,liver or heart disease,pre-gnant or lactating mothers,those taking medications or dietary supplements that affect body weight,lipid-lowering medica-tions or thyroid hormone substitution,or engaged regularly in heavy or vigorous physical activities were excluded from the study.Volunteers with known or suspected drug or alcohol abuse and tobacco users were also not recruited. We certify that all applicable institutional and govern-mental regulations concerning the ethical use of human volunteers were followed during this research.The trial was conducted at the Clinical Research Center(CRC)at Vander-bilt University,Nashville,Tennessee,USA and was approved by the Institutional Review Board of Vanderbilt University and followed the ethical principles of the Helsinki-II Declaration.Each participant provided written consent before the study.Study designBased on breath hydrogen test,lactose digesters and maldigesters were randomly assigned in a single-masked manner to one of two energy restriction diets:(1)dairy Ca in the form of dairy products and(2)non-dairy Ca in the form of food products excluding dairy.Each diet had two levels of dietary Ca:500mg(low Ca)and1500mg(high Ca).Non-dairy,high-Ca diet was supplemented with Ca citrate (1000mg of Ca).A sequence of the two levels of dietary Ca,either low–high Ca(500–1500mg)or high–low Ca (1500–500mg)was randomly assigned to each participant for12weeks(6weeks each diet)in a cross-over design. Adherence to the protocol was monitored by collecting self-reports of uneaten foods.Urinary nitrogen,sodium and potassium were measured weekly in24-h urine samples,as biomarkers of intake.DietsStudy participants received individualized energy-and nutrient-controlled diet for the whole study period provided by the CRC metabolic kitchen for consumption at home. The food items in these diets were similar to those regularly used in the US and were adjusted to individual preferences. Energy needs were calculated as sum of resting energy expenditure(REE)measured using metabolic cart(CPX Optima;MedGraphics,St Paul,MN,USA),EE of physical activity measured using accelerometer(RT3;StayHealthy, Monrovia,CA,USA)for one week before the study and thermic effect of food estimated as10%of REE.The individualized diet(10-day diet cycle)provided in daily portions contained approximately70%(±210kJ)of daily energy requirements,52–54%of energy from carbohydrates, 26–29%of energy from fat,17-21%of energy from protein and17-21g of fiber.To assure sufficient micronutrient content of the diet,participants received a multivitamin supplement daily(Nature Made,Mission Hills,CA,USA). After6weeks energy content of the diet was lowered(420–840kJ dayÀ1)to reflect changes in body weight.No restric-tions were imposed on the amounts of energy-free foods such as water,coffee(without sugar or milk),diet soft drinks, salt and pepper.All food items were marked(breakfast, lunch,dinner and snack)and foods for each day were packed in thermo-insulated bags.The dinner meals were pre-prepared and only needed to be heated.Each participant received a written,daily list of foods at every diet pick-up (four times a week).Any uneaten food and any additional food eaten by the participants were reported daily on sheets collected at food pick-up.The study dietitian met with each participant weekly to discuss the diet,resolve any barriers and concerns related to food or specimen collection,and encourage compliance.Each participant was allowed1or2 days(that is,birthday,holiday)on which additional foods could be eaten.Intake data were analyzed for energy and nutrient content using the NDS-R database(Nutrition Data System,St Paul,MN,USA).Lactose digestionLactose digestion was assessed by measuring alveolar breath hydrogen exhalation at30-min intervals for3h following a lactose oral challenge,as described previously.26Participants were classified as lactase deficient(lactose maldigesters) on the basis of a rise in breath hydrogen concentration of greater than0.90m mol lÀ1(420p.p.m.)after ingestion of25g of lactose in250ml of water.Body composition and anthropometric dataThe National Health and Nutrition Examination Survey (NHANES)protocols27were followed for all anthropome-trical measurements.Body weight was measured at baseline and thrice weekly to the nearest0.1kg using a calibrated beam platform scale(Detecto-Medic;Detecto Scales Inc.,Calcium and fecal fat excretionMS Buchowski et al 128International Journal of ObesityNorthbrook,IL,USA).Height was measured at baseline to the nearest0.5cm using a calibrated,wall-mounted stadi-ometer(Perspective Enterprises,Portage,MI,USA).Waist circumference was measured in standing position to the nearest0.1cm at the mid-axillary high point of the iliac crest at minimal respiration at baseline and after4,8,and 12weeks of energy restriction diet.The averages of the two readings were used for analysis.All measurements were performed by the same investigator.Body composition was determined by dual energy X-ray absorptiometry(DXA)at baseline and after12weeks using narrow fan-beam technol-ogy(GE Lunar Prodigy,Madison,WI,USA).Fat mass and fat-free mass were determined,and fat-free mass was further divided into lean body mass and bone mineral content.For quality assurance and equilibration,a calibration block was scanned each morning.A spine phantom was scanned on a weekly basis;the coefficient of variation(%)was0.7%.Total-body water was measured using bioelectrical impedance (Quantum-II Desktop;RJL Systems,Clinton Township,MI, USA).The measurement was performed promptly after DXA measurement by the same investigator.Data were entered into the software program provided by the manufacturer (Cypress;RLJ Systems,Clinton Township,MI,USA). Resting EEResting EE was measured at baseline and after12weeks,and was defined as the average EE during a30-min period of lying in a supine position after a30-min rest following an overnight fast(410h),using metabolic cart(CPX Ultima; MedGraphics,St Paul,MN,USA).Physical activityDaily physical activity was assessed using an RT3accelero-meter(StayHealthy;Monrovia,CA,US,USA).The partici-pants were instructed to maintain their habitual physical activity throughout the study.They wore the activity monitor on their right hip while awake for the duration of the study.The results were downloaded weekly and total and physical activity EE were calculated using energy calculated from the amount of movement measured by the monitor and REE measured at baseline.Physical activity levels were calculated by dividing total EE by REE for each monitored day. Blood pressureBlood pressure was measured three times a week in the reclining position after a10-min rest with an automatically inflating cuff(Dynamap;General Electric,Milwaukee,WI, USA).Urine analysesThe complete24-h urine samples were collected weekly. Urine volume and density were measured and a sample of 10ml was frozen atÀ701C until further analysis in the CRCCore laboratory.Urinary Ca,sodium and potassium were measured using Vitros250Analyzer(Ortho-clinical Diag-nostics,Rochester,NY,USA).Urinary nitrogen content was measured using a nitrogen analyzer(Antek instrument nitrogen system9000NS;Antek Instruments Inc.,Houston,TX,USA).The nitrogen excretion of the urine was used as a biological marker for protein intake by multiplying the content of nitrogen in the urine by the factor7.72.28The sodium content of the urine was used as a biological markerof sodium intake29and potassium content in the urine divided by0.77was used as a biological marker of potassium intake.30Blood analysesVenous blood samples were drawn in the morning after an overnight fast at baseline,at6weeks and on the last day ofthe study(12weeks).A basal metabolic panel including glucose and routine hematological indices(hemoglobin concentration,hematocrit,red and white blood cells count)was analyzed in the Vanderbilt University Hospital Labora-tory using standard methodologies.Blood for determinationof insulin,leptin,parathyroid hormone,and vitamin D was centrifuged at2800g for15min at41C.Serum was extractedand the samples were stored atÀ701C until later analyses atthe Vanderbilt Diabetes Research Center Hormone Assays Laboratory.Fecal fat analysesAll feces excreted during one weekend day(24h)were collected in plastic containers during all12weeks of the study.In addition,the subjects completed a questionnaireon daily defecation frequency during the whole study.Thefecal samples were weighed and frozen atÀ201C until sentto the analytical laboratory(Arup Laboratories,Salt LakeCity,UT,USA)for fecal fat analysis using gravimetric method.Statistical analysisData are presented as means,standard deviations(s.d.)or ranges.We considered the weekly measurements of fecal fat excretion calculated as percent of fat intake as well as their average over12weeks as the major outcomes.Since fecal fat excretion was consistent over6weeks within each Ca intakelevel and diet source(dairy or non-dairy),the average of fecalfat excretion over6weeks was used as the primary outcomein the final analysis.Random-effects models were used with generalized least-square estimators and Huber/White/sand-wich estimator of variance.As main effects in the model,Caintake level(500and1500mg dayÀ1),diet source(dairy andnon-dairy),lactose digestion status(digester and maldige-ster)and gender(male and female)were included.Differ-ences between means for body fat and weight loss,urinary Calcium and fecal fat excretionMS Buchowski et al129International Journal of Obesitybiomarkers,EE and physical activity were analyzed by paired t -test.All tests were two-tailed and a P -value less than 0.05was considered significant.Analyses were performed using STATA 9.2(StataCorp,College Station,TX,USA)and R ().ResultsA total of 51volunteers were recruited for the study;40were randomized and 34completed the study (19Caucasians,11African Americans and 4declaring other ethnicities).One participant was dropped due to noncompliance and five withdrew between week 1and 8.Baseline and end-of-the-study characteristics of participants who completed the study are shown in Table 1.There was no difference in initial weight and body composition between lactose mal-digesters and digesters,and between dairy and non-dairy diets (all P 40.05).Dietary intake and compliance with the study dietsThe participants had an average energy intake of 7.5±1.5MJ (Table 2).The average intake of energy from carbohydrates,fat and protein was 54.5±3.0,28.9±2.6and 18.4±1.85%,respectively.There were no differences between macronutrientand fiber content between the diets (dairy versus non-dairy).Average amount of Ca in low-Ca and high-Ca diets was 503±73and 1491±131mg day À1,respectively,and the level was not different between dairy and non-dairy diets.There were no significant differences between the intake of protein,sodium and potassium,and their respective biolo-gical markers in weekly urine collections (Table 3).The ratio of nitrogen in urine and corresponding protein intake were not significantly different between the dairy and non-dairy diets (1.13±0.41and 1.01±0.14;P ¼0.105).There were also no differences between the ratios of reported intake and excretion between dairy and non-dairy diets for sodium (0.96±0.20and 0.95±0.19;P ¼0.917)and potassium (1.15±0.23and 1.12±0.16;P ¼0.684).Fecal fat excretionThe average fecal fat loss (Table 4)over 6weeks was significantly higher with high-Ca diet than that with low-Ca diet after adjusting for gender,lactose digestion status and dairy or non-dairy diet source (mean:3.0%;95%confidence interval (CI):2.3–3.7%;P o 0.001).Fecal fat loss increased correspondingly with cross-over to high-Ca diet and vice versa (Figure 1).It was also significantly higher in females than in males after adjusting for Ca intake level,lactose digestion status and dairy or non-dairy diet source (mean:2.0%;95%CI:1.2–2.9%;P o 0.001).There was no significantTable 1Participant Characteristics at the baseline and after 12-week of energy restriction dietBaselineAfter 12-week dietDigester (n ¼18)Maldigester (n ¼16)Digesters (n ¼18)Maldigesters (n ¼16)Weight (kg)105.2±11.9(80.2–124.3)105.2±17.1(74.0–131.2)96.00±10.8a (72.3–113.2)98.65±16.9a (67.9–128.7)Body mass index (kg m À2)35.4±3.6(28.9–42.1)36.1±4.9(28.9–45.6)32.3±3.3a (25.6–38.2)34.2±4.9a (26.5–41.3)Body fat mass (kg)45.0±7.8(32.0–62.9)47.4±11.1(26.8–60.9)39.6±7.8a (27.3–58.4)42.6±12.1a (19.8–58.3)Total-body water (l)48.1±10.1(36.6–68.4)47.1±10.5(36.6–68.4)44.8±9.6a (32.9–61.7)43.8±9.6a (30.4–65.2)Waist circumference (cm)107.9±10.2(90–132)106.2±13.3(87–134)101.2±9.6a (84–123)104.2±14.6a (84–127)Bone mineral density (g cm À2) 1.319±0.105(1.149–1.542)1.355±0.107(1.212–1.628)1.302±0.096(1.137–1.486)1.321±0.096(1.145–1.526)All values are mean ±s.d.Values in parentheses are ranges.a Significantly different from the baseline (P o 0.05,paired t -test).Table 2Average daily intake of energy,macronutrients,fiber,vitamin D and calcium in study participantsDiet aEnergy (MJ)Fats (%energy)Carbohydrates (%energy)Proteins (%energy)Fiber (g)Vitamin D (mcg)Calcium (mg)Dairy diet (n ¼17)Low calcium (6weeks)7.47±1.429.3±2.654.1±3.218.5±1.619.0±3.9 2.29±1.3515±69High calcium (6weeks)7.55±1.327.8±2.353.0±2.421.3±2.216.7±3.4 5.8±2.01488±131Total diet (12weeks)7.51±1.328.6±2.553.5±2.827.8±2.319.9±1.9 4.0±1.661002±100Non-dairy diet (n ¼17)Low calcium (6weeks)7.46±1.529.1±2.854.3±3.418.2±2.118.4±3.9 1.6±0.9491±77High calcium (6weeks)7.52±1.528.7±2.454.7±2.718.6±1.618.8±4.1 3.9±1.91495±136Total diet (12weeks)7.49±1.528.9±2.654.5±3.018.4±1.818.6±4.0 2.7±1.4992±106All values are mean ±s.d.a Cross-over design with high-Ca diet (1500mg day À1)and low-Ca diet (500mg day À1)administered in random order for 6weeks (total 12weeks).The nutrient content was estimated using NDS-R dietary assessment software (NDS,St Paul,MN,USA).Calcium and fecal fat excretionMS Buchowski et al130International Journal of Obesitydifference in fecal fat loss between lactose digesters and maldigesters (Figure 2)after adjusting for gender,Ca intake level and dairy or non-dairy diet source (mean:0.2%;95%CI:0.5–1.0%;P ¼0.544).There was a significant positive correlation between Ca intake and fecal fat excretion in dairy (r ¼0.460)and non-dairy (r ¼0.555)diets and in lactose digesters (r ¼0.562)and maldigesters (r ¼0.463,all P 40.05).Although not statistically significant,the average fecal fat loss over 12weeks was higher in the non-dairy than that in the dairy diet group (Figure 1)after adjusting for Ca intake level,lactose digestion status and gender (mean:0.5%;95%CI:0.2–1.2%;P ¼0.150).In females,the average fecal fat loss over 6weeks tended to be higher with the non-dairy than that with the dairy diet after adjusting for Ca intake level and lactose digestion status (mean:0.8%;95%CI:À0.1–1.6%;P ¼0.067).Urinary Ca excretionUrinary Ca excretion (Table 5)was significantly higher with high Ca than low Ca (128.3±57.9and 146.4±77.9mg day À1;95%CI for difference: 3.8–31.1mg day À1;Table 3Comparison of the reported average (12weeks)intake of protein,sodium and potassium with the corresponding biological markers in urineIntake aUrinary excretion bRatio of intake to excretion P -value c Protein (g day À1)85.0±12.0(64.7–114.6)87.9±323.6(43.0–132.9) 1.04±0.32(0.67–2.10)0.496Sodium (g day À1) 3.03±0.44(2.21–4.01) 3.28±0.83(1.68-4.97)0.96±0.19(0.57–1.46)0.246Potassium (g day À1)2.83±0.43(2.01–3.81)2.53±0.53(1.74–3.58)1.13±0.19(0.94–1.68)0.432Data are presented as means ±s.d.Values in parentheses are ranges.a Average daily reported intakes of protein,sodium,and potassium assessed by NDSR (Nutrition Diet System,St Paul,MN,USA).b Nitrogen in 24-h urine samples (12weekly collections)multiplied by 7.72(Bingham and Cummings,1985)28and potassium in urine divided by 0.77(Johansson et al .,1992).30c P -values represent comparisons of the reported intakes of protein,sodium and potassium with the respective urinary excretion analyzed using the paired t -test.Table 4Dietary intake and fecal excretion of total fatLow-Ca dietHigh-Ca diet Fat intake a (g day À1)Fecal fat excretion b(g day À1)%of fat intakeFat intake a (g day À1)Fecal fat excretion b(g day À1)%of fat intakeDigesters (n ¼18)58.2±10.4(38.7–82.8) 3.8±0.7(2.5–5.2) 6.8±1.8(3.1–9.2)57.9±9.3(42.9–76.3) 5.8±1.0(3.6–7.1)10.2±1.5(7.1–12.6)Maldigesters (n ¼16)56.6±10.8(38.2–79.4) 4.4±0.8(2.8–6.1)7.9±1.7(4.8–11.3)56.7±12.4(36.1–83.1)5.9±1.4(4.1–8.7)10.5±2.1(5.6–14.0)Abbreviation:Ca,calcium.Data are presented as means ±s.d.Values in parentheses are ranges.a Average daily reported intake of fat assessed by NDS-R (Nutrition Diet System,St Paul,MN,USA).b Average daily fat excretion in 24-h stool samples (12weekly collections).%of fat intake was calculated as a %ratio of weekly fat excretion to average weekly fat intake.246810125101520DairyWeekF e c a l F a t (% o f F a t I n t a k e )••••••••••••••••••••••••High−Low Ca cross−over Low−High Ca cross−over246810125101520Non−dairyWeekF e c a l F a t (% o f F a t I n t a k e )••••••••••••••••••••••••High−Low Ca cross−over Low−High Ca cross−overFigure 1Patterns of individual and mean fecal fat excretion with high-and low-Ca cross-over for (a )dairy and (b )non-dairy diets.Calcium and fecal fat excretion MS Buchowski et al131International Journal of ObesityP ¼0.014).The differences in Ca excretion were not different between dairy versus non-dairy diets,and for digesters versus maldigesters (all P 40.05).Body weight and body compositionAfter following an energy-controlled diet for 12weeks (Table 1),there were no significant differences in weight loss between dairy and non-dairy diets (8.5±2.7and 7.2±2.8kg;P ¼0.116).However,there were significant differences in weight changes in lactose digesters versus maldigesters (9.2±2.2and 6.6±2.4;P ¼0.003).There was also significant differences between first and second 6-week study periods (5.6±1.8and 2.8±1.7kg;P ¼0.001).The differences between dairy and non-dairy diets were not significant during the first 6-week (5.7±1.9and 5.5±1.7kg)or second 6-week (2.9±1.9and 2.9±1.8kg)periods.There were also no significant differences in body fat changes across groups:dairy versus non-dairy (5.4±1.5and 4.1±1.5;P ¼0.393)or lactose digesters versus maldigesters (5.5±1.3versus 4.8±1.7;P ¼0.206).There were also no differences in the amount of total body water between the groups.Resting EE and physical activityThere was a difference in REE between the baseline and the end of the study (7.31±1.31versus 6.74±1.32MJ),which became insignificant when REE was adjusted for fat-free mass and fat mass (data not shown).There were not REE differences between digesters and maldigesters (Table 6).The differences in the amount of physical activity measured using RT3accelerometers during the entire study were also not significant.Participants did not change physical activity level during the study (Table 6).Blood pressure and blood parametersDiet had no significant effect on either systolic or diastolic blood pressure (Table 7).Basic hematological param-eters were not different between the groups (data is not shown).Diet did not have an effect on the serum concentrations of insulin and vitamin D.Leptin levels decreased significantly after 12weeks with the study diet independent of diet and lactose digestion status (40.6±20.3versus 27.3±16.7ng ml À1;P ¼0.001,paired t -test).Table 5Comparison of reported daily average calcium intake and urinary calcium excretion during 12-week dietLow-Ca dietHigh-Ca dietCa intake a (mg day À1)Urinary Ca b (mg day À1)%of intake Ca intake a (mg day À1)Urinary Ca b (mg day À1)%of intake Digesters (n ¼18)504.3±36.8(429–561)141.2±47.3(48.9–222.8)26.6±12.1(13.1–46.1)1498.9±33.8(1397–1543)160.9±69.5(54.8–295.6)10.9±6.1(6.1–17.8)Maldigesters (n ¼16)500.1±32.8(405–544)115.9±54.6(39.9–248.7)23.7±7.0(7.0–40.7)1508.8±72.5(1424–1756)130.9±85.5(24.1–365.6)8.9±7.3(4.6–17.1)Abbreviation:Ca,calcium.Data are presented as means ±s.d.Values in parentheses are ranges for weekly averages.a Average daily reported intake of calcium assessed using NDSR software (Nutrition Data System,St Paul,MN,USA).b Average daily calcium excretion in 24-h urine samples calculated from 12weekly collections.Table 6Resting energy expenditure,physical activity and physical activity levelBaselineAfter 12-week dietDigesters (n ¼18)Maldigesters (n ¼16)Digesters (n ¼18)Maldigesters (n ¼16)Resting energy expenditure (MJ day À1)b 7.38±1.3(5.53–9.64)7.25±1.4(5.09–9.97)7.05±1.4a (4.42–9.87) 6.38±1.2a (4.20–8.71)Physical activity (MJ day À1)b 3.40±1.5(1.98–6.28) 3.19±1.2(1.63-5.58) 2.81±1.2a (0.99–4.71) 2.85±1.2a (1.32–5.38)Physical activity level (PAL) 1.46±0.25(1.17–2.04)1.44±0.14(1.24–1.77)1.42±0.17(1.14–1.69)1.41±0.19(1.22–1.89)Data are presented as means ±s.d.Values in parentheses are ranges.a Significantly different from baseline values (P o 0.05,paired t -test).b Measured values (see the text for description of the methods).PAL is a ratio of total energy expenditure (resting energy expenditure plus physical activity)and resting energy expenditure.M e a n F e c a l F a t (% o f F a t I n t a k e )51015Low Calcium (800 mg)High Calcium (1500 mg)Low Calcium (800 mg)High Calcium(1500 mg)Lactose DigestersLactose MaldigestersM e a n F e c a l F a t (% o f F a t I n t a k e )51015Figure 2Mean fecal fat excretion for lactose digesters and maldigesters withhigh-and low-Ca diets.Calcium and fecal fat excretionMS Buchowski et al132International Journal of Obesity。