Protectin DX可以通过改善炎症和调节巨噬细胞表型提高脓毒症小鼠的存活率

合集下载
  1. 1、下载文档前请自行甄别文档内容的完整性,平台不提供额外的编辑、内容补充、找答案等附加服务。
  2. 2、"仅部分预览"的文档,不可在线预览部分如存在完整性等问题,可反馈申请退款(可完整预览的文档不适用该条件!)。
  3. 3、如文档侵犯您的权益,请联系客服反馈,我们会尽快为您处理(人工客服工作时间:9:00-18:30)。

•980•

sights from investigation of neurons and microglia [ J ].

Mol Cell Endocrinol,2016, 438:18-26.

[7] Lemus MB,Bayliss JA,Lockie SH,et al. A stereological

analysis of NPY, POMC, Orexin, GFAP astrocyte, and

Ibal microglia cell number and volume in diet-induced

obese male mice [ J ]. Endocrinology, 2015 , 156 ( 5 ):1701-1713.

[8 ] Cawley NX, Li Z, Loh YP. 60 years of POMC :biosynthe­

sis, trafficking, and secretion of pro-opiomelanocortin-de-

rived peptides [J]. J Mol Endocrinol, 2016, 56(4) :T77-

T97.

[9] Lowry P. 60 years of POMC :purification and biological

characterisation of melanotrophins and corticotrophins [ J ].

J Mol Endocrinol, 2016, 56(4) :T1-T12.

[10] Raffan E,Dennis RJ,0 ’ Donovan CJ,et al. A deletion in

the canine POMC gene is associated with weight and appe­

tite in obesity-prone labrador retriever dogs [ J ]. Cell

Metab, 2016, 23(5) :893-900.

[11] Low MJ. Neuroendocrinology :New hormone treatment for

obesity caused by POMC-deficiency[ J]. Nat Rev Endocri­

nol, 2016, 12(11) :627-628.

[12] Chronwall BM. Anatomy and physiology of the neuroendo­

crine arcuate nucleus [ J ]. Peptides, 1985 , 6 ( Suppl 2):1-11.

[13] Schwartz MW, Woods SC, Porte D Jr, et al. Central nerv­

ous system control of food intake [ J ]. Nature,2000,404

(6778) :661-671.

[14] Barsh GS, Schwartz MW. Genetic approaches to studying

energy balance :perception and integration [ J ]. Nat Rev

Genet, 2002, 3(8) :589-600.

[15] Lam TK,Schwartz GJ,Rossetti L. Hypothalamic sensing

of fatty acids[ J]. Nat Neurosci, 2005, 8(5) :579-584. [16] Waise TM, Toshinai K, Naznin F, et al. One-day high-fat

diet induces inflammation in the nodose ganglion and hypo­

thalamus of mice [ J ]. Biochem Biophys Res Commun,

2015, 464(4) :1157-1162.

(责任编辑:卢萍,罗森)

Protectin D X可以通过改善炎症和调节巨噬细胞表型

提局胺毒症小鼠的存活率

近期的一系列研究表明,源自Omega-3脂肪酸二十二碳六烯酸(docosahexaenoic acid, DHA)的脂质介质在多种炎症性疾 病中具有消炎或抗炎作用。因此,夏海发等试图评估Protectm DX(PDX;Pr〇tectm D1的异构体,一种新的脂质介质)是否可以 保护小鼠对抗脓毒症(sepsis),并探索其潜在机制。他们采用盲肠结扎穿孔(cecum ligation and puncture, CLP)建立脓毒症动 物模型,结果发现PDX可以提高脓毒症小鼠8d内的总体生存率,并减轻多器官损伤。除此之外,PDX可以在CLP术后24 h 减少促炎症因子和细菌载量。同时,PDX提高脓毒症小鼠腹腔巨噬细胞的吞噬能力,并增加M2型巨噬细胞的比例。在体外,PDX可以上调Raw264.7细胞中M2型巨噬细胞标志物(A rgl和Y m l)及其转录调节因子(过氧化物酶体增生物激活受体7,

peroxisome proliferator-activated receptor-7, PPAR-~y)的表达;反之,PPAR-~y 抑制剂 GW9662 和 PPAR-~y siRNA 可以消除 PDX 对 Raw264. 7细胞中A rgl和Y m l的诱导。综上所述,该研究结果表明PDX能够促进巨噬细胞的M2极化,增强其吞噬活性,加 快炎症消散,从而提高脓毒症小鼠的存活率。

Sci Rep, 2017, 7(1) :99(戴晓萌)

相关文档
最新文档