期刊文献+

葛脾煎剂调控单核细胞趋化蛋白-1水平逆转早期糖尿病肾病的实验研究 被引量:7

Study of Ge Pi Decoction on regulation of monocyte chemoattractant protein-1 level to reverse early diabetic nephropathy
原文传递
导出
摘要 目的:探讨葛脾煎剂对单核细胞趋化蛋白-1(MCP-1)的影响及其对逆转早期糖尿病肾病(DN)的作用。方法:选择Wistar雄性大鼠,采用高脂、高糖饮食联合小剂量链脲佐菌素(STZ)腹腔注射诱导的STZ糖尿病大鼠共41只,随机分为STZ糖尿病大鼠对照组14只,中药(葛脾煎剂)治疗组13只,西药(苯那普利)治疗组14只,分别观察8周;检测各组体重、肾重指数、血糖、尿微量白蛋白、血尿MCP-1、血8-异前列腺素F2α(8-iso-PGF2α)、肿瘤坏死因子-α(TNF-α),并进行肾脏病理学检查。结果:中药治疗组肾脏重量和肾重指数低于对照组(P<0.05),UAER、血尿MCP-1、血8-iso-PGF2α和TNF-α均明显低于对照组(P<0.01);而两治疗组,对上述指标的影响基本类似,两组间无明显差异(P>0.05)。另外,各组8-iso-PGF2α、MCP-1、TNF-α均与UAER呈正相关关系。中药葛脾煎剂能减轻肾脏肥大及肾小球系膜基质增生、硬化。结论:糖尿病肾病有自身免疫性炎症和氧化应激反应参入,中药葛脾煎剂对多种炎症因子具有抑制作用,从而可逆转早期糖尿病肾病。 Objective:To investigate the effect of Ge Pi decoction on regulation of monocyte chemoattractant protein-1(MCP-1)level to reverse early diabetic nephropathy(DN).Method: STZ diabetes model were induced by high lipoids and high glucose diet combined with intraperitoneal injection of small dose streptozotocin(STZ)(n = 41).STZ-induced diabetes model of Wistar male rats were divided into the control group(n = 14),the Traditional Chinese medicine(Ge Pi Decoction) treatment group(n = 13),and the western medicine(benazepril) treatment group(n = 14).After 8 weeks,detection of each group were carried out about weight,kidney weight index,blood glucose,urinary albumin microdosis,urinary albumin,blood and urine MCP-1,8-iso-prostaglandin F2a(8-iso-PGF2α)and tumor necrosis factor-α(TNF-α),and oservation were performed on the pathological change of the rats renal with light microscope.Result: Compared with those in the control group,the body weight and kidney weight index were decreased in the Ge Pi Decoction treatment(P 0.05).Microdosis urin-albumin,MCP-1,8-iso-PGF2α and TNF were decreased significantly(P 0.01).There was no significant difference between Ge Pi Decoction treatment group and benazepril treatment group(P 0.05).In addition,there were positive correlation between 8-iso-PGF2α,MCP-1,TNF-α and UAER in each group.Ge Pi Decoction can relieve kidney hypertrophy,mesangial matrix hyperplasia and sclerosis.Conclusion: There are autoimmunity inflammation and oxidative stress in diabetic nephropathy.Ge Pi Decoction can inhibit various inflammatory factors in diabetic nephropathy.
出处 《中国实验方剂学杂志》 CAS 北大核心 2010年第4期145-148,共4页 Chinese Journal of Experimental Traditional Medical Formulae
关键词 葛脾煎剂 单核细胞趋化蛋白-1 8-异前列腺素F2Α 糖尿病肾病 Ge Pi Decoction monocyte chemoattractant protein-1 8-iso-prostaglandin F2a diabetic nephropathy
  • 相关文献

参考文献9

  • 1Robert Toto. MD. Aagiotention II subtyPe 1 receptor blockers and reanl function[J]. Arch Intern Med,2001, 61 : 1492. 被引量:1
  • 2Banba N Y, Nakamura T, Matsumuka M, et al. Possible relationship of monocyte chemoattraetant protein-1 with diabetic nephropathy[ J]. Kidney Int, 2003, 58:684. 被引量:1
  • 3Wada T, Furuichi K, Sakai N, et al. Up-regulation of monocyte Chemoattreactant protein-lin tubulointerstitial lesions of human diabetic nephropathy [ J ]. Kidney International, 2000, 58 (4) : 1492. 被引量:1
  • 4Amann B, TinzmannR, AnqelkortB. ACE inhibitors improve diabetic nephropathy through suppression of renal MCP-1 [ J]. Diabetes Care ,2003, 26 (8) :2421. 被引量:1
  • 5Morii T, Fujita H, Narita T, et al. Increased urinary exretion of monocyte chemoattractant protein-1 in renal diseases[ J]. Renal Failure, 2003, 25 (3) :439. 被引量:1
  • 6Tashiro K, Koyanagi I, SaitohA, et al. Urinary levels of monocyte Chemoattractant protein-1 ( MCP-1 ) and interleuk in-8 (IL-8) , and renal injuries in patients with type 2 diabetic nephropathy[ J]. JClin Lab Anal,2002,16 (1):1. 被引量:1
  • 7Ha H, LeeH B. Reactiveoxygen speciesamplifyglucose signalling 615 in renal cells cultured under high glucose and in diabetic kidney [ J ]. Nephrology (Carhon) , 2005, 10(suppl) : 7. 被引量:1
  • 8Gu L, Hagiwara S, Fan Q. Role of receptor for advanced glycation End-products and signaling events in advanced glycation end-prod-Uct-induced monocyte ehemoattractant protein-1 expression in dif-Ferentiated mouse podocytes [ J]. Nephrol Dial Transplant,2006,21 (2) :299. 被引量:1
  • 9Forbes M, Cooper M E, Thallas V, et al. Reduction of the accumulation of advanced glycation end products by ACE inhibition in experimental diabetic nephropathy [ J ]. Diabetes, 2002, 51(11):3274. 被引量:1

同被引文献113

引证文献7

二级引证文献78

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部