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雷米普利抑制RAS后对糖尿病大鼠Reg3α表达的影响

Effect of blocking renin-angiotensin system by ramipril on Reg3α expression in diabetic rats
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摘要 目的观察雷米普利抑制肾素-血管紧张素系统(RAS)阻断后对糖尿病(DM)大鼠胰岛再生衍生因子3α(Reg3α)表达的影响。方法 SD大鼠10只采用链脲菌素40mg/kg腹腔注射建立DM模型:B组5只为模型对照(用生理盐水灌胃10周);C组5只采用雷米普利50mg·kg-1·d-1灌胃10周。另取5只大鼠腹腔注射等量柠檬酸缓冲液作为空白组(A组,用生理盐水灌胃10周)。基因芯片检测大鼠胰岛相关基因表达;实时定量PCR和Western blot验证相关基因mRNA和蛋白表达。结果 B组Reg3α表达较A组上调7.9倍,C组较B组Reg3α表达上调7.1倍。C组胰岛染色面积和胰岛形态结构较B组增加和改善。结论雷米普利抑制胰岛局部RAS系统,促进DM大鼠的胰岛再生;其作用可能部分通过影响Reg3α基因的表达实现。 Objective To observe the effect of blocking renin-angiotensin system(RAS) by ramipril on the expression of regenerating islet-derived 3 alpha(Reg3a) in diabetic rats. Methods The diabetic model was induced by intraperitoneal injection of streptozotocin 40 mg/kg in 10 rats, of which 5 rats (group C) were treated with ramipril 50 nag · kg-1· d-1 by lavage for 10 weeks and 5 rats (group B) were taken as model controls(treated with normal saline by lavage for 10 weeks). Another 5 ST) rats(group A) by intraperitoneal injection in the same volume of citrate butter were taken as blank controls (treated with normal saline by lavage for 10 weeks). The expressions of rat islet-related genes were detected by gene chip. qRT-PCR and Western blot were used to verify the mRNA and protein expressions of related genes. Results Compared to group A,Reg3a expression in group B was upregulated by 7. 9 times. Compared to group B, Reg3a expression in group C was upregulated by 7. 1 times. The area of islet dyeing was more and islet morphology structure was improved in group C than those in group B. Conclusion Ramipril may inhibit local RAS of pancreatic islet and promote islet regeneration of DM rats, which may be partially via influencing Reg3a gene expression.
出处 《江苏医药》 CAS 2015年第17期1999-2001,F0003,共4页 Jiangsu Medical Journal
基金 江苏省南通市科技局基金(K2009017)
关键词 肾素-血管紧张素系统 雷米普利 胰岛再生衍生因子3α 糖尿病 Renin-angiotensin system Ramipril Regenerating islet-derived 3 alpha Diabetes
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参考文献9

  • 1Cheng Q, Leung PS. An update on the islet rennin-angiotensin system[J]. Peptides, 2011,32(5) : 1087-1095.
  • 2Leung KK, Liang J, Zhao S, et al. Angiotensin lI type 2 receptor regulates the development of pancreatic endocrine cells in mouse embryos[J]. Dev Dyn, 2014,243 (3) .. 415-427.
  • 3Tikellis C, Wookey PJ, Candido R, et al. Improved islet morphology after blockade of the rennin-angiotensin system in the ZDF rat[J]. Diabetes, 2004,53(4) : 989-997.
  • 4Terazono K, Yamamoto H, Takasawa S, et al. A novel gene activated in regenerating islets[J]. J Biol Chem, 1988,263(5).. 2111-2114.
  • 5Jin CX, Hayakawa T, Ko SB, et al. Pancreatic stone protein/ regenerating protein family in pancreatic and gastrointestinal diseases[J]. Intem Med,2011,50(15) : 1507-1515.
  • 6Choi JH,Lee MY,Kim Y,et al. Isolation of genes involved in pancreas regeneration by subtractive hybriclization [J]. Biol Chem, 2010,391 (9) : 1019-1029.
  • 7Leung PS. Mechanisms of protective effects induced by blockade of the renin-angiotensin system., novel role of the pancreatic islet ring system in Type 2 diabetes[J]. Diabet Med, 2007,24(2) : 110-116.
  • 8Shao J, Iwashita N, Ikeda F, et al. Beneficial effects of cande- sartan,an angiotensin 11 type 1 receptor blocker, on beta-cell function and morphology in db/db miee[J]. Biochem Biophys Res Commun, 2006,344(4) : 1224-1233.
  • 9Chu KY, Lau T, Carlsson PO, et al. Angiotensin type 1 receptor blockade improves beta-cell function and glucose tolerance in a mouse model of type 2 diabetes[J]. Diabetes, 2006,55(2) : 367-374.

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