期刊文献+

糖尿病大鼠肾脏血管紧张素Ⅱ2型受体及Ⅳ型胶原mRNA表达初步研究 被引量:1

PRELIMINARY STUDY ON mRNA EXPRESSION OF TYPE 2 ANGIOTENSIN Ⅱ RECEPTOR AND COLLAGEN Ⅳ IN DIABETIC RATS'KIDNEY
下载PDF
导出
摘要 研究糖尿病大鼠肾脏血管紧张素Ⅱ 2型受体及Ⅳ型胶原的mRNA表达。方法 :大鼠随机分成两组 :单肾切组、糖尿病组。实验第 8周 ,应用RT -PCR检测大鼠肾皮质血管紧张素Ⅱ 2型受体 (AT2 )及Ⅳ型胶原mRNA表达。同时用放免法检测大鼠肾皮质血管紧张素Ⅱ含量。结果 :糖尿病组大鼠尿蛋白排泄率 (t=9.32 ,P <0 .0 1)、肾皮质血管紧张素Ⅱ水平 (t=2 .2 7,P <0 .0 5 )及Ⅳ型胶原mRNA表达 (t =3.71,P <0 .0 1)均较单肾切组明显升高 ;而AT2 的mRNA水平却下降 (t=2 .35 ,P <0 .0 5 )。结论 :糖尿病肾组织AT2 受体mRNA表达的下降及Ⅳ型胶原表达的增加参与了糖尿病肾病的发生、发展。 Objective:To investigate mRNA expression of the type 2 angiotensin Ⅱ receptor and collagen Ⅳ in diabetic rats'kidney.Methods:The rats were randomly divided into following groups: uninephrectomized (group C) and diabetic rats (group D). At 8 weeks' duration of study,mRNA expressions of the type 2 angiotensin Ⅱ receptor (AT 2) and collagen Ⅳ in rats'renal cortex were measured by quantitative reverse transcription polymerase chain reaction (RT-PCR), respectively. In addition, angiotensin Ⅱ level in renal cortex was determined by the radioimmunoassay.Results:In group D, urine protein excretion (t=9.32, P <0.01 ), angiotensin Ⅱ level (t=2.27, P <0.05) and mRNA expression of collagen Ⅳ (t=3.71, P <0.01 ) in rats'renal cortex were increased obviously in contrast to group C, however mRNA expressions of AT 2 in group D showed a significant decrease (t=2.35, P < 0.05 ).Conclusions: The decreased mRNA expressions of AT 2 and elevated collagen Ⅳ expression might play an important pathogenetic role in the initiation and progression of diabetic nephropathy.
出处 《中国现代医学杂志》 CAS CSCD 2002年第15期17-19,共3页 China Journal of Modern Medicine
基金 浙江省教委部分资助 (基金编号 2 0 0 0 0 666)
关键词 糖尿病紧病 血管紧张素Ⅱ2型受体 Ⅳ型胶原 放射免疫法 Diabetic Nephropathy Rats Losartan Type 2 Angiotensin Ⅱ Receptor Collagen Ⅳ
  • 相关文献

参考文献10

  • 1[1]Inagami T. Molecular biology and signalling of angiotensin receptors,an overview. J Am Soc Nephrol, 1999; 10:S2~S7
  • 2[2]Ozono R, Wang ZQ, Moore AF, et al. Expression of the subtype2 angiotensin Ⅱ (AT2) receptor protein in rat kidney. Hypertension, 1997 ;30:1238~1246
  • 3[3]Wang ZQ, Moore AF, Ozono R, et al. Immunolocalization of subtype 2 angiotensin Ⅱ (AT2) receptor protein in rat heart. Hypertension, 1998;32:78~83
  • 4[4]Ozono R,Wang ZQ, Moore AF, et al. Expression of the subtype2 angiotensin Ⅱ (AT2) receptor protein in rat kidney. Hypertension, 1997; 30:1238~1246
  • 5[5]Li JY, Avallet O, Berthelon MC,et al. Effects of growth factors on cell proliferation and angiotensir Ⅱ type ieceptor number and mRNA in PC12 and R3T3 cells. Mol Cell Endocrinol, 1998;139:61~69
  • 6[6]Nakamura T, Fukui M, Ebihara l, et al. mRNA expression of growth factors in glomeruli from diabetic rats. Diabetes, 1993;42:450~456
  • 7[7]Arendshorst WJ, Brannstrom K, Ruan X, et al. Actions of angiotensin Ⅱ on the renal microvasculature. J Am Soc Nephrol,1999;10:5149~5161
  • 8[8]Navar LG, Inscho EW, Majid SA, et al. Paracrine regulation of the renal microcirculation. Physiol Rev, 1996; 76: 425~536
  • 9[9]Maric C, Aldred GP, Harris P J, et al. Angiotensin Ⅱ inhibits growth of cultured embryoinc renomedullary interstitial cells through the AT2 receptor. Kidney Iht, 1998;53:92~96
  • 10[10]Kuizinga MC, Smits JFM, Arends JW, et al. AT2 receptor blockade reduces cardiac interstitial cell DNA synthesis and cardiac function at, er rat myocardial infarction. J Mol Cell Cardiol, 1998; 30:425~434

同被引文献5

引证文献1

二级引证文献8

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