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易卒中型自发性高血压大鼠肾脏中利钠肽受体亚型的基因表达改变

Altered gene expression of natriuretic peptide receptor subtypes in the kidney of stroke-prone spontaneously hypertensive rats.

作者信息

Goto M, Itoh H, Tanaka I, Suga S, Ogawa Y, Kishimoto I, Nakagawa M, Sugawara A, Yoshimasa T, Mukoyama M

机构信息

Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Japan.

出版信息

Clin Exp Pharmacol Physiol Suppl. 1995 Dec;22(1):S177-9. doi: 10.1111/j.1440-1681.1995.tb02871.x.

Abstract
  1. To elucidate the physiological and pathophysiological role of the natriuretic peptide system in the progression of hypertensive renal disease, we examined the gene expression of natriuretic peptide receptor subtypes, guanylate cyclase-A (GC-A), guanylate cyclase-B (GC-B) and clearance receptor (C receptor), in the kidney of stroke-prone spontaneously hypertensive rats (SHRSP) at 8 and 20 weeks of age, and compared them with their gene expression in age-matched Wistar-Kyoto (WKY) rats. 2. Northern blot analyses revealed that messages for three natriuretic peptide receptor subtypes were expressed in the kidney, and their expressions were higher in the glomeruli than in the whole kidney in each strain. 3. In 20 week old rats with established hypertension, the glomerular concentration of GC-A mRNA was significantly higher in SHRSP than in WKY. The concentrations of GC-B and C receptor mRNA in the glomeruli tended to increase and decrease, respectively, but they were not statistically significant in SHRSP. 4. In 8 week old rats, the glomerular concentrations of GC-A, GC-B and C receptor mRNA were not significantly different between SHRSP and WKY. 5. This study demonstrates that in the progression of hypertension, the expression of GC-A, which mediates biological actions of natriuretic peptides, is enhanced in the kidney of SHRSP compared to that of WKY. Together with the augmented secretion of the ligands previously revealed, altered expression of natriuretic peptide receptor subtypes in SHRSP may have a deterrent role in the development of hypertension and its renal complications.
摘要
  1. 为阐明利钠肽系统在高血压性肾病进展中的生理和病理生理作用,我们检测了易卒中型自发性高血压大鼠(SHRSP)8周龄和20周龄时肾脏中利钠肽受体亚型、鸟苷酸环化酶-A(GC-A)、鸟苷酸环化酶-B(GC-B)和清除受体(C受体)的基因表达,并将其与年龄匹配的Wistar-Kyoto(WKY)大鼠的基因表达进行比较。2. Northern印迹分析显示,三种利钠肽受体亚型的信使核糖核酸在肾脏中表达,且在每个品系中,其在肾小球中的表达均高于全肾。3. 在患有已确诊高血压的20周龄大鼠中,SHRSP肾小球中GC-A信使核糖核酸的浓度显著高于WKY。SHRSP肾小球中GC-B和C受体信使核糖核酸的浓度分别有升高和降低的趋势,但差异无统计学意义。4. 在8周龄大鼠中,SHRSP和WKY肾小球中GC-A、GC-B和C受体信使核糖核酸的浓度无显著差异。5. 本研究表明,在高血压进展过程中,与WKY相比,介导利钠肽生物学作用的GC-A在SHRSP肾脏中的表达增强。与先前揭示的配体分泌增加一起,SHRSP中利钠肽受体亚型的表达改变可能在高血压及其肾脏并发症的发生中起抑制作用。

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