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Klk1是导致 Dahl 盐敏感大鼠患高血压的基因之一。

Klk1 as one of the genes contributing to hypertension in Dahl salt-sensitive rat.

作者信息

Iwai Naoharu, Yasui Naomi, Naraba Hiroaki, Tago Naomi, Yamawaki Hideyuki, Sumiya Hiroshi

机构信息

Research Institute, National Cardiovascular Center, Suita, Osaka, Japan.

出版信息

Hypertension. 2005 May;45(5):947-53. doi: 10.1161/01.HYP.0000161969.65767.0d. Epub 2005 Apr 4.

Abstract

A genome-wide quantitative trait loci analysis for blood pressure was performed using 107 male F2 rats derived from Dahl salt-sensitive and Lewis rats. Blood pressure was assessed by telemetry, and >400 microsatellite markers were used for genotyping. Two major quantitative trait loci for blood pressure were identified at chromosome 1 and chromosome 10. The expression levels of 366 transcripts around the chromosome 1 quantitative trait loci were assessed by RT-PCR, and we found that the Klk1 (kallikrein 1) and Ngfg (nerve growth factor gamma) mRNA levels were significantly reduced in the kidneys of Dahl salt-sensitive rats compared with those in Lewis rats. The expression levels of kallikrein 1 protein were also suppressed in Dahl salt-sensitive rats compared with those in Lewis rats. Because the kallikrein-kinin system has been shown to be involved in renal function, including salt homeostasis, it is likely that the reduced expression of Klk1 contributes to salt-sensitive hypertension in Dahl salt-sensitive rats.

摘要

利用107只源自达尔盐敏感大鼠和刘易斯大鼠的雄性F2代大鼠进行了全基因组血压数量性状基因座分析。通过遥测评估血压,并使用400多个微卫星标记进行基因分型。在1号染色体和10号染色体上鉴定出两个主要的血压数量性状基因座。通过逆转录聚合酶链反应评估了1号染色体数量性状基因座周围366个转录本的表达水平,我们发现与刘易斯大鼠相比,达尔盐敏感大鼠肾脏中的激肽释放酶1(Klk1)和神经生长因子γ(Ngfg)的mRNA水平显著降低。与刘易斯大鼠相比,达尔盐敏感大鼠中激肽释放酶1蛋白的表达水平也受到抑制。由于激肽释放酶-激肽系统已被证明参与包括盐稳态在内的肾功能,Klk1表达降低很可能导致达尔盐敏感大鼠出现盐敏感性高血压。

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