• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

HSP27 locus cosegregates with left ventricular mass independently of blood pressure.

作者信息

Hamet P, Kaiser M A, Sun Y, Pagé V, Vincent M, Kren V, Pravenec M, Kunes J, Tremblay J, Samani N J

机构信息

Centre de Recherche Hôtel-Dieu de Montréal, Université de Montréal, Canada.

出版信息

Hypertension. 1996 Dec;28(6):1112-7.

PMID:8952607
Abstract

Left ventricular hypertrophy remains a significant clinical problem and a predictor of fatal outcome in hypertension. Blood pressure per se and environmental modifiers including stress affect cardiac mass. Heat shock proteins are involved in the stress response as well as in the regulation of cardiac growth and cytoprotection. The present study evaluates heat shock protein 27 as a locus marker or candidate gene of cardiac hypertrophy in hypertension. The spontaneously hypertensive rat allele of heat shock protein 27 was associated with about a 6% increase in relative left ventricular weight (P = .0112) in 30 recombinant inbred strains from crosses of Brown Norway and spontaneously hypertensive rats. In 336 F2 crosses of spontaneously hypertensive and Wistar-Kyoto rats, the hypertensive allele was dominant and cosegregated with a similar 6% increase in the ratio of left ventricular weight to body weight (P = .0058) in rats fed a normal salt diet, but its contribution to left ventricular weight decreased in rats kept on a high salt diet. The contribution of the heat shock protein 27 allele was independent of blood pressure. We suggest that heat shock protein 27 represents a candidate gene/locus marker of cardiac hypertrophy in hypertension.

摘要

相似文献

1
HSP27 locus cosegregates with left ventricular mass independently of blood pressure.
Hypertension. 1996 Dec;28(6):1112-7.
2
Failure of the heat-shock protein 70 locus to cosegregate with blood pressure in spontaneously hypertensive rat x Wistar-Kyoto rat cross.
J Hypertens. 1993 Oct;11(10):1047-51. doi: 10.1097/00004872-199310000-00007.
3
Cosegregation analysis in genetic crosses suggests a protective role for atrial natriuretic factor against ventricular hypertrophy.遗传杂交中的共分离分析表明,心房利钠因子对心室肥厚具有保护作用。
Circ Res. 1999 Jun 25;84(12):1453-8. doi: 10.1161/01.res.84.12.1453.
4
Locus for the inducible, but not a constitutive, nitric oxide synthase cosegregates with blood pressure in the Dahl salt-sensitive rat.在 Dahl 盐敏感大鼠中,诱导型而非组成型一氧化氮合酶的基因座与血压共分离。
J Clin Invest. 1995 May;95(5):2170-7. doi: 10.1172/JCI117906.
5
High salt intake accelerated cardiac remodeling in spontaneously hypertensive rats: time window of left ventricular functional transition and its relation to salt-loading doses.高盐摄入加速自发性高血压大鼠的心脏重构:左心室功能转换的时间窗口及其与盐负荷剂量的关系。
Clin Exp Hypertens. 2011;33(7):492-9. doi: 10.3109/10641963.2010.551795. Epub 2011 May 2.
6
Plzf as a candidate gene predisposing the spontaneously hypertensive rat to hypertension, left ventricular hypertrophy, and interstitial fibrosis.Plzf 作为候选基因,导致自发性高血压大鼠易患高血压、左心室肥厚和间质纤维化。
Am J Hypertens. 2014 Jan;27(1):99-106. doi: 10.1093/ajh/hpt156. Epub 2013 Aug 23.
7
Identification of quantitative trait loci for cardiac hypertrophy in two different strains of the spontaneously hypertensive rat.自发性高血压大鼠两个不同品系中心脏肥大数量性状基因座的鉴定。
Hypertens Res. 2005 Mar;28(3):273-81. doi: 10.1291/hypres.28.273.
8
Mapping and confirmation of a major left ventricular mass QTL on rat chromosome 1 by contrasting SHRSP and F344 rats.通过对比 SHRSP 和 F344 大鼠,定位和确认大鼠染色体 1 上的一个主要左心室质量数量性状位点。
Physiol Genomics. 2013 Sep 16;45(18):827-33. doi: 10.1152/physiolgenomics.00067.2013. Epub 2013 Jul 30.
9
Differential cardiotoxicity in response to chronic doxorubicin treatment in male spontaneous hypertension-heart failure (SHHF), spontaneously hypertensive (SHR), and Wistar Kyoto (WKY) rats.雄性自发性高血压心力衰竭(SHHF)、自发性高血压(SHR)和 Wistar Kyoto(WKY)大鼠慢性多柔比星治疗的心脏毒性差异。
Toxicol Appl Pharmacol. 2013 Nov 15;273(1):47-57. doi: 10.1016/j.taap.2013.08.012. Epub 2013 Aug 28.
10
Tetrahydrobiopterin reverse left ventricular hypertrophy and diastolic dysfunction through the PI3K/p-Akt pathway in spontaneously hypertensive rats.四氢生物蝶呤通过PI3K/p-Akt信号通路逆转自发性高血压大鼠的左心室肥厚和舒张功能障碍。
Biochem Biophys Res Commun. 2015 Aug 7;463(4):1012-20. doi: 10.1016/j.bbrc.2015.06.051. Epub 2015 Jun 18.

引用本文的文献

1
Research on Experimental Hypertension in Prague (1966-2009).布拉格实验性高血压研究(1966-2009)。
Physiol Res. 2024 Aug 31;73(Suppl 1):S49-S66. doi: 10.33549/physiolres.935425. Epub 2024 Jul 17.
2
Characterization of hsp27 kinases activated by elevated aortic pressure in heart.心脏中因主动脉压力升高而激活的 hsp27 激酶的特性。
Mol Cell Biochem. 2012 Dec;371(1-2):31-42. doi: 10.1007/s11010-012-1420-x. Epub 2012 Aug 10.
3
Distinct quantitative trait loci for kidney, cardiac, and aortic mass dissociated from and associated with blood pressure in Dahl congenic rats.
在 Dahl 同源近交系大鼠中,与血压分离并相关的肾脏、心脏和主动脉质量的不同数量性状基因座。
Mamm Genome. 2006 Dec;17(12):1147-61. doi: 10.1007/s00335-006-0086-7. Epub 2006 Dec 1.
4
A new framework marker-based linkage map and SDPs for the rat HXB/BXH strain set.一种基于标记的大鼠HXB/BXH品系集的新框架连锁图谱和SDPs。
Mamm Genome. 2003 Aug;14(8):537-46. doi: 10.1007/s00335-003-2266-z.
5
Congenic mapping of a blood pressure QTL on chromosome 16 of Dahl rats.Dahl大鼠16号染色体上血压数量性状位点的同源定位
Mamm Genome. 2002 Mar;13(3):153-6. doi: 10.1007/BF02684020.
6
Gene-environment interactions in hypertension.高血压中的基因-环境相互作用
Curr Hypertens Rep. 1999 Feb-Mar;1(1):42-50. doi: 10.1007/s11906-999-0072-z.
7
Heat shock protein expression in hearts hypertrophied by genetic and nongenetic hypertension.
Heart Vessels. 1998;13(1):30-9. doi: 10.1007/BF02750641.
8
Construction of a double congenic strain to prove an epistatic interaction on blood pressure between rat chromosomes 2 and 10.构建双同源导入系以证明大鼠2号和10号染色体之间对血压的上位相互作用。
J Clin Invest. 1998 Apr 15;101(8):1591-5. doi: 10.1172/JCI2251.