• 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

心肌疾病和心力衰竭中的β-肾上腺素能功能。

Beta-adrenergic function in heart muscle disease and heart failure.

作者信息

Bristow M R, Kantrowitz N E, Ginsburg R, Fowler M B

出版信息

J Mol Cell Cardiol. 1985 Jul;17 Suppl 2:41-52. doi: 10.1016/0022-2828(85)90007-0.

DOI:10.1016/0022-2828(85)90007-0
PMID:2863387
Abstract

Using data derived from clinical and experimental observations, we examine the role of the myocardial beta-adrenergic receptor system in pathophysiologic processes involved in heart muscle disease and heart failure. The available data suggest that the sympathetic nervous system exerts important influences on myocardial structure and function. As such the beta-adrenergic pathways represents an obvious locus for therapeutic intervention in evolving cardiomyopathic states.

摘要

利用来自临床和实验观察的数据,我们研究了心肌β-肾上腺素能受体系统在涉及心肌疾病和心力衰竭的病理生理过程中的作用。现有数据表明,交感神经系统对心肌结构和功能有重要影响。因此,β-肾上腺素能通路是对正在发展的心肌病状态进行治疗干预的一个明显靶点。

相似文献

1
Beta-adrenergic function in heart muscle disease and heart failure.心肌疾病和心力衰竭中的β-肾上腺素能功能。
J Mol Cell Cardiol. 1985 Jul;17 Suppl 2:41-52. doi: 10.1016/0022-2828(85)90007-0.
2
New views of human cardiac beta-adrenoceptors.人类心脏β-肾上腺素能受体的新观点。
J Mol Cell Cardiol. 1989 May;21(5):519-35. doi: 10.1016/0022-2828(89)90791-8.
3
Importance of receptor regulation in the pathophysiology and therapy of congestive heart failure.受体调节在充血性心力衰竭病理生理学及治疗中的重要性。
Am J Med. 1986 Feb 28;80(2B):67-72. doi: 10.1016/0002-9343(86)90148-8.
4
Rationale for beta-adrenergic blocking drugs in cardiomyopathy.β-肾上腺素能阻滞剂用于治疗心肌病的理论依据。
Am J Cardiol. 1985 Apr 26;55(10):120D-124D. doi: 10.1016/0002-9149(85)91066-5.
5
The molecular basis for distinct beta-adrenergic receptor subtype actions in cardiomyocytes.心肌细胞中不同β-肾上腺素能受体亚型作用的分子基础。
Circ Res. 1999 Nov 26;85(11):1101-11. doi: 10.1161/01.res.85.11.1101.
6
Beta-adrenergic receptor-G protein-adenylyl cyclase signal transduction in the failing heart.衰竭心脏中的β-肾上腺素能受体-G蛋白-腺苷酸环化酶信号转导
Am J Cardiol. 1999 Jun 17;83(12A):80H-85H. doi: 10.1016/s0002-9149(99)00266-0.
7
Molecular and biochemical mechanisms underlying the role of calcium ions in malignant ventricular arrhythmias.钙离子在恶性室性心律失常中作用的分子和生化机制。
Ann N Y Acad Sci. 1984;427:127-39. doi: 10.1111/j.1749-6632.1984.tb20780.x.
8
Calcium and catecholamines: relevance to cardiomyopathies and significance in therapeutic strategies.钙与儿茶酚胺:与心肌病的相关性及在治疗策略中的意义
J Mol Cell Cardiol. 1985 Jul;17 Suppl 2:21-34. doi: 10.1016/0022-2828(85)90005-7.
9
Activation of cardiac EP3 receptors by PGE1 reduces beta-adrenergic inotropic effects.
Adv Exp Med Biol. 1997;433:447-50. doi: 10.1007/978-1-4899-1810-9_99.
10
Mechanisms of beta adrenoceptor desensitisation in the failing human heart.
Cardiovasc Res. 1994 Oct;28(10):1451-60. doi: 10.1093/cvr/28.10.1451.

引用本文的文献

1
Baicalein Ameliorates Myocardial Ischemia Through Reduction of Oxidative Stress, Inflammation and Apoptosis via TLR4/MyD88/MAPK/NF-κB Pathway and Regulation of Ca Homeostasis by L-type Ca Channels.黄芩苷通过TLR4/MyD88/MAPK/NF-κB途径减轻氧化应激、炎症和凋亡以及通过L型钙通道调节钙稳态来改善心肌缺血。
Front Pharmacol. 2022 Mar 16;13:842723. doi: 10.3389/fphar.2022.842723. eCollection 2022.
2
[8]-Gingerol exerts anti-myocardial ischemic effects in rats via modulation of the MAPK signaling pathway and L-type Ca channels.[8]-姜辣素通过调节 MAPK 信号通路和 L 型钙通道发挥抗心肌缺血作用。
Pharmacol Res Perspect. 2021 Oct;9(5):e00852. doi: 10.1002/prp2.852.
3
Qi-Li-Qiang-Xin Alleviates Isoproterenol-Induced Myocardial Injury by Inhibiting Excessive Autophagy Activating AKT/mTOR Pathway.
芪苈强心通过抑制过度自噬激活AKT/mTOR信号通路减轻异丙肾上腺素诱导的心肌损伤。
Front Pharmacol. 2019 Nov 12;10:1329. doi: 10.3389/fphar.2019.01329. eCollection 2019.
4
Persistent increases in Ca(2+) influx through Cav1.2 shortens action potential and causes Ca(2+) overload-induced afterdepolarizations and arrhythmias.通过Cav1.2持续增加的钙离子内流会缩短动作电位,并导致钙离子过载引起的后去极化和心律失常。
Basic Res Cardiol. 2016 Jan;111(1):4. doi: 10.1007/s00395-015-0523-4. Epub 2015 Nov 26.
5
Cardiovascular function in large to small hibernators: bears to ground squirrels.从大型到小型冬眠动物的心血管功能:从熊到地松鼠
J Comp Physiol B. 2015 Apr;185(3):265-79. doi: 10.1007/s00360-014-0881-5. Epub 2014 Dec 27.
6
Repair of the injured adult heart involves new myocytes potentially derived from resident cardiac stem cells.成年心脏损伤的修复涉及潜在来源于心脏固有干细胞的新心肌细胞。
Circ Res. 2011 May 13;108(10):1226-37. doi: 10.1161/CIRCRESAHA.110.239046. Epub 2011 Mar 31.
7
Calcium influx through Cav1.2 is a proximal signal for pathological cardiomyocyte hypertrophy.钙内流通过 Cav1.2 是病理性心肌细胞肥大的近端信号。
J Mol Cell Cardiol. 2011 Mar;50(3):460-70. doi: 10.1016/j.yjmcc.2010.11.012. Epub 2010 Nov 25.
8
Cardiac gene therapy.心脏基因治疗。
Semin Thorac Cardiovasc Surg. 2010 Summer;22(2):127-39. doi: 10.1053/j.semtcvs.2010.09.009.
9
Enhanced basal contractility but reduced excitation-contraction coupling efficiency and beta-adrenergic reserve of hearts with increased Cav1.2 activity.心肌细胞钙通道 Cav1.2 活性增加导致基础收缩力增强,但兴奋-收缩耦联效率和β肾上腺素能储备降低。
Am J Physiol Heart Circ Physiol. 2010 Aug;299(2):H519-28. doi: 10.1152/ajpheart.00265.2010. Epub 2010 Jun 11.
10
c-Kit+ bone marrow stem cells differentiate into functional cardiac myocytes.c-Kit+ 骨髓干细胞分化为功能性心肌细胞。
Clin Transl Sci. 2009 Feb;2(1):26-32. doi: 10.1111/j.1752-8062.2008.00089.x.