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Differential effects of extended-release carvedilol and extended-release metoprolol on lipid profiles in patients with hypertension: results of the Extended-Release Carvedilol Lipid Trial.缓释卡维地洛与缓释美托洛尔对高血压患者血脂谱的不同影响:缓释卡维地洛血脂试验结果
J Am Soc Hypertens. 2009 May-Jun;3(3):210-20. doi: 10.1016/j.jash.2009.01.004. Epub 2009 Mar 29.
2
Arterial stiffness, hypertension, and rational use of nebivolol.动脉僵硬度、高血压与奈必洛尔的合理使用
Vasc Health Risk Manag. 2009;5(1):353-60. doi: 10.2147/vhrm.s3056.
3
Blood pressure-lowering effect of nebivolol in hypertensive patients with type 2 diabetes mellitus: the YESTONO study.奈必洛尔对2型糖尿病高血压患者的降压作用:YESTONO研究
Clin Drug Investig. 2007;27(12):841-9. doi: 10.2165/00044011-200727120-00006.
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The vasodilatory beta-blockers.血管舒张性β受体阻滞剂
Curr Hypertens Rep. 2007 Aug;9(4):269-77. doi: 10.1007/s11906-007-0050-2.
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The role of renin-angiotensin system blockade in the management of hypertension associated with the cardiometabolic syndrome.肾素-血管紧张素系统阻断在与心脏代谢综合征相关的高血压管理中的作用。
J Cardiometab Syndr. 2006 Winter;1(1):29-35. doi: 10.1111/j.0197-3118.2006.05422.x.
6
2007 Guidelines for the management of arterial hypertension: The Task Force for the Management of Arterial Hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC).2007年动脉高血压管理指南:欧洲高血压学会(ESH)和欧洲心脏病学会(ESC)动脉高血压管理特别工作组制定。
Eur Heart J. 2007 Jun;28(12):1462-536. doi: 10.1093/eurheartj/ehm236. Epub 2007 Jun 11.
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Metabolic profile of nebivolol, a beta-adrenoceptor antagonist with unique characteristics.奈必洛尔的代谢概况,一种具有独特特性的β-肾上腺素能受体拮抗剂。
Drugs. 2007;67(8):1097-107. doi: 10.2165/00003495-200767080-00001.
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Antioxidant activity of carvedilol in cardiovascular disease.卡维地洛在心血管疾病中的抗氧化活性。
J Hypertens. 2007 Apr;25(4):731-41. doi: 10.1097/HJH.0b013e3280127948.
9
Nebivovol and carvedilol induce NO-dependent coronary vasodilatation that is unlikely to be mediated by extracellular ATP in the isolated guinea pig heart.奈必洛尔和卡维地洛在离体豚鼠心脏中诱导一氧化氮依赖性冠状动脉血管舒张,这不大可能由细胞外三磷酸腺苷介导。
Pharmacol Rep. 2006;58 Suppl:103-10.
10
New hypertension guidelines from the National Institute for Health and Clinical Excellence and the British Hypertension Society.英国国家卫生与临床优化研究所和英国高血压学会发布的新高血压指南。
J Renin Angiotensin Aldosterone Syst. 2006 Jun;7(2):61-3. doi: 10.3317/jraas.2006.011.

高血压、血脂异常和糖尿病或代谢综合征患者的胰岛素抵抗:血管舒张β受体阻滞剂的益处。

Hypertension, dyslipidemia, and insulin resistance in patients with diabetes mellitus or the cardiometabolic syndrome: benefits of vasodilating β-blockers.

机构信息

Division of Cardiology, VACCHCS UCSF School of Medicine, University of California at San Francisco, Fresno, CA 93703, USA.

出版信息

J Clin Hypertens (Greenwich). 2011 Jan;13(1):52-9. doi: 10.1111/j.1751-7176.2010.00386.x. Epub 2010 Nov 8.

DOI:10.1111/j.1751-7176.2010.00386.x
PMID:21214722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8672984/
Abstract

Hypertension frequently coexists with diabetes and the cardiometabolic syndrome. β-Blockers have been a mainstay for controlling blood pressure for nearly 4 decades. However, β-blockers are perceived to cause glucose and lipid metabolism dysregulation, including hypoglycemia masking, reduced glycemic control, insulin resistance, and dyslipidemia. It should be noted, however, that β-blockers are diverse in their effects on glucose and lipid metabolism. Potential mechanisms that contribute to these metabolic effects include hemodynamic differences, anti-inflammatory and anti-oxidative pathways, and/or weight changes. Traditional β-blockers decrease cardiac output while peripheral vascular resistance increases or remains unchanged, which may result in glucose and lipid abnormalities. In contrast, vasodilating β-blockers reduce peripheral vascular resistance but have little effect on cardiac output. Vasodilating β-blockers may therefore result in less impact on insulin sensitivity and glycemic control, a reduced new-onset diabetes risk, and improved dyslipidemia compared with traditional β-blockers. Because of these effects, vasodilating β-blockers may represent a favorable option in the treatment of high-risk patients with hypertension.

摘要

高血压常与糖尿病和心脏代谢综合征并存。β受体阻滞剂作为控制血压的主要药物已经使用了近 40 年。然而,β受体阻滞剂被认为会导致糖脂代谢紊乱,包括低血糖掩盖、血糖控制降低、胰岛素抵抗和血脂异常。然而,需要注意的是,β受体阻滞剂在对糖脂代谢的影响方面存在差异。导致这些代谢作用的潜在机制包括血流动力学差异、抗炎和抗氧化途径以及/或体重变化。传统的β受体阻滞剂降低心输出量,同时外周血管阻力增加或保持不变,这可能导致葡萄糖和脂质异常。相比之下,血管扩张性β受体阻滞剂降低外周血管阻力,但对心输出量影响较小。因此,与传统的β受体阻滞剂相比,血管扩张性β受体阻滞剂可能对胰岛素敏感性和血糖控制的影响较小,新发糖尿病的风险降低,血脂异常得到改善。由于这些作用,血管扩张性β受体阻滞剂可能成为治疗高血压高危患者的一种有利选择。