• 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

特拉唑嗪:一种用于治疗高血压的新型长效α1肾上腺素能拮抗剂。

Terazosin: a new long-acting alpha 1-adrenergic antagonist for hypertension.

作者信息

Frishman W H, Eisen G, Lapsker J

机构信息

Albert Einstein College of Medicine, Bronx, New York.

出版信息

Med Clin North Am. 1988 Mar;72(2):441-8. doi: 10.1016/s0025-7125(16)30778-7.

DOI:10.1016/s0025-7125(16)30778-7
PMID:2894488
Abstract

Terazosin is a new long-acting, selective alpha 1-adrenergic antagonist. Its pharmacokinetic and pharmacodynamic profiles are similar to those of prazosin, but terazosin has a half-life three to four times longer. This allows once daily dosing of terazosin and a potential advantage in ensuring patient compliance to treatment. Terazosin has been evaluated alone and in combination with other drugs for the treatment of mild to moderate hypertension. Terazosin has been shown to have favorable lipid and side effect profiles. Unlike prazosin, the drug is available (but not yet marketed) in parenteral form. Its gradual onset of action with intravenous use would limit its potential application in hypertensive emergencies. Other possible uses for terazosin might include treatment of congestive heart failure and Raynaud's phenomenon, but definitive studies are needed.

摘要

特拉唑嗪是一种新型长效、选择性α1肾上腺素能拮抗剂。其药代动力学和药效学特征与哌唑嗪相似,但特拉唑嗪的半衰期长三至四倍。这使得特拉唑嗪可以每日给药一次,在确保患者治疗依从性方面具有潜在优势。特拉唑嗪已单独及与其他药物联合用于治疗轻至中度高血压。已证明特拉唑嗪具有良好的血脂和副作用特征。与哌唑嗪不同,该药物有肠胃外剂型(但尚未上市)。静脉使用时其作用起效缓慢,这将限制其在高血压急症中的潜在应用。特拉唑嗪的其他可能用途可能包括治疗充血性心力衰竭和雷诺现象,但需要进行确定性研究。

相似文献

1
Terazosin: a new long-acting alpha 1-adrenergic antagonist for hypertension.特拉唑嗪:一种用于治疗高血压的新型长效α1肾上腺素能拮抗剂。
Med Clin North Am. 1988 Mar;72(2):441-8. doi: 10.1016/s0025-7125(16)30778-7.
2
Terazosin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in essential hypertension.特拉唑嗪。对其药效学、药代动力学特性及在原发性高血压治疗中的疗效的综述。
Drugs. 1987 May;33(5):461-77. doi: 10.2165/00003495-198733050-00003.
3
Terazosin: a new alpha adrenoceptor blocking drug.特拉唑嗪:一种新型α肾上腺素能受体阻断药。
J Clin Pharmacol. 1992 Jun;32(6):520-3. doi: 10.1177/009127009203200605.
4
Terazosin: pharmacokinetics and the effect of age and dose on the incidence of adverse events.特拉唑嗪:药代动力学以及年龄和剂量对不良事件发生率的影响。
Am Heart J. 1991 Sep;122(3 Pt 2):901-5. doi: 10.1016/0002-8703(91)90809-v.
5
Terazosin: a new antihypertensive agent with favorable effects on lipids.特拉唑嗪:一种对脂质有良好作用的新型抗高血压药物。
Int J Clin Pharmacol Ther Toxicol. 1989 Jul;27(7):313-9.
6
Alpha-adrenergic receptor blockade with prazosin. Consideration of hypertension, heart failure, and potential new applications.
Ann Intern Med. 1982 Jul;97(1):67-77. doi: 10.7326/0003-4819-97-1-67.
7
Antihypertensive effects of doxazosin in systemic hypertension and comparison with terazosin.
Am J Cardiol. 1987 May 29;59(14):95G-98G. doi: 10.1016/0002-9149(87)90166-4.
8
Pharmacokinetics of terazosin.特拉唑嗪的药代动力学。
Am J Med. 1986 May 23;80(5B):20-4. doi: 10.1016/0002-9343(86)90847-8.
9
Alpha 2-agonist versus alpha 1-antagonist in mild-to-moderate hypertension: comparison of transdermal clonidine and terazosin monotherapies.
Am J Ther. 1997 Jan;4(1):9-15. doi: 10.1097/00045391-199701000-00003.
10
Terazosin: a new alpha 1-blocker for the treatment of hypertension: a review of randomized, controlled clinical trials of once-daily administration as monotherapy.特拉唑嗪:一种用于治疗高血压的新型α1受体阻滞剂:每日一次单药治疗的随机对照临床试验综述
J Hypertens Suppl. 1986 Dec;4(5):S494-7.

引用本文的文献

1
Pgk1 activation restores endothelial metabolic homeostasis to alleviate vascular aging and atherosclerosis.磷酸甘油酸激酶1(Pgk1)的激活可恢复内皮细胞代谢稳态,以减轻血管衰老和动脉粥样硬化。
Cardiovasc Diabetol. 2025 Nov 8;24(1):427. doi: 10.1186/s12933-025-02976-2.
2
Calcium and Neural Stem Cell Proliferation.钙与神经干细胞增殖。
Int J Mol Sci. 2024 Apr 6;25(7):4073. doi: 10.3390/ijms25074073.
3
Alpha-adrenergic blockers selectively antagonize the contractions induced by 6-nitrodopamine in the human vas deferens.α-肾上腺素能阻滞剂选择性地拮抗 6-硝基多巴胺引起的人输精管收缩。
Naunyn Schmiedebergs Arch Pharmacol. 2024 May;397(5):3227-3238. doi: 10.1007/s00210-023-02805-x. Epub 2023 Nov 1.
4
β- and β/β-adrenergic receptor antagonists block 6-nitrodopamine-induced contractions of the rat isolated epididymal vas deferens.β-和β/β-肾上腺素能受体拮抗剂可阻断 6-硝基多巴胺引起的大鼠离体附睾输精管收缩。
Naunyn Schmiedebergs Arch Pharmacol. 2022 Oct;395(10):1257-1268. doi: 10.1007/s00210-022-02268-6. Epub 2022 Jul 8.
5
Pharmacological tolerance to alpha 1-adrenergic receptor antagonism mediated by terazosin in humans.人类对特拉唑嗪介导的α1肾上腺素能受体拮抗作用的药理学耐受性。
J Clin Invest. 1992 Nov;90(5):1763-8. doi: 10.1172/JCI116050.