• 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

卡托普利对硝普钠血流动力学及激素效应的影响。

Impact of captopril on hemodynamic and hormonal effects of nitroprusside.

作者信息

Fahmy N R, Gavras H P

出版信息

J Cardiovasc Pharmacol. 1985 Sep-Oct;7(5):869-74. doi: 10.1097/00005344-198509000-00009.

DOI:10.1097/00005344-198509000-00009
PMID:2413294
Abstract

The impact of oral captopril, 2 mg . kg-1, on the dose and on the hemodynamic and hormonal effects of nitroprusside was studied in seven patients (Group II). A comparable group (Group I, n = 7) received nitroprusside alone. In both groups, nitroprusside produced comparable decreases in mean arterial pressure, systemic vascular resistance, and right atrial pressure; cardiac output increased because of a significant change in heart rate. Although plasma renin activity increased significantly (compared with control values) in both groups, it was greater (p = 0.01) through the operative period in patients pretreated with captopril. Plasma aldosterone concentration increased in Group I (p = 0.01) but decreased in Group II (p = 0.01). Plasma catecholamine concentrations increased (p = 0.01) with nitroprusside alone but were unchanged in captopril-treated patients. Plasma converting enzyme activity was markedly inhibited (p = 0.001) by captopril. Following cessation of nitroprusside infusion in Group I, rebound hypertension occurred in conjunction with a significant (p = 0.01) increase in systemic vascular resistance; it was associated with elevated plasma renin activity, catecholamines, and aldosterone concentrations. In contrast, captopril-treated patients showed no rebound hemodynamic changes. Nitroprusside dose was less (p = 0.01) with captopril pretreatment (2.1 +/- 0.3 vs. 4.8 +/- 0.9 microgram . kg-1 . min-1). Thus, captopril is a useful adjunct to nitroprusside-induced hypotension.

摘要

研究了口服卡托普利(2毫克·千克⁻¹)对硝普钠剂量以及血流动力学和激素效应的影响,共纳入7例患者(第二组)。设立了一个对照可比组(第一组,n = 7),该组仅接受硝普钠治疗。两组中,硝普钠均使平均动脉压、全身血管阻力和右心房压力出现了类似程度的下降;由于心率发生显著变化,心输出量增加。虽然两组的血浆肾素活性均显著升高(与对照值相比),但在手术期间,接受卡托普利预处理的患者其血浆肾素活性更高(p = 0.01)。第一组的血浆醛固酮浓度升高(p = 0.01),而第二组降低(p = 0.01)。单独使用硝普钠时血浆儿茶酚胺浓度升高(p = 0.01),但接受卡托普利治疗的患者血浆儿茶酚胺浓度未发生变化。卡托普利显著抑制了血浆转换酶活性(p = 0.001)。在第一组停止输注硝普钠后,出现了反弹性高血压,同时全身血管阻力显著增加(p = 0.01);这与血浆肾素活性、儿茶酚胺和醛固酮浓度升高有关。相比之下,接受卡托普利治疗的患者未出现反弹性血流动力学变化。卡托普利预处理后硝普钠剂量减少(p = 0.01)(2.1±0.3与4.8±0.9微克·千克⁻¹·分钟⁻¹)。因此,卡托普利是硝普钠诱导低血压的有用辅助药物。

相似文献

1
Impact of captopril on hemodynamic and hormonal effects of nitroprusside.卡托普利对硝普钠血流动力学及激素效应的影响。
J Cardiovasc Pharmacol. 1985 Sep-Oct;7(5):869-74. doi: 10.1097/00005344-198509000-00009.
2
The effects of captopril on the renin-angiotensin system and the sympathetic nervous system during sodium nitroprusside-induced hypotension in the halothane-anesthetized rabbit.
J Cardiovasc Pharmacol. 1990 Mar;15(3):465-71. doi: 10.1097/00005344-199003000-00017.
3
Captopril modifies the hemodynamic and neuroendocrine responses to sodium nitroprusside in hypertensive patients.
Hypertension. 1986 Mar;8(3):229-37. doi: 10.1161/01.hyp.8.3.229.
4
Quantitative differences in the hemodynamic effects of captopril and nitroprusside in severe chronic heart failure.卡托普利和硝普钠对重度慢性心力衰竭血流动力学影响的定量差异。
Am J Cardiol. 1983 Jan 1;51(1):183-8. doi: 10.1016/s0002-9149(83)80033-2.
5
Captopril reduces the dose requirement for sodium nitroprusside induced hypotension.
Anesthesiology. 1984 May;60(5):413-7. doi: 10.1097/00000542-198405000-00004.
6
Hormonal response to captopril pre-treatment during sodium nitroprusside-induced hypotension in man.
Eur J Anaesthesiol. 1987 Mar;4(2):101-12.
7
Effect of captopril on changes in plasma noradrenaline induced by sodium nitroprusside.卡托普利对硝普钠诱导的血浆去甲肾上腺素变化的影响。
Br J Clin Pharmacol. 1986 Oct;22(4):409-13. doi: 10.1111/j.1365-2125.1986.tb02910.x.
8
Angiotensin-converting enzyme inhibition, catecholamines and hemodynamics in essential hypertension.原发性高血压中的血管紧张素转换酶抑制、儿茶酚胺与血流动力学
Am J Cardiol. 1982 Apr 21;49(6):1420-4. doi: 10.1016/0002-9149(82)90354-x.
9
Comparison of intravenous nitroprusside, nitroprusside-captopril, and nitroglycerin for deliberate hypotension during posterior spine fusion in adults.
J Clin Anesth. 1988;1(2):87-95. doi: 10.1016/0952-8180(88)90027-x.
10
Plasma catecholamines, plasma renin activity and haemodynamics during sodium nitroprusside-induced hypotension and additional beta-blockage with bunitrolol.硝普钠诱导低血压期间及联合布尼洛尔额外β受体阻滞时的血浆儿茶酚胺、血浆肾素活性及血流动力学
Eur J Clin Pharmacol. 1981;19(5):317-22. doi: 10.1007/BF00544580.

引用本文的文献

1
Pharmacokinetic drug interactions with ACE inhibitors.与血管紧张素转换酶抑制剂的药代动力学药物相互作用。
Clin Pharmacokinet. 1993 Jul;25(1):20-58. doi: 10.2165/00003088-199325010-00003.
2
Nitrate tolerance. A relevant clinical problem?硝酸酯类药物耐受性:一个相关的临床问题?
Drugs. 1987;33 Suppl 4:51-4. doi: 10.2165/00003495-198700334-00011.
3
N-acetylcysteine fails to attenuate haemodynamic tolerance to glyceryl trinitrate in healthy volunteers.在健康志愿者中,N-乙酰半胱氨酸未能减弱对硝酸甘油的血流动力学耐受性。
Br J Clin Pharmacol. 1989 Oct;28(4):421-6. doi: 10.1111/j.1365-2125.1989.tb03522.x.
4
Nitrate tolerance in angina pectoris.心绞痛中的硝酸盐耐受性。
Cardiovasc Drugs Ther. 1989 Jan;2(6):823-9. doi: 10.1007/BF00133214.
5
Chronic administration of N-acetylcysteine fails to prevent nitrate tolerance in patients with stable angina pectoris.长期服用N-乙酰半胱氨酸不能预防稳定型心绞痛患者的硝酸盐耐受性。
Br J Clin Pharmacol. 1990 Oct;30(4):573-7. doi: 10.1111/j.1365-2125.1990.tb03815.x.
6
Mechanisms of nitrate tolerance: a review.硝酸盐耐受性的机制:综述
Cardiovasc Drugs Ther. 1990 Feb;4(1):247-52. doi: 10.1007/BF01857640.
7
Nitrates: why and how should they be used today? Current status of the clinical usefulness of nitroglycerin, isosorbide dinitrate and isosorbide-5-mononitrate.硝酸盐类药物:如今为何以及应如何使用?硝酸甘油、硝酸异山梨酯和5-单硝酸异山梨酯临床应用价值的现状。
Eur J Clin Pharmacol. 1990;38 Suppl 1:S35-51. doi: 10.1007/BF01417564.