• 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

肼屈嗪代谢产物的体外效应研究——羟基化、水解和结合产物的比较评估。

Study of in vitro effects of hydralazine metabolites--comparative evaluation of products of hydroxylation, hydrolysis and conjugation.

作者信息

McLean A J, du Souich P, Barron K, Carrier O, Haegele K D, McNay J L

出版信息

Arch Int Pharmacodyn Ther. 1978 Sep;235(1):19-25.

PMID:736689
Abstract

K+ contractures were induced in paired strips of rabbit aortic smooth muscle. The relationship between relaxant effects and the bath concentration of hydralazine acetone hydrazone (HA), 4-OH-hydralazine (HH) and phthalazine (P) was studied over the concentration range 10(-5)-10(-3)M. All compounds were active, HA = HH greater than P (p less than 0.05; n = 6) at concentrations in the range 10(-4)-10(-3M, HA greater than HH at a concentration of 10(-3M (pgreater than 0.01). The activity of HA did not depend on significant reconversion to hydralazine (H) in the bath ( less than 0.5%). A range of H derivatives may contribute to the hypotensive effects of administered H.

摘要

在兔主动脉平滑肌的成对条带上诱导产生钾离子挛缩。研究了在10⁻⁵ - 10⁻³M浓度范围内,肼屈嗪丙酮腙(HA)、4-羟基肼屈嗪(HH)和酞嗪(P)的浴液浓度与舒张作用之间的关系。所有化合物均有活性,在10⁻⁴ - 10⁻³M浓度范围内,HA = HH > P(p < 0.05;n = 6),在10⁻³M浓度时,HA > HH(p>0.01)。HA的活性并不依赖于其在浴液中显著再转化为肼屈嗪(H)(<0.5%)。一系列H衍生物可能有助于所给予的H的降压作用。

相似文献

1
Study of in vitro effects of hydralazine metabolites--comparative evaluation of products of hydroxylation, hydrolysis and conjugation.肼屈嗪代谢产物的体外效应研究——羟基化、水解和结合产物的比较评估。
Arch Int Pharmacodyn Ther. 1978 Sep;235(1):19-25.
2
Interaction of hydralazine and hydrazone derivatives with contractile mechanisms in rabbit aortic smooth muscle.肼屈嗪和腙衍生物与兔主动脉平滑肌收缩机制的相互作用。
J Pharmacol Exp Ther. 1978 May;205(2):418-25.
3
Comparative evaluation of the in vitro effects of hydralazine and hydralazine acetonide on arterial smooth muscle.肼屈嗪和肼屈嗪丙酮化物对动脉平滑肌体外作用的比较评价
Br J Pharmacol. 1977 Nov;61(3):345-9. doi: 10.1111/j.1476-5381.1977.tb08426.x.
4
Endogenous generation of hydralazine from labile hydralazine hydrazones.由不稳定的肼屈嗪腙内源性生成肼屈嗪。
J Pharmacol Exp Ther. 1982 Jul;222(1):159-65.
5
Identification of hydrallazine and hydrallazine hydrazone metabolites in human body fluids and quantitative in vitro comparisons of their smooth muscle relaxant activity.人体体液中肼屈嗪及其腙代谢物的鉴定以及它们平滑肌松弛活性的体外定量比较。
Br J Clin Pharmacol. 1978 Jun;5(6):489-94. doi: 10.1111/j.1365-2125.1978.tb01662.x.
6
Relaxant effects of pinacidil, nicorandil, hydralazine and nifedipine as studied in the porcine coronary artery and guinea-pig taenia coli.在猪冠状动脉和豚鼠结肠带中研究吡那地尔、尼可地尔、肼屈嗪和硝苯地平的舒张作用。
Arch Int Pharmacodyn Ther. 1986 Sep;283(1):124-33.
7
Interaction of hydralazine with tension development and mechanisms of calcium accumulation in K+-stimulated rabbit aortic strips.肼屈嗪与K⁺刺激的兔主动脉条张力发展及钙蓄积机制的相互作用
J Pharmacol Exp Ther. 1978 Oct;207(1):40-8.
8
Studies on the direct vasodilator effect of hydralazine in the isolated rabbit renal artery.关于肼屈嗪对离体兔肾动脉直接血管舒张作用的研究。
J Pharmacol Exp Ther. 1981 Feb;216(2):390-4.
9
Effects of cadralazine on contractions induced by norepinephrine, serotonin, angiotensin II and K+ in rabbit aortic and renal arterial strips.肼屈嗪对家兔主动脉和肾动脉条带中去甲肾上腺素、5-羟色胺、血管紧张素II和钾离子诱导的收缩作用。
Arzneimittelforschung. 1988 Mar;38(3):341-6.
10
Hydralazine-relaxing effect on rat aorta is not mediated through changes in ATPase activity.
Arch Int Pharmacodyn Ther. 1987 Jan;285(1):72-9.

引用本文的文献

1
Effect of N-Acetyltransferase 2 Genotype on the Pharmacokinetics of Hydralazine During Pregnancy.乙酰转移酶 2 基因型对妊娠期肼屈嗪药代动力学的影响。
J Clin Pharmacol. 2019 Dec;59(12):1678-1689. doi: 10.1002/jcph.1477. Epub 2019 Jun 30.