Suppr超能文献

四乙基秋兰姆二硫化物(双硫仑)和二乙基二硫代氨基甲酸钠(DDC)对去脑大鼠血管紧张素升压反应的选择性抑制作用。

Selective inhibition of angiotensin pressor responses in the pithed rat by tetraethylthiuram disulphide (disulfiram) and sodium diethyldithiocarbamate (DDC).

作者信息

Day M D, Hall J M, Owen D A

出版信息

Br J Pharmacol. 1972 Feb;44(2):192-202. doi: 10.1111/j.1476-5381.1972.tb07255.x.

Abstract
  1. Pressor responses to sympathetic outflow stimulation, noradrenaline and angiotensin have been recorded in pithed rats.2. Disulfiram (50 mg/kg) and sodium diethyldithiocarbamate (DDC) (5-100 mg/kg) both caused an initial increase in the pressor response to all three procedures followed by a selective inhibition of the angiotensin responses.3. Penicillamine (1-100 mg/kg) and ascorbic acid (1-500 mg/kg) increased the pressor responses to all three procedures without any subsequent blocking action.4. Reserpine (5 mg/kg daily for 3 days) abolished responses to sympathetic outflow stimulation but did not impair angiotensin or noradrenaline responses.5. In reserpinized rats, the initial enhancement of angiotensin responses after disulfiram and sodium diethyldithiocarbamate was absent or reduced and the onset of the subsequent block was accelerated.6. Possible mechanisms for the angiotensin-blocking action of disulfiram and sodium diethyldithiocarbamate are discussed.
摘要
  1. 在脊髓被横断的大鼠中记录了对交感神经流出刺激、去甲肾上腺素和血管紧张素的升压反应。

  2. 双硫仑(50毫克/千克)和二乙基二硫代氨基甲酸钠(DDC)(5 - 100毫克/千克)均使对所有三种操作的升压反应最初增强,随后选择性抑制血管紧张素反应。

  3. 青霉胺(1 - 100毫克/千克)和抗坏血酸(1 - 500毫克/千克)增强了对所有三种操作的升压反应,且无后续阻断作用。

  4. 利血平(每日5毫克/千克,共3天)消除了对交感神经流出刺激的反应,但不损害血管紧张素或去甲肾上腺素反应。

  5. 在利血平化的大鼠中,双硫仑和二乙基二硫代氨基甲酸钠给药后血管紧张素反应最初的增强不存在或减弱,且随后阻断的开始加快。

  6. 讨论了双硫仑和二乙基二硫代氨基甲酸钠血管紧张素阻断作用的可能机制。

相似文献

4
Modification of responses to sympathetic nerve stimulation by the renin-angiotensin system in rats.
Br J Pharmacol. 1974 Aug;51(4):541-7. doi: 10.1111/j.1476-5381.1974.tb09672.x.
6
The role of the sympathetic nervous system in the cardiovascular responses to angiotensin in the pithed rat.
Br J Pharmacol. 1969 Jul;36(3):481-8. doi: 10.1111/j.1476-5381.1969.tb08004.x.
9
Contribution of the sympathetic nervous system to the centrally-induced pressor action of angiotensin II in rats.
Clin Exp Pharmacol Physiol. 1982 Mar-Apr;9(2):193-201. doi: 10.1111/j.1440-1681.1982.tb00797.x.

本文引用的文献

1
Physiological effects of trihydroxy-N-methylindol and its reaction with copper ions.
Nature. 1950 Dec 30;166(4235):1116. doi: 10.1038/1661116a0.
3
INHIBITION OF DOPAMINE-BETA-HYDROXYLASE BY DISULFIRAM.
Life Sci (1962). 1964 Jul;3:763-7. doi: 10.1016/0024-3205(64)90031-1.
5
CINNARIZINE (R 516), A SPECIFIC ANGIOTENSINE-BLOCKING CORONARY VASODILATOR.
Life Sci (1962). 1963 Dec;12:963-74. doi: 10.1016/0024-3205(63)90066-3.
6
The in vitro reaction between tetraethylthiuram disulfide (antabuse) and glutathione.
Arch Biochem Biophys. 1953 May;44(1):249-51. doi: 10.1016/0003-9861(53)90034-4.
7
4,4,6-trimethyl-3,4-dihydropyrimidine-2-thiol, an effective inhibitor of dopamine-beta-hydroxylation in vivo.
Biochem Pharmacol. 1971 Jan;20(1):183-91. doi: 10.1016/0006-2952(71)90484-9.
8
The effect of reserpine on the pressor responses to angiotensin in the conscious cat.
Br J Pharmacol. 1970 Jun;39(2):414-27. doi: 10.1111/j.1476-5381.1970.tb12904.x.
9
A method of stimulating the complete sympathetic outflow from the spinal cord to blood vessels in the pithed rat.
Br J Pharmacol Chemother. 1967 May;30(1):78-87. doi: 10.1111/j.1476-5381.1967.tb02114.x.
10
Inhibition of valyl angiotensinamide II by osajin.
J Pharm Pharmacol. 1966 Jul;18(7):478-9. doi: 10.1111/j.2042-7158.1966.tb07912.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验