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The interaction between prazosin and clonidine at alpha-adrenoceptors in rats and cats.

作者信息

Timmermans P B, Lam E, Van Zwieten P A

出版信息

Eur J Pharmacol. 1979 Apr 1;55(1):57-66. doi: 10.1016/0014-2999(79)90147-x.

DOI:10.1016/0014-2999(79)90147-x
PMID:220064
Abstract
摘要

相似文献

1
The interaction between prazosin and clonidine at alpha-adrenoceptors in rats and cats.
Eur J Pharmacol. 1979 Apr 1;55(1):57-66. doi: 10.1016/0014-2999(79)90147-x.
2
Differential effects of prazosin on the pre- and postsynaptic alpha-adrenoceptors in the rat and dog [proceedings].哌唑嗪对大鼠和犬突触前及突触后α-肾上腺素能受体的不同作用[会议论文集]
Br J Pharmacol. 1977 Nov;61(3):469P.
3
Effects of prazosin and phentolamine on cardiac presynaptic alpha-adrenoceptors in the cat, dog and rat.哌唑嗪和酚妥拉明对猫、狗和大鼠心脏突触前α-肾上腺素能受体的作用。
Clin Exp Hypertens (1978). 1978;1(1):87-101. doi: 10.3109/10641967809068597.
4
Comparative effects of urapidil, prazosin, and clonidine on ligand binding to central nervous system receptors, arterial pressure, and heart rate in experimental animals.乌拉地尔、哌唑嗪和可乐定对实验动物中枢神经系统受体配体结合、动脉血压及心率的比较作用。
Am J Med. 1984 Oct 5;77(4A):87-95. doi: 10.1016/s0002-9343(84)80042-x.
5
Effects of prazosin and two of its derivatives (UK 18.596 and UK 33.274) on alpha-adrenoceptors [proceedings].哌唑嗪及其两种衍生物（UK 18.596和UK 33.274）对α-肾上腺素能受体的作用[会议论文集]
Br J Pharmacol. 1980 Jan;68(1):113P.
6
In vivo selectivity of prazosin but not of WB4101 for postsynaptic alpha-1 adrenoceptors.哌唑嗪对突触后α-1肾上腺素能受体具有体内选择性，而WB4101则没有。
J Pharmacol Exp Ther. 1981 May;217(2):467-74.
7
Comparison of cardiovascular actions of dihydralazine, phentolamine, and prazosin in spontaneously hypertensive rats.双肼屈嗪、酚妥拉明和哌唑嗪对自发性高血压大鼠心血管作用的比较。
J Cardiovasc Pharmacol. 1979 Jan-Feb;1(1):19-29. doi: 10.1097/00005344-197901000-00003.
8
Interaction of prazosin with alpha-adrenergic receptors--in vitro binding and in vivo antagonism.哌唑嗪与α-肾上腺素能受体的相互作用——体外结合与体内拮抗作用
Biochem Pharmacol. 1979 Aug 1;28(15):2409-11. doi: 10.1016/0006-2952(79)90711-1.
9
Interaction between prazosin and benzodioxan antihypertensives (R 28935 and R 29814); a competition for central alpha 1-adrenoceptors [proceedings].哌唑嗪与苯并二恶烷类抗高血压药（R 28935和R 29814）之间的相互作用；对中枢α1肾上腺素能受体的竞争[会议论文集]
Br J Pharmacol. 1980 Jan;68(1):138P-139P.
10
Effects of urapidil, clonidine, prazosin and propranolol on autonomic nerve activity, blood pressure and heart rate in anaesthetized rats and cats.乌拉地尔、可乐定、哌唑嗪和普萘洛尔对麻醉大鼠和猫自主神经活动、血压及心率的影响。
Eur J Pharmacol. 1985 Apr 2;110(2):181-90. doi: 10.1016/0014-2999(85)90210-9.

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Central and peripheral mechanisms underlying gastric distention inhibitory reflex responses in hypercapnic-acidotic rats.胃扩张抑制反射反应在高碳酸酸中毒大鼠中的中枢和外周机制。
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The I1-imidazoline receptor: from binding site to therapeutic target in cardiovascular disease.I1-咪唑啉受体：从结合位点到心血管疾病治疗靶点
J Hypertens Suppl. 1997 Jan;15(1):S9-23. doi: 10.1097/00004872-199715011-00002.
3
Hypotensive and bradycardic effects of talipexole (B-HT 920) in anaesthetized rabbits are antagonized by metoclopramide but not by yohimbine.
甲磺酸泰利必利（B-HT 920）对麻醉兔的降压和心动过缓作用可被甲氧氯普胺拮抗，但不能被育亨宾拮抗。
Naunyn Schmiedebergs Arch Pharmacol. 1993 Jul;348(1):58-64. doi: 10.1007/BF00168537.
4
Treatment with clorgyline and pargyline differentially decreases clonidine-induced hypotension and bradycardia.用氯吉兰和帕吉林治疗分别降低可乐定引起的低血压和心动过缓。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Sep;327(3):189-92. doi: 10.1007/BF00502448.
5
The influence of repeated administration of prazosin on its hypotensive effect and on renin release in conscious dogs. A comparison with urapidil.哌唑嗪重复给药对清醒犬降压作用及肾素释放的影响。与乌拉地尔的比较。
Basic Res Cardiol. 1984 Sep-Oct;79(5):579-87. doi: 10.1007/BF01910487.
6
Effects of prazosin and two of its derivatives (UK 18.596 and UK 33.274) on alpha-adrenoceptors [proceedings].哌唑嗪及其两种衍生物（UK 18.596和UK 33.274）对α-肾上腺素能受体的作用[会议论文集]
Br J Pharmacol. 1980 Jan;68(1):113P.
7
Pharmacology of combined alpha-beta-blockade. I.α-β联合阻滞的药理学。I.
Drugs. 1984;28 Suppl 2:16-34. doi: 10.2165/00003495-198400282-00003.
8
The cardiovascular effects of MPV 295 [4(5)-2-(2,6-dimethylphenyl)ethylimidazole], a new antihypertensive agent with alpha 2-adrenoceptor agonistic properties.MPV 295 [4(5)-2-(2,6-二甲基苯基)乙基咪唑] 是一种具有α2-肾上腺素能受体激动特性的新型抗高血压药物，其对心血管系统的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1983 May;322(4):279-85. doi: 10.1007/BF00508343.
9
A comparison of pre- and post-junctional potencies of several alpha-adrenoceptor agonists in the cardiovascular system and anococcygeus muscle of the rat. Evidence for two types of post-junctional alpha-adrenoceptor.几种α-肾上腺素能激动剂在大鼠心血管系统和尾骨肌中节前和节后效能的比较。两种节后α-肾上腺素能受体的证据。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Jun;312(2):107-16. doi: 10.1007/BF00569718.
10
Pharmacology of centrally acting hypotensive drugs.中枢性降压药的药理学
Br J Clin Pharmacol. 1980;10 Suppl 1(Suppl 1):13S-20S. doi: 10.1111/j.1365-2125.1980.tb04899.x.