突触前α-肾上腺素能受体参与FLA-136的心血管和镇静作用。 - Suppr | 超能文献

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突触前α-肾上腺素能受体参与FLA-136的心血管和镇静作用。 - Suppr | 超能文献

Involvement of presynaptic alpha-adrenoceptors in the cardiovascular and sedative effects of FLA-136.

作者信息

Timmermans P B, Lam E, van Zwieten P A

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1979 Mar;306(2):127-34. doi: 10.1007/BF00498982.

DOI:10.1007/BF00498982

Abstract

摘要

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Involvement of presynaptic alpha-adrenoceptors in the cardiovascular and sedative effects of FLA-136.突触前α-肾上腺素能受体参与FLA-136的心血管和镇静作用。

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引用本文的文献

1

A comparison of the cardiovascular and sedative actions of the alpha-adrenoceptor agonists, FLA-136 and clonidine, in the rat.大鼠体内α-肾上腺素能受体激动剂FLA - 136与可乐定的心血管及镇静作用比较

Br J Pharmacol. 1982 Jan;75(1):13-21. doi: 10.1111/j.1476-5381.1982.tb08753.x.

2

Selective stimulation of central alpha-autoreceptors following treatment with alpha-methyldopa and FLA 136.用α-甲基多巴和FLA 136治疗后对中枢α-自身受体的选择性刺激。

Naunyn Schmiedebergs Arch Pharmacol. 1979 Apr;306(3):263-6. doi: 10.1007/BF00507112.

本文引用的文献

1

[Pharmacological effects of 2-(2,6-dichlorophenylamino)-2-imidazoline hydrochloride, a new, antihypertensive substance].新型抗高血压物质2-（2,6-二氯苯基氨基）-2-咪唑啉盐酸盐的药理作用

Arzneimittelforschung. 1966 Aug;16(8):1038-50.

2

Evidence for a central noradrenaline receptor stimulation by clonidine.可乐定对中枢去甲肾上腺素受体刺激作用的证据。

Life Sci. 1970 May 1;9(9):513-23. doi: 10.1016/0024-3205(70)90207-9.

3

Involvement of alpha-receptors in clonidine-induced inhibition of transmitter release from central monoamine neurones.

α受体在可乐定诱导的中枢单胺能神经元递质释放抑制中的作用。

Neuropharmacology. 1973 Nov;12(11):1073-80. doi: 10.1016/0028-3908(73)90051-8.

4

Clonidine-induced inhibition of sympathetic nerve activity: no indication for a central presynaptic or an indirect sympathomimetic mode of action.可乐定诱导的交感神经活动抑制：无中枢突触前或间接拟交感神经作用模式的迹象。

Naunyn Schmiedebergs Arch Pharmacol. 1974;286(1):07-111. doi: 10.1007/BF00499107.

5

A further attempt to characterize sedative receptors activated by clonidine in chickens and mice.进一步尝试鉴定鸡和小鼠中由可乐定激活的镇静受体。

Eur J Pharmacol. 1973 Jun;22(3):355-9. doi: 10.1016/0014-2999(73)90038-1.

6

Drug-induced changes in the release of 3 H-monoamines from field stimulated rat brain slices.药物诱导的大鼠脑片经场刺激后3H-单胺释放的变化。

Acta Physiol Scand Suppl. 1971;371:35-44. doi: 10.1111/j.1748-1716.1971.tb05213.x.

7

The preparation and antihypertensive activity of 4-amino-3-(2,6-dichlorobenzylidenehydrazino)-1,2,4-triazole and some related compounds.4-氨基-3-(2,6-二氯亚苄基肼基)-1,2,4-三唑及一些相关化合物的制备与降压活性

Acta Pharm Suec. 1976;13(1):79-96.

8

Clinical pharmacology and pharmacokinetics of clonidine.可乐定的临床药理学与药代动力学

Clin Pharmacol Ther. 1976 Jan;19(1):11-7. doi: 10.1002/cpt197619111.

9

Hypotensive and bradycardic activities of clonidine and related imidazolidines; structure-activity relationship.可乐定及相关咪唑烷的降压和减慢心率作用；构效关系。

Arch Int Pharmacodyn Ther. 1977 Aug;228(2):237-50.

10

The effects of prazosin on the clonidine induced hypotension and bradycardia in rats and sedation in chicks [proceedings].哌唑嗪对大鼠可乐定诱导的低血压和心动过缓以及雏鸡镇静作用的影响[会议论文]

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