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5-HT1D receptor-mediated inhibition of forskolin-stimulated adenylate cyclase activity in calf substantia nigra.

作者信息

Hoyer D, Schoeffter P

机构信息

Preclinical Research, Sandoz Ltd., Basel, Switzerland.

出版信息

Eur J Pharmacol. 1988 Feb 16;147(1):145-7. doi: 10.1016/0014-2999(88)90645-0.

DOI:10.1016/0014-2999(88)90645-0
PMID:3371410
Abstract
摘要

相似文献

1
5-HT1D receptor-mediated inhibition of forskolin-stimulated adenylate cyclase activity in calf substantia nigra.5-羟色胺1D受体介导的对小牛黑质中福斯高林刺激的腺苷酸环化酶活性的抑制作用
Eur J Pharmacol. 1988 Feb 16;147(1):145-7. doi: 10.1016/0014-2999(88)90645-0.
2
5-Hydroxytryptamine 5-HT1B and 5-HT1D receptors mediating inhibition of adenylate cyclase activity. Pharmacological comparison with special reference to the effects of yohimbine, rauwolscine and some beta-adrenoceptor antagonists.介导腺苷酸环化酶活性抑制的5-羟色胺5-HT1B和5-HT1D受体。特别参照育亨宾、萝芙辛和某些β-肾上腺素能拮抗剂作用的药理学比较。
Naunyn Schmiedebergs Arch Pharmacol. 1989 Sep;340(3):285-92. doi: 10.1007/BF00168512.
3
The 5-hydroxytryptamine 5-HT1D receptor subtype is negatively coupled to adenylate cyclase in calf substantia nigra.5-羟色胺5-HT1D受体亚型在小牛黑质中与腺苷酸环化酶呈负偶联。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Jun;337(6):602-8. doi: 10.1007/BF00175784.
4
5-HT1B receptors are negatively coupled with adenylate cyclase in rat substantia nigra.5-羟色胺1B受体在大鼠黑质中与腺苷酸环化酶呈负偶联。
Eur J Pharmacol. 1988 Jul 7;151(2):189-96. doi: 10.1016/0014-2999(88)90799-6.
5
L-694,247: a potent 5-HT1D receptor agonist.L-694,247：一种强效的5-羟色胺1D受体激动剂。
Br J Pharmacol. 1993 Nov;110(3):1196-200. doi: 10.1111/j.1476-5381.1993.tb13941.x.
6
Interaction of arylpiperazines with 5-HT1A, 5-HT1B, 5-HT1C and 5-HT1D receptors: do discriminatory 5-HT1B receptor ligands exist?芳基哌嗪与5-HT1A、5-HT1B、5-HT1C和5-HT1D受体的相互作用：是否存在具有选择性的5-HT1B受体配体？
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Differential effects of somatostatin on adenylate cyclase as functional correlate for different brain somatostatin receptor subpopulations.生长抑素对腺苷酸环化酶的不同作用，作为不同脑内生长抑素受体亚群的功能关联。
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Chronic MAO A and MAO B inhibition decreases the 5-HT1A receptor-mediated inhibition of forskolin-stimulated adenylate cyclase.慢性单胺氧化酶A和单胺氧化酶B抑制作用会降低5-羟色胺1A受体介导的对福斯高林刺激的腺苷酸环化酶的抑制作用。
Eur J Pharmacol. 1988 Sep 23;154(3):255-61. doi: 10.1016/0014-2999(88)90199-9.
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Centrally acting hypotensive agents with affinity for 5-HT1A binding sites inhibit forskolin-stimulated adenylate cyclase activity in calf hippocampus.对5-HT1A结合位点具有亲和力的中枢性降压药可抑制小牛海马体中福斯高林刺激的腺苷酸环化酶活性。
Br J Pharmacol. 1988 Nov;95(3):975-85. doi: 10.1111/j.1476-5381.1988.tb11728.x.
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Inhibition of forskolin-stimulated adenylate cyclase activity by 5-HT receptor agonists.5-羟色胺受体激动剂对福斯高林刺激的腺苷酸环化酶活性的抑制作用。
Eur J Pharmacol. 1985 Dec 17;119(3):231-4. doi: 10.1016/0014-2999(85)90300-0.

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Autoradiographic characterisation and localisation of 5-HT1D compared to 5-HT1B binding sites in rat brain.大鼠脑中5-HT1D与5-HT1B结合位点的放射自显影表征及定位
Naunyn Schmiedebergs Arch Pharmacol. 1993 Jun;347(6):569-82. doi: 10.1007/BF00166939.
7
The 5-hydroxytryptamine 5-HT1D receptor subtype is negatively coupled to adenylate cyclase in calf substantia nigra.5-羟色胺5-HT1D受体亚型在小牛黑质中与腺苷酸环化酶呈负偶联。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Jun;337(6):602-8. doi: 10.1007/BF00175784.
8
Centrally acting hypotensive agents with affinity for 5-HT1A binding sites inhibit forskolin-stimulated adenylate cyclase activity in calf hippocampus.对5-HT1A结合位点具有亲和力的中枢性降压药可抑制小牛海马体中福斯高林刺激的腺苷酸环化酶活性。
Br J Pharmacol. 1988 Nov;95(3):975-85. doi: 10.1111/j.1476-5381.1988.tb11728.x.
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Interaction of arylpiperazines with 5-HT1A, 5-HT1B, 5-HT1C and 5-HT1D receptors: do discriminatory 5-HT1B receptor ligands exist?芳基哌嗪与5-HT1A、5-HT1B、5-HT1C和5-HT1D受体的相互作用：是否存在具有选择性的5-HT1B受体配体？
Naunyn Schmiedebergs Arch Pharmacol. 1989 Jun;339(6):675-83. doi: 10.1007/BF00168661.
10
5-Hydroxytryptamine 5-HT1B and 5-HT1D receptors mediating inhibition of adenylate cyclase activity. Pharmacological comparison with special reference to the effects of yohimbine, rauwolscine and some beta-adrenoceptor antagonists.介导腺苷酸环化酶活性抑制的5-羟色胺5-HT1B和5-HT1D受体。特别参照育亨宾、萝芙辛和某些β-肾上腺素能拮抗剂作用的药理学比较。
Naunyn Schmiedebergs Arch Pharmacol. 1989 Sep;340(3):285-92. doi: 10.1007/BF00168512.