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α1和α2肾上腺素能受体的激活抑制兔肾动脉去甲肾上腺素的释放:百日咳毒素和N-乙基马来酰亚胺的作用。

Activation of alpha 1- and alpha 2-adrenoceptors inhibits noradrenaline release in rabbit renal arteries: effects of pertussis toxin and N-ethylmaleimide.

作者信息

Rump L C, Wolk V, Ruff G, Schollmeyer P

机构信息

Universitätsklinik Freiburg, Innere Medizin IV, Germany.

出版信息

J Auton Pharmacol. 1992 Apr;12(2):97-108. doi: 10.1111/j.1474-8673.1992.tb00367.x.

Abstract
  1. The effects of selective alpha 1- and alpha 2-adrenoceptor agonists and antagonists on the stimulation-induced (S-I) outflow of radioactivity at 2 Hz were investigated in superfused rabbit renal arteries incubated with [3H]-noradrenaline. 2. The alpha 1-adrenoceptor agonist methoxamine (10 microM) inhibited S-I outflow of radioactivity and this effect was abolished by the alpha 1-adrenoceptor antagonist prazosin (0.1 microM) but not by the alpha 2-adrenoceptor antagonist rauwolscine (1 microM). Neither the prostaglandin synthesis inhibitor indomethacin (10 microM) nor the adenosine receptor antagonist 8-phenyl-theophylline (1 microM) prevented the inhibitory effect of methoxamine. 3. The alpha 2-adrenoceptor agonists clonidine (0.1 microM) and UK 14304 (0.1 microM) both inhibited S-I outflow of radioactivity. The inhibitory effect of clonidine was blocked by rauwolscine but not by prazosin. The inhibitory effect of UK 14304 was markedly reduced by rauwolscine. 4. Prazosin (0.1 microM) alone did not enhance the S-I outflow of radioactivity at 2 Hz and slightly enhanced S-I outflow at 4 Hz. Rauwolscine (1 microM) alone markedly enhanced S-I outflow of radioactivity at 2 and 4 Hz. 5. Pretreatment of the arteries with pertussis toxin (1 microgram ml-1) did not significantly alter the inhibitory effects of methoxamine or UK 14304 or the potentiation by rauwolscine. However, pretreatment of the arteries with a higher concentration of pertussis toxin (5 micrograms ml-1) prevented the inhibitory effect of methoxamine but still did not affect the responses to UK 14304 and rauwolscine. 6. Pretreatment of the arteries with N-ethylmaleimide (NEM, 10 microM) for 30 min did not alter the inhibitory effect of methoxamine but markedly attenuated the inhibitory effect of UK 14304 and the facilitatory effect of rauwolscine. 7. The results suggest that both alpha 1- and alpha 2-adrenoceptors take part in the modulation of noradrenaline release from sympathetic nerves in rabbit renal arteries. Alpha 1-adrenoceptor mediated inhibition may be coupled to G-proteins which are pertussis toxin sensitive and alpha 2-adrenoceptor mediated inhibition to G-proteins which are NEM-sensitive.
摘要
  1. 在与[3H]-去甲肾上腺素一起孵育的离体兔肾动脉中,研究了选择性α1和α2肾上腺素能受体激动剂及拮抗剂对2Hz刺激诱导(S-I)的放射性流出的影响。2. α1肾上腺素能受体激动剂甲氧明(10μM)抑制了放射性的S-I流出,这种作用被α1肾上腺素能受体拮抗剂哌唑嗪(0.1μM)消除,但未被α2肾上腺素能受体拮抗剂育亨宾(1μM)消除。前列腺素合成抑制剂吲哚美辛(10μM)和腺苷受体拮抗剂8-苯基茶碱(1μM)均未阻止甲氧明的抑制作用。3. α2肾上腺素能受体激动剂可乐定(0.1μM)和UK 14304(0.1μM)均抑制了放射性的S-I流出。可乐定的抑制作用被育亨宾阻断,但未被哌唑嗪阻断。UK 14304的抑制作用被育亨宾显著减弱。4. 单独使用哌唑嗪(0.1μM)在2Hz时并未增强放射性的S-I流出,而在4Hz时略有增强。单独使用育亨宾(1μM)在2Hz和4Hz时均显著增强了放射性的S-I流出。5. 用百日咳毒素(1μg/ml)预处理动脉并未显著改变甲氧明或UK 14304的抑制作用或育亨宾的增强作用。然而,用较高浓度的百日咳毒素(5μg/ml)预处理动脉可阻止甲氧明的抑制作用,但仍不影响对UK 14304和育亨宾的反应。6. 用N-乙基马来酰亚胺(NEM,10μM)预处理动脉30分钟并未改变甲氧明的抑制作用,但显著减弱了UK 14304的抑制作用和育亨宾的促进作用。7. 结果表明,α1和α2肾上腺素能受体均参与兔肾动脉交感神经去甲肾上腺素释放的调节。α1肾上腺素能受体介导的抑制可能与对百日咳毒素敏感的G蛋白偶联,而α2肾上腺素能受体介导的抑制与对NEM敏感的G蛋白偶联。

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