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儿茶酚胺可使正常大鼠和门静脉高压大鼠的门静脉和肠系膜静脉舒张。

Catecholamines relax portal and mesenteric veins from normal and portal hypertensive rats.

作者信息

Kaumann A J, Groszmann R J

机构信息

Veterans Administration Medical Center, West Haven 06516.

出版信息

Am J Physiol. 1989 Dec;257(6 Pt 1):G977-81. doi: 10.1152/ajpgi.1989.257.6.G977.

Abstract

The relaxation by catecholamines of superior mesenteric veins and portal veins, precontracted by 65 mM KCl, was studied after a 2-h exposure to phenoxybenzamine. The veins were obtained from portal-hypertensive and sham-operated rats. The beta 2-selective antagonist ICI 118551 attenuated the relaxation caused by epinephrine and isoproterenol but did not change the relaxation caused by norepinephrine in superior mesenteric veins. The beta 1-specific antagonist CGP 20712A reduced the relaxation caused by norepinephrine but only marginally attenuated those caused by epinephrine and isoproterenol in superior mesenteric veins. The combination of ICI 118551 and CGP 20712A abolished the relaxation caused by the catecholamines in superior mesenteric veins. The relaxation caused by norepinephrine, epinephrine, and isoproterenol was markedly reduced by ICI 118551 in portal veins. The pattern of antagonism was similar in veins from portal-hypertensive and sham-operated rats. The results suggest that both beta 1- and beta 2-adrenoceptors mediate relaxation induced by catecholamines in superior mesenteric veins. Relaxation of portal veins appears to be mediated mostly by beta 2-adrenoceptors.

摘要

在暴露于酚苄明2小时后,研究了儿茶酚胺对由65 mM氯化钾预收缩的肠系膜上静脉和门静脉的舒张作用。这些静脉取自门静脉高压大鼠和假手术大鼠。β2选择性拮抗剂ICI 118551减弱了肾上腺素和异丙肾上腺素引起的舒张,但不改变肠系膜上静脉中去甲肾上腺素引起的舒张。β1特异性拮抗剂CGP 20712A减少了去甲肾上腺素引起的舒张,但仅轻微减弱了肠系膜上静脉中肾上腺素和异丙肾上腺素引起的舒张。ICI 118551和CGP 20712A的组合消除了肠系膜上静脉中儿茶酚胺引起的舒张。ICI 118551显著降低了门静脉中去甲肾上腺素、肾上腺素和异丙肾上腺素引起的舒张。门静脉高压大鼠和假手术大鼠静脉中的拮抗模式相似。结果表明,β1和β2肾上腺素能受体均介导儿茶酚胺在肠系膜上静脉中诱导的舒张。门静脉的舒张似乎主要由β2肾上腺素能受体介导。

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