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肾上腺素对猪皮肤腺苷酸环化酶的体内激活作用及随后的激活不应性。

Epinephrine activation of pig skin adenylate cyclase in vivo and subsequent refractoriness to activation.

作者信息

Iizuka H, Adachi K, Halprin K M, Levine V

出版信息

J Invest Dermatol. 1978 Mar;70(3):119-22. doi: 10.1111/1523-1747.ep12258523.

Abstract

Epinephrine injected intradermally activated pig skin adenylate cyclase and increased the epidermal cyclic AMP level in vivo. This biphasic response reached a maximum in 5 min and gradually decreased thereafter. The simultaneous injection of a cyclic AMP phosphodiesterase inhibitor, isobutyl methyl xanthin (IBMX) potentiated the increase. The simultaneous injection of a specific beta-adrenergic receptor inhibitor, propranolol, inhibited this accumulation of cyclic AMP. After the first activation by epinephrine in vivo, there was a marked refractoriness of the skin (epidermal) adenylate cyclase to subsequent epinephrine stimulation vivo and in vitro. This refractoriness was specific for catecholamine stimulation as responses to histamine were normal. Recovery from refractoriness started at 48 hr and was completed at 1 week after the injection of epinephrine.

摘要

皮内注射肾上腺素可激活猪皮肤腺苷酸环化酶,并在体内提高表皮环磷酸腺苷(cAMP)水平。这种双相反应在5分钟时达到最大值,此后逐渐下降。同时注射环磷酸腺苷磷酸二酯酶抑制剂异丁基甲基黄嘌呤(IBMX)可增强这种增加。同时注射特异性β-肾上腺素能受体抑制剂普萘洛尔可抑制环磷酸腺苷的这种积累。在体内首次被肾上腺素激活后,皮肤(表皮)腺苷酸环化酶对随后体内和体外的肾上腺素刺激表现出明显的不应性。这种不应性对儿茶酚胺刺激具有特异性,因为对组胺的反应正常。不应性在注射肾上腺素后48小时开始恢复,1周后完成。

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