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甲氧明对大鼠大脑皮质切片中3',5'-环磷酸腺苷生成的刺激作用:与α肾上腺素能受体的相互作用

Stimulation of adenosine 3',5'-monophosphate formation in rat cerebral cortical slices by methoxamine: interaction with an alpha adrenergic receptor.

作者信息

Skolnick P, Daly J W

出版信息

J Pharmacol Exp Ther. 1975 May;193(2):549-58.

PMID:238025
Abstract

Methoxamine elicits a rapid accumulation of adenosine 3',5'-monophosphate (cyclic AMP) in rat cerebral cortical slices with maximal effects at 100 muM. The accumulations of cyclic AMP elicited by this amine are completely blocked by the alpha adrenergic antagonists, phenoxybenzamine and dihydroergokryptine, partially blocked by the alpha antagonist, phentolamine, and unaffected by the beta blocking agent, propranolol, or by the local anesthetic, tetracaine. The magnitude of the accumulations of cyclic AMP elicited by methoxamine in cerebral cortical slices of four rat strains (F-344, ACI, BUF, and Sprague-Dawley) exhibit a strong negative correlation with spontaneous motor activity and a positive correlation with the magnitude of norepinephrine-elicited accumulations of cyclic AMP. The stimulatory interaction of methoxamine with alpha adrenergically regulated cyclic AMP-generating systems differs from the interaction of norepinephrine with alpha receptors as evidenced by the following observations: 1) the stimulatory effects of methoxamine and norepinephrine are nearly additive; 2) the stimulatory effects of methoxamine and adenosine are nearly additive, whereas the effects of norepinephrine and adenosine are much more than additive. Methoxamine, however, does not increase further the magnitude of accumulation of cyclic AMP elicited by a combination of norepinephrine and adenosine. The results are consonant with the interaction of methoxamine with alpha adrenergic receptors which are normally activated by norepinephrine only to a marginal extent. However, in the presence of adenosine, these receptors are now sensitive to activation by norepinephrine.

摘要

甲氧明可使大鼠大脑皮质切片中的3',5'-单磷酸腺苷(环磷腺苷)迅速积累,在100μM时效果最佳。这种胺引起的环磷腺苷积累被α肾上腺素能拮抗剂酚苄明和二氢麦角隐亭完全阻断,被α拮抗剂酚妥拉明部分阻断,不受β阻滞剂普萘洛尔或局部麻醉药丁卡因的影响。甲氧明在四种大鼠品系(F-344、ACI、BUF和Sprague-Dawley)的大脑皮质切片中引起的环磷腺苷积累量与自发运动活性呈强烈负相关,与去甲肾上腺素引起的环磷腺苷积累量呈正相关。甲氧明与α肾上腺素能调节的环磷腺苷生成系统的刺激相互作用不同于去甲肾上腺素与α受体的相互作用,以下观察结果证明了这一点:1)甲氧明和去甲肾上腺素的刺激作用几乎是相加的;2)甲氧明和腺苷的刺激作用几乎是相加的,而去甲肾上腺素和腺苷的作用则远不止相加。然而,甲氧明不会进一步增加去甲肾上腺素和腺苷联合引起的环磷腺苷积累量。这些结果与甲氧明与α肾上腺素能受体的相互作用一致,这些受体通常仅在很小程度上被去甲肾上腺素激活。然而,在腺苷存在的情况下,这些受体现在对去甲肾上腺素的激活敏感。

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