Schimmel R J
Biochim Biophys Acta. 1980 Apr 17;629(1):83-94. doi: 10.1016/0304-4165(80)90267-6.
In the presence of either methyl xanthines or adenosine deaminase, isoproterenol elicited large dramatic increases in accumulation of cyclic AMPP. In contrast, cyclic AMP accumulation in response to epinephrine or norepinephrine was not potentiated by either methyl xanthines or by adenosine deaminase. Blocking the alpha adrenergic activity of norepinephrine and epinephrine with phentolamine established synergism between these catecholamines and methyl xanthines and adenosine deaminase. The activity of the particulate phosphodiesterase was not influenced by norepinephrine suggesting that the lack of synergism between the catecholamines norepinephrine and epinephrine and methyl xanthines is unrelated to this enzyme. The data are interpreted to suggest that the alpha adrenergic activity of catecholamines prevents the potentiation of cyclic AMP accumulation that occurs when the action of endogenously produced adenosine is interfered with, either by its degradation with adenosine deaminase or by receptor blockade with methyl xanthine. Because a major action of adenosine on fat cells is to inhibit adenylate cyclase it is suggested that alpha adrenergic receptor activation limits the extent to which the enzyme adenylate cyclase can be activated in a fashion similar to that of adenosine.
在存在甲基黄嘌呤或腺苷脱氨酶的情况下,异丙肾上腺素可引起环AMPP积累大幅显著增加。相比之下,甲基黄嘌呤或腺苷脱氨酶均未增强肾上腺素或去甲肾上腺素引起的环AMP积累。用酚妥拉明阻断去甲肾上腺素和肾上腺素的α肾上腺素能活性,证实了这些儿茶酚胺与甲基黄嘌呤和腺苷脱氨酶之间存在协同作用。颗粒性磷酸二酯酶的活性不受去甲肾上腺素影响,这表明儿茶酚胺去甲肾上腺素和肾上腺素与甲基黄嘌呤之间缺乏协同作用与该酶无关。这些数据被解释为表明,儿茶酚胺的α肾上腺素能活性可防止环AMP积累的增强,而环AMP积累增强发生在内源性产生的腺苷的作用被干扰时,这种干扰要么是通过腺苷脱氨酶对其降解,要么是通过甲基黄嘌呤对受体的阻断。由于腺苷对脂肪细胞的主要作用是抑制腺苷酸环化酶,因此有人提出,α肾上腺素能受体激活限制了腺苷酸环化酶以类似于腺苷的方式被激活的程度。