Schorderet M, Grosso A, de Sousa R C
Mol Cell Endocrinol. 1978 Jun;11(1):105-16. doi: 10.1016/0303-7207(78)90036-9.
Direct measurements of cyclic AMP were performed in the isolated epithelium of frog skin. Phosphodiesterase inhibitors (methylxanthines, papaverine) and activators of adenylyl cyclase (oxytocin, catecholamines) significantly increased the cyclic AMP content. Propranolol completely blocked the generation of cAMP induced by beta-adrenergic agonists but had little or no effect on that induced by oxytocin. Phentolamine enhanced the cAMP production by adrenalin and noradrenalin. At supramaximal concentrations, oxytocin and isoproterenol produced similar increments in cAMP, while exposure to both agents roughly doubled the increase in cAMP. The results suggest the presence of independent receptors for oxytocin and catecholamines in frog skin, with additive effects on cAMP generation.
在蛙皮分离上皮中进行了环磷酸腺苷(cAMP)的直接测量。磷酸二酯酶抑制剂(甲基黄嘌呤、罂粟碱)和腺苷酸环化酶激活剂(催产素、儿茶酚胺)显著增加了cAMP含量。普萘洛尔完全阻断了β-肾上腺素能激动剂诱导的cAMP生成,但对催产素诱导的cAMP生成几乎没有影响。酚妥拉明增强了肾上腺素和去甲肾上腺素的cAMP生成。在超最大浓度下,催产素和异丙肾上腺素使cAMP产生相似的增加,而同时暴露于这两种药物时,cAMP的增加大致翻倍。结果表明蛙皮中存在催产素和儿茶酚胺的独立受体,对cAMP生成具有相加作用。