Ferretti M E, Borasio P G, Biondi C, Campi A L, Pareschi M C, Portolan A
Institute of General Physiology, University of Ferrara, Italy.
Neurochem Res. 1991 May;16(5):583-9. doi: 10.1007/BF00974878.
The effects of Mn2+ and calmodulin were studied on the basal and agonist-modulated adenylate cyclase activity of the guinea pig superior cervical ganglion. The divalent cation strongly stimulates the basal and agonist-modulated enzyme in a concentration-dependent manner. Moreover, in the presence of Mn2+ the inhibitory effects of "high" GTP concentrations and of D-Ala2-Met-enkephalinamide on adenylate cyclase are eliminated, while the stimulation exerted by prostaglandin E2 and the supra-additive activation of the enzyme by the combination of the two drugs are unaffected. In EGTA-washed, calmodulin-depleted membrane preparations, Mn2+ still activates the cyclase but the enkephalin inhibition and the superactivation of the enzyme induced by the combination of opiate and prostaglandin are lost, both in the absence and in the presence of the cation. Reconstituting the depleted membranes with exogenous Ca2+/calmodulin fully restored the enzyme responsivity to the combination and, partially, to the enkephalin. The findings suggest the existence in the guinea pig superior cervical ganglion of both the calmodulin-sensitive and differently regulated calmodulin-insensitive adenylate cyclase.
研究了Mn2+和钙调蛋白对豚鼠颈上神经节基础状态及激动剂调节的腺苷酸环化酶活性的影响。二价阳离子以浓度依赖的方式强烈刺激基础状态及激动剂调节的酶。此外,在Mn2+存在的情况下,“高”浓度GTP和D - Ala2 - Met - 脑啡肽酰胺对腺苷酸环化酶的抑制作用被消除,而前列腺素E2的刺激作用以及两种药物联合对该酶的超加性激活作用不受影响。在经EGTA洗涤、钙调蛋白耗尽的膜制剂中,Mn2+仍能激活环化酶,但无论是在无阳离子还是有阳离子存在的情况下,脑啡肽的抑制作用以及阿片类药物与前列腺素联合诱导的酶的超激活作用均丧失。用外源性Ca2+/钙调蛋白重建耗尽的膜可完全恢复该酶对联合药物的反应性,并部分恢复对脑啡肽的反应性。这些发现提示豚鼠颈上神经节中存在钙调蛋白敏感且调节方式不同的钙调蛋白不敏感的腺苷酸环化酶。