Ferretti M E, Borasio P G, Biondi C, Capuzzo A, Fabbri E, Pareschi M C
Institute of General Physiology, University of Ferrara, Italy.
Neurochem Res. 1988 Sep;13(9):797-802. doi: 10.1007/BF00970745.
Crude membrane fractions, obtained from superior cervical ganglia of normal and sympathectomized guinea-pigs, have been used to investigate the role of prostaglandin E2 and D-ala2-met-enkephalinamide in the modulation of ganglionic adenylate cyclase as well as their functional interrelationship. In ganglia from normal animals the enzyme activity was stimulated and inhibited, respectively, by the prostaglandin (10(-4)M) and by the opiate pentapeptide (10(-4)M), while little or no effects were observed in denervated preparations. When the two substances were tested in combination, a supra-additive stimulation of adenylate cyclase activity was obtained both in normal and denervated ganglia. In the latter preparation the opiate increased prostaglandin E2 specific binding, suggesting that the mechanism of supra-additivity could involve interactions at receptors level. Furthermore, the supra-additive stimulation of adenylate cyclase activity by the combination of the two drugs was obtained in a narrow range of concentrations since at low prostaglandin E2 doses (10(-7)-10(-6)M) or at very high doses of the opiate (10(-3)M), only the inhibitory effect of D-ala2-met-enkephalinamide was evidenced.
从正常和交感神经切除的豚鼠颈上神经节获得的粗制膜组分,已被用于研究前列腺素E2和D-丙氨酸2-甲硫氨酸脑啡肽酰胺在神经节腺苷酸环化酶调节中的作用及其功能相互关系。在正常动物的神经节中,该酶活性分别受到前列腺素(10⁻⁴M)和阿片五肽(10⁻⁴M)的刺激和抑制,而在去神经支配的制剂中几乎没有观察到影响。当两种物质联合测试时,在正常和去神经支配的神经节中均获得了腺苷酸环化酶活性的超相加刺激。在后者的制剂中,阿片类药物增加了前列腺素E2的特异性结合,表明超相加的机制可能涉及受体水平的相互作用。此外,两种药物联合对腺苷酸环化酶活性的超相加刺激在很窄的浓度范围内获得,因为在低剂量前列腺素E2(10⁻⁷ - 10⁻⁶M)或非常高剂量的阿片类药物(10⁻³M)时,仅证明了D-丙氨酸2-甲硫氨酸脑啡肽酰胺的抑制作用。