Hansson E, Simonsson P, Alling C
Institute of Neurobiology, University of Göteborg, Sweden.
Neuropharmacology. 1990 Jun;29(6):591-8. doi: 10.1016/0028-3908(90)90072-y.
Astroglial cells in primary culture possess receptors with cyclic AMP and inositol phosphates (IP) as second messengers. The beta-receptor agonist, isoproterenol induces an increase in the accumulation of cyclic AMP, the alpha 2-receptor agonist clonidine inhibits the isoproterenol-induced accumulation of cyclic AMP, while the alpha 1-receptor agonist phenylephrine acts only on the inositol phosphate system. 5-Hydroxytryptamine (5-HT) stimulates, the formation of inositol phosphate, while isoproterenol and clonidine per se do not affect the inositol phosphate system. In the present paper the possibility of interactions between the cyclic AMP and the inositol phosphate transduction systems were investigated. In the presence of 10(-5) M 5-HT, in itself ineffective on the formation of cyclic AMP, isoproterenol stimulated the accumulation of cyclic AMP far more than in the absence of 5-HT. The potentiation was blocked by the 5-HT2 receptor antagonist ketanserin. On the other hand, there were no indications for a beta-receptor influence on the 5-HT-induced inositol phosphate formation. Stimulation of the alpha 2-receptor did not induce accumulation of inositol phosphate but significantly potentiated 5-HT2-receptor transduction, as measured by hydrolysis of phosphoinositide and formation of inositol phosphate. Stimulation by 5-HT also increased the formation of inositol phosphate after adrenergic stimulation and this effect was found to be synergistic at certain concentrations of adrenergic agonists. In addition, there was a statistically significant accumulation of cyclic AMP in the presence of both 5-HT and phenylephrine, none of which stimulated cyclic AMP alone. The results suggest specific interactions between the cyclic AMP and inositol phosphate systems on cultured astroglial cells.
原代培养的星形胶质细胞具有以环磷酸腺苷(cAMP)和肌醇磷酸(IP)作为第二信使的受体。β受体激动剂异丙肾上腺素可诱导cAMP积累增加,α2受体激动剂可乐定抑制异丙肾上腺素诱导的cAMP积累,而α1受体激动剂去氧肾上腺素仅作用于肌醇磷酸系统。5-羟色胺(5-HT)刺激肌醇磷酸的形成,而异丙肾上腺素和可乐定本身不影响肌醇磷酸系统。在本文中,研究了cAMP和肌醇磷酸转导系统之间相互作用的可能性。在存在10(-5)M 5-HT的情况下,5-HT本身对cAMP的形成无效,但异丙肾上腺素刺激cAMP积累的程度远超过不存在5-HT时。这种增强作用被5-HT2受体拮抗剂酮色林阻断。另一方面,没有迹象表明β受体对5-HT诱导的肌醇磷酸形成有影响。刺激α2受体不会诱导肌醇磷酸积累,但如通过磷酸肌醇水解和肌醇磷酸形成所测定的,可显著增强5-HT2受体转导。5-HT刺激还增加了肾上腺素能刺激后肌醇磷酸的形成,并且发现在某些浓度的肾上腺素能激动剂作用下这种效应具有协同性。此外,在同时存在5-HT和去氧肾上腺素的情况下,有统计学显著的cAMP积累,而它们单独均不刺激cAMP。结果表明培养的星形胶质细胞上cAMP和肌醇磷酸系统之间存在特异性相互作用。