Idres S, Delarue C, Lefebvre H, Larcher A, Feuilloley M, Vaudry H
Groupe de Recherche en Endocrinologie Moléculaire, URA CNRS 650, Université de Rouen, Mont-Saint-Aignan, France.
J Steroid Biochem. 1989;34(1-6):547-50. doi: 10.1016/0022-4731(89)90142-8.
The mechanism of action of serotonin (5-HT) on frog adrenal cortex has been investigated in vitro using the perifusion system technique. The direct effect of 5-HT on corticosteroid secreting cells was demonstrated, using enzymatically dispersed adrenocortical cells. Melatonin and 5-HTP appeared to be less potent than 5-HT to enhance corticosteroid secretion. In contrast Trp and 5-HIAA were totally devoid of effect on steroid secretion. To investigate the type of receptor involved in the stimulatory effect of 5-HT on adrenocortical cells, adrenal slices were stimulated with 5-HT in absence or presence of various antagonists. We observed that classical antagonists of 5-HT1, 5-HT2 and 5-HT3 type receptors failed to block 5-HT-induced corticosteroid secretion in our model. These results show that 5-HT exerts a direct effect on corticosteroid-secreting cells. Our data also indicates that the type of receptor involved in the action of 5-HT in frog adrenal cortex differs from mammalian 5-HT receptors.
利用灌流系统技术在体外研究了血清素(5-羟色胺,5-HT)对青蛙肾上腺皮质的作用机制。使用酶分散的肾上腺皮质细胞,证明了5-HT对皮质类固醇分泌细胞的直接作用。褪黑素和5-羟色氨酸(5-HTP)增强皮质类固醇分泌的作用似乎比5-HT弱。相比之下,色氨酸(Trp)和5-羟吲哚乙酸(5-HIAA)对类固醇分泌完全没有影响。为了研究参与5-HT对肾上腺皮质细胞刺激作用的受体类型,在存在或不存在各种拮抗剂的情况下,用5-HT刺激肾上腺切片。我们观察到,在我们的模型中,5-HT1、5-HT2和5-HT3型受体的经典拮抗剂未能阻断5-HT诱导的皮质类固醇分泌。这些结果表明,5-HT对皮质类固醇分泌细胞有直接作用。我们的数据还表明,参与5-HT对青蛙肾上腺皮质作用的受体类型与哺乳动物的5-HT受体不同。