Bunn S J, Marley P D, Livett B G
Department of Biochemistry, University of Melbourne, Parkville, Victoria, Australia.
Biochem Pharmacol. 1988 Feb 1;37(3):395-9. doi: 10.1016/0006-2952(88)90205-5.
The mammalian adrenal medulla expresses a variety of both opioid peptides and opioid receptors. The function of this adrenal opioid system is, however, largely unknown. We have examined the ability of a number of opioid compounds to influence basal and muscarinic stimulated accumulation of inositol phosphates in cultured bovine chromaffin cells. Muscarine produced a dose-dependent 1.5-fold increase in total inositol phosphates. This response was sensitive to atropine inhibition. The ten opioid compounds examined were chosen because between them they possess selectivity for all of the identified opioid receptor subtypes. However, none of these opioids in the concentration range 10nM-10 microM had any significant effect on either basal or muscarinic induced total inositol phosphate accumulation. We conclude that it is unlikely that opioid peptides released from either the chromaffin cells themselves or the splanchnic nerve can modulate the inositol phosphate second messenger system within the adrenal chromaffin cells.
哺乳动物的肾上腺髓质表达多种阿片肽和阿片受体。然而,这个肾上腺阿片系统的功能在很大程度上尚不清楚。我们研究了多种阿片类化合物影响培养的牛嗜铬细胞中肌醇磷酸基础积累和毒蕈碱刺激积累的能力。毒蕈碱使总肌醇磷酸产生了剂量依赖性的1.5倍增加。这种反应对阿托品抑制敏感。所研究的十种阿片类化合物被选中是因为它们对所有已鉴定的阿片受体亚型具有选择性。然而,在10nM - 10μM浓度范围内,这些阿片类药物对基础或毒蕈碱诱导的总肌醇磷酸积累均无任何显著影响。我们得出结论,嗜铬细胞自身或内脏神经释放的阿片肽不太可能调节肾上腺嗜铬细胞内的肌醇磷酸第二信使系统。