Lovenberg T W, Nichols D E, Nestler E J, Roth R H, Mailman R B
Department of Pharmacology, University of North Carolina School of Medicine, Chapel Hill 27599.
Brain Res. 1991 Aug 9;556(1):101-7. doi: 10.1016/0006-8993(91)90552-7.
D1 dopamine receptors on NS20Y neuroblastoma cells stimulate adenylate cyclase activity, whereas muscarinic receptors on the same cells negatively regulate adenylate cyclase. To determine the mechanisms which underlie these processes, cyclic AMP accumulation was measured in intact cells following either cholera or pertussis toxin treatment. Pretreatment with pertussis toxin (100 ng/ml), which ribosylated greater than 95% of inhibitory quinine nucleotide binding protein (Gi), caused the complete loss of muscarinic induced inhibition. Conversely, pertussis toxin did not affect the ability of dihydrexidine (1 microM, a full efficacy D1 agonist), PGE1 (100 nM), or forskolin (1 microM, a direct activator) to stimulate cAMP accumulation. Both the dihydrexidine-induced stimulation and the carbachol-induced inhibition of cyclic AMP accumulation were unaffected by either removal of extracellular calcium, or increased intracellular calcium caused by the addition of the calcium ionophore A23187. Cholera toxin dose- and time-dependently induced large accumulations of cAMP. At low cholera toxin concentrations, the effects of dihydrexidine (300 nM) were additive with those of cholera toxin. At cholera toxin concentrations greater than 100 ng/ml, dihydrexidine became ineffective in stimulating further cAMP synthesis. Conversely, forskolin (1 microM) still caused marked increases in cAMP accumulation after all cholera toxin treatments. Dihydrexidine-stimulated cAMP accumulation was additive with forskolin-stimulated cAMP accumulation at low forskolin concentrations (10 nM-3 microM), but synergistic at high concentrations (3-100 microM). Additionally, forskolin was much more potent after cholera toxin treatment, suggesting that an activated stimulatory guanine nucleotide binding protein (Gs) may be required for full activation of adenylate cyclase by forskolin in this cell type.(ABSTRACT TRUNCATED AT 250 WORDS)
NS20Y神经母细胞瘤细胞上的D1多巴胺受体可刺激腺苷酸环化酶活性,而同一细胞上的毒蕈碱受体则对腺苷酸环化酶起负调节作用。为确定这些过程背后的机制,在霍乱毒素或百日咳毒素处理后的完整细胞中测量了环磷酸腺苷(cAMP)的积累。用百日咳毒素(100 ng/ml)预处理,该毒素使超过95%的抑制性喹啉核苷酸结合蛋白(Gi)发生核糖基化,导致毒蕈碱诱导的抑制作用完全丧失。相反,百日咳毒素不影响二氢麦角隐亭(1 μM,一种完全有效的D1激动剂)、前列腺素E1(100 nM)或福斯可林(1 μM,一种直接激活剂)刺激cAMP积累的能力。无论是去除细胞外钙,还是添加钙离子载体A23187导致细胞内钙增加,二氢麦角隐亭诱导的cAMP积累刺激和卡巴胆碱诱导的抑制作用均不受影响。霍乱毒素剂量和时间依赖性地诱导cAMP大量积累。在低霍乱毒素浓度下,二氢麦角隐亭(300 nM)的作用与霍乱毒素的作用相加。在霍乱毒素浓度大于100 ng/ml时,二氢麦角隐亭刺激进一步cAMP合成的作用失效。相反,在所有霍乱毒素处理后,福斯可林(1 μM)仍能使cAMP积累显著增加。在低福斯可林浓度(10 nM - 3 μM)下,二氢麦角隐亭刺激的cAMP积累与福斯可林刺激的cAMP积累相加,但在高浓度(3 - 100 μM)下具有协同作用。此外,霍乱毒素处理后福斯可林的效力更强,这表明在这种细胞类型中,可能需要激活的刺激性鸟嘌呤核苷酸结合蛋白(Gs)才能使福斯可林完全激活腺苷酸环化酶。(摘要截短于250字)