Yang Ting-Ting, Tsao Chiung-Wen, Li Jin-Shiou, Wu Hung-Tsung, Hsu Chao-Tien, Cheng Juei-Tang
Department of Medicine, College of Medicine, China Medical University, Taichung City 40401, Taiwan.
Neurosci Lett. 2007 Oct 9;426(1):45-8. doi: 10.1016/j.neulet.2007.08.037. Epub 2007 Aug 24.
Pituitary adenylate cyclase-activating polypeptide (PACAP) is an endogenous neuropeptide observed in adrenal gland and sympathetic ganglia to regulate catecholamine synthesis and release. Both PACAP and glucocorticoid showed the activity to elevate catecholamine level through the stimulation of biosynthesis. However, the relationship of glucocorticoid and PACAP for this action is still unclear. Thus, alterations of gene expression, dopamine (DA) content, and cell proliferation in rat pheochromocytoma PC12 cells are employed as indicators to clarify this relationship in the present study. From the analysis of RT-PCR, the mRNA level of PACAP was observed to be raised by dexamethasone (DEX) and this action was blocked in cells treated with RU486 (mifepristone), a glucocorticoid receptor (GR) antagonist, or actinomycin D, a transcriptional inhibitor. An increase of DA content by HPLC analysis and/or cell proliferation identified by MTT assay by DEX was also observed which could be inhibited by PACAP (6-38) at concentration sufficient to block PACAP type 1 (PAC1) receptor. These results suggest that PACAP is involved in DEX-induced DA biosynthesis and cell proliferation in PC12 cells.
垂体腺苷酸环化酶激活多肽(PACAP)是一种在内分泌腺和交感神经节中发现的内源性神经肽,可调节儿茶酚胺的合成与释放。PACAP和糖皮质激素都具有通过刺激生物合成来提高儿茶酚胺水平的活性。然而,糖皮质激素与PACAP在此作用中的关系仍不清楚。因此,本研究采用大鼠嗜铬细胞瘤PC12细胞中基因表达的改变、多巴胺(DA)含量及细胞增殖作为指标来阐明这种关系。通过逆转录-聚合酶链反应(RT-PCR)分析发现,地塞米松(DEX)可使PACAP的mRNA水平升高,而这种作用在用糖皮质激素受体(GR)拮抗剂RU486(米非司酮)或转录抑制剂放线菌素D处理的细胞中受到阻断。通过高效液相色谱(HPLC)分析还观察到DEX可使DA含量增加,和/或通过MTT法检测发现DEX可促进细胞增殖,而在足以阻断1型PACAP(PAC1)受体的浓度下,PACAP(6-38)可抑制上述作用。这些结果表明,PACAP参与了DEX诱导的PC12细胞中DA生物合成及细胞增殖过程。