Huang Hai-Shan, Han Xiang-Hua, Hwang Bang-Yeon, Park Jae-In, Yoo Se-Kuel, Choi Hyun-Sook, Lim Sung-Cil, Lee Myung-Koo
College of Pharmacy and Research Center for Bioresource and Health, Chungbuk National University, Cheongju 361-763, South Korea.
J Asian Nat Prod Res. 2009 Oct;11(10):867-75. doi: 10.1080/10286020903193094.
The effects of catalponol (1) on dopamine biosynthesis and L-DOPA-induced cytotoxicity in PC12 cells were investigated. Catalponol at concentration ranges of 1-5 microM increased the intracellular levels of dopamine at 12-48 h. Catalponol at concentrations of up to 10 microM did not alter cell viability. Tyrosine hydroxylase (TH) activity was enhanced by 1 at 3 microM in a time-dependent manner, but aromatic L-amino acid decarboxylase activity was not. Catalponol also increased the intracellular levels of cyclic AMP and TH phosphorylation. In addition, catalponol at 3 microM associated with L-DOPA (20-50 microM) further enhanced the increases in dopamine levels induced by L-DOPA (50-100 microM) at 24 h. Catalponol at 2-5 microM inhibited L-DOPA (100-200 microM)-induced cytotoxicity at 48 h. These results suggest that 1 enhanced dopamine biosynthesis by inducing TH activity and protected against L-DOPA-induced cytotoxicity in PC12 cells, which was mediated by the increased levels of cyclic AMP.
研究了梓醇(1)对PC12细胞中多巴胺生物合成及左旋多巴(L-DOPA)诱导的细胞毒性的影响。浓度范围为1-5微摩尔的梓醇在12-48小时内增加了细胞内多巴胺水平。浓度高达10微摩尔的梓醇未改变细胞活力。3微摩尔的梓醇(1)以时间依赖性方式增强了酪氨酸羟化酶(TH)的活性,但未增强芳香族L-氨基酸脱羧酶的活性。梓醇还增加了细胞内环磷酸腺苷(cAMP)水平和TH磷酸化。此外,3微摩尔的梓醇与L-DOPA(20-50微摩尔)联合使用,在24小时时进一步增强了L-DOPA(50-100微摩尔)诱导的多巴胺水平升高。2-5微摩尔的梓醇在48小时时抑制了L-DOPA(100-200微摩尔)诱导的细胞毒性。这些结果表明,梓醇(1)通过诱导TH活性增强了多巴胺生物合成,并在PC12细胞中保护细胞免受L-DOPA诱导的细胞毒性,这是由cAMP水平升高介导的。