胶质细胞源性神经生长因子
多巴胺能
酪氨酸羟化酶
化学
药理学
细胞内
活力测定
碘化丙啶
细胞生物学
神经营养因子
细胞凋亡
生物
内分泌学
多巴胺
程序性细胞死亡
生物化学
受体
作者
Shima Tavakol,Elham Hoveizi,Behnaz Tavakol,Fereshteh Azedi,Somayeh Ebrahimi‐Barough,Peyman Keyhanvar,Mohammad Taghi Joghataei
摘要
Multiple sclerosis (MS) patients should take medication such as fingolimod (FTY-720) for a long time, hence pharmaceutical effects on other neural cells such as dopaminergic cells are important. Dopaminergic cell line, BE(2)-M17, was treated by FTY-720 and then cell viability and genes involve in neurosurvival were investigated. It was disclosed that FTY-720 significantly stimulates Bcl2 overexpression. Whereas, it decreased intracellular reactive oxygen species production and cell membrane damage of dopaminergic cells. The increase in Bcl2/Bax ratio increased the cell metabolic activity and decreased propidium iodide-positive cells. Besides, FTY-720 induced the overexpression of CACNA1C, nNOS gene, and nitric oxide production. However, FTY-720 induced GABARA1 overexpression and eventually it could overcame to the cytotoxic effect of intracellular calcium. This cascade led to tyrosine hydroxylase and BDNF genes overexpression whereas FTY-720 did not change GDNF concentration in BE(2)-M17 cells. Concluding, it might be said that taking FTY-720 in MS patients did not induce adverse effect on dopaminergic cells.
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