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尼古丁可使PC12细胞免受因神经生长因子剥夺而导致的死亡。

Nicotine rescues PC12 cells from death induced by nerve growth factor deprivation.

作者信息

Yamashita H, Nakamura S

机构信息

Third Department of Internal Medicine, Hiroshima University School of Medicine, Japan.

出版信息

Neurosci Lett. 1996 Aug 2;213(2):145-7. doi: 10.1016/0304-3940(96)12829-9.

Abstract

We examined the protective effect of nicotine against neuronal cell death in the model system of serum- and nerve growth factor (NGF)-free cultures of PC12 cells. Serum deprivation induced massive death of undifferentiated PC12 cells, which was inhibited by the addition of NGF, but not by the addition nicotine (100 microM). Even after PC12 cells had been differentiated by the treatment with NGF, serum and NGF deprivation induced rapid and massive death of these cells. The addition of nicotine (1-100 microM) to the deprivation system prevented such cell death almost completely. The protective effect of nicotine was abolished by hexamethonium or mecamylamine, inhibitors of nicotinic acetylcholine (nACh) receptors. Treatment with reserpine to deplete intracellular catecholamines did not influence the effect. The results suggest that the protective effect of nicotine against neuronal cell death is exerted through nACh receptors.

摘要

我们在无血清和无神经生长因子(NGF)的PC12细胞培养模型系统中,研究了尼古丁对神经元细胞死亡的保护作用。血清剥夺诱导未分化PC12细胞大量死亡,添加NGF可抑制这种死亡,但添加尼古丁(100微摩尔)则不能。即使PC12细胞经NGF处理已分化,血清和NGF剥夺仍会诱导这些细胞迅速大量死亡。向剥夺系统中添加尼古丁(1 - 100微摩尔)几乎可完全防止这种细胞死亡。尼古丁的保护作用被烟碱型乙酰胆碱(nACh)受体抑制剂六甲铵或美加明消除。用利血平处理以耗尽细胞内儿茶酚胺并不影响该作用。结果表明,尼古丁对神经元细胞死亡的保护作用是通过nACh受体发挥的。

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