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尼古丁会抑制海马体和纹状体中的乙酰胆碱酯酶活性,并对成年神经元的增殖和成熟表现出双重作用。

Nicotine inhibits hippocampal and striatal acetylcholinesterase activities, and demonstrates dual action on adult neuronal proliferation and maturation.

作者信息

Ijomone Omamuyovwi M, Nwoha Polycarp U

机构信息

Department of Human Anatomy, Cross River University of Technology, Okuku Campus, Cross River, Nigeria; Department of Anatomy and Cell Biology, Obafemi Awolowo University, Ile-Ife, Osun, Nigeria.

Department of Anatomy and Cell Biology, Obafemi Awolowo University, Ile-Ife, Osun, Nigeria.

出版信息

Pathophysiology. 2015 Dec;22(4):231-9. doi: 10.1016/j.pathophys.2015.09.002. Epub 2015 Sep 25.

Abstract

AIM

The present study investigated the effects of nicotine on acetylcholinesterase (AChE) activities in the hippocampus and striatum; and on immunoreactivity of certain neurogenic markers in the dentate gyrus (DG) of the hippocampus.

METHODS

Male rats were given daily subcutaneous injections of nicotine at doses of 0.25, 2 or 4mg/kg body weight for 28 days. Animals were euthanized by cervical dislocation at the end of administration. Brains were excised and processed for histochemical demonstration of AChE and immunohistochemical studies of Ki67, GFAP and NSE.

RESULTS

There was significant decrease (P<0.001) in AChE positive cells in the hippocampus and striatum following 2 and 4mg/kg nicotine but not at 0.25mg/kg. Nicotine treatment at 0.25 and 4mg/kg significantly decrease (P<0.05) immunoreactivity of Ki67 and NSE in DG. Contrastingly, 2mg/kg nicotine did not alter Ki67 immunoreactivity but rather significantly increased (P<0.05) NSE immunoreactivity in DG compared to control.

CONCLUSION

This study suggests that nicotine may inhibit AChE activities in the brain, thereby having a direct or indirect influence on prevention of central acetylcholine degradation, as well as either improve or retard maturation adult born neurons in DG, at different doses.

摘要

目的

本研究调查了尼古丁对海马体和纹状体中乙酰胆碱酯酶(AChE)活性的影响;以及对海马齿状回(DG)中某些神经源性标志物免疫反应性的影响。

方法

雄性大鼠每天皮下注射剂量为0.25、2或4mg/kg体重的尼古丁,持续28天。给药结束时通过颈椎脱臼法对动物实施安乐死。取出大脑并进行处理,以进行AChE的组织化学检测以及Ki67、GFAP和NSE的免疫组织化学研究。

结果

2mg/kg和4mg/kg尼古丁处理后,海马体和纹状体中AChE阳性细胞显著减少(P<0.001),但0.25mg/kg剂量时未出现此现象。0.25mg/kg和4mg/kg尼古丁处理显著降低(P<0.05)DG中Ki67和NSE的免疫反应性。相反,与对照组相比,2mg/kg尼古丁并未改变DG中Ki67的免疫反应性,反而显著增加(P<0.05)了DG中NSE的免疫反应性。

结论

本研究表明,尼古丁可能抑制大脑中的AChE活性,从而对预防中枢乙酰胆碱降解产生直接或间接影响,并且在不同剂量下,要么促进要么延缓DG中成年新生神经元的成熟。

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