目的:探讨次声对成年大鼠海马齿状回颗粒细胞下层(subgranular zone,SGZ)神经干细胞增殖抑制作用的细胞学机制。方法:成年雄性Sprague-Dawley大鼠置于次声压力舱,连续暴露于16Hz、130dB次声7d(2h/d)后,给与小胶质细胞抑制剂米诺环素(50mg/kg,药物组,n=16)或等体积生理盐水(对照组,n=16),同时设立不经次声作用的正常对照组(n=16);分别于1、3、7和14d处死大鼠,利用免疫组织化学法以Iba1、OX42标记小胶质细胞,Brdu标记增殖的神经干细胞。结果:小胶质细胞在SGZ区分布较为密集;与正常对照组相比,次声暴露后3d时OX42免疫反应性明显增强、SGZ区BrdU阳性细胞数目减少最为明显(P〈0.01);米诺环素可显著改善次声暴露后BrdU阳性细胞数目的减少(P〈0.01)。结论:小胶质细胞活化参与次声抑制成年大鼠海马SGZ区神经干细胞的增殖。
Objective: To explore the cellular mechanisms underlying infrasound-induced suppression of neural stem cell proliferation in the subgranular zone (SGZ) of hippocampal dentate gyrus of adult rats. Methods: Male Sprague-Dawley rats were placed in a infrasonic chamber and exposed to 16 Hz at 130 dB infrasound for 2 h/d in consecutive 7 days. Then rats were treated with microglia inhibitor minocycline ( the drug group, 50 mg/kg, n = 16) or same volume of saline ( the control group, n = 16) intraperitoneally. The rats without infrasound exposure and drugs treatment were established as the normal control group ( n = 16). At 1,3, 7 or 14 d following infrasound exposure, the rats were sacrificed and their brain sections were subjected to immunostaining of Iba1, OX42 ( two markers for mieroglia), and BrdU ( a marker for proliferating cells). Results: Microglia was distributed abundantly in the SGZ region. Relative to the normal controls, at 3 d following infrasound exposure, OX42 immunoreactivity was most enhanced and BrdU-positive cells were decreased to the lowest number in the SGZ ( P 〈 0.01 ). Minocycline attenuated the infrasound-induced decrease of BrdU-positive cell number significantly (P 〈0.01 ). Conclusion: Microglial activation was involved in infrasound-induced suppression of neural stem cell proliferation in hippocampal SGZ of adult rats.