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次声可增加成年大鼠海马细胞内钙离子浓度并诱导其凋亡。

Infrasound increases intracellular calcium concentration and induces apoptosis in hippocampi of adult rats.

机构信息

Department of Physiotherapy and Rehabilitation Medicine, Tangdu Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, PR China.

出版信息

Mol Med Rep. 2012 Jan;5(1):73-7. doi: 10.3892/mmr.2011.597. Epub 2011 Sep 23.

Abstract

In the present study, we determined the effect of infrasonic exposure on apoptosis and intracellular free Ca²⁺ ([Ca²⁺]i) levels in the hippocampus of adult rats. Adult rats were randomly divided into the control and infrasound exposure groups. For infrasound treatment, animals received infrasonic exposure at 90 (8 Hz) or 130 dB (8 Hz) for 2 h per day. Hippocampi were dissected, and isolated hippocampal neurons were cultured. The [Ca²⁺]i levels in hippocampal neurons from adult rat brains were determined by Fluo-3/AM staining with a confocal microscope system on days 1, 7, 14, 21 and 28 following infrasonic exposure. Apoptosis was evaluated by Annexin V-FITC and propidium iodide double staining. Positive cells were sorted and analyzed by flow cytometry. Elevated [Ca²⁺]i levels were observed on days 14 and 21 after rats received daily treatment with 90 or 130 dB sound pressure level (SPL) infrasonic exposure (p<0.01 vs. control). The highest levels of [Ca²⁺]i were detected in the 130 dB SPL infrasonic exposure group. Meanwhile, apoptosis in hippocampal neurons was found to increase on day 7 following 90 dB SPL infrasound exposure, and significantly increased on day 14. Upon 130 dB infrasound treatment, apoptosis was first observed on day 14, whereas the number of apoptotic cells gradually decreased thereafter. Additionally, a marked correlation between cell apoptosis and [Ca²⁺]i levels was found on day 14 and 21 following daily treatment with 90 and 130 dB SPL, respectively. These results demonstrate that a period of infrasonic exposure induced apoptosis and upregulated [Ca²⁺]i levels in hippocampal neurons, suggesting that infrasound may cause damage to the central nervous system (CNS) through the Ca²⁺‑mediated apoptotic pathway in hippocampal neurons.

摘要

在本研究中,我们测定了次声暴露对成年大鼠海马细胞凋亡和细胞内游离 Ca²⁺([Ca²⁺]i)水平的影响。成年大鼠被随机分为对照组和次声暴露组。次声处理时,动物每天接受 90(8Hz)或 130dB(8Hz)次声暴露 2 小时。分离海马后,培养海马神经元。用 Fluo-3/AM 染色,用共聚焦显微镜系统在次声暴露后第 1、7、14、21 和 28 天测定成年大鼠脑内海马神经元的[Ca²⁺]i 水平。用 Annexin V-FITC 和碘化丙啶双重染色评价细胞凋亡。用流式细胞术对阳性细胞进行分选和分析。大鼠接受 90 或 130dB 声压级(sound pressure level,SPL)次声暴露后,第 14 天和第 21 天[Ca²⁺]i 水平升高(p<0.01,与对照组比较)。130dB SPL 次声暴露组[Ca²⁺]i 水平最高。同时,90dB SPL 次声暴露后第 7 天海马神经元凋亡增加,第 14 天显著增加。130dB 次声处理后,第 14 天首次观察到细胞凋亡,此后凋亡细胞数逐渐减少。此外,在分别接受 90 和 130dB SPL 每天处理后第 14 天和第 21 天,细胞凋亡与[Ca²⁺]i 水平之间存在显著相关性。这些结果表明,一段时间的次声暴露诱导海马神经元凋亡和[Ca²⁺]i 水平升高,提示次声可能通过海马神经元 Ca²⁺介导的凋亡途径对中枢神经系统(central nervous system,CNS)造成损伤。

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