Department of ENT, First Affiliated Hospital of Chongqing Medical University, Chongqing, People's Republic of China.
J Neurophysiol. 2021 Oct 1;126(4):1112-1121. doi: 10.1152/jn.00240.2021. Epub 2021 Sep 1.
This study explored the role of the p38 mitogen-activated protein kinase (MAPK) signaling pathway in hippocampal neuron autophagy in rats with chronic intermittent hypoxia (CIH). Male Sprague-Dawley rats were randomly divided to normoxic control (CON), CIH (optimal modeling time was determined prior by measuring the expression of several proteins after 2-, 4-, and 6-wk intermittent hypoxia), solvent (CIH+Veh), or p38MAPK inhibitor (CIH+SB203580) groups. DMSO and SB203580 were injected intraperitoneally 30 min before hypoxia in CIH+Veh and CIH+SB203580 group rats, respectively. Rat learning and memory were evaluated via the Morris water maze test. Ultrastructural changes in the hippocampal CA1 region autophagic vesicles and neurons were observed under transmission electron and light microscopy. Hippocampal microtubule-associated proteins were detected by western blot. Morris water maze test showed that CIH+SB203580 group rats spent significantly more time on the platform quadrant and crossed the platform more times than CIH+Veh group rats ( < 0.01). Hematoxylin-eosin (HE) staining showed greater rat cell damage in the CIH+SB group than in the CIH and CIH+Veh groups. Western blot analysis showed that CIH+SB group rats had significantly lower p-p38MAPK/p38MAPK, LC3I, and p62 expression and higher beclin-1 expression than CIH+Veh group rats ( < 0.01). Electron microscopy showed that CIH+SB203580 group rats had several small hippocampal neuron autophagic vesicles. On immunofluorescence analyses, it showed a higher LC3II expression in CIH+SB203580 group rats than in CIH+Veh group rats ( < 0.01). These results indicate that inhibition of the CIH p38MAPK signaling pathway can activate autophagy and protect hippocampal neurons in rats. The pathophysiological processes related to autophagy obstructive sleep apnea-hypopnea syndrome (OSAHS) are unclear. This study clarified that the inhibition of the p38MAPK signaling pathway could further activate autophagy in hippocampal nerve cells, thus reducing nerve cell injury.
本研究探讨了 p38 丝裂原活化蛋白激酶(MAPK)信号通路在慢性间歇性低氧(CIH)大鼠海马神经元自噬中的作用。雄性 Sprague-Dawley 大鼠随机分为常氧对照组(CON)、CIH(通过测量 2、4 和 6 周间歇性低氧后几种蛋白质的表达来确定最佳建模时间)、溶剂(CIH+Veh)或 p38MAPK 抑制剂(CIH+SB203580)组。在 CIH+Veh 和 CIH+SB203580 组大鼠中,分别在缺氧前 30 分钟腹腔注射 DMSO 和 SB203580。通过 Morris 水迷宫试验评估大鼠学习和记忆能力。透射电镜和光镜观察海马 CA1 区自噬小体和神经元的超微结构变化。Western blot 检测海马微管相关蛋白。Morris 水迷宫试验显示,与 CIH+Veh 组相比,CIH+SB203580 组大鼠在平台象限花费的时间显著增加,穿过平台的次数也显著增加(<0.01)。苏木精-伊红(HE)染色显示 CIH+SB 组大鼠的细胞损伤明显大于 CIH 组和 CIH+Veh 组。Western blot 分析显示,与 CIH+Veh 组相比,CIH+SB 组大鼠的 p-p38MAPK/p38MAPK、LC3I 和 p62 表达显著降低,beclin-1 表达显著升高(<0.01)。电镜显示 CIH+SB203580 组大鼠海马神经元自噬小泡较小。免疫荧光分析显示,CIH+SB203580 组大鼠的 LC3II 表达明显高于 CIH+Veh 组(<0.01)。这些结果表明,抑制 CIH p38MAPK 信号通路可激活自噬,保护大鼠海马神经元。与自噬相关的阻塞性睡眠呼吸暂停低通气综合征(OSAHS)的病理生理过程尚不清楚。本研究阐明,抑制 p38MAPK 信号通路可进一步激活海马神经细胞自噬,从而减轻神经细胞损伤。