Electroacupuncture treatment ameliorated the long-term cognitive impairment via activating eNOS/NO pathway and related Aβ downregulation in sepsis-survivor mice.
Electroacupuncture treatment ameliorated the long-term cognitive impairment via activating eNOS/NO pathway and related Aβ downregulation in sepsis-survivor mice.
复制标题
电针治疗通过激活 eNOS/NO 途径和相关 Aβ 下调脓毒症幸存者小鼠改善长期认知障碍。
DOI:
10.1016/j.physbeh.2021.113646
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发表时间:
2022
影响因子:
2.9
通讯作者:
Song Jiangang
中科院分区:
文献类型:
--
作者:
Jun Guo;Yong Yue;Lu Liyue;Gao Hao;Yin Zhiyu;Wei Pan;Sun Long;Ruan Wenqing;Zou Yinghua;He He;Song Wei;Tong Qiuyu;Wang Xiongbiao;Wang Yongqiang;Song Jiangang
ObjectiveSepsis is a major challenge in intensive care unit worldwide and the septic survivors are left with long-term cognitive deficits. This work aims to explore the effects of electroacupuncture (EA) on long-term cognitive function and its underlying mechanism in sepsis-survivor mice.MethodsSepsis was induced by cecal ligation and puncture in C57BL/6 male mice. Seven days post-surgery, sepsis-survivor mice were treated with EA or nonacupoint EA for 17 days twice daily. Then, cognitive function was evaluated by Morris water maze task. The hippocampus tissue were collected from the mice at 30 days post-surgery. The level of nitric oxide and the expression of endothelial nitric oxide (eNOS), phospho-eNOS (p-eNOS), and amyloid β–peptide (Aβ) were measured.ResultsCompared with the sham-operated control, sepsis-survivors had significant cognitive deficits evidenced by the increased time of escape latency and reduced crossing number in Morris water maze task, as well as lower NO and p-eNOS level and higher Aβ level. EA treatment at GV20 and ST36 acupoints but not at a nonacupoint improved the cognitive function, increased the NO and p-eNOS level, and decreased Aβ generation; while eNOS inhibitor (l-NAME) undermined the efficacy of EA treatment.ConclusionIn conclusion, repeated EA treatment could ameliorate the long-term cognitive impairment via manipulating the expression of p-eNOS and related Aβ in sepsis-survivor mice.