Anesthesia/surgery-induced learning and memory dysfunction by inhibiting mitophagy-mediated NLRP3 inflammasome inactivation in aged mice

被引:2
|
作者
Lu, Jian [1 ]
Zong, Youming [1 ]
Tao, Xiaoyan [2 ]
Dai, Hongyu [1 ]
Song, Jiale [1 ]
Zhou, Hongmei [1 ]
机构
[1] Jiaxing Univ, Hosp Jiaxing 2, Affiliated Hosp 2, Dept Anesthesiol, Jiaxing, Zhejiang, Peoples R China
[2] Jiaxing Univ, Hosp Jiaxing 2, Affiliated Hosp 2, Dept Nursing, Jiaxing, Zhejiang, Peoples R China
关键词
Postoperative cognitive deficit; Mitophagy; Aged mice; NLRP3; Neuroinflammation; POSTOPERATIVE COGNITIVE DYSFUNCTION; ALZHEIMERS-DISEASE; ACTIVATION; MITOCHONDRIAL;
D O I
10.1007/s00221-023-06724-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Postoperative cognitive dysfunction (POCD) is a common postoperative complication, not only affects the quality of life of the elderly and increases the mortality rate, but also brings a greater burden to the family and society. Previous studies demonstrated that Nod-like receptor protein 3 (NLRP3) inflammasome participates in various inflammatory and neurodegenerative diseases. However, possible mitophagy mechanism in anesthesia/surgery-elicited NLRP3 inflammasome activation remains to be elucidated. Hence, this study clarified whether mitophagy dysfunction is related to anesthesia/surgery-elicited NLRP3 inflammasome activation. POCD model was established in aged C57BL/6 J mice by tibial fracture fixation under isoflurane anesthesia. Morris Water Maze (MWM) was used to evaluate learning and memory abilities. We found that in vitro experiments, lipopolysaccharide (LPS) significantly facilitated NLRP3 inflammasome activation and mitophagy inhibition in BV2 cells. Rapamycin restored mitophagy and improved mitochondrial function, and inhibited NLRP3 inflammasome activation induced by LPS. In vivo experiments, anesthesia and surgery caused upregulation of hippocampal NLRP3, caspase recruitment domain (ASC) and interleukin-1 beta (IL-1 beta), and downregulation of microtubule-associated protein light chain 3II (LC3II) and Beclin1 in aged mice. Olaparib inhibited anesthesia/surgery-induced NLRP3, ASC, and IL-1 beta over-expression in the hippocampus, while upregulated the expression of LC3II and Beclin1. Furthermore, Olaparib improved cognitive impairment in older mice. These results revealed that mitophagy was involved in NLRP3 inflammasome-mediated anesthesia/surgery-induced cognitive deficits in aged mice. Overall, our results suggested that mitophagy was related in NLRP3 inflammasome-induced cognitive deficits after anesthesia and surgery in aged mice. Activating mitophagy may have clinical benefits in the prevention of cognitive impairment induced by anesthesia and surgery in elderly patients.
引用
收藏
页码:417 / 427
页数:11
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