Hippocampal estrogens rescued the decline of synaptic plasticity after surgery and anesthesia by inhibiting microglia overactivation

• Published in: Behavioural brain research Vol. 459; p. 114794
• Main Authors: Tan, Xiao-Xiang, Dai, Hong-Yu, Yao, Juan, Wang, Jia-Jia, Dai, Yu-Chen, Zhang, Tian-Hao, Qiu, Li-Li, Sun, Jie
• Format: Journal Article
• Language: English
• Published: Netherlands 29.02.2024
• Subjects: Aged; Anesthesia - adverse effects; Animals; Cognitive Dysfunction - etiology; Estrogens - metabolism; Estrogens - pharmacology; Female; Hippocampus - metabolism; Humans; Infant; Male; Mice; Mice, Inbred C57BL; Microglia; Receptors, Estrogen - metabolism; Postoperative cognitive dysfunction; Estrogens; Synaptic plasticity; Microglia
• ISSN: 0166-4328; 1872-7549
• DOI: 10.1016/j.bbr.2023.114794

Elderly patients experience postoperative cognitive impairment frequently; therefore, effective interventions are urgently needed. Central nervous inflammation characterized by microglia may promote the progression of POCD by reducing synaptic plasticity. Notably, clinical studies revealed that the incidence of female patients was significantly lower than that of male patients. Besides, the brain estrogens have an anti-inflammatory effect and regulate the microglia at the same times. This study aimed to determine whether suppressing microglia overactivation by hippocampal estrogens can rescue the decrease of synaptic plasticity after surgery and anesthesia. Exploratory laparotomy was used to establish the POCD model in 15-month-old male or female C57BL/6 J mice and animal behavioral tests were performed to test hippocampal-dependent memory capacity. Western blot and immunofluorescence were used to detect the microglial activation and plasticity related protein expressions. Elisa was used to detect the content of estrogens in the hippocampus. Estrogens and estrogen receptor inhibitor were used to replenish the estrogens in the brain and inhibit the effect of estrogens. Surgery and anesthesia did not cause POCD in female mice (P > 0.05), while the cognitive function decreased significantly after estrogen receptor inhibitor was given(P < 0.05). Male mice experienced cognitive dysfunction after surgery and anesthesia, and their cognitive function improved after estrogens supplementation (P < 0.05). Given estrogens and estrogen receptor inhibitors at the same time, the cognitive function of male mice could not be saved (P < 0.05). By correlation analysis, there was a negative correlation between the content of hippocampal estrogens and microglia (P < 0.05). The number or degree of activation of microglia affected the synaptic plasticity, which ultimately regulated the cognitive function of mice. Hippocampal estrogens rescued the decline of synaptic plasticity after surgery and anesthesia by inhibiting microglia overactivation.