a. Department of Anesthesiology, Peking University Third Hospital, No. 49 North Garden Road, Haidian District, Beijing 100191, China;
b. National Institute on Drug Dependence and Beijing Key Laboratory on Drug Dependence Research, Peking University, Beijing 100191, China;
c. The Key Laboratory for Neuroscience of the Ministry of Education and Health, Peking University, Beijing 100191, China;
d. Executive Office, Beijing Center of Quality Control and Improvement on Clinical Anesthesia, Beijing 100191, China;
e. Laboratory of Integrative Physiology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100191, China;
f. University of Chinese Academy of Sciences, Beijing 100191, China;
g. State Key Laboratory of Vascular Homeostasis and Remodeling, Department of Anesthesiology, Peking University Third Hospital, Beijing 100191, China
Funds:
This work was supported by the Ministry of Science and Technology of the People's Republic of China (STI2030-Major Projects, 2021ZD0204300 to X.G.), the National Natural Science Foundation of China (82271222 and 82571443 to Z.L.
32422031 to Z.W.), the Research Project of Peking University Third Hospital in State Key Laboratory of Vascular Homeostasis and Remodeling (Peking University) (2024-VHR-SY-10 to Z.L.), the Peking University Clinical Scientist Training Program (BMU2025PYJH008 to Z.L.), and the special fund of the National Clinical Key Specialty Construction Program, P. R. China (2025). Z.W. is supported by the Xiaomi Foundation.
General anesthetics profoundly alter brain function and consciousness, yet the mechanisms underlying these effects remain incompletely understood. Although traditional studies have primarily focused on neuronal targets, accumulating evidence suggests that microglia dynamically respond to anesthetic exposure and may participate in anesthesia-associated neurophysiological changes. Beyond their established immune functions, microglia are increasingly implicated in synaptic remodeling, metabolic regulation, neuronal activity surveillance, and neuron–glia communication. Recent studies indicate that different classes of anesthetic agents modulate microglial activity through diverse and context-dependent mechanisms involving inflammatory signaling, purinergic pathways, calcium dynamics, mitochondrial metabolism, and neural circuit interactions. These responses are associated with postoperative neurocognitive disorders, altered synaptic plasticity, and anesthesia-related changes in brain states. In this review, we summarize current evidence regarding the effects of volatile anesthetics, intravenous anesthetics, and analgesics on microglial function and discuss the molecular, functional, and circuit-level mechanisms underlying anesthesia-associated neuron–microglia interactions. We further highlight the dynamic and heterogeneous nature of microglial responses during anesthesia and discuss current limitations in the field, including the lack of temporally resolved and cell-specific approaches. Understanding these processes may provide insights into anesthesia-associated neurocognitive dysfunction and support the development of neuroimmune-targeted strategies in anesthesiology.