Anesthetic Agents and Neuronal Autophagy. What We Know and What We Don't.

Title:Anesthetic Agents and Neuronal Autophagy. What We Know and What We Don't.

Volume: 25 Issue: 8

Author(s): Lili Xu, Jianjun Shen, Patrick M. McQuillan and Zhiyong Hu*

Affiliation:

• Department of Anesthesiology, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou,China

Keywords: Immature brain, general anesthetic agents, autophagy, neurotoxicity, ethanol, neuronal cell.

Abstract: Background: Ethanol is known to have both γ-Aminobutyric acid agonist and Nmethyl- D-aspartate antagonist characteristics similar to commonly used volatile anesthetic agents. Recent evidence demonstrates that autophagy can reduce the development of ethanol induced neurotoxicity. Recent studies have found that general anesthesia can cause longterm impairment of both mitochondrial morphogenesis and synaptic transmission in the developing rat brain, both of which are accompanied by enhanced autophagy activity. Autophagy may play an important role in general anesthetic mediated neurotoxicity.

Methods: This review outlines the role of autophagy in the development of anesthetic related neurotoxicity and includes an explanation of the role of autophagy in neuronal cell survival and death, the relationship between anesthetic agents and neuronal autophagy, possible molecular and cellular mechanisms underlying general anesthetic agent induced activation of neuronal autophagy in the developing brain, and potential therapeutic approaches aimed at modulating autophagic pathways.

Results: In a time- and concentration-dependent pattern, general anesthetic agents can disrupt intracellular calcium homeostasis which enhances both autophagy and apoptosis activation. The degree of neural cell injury may be ultimately determined by the interplay between autophagy and apoptosis. It appears likely that the increase in calcium flux associated with some anesthetic agents disrupts lysosomal function. This results in an over-activation of endosomal- lysosomal trafficking causing mitochondrial damage, reactive oxygen species upregulation, and lipid peroxidation.

Conclusion: Autophagy may play a role in the development of anesthetic related neurotoxicity. Understanding this may lead to strategies or therapies aimed at preventing or ameliorating general anesthetic agent mediated neurotoxicity.

Cite this article as:

Xu Lili, Shen Jianjun, McQuillan M. Patrick and Hu Zhiyong *, Anesthetic Agents and Neuronal Autophagy. What We Know and What We Don't., Current Medicinal Chemistry 2018; 25 (8) . https://dx.doi.org/10.2174/0929867324666171009123605