[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Dept Anesthesiol, Shanghai, Peoples R China
来源:
FRONTIERS IN MOLECULAR NEUROSCIENCE
|
2022年
/
15卷
基金:
中国国家自然科学基金;
上海市自然科学基金;
关键词:
general anesthesia;
neurotoxicity;
neurodevelopmental impairment;
cognitive dysfunction;
developing brain;
REQUIRING GENERAL-ANESTHESIA;
TERM COGNITIVE DYSFUNCTION;
AWAKE-REGIONAL ANESTHESIA;
PROTEIN INTERACTIONS;
INFANCY GAS;
EXPOSURE;
SEVOFLURANE;
AGE;
NEUROTOXICITY;
OUTCOMES;
D O I:
10.3389/fnmol.2022.1017578
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Anesthesia is unavoidable in surgical procedures. However, whether the general anesthetics are neurotoxic to immature brains remains undefined. Neurodevelopmental impairment induced by anesthesia has been a critical health issue and topic of concern. This review summarizes recent progress made in clinical and preclinical studies to provide useful suggestions and potential therapeutic targets for the protection of the immature brain. On the one hand, clinical researchers continue the debate about the effect of single and multiple exposures to anesthesia on developing brains. On the other hand, preclinical researchers focus on exploring the mechanisms of neurotoxic effects of general anesthesia on immature brains and seeking novel solutions. Rodent models have always been used in preclinical studies, but it is still unclear whether the mechanisms observed in rodent models have clinical relevance. Compared with these models, non-human primates (NHPs) are more genetically similar to humans. However, few research institutions in this area can afford to use NHP models in their studies. One way to address both problems is by combining single-cell sequencing technologies to screen differential gene expression in NHPs and perform in vivo validation in rodents. The mechanism of anesthesia-induced neurotoxicity still requires further elucidation in primates.
机构:
Emory Univ, Yerkes Natl Primate Res Ctr, Div Dev & Cognit Neurosci, Atlanta, GA 30322 USAEmory Univ, Yerkes Natl Primate Res Ctr, Div Dev & Cognit Neurosci, Atlanta, GA 30322 USA
Alvarado, M. C.
Murphy, K. L.
论文数: 0引用数: 0
h-index: 0
机构:
Newcastle Univ, Comparat Biol Ctr, Newcastle Upon Tyne, Tyne & Wear, EnglandEmory Univ, Yerkes Natl Primate Res Ctr, Div Dev & Cognit Neurosci, Atlanta, GA 30322 USA
Murphy, K. L.
Baxter, M. G.
论文数: 0引用数: 0
h-index: 0
机构:
Icahn Sch Med Mt Sinai, Dept Neurosci, New York, NY 10029 USA
Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USAEmory Univ, Yerkes Natl Primate Res Ctr, Div Dev & Cognit Neurosci, Atlanta, GA 30322 USA
机构:
Emory Univ, Yerkes Natl Primate Res Ctr, Div Dev & Cognit Neurosci, Atlanta, GA 30322 USAEmory Univ, Yerkes Natl Primate Res Ctr, Div Dev & Cognit Neurosci, Atlanta, GA 30322 USA
Alvarado, M. C.
Murphy, K. L.
论文数: 0引用数: 0
h-index: 0
机构:
Newcastle Univ, Comparat Biol Ctr, Newcastle Upon Tyne, Tyne & Wear, EnglandEmory Univ, Yerkes Natl Primate Res Ctr, Div Dev & Cognit Neurosci, Atlanta, GA 30322 USA
Murphy, K. L.
Baxter, M. G.
论文数: 0引用数: 0
h-index: 0
机构:
Icahn Sch Med Mt Sinai, Dept Neurosci, New York, NY 10029 USA
Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USAEmory Univ, Yerkes Natl Primate Res Ctr, Div Dev & Cognit Neurosci, Atlanta, GA 30322 USA