Rosiglitazone Promotes Oligodendrocyte Development and Myelin Formation of Repeated Neonatal Sevoflurane Exposure via PPARγ Signaling

被引:1
作者
Cao, Tianyu [1 ]
Jiang, Sufang [1 ]
Wang, Xueji [1 ]
Huang, Peiying [1 ]
Zhou, Lijie [2 ]
Di, Lichao [1 ]
Han, Shuang [3 ]
Huang, Lining [1 ,4 ]
机构
[1] Hebei Med Univ, Hosp 2, Dept Anesthesiol, Shijiazhuang, Hebei, Peoples R China
[2] First Hosp Qinhuangdao, Dept Anesthesiol, Qinhuangdao, Hebei, Peoples R China
[3] Hebei Gen Hosp, Dept Anesthesiol, Shijiazhuang, Hebei, Peoples R China
[4] Minist Educ, Key Lab Clin Neurol, Shijiazhuang, Hebei, Peoples R China
关键词
Sevoflurane; Rosiglitazone; Myelination; Oligodendrocyte; PPAR gamma signaling; Neurotoxicity; GENERAL-ANESTHESIA; BRAIN; CNS; NEUROTOXICITY; REMYELINATION; MECHANISMS;
D O I
10.1007/s12035-024-04413-z
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sevoflurane is one of the most commonly used general anesthetics for children and infants. Recent research indicates that repeated exposure to sevoflurane in neonates induces cognitive and fine motor deficits. Peroxisome proliferator-activated receptor-gamma (PPAR gamma) agonists have garnered significant attention as potential therapies for a variety of neurological conditions. In this research, we evaluated whether pretreatment with rosiglitazone in neonatal mice could address myelination defects, cognitive impairment, and fine motor dysfunction via PPAR gamma. The mice were exposed to 3% sevoflurane for 2 h on postnatal days 6-8 (P6-P8). Behavioral tests were conducted from P29 to P34. Additionally, we evaluated morphological and functional changes related to myelin. Our results showed that rosiglitazone pretreatment significantly ameliorated the cognitive and fine motor impairments of repeated neonatal sevoflurane exposure. In addition, rosiglitazone pretreatment promoted oligodendrocyte precursor cells (OPCs) differentiation and myelination. This suggests that rosiglitazone may be used in clinical settings to enhance the security of neonatal sevoflurane exposure. Furthermore, PPAR gamma and fatty acid synthase (FASN) may be mediators for rosiglitazone, which alleviates myelination defects, cognitive impairment, and fine motor dysfunction.
引用
收藏
页码:2348 / 2361
页数:14
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