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辛二酰苯胺异羟肟酸(SAHA)可减轻暴露于七氟醚麻醉的大鼠后代的记忆损伤。

Suberoylanilide hydroxamic acid (SAHA) attenuates memory impairment in the offspring of rats exposed to sevoflurane anesthesia.

作者信息

Song Xiao-Yuan, Liu Xiu-Wen, Wang Jia

机构信息

Department of Anesthesiology, Shanxi Provincial People's Hospital, Taiyuan, Shanxi, 030012, China.

Department of Anesthesiology, Shanxi Provincial People's Hospital, Taiyuan, Shanxi, 030012, China.

出版信息

Biochem Biophys Res Commun. 2023 Feb 5;643:139-146. doi: 10.1016/j.bbrc.2022.11.073. Epub 2022 Nov 25.

Abstract

BACKGROUND

SAHA was reported to enhance the expression of miR-129-5p, which was predicted to bind to 3' UTR of CASP-6, a gene playing crucial roles in the pathogenesis of memory impairment. Whether SAHA/miR-129-5p/CASP-6 is involved in the pathogenesis of prenatal exposure to sevoflurane remains to be explored.

METHODS

Morris water maze test was performed to evaluate the functional parameters of learning and memory. Quantitative real-time qPCR was carried out to analyze the expression of miRNAs and CASP-6 mRNA under different conditions.

RESULTS

Sevoflurane exposure of pregnant rats and SAHA treatment of the offspring had no effect on the blood gases, litter size, survival rate and weight. SAHA administration remarkably reversed the learning and memory impairment in prenatal rats caused by sevoflurane exposure. Mechanistically, the abnormal expression of miR-129-5p and CASP-6 in the offspring of pregnant rats exposed to sevoflurane was effectively restored by SAHA treatment. The luciferase activity of CASP-6 vector was effectively inhibited by miR-129-5p in primary neuron cells of rats. Moreover, the expression of CASP-6 mRNA and protein was significantly suppressed by miR-129-5p and SAHA treatment in a dose-dependent manner.

CONCLUSION

Our work demonstrated that the administration of SAHA suppressed the expression of CASP-6 via modulating the expression of miR-129-5p, and SAHA may rescue the apoptosis of neurons caused by exposure to sevoflurane. The underlying mechanism might be the ability of SAHA to relieve learning and memory impairment in the offspring of the pregnant rats exposed to sevoflurane.

摘要

背景

据报道,SAHA可增强miR-129-5p的表达,预测该miRNA可与CASP-6基因的3'UTR结合,而CASP-6基因在记忆障碍的发病机制中起关键作用。SAHA/miR-129-5p/CASP-6是否参与产前暴露于七氟醚的发病机制仍有待探索。

方法

进行Morris水迷宫试验以评估学习和记忆的功能参数。采用定量实时qPCR分析不同条件下miRNA和CASP-6 mRNA的表达。

结果

孕鼠暴露于七氟醚以及对其后代进行SAHA处理对血气、窝仔数、存活率和体重均无影响。SAHA给药显著逆转了七氟醚暴露所致产前大鼠的学习和记忆障碍。机制上,SAHA处理有效恢复了孕鼠暴露于七氟醚后其后代中miR-129-5p和CASP-6的异常表达。在大鼠原代神经元细胞中,miR-129-5p有效抑制了CASP-6载体的荧光素酶活性。此外,miR-129-5p和SAHA处理以剂量依赖方式显著抑制了CASP-6 mRNA和蛋白的表达。

结论

我们的研究表明,SAHA通过调节miR-129-5p的表达抑制了CASP-6的表达,并且SAHA可能挽救七氟醚暴露所致的神经元凋亡。潜在机制可能是SAHA缓解了孕鼠暴露于七氟醚后其后代的学习和记忆障碍。

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