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单唾液酸神经节苷脂1可能减轻丙泊酚联合瑞芬太尼对神经干细胞诱导的神经毒性。

Monosialoganglioside 1 may alleviate neurotoxicity induced by propofol combined with remifentanil in neural stem cells.

作者信息

Lu Jiang, Yao Xue-Qin, Luo Xin, Wang Yu, Chung Sookja Kim, Tang He-Xin, Cheung Chi Wai, Wang Xian-Yu, Meng Chen, Li Qing

机构信息

Anesthesiology Research Institute of Hubei University of Medicine, Shiyan, Hubei Province, China.

Department of Anesthesiology, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei Province, China.

出版信息

Neural Regen Res. 2017 Jun;12(6):945-952. doi: 10.4103/1673-5374.208589.

Abstract

Monosialoganglioside 1 (GM1) is the main ganglioside subtype and has neuroprotective properties in the central nervous system. In this study, we aimed to determine whether GM1 alleviates neurotoxicity induced by moderate and high concentrations of propofol combined with remifentanil in the immature central nervous system. Hippocampal neural stem cells were isolated from newborn Sprague-Dawley rats and treated with remifentanil (5, 10, 20 ng/mL) and propofol (1.0, 2.5, 5.0 μg/mL), and/or GM1 (12.5, 25, 50 μg/mL). GM1 reversed combined propofol and remifentanil-induced decreases in the percentage of 5-bromodeoxyuridine(+) cells and also reversed the increase in apoptotic cell percentage during neural stem cell proliferation and differentiation. However, GM1 with combined propofol and remifentanil did not affect β-tubulin(+) or glial fibrillary acidic protein(+) cell percentage during neural stem cell differentiation. In conclusion, we show that GM1 alleviates the damaging effects of propofol combined with remifentanil at moderate and high exposure concentrations in neural stem cells , and exerts protective effects on the immature central nervous system.

摘要

单唾液酸神经节苷脂1(GM1)是主要的神经节苷脂亚型,在中枢神经系统中具有神经保护特性。在本研究中,我们旨在确定GM1是否能减轻中高浓度丙泊酚联合瑞芬太尼对未成熟中枢神经系统诱导的神经毒性。从新生Sprague-Dawley大鼠中分离海马神经干细胞,并用瑞芬太尼(5、10、20 ng/mL)和丙泊酚(1.0、2.5、5.0 μg/mL)和/或GM1(12.5、25、50 μg/mL)进行处理。GM1可逆转丙泊酚和瑞芬太尼联合诱导的5-溴脱氧尿苷(+)细胞百分比的降低,并且还能逆转神经干细胞增殖和分化过程中凋亡细胞百分比的增加。然而,GM1与丙泊酚和瑞芬太尼联合使用时,在神经干细胞分化过程中并不影响β-微管蛋白(+)或胶质纤维酸性蛋白(+)细胞的百分比。总之,我们表明GM1可减轻中高暴露浓度下丙泊酚联合瑞芬太尼对神经干细胞的损伤作用,并对未成熟中枢神经系统发挥保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/085b/5514870/45a3f5fd43ad/NRR-12-945-g003.jpg

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