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成纤维细胞生长因子 21 通过调节肠道微生物群和代谢稳态改善帕金森病小鼠模型的行为缺陷。

Fibroblast growth factor 21 ameliorates behavior deficits in Parkinson's disease mouse model via modulating gut microbiota and metabolic homeostasis.

机构信息

Institute of Metabonomics & Medical NMR, School of Pharmaceutical Science, Wenzhou Medical University, Wenzhou, China.

School of Public health, Fujian Medical University, Fuzhou, China.

出版信息

CNS Neurosci Ther. 2023 Dec;29(12):3815-3828. doi: 10.1111/cns.14302. Epub 2023 Jun 19.

DOI:10.1111/cns.14302
PMID:37334756
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10651963/
Abstract

AIMS

The effects of FGF21 on Parkinson's disease (PD) and its relationship with gut microbiota have not been elucidated. This study aimed to investigate whether FGF21 would attenuate behavioral impairment through microbiota-gut-brain metabolic axis in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) induced PD mice model.

METHODS

Male C57BL/6 mice were rendomized into 3 groups: vehicle (CON); MPTP 30 mg/kg/day i.p. injection (MPTP); FGF21 1.5 mg/kg/d i.p. injection plus MPTP 30 mg/kg/day i.p. injection (FGF21 + MPTP). The behavioral features, metabolimics profiling, and 16 s rRNA sequencing were performed after FGF21 treatment for 7 days.

RESULTS

MPTP-induced PD mice showed motor and cognitive deficits accompanied by gut microbiota dysbiosis and brain-region-specific metabolic abnormalities. FGF21 treatment dramatically attenuated motor and cognitive dysfunction in PD mice. FGF21 produced a region-specific alteration in the metabolic profile in the brain in ways indicative of greater ability in neurotransmitter metabolism and choline production. In addition, FGF21 also re-structured the gut microbiota profile and increased the relative abundance of Clostridiales, Ruminococcaceae, and Lachnospiraceae, thereby rescuing the PD-induced metabolic disorders in the colon.

CONCLUSION

These findings indicate that FGF21 could affect behavior and brain metabolic homeostasis in ways that promote a favorable colonic microbiota composition and through effects on the microbiota-gut-brain metabolic axis.

摘要

目的

成纤维细胞生长因子 21(FGF21)对帕金森病(PD)的影响及其与肠道微生物群的关系尚未阐明。本研究旨在探讨 FGF21 是否通过微生物群-肠道-脑代谢轴在 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的 PD 小鼠模型中减轻行为损伤。

方法

雄性 C57BL/6 小鼠随机分为 3 组:对照组(CON);MPTP30mg/kg/天腹腔注射(MPTP);FGF211.5mg/kg/天腹腔注射加 MPTP30mg/kg/天腹腔注射(FGF21+MPTP)。在 FGF21 治疗 7 天后进行行为特征、代谢组学分析和 16s rRNA 测序。

结果

MPTP 诱导的 PD 小鼠表现出运动和认知功能障碍,同时伴有肠道微生物群失调和脑区特异性代谢异常。FGF21 治疗可显著改善 PD 小鼠的运动和认知功能障碍。FGF21 对脑代谢谱产生了特定的区域改变,表明其在神经递质代谢和胆碱生成方面具有更强的能力。此外,FGF21 还重构了肠道微生物群谱,增加了厚壁菌门、瘤胃球菌科和毛螺菌科的相对丰度,从而挽救了 PD 诱导的结肠代谢紊乱。

结论

这些发现表明,FGF21 可以通过影响微生物群-肠道-脑代谢轴,影响行为和大脑代谢稳态,从而促进有利的结肠微生物群组成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/3a2fba784389/CNS-29-3815-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/06d6e23e886f/CNS-29-3815-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/555a8686954e/CNS-29-3815-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/a0e469157f90/CNS-29-3815-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/95c81cc0c712/CNS-29-3815-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/2d8c660aa2fe/CNS-29-3815-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/d8d7f7fb7c2b/CNS-29-3815-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/3a2fba784389/CNS-29-3815-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/06d6e23e886f/CNS-29-3815-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/555a8686954e/CNS-29-3815-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/a0e469157f90/CNS-29-3815-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/95c81cc0c712/CNS-29-3815-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/2d8c660aa2fe/CNS-29-3815-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/d8d7f7fb7c2b/CNS-29-3815-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379f/10651963/3a2fba784389/CNS-29-3815-g006.jpg

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