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姜黄素通过调节肠道微生物群和短链脂肪酸减轻1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的小鼠帕金森病。

Curcumin alleviates 1-methyl- 4-phenyl- 1,2,3,6-tetrahydropyridine- induced Parkinson's disease in mice via modulating gut microbiota and short-chain fatty acids.

作者信息

Cai Benchi, Zhong Lifan, Wang Qitong, Xu Wendi, Li Xi, Chen Tao

机构信息

Affiliation Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan, China.

出版信息

Front Pharmacol. 2023 Jun 14;14:1198335. doi: 10.3389/fphar.2023.1198335. eCollection 2023.

DOI:10.3389/fphar.2023.1198335
PMID:37388445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10303117/
Abstract

The microbiota-gut-brain axis has been proposed as a potential therapeutic target of PD. The effects of curcumin against Parkinson's disease have been demonstrated; however, its neuroprotective mechanisms remain unknown. Our study investigated the potential mechanisms through which curcumin ameliorates Parkinson's disease via the microbiota-gut-brain axis. Mice were randomly divided into four groups: control, Curcumin, MPTP, and MPTP + Curcumin. Motor deficits and gastrointestinal dysfunction were assessed using behavioral test, intestinal motility test, and fecal parameter measurement. The loss of dopaminergic neurons and intestinal barrier function was measured using Western blot and immunofluorescence. Shotgun metagenomic sequencing and LC-MS were parallelly performed on mice feces to investigate alterations in microbiota and metabolites. Curcumin alleviated motor deficits and the loss of dopaminergic neurons in MPTP-induced mice. Curcumin ameliorated gastrointestinal and intestinal barrier dysfunctions in MPTP-induced mice. Curcumin reduced gut microbial dysbiosis and modulated carbohydrate metabolism in MPTP-induced mice. Curcumin restored short-chain fatty acid (SCFA) profiles in MPTP-induced mice. Concurrently, these results indicate that curcumin inhibits Parkinson's disease by regulating the gut microbiota and short-chain fatty acids.

摘要

微生物群-肠道-脑轴已被提出作为帕金森病的一个潜在治疗靶点。姜黄素对帕金森病的作用已得到证实;然而,其神经保护机制仍不清楚。我们的研究调查了姜黄素通过微生物群-肠道-脑轴改善帕金森病的潜在机制。将小鼠随机分为四组:对照组、姜黄素组、MPTP组和MPTP+姜黄素组。使用行为测试、肠道运动测试和粪便参数测量来评估运动功能障碍和胃肠功能障碍。使用蛋白质免疫印迹法和免疫荧光法检测多巴胺能神经元的损失和肠道屏障功能。对小鼠粪便同时进行鸟枪法宏基因组测序和液相色谱-质谱联用,以研究微生物群和代谢产物的变化。姜黄素减轻了MPTP诱导小鼠的运动功能障碍和多巴胺能神经元的损失。姜黄素改善了MPTP诱导小鼠的胃肠和肠道屏障功能障碍。姜黄素减少了MPTP诱导小鼠的肠道微生物群失调并调节了碳水化合物代谢。姜黄素恢复了MPTP诱导小鼠的短链脂肪酸(SCFA)谱。同时,这些结果表明姜黄素通过调节肠道微生物群和短链脂肪酸来抑制帕金森病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc53/10303117/f46ce2ef3e3c/fphar-14-1198335-g007.jpg
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