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评价艾灸治疗多囊卵巢综合征的潜力:基于肠道微生物群和代谢物相互作用的大鼠模型研究。

Evaluating the therapeutic potential of moxibustion on polycystic ovary syndrome: a rat model study on gut microbiota and metabolite interaction.

机构信息

Department of Traditional Chinese Medicine Specialty Diagnosis and Treatment, Xiamen Hospital of Traditional Chinese Medicine, Xiamen, China.

Department of Traditional Chinese Medicine, School of Medicine, Xiamen University, Xiamen, China.

出版信息

Front Cell Infect Microbiol. 2024 Apr 11;14:1328741. doi: 10.3389/fcimb.2024.1328741. eCollection 2024.

Abstract

Polycystic ovary syndrome (PCOS) is a common systemic disorder related to endocrine disorders, affecting the fertility of women of childbearing age. It is associated with glucose and lipid metabolism disorders, altered gut microbiota, and insulin resistance. Modern treatments like pioglitazone, metformin, and spironolactone target specific symptoms of PCOS, while in Chinese medicine, moxibustion is a common treatment. This study explores moxibustion's impact on PCOS by establishing a dehydroepiandrosterone (DHEA)-induced PCOS rat model. Thirty-six specific pathogen-free female Sprague-Dawley rats were divided into four groups: a normal control group (CTRL), a PCOS model group (PCOS), a moxibustion treatment group (MBT), and a metformin treatment group (MET). The MBT rats received moxibustion, and the MET rats underwent metformin gavage for two weeks. We evaluated ovarian tissue changes, serum testosterone, fasting blood glucose (FBG), and fasting insulin levels. Additionally, we calculated the insulin sensitivity index (ISI) and the homeostasis model assessment of insulin resistance index (HOMA-IR). We used 16S rDNA sequencing for assessing the gut microbiota, H NMR spectroscopy for evaluating metabolic changes, and Spearman correlation analysis for investigating the associations between metabolites and gut microbiota composition. The results indicate that moxibustion therapy significantly ameliorated ovarian dysfunction and insulin resistance in DHEA-induced PCOS rats. We observed marked differences in the composition of gut microbiota and the spectrum of fecal metabolic products between CTRL and PCOS rats. Intriguingly, following moxibustion intervention, these differences were largely diminished, demonstrating the regulatory effect of moxibustion on gut microbiota. Specifically, moxibustion altered the gut microbiota by increasing the abundance of and , as well as decreasing the abundance of . Concurrently, we also noted that moxibustion promoted an increase in levels of short-chain fatty acids (including acetate, propionate, and butyrate) associated with the gut microbiota of PCOS rats, further emphasizing its positive impact on gut microbes. Additionally, moxibustion also exhibited effects in lowering FBG, testosterone, and fasting insulin levels, which are key biochemical indicators associated with PCOS and insulin resistance. Therefore, these findings suggest that moxibustion could alleviate DHEA-induced PCOS by regulating metabolic levels, restoring balance in gut microbiota, and modulating interactions between gut microbiota and host metabolites.

摘要

多囊卵巢综合征(PCOS)是一种常见的与内分泌紊乱相关的系统性疾病,影响育龄妇女的生育能力。它与葡萄糖和脂质代谢紊乱、肠道微生物群改变和胰岛素抵抗有关。现代治疗方法,如吡格列酮、二甲双胍和螺内酯,针对 PCOS 的特定症状,而在中医中,艾灸是一种常见的治疗方法。本研究通过建立脱氢表雄酮(DHEA)诱导的 PCOS 大鼠模型,探讨艾灸对 PCOS 的影响。将 36 只特定病原体无特定病原体雌性 Sprague-Dawley 大鼠分为四组:正常对照组(CTRL)、PCOS 模型组(PCOS)、艾灸治疗组(MBT)和二甲双胍治疗组(MET)。MBT 组大鼠接受艾灸治疗,MET 组大鼠进行二甲双胍灌胃治疗两周。我们评估了卵巢组织变化、血清睾丸酮、空腹血糖(FBG)和空腹胰岛素水平。此外,我们计算了胰岛素敏感指数(ISI)和稳态模型评估的胰岛素抵抗指数(HOMA-IR)。我们使用 16S rDNA 测序评估肠道微生物群,使用 H NMR 光谱评估代谢变化,并使用 Spearman 相关分析研究代谢产物与肠道微生物群组成之间的关系。结果表明,艾灸治疗显著改善了 DHEA 诱导的 PCOS 大鼠的卵巢功能障碍和胰岛素抵抗。我们观察到 CTRL 和 PCOS 大鼠之间肠道微生物群组成和粪便代谢产物谱存在显著差异。有趣的是,艾灸干预后,这些差异在很大程度上得到了缩小,表明艾灸对肠道微生物群具有调节作用。具体而言,艾灸通过增加和的丰度以及降低的丰度来改变肠道微生物群。同时,我们还注意到艾灸促进了与 PCOS 大鼠肠道微生物群相关的短链脂肪酸(包括乙酸盐、丙酸盐和丁酸盐)水平的升高,进一步强调了它对肠道微生物群的积极影响。此外,艾灸还降低了 FBG、睾丸酮和空腹胰岛素水平,这些是与 PCOS 和胰岛素抵抗相关的关键生化指标。因此,这些发现表明,艾灸可能通过调节代谢水平、恢复肠道微生物群平衡以及调节肠道微生物群与宿主代谢物之间的相互作用来缓解 DHEA 诱导的 PCOS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab06/11043641/ffefc24d4c45/fcimb-14-1328741-g001.jpg

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