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生酮饮食通过调节巨噬细胞增殖缓解 UUO 小鼠的肾间质纤维化。

Ketogenic diet alleviates renal interstitial fibrosis in UUO mice by regulating macrophage proliferation.

机构信息

Institute of Organ Transplantation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

J Nutr Biochem. 2023 Aug;118:109335. doi: 10.1016/j.jnutbio.2023.109335. Epub 2023 Apr 5.

Abstract

The ketogenic diet (KD), a high-fat and extremely low-carbohydrate dietary regimen, has long been acknowledged as a highly beneficial dietary therapy for the treatment of intractable epilepsy throughout the last decade. Because of its significant therapeutic potential for a variety of ailments, KD is increasingly attracting study interest. In renal fibrosis, KD has received little attention. This study aimed to determine whether KD protects against renal fibrosis in unilateral ureteral obstruction (UUO) models and the possible mechanisms. The ketogenic diet, according to our findings, reduces UUO-induced kidney injury and fibrosis in mice. KD dramatically decreased the number of F4/80macrophages in kidneys. Next, immunofluorescence results revealed a reduction in the number of F4/80Ki67macrophages in the KD group. Furthermore, our study evaluated the impact of β-hydroxybutyric acid (β-OHB) in RAW246.7 macrophages in vitro. We found that β-OHB inhibits macrophage proliferation. Mechanistically, β-OHB inhibits macrophage proliferation may be via the FFAR3-AKT pathway. Collectively, our study indicated that KD ameliorates UUO-induced renal fibrosis by regulating macrophage proliferation. KD may be an effective therapy method for renal fibrosis due to its protective impact against the disorder.

摘要

生酮饮食(KD)是一种高脂肪、极低碳水化合物的饮食方案,在过去十年中,它一直被认为是治疗难治性癫痫的一种非常有效的饮食疗法。由于其对多种疾病的显著治疗潜力,KD 越来越受到研究关注。在肾纤维化方面,KD 受到的关注较少。本研究旨在确定 KD 是否能预防单侧输尿管梗阻(UUO)模型中的肾纤维化以及可能的机制。根据我们的研究结果,KD 可减轻 UUO 诱导的小鼠肾脏损伤和纤维化。KD 可显著减少肾脏中 F4/80 巨噬细胞的数量。接下来,免疫荧光结果显示 KD 组 F4/80Ki67 巨噬细胞数量减少。此外,我们还评估了 β-羟基丁酸(β-OHB)在体外 RAW246.7 巨噬细胞中的作用。我们发现 β-OHB 可抑制巨噬细胞增殖。在机制上,β-OHB 可能通过 FFAR3-AKT 通路抑制巨噬细胞增殖。综上所述,本研究表明 KD 通过调节巨噬细胞增殖来改善 UUO 诱导的肾纤维化。由于 KD 对该疾病具有保护作用,因此它可能是治疗肾纤维化的有效方法。

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