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柚皮苷通过塑造肠道微生物群激活高脂肪饮食喂养的 C57BL/6 小鼠的米色脂肪细胞棕色化。

Naringenin activates beige adipocyte browning in high fat diet-fed C57BL/6 mice by shaping the gut microbiota.

机构信息

Department of the Third Health Care, Second Medical Centre of Chinese PLA General Hospital, Medical School of Chinese PLA, Beijing 100039, China.

Centre of Sport Nutrition and Health, Zhengzhou University, Zhengzhou 450001, China.

出版信息

Food Funct. 2022 Oct 3;13(19):9918-9930. doi: 10.1039/d2fo01610a.

Abstract

Naringenin is a kind of natural citrus flavonoid with various biological and pharmacological functions. Several studies have reported the anti-obesity effect of naringenin, but its potential mechanism of action (MoA) on beige adipose browning remains unclear. Here, we investigated whether naringenin induces gut microbe-host interactions to promote beige adipose thermogenesis and browning. Naringenin treatment alleviated obesity, increased body's energy expenditure and activated inguinal white adipose tissue thermogenesis and browning in high fat diet (HFD) fed mice. In addition, naringenin improved HFD-induced gut microbiota dysbiosis and increased short-chain fatty acid (SCFA) levels (especially acetic acid) in a host's cecum and serum. Furthermore, using antibiotic treatment and gut microbe transplantation, we found that gut microbes played an indispensable role in naringenin-induced beige fat browning and naringenin-exerted anti-obesity effects. Our study suggests that naringenin activated beige adipose thermogenesis and browning by gut microbe-SCFA-host interactions, which increase energy expenditure and prevent HFD-induced obesity.

摘要

柚皮素是一种天然的柑橘类黄酮,具有多种生物和药理功能。有几项研究报道了柚皮素的抗肥胖作用,但它对米色脂肪褐变的潜在作用机制(MoA)尚不清楚。在这里,我们研究了柚皮素是否通过肠道微生物-宿主相互作用促进米色脂肪产热和褐变。柚皮素治疗可缓解肥胖,增加机体能量消耗,并激活高脂饮食(HFD)喂养小鼠腹股沟白色脂肪产热和褐变。此外,柚皮素改善了 HFD 诱导的肠道微生物失调,并增加了宿主盲肠和血清中的短链脂肪酸(SCFA)水平(尤其是乙酸)。此外,通过抗生素处理和肠道微生物移植,我们发现肠道微生物在柚皮素诱导的米色脂肪褐变和柚皮素发挥抗肥胖作用中起着不可或缺的作用。我们的研究表明,柚皮素通过肠道微生物-SCFA-宿主相互作用激活米色脂肪产热和褐变,从而增加能量消耗并预防 HFD 诱导的肥胖。

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