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Antibiotic Azithromycin inhibits brown/beige fat functionality and promotes obesity in human and rodents

  • Jian Yu
  • , Xin Chen
  • , Yuanjin Zhang
  • , Xiangdi Cui
  • , Zhe Zhang
  • , Wenxiu Guo
  • , Dongmei Wang
  • , Shengbo Huang
  • , Yanru Chen
  • , Yepeng Hu
  • , Cheng Zhao
  • , Jin Qiu
  • , Yu Li
  • , Meiyao Meng
  • , Mingwei Guo
  • , Fei Shen
  • , Mengdi Zhang
  • , Ben Zhou
  • , Xuejiang Gu
  • , Jiqiu Wang
  • Xin Wang*, Xinran Ma*, Lingyan Xu*
*此作品的通讯作者
  • East China Normal University
  • Shanghai Jiao Tong University
  • Wenzhou Medical University
  • CAS - Shanghai Institute of Nutrition and Health

科研成果: 期刊稿件文章同行评审

摘要

Obesity, a metabolic disease caused by multiple factors, has become a global health problem. In addition to nutrient intake and sedentary lifestyle, environmental pollutants exposure has been shown to be involved in obesity epidemics. Antibiotics, a new type of environmental pollutant, have been widely used in animal husbandry, aquaculture and microorganism. However, the effects of antibiotics exposure on fat metabolism and metabolic diseases are largely unknown. Methods: We screened major types of antibiotics to examine their effects on the differentiation capacity and thermogenic functionality of brown and beige adipocytes, and found that azithromycin, one major kind of macrolide antibiotics suppressed brown and beige adipocyte functionality. We thus examined azithromycin accretion in adipose tissues of obese patients that correlates with BMI by high performance liquid chromatography-tandem mass spectrometry and systematically explore the influences of azithromycin on adiposity and metabolic performance in mice under high diet. Results: Azithromycin (macrolides) inhibits the mitochondrial and thermogenic gene programs of brown and beige adipocytes, thus disrupting their mitochondrial function and thermogenic response. Consistently, azithromycin treatment are more prone to diet-induced obesity in mice, and this was associated with impaired energy expenditure. Importantly, azithromycin is more accumulated in adipose tissue of obese patients and correlates with BMI and body weight. Mechanistically, we found that azithromycin inhibits mitochondria respiratory complex I protein levels and increases reactive oxidative species (ROS) levels, which causes damage of mitochondrial function in brown and beige adipocytes. The deleterious effects of azithromycin can be ameliorated by antioxidant N-acetyl-L-cysteine. Conclusions: Taken together, this work highlights the possible role of azithromycin in obesity epidemic and presents strategies for safe applications of antibiotics in the future.

源语言英语
页(从-至)1187-1203
页数17
期刊Theranostics
12
3
DOI
出版状态已出版 - 2022

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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