4.7 Article

Hypothalamic miR-219 regulates individual metabolic differences in response to diet-induced weight cycling

期刊

MOLECULAR METABOLISM
卷 9, 期 -, 页码 176-186

出版社

ELSEVIER
DOI: 10.1016/j.molmet.2018.01.015

关键词

Weight cycling; Metabolic syndrome; miRNAs; Ventromedial hypothalamus; High fat diet; Diabetes

资金

  1. European Research Council [260463]
  2. Israel Science Foundation [1565/15, 1916/12]
  3. Chief Scientist Office of the Israeli Ministry of Health [311389]
  4. Federal Ministry of Education and Research [01KU1501A]
  5. I-CORE Program of the Planning and Budgeting Committee
  6. Nella and Leon Benoziyo Center for Neurological Diseases
  7. Henry Chanoch Krenter Institute for Biomedical Imaging and Genomics
  8. Perlman Family Foundation
  9. Adelis Foundation
  10. Marc Besen and the Pratt Foundation
  11. Irving I. Moskowitz Foundation
  12. Bruno and Simone Licht

向作者/读者索取更多资源

Consumption of a low calorie diet is the most common approach to lose weight. While generally effective at first, it is frequently followed by a relapse where the pre-diet weight is regained, and often exceeded. This pattern of repeated weight loss/regain is referred to as weight cycling and the resulting metabolic response varies greatly between individuals. Objective: We attempted to address the issue of individual differences in the response to weight cycling in male mice. Methods: We first exposed adult wild type mice to repeated cycles of high/low fat food. Next, using a lentiviral approach, we knocked-down or over-expressed miR-219 in the ventromedial hypothalamus (VMH) of an additional mouse cohort and performed a full metabolic assessment. Results: Exposure of wild type males to weight cycling resulted in the division of the cohort into subsets of resistant versus metabolic syndrome-prone (MS) animals, which differed in their metabolic profile and hypothalamic miR-219 levels. Lentiviral knock-down of miR-219 in the VMH led to exacerbation of metabolic syndrome. In contrast, over-expression of miR-219 resulted in moderation of the metabolic syndrome phenotype. Conclusions: Our results suggest a role for miR-219 in the mediation of the metabolic phenotype resulting from repeated weight cycling. (C) 2018 The Authors. Published by Elsevier GmbH.

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