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Here we tested the hypothesis that the genetic deletion of metabotropic glutamate receptor 5 (mGluR5) may rescue metabolic and inflammatory features present in BACHD mice, a mouse model of Huntington\u2019s disease (HD) with an obese phenotype. For that, we crossed BACHD and mGluR5 knockout mice (mGluR5<jats:sup>\u2212\/\u2212<\/jats:sup>) in order to obtain the following groups: Wild type (WT), mGluR5<jats:sup>\u2212\/\u2212<\/jats:sup>, BACHD and BACHD\/mGluR5<jats:sup>\u2212\/\u2212<\/jats:sup> (double mutant mice). Our results showed that the double mutant mice present decreased body weight as compared to BACHD mice in all tested ages and reduced visceral adiposity as compared to BACHD at 6\u00a0months of age. Additionally, 12-month-old double mutant mice present increased adipose tissue levels of adiponectin, decreased leptin levels, and increased IL-10\/TNF ratio as compared to BACHD mice. Taken together, our preliminary data propose that the absence of mGluR5 reduce weight gain and visceral adiposity in BACHD mice, along with a decrease in the inflammatory state in the visceral adipose tissue (VAT), which may indicate that mGluR5 may play a role in adiposity modulation.<\/jats:p>","DOI":"10.1038\/s41598-022-08924-4","type":"journal-article","created":{"date-parts":[[2022,4,5]],"date-time":"2022-04-05T09:33:05Z","timestamp":1649151185000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":10,"title":["Metabotropic glutamate receptor 5 knockout rescues obesity phenotype in a mouse model of Huntington\u2019s disease"],"prefix":"10.1038","volume":"12","author":[{"given":"Rebeca P. 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