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September 18, 2025Aging Cell6 citationsOpen Access

Repeated Withdrawal of a GLPR Agonist Induces Hyperleptinemia and Deteriorates Metabolic Health in Obese Aging UM‐HET3 Mice

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NJNisi JiangJYJiyuan YinNLNatalia Lawrence

Key Points

  • Withdrawn GLP-1 therapy led to hyperleptinemia and metabolic decline in aged obese mice, showing significant health risks.
  • Mice undergoing intermittent liraglutide treatment regained fat but failed to restore lean mass, indicating an adverse body composition shift.
  • Continuous treatment with liraglutide resulted in weight reduction and improved metabolic health, contrasting with cyclic treatment groups.
  • Results suggest the importance of sustained GLP-1 therapy to prevent age-associated metabolic deterioration and sarcopenia.

Abstract

ABSTRACT GLP‐1‐based therapy is highly effective in combating aging‐associated metabolic diseases. However, the metabolic effects of frequent withdrawal from this therapy in aged, obese mice have not been previously studied. In this study, aged obese UM‐HET3 mice were assigned to three groups: Group 1 received no liraglutide treatment (Lira OFF); Group 2 underwent 3 cycles of treatment followed by withdrawal (Lira ON/OFF); and Group 3 remained on continuous treatment (Lira ON). As expected, mice in Group 3 showed reduced body weight and food intake, along with improved metabolic health. In contrast, mice in Group 2 developed hyperleptinemia and visceral fat expansion, leading to impaired metabolic health. Importantly, although these mice regained their fat mass after each treatment cycle, they failed to restore lean mass, an unfavorable shift in body composition that may increase vulnerability to aging‐related sarcopenia. These findings suggest that continuous GLP‐1‐based therapy is necessary to sustain metabolic benefits, while intermittent use may promote age‐associated sarcopenia and metabolic decline.

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Cite This Study

Jiang et al. (2025) studied this question.

synapsesocial.com/papers/68d461cb31b076d99fa612cdhttps://doi.org/10.1111/acel.70210
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