The <scp>NLRP3</scp> inhibitor <scp>NT</scp>‐0796 enhances and sustains <scp>GLP</scp>‐<scp>1R</scp> agonist‐mediated weight loss in a murine diet‐induced obesity model

Alleviation of obesity-associated inflammation via NLRP3 inhibition 1) constitutes an effective weight-loss strategy as monotherapy in mice with DIO, 2) augments the weight-loss efficacy of a subtherapeutic dose of semaglutide, and 3) blocks recovery of lost weight following cessation of semaglutide.

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Publication Details

Journal
Obesity
Published
2025-04-30
DOI
https://doi.org/10.1002/oby.24305
Citations
4
Primary Topic
Diabetes Treatment and Management
Type
article
Field-Weighted Citation Impact
5.18

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article

The NLRP3 inhibitor NT‐0796 enhances and sustains GLP‐1R agonist‐mediated weight loss in a murine diet‐induced obesity model

John R. Doedens, Valérie Reader, Nicola Lindsay, Zsofia Digby et al.
4 citations
Obesity
Diabetes Treatment and Management
5.18
article

The NLRP3 inhibitor NT‐0796 enhances and sustains GLP‐1R agonist‐mediated weight loss in a murine diet‐induced obesity model

John R. Doedens, Valérie Reader, Nicola Lindsay, Zsofia Digby, Peter Thornton, Nicholas Clarke, Alan P. Watt
article en
4 citations

Abstract

Alleviation of obesity-associated inflammation via NLRP3 inhibition 1) constitutes an effective weight-loss strategy as monotherapy in mice with DIO, 2) augments the weight-loss efficacy of a subtherapeutic dose of semaglutide, and 3) blocks recovery of lost weight following cessation of semaglutide.

ObesityVol. 33(7)
University of Washington
Responsible consumption and production
Openalex Percentile: Top 5%
Diabetes Treatment and Management
5.18
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