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Pathogenic hypothalamic extracellular matrix promotes metabolic disease.
- Source :
-
Nature [Nature] 2024 Sep; Vol. 633 (8031), pp. 914-922. Date of Electronic Publication: 2024 Sep 18. - Publication Year :
- 2024
-
Abstract
- Metabolic diseases such as obesity and type 2 diabetes are marked by insulin resistance <superscript>1,2</superscript> . Cells within the arcuate nucleus of the hypothalamus (ARC), which are crucial for regulating metabolism, become insulin resistant during the progression of metabolic disease <superscript>3-8</superscript> , but these mechanisms are not fully understood. Here we investigated the role of a specialized chondroitin sulfate proteoglycan extracellular matrix, termed a perineuronal net, which surrounds ARC neurons. In metabolic disease, the perineuronal net of the ARC becomes augmented and remodelled, driving insulin resistance and metabolic dysfunction. Disruption of the perineuronal net in obese mice, either enzymatically or with small molecules, improves insulin access to the brain, reversing neuronal insulin resistance and enhancing metabolic health. Our findings identify ARC extracellular matrix remodelling as a fundamental mechanism driving metabolic diseases.<br /> (© 2024. The Author(s).)
- Subjects :
- Animals
Male
Mice
Rats
Insulin metabolism
Mice, Inbred C57BL
Mice, Obese
Neurons metabolism
Neurons pathology
Obesity metabolism
Obesity pathology
Obesity therapy
Rats, Sprague-Dawley
Arcuate Nucleus of Hypothalamus drug effects
Arcuate Nucleus of Hypothalamus metabolism
Arcuate Nucleus of Hypothalamus pathology
Chondroitin Sulfate Proteoglycans metabolism
Extracellular Matrix drug effects
Extracellular Matrix metabolism
Extracellular Matrix pathology
Insulin Resistance
Metabolic Diseases metabolism
Metabolic Diseases pathology
Metabolic Diseases therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1476-4687
- Volume :
- 633
- Issue :
- 8031
- Database :
- MEDLINE
- Journal :
- Nature
- Publication Type :
- Academic Journal
- Accession number :
- 39294371
- Full Text :
- https://doi.org/10.1038/s41586-024-07922-y