Sunday, January 18, 2026

Skeletal Muscle 11beta-HSD1 Controls Glucocorticoid-Induced Proteolysis and Expression of E3 Ubiquitin Ligases Atrogin-1 and MuRF-1

Authors: Katrin Biedasek, Janin Andres, Knut Mai, Stephanie Adams, Simone Spuler, Jens Fielitz, Joachim Spranger

DOI: 10.1371/journal.pone.0016674

Abstract Summary

Researchers found that the enzyme 11β-HSD1, which converts inactive cortisone to active cortisol in muscle cells, plays a key role in glucocorticoid-induced muscle wasting. Blocking this enzyme with an inhibitor completely prevented cortisone-triggered protein breakdown and suppressed genes linked to muscle atrophy. This discovery suggests 11β-HSD1 inhibitors could offer a therapeutic strategy to combat muscle loss.

Why Brain? 🧠

Blocking 11beta-HSD1 enzyme prevents steroid-induced muscle wasting by stopping protein breakdown, offering a potential therapeutic target to preserve muscle mass in patients on glucocorticoid therapy.

License: CC BY.


The image is AI-generated for illustrative purposes only. Courtesy of Midjourney.

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