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A combination of metformin and galantamine exhibits synergistic benefits in the treatment of sarcopenia
Caterina Tezze, … , Marco Sandri, Evi M. Mercken
Caterina Tezze, … , Marco Sandri, Evi M. Mercken
Published August 8, 2023
Citation Information: JCI Insight. 2023;8(15):e168787. https://doi.org/10.1172/jci.insight.168787.
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Research Article Aging Muscle biology

A combination of metformin and galantamine exhibits synergistic benefits in the treatment of sarcopenia

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Abstract

Age-associated sarcopenia, characterized by a progressive loss in muscle mass and strength, is the largest cause of frailty and disability in the elderly worldwide. Current treatments involve nonpharmacological guidelines that few subjects can abide by, highlighting the need for effective drugs. Preclinical models were employed to test the benefits of RJx-01, a combination drug composed of metformin and galantamine, on sarcopenia. In worms, RJx-01 treatment improved lifespan, locomotion, pharyngeal pumping, and muscle fiber organization. The synergistic effects of RJx-01 were recapitulated in a transgenic mouse model that displays an exacerbated aging phenotype (Opa1–/–). In these mice, RJx-01 ameliorated physical performance, muscle mass and force, neuromuscular junction stability, and systemic inflammation. RJx-01 also improved physical performance and muscle strength in 22-month-old WT mice and also improved skeletal muscle ultrastructure, mitochondrial morphology, autophagy, lysosomal function, and satellite cell content. Denervation and myofiber damage were decreased in RJx-01–treated animals compared with controls. RJx-01 improved muscle quality rather than quantity, indicating that the improvement in quality underlies the beneficial effects of the combination drug. The studies herein indicate synergistic beneficial effects of RJx-01 in the treatment of sarcopenia and support the pursuit of RJx-01 in a human clinical trial as a therapeutic intervention for sarcopenia.

Authors

Caterina Tezze, Francesco Ivan Amendolagine, Leonardo Nogara, Martina Baraldo, Stefano Ciciliot, Diletta Arcidiacono, Alice Zaramella, Giulio Masiero, Giulia Ferrarese, Stefano Realdon, Bert Blaauw, Giel Detienne, Ann T.J. Beliën, Marco Sandri, Evi M. Mercken

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Figure 2

RJx-01 treatment suppresses muscle mass and quality loss and enhances functional outcomes in muscle-specific Opa1–/– mice.

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RJx-01 treatment suppresses muscle mass and quality loss and enhances fu...
(A) Percentage of lean mass of Opa1–/– mice fed a control diet or a diet supplemented with RJx-01 (Opa1–/–, n = 11; Opa1–/– RJx-01, n = 8). (B) Weights of gastrocnemius muscles of Opa1–/– mice were fed a control diet, a control diet supplemented with metformin (Met), a control diet supplemented with galantamine (Gal), and a control diet supplemented with RJx-01 (Opa1–/–, n = 11; Opa1–/– Met, n = 6; Opa1–/– Gal, n = 9; Opa1–/– RJx-01, n = 8). (C) Myofibers cross-sectional area analysis (Opa1–/–, n=11; Opa1–/– Met, n = 6; Opa1–/– Gal, n = 9; Opa1–/– RJx-01, n = 8). Scale bar: 50 μm. (D) Representative images of immunostaining for NCAM expression, and quantification of denervated NCAM+ fibers in the respective groups (Opa1–/–, n = 10; Opa1–/– Met, n = 6; Opa1–/– Gal, n = 8; Opa1–/– RJx-01, n = 8). (E) Exercise performance on the treadmill expressed as running time (Opa1–/–, n = 11; Opa1–/– Met, n = 5; Opa1–/– Gal, n = 8; Opa1–/– RJx-01, n = 8). (F) Force-frequency curves were performed in vivo on gastrocnemius muscles. Absolute force and maximal specific force generated during tetanic contraction in the respective groups (Opa1–/–, n = 6; Opa1–/– Met, n = 3; Opa1–/– Gal, n = 5; Opa1–/– RJx-01, n = 5). Data are shown as mean ± SEM. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001; ####P < 0.0001 compared with Opa1–/– RJx-01. In A and F, a linear mixed-effects model was used, and 1-way ANOVA followed by Holm step-down method (2-tailed Student’s t test) was performed in B–E.

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