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 PMID:33627403  

Mitochondrial hydrogen sulfide supplementation improves health in the C. elegans Duchenne muscular dystrophy model.

Rebecca A Ellwood | Jennifer E Hewitt | Roberta Torregrossa | Ashleigh M Philp | Justin P Hardee | Samantha Hughes | David van de Klashorst | Nima Gharahdaghi | Taslim Anupom | Luke Slade | Colleen S Deane | Michael Cooke | Timothy Etheridge | Mathew Piasecki | Adam Antebi | Gordon S Lynch | Andrew Philp | Siva A Vanapalli | Matthew Whiteman | Nathaniel J Szewczyk
Proceedings of the National Academy of Sciences of the United States of America | 2021

Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder characterized by progressive muscle degeneration and weakness due to mutations in the dystrophin gene. The symptoms of DMD share similarities with those of accelerated aging. Recently, hydrogen sulfide (H2S) supplementation has been suggested to modulate the effects of age-related decline in muscle function, and metabolic H2S deficiencies have been implicated in affecting muscle mass in conditions such as phenylketonuria. We therefore evaluated the use of sodium GYY4137 (NaGYY), a H2S-releasing molecule, as a possible approach for DMD treatment. Using the dys-1(eg33) Caenorhabditis elegans DMD model, we found that NaGYY treatment (100 µM) improved movement, strength, gait, and muscle mitochondrial structure, similar to the gold-standard therapeutic treatment, prednisone (370 µM). The health improvements of either treatment required the action of the kinase JNK-1, the transcription factor SKN-1, and the NAD-dependent deacetylase SIR-2.1. The transcription factor DAF-16 was required for the health benefits of NaGYY treatment, but not prednisone treatment. AP39 (100 pM), a mitochondria-targeted H2S compound, also improved movement and strength in the dys-1(eg33) model, further implying that these improvements are mitochondria-based. Additionally, we found a decline in total sulfide and H2S-producing enzymes in dystrophin/utrophin knockout mice. Overall, our results suggest that H2S deficit may contribute to DMD pathology, and rectifying/overcoming the deficit with H2S delivery compounds has potential as a therapeutic approach to DMD treatment.

Pubmed ID: 33627403

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: Department of Health, United Kingdom
  • Agency: Medical Research Council, United Kingdom
    Id: MR/S002626/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/P021220/1
  • Agency: Medical Research Council, United Kingdom
    Id: MC_PC_16072
  • Agency: Biotechnology and Biological Sciences Research Council, United Kingdom
    Id: BB/N015894/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/P021220/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/T026014/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/K00414X/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/R502364/1

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Cell Signaling Technology (tool)

RRID:SCR_004431

Privately held company that develops and produces antibodies, ELISA kits, ChIP kits, proteomic kits, and other related reagents used to study cell signaling pathways that impact human health.

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Abcam (tool)

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A commercial antibody supplier which supplies primary and secondary antibodies, biochemicals, proteins, peptides, lysates, immunoassays and other kits.

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BZ33 (tool)

RRID:WB-STRAIN:WBStrain00004037

Caenorhabditis elegans with name dys-1(eg33) I. from WB.

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C57BL/10ScSn (tool)

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laboratory mouse with name C57BL/10ScSn from MGI.

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