» Articles » PMID: 35803994

A Medium-chain Triglyceride Containing Ketogenic Diet Exacerbates Cardiomyopathy in a CRISPR/Cas9 Gene-edited Rat Model with Duchenne Muscular Dystrophy

Overview
Journal Sci Rep
Specialty Science
Date 2022 Jul 8
PMID 35803994
Authors
Affiliations
Soon will be listed here.
Abstract

Duchenne muscular dystrophy (DMD) is an X-linked recessive myopathy caused by dystrophin mutations. Although respiratory management has improved the prognosis of patients with DMD, inevitable progressive cardiomyopathy is a current leading cause of premature death. Recently, we showed that a medium-chain triglyceride containing ketogenic diet (MCTKD) improves skeletal muscle function and pathology in a CRISPR/Cas9 gene-edited rat model with DMD. In this study, we sought to clarify whether MCTKD also improves the cardiomyopathy in these rats. DMD rats were fed either the MCTKD or normal diet (ND) from ages of 3 weeks to 9 months old. Compared with the ND-fed rats, MCTKD-fed rats showed significantly prolonged QRS duration, decreased left ventricular fractional shortening, an increased heart weight/body weight ratio, and progression of cardiac fibrosis. In contrast to our previous study which found that MCTKD improved skeletal myopathy, the current study showed unexpected exacerbation of the cardiomyopathy. Further studies are needed to explore the underlying mechanisms for these differences and to explore modified dietary options that improve skeletal and cardiac muscles simultaneously.

Citing Articles

Developing hydrogels for gene therapy and tissue engineering.

Su C, Lin D, Huang X, Feng J, Jin A, Wang F J Nanobiotechnology. 2024; 22(1):182.

PMID: 38622684 PMC: 11017488. DOI: 10.1186/s12951-024-02462-z.


Rodent Models of Dilated Cardiomyopathy and Heart Failure for Translational Investigations and Therapeutic Discovery.

Ponzoni M, Coles J, Maynes J Int J Mol Sci. 2023; 24(4).

PMID: 36834573 PMC: 9963155. DOI: 10.3390/ijms24043162.


Functional Nutrients to Ameliorate Neurogenic Muscle Atrophy.

Moresi V, Renzini A, Cavioli G, Seelaender M, Coletti D, Gigli G Metabolites. 2022; 12(11).

PMID: 36422289 PMC: 9693586. DOI: 10.3390/metabo12111149.

References
1.
Grady R, Teng H, Nichol M, Cunningham J, WILKINSON R, Sanes J . Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy. Cell. 1997; 90(4):729-38. DOI: 10.1016/s0092-8674(00)80533-4. View

2.
Bergmann O, Zdunek S, Felker A, Salehpour M, Alkass K, Bernard S . Dynamics of Cell Generation and Turnover in the Human Heart. Cell. 2015; 161(7):1566-75. DOI: 10.1016/j.cell.2015.05.026. View

3.
Stafstrom C, Rho J . The ketogenic diet as a treatment paradigm for diverse neurological disorders. Front Pharmacol. 2012; 3:59. PMC: 3321471. DOI: 10.3389/fphar.2012.00059. View

4.
Sugihara H, Teramoto N, Nakamura K, Shiga T, Shirakawa T, Matsuo M . Cellular senescence-mediated exacerbation of Duchenne muscular dystrophy. Sci Rep. 2020; 10(1):16385. PMC: 7550355. DOI: 10.1038/s41598-020-73315-6. View

5.
Hourde C, Joanne P, Medja F, Mougenot N, Jacquet A, Mouisel E . Voluntary physical activity protects from susceptibility to skeletal muscle contraction-induced injury but worsens heart function in mdx mice. Am J Pathol. 2013; 182(5):1509-18. DOI: 10.1016/j.ajpath.2013.01.020. View