Mitochondrial respiration in C57BL/6 substrains varies in response to myocardial infarction
- PMID: 33630237
- DOI: 10.1007/s10863-021-09884-6
Mitochondrial respiration in C57BL/6 substrains varies in response to myocardial infarction
Abstract
The C57BL/6 mouse strain have been commonly used for the genetic background animal models and experimental research. There are several major sources of C57BL/6 substrains for the biomedical research community which display genetic and phenotypic differences. Previous studies have suggested that the varies in baseline of cardiovascular phenotypes as well as in response to pressure overload by transverse aortic constriction (TAC). To investigate whether there exist substrain specific differences in response to heart failure post myocardial infarction (MI), consequently the impaired mitochondrial respiration, we performed MI surgery on two commonly used C57BL/6 substrains: C57BL/6J (BL/6J) and C57BL/6NCrl (BL/6N) mice. Subsequently, measurements about cardiac function, histology and mitochondrial respiration capacities were conducted to evaluate the differences. The data showed that C57BL/6J(BL/6J) mice is more resistant to the attack of MI, evidenced by lower mortality, less infarct size and better preserved cardiac function after MI, especially exhibited better mitochondrial respiration capacities, compared with the C57BL/6NCrl(BL/6N) mice.
Keywords: C57BL/6 mouse; Heart failure; Mitochondrial respiration; Myocardial infarction; OXPHOS.
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References
-
- Almodovar AJ, Luther RJ, Stonebrook CL, Wood PA (2013) Genomic structure and genetic drift in C57BL/6 congenic metabolic mutant mice. Mol Genet Metab 110:396–400. https://doi.org/10.1016/j.ymgme.2013.06.019 - DOI - PubMed
-
- Arkblad EL, Betsholtz C, Rydstrom J (1996) The cDNA sequence of proton-pumping nicotinamide nucleotide transhydrogenase from man and mouse. Biochim Biophys Acta 1273:203–205. https://doi.org/10.1016/0005-2728(95)00159-x - DOI - PubMed
-
- Ashworth A, Bardgett ME, Fowler J, Garber H, Griffith M, Curran CP (2015) Comparison of neurological function in males and females from two substrains of C57BL/6. Mice Toxics 3:1–17. https://doi.org/10.3390/toxics3010001 - DOI - PubMed
-
- Bothe GW, Bolivar VJ, Vedder MJ, Geistfeld JG (2004) Genetic and behavioral differences among five inbred mouse strains commonly used in the production of transgenic and knockout mice. Genes Brain Behav 3:149–157. https://doi.org/10.1111/j.1601-183x.2004.00064.x - DOI - PubMed
-
- Cooper MA et al (2018) Intrinsic activity of C57BL/6 substrains associates with high-fat diet-induced mechanical sensitivity in mice. J Pain 19:1285–1295. https://doi.org/10.1016/j.jpain.2018.05.005 - DOI - PubMed - PMC
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