Literature DB >> 33630237

Mitochondrial respiration in C57BL/6 substrains varies in response to myocardial infarction.

Zhou Zhou1, Zhiheng Liu1, Xu Gao1, Qinqiang Long2.   

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.

Entities:  

Keywords:  C57BL/6 mouse; Heart failure; Mitochondrial respiration; Myocardial infarction; OXPHOS

Mesh:

Year:  2021        PMID: 33630237     DOI: 10.1007/s10863-021-09884-6

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  28 in total

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Journal:  Cell Metab       Date:  2006-01       Impact factor: 27.287

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Journal:  Compr Physiol       Date:  2015-09-20       Impact factor: 9.090

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Journal:  Nature       Date:  2012-12-05       Impact factor: 49.962

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Journal:  Genes Brain Behav       Date:  2004-06       Impact factor: 3.449

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Journal:  Mol Genet Metab       Date:  2013-07-02       Impact factor: 4.797

7.  Muscone improves cardiac function in mice after myocardial infarction by alleviating cardiac macrophage-mediated chronic inflammation through inhibition of NF-κB and NLRP3 inflammasome.

Authors:  Yingqiang Du; Xin Gu; Haoyu Meng; Nan Aa; Shuiyuan Liu; Chengyi Peng; Yingbin Ge; Zhijian Yang
Journal:  Am J Transl Res       Date:  2018-12-15       Impact factor: 4.060

8.  The cDNA sequence of proton-pumping nicotinamide nucleotide transhydrogenase from man and mouse.

Authors:  E L Arkblad; C Betsholtz; J Rydström
Journal:  Biochim Biophys Acta       Date:  1996-03-28

9.  Comparison of Neurological Function in Males and Females from Two Substrains of C57BL/6 Mice.

Authors:  Amy Ashworth; Mark E Bardgett; Jocelyn Fowler; Helen Garber; Molly Griffith; Christine Perdan Curran
Journal:  Toxics       Date:  2014-12-25

10.  LXR/RXR signaling and neutrophil phenotype following myocardial infarction classify sex differences in remodeling.

Authors:  Kristine Y DeLeon-Pennell; Alan J Mouton; Osasere K Ero; Yonggang Ma; Rugmani Padmanabhan Iyer; Elizabeth R Flynn; Ingrid Espinoza; Solomon K Musani; Ramachandran S Vasan; Michael E Hall; Ervin R Fox; Merry L Lindsey
Journal:  Basic Res Cardiol       Date:  2018-08-21       Impact factor: 17.165

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