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Cardiomyocyte β 2 ‐Adrenergic Receptor Plays A Protective Role in Cardiac Fibrosis
Author(s) -
Zhu Chaoqun,
Deng Bingqing,
Zhang Yu,
Wang Ying,
Xu Bing,
Xiang Yang Kevin
Publication year - 2020
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2020.34.s1.05028
Subject(s) - cardiac function curve , medicine , cardiac fibrosis , endocrinology , contractility , fibrosis , heart failure , diabetic cardiomyopathy , cardiomyopathy , diastole , diabetes mellitus , receptor , muscle hypertrophy , blood pressure
Background Chronic stimulation of β adrenergic receptor (βAR) has been implicated in cardiac remodeling including hypertrophy and fibrosis associated with heart failure. Previous studies indicate a role of β 2 AR on inhibiting collagen production in cultured cardiac fibroblasts, however, our recent studies show that global deletion of β 2 AR prevent cardiac fibrosis in diabetic cardiomyopathy. Therefore, this study aims to determine the specific role of cardiomyocyte β 2 AR in cardiac function and the development of cardiac fibrosis in vivo . Methods 2‐month old male β 2 AR flox/flox (f/f) mice (n=10) and cardiomyocyte‐specific knockout of β 2 AR (CKO) mice (n=10) were fed with either normal chow (NC), or high fat diet (HFD) for 6 months to induce obesity and diabetes. Echocardiography was performed using a Vevo 2100 imaging system from VisualSonics. Biochemistry and histological analyses were performed on heart tissues. Real‐time PCR was performed for mRNA expression examination. Results While cardiac function was normal at 2‐month old CKO mice, a significant decrease in cardiac contractility was observed in CKO mice compared to f/f mice at 8‐month old age (EF%: CKO 48.43 ± 1.314 vs . f/f 52.69 ± 0.8270, p<0.05). Moreover, HFD feeding exacerbated cardiac dysfunction in CKO mice when compared to f/f mice (EF%: CKO 42.93 ± 0.69 vs . f/f 46.79 ± 0.76, p<0.001). CKO mice also exhibited diastolic dysfunction (IVRT: CKO 20.23 ± 0.30 vs . f/f 16.83 ± 0.23, p<0.0001), which was exacerbated after HFD feeding (IVRT, CKO 24.75 ± 0.50 vs . f/f 19.94 ± 0.45, p<0.0001). The observed cardiac dysfunction was associated with severe cardiac fibrosis in 8‐month old CKO mice, and HFD feeding leads to further exacerbation in cardiac fibrosis. Cardiac fibrosis was validated with elevated protein expression of connective tissue growth factor (CTGF), and significant upregulations of mRNA expression of CTGF, α smooth muscle actin (α‐SMA), and collagen 1 in CKO HFD mice. Conclusions This study elucidates that cardiomyocyte β 2 AR is essential to maintain normal cardiac function and plays a protective role against the development of cardiac fibrosis in aging and HFD feeding in vivo . Support or Funding Information NIH HL113413, HL147264, VABX002900