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. 2024 May 15;9:133. doi: 10.1038/s41392-024-01816-1

Fig. 2.

Fig. 2

2-APQC improves heart failure (HF) by relieving myocardial hypertrophy and inhibiting myocardial fibrosis in ISO-induced HF model in vitro and in vivo. a H9c2 cells were treated with the indicated concentration 2-APQC for 24 h, and then ISO treated for 48 h. Determine the size of cardiomyocytes by β-actin tracker staining (red). The position of the nucleus is marked by 4’,6-diamidino-2-phenylindole (DAPI) staining. Scale bar = 10 μm. Data are present as mean ± s.e.m, n = 3. b, c Immunostaining of cells with α-SMA and Collagen. The position of the nucleus is marked by DAPI staining. The representative image is shown, and the Scale bar = 10 μm. Data are present as mean ± s.e.m, n = 3. d Detection and quantification of the expression of fibronectin and collagen I by Western blot. e, f Representative image of echocardiogram of indicated groups. gl ejection fraction (EF), fractional shortening (FS), left ventricular posterior wall dimension (LVPWD) (mean ± s.e.m, con group, ISO group,ISO + Met group, ISO + 10 μM 2-APQC group, ISO + 20 μM 2-APQC group, ISO + 30 μM 2-APQC group, n = 6; ISO + Hon group, n = 10), LVESd, HWI (mean ± s.e.m, con group, n = 6; ISO group, ISO + Met group, ISO+Hon group, ISO + 10 μM 2-APQC group, ISO + 20 μM 2-APQC group, ISO + 30 μM 2-APQC group, n = 10), BNP (mean±s.e.m, con group, ISO group, ISO + Met group, ISO + Hon group, ISO + 10 μM 2-APQC group, ISO + 30 μM 2-APQC group, n = 8; ISO + 20 μM 2-APQ group, n = 10) were assessed by quantitative echocardiography, HWI was calculated by heart weight/body weight and Enzyme-linked immunosorbent assay was used to detect BNP levels. m Representative heart tissue in each group. n Represents the result of HE staining in heart tissues, scale bar = 4 mm. o Sirius Red staining in heart tissues, scale bar = 4 mm. n = 3. p Wheat germ agglutinin (WGA) staining in heart tissues, scale bar = 10 μm. q The percentage of fibrosis in heart tissue. The analysis of myocyte cross-sectional area in heart tissue. Data are present as mean ± s.e.m, n = 3. rv Analysis of serum biochemical indicators. Use enzymatic reagent kit to measure serum AST (mean ± s.e.m, con group, ISO group, ISO + Met group, ISO + Hon group, ISO + 10 μM 2-APQC group, ISO + 20 μM 2-APQC group, n = 7; ISO + 30 μM 2-APQ group, n = 6), LDH (mean ± s.e.m, con group, ISO + Hon group, n = 7; ISO group, ISO + 10 μM 2-APQC group, ISO + 20 μM 2-APQC group, n = 9; ISO + Met group, ISO + 30 μM 2-APQ group, n = 6;), α-HBDH (mean ± s.e.m, con group, ISO + Hon group, n = 8; ISO group, n = 9; ISO + Met group, n = 7; ISO + 10 μM 2-APQC group, ISO + 20 μM 2-APQC group, n = 6; ISO + 30 μM 2-APQ group, n = 7;) and creatine kinase-MB (CK-MB) (mean ± s.e.m, con group, ISO + 30 μM 2-APQ group, n = 8; ISO group, n = 10; ISO + Met group, n = 6; ISO + Hon group, ISO + 10 μM 2-APQC group, ISO + 20 μM 2-APQC group, n = 7;). w The body weight changes during the experiment of the indicated groups. β-actin, loading control. ns, no significance, *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001, compared with ISO group; #p < 0.05, ##p < 0.01, ###p < 0.001, ####p < 0.0001, compared with control group. Nico nicotinamide, Hon Honokiol, ISO isoproterenol