Skip to main content
Fig. 2 | Journal of Biomedical Science

Fig. 2

From: Baicalin attenuates chronic hypoxia-induced pulmonary hypertension via adenosine A2A receptor-induced SDF-1/CXCR4/PI3K/AKT signaling

Fig. 2

The A2AR and baicalin attenuated right ventricular remodeling and pulmonary congestion in the hypoxia-induced PAH mouse model. Effects of baicalin (+Bai, 60 mg/kg/day) and CGS21680 (+CGS, 0.25 mg/kg/day) on RV/(LV + S) (a; n = 8), RV/BW (b; n = 8), and Lung/BW (c; n = 8) in WT and A2AR−/− mice. The mice were subjected to 4 weeks of hypoxia. Data are presented as the mean ± SD. #Value significantly greater than the corresponding value in saline-treated normoxic mice (# P < 0.05, ## P < 0.01). *Value significantly less than the corresponding value in hypoxic mice (*P < 0.05, **P < 0.01). §Value significantly less than the corresponding value in baicalin-treated mice (§ P < 0.05, §§ P < 0.01). +Value significantly greater than the corresponding value in WT saline-treated mice, WT hypoxic mice, and WT baicalin-treated mice (++ P < 0.01). WTH, wild-type hypoxic; A2AR−/−H, A2AR−/− hypoxic; s, saline-treated

Back to article page