TY - JOUR
T1 - Punicalagin Prevents Hypoxic Pulmonary Hypertension via Anti-Oxidant Effects in Rats
AU - Shao, Jingyun
AU - Wang, Peng
AU - Liu, An
AU - Du, Xusheng
AU - Bai, Jie
AU - Chen, Mingwei
N1 - Publisher Copyright:
© 2016 World Scientific Publishing Company.
PY - 2016
Y1 - 2016
N2 - Punicalagin (PG), a major bioactive ingredient in pomegranate juice, has been proven to have anti-oxidative stress properties and to exert protective effects on acute lung injuries induced by lipopolysaccharides. This study aimed to investigate the effects of PG treatment on hypoxic pulmonary hypertension (HPH) and the underlying mechanisms responsible for the effects. Rats were exposed to 10% oxygen for 2 wk (8 h/day) to induce the HPH model. PG (5, 15, 45mg/kg) was orally administered 10min before hypoxia each day. PG treatments at the doses of 15 and 45mg/kg/d decreased the mean pulmonary arterial pressure (mPAP) and alleviated right ventricular hypertrophy and vascular remodeling in HPH rats. Meanwhile, PG treatment attenuated the hypoxia-induced endothelial dysfunction of pulmonary artery rings. The beneficial effects of PG treatment were associated with improved nitric oxide (NO)-cGMP signaling and reduced oxidative stress, as evidenced by decreased superoxide generation, gp91phox expression and nitrotyrosine content in the pulmonary arteries. Furthermore, tempol's scavenging of oxidative stress also increased NO production and attenuated endothelial dysfunction and pulmonary hypertension in HPH rats. Combining tempol and PG did not exert additional beneficial effects compared to tempol alone. Our study indicated for the first time that PG treatment can protect against hypoxia-induced endothelial dysfunction and pulmonary hypertension in rats, which may be induced via its anti-oxidant actions.
AB - Punicalagin (PG), a major bioactive ingredient in pomegranate juice, has been proven to have anti-oxidative stress properties and to exert protective effects on acute lung injuries induced by lipopolysaccharides. This study aimed to investigate the effects of PG treatment on hypoxic pulmonary hypertension (HPH) and the underlying mechanisms responsible for the effects. Rats were exposed to 10% oxygen for 2 wk (8 h/day) to induce the HPH model. PG (5, 15, 45mg/kg) was orally administered 10min before hypoxia each day. PG treatments at the doses of 15 and 45mg/kg/d decreased the mean pulmonary arterial pressure (mPAP) and alleviated right ventricular hypertrophy and vascular remodeling in HPH rats. Meanwhile, PG treatment attenuated the hypoxia-induced endothelial dysfunction of pulmonary artery rings. The beneficial effects of PG treatment were associated with improved nitric oxide (NO)-cGMP signaling and reduced oxidative stress, as evidenced by decreased superoxide generation, gp91phox expression and nitrotyrosine content in the pulmonary arteries. Furthermore, tempol's scavenging of oxidative stress also increased NO production and attenuated endothelial dysfunction and pulmonary hypertension in HPH rats. Combining tempol and PG did not exert additional beneficial effects compared to tempol alone. Our study indicated for the first time that PG treatment can protect against hypoxia-induced endothelial dysfunction and pulmonary hypertension in rats, which may be induced via its anti-oxidant actions.
KW - Endothelial Function
KW - Hypoxic Pulmonary Hypertension
KW - Nitric Oxide
KW - Oxidative Stress
KW - Punicalagin
UR - https://www.scopus.com/pages/publications/84969931447
U2 - 10.1142/S0192415X16500439
DO - 10.1142/S0192415X16500439
M3 - 文章
C2 - 27222062
AN - SCOPUS:84969931447
SN - 0192-415X
VL - 44
SP - 785
EP - 801
JO - American Journal of Chinese Medicine
JF - American Journal of Chinese Medicine
IS - 4
ER -