scholarly journals Grape seed proanthocyanidin extract supplementation affects exhaustive exercise-induced fatigue in mice

2018 ◽  
Vol 62 (0) ◽  
Author(s):  
Liu Xianchu ◽  
Liu Ming ◽  
Liu Xiangbin ◽  
Zheng Lan
Appetite ◽  
2015 ◽  
Vol 91 ◽  
pp. 432
Author(s):  
J. Serrano ◽  
À. Casanova-Martí ◽  
M.T. Blay ◽  
X. Terra ◽  
M. Pinent ◽  
...  

2020 ◽  
Vol 64 (16) ◽  
pp. 2000303 ◽  
Author(s):  
Àngela Casanova‐Martí ◽  
Noemi González‐Abuín ◽  
Joan Serrano ◽  
Maria Teresa Blay ◽  
Ximena Terra ◽  
...  

RSC Advances ◽  
2019 ◽  
Vol 9 (21) ◽  
pp. 11842-11850 ◽  
Author(s):  
Er Hui Wang ◽  
Zeng Li Yu ◽  
Yong Jun Bu ◽  
Peng Wei Xu ◽  
Jin Yan Xi ◽  
...  

GSPE alleviates high-fat diet induced testicular toxicity in rats by promoting anti-apoptotic activity.


2020 ◽  
Vol 11 ◽  
Author(s):  
Yongxue Ruan ◽  
Qike Jin ◽  
Jingjing Zeng ◽  
Fangfang Ren ◽  
Zuoyi Xie ◽  
...  

Myocardial infarction is one of the most serious fatal diseases in the world, which is due to acute occlusion of coronary arteries. Grape seed proanthocyanidin extract (GSPE) is an active compound extracted from grape seeds that has anti-oxidative, anti-inflammatory and anti-tumor pharmacological effects. Natural products are cheap, easy to obtain, widely used and effective. It has been used to treat numerous diseases, such as cancer, brain injury and diabetes complications. However, there are limited studies on its role and associated mechanisms in myocardial infarction in mice. This study showed that GSPE treatment in mice significantly reduced cardiac dysfunction and improved the pathological changes due to MI injury. In vitro, GSPE inhibited the apoptosis of H9C2 cells after hypoxia culture, resulting in the expression of Bax decreased and the expression of Bcl-2 increased. The high expression of p-PI3K and p-AKT was detected in MI model in vivo and in vitro. The use of the specific PI3K/AKT pathway inhibitor LY294002 regressed the cardio-protection of GSPE. Our results showed that GSPE could improve the cardiac dysfunction and remodeling induced by MI and inhibit cardiomyocytes apoptosis in hypoxic conditions through the PI3K/AKT signaling pathway.


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