Agkistrodon acutus-purified protein C activator protects human umbilical vein endothelial cells against H 2 O 2 -induced apoptosis

Recent studies show that the Agkistrodon acutus (Viperidae) (syn. Deinagkistrodon acutus) protein C activator (PCA) treats acute myocardial infarction and ischaemia-reperfusion animal models effectively, while the underlying mechanism remains unknown. To study the effect of PCA on the injury of huma...

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Veröffentlicht in:Pharmaceutical biology 2016-12, Vol.54 (12), p.3285-3291
Hauptverfasser: Li, Shu, Hong, Yun, Jin, Xin, Li, Xianwei, Sun, Entao, Zhang, Genbao, Lu, Linming, Nie, Liuwang
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Sprache:eng
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Zusammenfassung:Recent studies show that the Agkistrodon acutus (Viperidae) (syn. Deinagkistrodon acutus) protein C activator (PCA) treats acute myocardial infarction and ischaemia-reperfusion animal models effectively, while the underlying mechanism remains unknown. To study the effect of PCA on the injury of human umbilical vein endothelial cells (HUVECs) induced by H O and the underlying mechanism. Primary cultured HUVECs were pretreated with PCA (20, 40 and 80 μg/mL) for 1 h, then HUVEC apoptosis was induced by 300 μmol/mL H O . Apoptosis was analyzed by AnnexinV-FITC/PI, and reactive oxygen species (ROS) level was tested by flow cytometry. Colorimetric methods were used to detect the levels of NO and IL-1. In addition, real-time PCR and western blot analyses were used to detect the expression of eNOS and phospho-p38/MAPK. Morphological changes were induced by H O in HUVECs. The cell survival rate was increased by 43.9, 64.0 and 80.6% in each PCA pretreated group (20, 40 and 80 μg/mL) compared to the model group. In each PCA pretreated group, oxidative stress level was also decreased to 54.7, 42.7 and 25.1%. Moreover, the level of IL-1 was decreased to 83.3, 62.2 and 30.7%. The level of NO was increased by 155.9, 232.4 and 317.6%. Apoptosis rate was decreased to 59.0, 47.7 and 32.7%. Phospho-p38 expression was downregulated, but eNOS expression was upregulated. The results suggest that PCA can effectively protect the endothelial cells from injury induced by H O , which may be associated with antioxidation, upregulation of eNOS and downregulation of p38-MAPK.
ISSN:1388-0209
1744-5116
DOI:10.1080/13880209.2016.1224259