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西洋参皂苷联合双联抗血小板药物通过PI3K/AKT和COX途径抑制血小板黏附于损伤的人脐静脉内皮细胞。

Panax quinquefolium saponin combined with dual antiplatelet drugs inhibits platelet adhesion to injured HUVECs via PI3K/AKT and COX pathways.

作者信息

Wang Ming-Ming, Xue Mei, Miao Yu, Kou Na, Xu Yong-Gang, Yang Lin, Zhang Ying, Shi Da-Zhuo

机构信息

Center for Cardiovascular Disease, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.

Center for Cardiovascular Disease, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.

出版信息

J Ethnopharmacol. 2016 Nov 4;192:10-19. doi: 10.1016/j.jep.2016.07.015. Epub 2016 Jul 8.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Panax quinquefolium saponin (PQS) is the active component extracted from traditional Chinese medicine Panax quinquefolius L. and has been widely used as a supplement to dual antiplatelet drugs (DA) for treatment of coronary artery disease (CAD) for two decades; however, the efficacy of PQS combined with DA against platelet adhesion to endothelial cells (ECs), an essential step in thrombosis, remains unclear.

AIM OF THE STUDY

To compare PQS combined with DA and DA alone in inhibiting platelet adhesion to injured human umbilical vein endothelial cells (HUVECs) and to explore the possible mechanisms focusing on PI3K/AKT, COX-2/6-keto-PGF, and COX-1/TXB pathways.

METHODS

HUVECs injured by oxidized low-density lipoprotein (ox-LDL) were randomly allocated into control, model, DA, PQS+DA (P+DA), LY294002 (a PI3K inhibitor)+DA (L+DA), and LY294002+PQS+DA (LP+DA) groups. HUVEC apoptosis, platelet adhesion to injured HUVECs, and platelet CD62p expression were assayed by fluorescence activated cell sorting (FACS). The concentrations of 6-keto-PGF and TXB in the supernatant were measured by radioimmunoassay. Protein expression of phosphorylated-PI3K, PI3K, phosphorylated-AKT, AKT, COX-1, and COX-2 in both platelets and HUVECs was evaluated by western blot.

RESULTS

Compared to DA alone, PQS combined with DA reduced platelet adhesion to HUVECs and HUVEC apoptosis more potently, increased the concentration of supernatant 6-keto-PGF and up-regulated phospho-AKT protein in HUVECs. LY294002 mitigated the effects of PQS on HUVEC apoptosis and platelet adhesion.

CONCLUSIONS

These findings show that PQS as a powerful supplement to DA, attenuated HUVEC apoptosis and improved the DA-mediated reduction of platelet adhesion to injured HUVECs and the underlying mechanisms may be associated with PI3K/AKT and COX pathways in HUVECs and platelets. PQS might provide a new complementary approach to improve the prognosis of thrombotic diseases in future.

摘要

民族药理学相关性

西洋参皂苷(PQS)是从传统中药西洋参中提取的活性成分,二十年来一直被广泛用作双重抗血小板药物(DA)的补充剂,用于治疗冠状动脉疾病(CAD);然而,PQS联合DA对血小板黏附于内皮细胞(ECs)(血栓形成的关键步骤)的疗效仍不清楚。

研究目的

比较PQS联合DA与单独使用DA对抑制血小板黏附于损伤的人脐静脉内皮细胞(HUVECs)的作用,并探讨聚焦于PI3K/AKT、COX-2/6-酮-前列腺素F1α(6-keto-PGF)和COX-1/血栓素B2(TXB)途径的可能机制。

方法

将经氧化低密度脂蛋白(ox-LDL)损伤的HUVECs随机分为对照组、模型组、DA组、PQS+DA(P+DA)组、LY294002(一种PI3K抑制剂)+DA(L+DA)组和LY294002+PQS+DA(LP+DA)组。通过荧光激活细胞分选(FACS)检测HUVEC凋亡、血小板对损伤的HUVECs的黏附以及血小板CD62p表达。采用放射免疫分析法测定上清液中6-酮-前列腺素F1α和血栓素B2的浓度。通过蛋白质印迹法评估血小板和HUVECs中磷酸化-PI3K、PI3K、磷酸化-AKT、AKT、COX-1和COX-2的蛋白表达。

结果

与单独使用DA相比,PQS联合DA更有效地降低了血小板对HUVECs的黏附和HUVEC凋亡,增加了上清液中6-酮-前列腺素F1α的浓度,并上调了HUVECs中磷酸化-AKT蛋白的表达。LY294002减轻了PQS对HUVEC凋亡和血小板黏附的影响。

结论

这些发现表明,PQS作为DA的有力补充剂,减轻了HUVEC凋亡,改善了DA介导的血小板对损伤的HUVECs黏附的降低,其潜在机制可能与HUVECs和血小板中的PI3K/AKT以及COX途径有关。PQS可能为未来改善血栓性疾病的预后提供一种新的补充方法。

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