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油酸抑制胶原蛋白刺激的血小板活化的机制。

The mechanism of oleic acid inhibiting platelet activation stimulated by collagen.

机构信息

Department of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Avenue, Wuhan, 430022, Hubei Province, China.

Collaborative Innovation Center of Hematology, Huazhong University of Science and Technology, Wuhan, 430022, China.

出版信息

Cell Commun Signal. 2023 Oct 10;21(1):278. doi: 10.1186/s12964-023-01276-0.

Abstract

BACKGROUND

Abnormal platelet activation is a key factor in the occurrence and development of thrombotic diseases. However, the physiological mechanisms that underlie platelet homeostasis remain unclear. Oleic acid, one of the most abundant lipids in the human diet, has potential antithrombotic effects. This study aimed to investigate the effects of oleic acid on platelet activation and thrombosis.

METHODS

Platelet aggregation, ATP release, and fibrinogen spread were evaluated to determine the role of oleic acid in platelet activation. A ferric chloride-induced carotid injury model was used to establish the effect of oleic acid on thrombus formation in vivo. Western blotting analysis and transfection experiments were performed to determine the mechanisms involved in this process.

RESULTS

Oleic acid inhibited platelet aggregation, granule release, and calcium mobilization. Furthermore, it inhibited the spread of platelets on fibrinogen. We also found that oleic acid delayed arterial thrombosis in mice, as demonstrated in a murine model of ferric chloride-induced carotid artery thrombosis. The molecular mechanism of its inhibition of platelet activity may be through the Syk-PLCγ2 and CaMKKβ/AMPKα/VASP pathways. In addition, we demonstrated that the phosphorylation of AMPK at Ser496 was an important mechanism of platelet activation.

CONCLUSIONS

Our study showed that oleic acid inhibits platelet activation and reduces thrombogenesis by inhibiting the phosphorylation of multiple signaling molecules, offering new insights into the research and development of antiplatelet drugs. Video Abstract.

摘要

背景

血小板异常激活是血栓性疾病发生和发展的关键因素。然而,血小板稳态的生理机制仍不清楚。油酸是人类饮食中最丰富的脂质之一,具有潜在的抗血栓作用。本研究旨在探讨油酸对血小板激活和血栓形成的影响。

方法

通过评估血小板聚集、ATP 释放和纤维蛋白原扩散来确定油酸在血小板激活中的作用。采用三氯化铁诱导颈动脉损伤模型,建立油酸在体内血栓形成中的作用。通过 Western blot 分析和转染实验,确定了这一过程涉及的机制。

结果

油酸抑制血小板聚集、颗粒释放和钙动员。此外,它还抑制血小板在纤维蛋白原上的扩散。我们还发现,油酸可延迟小鼠动脉血栓形成,在三氯化铁诱导的颈动脉血栓形成小鼠模型中得到证实。其抑制血小板活性的分子机制可能是通过 Syk-PLCγ2 和 CaMKKβ/AMPKα/VASP 途径。此外,我们证明了 AMPK 在 Ser496 位点的磷酸化是血小板激活的一个重要机制。

结论

我们的研究表明,油酸通过抑制多个信号分子的磷酸化来抑制血小板激活和减少血栓形成,为抗血小板药物的研究和开发提供了新的思路。

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