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饮食中的 α-亚麻酸可抑制动脉血栓形成、组织因子表达和血小板活化。

Dietary α-linolenic acid inhibits arterial thrombus formation, tissue factor expression, and platelet activation.

机构信息

Cardiovascular Research, Institute of Physiology, Center for Integrative Human Physiology, University of Zurich, Switzerland.

出版信息

Arterioscler Thromb Vasc Biol. 2011 Aug;31(8):1772-80. doi: 10.1161/ATVBAHA.111.226118. Epub 2011 May 12.

Abstract

OBJECTIVE

Plant-derived α-linolenic acid (ALA) may constitute an attractive cardioprotective alternative to fish-derived n-3 fatty acids. However, the effect of dietary ALA on arterial thrombus formation remains unknown.

METHODS AND RESULTS

Male C57Bl/6 mice were fed a high-ALA or low-ALA diet for 2 weeks. Arterial thrombus formation was delayed in mice fed a high-ALA diet compared with those on a low-ALA diet (n=7; P<0.005). Dietary ALA impaired platelet aggregation to collagen and thrombin (n=5; P<0.005) and decreased p38 mitogen-activated protein kinase activation in platelets. Dietary ALA impaired arterial tissue factor (TF) expression, TF activity, and nuclear factor-κB activity (n=7; P<0.05); plasma clotting times and plasma thrombin generation did not differ (n=5; P=not significant). In cultured human vascular smooth muscle and endothelial cells, ALA inhibited TF expression and activity (n=4; P<0.01). Inhibition of TF expression occurred at the transcriptional level via the mitogen-activated protein kinase p38 in smooth muscle cells and p38, extracellular signal-regulated kinases 1 and 2, and c-Jun N-terminal kinases 1 and 2 in endothelial cells.

CONCLUSIONS

ALA impairs arterial thrombus formation, TF expression, and platelet activation and thereby represents an attractive nutritional intervention with direct dual antithrombotic effects.

摘要

目的

植物来源的α-亚麻酸(ALA)可能构成一种有吸引力的心脏保护替代物,替代鱼源 n-3 脂肪酸。然而,饮食中 ALA 对动脉血栓形成的影响尚不清楚。

方法和结果

雄性 C57Bl/6 小鼠用高 ALA 或低 ALA 饮食喂养 2 周。与低 ALA 饮食组相比,高 ALA 饮食组的动脉血栓形成时间延迟(n=7;P<0.005)。饮食 ALA 可损害血小板对胶原蛋白和凝血酶的聚集(n=5;P<0.005),并降低血小板中 p38 丝裂原活化蛋白激酶的激活。饮食 ALA 可损害动脉组织因子(TF)的表达、TF 活性和核因子-κB 活性(n=7;P<0.05);血浆凝血时间和血浆凝血酶生成没有差异(n=5;P=无显著性)。在培养的人血管平滑肌和内皮细胞中,ALA 抑制 TF 的表达和活性(n=4;P<0.01)。在平滑肌细胞中,通过丝裂原活化蛋白激酶 p38 发生在转录水平上抑制 TF 表达,在内皮细胞中通过 p38、细胞外信号调节激酶 1 和 2 以及 c-Jun N-末端激酶 1 和 2 发生。

结论

ALA 可损害动脉血栓形成、TF 表达和血小板激活,因此代表了一种具有直接双重抗血栓作用的有吸引力的营养干预措施。

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