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抗磷脂综合征中的动脉疾病与血栓形成:内皮素-1的致病作用

Arterial disease and thrombosis in the antiphospholipid syndrome: a pathogenic role for endothelin 1.

作者信息

Atsumi T, Khamashta M A, Haworth R S, Brooks G, Amengual O, Ichikawa K, Koike T, Hughes G R

机构信息

The Rayne Institute, St. Thomas' Hospital, London, UK.

出版信息

Arthritis Rheum. 1998 May;41(5):800-7. doi: 10.1002/1529-0131(199805)41:5<800::AID-ART5>3.0.CO;2-J.

Abstract

OBJECTIVE

To explore a possible correlation between endothelin 1 (ET-1), the most potent endothelium-derived contracting factor that modulates vascular smooth muscle tone, and arterial disease in patients with the antiphospholipid syndrome (APS).

METHODS

Plasma levels of ET-1 were measured in APS patients with (n = 16) and without (n = 11) arterial thrombosis and in non-APS patients with arterial thrombosis (n = 9). In addition, steady-state prepro-ET-1 messenger RNA (mRNA) levels were determined in endothelial cells treated with a range of human monoclonal anticardiolipin antibodies (aCL) (as anti-beta2-glycoprotein I antibodies) by semiquantitative 32P-dCTP-labeled reverse transcription-polymerase chain reaction.

RESULTS

Compared with healthy controls, markedly increased plasma levels of ET-1 were found in APS patients with arterial thrombosis (2.00 +/- 0.87 versus 0.96 +/- 0.37 pg/ml; P = 0.0001) but not in other groups. Three human monoclonal aCL induced prepro-ET-1 mRNA levels significantly more than did control monoclonal antibody lacking aCL activity.

CONCLUSION

Plasma ET-1 levels correlated significantly with a history of arterial thrombosis in patients with APS. Prepro-ET-1 mRNA was induced by human monoclonal aCL in the in vitro experimental system. The induction of ET-1 by antiphospholipid antibodies might contribute to increased arterial tone, leading to vasospasm and, ultimately, to arterial occlusion.

摘要

目的

探讨内皮素1(ET-1)这一调节血管平滑肌张力的最强大的内皮源性收缩因子与抗磷脂综合征(APS)患者动脉疾病之间可能存在的相关性。

方法

检测了伴有(n = 16)和不伴有(n = 11)动脉血栓形成的APS患者以及伴有动脉血栓形成的非APS患者(n = 9)血浆中的ET-1水平。此外,通过半定量32P-dCTP标记的逆转录-聚合酶链反应,测定了用一系列人单克隆抗心磷脂抗体(aCL)(作为抗β2-糖蛋白I抗体)处理的内皮细胞中前内皮素原-1信使核糖核酸(mRNA)的稳态水平。

结果

与健康对照相比,伴有动脉血栓形成的APS患者血浆ET-1水平显著升高(2.00±0.87对0.96±0.37 pg/ml;P = 0.0001),而其他组未见升高。三种人单克隆aCL诱导前内皮素原-1 mRNA水平的作用显著强于缺乏aCL活性的对照单克隆抗体。

结论

APS患者血浆ET-1水平与动脉血栓形成病史显著相关。在体外实验系统中,人单克隆aCL可诱导前内皮素原-1 mRNA。抗磷脂抗体诱导ET-1可能导致动脉张力增加,引起血管痉挛,并最终导致动脉闭塞。

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