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脂氧合酶途径在去氧肾上腺素诱导的血管平滑肌细胞增殖和迁移中的作用。

Role of the lipoxygenase pathway in phenylephrine-induced vascular smooth muscle cell proliferation and migration.

作者信息

Nishio E, Watanabe Y

机构信息

Department of Pharmacology, National Defense Medical College, Tokorozawa, Saitama, Japan.

出版信息

Eur J Pharmacol. 1997 Oct 8;336(2-3):267-73. doi: 10.1016/s0014-2999(97)01259-4.

Abstract

We studied the effects of phenylephrine-stimulated proliferation and migration of vascular smooth muscle cells and the role of 12-lipoxygenase-mediated pathways under normal as well as high glucose conditions. Phenylephrine-induced increases in cellular proliferation and migration were attenuated by the specific 12-lipoxygenase inhibitor baicalein. In contrast, neither of the cyclo-oxygenase inhibitors, indomethacin or ibuprofen, had any effect. Direct addition of the 12-lipoxygenase product, 12-S-hydroxyeicosatetraenoic acid (12-HETE), increased the proliferation and migration of vascular smooth muscle cells treated with both phenylephrine and nordihydroguaiaretic acid. Furthermore, we observed that phenylephrine induced greater increases in the proliferation and migration of vascular smooth muscle cells and also that the 12-lipoxygenase inhibitor prevented the enhancement of proliferation and migration of vascular smooth muscle cells induced by phenylephrine in the presence of high glucose (25 mmol/l). These results suggest that 12-lipoxygenase activation plays a key role in phenylephrine-induced responses of vascular smooth muscle cells under normal and hyperglycemic conditions. 12-lipoxygenase may be a good pharmacological target for treatment of vascular disease of hypertension and diabetes mellitus.

摘要

我们研究了去氧肾上腺素刺激下血管平滑肌细胞增殖和迁移的影响,以及在正常和高糖条件下12-脂氧合酶介导途径的作用。去氧肾上腺素诱导的细胞增殖和迁移增加被特异性12-脂氧合酶抑制剂黄芩苷减弱。相比之下,环氧化酶抑制剂吲哚美辛或布洛芬均无任何作用。直接添加12-脂氧合酶产物12-S-羟基二十碳四烯酸(12-HETE),可增加用去氧肾上腺素和去甲二氢愈创木酸处理的血管平滑肌细胞的增殖和迁移。此外,我们观察到去氧肾上腺素诱导血管平滑肌细胞的增殖和迁移增加得更多,并且12-脂氧合酶抑制剂可阻止在高糖(25 mmol/L)存在下去氧肾上腺素诱导的血管平滑肌细胞增殖和迁移增强。这些结果表明,12-脂氧合酶激活在正常和高血糖条件下去氧肾上腺素诱导的血管平滑肌细胞反应中起关键作用。12-脂氧合酶可能是治疗高血压和糖尿病血管疾病的良好药理学靶点。

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