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二甲基亚砜对内皮细胞的抗血管生成作用。

Anti-angiogenic effects of dimethyl sulfoxide on endothelial cells.

作者信息

Koizumi Keiichi, Tsutsumi Yasuo, Yoshioka Yasuo, Watanabe Masaki, Okamoto Takayuki, Mukai Yohei, Nakagawa Shinsaku, Mayumi Tadanori

机构信息

Graduate School of Pharmaceutical Sciences, Osaka University, Osaka, Japan.

出版信息

Biol Pharm Bull. 2003 Sep;26(9):1295-8. doi: 10.1248/bpb.26.1295.

Abstract

Dimethyl sulfoxide (DMSO) has anti-inflammatory and analgesic properties and is the only intravesical agent approved by the FDA for the treatment of interstitial cystitis. While it is known that DMSO has numerous biological effects on cell differentiation and alteration of cell-surface carbohydrate structures, the anti-inflammatory mechanism of DMSO has been not clear yet. Therefore, further investigation of DMSO in terms of inflammation therapy is needed. This study assessed the in vitro anti-angiogenic effects of DMSO on human aorta endothelial cells to clarify one of the mechanisms of its anti-inflammatory activity. DMSO did not affect expression of E-selectin on endothelial cells in the presence of TNF-alpha. Furthermore, DMSO effectively inhibited capillary tube formation; this mechanism would be due to suppression of matrix metalloproteinase-2 (MMP-2) production. These results provide useful knowledge about the anti-inflammatory effects of DMSO and the regulatory mechanism of MMP-2.

摘要

二甲基亚砜(DMSO)具有抗炎和镇痛特性,是美国食品药品监督管理局(FDA)批准用于治疗间质性膀胱炎的唯一膀胱内用药。虽然已知DMSO对细胞分化和细胞表面碳水化合物结构改变具有多种生物学效应,但其抗炎机制尚不清楚。因此,需要进一步研究DMSO在炎症治疗方面的作用。本研究评估了DMSO对人主动脉内皮细胞的体外抗血管生成作用,以阐明其抗炎活性的机制之一。在存在肿瘤坏死因子-α(TNF-α)的情况下,DMSO不影响内皮细胞上E-选择素的表达。此外,DMSO有效抑制毛细血管管形成;这一机制可能是由于基质金属蛋白酶-2(MMP-2)产生受到抑制。这些结果为DMSO的抗炎作用及MMP-2的调节机制提供了有用的知识。

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