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曲尼司特对中性粒细胞体外产生基质金属蛋白酶的影响。

Effect of tranilast on matrix metalloproteinase production from neutrophils in-vitro.

作者信息

Shimizu Toshiyuki, Kanai Ken-Ichi, Kyo Yoshiyuki, Asano Kazuhito, Hisamitsu Tadashi, Suzaki Harumi

机构信息

Department of Otorhinolaryngology, School of Medicine, Showa University, Tokyo, Japan.

出版信息

J Pharm Pharmacol. 2006 Jan;58(1):91-9. doi: 10.1211/jpp.58.1.0011.

Abstract

Tranilast is an anti-allergic agent that blocks the release of chemical mediators, such as histamine and leukotrienes from mast cells, and has been reported to suppress keloid and hypertrophic scar formation. Since matrix metalloproteinases (MMPs) play an essential role in tissue remodelling, this study was undertaken to determine whether tranilast suppresses MMP production from neutrophils after lipopolysaccharide (LPS) stimulation in-vitro. Neutrophils from five healthy donors (1 x 10(5) cells/mL) were stimulated with 1.0 microg mL(-1) LPS in the presence or absence of various concentrations of tranilast for 24 h. MMP-7, MMP-8, MMP-9 and tissue inhibitor of metalloproteinase (TIMP)-1 levels in the culture supernatants were assayed by ELISA. In addition, the influence of tranilast on MMP mRNA expression and transcriptional factor activation in cells cultured for 12 h and 4 h was also evaluated by reverse transcriptase-polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay (ELISA), respectively. Tranilast inhibited MMP and TIMP-1 production from neutrophils when cells were treated with the agent at more than 5.0 x 10(-5) M. It also suppressed MMP mRNA expression and transcriptional factor activation induced in neutrophils by LPS stimulation. The results suggest that tranilast inhibits the formation of keloid scarring through the suppression of factors such as MMPs and TIMP, which are essential for tissue remodelling, from inflammatory cells.

摘要

曲尼司特是一种抗过敏药物,可阻止肥大细胞释放组胺和白三烯等化学介质,据报道它能抑制瘢痕疙瘩和增生性瘢痕的形成。由于基质金属蛋白酶(MMPs)在组织重塑中起重要作用,因此开展本研究以确定曲尼司特在体外脂多糖(LPS)刺激后是否能抑制中性粒细胞产生MMPs。将来自5名健康供者的中性粒细胞(1×10⁵个细胞/mL)在存在或不存在不同浓度曲尼司特的情况下,用1.0μg/mL LPS刺激24小时。通过酶联免疫吸附测定(ELISA)检测培养上清液中MMP-7、MMP-8、MMP-9和金属蛋白酶组织抑制剂(TIMP)-1的水平。此外,还分别通过逆转录-聚合酶链反应(RT-PCR)和酶联免疫吸附测定(ELISA)评估了曲尼司特对培养12小时和4小时的细胞中MMP mRNA表达和转录因子激活的影响。当用高于5.0×10⁻⁵M的曲尼司特处理细胞时,它能抑制中性粒细胞产生MMPs和TIMP-1。它还能抑制LPS刺激诱导的中性粒细胞中MMP mRNA表达和转录因子激活。结果表明,曲尼司特通过抑制炎症细胞中对组织重塑至关重要的MMPs和TIMP等因子的形成,从而抑制瘢痕疙瘩的形成。

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