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齿槽口线虫:谷胱甘肽 S-转移酶 (GST) 抑制剂对 GST 活性和幼虫发育的影响。

Oesophagostomum dentatum: effect of glutathione S-transferase (GST) inhibitors on GST activity and larval development.

机构信息

Institute of Parasitology, Department of Pathobiology, University of Veterinary Medicine Vienna, Veterinaerplatz 1, A-1210 Vienna, Austria.

出版信息

Exp Parasitol. 2011 Apr;127(4):762-7. doi: 10.1016/j.exppara.2011.01.005. Epub 2011 Jan 15.

Abstract

Sulphobromophthalein (SBP) inhibits isolated glutathione S-transferase of the porcine nodule worm Oesophagostomum dentatum (Od-GST) and reduces larval development in vitro. In this study possible inhibitory effects of various inhibitors were evaluated in an enzymatic (CDNB) assay with isolated Od-GST and in a larval development assay (LDA). Reversibility was tested in the LDA by removing the inhibitor from culture halfway through the cultivation period. SBP, indomethacin and ethacrynic acid inhibited both enzyme activity and larval development in a dose-dependent and reversible manner. HQL-79 also reduced larval development but had only a minor effect on the isolated enzyme. The phospholipase A(2) inhibitors dexamethasone and hydrocortisone had no major effect. High thermal stability of Od-GST was demonstrated with increasing activity between 4 and 50°C. Differences between Od-GST and GST of other organisms indicate structural and possibly functional peculiarities and highlight the potential of such enzymes as targets of intervention.

摘要

磺溴酞(SBP)抑制猪结节虫 Oesophagostomum dentatum(Od-GST)的分离谷胱甘肽 S-转移酶,并减少体外幼虫发育。在这项研究中,用分离的 Od-GST 在酶(CDNB)测定和幼虫发育测定(LDA)中评估了各种抑制剂的可能抑制作用。通过在培养期间的中途从培养物中除去抑制剂来测试可逆性。SBP、吲哚美辛和依他尼酸以剂量依赖和可逆的方式抑制酶活性和幼虫发育。HQL-79 也减少了幼虫发育,但对分离的酶只有轻微影响。磷脂酶 A(2)抑制剂地塞米松和氢化可的松没有产生重大影响。Od-GST 的高热稳定性表现为在 4 至 50°C 之间活性增加。Od-GST 与其他生物体的 GST 之间的差异表明结构和功能上的特殊性,并突出了这些酶作为干预目标的潜力。

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