De Brabander M, Aerts F, Geuens G, van Ginckel R, van de Veire R, van Belle H
Chem Biol Interact. 1978 Oct;23(1):45-63. doi: 10.1016/0009-2797(78)90041-8.
DL-2-Oxo-3-(2-mercaptoethyl)-5-phenylimidazolidine (OMPI) a sulfhydryl metabolite of levamisole, unlike the parent compound, is shown to interfere with the morphological and functional integrity of microtubules in cultured cells at high concentrations (1.6-10(-4) M). Lower concentrations do not affect the cell morphology, viability or growth rate in any appreciable way. Both levamisole and OMPI, at low concentrations (10(-5)-10(-6) m), markedly enhance the antimicrotubular effect of mercaptoethanol. High concentrations of OMPI (+/- 10(-4) M) inhibit the self-assembly of microtubules in a cell free system. Low concentrations (+/- 10(-6) M) markedly enhance the polymerization rate of tubulin. Levamisole has no effect on tubulin polymerization. The effects of OMPI on microtubules in cells and in the polymerization system can be reversed by reduced glutathione, cysteine and dithiothreitol. The data indicate that OMPI interacts in a biphasic manner with microtubule formation probably through interaction with critical SH-groups on the tubulin molecule. It seems of interest to further investigate the hypothesis that the immunomodulating properties of levamisole are at least partially due to the formation of its metabolite (OMPI) which could enhance microtubule integrity and function in leukocytes.
左旋咪唑的巯基代谢产物DL-2-氧代-3-(2-巯基乙基)-5-苯基咪唑烷(OMPI),与母体化合物不同,在高浓度(1.6 - 10(-4)M)时可干扰培养细胞中微管的形态和功能完整性。较低浓度对细胞形态、活力或生长速率没有明显影响。左旋咪唑和OMPI在低浓度(10(-5)-10(-6)m)时,均可显著增强巯基乙醇的抗微管作用。高浓度的OMPI(±10(-4)M)在无细胞体系中抑制微管的自我组装。低浓度(±10(-6)M)则显著提高微管蛋白的聚合速率。左旋咪唑对微管蛋白聚合无影响。OMPI对细胞内和聚合体系中微管的作用可被还原型谷胱甘肽、半胱氨酸和二硫苏糖醇逆转。数据表明,OMPI可能通过与微管蛋白分子上的关键巯基相互作用,以双相方式与微管形成相互作用。进一步研究左旋咪唑的免疫调节特性至少部分归因于其代谢产物(OMPI)的形成这一假说似乎很有意义,该代谢产物可增强白细胞中微管的完整性和功能。