Mikami Y, Fukushima K, Arai T, Abe F, Shibuya H, Ommura Y
Zentralbl Bakteriol Mikrobiol Hyg A. 1984 Jul;257(2):275-83.
Peptide mycotoxins "leucinostatins" were obtained from the culture strains of Paecilomyces lilacinus, which were isolated both from soil and a case of human oculomycosis. Comparative studies of the symptoms of experimental keratomycosis caused both by the inoculation of P. lilacinus and by direct administration of leucinostatins into the infection model in rabbit suggested the possible role of leucinostatins in the inflammatory response of invaded tissues. Leucinostatin was formerly reported as a single entity. However, in the course of the structural studies, leucinostatin was found to be a complex of two closely related components, and the structures of the both mycotoxins were determined. Both of the mycotoxins possessed high toxicity to experimental animals. The intraperitoneal and oral LD50 values in mice were 1.8 and 5.4 to 6.3 mg/kg by a single administration. Toxicological studies showed that leucinostatins have some potent effects on liver cells after oral administration. It was also found that leucinostatins exhibit strong uncoupling activity on rat liver mitochondrial system.
肽类霉菌毒素“亮抑菌素”是从淡紫拟青霉的培养菌株中获得的,这些菌株是从土壤和一例人类眼部真菌病病例中分离出来的。对由接种淡紫拟青霉以及将亮抑菌素直接注入兔感染模型所引起的实验性角膜真菌病症状的比较研究表明,亮抑菌素在受侵染组织的炎症反应中可能发挥作用。亮抑菌素以前被报道为单一物质。然而,在结构研究过程中,发现亮抑菌素是两种密切相关成分的复合物,并确定了这两种霉菌毒素的结构。这两种霉菌毒素对实验动物均具有高毒性。单次给药时,小鼠腹腔注射和口服的半数致死量(LD50)值分别为1.8和5.4至6.3毫克/千克。毒理学研究表明,口服亮抑菌素对肝细胞有一些强效作用。还发现亮抑菌素对大鼠肝脏线粒体系统表现出强烈的解偶联活性。