Faculty of Science and Technology, Keio University, Kanagawa, Japan.
Planta Med. 2012 Jun;78(10):957-61. doi: 10.1055/s-0031-1298538. Epub 2012 May 15.
Lysenin is a pore-forming toxin derived from coelomic fluid of the earthworm Eisenia foetida. The model of lysenin-induced hemolysis includes the specific binding of lysenin to sphingomyelin, oligomerization of the pore proteins, and pore formation. Although the mechanism of lysenin-induced hemolysis is unique, its precise mechanism of action and its inhibitors are poorly understood. In the present study, we screened for inhibitors of lysenin-induced hemolysis by using an optimized screening system and found a methanolic extract of Dalbergia latifolia leaves to be a potential candidate. After isolation and identification, all-E-lutein was identified as the hemolysis inhibitor with an effective dose of 0.025-2.5 ng/mL without any toxicity. The inhibition by all-E-lutein is likely to occur during the receptor binding and/or pore-forming protein oligomerization.
Lysenin 是一种由蚯蚓(Eisenia foetida)体腔液中提取的形成孔道的毒素。lysenin 诱导溶血的模型包括 lysenin 与神经鞘磷脂的特异性结合、孔道蛋白的寡聚化和孔道形成。尽管 lysenin 诱导溶血的机制是独特的,但它的确切作用机制及其抑制剂知之甚少。在本研究中,我们通过优化的筛选系统筛选了 lysenin 诱导溶血的抑制剂,并发现黄檀叶甲醇提取物是一种潜在的候选物。经过分离和鉴定,全-E-叶黄素被鉴定为溶血抑制剂,有效剂量为 0.025-2.5ng/mL,且无任何毒性。全-E-叶黄素的抑制作用可能发生在受体结合和/或形成孔道蛋白寡聚化过程中。