Sawyer T W, Hancock J R, D'Agostino P A
Detection and Identification Section, Defense Research Establishment Suffield, Medicine Hat, Alberta, T1A 8K6, Canada.
Toxicol Appl Pharmacol. 1998 Aug;151(2):340-6. doi: 10.1006/taap.1998.8457.
Previous studies in this laboratory have shown that the well-characterized arginine analogue nitric oxide synthase (NOS) inhibitor, l-nitroarginine methyl ester (l-NAME) is protective against the cytotoxicity of the vesicating agent bis (2-chloroethyl) sulphide (HD). Furthermore, these protective effects were not mediated through the inhibition of NOS. In studies designed to investigate the efficacy of additional arginine analogue NOS inhibitors as protective agents against this compound, l-thiocitrullline (l-TC) was identified as being extremely potent. In contrast to the protection conferred by l-NAME, however, l-TC was found to protect immature cultures of neurons against HD, as well as mature cultures. In addition, l-TC was found to exert its effects prophylactically, as opposed to the therapeutic characteristics of l-NAME. l-TC gave approximately 800% protection against HD with a one-h pretreatment compared to approximately 1500% protection with a 24-h pretreatment. The protection conferred by l-TC against HD was persistent, and did not require the continued presence of l-TC after the initial HD lesion was expressed. The protective characteristics of l-TC against HD are very different than those of l-NAME and suggest that these closely related arginine analogues act at as yet unidentified and different sites to exert their effects.
本实验室之前的研究表明,特征明确的精氨酸类似物一氧化氮合酶(NOS)抑制剂L-硝基精氨酸甲酯(L-NAME)对发泡剂双(2-氯乙基)硫化物(HD)的细胞毒性具有保护作用。此外,这些保护作用并非通过抑制NOS介导。在旨在研究其他精氨酸类似物NOS抑制剂作为针对该化合物的保护剂的功效的研究中,L-硫代瓜氨酸(L-TC)被确定具有极强的效力。然而,与L-NAME所提供的保护作用不同,L-TC被发现不仅能保护成熟神经元培养物免受HD损伤,还能保护未成熟神经元培养物。此外,与L-NAME的治疗特性相反,L-TC被发现具有预防性作用。与24小时预处理约1500%的保护率相比,L-TC在1小时预处理时对HD的保护率约为800%。L-TC对HD的保护作用具有持续性,在最初的HD损伤表现出来后,并不需要L-TC持续存在。L-TC对HD的保护特性与L-NAME的保护特性非常不同,这表明这些密切相关的精氨酸类似物在尚未明确的不同位点发挥作用以产生其效果。