Division of Pulmonary and Critical Care Medicine, Department of Medicine, Pennsylvania State University, College of Medicine, Hershey, Pennsylvania.
Center for Translational Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania.
Ann N Y Acad Sci. 2020 Nov;1479(1):108-121. doi: 10.1111/nyas.14353. Epub 2020 May 6.
The aim of the present study was to determine whether methylene blue (MB) could directly oppose the neurological toxicity of a lethal cyanide (CN) intoxication. KCN, infused at the rate of 0.375 mg/kg/min intravenously, produced 100% lethality within 15 min in unanaesthetized rats (n = 12). MB at 10 (n = 5) or 20 mg/kg (n = 5), administered 3 min into CN infusion, allowed all animals to survive with no sequelae. No apnea and gasping were observed at 20 mg/kg MB (P < 0.001). The onset of coma was also significantly delayed and recovery from coma was shortened in a dose-dependent manner (median of 359 and 737 seconds, respectively, at 20 and 10 mg/kg). At 4 mg/kg MB (n = 5), all animals presented faster onset of coma and apnea and a longer period of recovery than at the highest doses (median 1344 seconds, P < 0.001). MB reversed NaCN-induced resting membrane potential depolarization and action potential depression in primary cultures of human fetal neurons intoxicated with CN. MB restored calcium homeostasis in the CN-intoxicated human SH-SY5Y neuroblastoma cell line. We conclude that MB mitigates the neuronal toxicity of CN in a dose-dependent manner, preventing the lethal depression of respiratory medullary neurons and fatal outcome.
本研究旨在确定亚甲蓝(MB)是否可以直接对抗致死剂量氰化物(CN)中毒引起的神经毒性。在未麻醉大鼠中,静脉内以 0.375 mg/kg/min 的速度输注 KCN,在 15 分钟内产生 100%的致死率(n=12)。在 CN 输注开始后 3 分钟给予 10(n=5)或 20 mg/kg(n=5)MB,使所有动物均存活且无后遗症。在 20 mg/kg MB 时未观察到呼吸暂停和喘息(P<0.001)。MB 以剂量依赖的方式显著延迟昏迷的发作并缩短从昏迷中恢复的时间(20 和 10 mg/kg 时分别为 359 和 737 秒的中位数)。在 4 mg/kg MB(n=5)时,所有动物的昏迷发作更快,出现呼吸暂停和恢复时间更长,与最高剂量相比(中位数 1344 秒,P<0.001)。MB 逆转了原发性人胎神经元培养物中 CN 引起的静息膜电位去极化和动作电位抑制。MB 恢复了 CN 中毒的人 SH-SY5Y 神经母细胞瘤细胞系中的钙稳态。我们得出结论,MB 以剂量依赖的方式减轻 CN 引起的神经元毒性,防止呼吸髓质神经元的致命抑制和致命结局。