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亚甲蓝对抗氰化物神经毒性的解毒作用:体内和体外研究。

Antidotal effects of methylene blue against cyanide neurological toxicity: in vivo and in vitro studies.

机构信息

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.

出版信息

Ann N Y Acad Sci. 2020 Nov;1479(1):108-121. doi: 10.1111/nyas.14353. Epub 2020 May 6.

DOI:10.1111/nyas.14353
PMID:32374444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7644644/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/dea9fa4c4a26/nihms-1606217-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/9d1769bbf467/nihms-1606217-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/98d8e94261fd/nihms-1606217-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/f1c19456e462/nihms-1606217-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/8095f1a3c146/nihms-1606217-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/196186e0fdda/nihms-1606217-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/dea9fa4c4a26/nihms-1606217-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/9d1769bbf467/nihms-1606217-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/98d8e94261fd/nihms-1606217-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/f1c19456e462/nihms-1606217-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/8095f1a3c146/nihms-1606217-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/196186e0fdda/nihms-1606217-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/038d/7644644/dea9fa4c4a26/nihms-1606217-f0006.jpg

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Alcohol exposure alters pre-mRNA splicing of antiapoptotic Mcl-1L isoform and induces apoptosis in neural progenitors and immature neurons.酒精暴露会改变抗凋亡 Mcl-1L 异构体的前体 mRNA 剪接,从而诱导神经祖细胞和未成熟神经元凋亡。
Cell Death Dis. 2019 Jun 6;10(6):447. doi: 10.1038/s41419-019-1673-3.
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Hydrogen sulfide intoxication induced brain injury and methylene blue.
Toxicol Rep. 2020 Oct 20;7:1459-1464. doi: 10.1016/j.toxrep.2020.10.015. eCollection 2020.
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Neurobiol Dis. 2020 Jan;133:104474. doi: 10.1016/j.nbd.2019.05.013. Epub 2019 May 16.
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