Acute administration of diazepam or midazolam minimally alters long-term neuropathological effects in the rat brain following acute intoxication with diisopropylfluorophosphate
European Journal of Pharmacology, ISSN: 0014-2999, Vol: 886, Page: 173538
2020
- 24Citations
- 29Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations24
- Citation Indexes24
- 24
- CrossRef21
- Captures29
- Readers29
- 29
Article Description
Acute intoxication with organophosphorus cholinesterase inhibitors (OPs) can trigger seizures that rapidly progress to life-threatening status epilepticus. Diazepam, long considered the standard of care for treating OP-induced seizures, is being replaced by midazolam. Whether midazolam is more effective than diazepam in mitigating the persistent effects of acute OP intoxication has not been rigorously evaluated. We compared the efficacy of diazepam vs. midazolam in preventing persistent neuropathology in adult male Sprague-Dawley rats acutely intoxicated with the OP diisopropylfluorophosphate (DFP). Subjects were administered pyridostigmine bromide (0.1 mg/kg, i.p. ) 30 min prior to injection with DFP (4 mg/kg, s.c. ) or vehicle (saline) followed 1 min later by atropine sulfate (2 mg/kg, i.m. ) and pralidoxime (25 mg/kg, i.m. ), and 40 min later by diazepam (5 mg/kg, i.p. ), midazolam (0.73 mg/kg, i.m. ), or vehicle. At 3 and 6 months post-exposure, neurodegeneration, reactive astrogliosis, microglial activation, and oxidative stress were assessed in multiple brain regions using quantitative immunohistochemistry. Brain mineralization was evaluated by in vivo micro-computed tomography (micro-CT). Acute DFP intoxication caused persistent neurodegeneration, neuroinflammation, and brain mineralization. Midazolam transiently mitigated neurodegeneration, and both benzodiazepines partially protected against reactive astrogliosis in a brain region-specific manner. Neither benzodiazepine attenuated microglial activation or brain mineralization. These findings indicate that neither benzodiazepine effectively protects against persistent neuropathological changes, and suggest that midazolam is not significantly better than diazepam. Overall, this study highlights the need for improved neuroprotective strategies for treating humans in the event of a chemical emergency involving OPs.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0014299920306300; http://dx.doi.org/10.1016/j.ejphar.2020.173538; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85090695432&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/32898549; https://linkinghub.elsevier.com/retrieve/pii/S0014299920306300; https://dx.doi.org/10.1016/j.ejphar.2020.173538
Elsevier BV
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