The benefit of combinations of oximes for the ability of antidotal treatment to counteract sarin-induced brain damage in rats-Reference-Cited by-同舟云学术

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The benefit of combinations of oximes for the ability of antidotal treatment to counteract sarin-induced brain damage in rats

Published:2018-06-28 Issue:1 Volume:19 Page:
ISSN:2050-6511
Container-title:BMC Pharmacology and Toxicology
language:en
Short-container-title:BMC Pharmacol Toxicol

Author:

Caisberger Filip,Pejchal Jaroslav,Misik Jan,Kassa Jiri,Valis Martin,Kuca Kamil

Funder

University of Defence, Faculty of Military Health Sciences in Hradec Kralove

University Hospital Hradec Kralove

University of Hradec Kralove

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Link

http://link.springer.com/content/pdf/10.1186/s40360-018-0227-0.pdf

Reference41 articles.

1. Antonijevic E, Musilek K, Kuca K, Djukic-Cosic D, Vucinic S, Antonijevic B. Therapeutic and reactivating efficacy of oximes K027 and K203 against a direct acetylcholinesterase inhibitor. Neurotoxicology. 2016;55:33–9.

2. Baille V, Clarke PG, Brochier G, Dorandeu F, Verna JM, Four E, Lallement G, Carpentier P. Soman-induced convulsions: the neuropathology revisited. Toxicology. 2005;215:1–24.

3. Ben-Ari Y, Zigmond RE, Shute CC, Lewis PR. Regional distribution of choline acetyltransferase and acetylcholinesterase within the amygdaloid complex and stria terminalis system. Brain Res. 1977;120:435–44.

4. Brown MA, Brix KA. Review of health consequences from high-, intermediate- and low-level exposure to organophosphorus nerve agents. J Appl Toxicol. 1998;18:393–408.

5. Cayre M, Canoll P, Goldman JE. Cell migration in the normal and pathological postnatal mammalian brain. Prog Neurobiol. 2009;88:41–63.

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