Pregled bibliografske jedinice broj: 479475
Comparative determination of the efficacy of bispyridinium oximes in paraoxon poisoning
Comparative determination of the efficacy of bispyridinium oximes in paraoxon poisoning // Toxicology Letters, Abstracts of the XII International Congress of Toxicology
Barcelona, Španjolska, 2010. (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Comparative determination of the efficacy of bispyridinium oximes in paraoxon poisoning
Autori
Lucić Vrdoljak, Ana ; Berend, Suzana ; Radić, Božica ; Kuča, Kamil
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Toxicology Letters, Abstracts of the XII International Congress of Toxicology
/ - , 2010
Skup
XII International Congress of Toxicology
Mjesto i datum
Barcelona, Španjolska, 19.07.2010. - 23.07.2010
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Bispyridinium oximes; paraoxon; therapy
Sažetak
Organophosphorous compounds (OP) are widely used in agriculture and in public health, but also developed as nerve warfare agents. The mechanism of OP poisoning involves phosphorylation of the serine hydroxyl group in the active site of acetylcholinesterase (AChE) leading to the inactivation of this essential enzyme which has an important role in neurotransmission. The clinical signs of AChE inhibition manifest as hypersalivation, lacrimation, diarrhoea, tremor, respiratory distress, convulsion and seizures. Together with atropine, pyridinium oximes are known to be successfully used to treat OP poisoning. The use of organophosphorous pesticides as highly toxic compounds is restricted in most parts of the world. Despite regulatory efforts some of them like parathion are still widely (mis)used. Paraoxon, the active metabolite of the insecticide parathion, is one of the most potent acetylcholinesterase-inhibiting compounds available. The present study was performed to assess and compare a therapeutic efficacy of six experimental bispyridinium oximes (K027, K033, K048, K074, K075 and K203) combined with atropine in paraoxon-poisoned mice. Currently used oximes HI-6 and TMB-4 were included for comparison. The studied oximes (5% or 25% of their LD50) plus atropine (10 mg/kg) were given intraperitoneally one minute after paraoxon (given subcutaneously). Their therapeutic efficacywasexpressed as protective index (PI) and maximal dose of poison (MDP). Except K033, all experimental oximes showed better antidotal activity than HI-6 and TMB-4 in paraoxon-poisoned mice. Doseresponse relationship was obtained for oximes K074, K075 and K203. Considering the lower dose K027 and K048 were the mostpotent against paraoxon intoxication, while from the point of acute toxicity the most effective were K075 and K203. Convenient stereochemical arrangements (functional aldoxime group at position four ; propane-, butane- or butene-like linker) along with excellent results of this study are in agreement with already shown reactivating potency of these oximes.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
022-0222148-2139 - Terapijski učinak novosintetiziranih spojeva pri otrovanju organofosfatima (Lucić Vrdoljak, Ana, MZOS ) ( CroRIS)
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE