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Pregled bibliografske jedinice broj: 1214335

Counteracting organophosphate-induced toxicity by improved bioscavenging capacity of BChE and damage prevention at cell level


Čadež, Tena; Zandona, Antonio; Katalinić, Maja; Kovarik, Zrinka
Counteracting organophosphate-induced toxicity by improved bioscavenging capacity of BChE and damage prevention at cell level // Journal of Neurochemistry. 2022 ; 162(Suppl. 1)
Honolulu (HI), Sjedinjene Američke Države, 2022. str. 58-59 doi:10.1111/jnc.15674 (poster, međunarodna recenzija, sažetak, znanstveni)


CROSBI ID: 1214335 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Counteracting organophosphate-induced toxicity by improved bioscavenging capacity of BChE and damage prevention at cell level

Autori
Čadež, Tena ; Zandona, Antonio ; Katalinić, Maja ; Kovarik, Zrinka

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
Journal of Neurochemistry. 2022 ; 162(Suppl. 1) / - , 2022, 58-59

Skup
ISN-APSN 2022 Meeting

Mjesto i datum
Honolulu (HI), Sjedinjene Američke Države, 28.08.2022. - 01.09.2022

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Cyclosarin, butyrylcholesterase, pyridinium oximes, neuroblastoma, bioscavenging

Sažetak
The phosphylation of acetylcholinesterase (AChE), a pivotal enzyme in hydrolysis of the neurotransmitter acetylcholine, by nerve agents (NAs) still has no adequate or fully efficient medical countermeasures. Furthermore, oxime antidotes known for their nucleophilic properties have limited potency in the reactivation of phosphylated AChE in the central nervous system (CNS), so even after survival, long- term effects of poisoning could occur. However, the AChE related enzyme butyrylcholinesterase (BChE), typically present in the blood, serves as bioscavenger of OPs, before they reach the crucial AChE in CNS. In our study, we wanted to investigate with a combination of in silico, in vitro, and ex vivo methods, the feasibility of an approach to develop a safe bioscavenger of NAs, based on the oxime-assisted reactivation of BChE. Firstly, we identified a promising reactivator of cyclosarin- inhibited BChE as a model system with no impact on the viability of neuroblastoma cells upon 4-hour treatment. Herein, the efficient oxime-assisted catalytic BChE degradation of cyclosarin was demonstrated ex vivo. This pair was then applied to OP-treated cells and, as the result shows, it acted by, protecting cells’ homeostasis by preserving from 50% to nearly 100% of neural cells. The most significant result was obtained if the oxime and BChE pair were applied to cells before exposure to cyclosarin or in other words, as pretreatment. This result is in accordance with ex vivo effects determined in the whole blood showing up to 80% of restored phosphylated cholinesterase activity within two minutes. In conclusion, our findings showed that an antidote should act on two levels—on cholinesterase reactivity and prevention of the long- term effects of poisoning.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Temeljne medicinske znanosti, Farmacija



POVEZANOST RADA


Projekti:
IP-2018-01-7683 - Analiza interakcija butirilkolinesteraze s novim inhibitorima i reaktivatorima (AnalyseBChE) (Kovarik, Zrinka, HRZZ - 2018-01) ( CroRIS)

Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb

Profili:

Avatar Url Tena Čadež (autor)

Avatar Url Maja Katalinić (autor)

Avatar Url Antonio Zandona (autor)

Avatar Url Zrinka Kovarik (autor)

Poveznice na cjeloviti tekst rada:

doi

Citiraj ovu publikaciju:

Čadež, Tena; Zandona, Antonio; Katalinić, Maja; Kovarik, Zrinka
Counteracting organophosphate-induced toxicity by improved bioscavenging capacity of BChE and damage prevention at cell level // Journal of Neurochemistry. 2022 ; 162(Suppl. 1)
Honolulu (HI), Sjedinjene Američke Države, 2022. str. 58-59 doi:10.1111/jnc.15674 (poster, međunarodna recenzija, sažetak, znanstveni)
Čadež, T., Zandona, A., Katalinić, M. & Kovarik, Z. (2022) Counteracting organophosphate-induced toxicity by improved bioscavenging capacity of BChE and damage prevention at cell level. U: Journal of Neurochemistry. 2022 ; 162(Suppl. 1) doi:10.1111/jnc.15674.
@article{article, author = {\v{C}ade\v{z}, Tena and Zandona, Antonio and Katalini\'{c}, Maja and Kovarik, Zrinka}, year = {2022}, pages = {58-59}, DOI = {10.1111/jnc.15674}, keywords = {Cyclosarin, butyrylcholesterase, pyridinium oximes, neuroblastoma, bioscavenging}, doi = {10.1111/jnc.15674}, title = {Counteracting organophosphate-induced toxicity by improved bioscavenging capacity of BChE and damage prevention at cell level}, keyword = {Cyclosarin, butyrylcholesterase, pyridinium oximes, neuroblastoma, bioscavenging}, publisherplace = {Honolulu (HI), Sjedinjene Ameri\v{c}ke Dr\v{z}ave} }
@article{article, author = {\v{C}ade\v{z}, Tena and Zandona, Antonio and Katalini\'{c}, Maja and Kovarik, Zrinka}, year = {2022}, pages = {58-59}, DOI = {10.1111/jnc.15674}, keywords = {Cyclosarin, butyrylcholesterase, pyridinium oximes, neuroblastoma, bioscavenging}, doi = {10.1111/jnc.15674}, title = {Counteracting organophosphate-induced toxicity by improved bioscavenging capacity of BChE and damage prevention at cell level}, keyword = {Cyclosarin, butyrylcholesterase, pyridinium oximes, neuroblastoma, bioscavenging}, publisherplace = {Honolulu (HI), Sjedinjene Ameri\v{c}ke Dr\v{z}ave} }

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