Pregled bibliografske jedinice broj: 256054
Protective effect of IL-1 alpha and beta on the acetaminophen induced liver toxicity relies on their early induction by acetaminophen itself
Protective effect of IL-1 alpha and beta on the acetaminophen induced liver toxicity relies on their early induction by acetaminophen itself // European Cytokine Network / Fradelizzi, Didier (ur.).
Pariz: John Libbey Eurotext, 2006. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 256054 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Protective effect of IL-1 alpha and beta on the acetaminophen induced liver toxicity relies on their early induction by acetaminophen itself
(Protective effect of IL-1 alpha and beta on the acetaminophen induced liver toxicity relies on their early induction by acetaminophen itself.)
Autori
Aleksić, Joško ; Čulo, Melanie Ivana ; Poljak, Ljiljana ; Matić, Tomas ; Čulo, Filip ;
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
European Cytokine Network
/ Fradelizzi, Didier - Pariz : John Libbey Eurotext, 2006
Skup
6th International Cytokine Conference, Vienna, Austria
Mjesto i datum
Beč, Austrija, 27.08.2006. - 31.08.2006
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
acetaminophen; IL-1 hepatoprotective effect; RT-PCR analysis
(acetaminphen; IL-1 hepatoprotective effect; RT-PCR analysis)
Sažetak
We have previoulsy shown that both IL-1 alpha and IL-6 exhibit heaptopreotective effect if given before administration of acetaminophen (APAP) that is partially mediated by PGE2. When the effect of IL-1 beta was investigated using the same model, IL (1500IU/mouse)or anti-IL-1beta antibody (0.5ml of rabbit to mouse IL-1, obtained by three constitutive injection of Il-1 beta, first incomplete FCA) were given i.p. 3 hours before APAP. The survival of mice has been followed for 72 hours and the serum concetration of aminotransfereses (AST and ALT) were determined 18-24 hours after APAP administration. IL-1beta significantl< increased the survival of mice and decreased serum level of AST and ALT (p<0.05. As expected, when anti IL-1Ra antibody was administered, significant increase in the serum concentrations of AST and ALT (p<0.05 or better) were observed. The survival of animals hasn't been followed in this experiment. The finding that anti-IL-1R alpha antiobdy treatment causes increased AST and ALT serumlevel, the same effect as anti-IL-1 beta therapy dose, prompted us to analyze the endogenous synthesis of Il-1 cytokine in liver samples from IL-1 non-exposed but APAP intocicated animals. RT_PCR analysis of the IL-1a alpha nd IL-1 beta expression level in liver smaples from APAP inotxicated mice has revealed that acetaminophen induces the expression of both cytokines though of somewhat different pattern, already 1 hour after its intragastric administration. This expression was even higher at 6 hours following APAP adminsitration and could be blocked by intraperitoneal injection of aspirin at the dose which inhibits NF-kB activity. Based on this we hypothesized that oganism intoxicated with APAP synthesize its own IL-1 realy on following APAP administration which may represent a host defense raction that could be halped by applying appropriate dose of exogenous cytokines.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti