Pregled bibliografske jedinice broj: 347697
The role of prostaglandins in acute hepatotoxicity
The role of prostaglandins in acute hepatotoxicity // Annual Meeting of the Croatian Immunological Society. Rovinj , Book of Abstracts 2007
Rovinj, Hrvatska, 2007. (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 347697 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The role of prostaglandins in acute hepatotoxicity
Autori
Ćavar, Ivan ; Renić, Marija ; Kelava, Tomislav ; Aleksić, Joško ; Čulo, Filip
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Annual Meeting of the Croatian Immunological Society. Rovinj , Book of Abstracts 2007
/ - , 2007
Skup
2007 Annual Meeting of the Croatian Immunological Society
Mjesto i datum
Rovinj, Hrvatska, 19.10.2007. - 21.10.2007
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
prostaglandin; acetaminophen; hepatotoxicity
Sažetak
Previously we have shown that liver cells of mice intoxicated with high dose of acetaminophen (Paracetamol, APAP) synthesize increased quantities of prostaglandin E2 (PGE2), prostaglandin I2 (PGI2) and thromboxane (TXA2). The aim of study was to determine which of these prostanoids contribute to defensive reaction of host to toxic effect of APAP (i.e. is hepatoprotective) and those which increase the toxic effect of APAP (i.e. is pathogenic). The toxicity of APAP was determined by observing the survival of mice given a lethal dose of APAP by gastric lavage and concentration of serum aminotransferases (AST and ALT) in mice given a sublethal dose of APAP. The concentration of particular prostanoid in body fluid of mice was modulated either by giving exogenously its stabile analog or giving specific anti-PG antibodies or inhibitors of specific receptors. In previous investigations we have shown that 16-16-dimethyl-PGE2 (a stable analogue of PGE2) had a strong protective effect if given to mice before or after APAP ; in contrast, application of specific anti- PGE2 antibodies increased toxic effect of APAP. Here we have shown that anti-TXB2 antibodies have opposite effect than anti-PGE2 antibodies, i.e., when given to APAP intoxicated mice, they decreased significantly serum AST and ALT levels. Recombinant TXB2 (0, 2 mg/kg) had no significant effect on AST and ALT levels in same mice. Presently we are testing the effect of various prostanoids agonists and antagonist on survival of intoxicated mice. The effect protective PG-s on synthesis of hepatotrophic cytokine, IL-6 and induction of Stat3 protein will also be tested.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
219-0000000-0328 - Uloga proupalnih citokina i prostaglandina u akutnom oštećenju jetre (Čulo, Filip, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb,
Medicinski fakultet, Osijek