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Expression of hsp70 in LLC-PK1 and MDCK cells exposed to ochratoxin A (CROSBI ID 486104)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | domaća recenzija

Barišić, Karmela ; Petrik, Jozsef ; Rumora, Lada ; Čepelak, Ivana ; Žanić Grubišić, Tihana Expression of hsp70 in LLC-PK1 and MDCK cells exposed to ochratoxin A // Periodicum Biologorum, 3rd Croatian Congress of Pharmacology with International Participation, Abstract book / Vitale, Branko (ur.). Zagreb: Societas Scientiarum Naturalium Croatica, 2001. str. 102-x

Podaci o odgovornosti

Barišić, Karmela ; Petrik, Jozsef ; Rumora, Lada ; Čepelak, Ivana ; Žanić Grubišić, Tihana

engleski

Expression of hsp70 in LLC-PK1 and MDCK cells exposed to ochratoxin A

Introduction: Ochratoxin A (OTA) is a possible etiological agent of endemic nephropathy, a chronic renal disease with high prevalence in limited geographic areas. Ochratoxicosis has many characteristics of different pathological states in which heat shock proteins (Hsps) are usually induced. The most inducible heat shock proteins belong to the Hsp70 family. Material and Methods: Hsp70 was determined by the Western blot in kidneys of rats chronically treated with a low dose of OTA and in LLC-PK1 and MDCK cells exposed to OTA. Estimation of cell viability and release of lactate dehydrogenase (LDH) confirmed the toxic effects of OTA on cultured cells. Results: OTA affects quantitative distribution between two Hsp70s isoforms (68kDa- and 74kDa- isoforms) but does not induce Hsp70 in rat kidney. No changes in the Hsp70 level were detected in LLC-PK1 and MDCK cells treated with OTA, although the cells were seriously injured, as seen from the reduced cell viability and increased release of LDH. Both cell lines were capable of inducing Hsp70 following a heat shock. However, exposure of the cells to OTA before the heat shock challenge prevented Hsp70 induction. Conclusion: Results of the presented study show that OTA does not induce Hsp70 in rat kidney and in cultured kidney cells. The absence of Hsp70 protective effects in the cells and tissues might be a possible explanation for the cumulative destructive effects of OTA and a silent onset of endemic nephropathy in humans and OTA-induced experimental nephrotoxicity in animals.

ochratoxin A; hsp70; LLCPK-1; MDCK

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o prilogu

102-x.

2001.

objavljeno

Podaci o matičnoj publikaciji

Periodicum Biologorum, 3rd Croatian Congress of Pharmacology with International Participation, Abstract book

Vitale, Branko

Zagreb: Societas Scientiarum Naturalium Croatica

Podaci o skupu

3rd Croatian Congress Of Pharmacology with international participation

poster

01.09.2001-04.09.2001

Zagreb, Hrvatska

Povezanost rada

Temeljne medicinske znanosti