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Subchronic exposure of individual and combined ochratoxin A and citrinin selectively affects the expression of rat renal organic cation transporters (CROSBI ID 303994)

Prilog u časopisu | pregledni rad (znanstveni) | međunarodna recenzija

Karaica, Dean ; Micek, Vedran ; Rašić, Dubravka ; Peraica, Maja ; Šegvić Klarić, Maja ; Breljak, Davorka Subchronic exposure of individual and combined ochratoxin A and citrinin selectively affects the expression of rat renal organic cation transporters // Mycotoxin research, 38 (2022), 1; 339-352. doi: 10.1007/s12550-022-00450-6

Podaci o odgovornosti

Karaica, Dean ; Micek, Vedran ; Rašić, Dubravka ; Peraica, Maja ; Šegvić Klarić, Maja ; Breljak, Davorka

engleski

Subchronic exposure of individual and combined ochratoxin A and citrinin selectively affects the expression of rat renal organic cation transporters

Ochratoxin A (OTA) and citrinin (CIT) are nephrotoxins found co-occurring in various human/animal food/feed and recog- nized as a health threat. However, most studies investigate individual effects and neglect their combined nephrotoxic effects in mammals. Previous studies have indicated that organic anion/cation transporters (OATs/OCTs) localized in renal proximal tubules mediate the transport of OTA and CIT. Still, little is known about the in vivo effects of individual/combined OTA and CIT on protein localization/expression of OCTs, physiologically/pharmacologically important renal transporters. Here, we used Western blot and immunofluorescence microscopy to study the effects of subchronic (21-day) exposure to individual/ combined OTA (0.125 and 0.250 mg kg−1 b.w.) and CIT (20 mg kg−1 b.w.) on protein localization/expression of organic cation transporters (rOct1/Slc22a1 and rOct2/Slc22a2) in kidneys of Wistar rats. Since the antioxidant resveratrol (RSV) has shown measurable protective effects against OTA- and CIT-related oxidative stress toxicity in vitro, we investigated the effects of an OTA + CIT + RSV combination on rOct1/2 localization/expression in the same model. Individual OTA induced a dose-dependent decrease of rOct1 but not rOct2 protein expression, whereas their localization pattern remained unchanged. Individual CIT did not affect the renal rOct1/2 protein localization/expression. Combined OTA + CIT exposure induced a significant decrease of rOct1 protein expression by an OTA250 dose, whereas oral co-administration of OTA + CIT + RSV resulted in a significant decrease of rOct1/2 protein expression. Thus, we revealed an OTA- related selective effect on the rOct1/2 protein expression and a non-specific adverse effect of RSV in the OTA + CIT + RSV combination on the renal organic cation transport system in rat.

In vivo ; Kidney, Mycotoxin ; Nephrotoxicity ; Resveratrol ; Slc22 family

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

38 (1)

2022.

339-352

objavljeno

0178-7888

1867-1632

10.1007/s12550-022-00450-6

Povezanost rada

Biologija, Farmacija, Temeljne medicinske znanosti

Poveznice
Indeksiranost