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Pregled bibliografske jedinice broj: 957129

Sterigmatocystin induces oxidative stress in male Wistar rats


Rašić, Dubravka; Želježić, Davor; Micek, Vedran; Kifer, Domagoj; Jakšić, Daniela; Peraica, Maja; Kopjar, Nevenka; Šegvić Klarić, Maja
Sterigmatocystin induces oxidative stress in male Wistar rats // Toxicology Letters / Dekant, Wolfgang (ur.).
Brussels: Elsevier, 2018. str. S199-S200 doi:10.1016/j.toxlet.2018.06.887 (poster, međunarodna recenzija, sažetak, znanstveni)


Naslov
Sterigmatocystin induces oxidative stress in male Wistar rats

Autori
Rašić, Dubravka ; Želježić, Davor ; Micek, Vedran ; Kifer, Domagoj ; Jakšić, Daniela ; Peraica, Maja ; Kopjar, Nevenka ; Šegvić Klarić, Maja

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

Izvornik
Toxicology Letters / Dekant, Wolfgang - Brussels : Elsevier, 2018, S199-S200

Skup
54th Congress of the European Societies of Toxicology (EUROTOX 2018) TOXICOLOGY OUT OF THE BOX

Mjesto i datum
Brisel, Belgija, 2.-5.9.2018

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
DNA damage, glutathione, malondialdehyde, sterigmatocystin, superoxide dismutase

Sažetak
Sterigmatocystin (STC) is a polyketide mycotoxin with a bifuran ring structurally similar to aflatoxin. It is a precursor in aflatoxin biosynthesis in some Aspergillus species from the section Flavi and the final product in a number of Aspergilli from the section Versicolores. STC has been detected in various foodstuffs as well as indoor environments such as damp, moldy dwellings, carpets, and grain dust. In acute oral exposure it targets the liver and the kidneys. Its oral LD50 in male rats is about 160 mg kg-1 b.w. Similar to aflatoxin, STC's mechanism of action has been linked to the formation of exo- epoxide, which readily forms DNA adducts. Considering that aflatoxin toxicity has also been associated with oxidative stress, the aim of this study was to check whether the same is true for STC toxicity. With that in mind, we treated male Wistar rats with single oral STC doses of 1/4, 1/8, and 1/16 of LD50 (40, 20, and 10 mg kg-1 b.w., respectively) and measured superoxide dismutase (SOD) activity in plasma on a plate reader using a commercial kit. We also measured glutathione (GSH) and malondialdehyde (MDA) in plasma, kidney, and liver tissue using a spectrophotometer and HPLC, respectively. To assess oxidative DNA damage in the liver and kidneys we used comet tail intensity (i. e. DNA % in tail) obtained with the hOGG1-modified comet assay. STC did not affect GSH concentrations. SOD activity in plasma dropped significantly only in rats treated with 1/8 of LD50 (9.26±0.26 vs. 10.08±0.82 U mL-1 in control). All doses significantly increased MDA concentrations in plasma and kidney, but not in the liver. Oxidative DNA damage showed up in the liver and kidney cells, and was more pronounced in the kidneys, particularly at 1/8 of LD50. Our findings suggest that acute oral exposure to STC causes greater oxidative stress in the kidneys than the liver. This work has been fully supported by the Croatian Science Foundation under the project MycotoxA (HRZZ-IP- 09-2014-5982).

Izvorni jezik
Engleski

Znanstvena područja
Interdisciplinarne prirodne znanosti, Temeljne medicinske znanosti, Javno zdravstvo i zdravstvena zaštita



POVEZANOST RADA


Projekt / tema
HRZZ-IP-2014-09-5982 - Štetni učinci pojedinačnih i kombiniranih mikotoksina Aspergillus vrsta

Ustanove
Farmaceutsko-biokemijski fakultet, Zagreb,
Institut za medicinska istraživanja i medicinu rada, Zagreb

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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