Dergiler / Medicine Science / 2014 / Cilt: 3 - Sayı: 1

Effects of Benzo(a)pyrene and Ethanol on Morphology and Antioxidant Status and Transaminases in Rat Liver

Sayfa
1054–1067
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Additionally, we noted [B(a)P] induced hepatocellular changes in the periportal area.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Ethanol and benzo(a)pyrene cause an increase in lipid peroxidation either by producing the reactive oxygen species or decreasing the level of endogenous antioxidant enzymes that leads to cellular damage and cellular dysfunction.
📊
Temel Bulgular & Veri:Superoxide dismutase (SOD), alanin aminotransferase (ALT), aspartat aminotransferase (AST), gamma-glutamyl transferase (GGT), glutathione (GSH), malondialdehyde (MDA) levels as well as histological examination were evaluated to demonstrate the liver response following administration of [B(a)P] and (EtOH) separately and together.
💡
Sonuç & Katkı:Additionally, we noted [B(a)P] induced hepatocellular changes in the periportal area.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Ethanol and benzo(a)pyrene cause an increase in lipid peroxidation either by producing the reactive oxygen species or decreasing the level of endogenous antioxidant enzymes that leads to cellular damage and cellular dysfunction. The aim of this study was to investigate both physiological and histological changes in liver tissue after administration of benzo(a)pyrene and ethanol. Male Sprague Dawley rats were divided into four groups. First group (control group). Second group treated with benzo(a)pyrene [B(a)P], third group treated with benzo(a)pyrene[B(a)P] plus ethanol (EtOH) and fourth group was given ethanol(EtOH). Superoxide dismutase (SOD), alanin aminotransferase (ALT), aspartat aminotransferase (AST), gamma-glutamyl transferase (GGT), glutathione (GSH), malondialdehyde (MDA) levels as well as histological examination were evaluated to demonstrate the liver response following administration of [B(a)P] and (EtOH) separately and together. SOD activities of the liver tissue in the experimental groups were decreased when compared to the first group. Activities of ALT, AST and GGT of the liver tissue in all experimental groups were found significantly higher than that of the first group. GSH levels of the liver tissue of the experimental groups were lower than the first group especially in fourth group. When we compared MDA levels among study groups, MDA levels of experimental groups were found significantly higher than the first group. Exposure [B(a)P] to resulted in hepatocellular changes in the periportal area and inflammatory cell infiltration . On the other hand, liver tissue in third group and fourth group, which was treated with [B(a)P] plus EtOH and EtOH alone respectively, showed seldom inflammatory cell infiltrations. [B(a)P] and EtOH administration alone or together discretely determined changes in the GSH, MDA levels and SOD ALT, AST and GGT enzyme activities in the liver tissues. Additionally, we noted [B(a)P] induced hepatocellular changes in the periportal area.

🔖

Bu Makaleye Atıf Yap

EMRE, M. H., AKTAY, G., POLAT, A., ÖZTÜRK, F. (2014). Effects of Benzo(a)pyrene and Ethanol on Morphology and Antioxidant Status and Transaminases in Rat Liver. Medicine Science, Cilt: 3 - Sayı: 1, 1054–1067. https://ajindex.com/articles/277804

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (13)

  1. Jurczuk M, Brzosk, MM, Moniuszko-Jakoniuk J, Galazyn-Sidorczuk M, KulikowskaKarpinska, E. Antioxidant enzymes activity and lipid peroxidation in liver and kidney of rats exposed to cadmium and ethanol. Food Chem Toxicol. 2004;42(3):429-38
  2. Onaran I, Guven G, Ozaydin A, Ulutin T. The influence of GSTM1 null genotype on susceptibility to in vitro oxidative stress. Toxicology. 2001;157(3):195-205
  3. Gosset P, Garcon G, Casset A, Fleurisse L, Hannothiaux MH, Creusy C, Shirali P. Benzo(a)pyrene-coated onto Fe2O3 particles-induced apoptotic events in the lungs of Sprague-Dawley rats. Toxicol Lett. 2003;143(2):223-32
  4. Sivaram AG, Suresh MV, Indira M. Combined effect of ascorbic acid and selenium supplementation on alcohol-induced oxidative stress in guinea pigs. Comp Biochem Physiol C Toxicol Pharmacol. 2003;134(3):397-401
  5. Pushpakiran G, Mahalakshmi K, Anuradha CV. Taurine restores ethanol-induced depletion of antioxidants and attenuates oxidative stress in rat tissues. Amino Acids. 2004;27(1):91-6
  6. Thirunavukkarasu V, Anuradha CV, Viswanathan P. Protective effect of fenugreek (Trigonella foenum graecum) seeds in experimental ethanol toxicity Phytother Res. 2003;17(7):737-43
  7. Vidyashankara S, Nandakumara KS, Patkib PS. Alcohol depletes coenzyme-Q10 associated with increased TNF-alpha secretion to induce cytotoxicity in HepG2 cells. Toxicology. 2012;302(1):34-9
  8. Lieber CS. ALCOHOL: its metabolism and interaction with nutrients. Annu Rev Nutr. 2000;20:395-430
  9. Oh SI, Kim CI, Chun, HJ, Lee M.S, Park SC. Glutathione recycling is attenuated by acute ethanol feeding in rat liver. J Korean Med Sci. 1997;12(4):316-21
  10. Singletary KW, Barnes SL, van Breemen RB. Ethanol inhibits benzo[a]pyrene-DNA adduct removal and increases 8-oxo-deoxyguanosine formation in human mammary epithelial cells. Cancer Lett. 2004;203(2):139-44
  11. Gomez-Mendikute A, Etxeberria A, Olabarrieta I, Cajaraville MP. Oxygen radicals production and actin filament disruption in bivalve haemocytes treated with benzo(a)pyrene. Mar Environ Res. 2002;54(3-5):431-6
  12. Kasapinovic S, McCallum GP, Wiley MJ, Wells PGThe peroxynitrite pathway in development: phenytoin and benzo[a]pyrene embryopathies in inducible nitric oxide synthase knockout mice. Free Radic Biol Med. 2004;37(11):1703-11
  13. Seagrave JC, Burchiel SW. Interactions between benzo[a]pyrene and UVA light affecting ATP levels, cytoskeletal organization, and resistance to trypsinization. Toxicol Lett. 2000;117(1-2):1