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Sıçanlarda Gebelik Süresince Yeşil Çay Tüketiminin Maternal ve Neonatal Hepatositlerde Sitokeratin-18 Üzerindeki Etkisi

Yıl 2021, , 233 - 238, 27.09.2021
https://doi.org/10.21673/anadoluklin.881516

Öz

Amaç: Bu çalışmada, gebelikleri süresince yeşil çay ekstraktıyla beslenen sıçanların ve yavrularının karaciğer dokularında sSitokeratin-18 (SK-18) düzey ve ekspresyonunu değerlendirmek amaçlanmıştır.
Yöntem: On sekiz adet Wistar albino gebe sıçan, iki gruba ayrıldı: kontrol grubu ve (oral gavaj ile 50 mg/kg yeşil çay ekstraktı verilenuygulanan) yeşil çay grubu. Yirmi bir günlük gebelikten sonra, her iki gruptaki anne sıçanların ve doğdukları ilk gün yavruların karaciğer dokuları çıkarıldı. Bu doku örneklerinde SK-18 ekspresyonu ve düzeyi immünohistokimyasal olarak ve enzime bağlı immünosorbent analiz (ELISA) ile değerlendirildi.
Bulgular: İki grupta da maternal dokularda santral venlerin çevresindeki hepatositlerin hücre zarları yakınında kuvvetli SK-18 immünoreaksiyonu gözlendi. Kontrol grubu yenidoğan dokularında santral ven çevresindeki hepatositlerde zayıf SK-18 immünoreaksiyonu gözlenirken, yeşil çay grubunda hepatositlerin hücre zarı yakınında oldukça kuvvetli SK-18 immünoreaksiyonu gözlendi. Biyokimyasal incelemede de, maternal SK-18 düzeyleri her iki grupta da yüksek olup birbirinden istatistiksel olarak anlamlı farklılık göstermezken, neonatal SK-18 düzeyleri kontrol grubuna kıyasla yeşil çay grubunda anlamlı biçimde daha yüksekti.
Sonuç: İmmünohistokimya ve ELISA sonuçlarımız gebelik süresince maternal yeşil çay tüketiminin yenidoğan karaciğerinde hücre hasarına neden olabileceğini düşündürmektedir.

Kaynakça

  • Singh BN, Shankar S, Srivastava RK. Green tea catechin, epigallocatechin-3-gallate (EGCG): mechanisms, perspectives and clinical applications. Biochem Pharmacol. 2011;82(12):1807–21.
  • Bun SS, Bun H, Guédon D, Rosier C, Ollivier E. Effect of green tea extracts on liver functions in Wistar rats. Food Chem Toxicol. 2006;44(7):1108–13.
  • Nakamoto K, Takayama F, Mankura M, Hidaka Y, Egashira T, Ogino T, ve ark. Beneficial effects of fermented green tea extract in a rat model of non-alcoholic steatohepatitis. J Clin Biochem Nutr. 2009;44(3):239–46.
  • Zhi Z, Froh M, Connor HD, Li X, Conzelmann LO, Mason RP, ve ark. Prevention of hepatic ischemia-reperfusion injury by green tea extract. Am J Physiol Gastrointest Liver Physiol. 2002;283:957–64.
  • Zhong Z, Froh M, Lehnert M, Schoonhoven R, Yang L, Lind H, ve ark. Polyphenols from Camellia sinenesis attenuate experimental cholestasis induced liver fibrosis in rats. Am J Physiol Gastrointest Liver Physiol. 2003;285:1004–13.
  • Li YM, Zhang XG, Zhou HL, Chen SH, Zhang Y, Yu CH. Effects of tea polyphenols on hepatic fibrosis in rats with alcoholic liver disease. Hepatobiliary Pancreat Dis Int. 2004;3:577–9.
  • Arteel GE, Uesugi T, Bevan LN, Gäbele E, Wheeler MD, McKim SE, ve ark. Green tea extract protects against early alcohol-induced liver injury in rats. Biol Chem. 2002;383(3–4):663–70.
  • Chen JH, Tipoe GL, Liong EC, So HSH, Leung KM, Tom WM, ve ark. Green tea polyphenols prevent toxin-induced hepatotoxicity in mice by down-regulating inducible nitric oxide-derived prooxidants. Am J Clin Nutr. 2004;80:742–51.
  • Oz HS, McClain CJ, Nagasawa HT, Ray MB, Villiers WJ, Chen TS. Diverse antioxidants protect against acetaminophen hepatotoxicity. J Biochem Mol Toxicol. 2004;18:361–8.
  • Mazzanti G, Menniti-Ippolito F, Moro PA, Cassetti F, Raschetti R, Santuccio C, ve ark. Hepatotoxicity from green tea: a review of the literature and two unpublished cases. Eur J Clin Pharmacol. 2009;65:331–41.
  • Lambert JD, Kennett MJ, Sang S, Reuhl KR, Ju J, Yang CS. Hepatotoxicity of high oral dose (-)-epigallocatechin-3-gallate in mice. Food Chem Toxicol. 2010;48(1):409–16.
  • Galati G, Lin A, Sultan AM, O’Brien PJ. Cellular and in vivo hepatotoxicity caused by green tea phenolic acids and catechins. Free Radic Biol Med. 2006;15:40(4):570–80.
  • Chow HHS, Cai Y, Hakim IA, Crowell JA, Shahi F, Brooks CA, ve ark. Pharmacokinetics and safety of green tea polyphenols after multiple-dose administration of epigallocatechin gallate and polyphenon E in healthy individuals. Clin Cancer Res. 2003;9(9):3312–9.
  • Chengelis CP, Kirkpatrick JB, Regan KS, Radovsky AE, Beck MJ, Morita O, ve ark. 28-day oral gavage toxicity studies of green tea catechins prepared for beverages in rats. Food Chem Toxicol. 2008;46(3):978–89.
  • Morita O, Kirkpatrick JB, Tamaki Y, Chengelis CP, Beck MJ, Bruner RH. Safety assessment of heat-sterilized green tea catechin preparation: a 6-month repeat-dose study in rats. Food Chem Toxicol. 2009;47(8):1760–70.
  • Wang CC, Chu KO, Chong WS, Li WY, Pang CP, Shum ASW, ve ark. Tea epigallocatechin-3-gallate increases 8-isoprostane level and induces caudal regression in developing rat embryos. Free Radic Biol Med. 2007;43(4):519–27.
  • Correa A, Stolley A, Liu Y. Prenatal tea consumption and risks of anencephaly and spina bifida. Ann Epidemiol. 2000;10(7):476–7.
  • Ismail SA, El-Saadany S, Ziada DH, Zakaria SS, Mayah WW, Elashry H, ve ark. Cytokeratin-18 in diagnosis of HCC in patients with liver cirrhosis. Asian Pac J Cancer Prev. 2017;18(4):1105–11.
  • Yilmaz Y. Systematic review: caspase-cleaved fragments of cytokeratin 18—the promises and challenges of a biomarker for chronic liver disease. Aliment Pharmacol Ther. 2009;30(11–12):1103–9.
  • Abdel-Majeed S, Mohammad A, Shaima AB, Mohammad R, Mousa SA. Inhibition property of green tea extract in relation to reserpine-induced ribosomal strips of rough endoplasmic reticulum (rER) of the rat kidney proximal tubule cells. J Toxicol Sci. 2009;34(6):637–45.
  • Gürgen SG, Sayın O, Cetin F, Tuç Yücel A. Transcutaneous electrical nerve stimulation (TENS) accelerates cutaneous wound healing and inhibits pro-inflammatory cytokines. Inflammation. 2014;37(3):775–84.
  • Gürgen SG, Karakuş AÇ, Çeçen D, Özen G, Koçtürk S. Usage of whey protein may cause liver damage via inflammatory and apoptotic responses. Hum Exp Toxicol. 2015;34(7):769–79.
  • Morita O, Knapp JF, Tamaki Y, Stump DG, Moore JS, Nemec MD. Effects of green tea catechin on embryo/fetal development in rats. Food Chem Toxicol. 2009;47(6):1296–303.
  • Chu KO, Wang CC, Chu CY, Chan KP, Rogers MS, Choy KW, ve ark. Pharmacokinetic studies of green tea catechins in maternal plasma and fetuses in rats. J Pharm Sci. 2006;95:1372–81.
  • Chu KO, Wang CC, Chu CY, Choy KW, Pang CP, Rogers MS. Uptake and distribution of catechins in fetal organs following in utero exposure in rats. Hum Reprod. 2006;22:280–7.
  • Isbrucker RA, Edwards JA, Wolz E, Davidovich A, Bausch J. Safety studies on epigallocatechin gallate (EGCG) preparations. Part 3: teratogenicity and reproductive toxicity studies in rats. Food Chem Toxicol. 2006;44(5):6516–61.

The Effects of Green Tea Consumption during Pregnancy on the Cytokeratin-18 in Maternal and Neonatal Hepatocytes in Rats

Yıl 2021, , 233 - 238, 27.09.2021
https://doi.org/10.21673/anadoluklin.881516

Öz

Aim: In this study, we aimed to evaluate the cCytokeratin-18 (CK-18) levels and expression in liver tissues of rats that were fed with green tea extract during pregnancy and their pups.
Methods: Eighteen pregnant Wistar albino rats were divided into two groups: the control group and the green tea group (orally gavaged with 50 mg/kg of green tea extract). After 21- days of gestation, liver tissues were removed from the mother rats and their pups on the first postnatal day in both groups. The CK-18 levels and expression in these tissue samples were evaluated immunohistochemically and by use of enzyme-linked immunosorbent assay (ELISA).
Results: Strong CK-18 immunoreaction was observed near the cell membranes of hepatocytes around the central veins in maternal liver tissues in both groups. While a weak CK-18 immunoreaction was observed in hepatocytes around the central veins in the control group neonatal tissues, a strong CK-18 immunoreaction was observed near the cell membranes of hepatocytes in the green tea group. Biochemically also, while maternal CK-18 levels were high in both groups with no statistically significant difference, neonatal CK-18 levels were significantly higher in the green tea group than in the control group.
Conclusion: Our immunohistochemical and ELISA results suggest that maternal consumption of green tea during pregnancy may lead to cell injury in the neonatal liver.

Kaynakça

  • Singh BN, Shankar S, Srivastava RK. Green tea catechin, epigallocatechin-3-gallate (EGCG): mechanisms, perspectives and clinical applications. Biochem Pharmacol. 2011;82(12):1807–21.
  • Bun SS, Bun H, Guédon D, Rosier C, Ollivier E. Effect of green tea extracts on liver functions in Wistar rats. Food Chem Toxicol. 2006;44(7):1108–13.
  • Nakamoto K, Takayama F, Mankura M, Hidaka Y, Egashira T, Ogino T, ve ark. Beneficial effects of fermented green tea extract in a rat model of non-alcoholic steatohepatitis. J Clin Biochem Nutr. 2009;44(3):239–46.
  • Zhi Z, Froh M, Connor HD, Li X, Conzelmann LO, Mason RP, ve ark. Prevention of hepatic ischemia-reperfusion injury by green tea extract. Am J Physiol Gastrointest Liver Physiol. 2002;283:957–64.
  • Zhong Z, Froh M, Lehnert M, Schoonhoven R, Yang L, Lind H, ve ark. Polyphenols from Camellia sinenesis attenuate experimental cholestasis induced liver fibrosis in rats. Am J Physiol Gastrointest Liver Physiol. 2003;285:1004–13.
  • Li YM, Zhang XG, Zhou HL, Chen SH, Zhang Y, Yu CH. Effects of tea polyphenols on hepatic fibrosis in rats with alcoholic liver disease. Hepatobiliary Pancreat Dis Int. 2004;3:577–9.
  • Arteel GE, Uesugi T, Bevan LN, Gäbele E, Wheeler MD, McKim SE, ve ark. Green tea extract protects against early alcohol-induced liver injury in rats. Biol Chem. 2002;383(3–4):663–70.
  • Chen JH, Tipoe GL, Liong EC, So HSH, Leung KM, Tom WM, ve ark. Green tea polyphenols prevent toxin-induced hepatotoxicity in mice by down-regulating inducible nitric oxide-derived prooxidants. Am J Clin Nutr. 2004;80:742–51.
  • Oz HS, McClain CJ, Nagasawa HT, Ray MB, Villiers WJ, Chen TS. Diverse antioxidants protect against acetaminophen hepatotoxicity. J Biochem Mol Toxicol. 2004;18:361–8.
  • Mazzanti G, Menniti-Ippolito F, Moro PA, Cassetti F, Raschetti R, Santuccio C, ve ark. Hepatotoxicity from green tea: a review of the literature and two unpublished cases. Eur J Clin Pharmacol. 2009;65:331–41.
  • Lambert JD, Kennett MJ, Sang S, Reuhl KR, Ju J, Yang CS. Hepatotoxicity of high oral dose (-)-epigallocatechin-3-gallate in mice. Food Chem Toxicol. 2010;48(1):409–16.
  • Galati G, Lin A, Sultan AM, O’Brien PJ. Cellular and in vivo hepatotoxicity caused by green tea phenolic acids and catechins. Free Radic Biol Med. 2006;15:40(4):570–80.
  • Chow HHS, Cai Y, Hakim IA, Crowell JA, Shahi F, Brooks CA, ve ark. Pharmacokinetics and safety of green tea polyphenols after multiple-dose administration of epigallocatechin gallate and polyphenon E in healthy individuals. Clin Cancer Res. 2003;9(9):3312–9.
  • Chengelis CP, Kirkpatrick JB, Regan KS, Radovsky AE, Beck MJ, Morita O, ve ark. 28-day oral gavage toxicity studies of green tea catechins prepared for beverages in rats. Food Chem Toxicol. 2008;46(3):978–89.
  • Morita O, Kirkpatrick JB, Tamaki Y, Chengelis CP, Beck MJ, Bruner RH. Safety assessment of heat-sterilized green tea catechin preparation: a 6-month repeat-dose study in rats. Food Chem Toxicol. 2009;47(8):1760–70.
  • Wang CC, Chu KO, Chong WS, Li WY, Pang CP, Shum ASW, ve ark. Tea epigallocatechin-3-gallate increases 8-isoprostane level and induces caudal regression in developing rat embryos. Free Radic Biol Med. 2007;43(4):519–27.
  • Correa A, Stolley A, Liu Y. Prenatal tea consumption and risks of anencephaly and spina bifida. Ann Epidemiol. 2000;10(7):476–7.
  • Ismail SA, El-Saadany S, Ziada DH, Zakaria SS, Mayah WW, Elashry H, ve ark. Cytokeratin-18 in diagnosis of HCC in patients with liver cirrhosis. Asian Pac J Cancer Prev. 2017;18(4):1105–11.
  • Yilmaz Y. Systematic review: caspase-cleaved fragments of cytokeratin 18—the promises and challenges of a biomarker for chronic liver disease. Aliment Pharmacol Ther. 2009;30(11–12):1103–9.
  • Abdel-Majeed S, Mohammad A, Shaima AB, Mohammad R, Mousa SA. Inhibition property of green tea extract in relation to reserpine-induced ribosomal strips of rough endoplasmic reticulum (rER) of the rat kidney proximal tubule cells. J Toxicol Sci. 2009;34(6):637–45.
  • Gürgen SG, Sayın O, Cetin F, Tuç Yücel A. Transcutaneous electrical nerve stimulation (TENS) accelerates cutaneous wound healing and inhibits pro-inflammatory cytokines. Inflammation. 2014;37(3):775–84.
  • Gürgen SG, Karakuş AÇ, Çeçen D, Özen G, Koçtürk S. Usage of whey protein may cause liver damage via inflammatory and apoptotic responses. Hum Exp Toxicol. 2015;34(7):769–79.
  • Morita O, Knapp JF, Tamaki Y, Stump DG, Moore JS, Nemec MD. Effects of green tea catechin on embryo/fetal development in rats. Food Chem Toxicol. 2009;47(6):1296–303.
  • Chu KO, Wang CC, Chu CY, Chan KP, Rogers MS, Choy KW, ve ark. Pharmacokinetic studies of green tea catechins in maternal plasma and fetuses in rats. J Pharm Sci. 2006;95:1372–81.
  • Chu KO, Wang CC, Chu CY, Choy KW, Pang CP, Rogers MS. Uptake and distribution of catechins in fetal organs following in utero exposure in rats. Hum Reprod. 2006;22:280–7.
  • Isbrucker RA, Edwards JA, Wolz E, Davidovich A, Bausch J. Safety studies on epigallocatechin gallate (EGCG) preparations. Part 3: teratogenicity and reproductive toxicity studies in rats. Food Chem Toxicol. 2006;44(5):6516–61.
Toplam 26 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Sağlık Kurumları Yönetimi
Bölüm ORJİNAL MAKALE
Yazarlar

Oya Sayın 0000-0003-0879-9091

Seren Gülşen Gürgen 0000-0002-5514-1404

Ferihan Çetin 0000-0003-1852-4622

Ayşe Tuç Yücel 0000-0001-8374-538X

Selda İldan Çalım 0000-0001-8500-4251

Yayımlanma Tarihi 27 Eylül 2021
Kabul Tarihi 10 Nisan 2021
Yayımlandığı Sayı Yıl 2021

Kaynak Göster

Vancouver Sayın O, Gürgen SG, Çetin F, Tuç Yücel A, İldan Çalım S. Sıçanlarda Gebelik Süresince Yeşil Çay Tüketiminin Maternal ve Neonatal Hepatositlerde Sitokeratin-18 Üzerindeki Etkisi. Anadolu Klin. 2021;26(3):233-8.

13151 This Journal licensed under a CC BY-NC (Creative Commons Attribution-NonCommercial 4.0) International License.