open access

Vol 76, No 4 (2017)
Original article
Submitted: 2017-02-17
Accepted: 2017-05-15
Published online: 2017-05-25
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Effect of subchronic intake of green tea extract on liver of albino rat histomorphometric, ultrastructural and biochemical study

S. M. Zaki1, S. H. Ahmed1, W. M. Sayed1, A. A. Ali1
·
Pubmed: 28553849
·
Folia Morphol 2017;76(4):642-649.
Affiliations
  1. Faculty of Medicine, Cairo University, Egypt

open access

Vol 76, No 4 (2017)
ORIGINAL ARTICLES
Submitted: 2017-02-17
Accepted: 2017-05-15
Published online: 2017-05-25

Abstract

Background: There are conflicting reports on the effect of green tea extract (GTE) on the liver of animals. Some studies failed to show any adverse hepatic effects following administration of GTE to mice, rats, and dogs. Others reported severe hepatic necrosis, resulting in death in female Swiss-Webster mice following its administration. The aim of the study was to examine the subchronic toxicity of GTE on the liver of the adult male albino rats.

Materials and methods: Forty male adult Wistar albino rats were used in the study. The rats were divided into four groups; group I (control), group II (low-dose green tea), group III (medium-dose green tea) and group IV (high-dose green tea). Histological, biochemical and histomorphometric analyses were done.

Results: Mild hepatic affections were observed in group II. The affections were severe in groups III and IV. The central veins and hepatic sinusoids were congested. The hepatocytes were degenerated. Hypertrophy of the hepatic arteries, dilation of the bile ducts and cellular infiltration were clearly observed in the last two groups. Mild degenerative changes were observed in the hepatocytes in rat’s group II; the cytoplasm was rarefied and vacuolated. Some mitochondria were ruptured. The blood sinusoids were congested. The rough endoplasmic retinaculum was fragmented in group III. More degenerative changes were observed in group IV; the hepatic architectures were lost with disruption of cell membranes. Most of the cell organelles were degenerated and most of mitochondria were ballooned. As compared to that of the control groups: the total serum protein values in groups II, III and IV showed a statistically significant decrease (12%, 20% and 21%, respectively), the mean area per cent of collagen fibres in groups III and IV increased 5 and 7 folds.

Conclusions: Subchronic administration of GTE resulted in structural and functional affection of the rats’ liver. The dose of 250 mg/kg/day seemed to be safe, while the doses of 500 mg/kg/day and 1000 mg/kg/day had deleterious effect being more evident in the latter dose.

Abstract

Background: There are conflicting reports on the effect of green tea extract (GTE) on the liver of animals. Some studies failed to show any adverse hepatic effects following administration of GTE to mice, rats, and dogs. Others reported severe hepatic necrosis, resulting in death in female Swiss-Webster mice following its administration. The aim of the study was to examine the subchronic toxicity of GTE on the liver of the adult male albino rats.

Materials and methods: Forty male adult Wistar albino rats were used in the study. The rats were divided into four groups; group I (control), group II (low-dose green tea), group III (medium-dose green tea) and group IV (high-dose green tea). Histological, biochemical and histomorphometric analyses were done.

Results: Mild hepatic affections were observed in group II. The affections were severe in groups III and IV. The central veins and hepatic sinusoids were congested. The hepatocytes were degenerated. Hypertrophy of the hepatic arteries, dilation of the bile ducts and cellular infiltration were clearly observed in the last two groups. Mild degenerative changes were observed in the hepatocytes in rat’s group II; the cytoplasm was rarefied and vacuolated. Some mitochondria were ruptured. The blood sinusoids were congested. The rough endoplasmic retinaculum was fragmented in group III. More degenerative changes were observed in group IV; the hepatic architectures were lost with disruption of cell membranes. Most of the cell organelles were degenerated and most of mitochondria were ballooned. As compared to that of the control groups: the total serum protein values in groups II, III and IV showed a statistically significant decrease (12%, 20% and 21%, respectively), the mean area per cent of collagen fibres in groups III and IV increased 5 and 7 folds.

Conclusions: Subchronic administration of GTE resulted in structural and functional affection of the rats’ liver. The dose of 250 mg/kg/day seemed to be safe, while the doses of 500 mg/kg/day and 1000 mg/kg/day had deleterious effect being more evident in the latter dose.

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Keywords

green tea extract, liver

About this article
Title

Effect of subchronic intake of green tea extract on liver of albino rat histomorphometric, ultrastructural and biochemical study

Journal

Folia Morphologica

Issue

Vol 76, No 4 (2017)

Article type

Original article

Pages

642-649

Published online

2017-05-25

Page views

1638

Article views/downloads

1661

DOI

10.5603/FM.a2017.0050

Pubmed

28553849

Bibliographic record

Folia Morphol 2017;76(4):642-649.

Keywords

green tea extract
liver

Authors

S. M. Zaki
S. H. Ahmed
W. M. Sayed
A. A. Ali

References (30)
  1. Bajerska J, Wozniewicz M, Jeszka J, et al. Green tea aqueous extract reduces visceral fat and decreases protein availability in rats fed with a high-fat diet. Nutr Res. 2011; 31(2): 157–164.
  2. Bun SS, Bun H, Guédon D, et al. Effect of green tea extracts on liver functions in Wistar rats. Food Chem Toxicol. 2006; 44(7): 1108–1113.
  3. Chan PoC, Ramot Y, Malarkey DE, et al. Fourteen-week toxicity study of green tea extract in rats and mice. Toxicol Pathol. 2010; 38(7): 1070–1084.
  4. Ding SP, Li JC, Jin C. A mouse model of severe acute pancreatitis induced with caerulein and lipopolysaccharide. World J Gastroenterol. 2003; 9(3): 584–589.
  5. Emoto Y, Yoshizawa K, Kinoshita Y, et al. Green Tea Extract-induced Acute Hepatotoxicity in Rats. J Toxicol Pathol. 2014; 27(3-4): 163–174.
  6. Fausther M, Lavoie EG, Dranoff JA. Contribution of myofibroblasts of different origins to liver fibrosis. Curr Pathobiol Rep. 2013; 1(3): 225–230.
  7. Forbes SJ, Parola M. Liver fibrogenic cells. Best Pract Res Clin Gastroenterol. 2011; 25(2): 207–217.
  8. Fujimoto T, Ohsaki Y, Suzuki M, et al. Imaging lipid droplets by electron microscopy. Methods Cell Biol. 2013; 116: 227–251.
  9. Galati G, Lin A, Sultan AM, et al. Cellular and in vivo hepatotoxicity caused by green tea phenolic acids and catechins. Free Radic Biol Med. 2006; 40(4): 570–580.
  10. Goodin MG, Rosengren RJ. Epigallocatechin gallate modulates CYP450 isoforms in the female Swiss-Webster mouse. Toxicol Sci. 2003; 76(2): 262–270.
  11. Higdon JV, Frei B. Tea catechins and polyphenols: health effects, metabolism, and antioxidant functions. Crit Rev Food Sci Nutr. 2003; 43(1): 89–143.
  12. Hsu YW, Tsai CF, Chen WK, et al. A subacute toxicity evaluation of green tea (Camellia sinensis) extract in mice. Food Chem Toxicol. 2011; 49(10): 2624–2630.
  13. Klaassen CD, Watkins JB, Casarett LJ. Casarett & Doull's essentials of toxicology. 2nd ed. McGraw-Hill Medical Pub. Division, New York: 2010: pxi, 459.
  14. Kühnlein RP. Thematic review series: Lipid droplet synthesis and metabolism: from yeast to man. Lipid droplet-based storage fat metabolism in Drosophila. J Lipid Res. 2012; 53(8): 1430–1436.
  15. Lambert JD, Kennett MJ, Sang S, et al. Hepatotoxicity of high oral dose (-)-epigallocatechin-3-gallate in mice. Food Chem Toxicol. 2010; 48(1): 409–416.
  16. Mazzanti G, Di Sotto A, Vitalone A. Hepatotoxicity of green tea: an update. Arch Toxicol. 2015; 89(8): 1175–1191.
  17. Mehdipour M, Daghigh Kia H, Najafi A, et al. Effect of green tea (Camellia sinensis) extract and pre-freezing equilibration time on the post-thawing quality of ram semen cryopreserved in a soybean lecithin-based extender. Cryobiology. 2016 [Epub ahead of print]; 73(3): 297–303.
  18. Molinari M, Watt KDS, Kruszyna T, et al. Acute liver failure induced by green tea extracts: case report and review of the literature. Liver Transpl. 2006; 12(12): 1892–1895.
  19. Nagao T, Komine Y, Soga S, et al. Ingestion of a tea rich in catechins leads to a reduction in body fat and malondialdehyde-modified LDL in men. Am J Clin Nutr. 2005; 81(1): 122–129.
  20. Nagata T. Senescence. Rijeka (HR): InTech,; 2012. Available from: . http://www.ncbi.nlm.nih.gov/books/NBK402330/.
  21. Patel SS, Beer S, Kearney DL, et al. Green tea extract: a potential cause of acute liver failure. World J Gastroenterol. 2013; 19(31): 5174–5177.
  22. Saleh IG, Ali Z, Abe N, et al. Effect of green tea and its polyphenols on mouse liver. Fitoterapia. 2013; 90: 151–159.
  23. Salminen WF, Yang Xi, Shi Q, et al. Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice. Food Chem Toxicol. 2012; 50(5): 1439–1446.
  24. Sarma DN, Barrett ML, Chavez ML, et al. Safety of green tea extracts : a systematic review by the US Pharmacopeia. Drug Saf. 2008; 31(6): 469–484.
  25. Sell S. The hepatocyte: heterogeneity and plasticity of liver cells. Int J Biochem Cell Biol. 2003; 35(3): 267–271.
  26. Serov VV. [Nature of cloudy swelling and granular degeneration of parenchymatous organs]. Arkh Patol. 1991; 53(2): 3–6.
  27. Shi J, Hao JH, Ren WH, et al. Effects of heparin on liver fibrosis in patients with chronic hepatitis B. World J Gastroenterol. 2003; 9(7): 1611–1614.
  28. Slott PA, Liu MH, Tavoloni N. Origin, pattern, and mechanism of bile duct proliferation following biliary obstruction in the rat. Gastroenterology. 1990; 99(2): 466–477.
  29. Zhang F, Xu X, Li T, et al. Shellfish toxins targeting voltage-gated sodium channels. Mar Drugs. 2013; 11(12): 4698–4723.
  30. Zheng EX, Rossi S, Fontana RJ, et al. Risk of Liver Injury Associated with Green Tea Extract in SLIMQUICK(®) Weight Loss Products: Results from the DILIN Prospective Study. Drug Saf. 2016; 39(8): 749–754.

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