You are here

Diisobutyl Phthalate’ ın (DIBP) Sıçan Karaciğeri Üzerine Histopatolojik Etkileri

Histopathological effects of Diisobutyl Phthalate (DIBP) on Rat Liver

Journal Name:

Publication Year:

DOI: 
http://dx.doi.org/10.17776/csj.49560

Keywords (Original Language):

Abstract (2. Language): 
The aim of this study is to investigate the histopathological effects on the liver tissues of widely used as plasticizer Diisobutyl phthalate (DIBP). In this study Wistar albino (n=10) rats were used. Three study groups were created: an experimental group, a control group fed with corn oil and a control group. The experimental group were administered by gavaj daily with 3 different dosages (0.25 - 0.5 - 1 ml/kg/day) of DIBP mixed with corn oil for 28 days. The liver tissue sections after rutin histological preparation processes were examined and photographed using an Olympus BX51 light microscope. It was determined from the analyses that there was no significant histological difference between the control and the corn-oil fed control group. The group which was administered DIBP displayed deterioration in lobulation, focal hepatocellular necrosis, oedema in hepatic artery and vena centralis, decrease in glycogen and distortion of nucleus shape in relation to the dosage of DIBP they received. As a result, it has been determined that DIBP is a hepatotoxic substance and has been found to cause irreversible serious histopathological changes in liver tissue.
Abstract (Original Language): 
Bu çalışmada, plastikleştirici olarak yaygın kullanılan fitalatlardan Diisobutyl phthalate’ın (DIBP) karaciğer dokusu üzerine etkilerinin histopatolojik yönden belirlenmesi amaçlanmıştır. Araştırmada Wistar albino cinsi sıçanlar (n=10/grup) kullanılmıştır. Çalışma kontrol, mısır yağı verilen kontrol ve deney grubu olarak üçe ayrılmıştır. Deney grubu hayvanlara 28 gün boyunca her gün üç farklı dozda (0.25-0.5-1ml/kg/gün) DIBP mısır yağı ile karıştırılarak gavaj yolu ile verilmiştir. Deneyin sonunda kontrol ve deney gruplarına ait tüm hayvanlardan alınan karaciğer doku örnekleri rutin ışık mikroskop histolojik preparasyon işlemlerinden (fiksasyon, dehidrasyon, bloklama, kesit alma, boyama, kapatma) sonra ışık mikroskobunda (Olympus BX51) incelenip değerlendirilmiştir. Histolojik incelemelerde kontrol ve mısır yağı kontrol grupları arasında histolojik açıdan farklılık olmadığı görülmüştür. DIBP uygulama gruplarında ise doza bağlı olarak artış gösteren lobulasyonda bozulma, fokal hepatoselüler nekroz, hepatik arter ve merkezi venlerde ödem, kongesyon, sinuzoidlerde genişleme, hepatositlerde sitoplazmik eosinofili, vakuolizasyon, glikojende azalma ve nükleuslarda şekil değişimi belirlenmiştir. Sonuç olarak DIBP’ın hepatotoksik olduğu ve karaciğer dokusunda geri dönüşümü olmayan ciddi histopatolojik değişikliklere yol açtığı tespit edilmiştir.
67
78

REFERENCES

References: 

[1] Ahbab M: Di-N-Hekzil fitalat ve disiklohekzil fitalat’a prenatal maruziyetin erkek sıçanların üreme sisteminin gelişimi üzerindeki etkilerinin incelenmesi. Hacettepe Üniversitesi, Fen Bilm Enst., Doktora Tezi, Ankara, 2010.
[2] Solomon GM, Schettler T: Environment and health: Endocrine disruption and potential human health implications. Canadian Medical Association Journal, 1116, 1467-74, 2000.
[3] Lee MM: Endocrine disrupters. Pediatric Endocrinology, 109, 18-37, 2007.
[4] Saito I, Onuki A, Seto H: Determination of organic phosphate triesters in indoor and outdoor air. J Aerosol Research, 16, 209-216, 2001.
[5] Shen H: Simultaneous screening and determination eight phthalates in plastic products for food use by sonication-assisted extraction/GC-MS methods. Talanta, 66: 734-739, 2005.
[6] Castle L, Mayo A, Gilbert J: Migration of plasticizers from printing inks into foods. Food Add Contam, 6, 437-443, 1989.
[7] Okubo T, Suzuki T, Yokoyama Y, Kano K, Kano I: Estimation of estrogenic and anti-estrogenic activites of some phthalate diesters and monoesters by MCF-7 cell proliferation assay in Vitro. Biol Pharm Bull, 26, 1219-1224, 2003.
[8] Environmental Protection Agency (EPA): Phthalates Action Plan, 2009. [http://www.epa.gov/oppt/existingchemicals/pubs/phthalates_ap_2009_1230_f..., Erişim Tarihi: 02.30.2011.
Diisobutyl Phthalate’ ın (DIBP) Sıçan Karaciğeri Üzerine
77
[9] European Chemicals Agency (ECHA): Annex IV Dossier, proposal for identification of a substance as SVHC/CMR (substances of very high concern/carcinogenic, mutagenic, or toxic to reproduction). [http://echa.europa.eu/doc/consultations/svhc/svhc_axvrep_germany_cmr_dii... 090831.pdf], 2009. Erişim Tarihi: 02.30.2011.
[10] European Commission: Diisobutyl phthalate. IUCLID Dataset. European Commission. European Chemicals Bureau, 2000. Substance ID: 84-69-5.
[ http://ecb.jrc.ec.europa.eu/iuclid-datasheet/84695.pdf], Erişim Tarihi: 04.13.2012.
[11] European Commission: Diisobutyl phthalate. Commission of the European Communities. European Chemicals Bureau, 2004. ECBI/116/04. [http://ecb.jrc.it/classlab/agenda/_ag_Health_0305.htm], Erişim Tarihi: 01.19.2012.
[12] Organization for Economic Cooperation and Development (OECD): Guidelines for Testing of Chemicals No: 407. Repeated Dose 28-day oral toxicity study in rodents. Paris, France, 1995.
[13] Bancroft JD, Cook HC: Manual of histological techniques and their diagnostic application. Churchill Livingstone, pp 457, London, 1994.
[14] Mann AH, Price SC, Mitchel FE, Grasso P, Hinton RH, Bridges JW: Comparison of the short-term effects of di(2-ethylhexyl) phthalate, di(n-hexyl) phthalate, and di(n-octyl) phthalate in rats. Toxicol Appl Pharmacol, 77, 116-132, 1985.
[15] David RM, Moore MR, Finney DC, Guest D: Chronic toxicity of di (2-ethylhexyl) phthalate in rats. Toxicol Sci, 55, 433-443, 2000.
[16] Rusyn I, Peters JM, Cunningham ML: Modes of action and speciesspecific effects of di (2-ethylhexyl) phthalate in the liver. Crit Rev Toxicol, 36, 459-479, 2006.
[17] Üçüncü Sİ, Ergen G, Önen Ö, Tekkan B, Üreten M, Boz E, Seferoğlu K, Gökçe B: Dioktil Adipat’ın (DOA) Labidochromis caeruleus Fryer, 1956 (Cichlidae, Teleostei) Karaciğer Histolojisi Üzerindeki Etkileri. Kafkas Univ. Vet. Fak. Derg, 16 (Suppl-B): 197-203, 2010.
[18] Peters N, Köhler A, Kranz H: Liver pathology in fishes from the lower Elbe as a consequence of pollution. Dis Aquat Org., 2, 87-97, 1987.
[19] Kranz H, Dethlefsen V: Liver anomalies in dab Limanda limanda from the southern North Sea with special consideration given to neoplastic lesions. Dis Aquat Org., 9, 171-185, 1990.
[20] Romano S., Donatti L., Freitas M., Teixeira J., Kusma J. 2006. Blood parameter analysis and morphological alterations as biomarkers on health of Hoplias malabaricus and Geophagus brasiliensis. Brazil Arch. Biol. Technol., 49, 441-448, 2006.
[21] Hoivik DJ, Qualls CWJr, Mirabile RC, Cariello NF, Kimbrough CL, Colton HM, Anderson SP, Santostefano MJ, Morgan RJ, Dahl RR, Brown AR, Zhao Z, Mudd PNJr, Oliver WBJr, Brown HR, Miller RT: Fibrates induce hepatic peroxisome and mitochondrial proliferation without overt evidence for cellular proliferation and oxidative stress in cynomolgus monkeys. Carcinogenesis, 25, 1757-69, 2004.
[22] Carthew P, Nolan BM, Edwards RE, Smith LL: The role of cell death and cell proliferation in the promotion of rat liver tumours by tamoxifen. Cancer Lett, 10, 163-69,1996.
AKYILDIZ, BAŞIMOĞLU KOCA
78
[23] Greaves P: Liver and pancreas. In Histopathology of Preclinical Toxicity Studies, 3rd ed., pp. 457-504. Elsevier, London, UK, 2007.
[24] Maronpot RR, Yoshizawa K, Nyska A, Harada T, Flake G, Mueller G, Singh B, Ward JM: Hepatic enzyme induction: Histopathology. Toxicol Pathol, 38, 776-95, 2010.
[25] Hall AP, Elcombe CR, Foster JR, Harada T, Kaufmann W, Knippel A, Küttler K, Malarkey DE, Maronpot RR, Nishikawa A, Nolte T, Schulte A, Strauss V, York MJ: Liver hypertrophy: A Review of adaptive (Adverse and non-adverse) changes conclusions from the 3rd international ESTP expert work shop. Toxicologic Pathology, 40, 971-994, 2012.
[26] Tamaru CS, Cole B, Bairley R, Brown C, Ako H: A manural for commercial production of Swordtail, Xiphophorus Helleri. University Of Hawaii Sea Grant Extension Service, School of Ocean Earth Science and Technology, CTSA Publication Number 128, pp; 1-38. Honululu, Hawaii, 2001.
[27] Weisman JL, Miller DL: Lipoid Liver Disease and Steatitis in Captive Sapphire Damsel Pomacentrus Pavo. Acta Lchtiyol Piscatoria, 36 (2): 99-104, 2006.
[28] Arellano JM, Storch V, Sarasquete C: Histological changes and copper accumulation in liver and gills of the Senegales Sole, Solea Senegalensis. Ecotoxicol Environ Saf, 44, 62-72, 1999.
[29] Manahan SE. Water pollution environment chermistry. First Ed., Lewis Publishers. London, 1991.
[30] Shehata AS, Abd El-Rehim Mohamed Z, Abd El-Haleem MR, Samak AM: Effects of exposure to plasticizers di-(2-Ethylhexyl) phthalate and trioctyltrimellitate on the histological structure of adult male albino rats’ Liver. Clinical Toxicology, 3, 4, 2013.

Thank you for copying data from http://www.arastirmax.com