Effect of short-term exposure to dichlorvos on rat hepatocyte: molecular and histopathological approach
Autor: | Ayse Kurtulus, Goksin Nilufer Yonguc, Yavuz Dodurga, Bora Boz, Kemalettin Acar, Hülya Çetin Sorkun |
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Jazyk: | angličtina |
Rok vydání: | 2012 |
Předmět: |
Pathology
gene amplification Apoptosis animal cell chemistry.chemical_compound interleukin 1beta converting enzyme Organophosphate Gene expression caspase 3 rat tumor suppressor gene tumor necrosis factor alpha Liver cell article liver cell tumor necrosis factor alpha gene hypoxia inducible factor 1 alpha gene liver toxicity Reverse transcription polymerase chain reaction liver histology caspase 3 gene RNA isolation medicine.anatomical_structure female Liver Hepatocyte histopathology medicine.medical_specialty animal experiment Intoxication Caspase 3 Hepatocyte density Pathology and Forensic Medicine animal tissue Andrology reverse transcription polymerase chain reaction Dichlorvos medicine controlled study hypoxia inducible factor 1alpha gene nonhuman dichlorvos liver examination caspase 1 gene RNA extraction chemistry molecular genetics gene expression cytotoxicity test Corn oil |
Popis: | Organophosphate (OP) insecticides are the most widely used in both agricultural and landscape pest control. The mortality and morbidity rate of OP poisoning is high. The aim of the present study is to investigate the effect of acute organophosphate exposure on hepatocyte and to examine caspase 1 and caspase-3 gene expression, and cell apoptosis related genes as p53, Tumor Necrosis Factor-alpha, Hypoxia Inducible Factor 1-alpha expression changes in rat hepatocyte. Material and Methods: 10 adult Wistar Albino female rats weighing 250-300 g were divided into control (n=5) and experiment (n=5) groups. In experimental group, rats were treated 25 mg/kg of dichlorvos (Bayer DDVP EC 550, Bayer) in corn oil by 16 gauge oral gavage tube. In control group, rats were treated only 2.5 ml corn oil by oral gavage. After seven days, all of the rats were sacrificed by cervical dislocation under anesthesia. The liver was removed and divided into fragments. Hepatocyte density and histopathological examination were performed in fixed liver tissues. For this purpose, sections were taken and stained with hematoxylin-eosin. A part of the liver was used for gene expression analysis. Total RNA was extracted from the liver tissue using an RNA isolation reagent via manufacturer's instruction. Changes in mRNA levels, detected using semi-quantitative reverse transcription-polymerase chain reaction, were calculated as the proportion of the target gene amplification products to the amplification products of the housekeeping gene GAPDH. Results: Hepatocyte density were decreased in experimental group compared to control group (p |
Databáze: | OpenAIRE |
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