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
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