Immunohistochemical distribution of Bcl-2 and p53 apoptotic markers in acetamiprid-induced nephrotoxicity

Gokhan Nur; Emrah Caylak; Pinar Aksu Kilicle; Safak Sandayuk; Ozlem Onen Celebi

doi:10.1515/med-2022-0603

Immunohistochemical distribution of Bcl-2 and p53 apoptotic markers in acetamiprid-induced nephrotoxicity

Open Med (Wars). 2022 Nov 21;17(1):1788-1796. doi: 10.1515/med-2022-0603. eCollection 2022.

Authors

Gokhan Nur¹, Emrah Caylak², Pinar Aksu Kilicle³, Safak Sandayuk³, Ozlem Onen Celebi⁴

Affiliations

¹ Department of Biomedical Engineering, Faculty of Engineering and Natural Sciences, Iskenderun Technical University, Hatay, Turkey.
² Department of Biochemistry, Faculty of Medicine, Girne American University, Kyrenia, Cyprus.
³ Department of Molecular Biology, Faculty of Science and Arts, Kafkas University, Kars, Turkey.
⁴ Department of Zoology, Faculty of Science and Arts, Kafkas University, Kars, Turkey.

Abstract

Pesticides, which adversely affect the critical metabolic processes of organisms, disrupt the physiological balance by specifically targeting enzymes and may lead to such consequences that may lead to death. It provides benefits in agricultural activities. The p53 protein antagonizes bcl-2, an anti-apoptotic protein character, and induces apoptosis by causing mitochondrial membrane permeability. This study aims to show the effect of acetamiprid, which is an insecticide from the neonicotinoid class, on bcl-2 and p53 immunoreactivity, which has an important place in the apoptotic mechanism in kidney tissue. A total of four groups including control and three experimental groups (the acetamiprid was administered 5, 10, and 15 mg kg^-1) were formed in the study. After acetamiprid was administered via gavage for 14 days, the kidney tissues taken from the mice, which were sacrificed by cervical dislocation, were fixed in 10% formaldehyde solution for histological and immunohistochemical analyses, and as a result of routine tissue follow-up, the sections were blocked in paraffin and stained with haematoxylin-eosin and immunostaining. The histopathological examinations revealed that while the kidney tissue had a normal structure in the control group, degeneration in the distal and proximal tubules, glomerular degeneration, increase in the capsular area, glomerular atrophy, and haemorrhage were determined in the acetamiprid groups at increasing severity and frequency depending on the dose of the applied substance. In the kidney tissue, Bcl-2 and p53 immunoreactivity was observed in glomerular cells, sinusoidal epithelium, and proximal and distal tubule cells. The acetamiprid caused pathological changes in the kidneys in the dose range used. This effect also affects the expression of bcl-2 and p53 genes, which are biomarkers in the apoptotic mechanism. As acetamiprid accumulates in tissues, it increases the expression of p53 from cell death receptors, while suppressing the anti-apoptotic bcl-2 expression.

Keywords: acetamiprid; bcl-2; histopathology; immunoreactivity; kidney; p53.