Indian Journal of Public Health Research & Development
  • Year: 2019
  • Volume: 10
  • Issue: 8

Nickel Induced Alteration of Pathophysiology of Lungs in Experimental Rats

1Department of Biochemistry, Shri B.M. Patil Medical College, Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura, Karnataka, India

2Laboratory of Vascular Physiology and Medicine, Department of Physiology, Shri B.M. Patil Medical College, Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura, Karnataka, India

*Corresponding Author: Kusal K Das Professor, Laboratory of Vascular Physiology and Medicine, Department of Physiology, Shri B. M. Patil Medical College, Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura-586103, Karnataka, India. Email: kusaldas@bldedu.ac.in, Telephone: +91-9611825998

Online published on 26 September, 2019.

Abstract

Nickel and its compounds are known lung carcinogens, hypoxia mimicking effect of divalent nickel (Ni (II)) plays a crucial role in transformation of cells and the progression of tumours. In this study we aimed to evaluate the possible pathophysiological alterations of lung tissues of rats exposed to nickel sulphate.

For this study 12 male albino rats were randomly divided into two groups: control (placebo), NiSO4 and given respective interventions for 21 days. % body weight gain, pulmonarysomatic index was calculated. In lung tissue homogenates of all groups of animals, concentration of lipid peroxidation product malondialdehyde (MDA), nitric oxide (NO) and antioxidant l-ascorbic acid was estimated spectrophotometrically and lung tissue histopathological observations were also made.

Our results shows significantly decreased % body weight gain, elevated lung tissue MDA, NO and concomitant decrease of l-ascorbic acid concentration in NiSO4 treated groups when compared to control group. Histopathological observations of lung tissue sections of NiSO4 treated group showed eosinophilic oedema fluid filled alveoli, cystic macrophages, thickened interstitial septa, leucocytic infiltration, haemorrhage and acute bronchiolitis.

Our results demonstrate that heavy metal nickel exposure leads to increased pulmonary oxidative and nitrosative stress, decreased concentrations of antioxidants like l-ascorbic acid and histopathological alterations in lungs. So we can conclude that people exposed to heavy metals like nickel may be more prone for lung disorders irrespective of the route of exposure.

Keywords

Nickel, lungs, histopathology, malondialdehyde, nitric oxide, l-ascorbic acid, lipid peroxidation