Protective effects of boron on cyclophosphamide induced lipid peroxidation and genotoxicity in rats

Chemosphere. 2014 Aug:108:197-204. doi: 10.1016/j.chemosphere.2014.01.038. Epub 2014 Feb 14.

Abstract

The aim of the present study was to evaluate the possible protective effect of boron (B) on cyclophosphamide (CYC) induced oxidative stress in rats. Totally, thirty Wistar albino male rats were fed standard rodent diet and divided into 5 equal groups: physiological saline was given intraperitoneally (i.p.) to the control group (vehicle treated), to the second group only 75 mg kg(-1) CYC was given i.p. on the 14th d, and boron was administered (5, 10, and 20 mg kg(-1), i.p.) to the other groups for 14 d and CYC (75 mg kg(-1), i.p.) on the 14th d. CYC caused increase of malondialdehyde and decrease of glutathione levels, decrease of superoxide dismutase activities in erythrocyte and tissues, decrease of erythrocyte, heart, lung, and brain catalase, and plasma antioxidant activities. Also, CYC treatment caused to DNA damage in mononuclear leukocytes. Moreover, B exhibited protective action against the CYC-induced histopathological changes in tissues. However, treatment of B decreased severity of CYC-induced lipid peroxidation and genotoxicity on tissues. In conclusion, B has ameliorative effects against CYC-induced lipid peroxidation and genotoxicity by enhancing antioxidant defence mechanism in rat.

Keywords: Boron; Cyclophosphamide; Genotoxicity; Lipid peroxidation; Rat.

MeSH terms

  • Animals
  • Boron / chemistry
  • Boron / pharmacology*
  • Catalase / metabolism
  • Cyclophosphamide / toxicity
  • DNA Damage / drug effects
  • Erythrocytes / drug effects
  • Erythrocytes / enzymology
  • Erythrocytes / metabolism
  • Glutathione / metabolism
  • Glutathione Peroxidase / metabolism
  • Lipid Peroxidation / drug effects*
  • Male
  • Malondialdehyde / metabolism
  • Nitric Oxide / analysis
  • Nitric Oxide / blood
  • Protective Agents / chemistry
  • Protective Agents / pharmacology*
  • Rats
  • Rats, Wistar
  • Superoxide Dismutase / metabolism

Substances

  • Protective Agents
  • Nitric Oxide
  • Malondialdehyde
  • Cyclophosphamide
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Glutathione
  • Boron