Iranian J Pharmacol Ther. 2017 (June);15:1-7. This paper is available online at: http://ijpt.iums.ac.ir
Experimental study of cerium oxide nanoparticles (CeNP) against
malathion induced lung oxidative toxic stress in rats
Maziar Ganji
1
, Jamshid Karimi
2
, Seyed Abdolhakim Hosseini
3
, Heresh Moridi
2,3
, Asieh Hosseini
4
,
Davoud Ahmadimoghaddam
5
, Akram Ranjbar
5
*
1
Student Research Center, Hamadan University of Medical Sciences, Hamadan, Iran, & Department of Medical Genetics,
Faculty of Medicine, Shahid Beheshti University of Sciences, Tehran, Iran
2
Department of Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
3
Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
4
Razi Drug Research Center, Iran University of Medical Sciences, Tehran, Iran
5
Department of Toxicology and Pharmacology, School of Pharmacy, Hamadan University of Medical Sciences,
Hamadan, Iran
Please cite this article as:
Ganji M, Karimi J, Hosseini SA, Moridi H, Hosseini A, Ahmadimoghaddam D, Ranjbar A. Experimental study of cerium oxide
nanoparticles (CeNP) against malathion induced lung oxidative toxic stress in rats. Iranian J Pharmacol Ther. 2017 (July);15: 1-7.
ABSTRACT
Regardless of toxicity of nanoparticles, cerium oxide nanoparticles (CeNPs) are emerging
as a multi-functional agent for biomedical purposes. On the other hand, Organophosphorus
pesticides, like malathion, are inevitably found in the environment. The common involving
pathway CeNPs and malathion share is oxidative stress. Therefore, we conducted this study
to find the possible neutralizing or synergistic effects of CeNPs on oxidative stress responses
in malathion-induced toxicity by intraperitoneal (IP) injection. In this experimental study, 40
Wistar male rats with the weight range of 200-250 g were randomly selected and divided
into eight groups. Group1 (control, normal saline), group2 (100 mg/kg/day malathion /IP),
group3 (15 mg/kg/day CeNPs/IP), group4 (30 mg/kg/day CeNPs /IP), group5 (60 mg/kg/day
CeNPs /IP), group6 (100 mg/kg/day malathion+15 mg/kg/day CeNPs /IP), group7 (100
mg/kg/day malathion+30 mg/kg/day CeNPs /IP) and group8 (100mg/kg/day malathion+60
mg/kg/day CeNPs /IP). After 4 weeks of treatment, the levels of lipid peroxidation (LPO),
total antioxidant capacity (TAC), total thiol molecules (TTM) and activity of catalase (CAT)
in lung tissue were measured. All data were analyzed by SPSS V16 and One way ANOVA
with Tukey post hoc test. The results demonstrated that CeNPs caused significant increases
in LPO and TAC, in a dose-dependent-manner. For TTM level, none of the groups presented
any significant change compared to control. Significantly decreased levels of CAT, also,
were seen in all treatment groups. Surprisingly, all animals of group 8 died. Worth of noting,
groups receiving combined CeNPs and malathion showed severe responses for these
parameters. These results discovered that CeNPs induces oxidative stress parameters and
ROS production, especially combined with malathion in lung tissue. Groups receiving both
CeNPs and malathion displayed synergistic toxic properties. LPO, TAC and CAT seem to be
better parameters for measuring CeNPs-induced responses. Further investigations are
required to shed light on clear mechanisms involved.
Conflicts of Interest: Declared None
Funding: None
Keywords
Cerium oxide nanoparticle,
Lung,
Oxidative Stress,
Rat,
Malathion
Corresponding to:
Akram Ranjbar,
Department of Toxicology and
Pharmacology, School of
Pharmacy, Hamadan University
of Medical Sciences, Hamadan,
Iran
Email:
akranjbar2015@gmail.com
Received: 6 May 2016
Revised: 2 July 2016,
Accepted: 25 July 2016
INTRODUCTION
Organophosphorus compounds are known to be one of
the most widely utilized pesticides all over the world.
Residual amounts of these pesticides can be detected in the
Original Article
IRANIAN JOURNAL OF PHARMACOLOGY & THERAPEUTICS
Copyright © 2017 by Iran University of Medical Sciences
Iranian J Pharmacol Ther. 2017 (July);15:1-7.
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