Effect of Petroleum Products Inhalation on Oxidative Stress Parameters of Male Wistar Albino Rats
Main Article Content
Abstract
Background: The widespread use of petroleum products in modern industries has raised concerns about their potential toxic effects on biological systems. The study explored the effect of petroleum product inhalation on the oxidative stress parameters of the male Wistar albino rats.
Method: Forty-five rats, aged three months and weighing 180–220 g, were divided into five groups: Group A (Control), Group B (PMS exposure - 500 ml), Group C (Kerosene exposure - 500 ml), Group D (Diesel exposure - 500 ml), and Group E (Mixed petroleum products - 500 ml). The exposure lasted for 28 days, with lungs and hippocampal tissue homogenate samples collected at day 0, 14, and 28 to measure hydrogen peroxide (H2O2) scavenging activity, nitric oxide (NO) activity, reduced glutathione (GSH) level, superoxide dismutase (SOD) activity, and malondialdehyde (MDA) level.
Results: The results showed that H2O2 scavenging activity, NO activity and MDA level were significantly increased (p>0.05) (24.34 ± 1.19, 4.90 ± 0.54, and 1.20 ± 0.14 mg/dl) when compared to control (31,04 ± 1.11, 4.15 ± 0.59 and 1.46 ± 0.20 mg/dl) while GSH level and SOD activity were significantly decreased (p<0.05) (1.93 ± 0.31 and 11.12 ± 0.48 mg/L) when compared with the control (3.28 ± 0.30 and 12.87 ± 0.93 µ/mg).
Conclusion: The results inferred the detrimental effects of inhaling petroleum products on critical organ systems, particularly the brain and lungs.
Downloads
Article Details
Section

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
The Journal is owned, published and copyrighted by the Nigerian Medical Association, River state Branch. The copyright of papers published are vested in the journal and the publisher. In line with our open access policy and the Creative Commons Attribution License policy authors are allowed to share their work with an acknowledgement of the work's authorship and initial publication in this journal.
This is an open access journal which means that all content is freely available without charge to the user or his/her institution. Users are allowed to read, download, copy, distribute, print, search, or link to the full texts of the articles in this journal without asking prior permission from the publisher or the author.
The use of general descriptive names, trade names, trademarks, and so forth in this publication, even if not specifically identified, does not imply that these names are not protected by the relevant laws and regulations. While the advice and information in this journal are believed to be true and accurate on the date of its going to press, neither the authors, the editors, nor the publisher can accept any legal responsibility for any errors or omissions that may be made. The publisher makes no warranty, express or implied, with respect to the material contained herein.
TNHJ also supports open access archiving of articles published in the journal after three months of publication. Authors are permitted and encouraged to post their work online (e.g, in institutional repositories or on their website) within the stated period, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access). All requests for permission for open access archiving outside this period should be sent to the editor via email to editor@tnhjph.com.
How to Cite
References
1.Robinson PR, Hsu CS. Petroleum and its products. In: Meyers RA, editor. Handbook of Industrial Chemistry and Biotechnology. New York: Springer; 2017. p. 13–106.
2.Ahmed F, Fakhruddin ANM. A review on environmental contamination of petroleum hydrocarbons and its biodegradation. Int J Environ Sci Nat Resour. 2018; 11(3):1–7.
3.Ekpenyong CE, Asuquo AE. Recent advances in occupational and environmental health hazards of workers exposed to gasoline compounds. Int J Occup Med Environ Health. 2017; 30(1):1–26.
4.Unsal V, Dalkiran T, Cicek M, Kolukcu E. The role of natural antioxidants against reactive oxygen species produced by cadmium toxicity: a review. Adv Pharm Bull. 2020; 10(2):184–190.
5.Kemabonta KA, Ikerodah AA, Anumudu PC. Toxicological effects of petrol, xylene and thinner on Mus musculus (albino mice). Pan Afr J Life Sci. 2020; 4(2):98–103.
6.Schiavone S, Jaquet V, Trabace L, Krause KH. Severe life stress and oxidative stress in the brain: from animal models to human pathology. Antioxid Redox Signal. 2013; 18(12):1475–1490.
7.Heusinkveld HJ, Wahle T, Campbell A, Westerink RHS, Tran L, Johnston H, et al. Neurodegenerative and neurological disorders by small inhaled particles. Neurotoxicology. 2016; 56:94–106.
8.Olasehinde TA, Olaniran AO. Neurotoxicity of polycyclic aromatic hydrocarbons: a systematic mapping and review of neuropathological mechanisms. Toxics. 2022; 10(8):417.
9.Zhao Q, Li Y, Chai X, Xu L, Zhang L, Ning P. Interaction of inhalable volatile organic compounds and pulmonary surfactant: potential hazards of VOC exposure to lung. J Hazard Mater. 2019; 369:512–520.
10.Krubaa P, Yogitha PS. Albino Wistar rats: advantages and limitations in biomedical research. SBV J Basic Clin Appl Health Sci. 2024; 7(2):61–65.
11.Ruch RJ, Cheng SJ, Klaunig JE. Prevention of cytotoxicity and inhibition of intercellular communication by antioxidant catechins isolated from Chinese green tea. Carcinogenesis. 1989; 10:1003–1008.
12.Marcocci L, Maguire JJ, Droy-Lefaix MT, Packer L. The nitric oxide-scavenging properties of Ginkgo biloba extract EGb 761. Biochem Biophys Res Commun. 1994; 201:748–755.
13.Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959; 82(1):70–77.
14.McCord JM, Fridovich I. Superoxide dismutase: an enzymic function for erythrocuprein (hemocuprein). J Biol Chem. 1969; 244(22):6049–6055.
15.Donnan SK. The thiobarbituric acid test applied to tissues from rats treated in various ways. J Biol Chem. 1950; 182(1):415–420.
16.Moronkeji A, Olayanju A, Adeniyi TD, Atere AD, Moronkeji AI, Igunbor MC. Oxidative stress response to gasoline generator exhaust emission in adult male Wistar rats. Environ Anal Health Toxicol. 2024; 39(4):030.
17.Oni AA, Osoh MO, Obikoya AO, Ohore OG. Oxidative stress responses as a marker of toxicity in mice exposed to polluted groundwater from an automobile junk market in South-Western Nigeria. Cell Stress Chaperones. 2022; 27(6):685–702.
18.Khan RA, Khan MR, Sahreen S, Bokhari J. Prevention of CCl4-induced liver alterations in reduced glutathione-deficient rats by diltiazem. Environ Toxicol Pharmacol. 2017; 52:200–213.
19.Azeez OM, Akhigbe RE, Anigbogu CN. Oxidative status in rat kidney exposed to petroleum hydrocarbons. J Nat Sci Biol Med. 2013; 4(1):149–154.
20.Owagboriaye FO, Dedeke GA, Aladesida AA, Bamidele JA, Olooto WE. Assessment of the effect of gasoline fume on stress hormones, antioxidant status and lipid peroxidation in albino rats. J King Saud Univ Sci. 2018; 30(3):393–399.
21.Fang J, Xu X, Jiang L, Qiao J, Zhou H, Li K. Preliminary results of toxicity studies in rats following low-dose and short-term exposure to methyl mercaptan. Toxicol Rep. 2019; 6:431–438.