Benha University

Taghrid Gamaleldin Abdelrahman

Professor

Faculty of Medicine MICROBIOIOGY & IMMUNOIOGY

PROTECTIVE EFFECT OF N-ACETYLCYSTEINE (NAC) AGAINST DIETHYLHEXYL PHTHALATE (DEHP) INDUCED PULMONARY TOXICITY IN MALE ALBINO RATS (HISTOLOGICAL AND IMMUNOHISTOCHEMICAL STUDY)

Egypt J. Forensic Sci. Appli. Toxicol. • 2021
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Publication Information
Authors Amina A. Farag1*, Eman M. Faruk2, Taghrid G. Kharboush 3, Nashwa H. Abu-Raia 4, Haidy M. Fakher
Keywords Di-Ethylhexyl Phthalate, N-acetylcysteine, lung, lipid peroxidation; glutathione.
Journal Egypt J. Forensic Sci. Appli. Toxicol.
Publisher Not Available
Volume 21
Issue Not Available
Pages Not Available
publication.type Local
Paper Link Not Available
Supplementary Materials Not Available
Abstract
i-Ethylhexyl phthalate (DEHP) is a global environmental pollutant. Human exposure to
DEHP occurs through environmental sources. Community exposure (food, air, water), as well as
medical settings’ exposure, impose crucial effects on human health. DEHP had been reported to
have cytotoxic, immunotoxic, genotoxic, and reproductive toxic properties. This work aims to
assess the possible toxic effects of DEHP on adult albino rats' lungs and to evaluate the possible
protective effects of N-acetylcysteine (NAC) using bodyweight and relative lung weight
parameters. Assessment of DHEP toxicity is measured by biochemical, histopathological, and
immunohistochemical methods. Fifty male adult albino rats were divided into five equal groups
as follows: Group Ι (Negative control group), Group ΙΙ (Positive control group), Group IΙΙ
(NAC-treated group): was given NAC orally (200 mg/kg/day), Group IV (DEHP-treated group):
was given DEHP orally (3gm/kg once daily for 4 weeks) and Group V: (DEHP + NAC-treated
group): was treated with DEHP concomitantly with NAC at the same previous doses. The results
of the present study revealed that DEHP has significantly increased the lipid peroxidation level
and significantly reduced glutathione content (GSH), superoxide dismutase (SOD) activity, and
catalase activity. The histological results of group IV showed inflammatory cellular infiltration
of the lungs associated with interstitial edema, hemorrhage, and inter-alveolar septal thickening
that were markedly reduced in group V. Also, group V, showed a significant decrease in the
collagen fibers accumulation and caspase-3 expression as compared to group IV. Conclusion:
treatment with NAC can protect against DEHP induced pulmonary toxicity in rats by decreasing
oxidative stress, inflammation, and apoptosis.
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