Assessment of Cytotoxic, Genotoxic, and Oxidative Stress of Dibutyl Phthalate on Cultured Bovine Peripheral Lymphocytes

Author:

Ali Muhammad Muddassir1ORCID,Sahar Taha1,Firyal Sehrish1ORCID,Ijaz Muhammad2ORCID,Majeed Khalid Abdul3ORCID,Awan Furqan4ORCID,Adil Memoona1,Akbar Haroon5ORCID,Rashid Muhammad Imran5ORCID,Ciğerci İbrahim Hakki6ORCID

Affiliation:

1. Institute of Biochemistry and Biotechnology, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan

2. Department of Veterinary Medicine, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan

3. Department of Physiology, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan

4. Department of Epidemiology and Public Health, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan

5. Department of Parasitology, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan

6. Department of Molecular Biology and Genetics, Afyon Kocatepe University, Afyonkarahisar, Turkey

Abstract

Recently, there have been numerous reports showing that phthalates have negative human health impacts and may cause several diseases such as asthma, breast cancer, obesity, type II diabetes, and male infertility. Animals are also exposed to phthalates through the environment and can cause adverse health effects on them. Several studies have been found on the cytogenetic effects of dibutyl phthalate (DBP) on different organisms but no documented evidence has been found on the cytotoxic and genotoxic effects of dibutyl phthalate (DBP) on bovine cultured lymphocytes. MTT assay was performed on different series of DBP concentrations (10 μM, 20 μM, 30 μM, 50 μM, 70 μM, 100 μM). A concentration-dependent decrease in cell viability was observed by the DBP. The LD50, LD50/2, and 2 LD50 were found to be 50 μM, 30 μM, and 80 μM on bovine lymphocytes, respectively. Then, these concentrations of DBP were utilized to perform comet, micronucleus assays, and oxidative stress. A concentration-dependent increase in DNA damage, oxidative stress, and micronuclei formation was observed in lymphocytes by the DBP as compared to the control group. Highest genotoxic effects were observed at a concentration of 2 LD50. Similarly, total oxidative stress was found higher, and antioxidative stress was lower in concentration-dependent manner by the DBP. The current study revealed a significant cytotoxic, genotoxic, and oxidative stress of DBP on cultured bovine lymphocytes.

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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