Green Synthesized Zinc Oxide Nanoparticles Using Moringa olifera Ethanolic Extract Lessens Acrylamide-Induced Testicular Damage, Apoptosis, and Steroidogenesis-Related Gene Dysregulation in Adult Rats

Author:

Mostafa-Hedeab Gomaa1ORCID,Behairy Amany2,Abd-Elhakim Yasmina M.3ORCID,Mohamed Amany Abdel-Rahman3,Noreldin Ahmed E.4ORCID,Dahran Naief5ORCID,Gaber Rasha A.6,Alqahtani Leena S.7,Essawi Walaa M.8ORCID,Eskandrani Areej A.9,El-Shetry Eman S.10

Affiliation:

1. Pharmacology Department & Health Research Unit, Medical College, Jouf University, Sakaka 72446, Saudi Arabia

2. Department of Physiology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44511, Egypt

3. Department of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt

4. Department of Histology and Cytology, Faculty of Veterinary Medicine, Damanhour University, Damanhour 22511, Egypt

5. Department of Anatomy, Faculty of Medicine, University of Jeddah, Jeddah 23218, Saudi Arabia

6. Medical Biochemistry Department, Faculty of Medicine, Tanta University, Tanta 31527, Egypt

7. Department of Biochemistry, College of Science, University of Jeddah, Jeddah 80203, Saudi Arabia

8. Department of Theriogenology, Faculty of Veterinary Medicine, Aswan University, Aswan 81528, Egypt

9. Chemistry Department, College of Science, Taibah University, Medina 30002, Saudi Arabia

10. Department of Human Anatomy and Embryology, Faculty of Medicine, Zagazig University, Zagazig 44511, Egypt

Abstract

This study assessed the possible protective role of green synthesized zinc oxide nanoparticles using Moringa olifera leaf extract (MO-ZNPs) in acrylamide (ACR)-induced reproductive dysfunctions in male rats. ACR (20 mg/kg b.wt/day) and/or MO-ZNPs (10 mg/kg b.wt/day) were given orally by gastric gavage for 60 days. Then, sperm parameters; testicular enzymes; oxidative stress markers; reproductive hormones including testosterone, luteinizing hormone (LH)-estradiol, and follicle-stimulating hormone (FSH) concentration; testis histology; steroidogenesis-related gene expression; and apoptotic markers were examined. The findings revealed that MO-ZNPs significantly ameliorated the ACR-induced decline in the gonadosomatic index and altered the pituitary–gonadal axis, reflected by decreased serum testosterone and FSH with increased estradiol and LH, and sperm analysis disruption. Furthermore, a notable restoration of the tissue content of antioxidants (catalase and reduced glutathione) but depletion of malondialdehyde was evident in MO-ZNPs+ACR-treated rats compared to ACR-exposed ones. In addition, MO-ZNPs oral dosing markedly rescued the histopathological changes and apoptotic caspase-3 reactions in the testis resulting from ACR exposure. Furthermore, in MO-ZNPs+ACR-treated rats, ACR-induced downregulation of testicular steroidogenesis genes and proliferating cell nuclear antigen (PCNA) immune-expression were reversed. Conclusively, MO-ZNPs protected male rats from ACR-induced reproductive toxicity by suppressing oxidative injury and apoptosis while boosting steroidogenesis and sex hormones.

Publisher

MDPI AG

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Biochemistry,Physiology

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