Manal Mohammad Morsy
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Manal Mohammad Morsy has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Marwa Mahmood Ahmad
Department of Human Anatomy and Embryology, Faculty of Medicine, Zagazig University, Zagazig, Egypt
2 shared publications - Amal Fawzy
Medical Biochemistry Department, Faculty of Medicine-Zagazig University, Zagazig, Egypt
1 shared publication Azza I. Farag
Department of human anatomy and embryology, Faculty of medicine, Zagazig University, Egypt
1 shared publication- Dalia A. Mandour
Department of human anatomy and embryology, Faculty of medicine, Zagazig University, Egypt
1 shared publication - Eman El-Sayed Khayal
Department of Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Zagazig University, Egypt
1 shared publication - Mona G. Elhadidy
Medical Physiology, Faculty of Medicine, Mansoura University, Mansoura City 35516, Egypt
1 shared publication
Latest Publications
- Open Access
- 27 December 2024
- Published by Elsevier in Toxicology Reports
- Vol. 14, 101882
Podocyte-related biomarkers' role in evaluating renal toxic effects of silver nanoparticles with the possible ameliorative role of resveratrol in adult male albino rats
- 27 December 2024
- Published by Elsevier in Toxicology Reports
- Vol. 14, 101882
Open AccessPodocyte-related biomarkers' role in evaluating renal toxic effects of silver nanoparticles with the possible ameliorative role of resveratrol in adult male albino rats
- 3 August 2024
- Published by Elsevier in Tissue and Cell
- Vol. 90, 102503
Maternal exposure to low-dose bisphenol A and its potential neurotoxic impact on male pups: A histological, immunohistochemical, and ultrastructural study
- 3 August 2024
- Published by Elsevier in Tissue and Cell
- Vol. 90, 102503
Maternal exposure to low-dose bisphenol A and its potential neurotoxic impact on male pups: A histological, immunohistochemical, and ultrastructural study
- Open Access
- 27 June 2023
- Published by Springer Nature in Journal of Molecular Histology
- Vol. 54 (4) , 283-296
Structural and molecular changes in the rat myocardium following perfluoroctane sulfonate (PFOS) exposure are mitigated by quercetin via modulating HSP 70 and SERCA 2
Perfluorooctane sulfonate (PFOS) is a man-made fluorinated compound employed in a variety of industrial and civilian applications. Due to its long elimination half-life and promotion of oxidative stress and inflammation, it is one of the most abundant organic contaminants. The present study was designed to determine the cytotoxic effect of PFOS on adult male rat cardiac tissue and to assess the cardioprotective role of the flavonoid quercetin (Que), which possesses antioxidant, anti-inflammatory, and anti-apoptotic properties. Twenty-four adult male Sprague–Dawley rats were randomly divided into four equal groups: Group I (Control). Group II (Que) received Que (75 mg/kg/day for 4 weeks) by oral gavage. Group III (PFOS group): supplemented orally with PFOS (20 mg/kg/day for 4 weeks) and Group IV (PF OS/Que). The rat heart was processed for histological, immunohistochemical, and gene expression studies. The PFOS group showed histological alterations in the myocardium that were partially reversed by the administration of Que. The inflammatory biomarkers (TNF, IL-6, and IL-1), lipid profile, TSH, MDA, and serum cardiac enzymes (LDH and CK-MB) were all altered. These findings collectively suggest that PFOS had adverse effects on the cardiac muscle structure, and these effects were alleviated by quercetin, which is a promising cardioprotective flavonoid.
- 27 June 2023
- Published by Springer Nature in Journal of Molecular Histology
- Vol. 54 (4) , 283-296
Open AccessStructural and molecular changes in the rat myocardium following perfluoroctane sulfonate (PFOS) exposure are mitigated by quercetin via modulating HSP 70 and SERCA 2
Perfluorooctane sulfonate (PFOS) is a man-made fluorinated compound employed in a variety of industrial and civilian applications. Due to its long elimination half-life and promotion of oxidative stress and inflammation, it is one of the most abundant organic contaminants. The present study was designed to determine the cytotoxic effect of PFOS on adult male rat cardiac tissue and to assess the cardioprotective role of the flavonoid quercetin (Que), which possesses antioxidant, anti-inflammatory, and anti-apoptotic properties. Twenty-four adult male Sprague–Dawley rats were randomly divided into four equal groups: Group I (Control). Group II (Que) received Que (75 mg/kg/day for 4 weeks) by oral gavage. Group III (PFOS group): supplemented orally with PFOS (20 mg/kg/day for 4 weeks) and Group IV (PF OS/Que). The rat heart was processed for histological, immunohistochemical, and gene expression studies. The PFOS group showed histological alterations in the myocardium that were partially reversed by the administration of Que. The inflammatory biomarkers (TNF, IL-6, and IL-1), lipid profile, TSH, MDA, and serum cardiac enzymes (LDH and CK-MB) were all altered. These findings collectively suggest that PFOS had adverse effects on the cardiac muscle structure, and these effects were alleviated by quercetin, which is a promising cardioprotective flavonoid.