Salem, Mahmoud Elsayed Mohamed

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Job Title
Doktor Öğretim Üyesi
Email Address
mahmoudsalem17572@gmail.com
Main Affiliation
Department of Nursing / Hemşirelik Bölümü
Status
Current Staff
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Sustainable Development Goals

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NO POVERTY
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8

DECENT WORK AND ECONOMIC GROWTH
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7

AFFORDABLE AND CLEAN ENERGY
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17

PARTNERSHIPS FOR THE GOALS
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13

CLIMATE ACTION
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2

ZERO HUNGER
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4

QUALITY EDUCATION
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3

GOOD HEALTH AND WELL-BEING
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9

INDUSTRY, INNOVATION AND INFRASTRUCTURE
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PEACE, JUSTICE AND STRONG INSTITUTIONS
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GENDER EQUALITY
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RESPONSIBLE CONSUMPTION AND PRODUCTION
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REDUCED INEQUALITIES
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LIFE BELOW WATER
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SUSTAINABLE CITIES AND COMMUNITIES
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LIFE ON LAND
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CLEAN WATER AND SANITATION
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This researcher does not have a Scopus ID.
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Scholarly Output

2

Articles

2

Views / Downloads

8/0

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Supervised PhD Theses

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WoS Citation Count

2

Scopus Citation Count

2

WoS h-index

1

Scopus h-index

1

Patents

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Projects

0

WoS Citations per Publication

1.00

Scopus Citations per Publication

1.00

Open Access Source

2

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0

JournalCount
Experimental Biomedical Research1
Turkish Journal of Medical Sciences1
Current Page: 1 / 1

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Now showing 1 - 2 of 2
  • Article
    Citation - WoS: 2
    Citation - Scopus: 2
    Ascorbic Acid Exhibits More of a Protective Effect Than Estradiol Against Nephrotoxicity Induced by Malathion in Rats: a Histopathological and Molecular Docking Study
    (TUBITAK Scientific & Technological Research Council Turkey, 2025) Alhilal, Mohammad; Salem, Mahmoud E. L. S. A. Y. E. D. M. O. H. A. M. E. D.; Ali Albakoush, Ahmed; Alhilal, Suzan; Farag, Basant; Gomha, Sobhi M.; Albakoush, Ahmed; Elsayed Mohamed Salem, Mahmoud; M.gomha, Sobhi
    Background/aim: Despite the known harmful effects associated with malathion toxicity in various organs, it continues to be widely used for plant protection and insect control. This study is the first to compare the protective effects of estradiol and ascorbic acid against malathion-induced nephrotoxicity through histopathological assessment and molecular docking analyses. Materials and methods: This study was conducted using 20 female albino rats that were distributed into sham, malathion, malathion + estradiol, and malathion + ascorbic acid groups. Nephrotoxicity was induced by daily treatment with malathion and the effects of estradiol and ascorbic on nephrotoxicity were evaluated. After 4 weeks of treatment, the animals were sacrificed and the kidneys were examined following hematoxylin and eosin (H&E) staining. Histopathology results were supported by molecular docking studies of estradiol and ascorbic acid against a target protein (PDB ID: 2YMX), the peptide inhibitor Fab408 inhibiting acetylcholinesterase (AChE). The inhibition of AChE is the primary mechanism of the toxic effects of malathion. Results: Histopathological examination revealed a notable elevation (p < 0.001) in degeneration and necrosis within the tubular epithelium and interstitial nephritis in the malathion group compared to the sham group. Daily administration of estradiol and ascorbic acid resulted in a notable reduction (p = 0.0022) in the severity of these histopathological changes in the malathion + estradiol and malathion + ascorbic acid groups compared to the malathion group. Of these, the most significant decreases were observed in the malathion + ascorbic acid group. Docking studies of these compounds against the selected protein (PDB ID: 2YMX) revealed promising binding scores. Ascorbic acid exhibited the highest docking score (-6.44 kcal/mol), indicating a favorable binding interaction with this protein. Conclusion: Estradiol and ascorbic acid exert protective effects against malathion-induced nephrotoxicity, whereas ascorbic acid showed superior efficacy compared to estradiol. This result was further supported by molecular docking studies.
  • Article
    Estradiol and Ascorbic Acid Alleviate Malathion-Induced Lung Damage in Albino Wistar Rats: a Histopathological Study
    (2024) Alhılal, Mohammad; Salem, Mahmoud Elsayed Mohamed
    Aim: To assess the modulatory role of estradiol and ascorbic acid in malathion-induced pulmonary toxicity in albino Wistar rats. Methods: A total of twenty albino Wistar rats were randomly divided into four groups; the control group (group 1) was given corn oil alone, the test group (group 2) received a daily dose of malathion 20 mg/kg in corn oil, treatment group A (group 3) was administered a daily dose of malathion 20 mg/kg in corn oil plus estradiol 40 μg/100 g (gram), and treatment group B (group 4) received a daily dose of malathion 20 mg/kg in corn oil plus ascorbic acid 100 mg/kg. Experimental rats were administered once daily for four weeks. The lungs were examined histopathologically using two staining methods (Hematoxylin and Eosin, Masson Trichrome). Results: There were significant reductions in degeneration, interstitial pneumonia and interstitial fibrosis for group 3 (treatment group A) compared to group 2 (test group) (p<0.05). These reductions were more statistically significant for group 4 (treatment group B) compared to group 2 (test group) (p<0.01). Therefore, the damage was less pronounced and injury severity was moderate in group 3 treated with estradiol. Group 4, with ascorbic acid, showed the most improvement with significant tissue repair under microscopic examination and mild injury compared to group 3. Conclusions: The results of our present study suggest that both estradiol and ascorbic acid have clear protective effects against malathion-induced lung injury. However, ascorbic acid exhibited more pronounced protective effects compared to estradiol. With more comprehensive studies, the positive effects of ascorbic acid and estradiol can be used to prevent lung damage in individuals exposed to malathion.