Maged Abdel-Kader

Prof. Dr. Maged Abdel-Kader

Prince Sattam bin Abdulaziz University, Saudi Arabia
orcid

Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 May 2014 in Journal of Chemical & Engineering Data
Verified
Journal Article
Closed access
Md Khalid AnwerMd Khalid Anwer
Md Khalid Anwer
RARamadan Al-Shdefat
Ramadan Al-Shdefat
SJShahid Jamil
Shahid Jamil
PAPrawez Alam
Prawez Alam
MAMaged Abdel-Kader
Maged Abdel-Kader
FSFaiyaz Shakeel
Faiyaz Shakeel

3 June 1999 in Journal of Natural Products
Verified
Journal Article
Closed access
SYShu-Wei Yang
Shu-Wei Yang
MAMaged Abdel-Kader
Maged Abdel-Kader
SMStan Malone
Stan Malone
MWMarga C. M. Werkhoven
Marga C. M. Werkhoven
JWJan H. Wisse
Jan H. Wisse
DKDavid G. I. Kingston
David G. I. Kingston

1 August 2002 in Phytochemistry
Verified
Journal Article
Closed access
SESawsan El-Masry
Sawsan El-Masry
MAMasouda E Amer
Masouda E Amer
MAMaged Abdel-Kader
Maged Abdel-Kader
HZHala Zaatout
Hala Zaatout

29 March 2001 in Journal of Natural Products
Verified
Journal Article
Closed access
MAMaged Abdel-Kader
Maged Abdel-Kader
JHJeannine Hoch
Jeannine Hoch
JBJohn M. Berger
John M. Berger
RERandy Evans
Randy Evans
JMJames S. Miller
James S. Miller
DKDavid G. I. Kingston
David G. I. Kingston

25 September 1998 in Journal of Natural Products
Verified
Journal Article
Closed access
MAMaged Abdel-Kader
Maged Abdel-Kader
BBBrian D. Bahler
Brian D. Bahler
SMStan Malone
Stan Malone
MWMarga C. M. Werkhoven
Marga C. M. Werkhoven
FTFrits van Troon
Frits van Troon
DKDavid G. I. Kingston
David G. I. Kingston

1 March 2019 in Saudi Pharmaceutical Journal
Verified
Journal Article
Open access
GSGamal A. Soliman
Gamal A. Soliman
ASAbdulaziz S. Saeedan
Abdulaziz S. Saeedan
Rehab Fawzy Abdel-RahmanRehab Fawzy Abdel-Rahman
Rehab Fawzy Abdel-Rahman
HOHanan Ogaly
Hanan Ogaly
REReham Abd elsalam
Reham Abd elsalam
MAMaged Abdel-Kader
Maged Abdel-Kader
Diabetes mellitus (DM) has emerged as a public healthcare problem. Sustained hyperglycemia has been linked with many complications including impaired male fertility Olive tree (Olea europaea L.) leaves have been extensively used in traditional remedies worldwide to control blood glucose level in DM. In this study, the beneficial role of olive leaves extract (OLE) was investigated to combat diabetes-induced adverse effect on testicular tissues. Thirty male Wistar rats were divided into 5 equal groups: normal control group, streptozotocin (STZ)-diabetic group and diabetic groups which were given glibenclamide (GLB) or OLE at 250 and 500 mg/kg for 9 weeks to investigate the efficiency of olive leaves extract (OLE) in reducing the deleterious effect of diabetes on the reproductive system of male rats. Rats were checked for serum glucose, insulin, testosterone and gonadotropins. Also, testicular antioxidants, epididymal sperm characteristics and testicular histopathology were assessed. Expression of the testicular steroidogenic enzymes, cholesterol side-chain cleavage enzyme (P450 scc) and 17β-hydroxysteroid dehydrogenase (17β-HSD) was examined. Moreover, androgen receptor and proliferating cell nuclear antigen (PCNA) protein immunohistochemistry were assessed in testes. STZ-induced diabetes significantly increased serum glucose. However, STZ significantly decreased serum levels of insulin, testosterone, follicle stimulating hormone (FSH) and luteinizing hormone (LH). Marked reductions in testicular antioxidants with elevated malondialdehyde (MDA) parallel with deterioration of the testicular histoarchitecture and epididymal sperm characteristics were recorded. Administration of GLB or OLE (250 and 500 mg/kg) resulted in a significant recovery of the above mentioned parameters in STZ-diabetic rats. Interestingly, OLE shows greater glycemic improvement and testicular protection than GLB with the highest percentage protection exhibited by the OLE high dose. Furthermore, OLE significantly induced testicular steroidogenesis in diabetic rat as evidenced by elevated P450 scc and 17β-HSD mRNA expression. The study proves that OLE possesses a potential protective role against diabetes-induced reproductive disorders, which may be due to its antioxidant activity and its ability to normalize testicular steroidogenesis.