SUAT TEKİN

Prof. Dr. SUAT TEKİN


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

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

Representative Publications

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1 April 2017 in Neuroscience Letters
Verified
Journal Article
Closed access
STSUAT TEKİN
SUAT TEKİN
YEYavuz Erden
Yavuz Erden
FOFatma Ozyalin
Fatma Ozyalin
YCYilmaz Cigremis
Yilmaz Cigremis
Cemil ColakCemil Colak
Cemil Colak
SSSüleyman Sandal
Süleyman Sandal

7 June 2022 in Journal of Biochemical and Molecular Toxicology
Verified
Journal Article
Closed access
ZZZineddine Zebbiche
Zineddine Zebbiche
GŞGüldeniz Şekerci
Güldeniz Şekerci
Houssem BOULEBDHoussem BOULEBD
Houssem BOULEBD
FKFatümetüzzehra Küçükbay
Fatümetüzzehra Küçükbay
STSUAT TEKİN
SUAT TEKİN
BBBoudjemaa Boumoud
Boudjemaa Boumoud

1 May 2018 in Neuroscience Letters
Verified
Journal Article
Closed access
STSUAT TEKİN
SUAT TEKİN
YEYavuz Erden
Yavuz Erden
FOFatma Ozyalin
Fatma Ozyalin
EOEbru Etem Onalan
Ebru Etem Onalan
YCYilmaz Cigremis
Yilmaz Cigremis
SSSüleyman Sandal
Süleyman Sandal

1 December 2021 in Molecular and Cellular Endocrinology
Verified
Journal Article
Closed access
TKTuba Keskin
Tuba Keskin
YEYavuz Erden
Yavuz Erden
STSUAT TEKİN
SUAT TEKİN

24 January 2020 in Archives of Physiology and Biochemistry
Verified
Journal Article
Closed access
STSUAT TEKİN
SUAT TEKİN
ABAsiye Beytur
Asiye Beytur
MÇMURAT ÇAKIR
MURAT ÇAKIR
ATAslı Taslıdere
Aslı Taslıdere
YEYavuz Erden
Yavuz Erden
SSSüleyman Sandal
Süleyman Sandal
Saxagliptin is an effective and selective dipeptidyl peptidase-4 (DPP-4) inhibitor. This study was designed to determine possible protective effects of saxagliptin against damage caused by renal ischaemia/reperfusion (I/R) in rats. In this study, 40 rats were divided into 4 groups (n = 10 for each). Group 1 (Control), Group 2 (I/R) in both kidneys ischaemia of 45 min was performed, and then reperfusion was applied for 24 h. Saxagliptin (Group 3: 2 mg/kg and Group 4: 10 mg/kg) was administered by oral gavage to the animals in treatment groups, before the I/R. Saxagliptin decreased the markers (BUN, Cre, NGAL, KIM-1 and IL-18) of acute renal damage in blood and kidney tissue. Saxagliptin provided increase in antioxidant enzyme levels and decrease in MDA and apoptosis. Histological results showed that the administration of saxagliptin exhibited a protective effect against renal damage caused by I/R. These results indicates that saxagliptin provide protection against kidney injury caused by I/R.

24 March 2022 in Molecular Biology Reports
Verified
Journal Article
Closed access
PDF file
GŞGüldeniz Şekerci
Güldeniz Şekerci
YEYavuz Erden
Yavuz Erden
STSUAT TEKİN
SUAT TEKİN