Person:
TOK, OLGU ENİS

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OLGU ENİS
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TOK
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Now showing 1 - 10 of 15
  • PublicationOpen Access
    Comparison of Small-diameter-hole and Traditional Microfracture in Cartilage Repair and the Effect of Adding a Hyaluronic Acid-based Acellular Matrix Scaffold: An Animal Study
    (2021-03-01T00:00:00Z) UÇAN, VAHDET; YILDIZ, FATİH; ELMADAĞ, Nuh Mehmet; UZER, GÖKÇER; GÜZEL, YUNUS; TOK, OLGU ENİS; Mukaddes, E.; UÇAN, VAHDET; YILDIZ, FATİH; ELMADAĞ, NUH MEHMET; UZER, GÖKÇER; TOK, OLGU ENİS; EŞREFOĞLU, MUKADDES
    Objective: Since, there is no standardized technique for the treatment of focal cartilage defects that can recreate original cartilage tissue; researchers continue to explore and evaluate various treatment modalities. This study compared post-operatke healing of cartilage defects after treatment with small-diameter-hole microfracture (SDHM) technique with that of traditional microfracture technique. The effects of the hole density and augmentation with hyaluronic acid-based acellular matrix (HA-based AM) on cartilage healing were also investigated. Methods: Articular cartilage defects measuring 5 mm in diameter and 3 mm in depth were created in each femoral trochlear groove of 21 New Zealand rabbits. Rabbits were assigned to seven groups comprising six knees each. The rabbits were sacrificed 12 weeks later, and the regenerated cartilage was harvested for histological evaluation using the Wakitani scoring system. Results: All defects were filled with regenerated tissue macroscopically. Group I (14; range 10-14 points) had significantly higher Wakitani score than in groups VI (6; range 1-11 points) and VII (5; range 3-10 points) (p=0.043 and p=0.016, respectively). No significant differences were observed among the other groups. Augmentation with HA-based AM did not contribute to cartilage healing. Conclusion: Improved cartilage healing was observed with increasing SDHM density than with traditional microfracture technique. SDHM combined with HA-based AM implantation did not improve the quality of the regenerated cartilage.
  • PublicationMetadata only
    Shea Yağının Yara İyileşmesi Üzerine Etkisi.
    (2016-05-03) BAYINDIR, NİHAN; TOK, OLGU ENİS; EŞREFOĞLU, MUKADDES; Kılıç, Elif; BULUT, HURİ; BAYINDIR, NİHAN; TOK, OLGU ENİS; EŞREFOĞLU, MUKADDES; BULUT, HURI
  • PublicationMetadata only
    Genç Ve Yaşlı Sprague-Dawley Sıçanlarda Parsiyel Hepatektomi Sonrası Melatoninin Karaciğer Rejenerasyonuna Etkisi.
    (2016-05-03) TOK, OLGU ENİS; AYDIN, M. S.; ESREFOGLU, MUKADDES; IRAZ, M.; KESKİN, Sıdıka; KOÇYİĞİT, ABDÜRRAHİM; TOK, OLGU ENİS; EŞREFOĞLU, MUKADDES; KOÇYİĞİT, ABDÜRRAHİM
  • PublicationMetadata only
    Uzun Süreli ve Düşük Doz Siklosporin Kullanımının Böbrek Dokusu Üzerine Apopitotik Etkileri
    (2014-03-09) Garip, Aylin; Uzak, Emirhan; TOK, OLGU ENİS; ESREFOGLU, MUKADDES; AKTAS, R. G.; TOK, OLGU ENİS; EŞREFOĞLU, MUKADDES
  • PublicationMetadata only
    Effects of beta-glucan on protection of young and aged rats from renal ischemia and reperfusion injury
    (2016-01-01) ESREFOGLU, MUKADDES; Tok, OLGU ENİS; AYDIN, M. S.; OZER, O. F.; SELEK, S.; Iraz, M.; EŞREFOĞLU, MUKADDES; TOK, OLGU ENİS; ÖZER, ÖMER FARUK; SELEK, ŞAHABETTİN
    BACKGROUND: Ischemia reperfusion injury is one of the leading causes of acute renal failure which is a common clinical event leading to development of chronic kidney disease and a high mortality; especially in elderly people. beta-glucans are glucose polymer groups with free-radical scavenger, macrophage activator, and immune defense inducer functions. We designed this study to determine the possible protective effects of beta-glucan against renal ischemia reperfusion injury comparatively in young and aged rats.
  • PublicationMetadata only
    Fluoxetine prevents ischemia perfusion induced acute cardiac inflammation and injury.
    (2016-08-25) Sahin, G.; Yaman, OM; Guner, I.; TOK, OLGU ENİS; Pala, M.; EŞREFOĞLU, MUKADDES; Yelmen, N.; TOK, OLGU ENİS; EŞREFOĞLU, MUKADDES
  • PublicationMetadata only
    Protective effect of beta-glucan on renal ischemia and reperfusion injury in young and aged rats.
    (2014-09-12) EŞREFOĞLU, MUKADDES; TOK, OLGU ENİS; AYDIN, M. S.; IRAZ, M.; SELEK, ŞAHBETTİN; ÖZER, ÖMER FARUK; KOÇYİĞİT, ABDÜRRAHİM; EŞREFOĞLU, MUKADDES; TOK, OLGU ENİS; SELEK, ŞAHABETTİN; ÖZER, ÖMER FARUK; KOÇYİĞİT, ABDÜRRAHİM
  • PublicationMetadata only
    Remote Myocardial Injury: The Protective Role of Fluoxetine
    (2017-09-01) Yaman, Onur; Erman, Hayriye; Güner, İbrahim; TOK, OLGU ENİS; EŞREFOĞLU, MUKADDES; Pala, Mukaddes; Gelisgen, Remise; Uzun, Hafize; Uğur, Aksu; Yelmen, Nermin; Şahin, Gülderen; TOK, OLGU ENİS; EŞREFOĞLU, MUKADDES
  • PublicationMetadata only
    Effects of Cichorium intybus on seizure development in pentyleneterazole kindling model of epilepsy
    (2015-05-03) ERKEC, OZLEM ERGUL; MERAL, İSMAİL; KARA, MEHMET; ESREFOGLU, MUKADDES; TOK, OLGU ENİS; MERAL, İSMAİL; EŞREFOĞLU, MUKADDES; TOK, OLGU ENİS
  • PublicationOpen Access
    Can Coenzyme Q10 supplementation protect the ovarian reserve against oxidative damage?
    (2016-09-01) OZCAN, PINAR; Ficicioglu, Cem; Kizilkale, Ozge; Yesiladali, Mert; Tok, OLGU ENİS; Ozkan, Ferda; Esrefoglu, MUKADDES; ÖZCAN, PINAR; TOK, OLGU ENİS; EŞREFOĞLU, MUKADDES
    Purpose: We investigated antioxidant effects of CoQ10 supplementation on the prevention of OS-induced ovarian damage and to evaluate the protective effect of such supplementation against OS-related DNA damage. Methods: Twenty-four adult female Sprague-Dawley rats were randomly divided into three groups (8 rats per group): group 1 (control): saline, ip, and orally; group 2 (cisplatin group): cisplatin, 4.5 mg/kg ip, two times with an interval of 7 days; and group 3 (cisplatin + CoQ10 group): cisplatin, 4.5 mg/kg ip, two times with an interval of 7 days, and 24 h before cisplatin, 150 mg/kg/day orally in 1 mL of saline daily for 14 days. Serum concentrations of anti-Mullerian hormone (AMH), number of AMH-positive follicles, the assessment of the intensity of 8'OHdG immunoreactivity, the primordial, antral and atretic follicle counts in the ovary were assessed. Result(s): The mean serum AMH concentrations were 1.3 ± 0.19, 0.16 ± 0.03, and 0.27 ± 0.20 ng/mL in groups 1, 2, and 3, respectively (p < 0.01). Serum AMH levels were significantly higher in group 1 compared to groups 2 and 3 (p < 0.01 and p = 0.01, respectively). There was a statistically significant difference in AMH-positive follicle count between the groups (p < 0.01). Group 1 showed higher numbers of AMH-positive granulosa cells compared to group 2 (p = 0.01). A significant difference was found in the primordial, the atretic, and antral follicle counts between the three groups (p < 0.01, p < 0.01, and p < 0.01, respectively). The atretic follicle count was significantly lower in the cisplatin plus CoQ10 group compared to the cisplatin group (p < 0.01). The antral follicle counts were significantly higher in the cisplatin plus CoQ10 group compared with the cisplatin group (p < 0.01). There was a statistically significant difference in the intensity of staining of the follicles that were positive for anti-8'OHdG between the groups (p = 0.02). Group 1 showed a significant lower intensity of staining of the follicles positive for anti-8'OHdG compared with group 2 (p = 0.03). Conclusion(s): CoQ10 supplementation may protect ovarian reserve by counteracting both mitochondrial ovarian ageing and physiological programmed ovarian ageing although the certain effect of OS in female infertility is not clearly known.