The Protective Effects of Thymol Against Ketoprofen Induced Damages on Pancreatic Acinar and Islet of Langerhans Cells in Rats


YILDIZ DENİZ G.

JOURNAL OF ESSENTIAL OIL BEARING PLANTS, cilt.22, sa.3, ss.604-613, 2019 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 22 Sayı: 3
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1080/0972060x.2019.1625814
  • Dergi Adı: JOURNAL OF ESSENTIAL OIL BEARING PLANTS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.604-613
  • Anahtar Kelimeler: Caspase-3, ketoprofen, pancreas, thymol, 8-OHdG, OXIDATIVE STRESS, ANTIOXIDANT, HEPATOTOXICITY
  • Atatürk Üniversitesi Adresli: Evet

Özet

This study was conducted to determine protective effects of thymol against non-steroidal anti-inflammatory drug induced damages on pancreas of rats. For this aim, thirty five Sprague-Dawley male rats were randomly allocated into five groups including control group, ketoprofen (Keto)-treated group (50 mg/kg) and the other three remaining groups received orally 100-400 mg/kg thymol before Keto administration, respectively. Thymol was orally administrated for 2 days before Keto administration, and continued for 4 days. To evaluate the antioxidative and anti-apoptotic effects of thymol against Keto induced damages in rat pancreatic cells, total antioxidant (TAS) and total oxidative stress (TOS) statuses, 8-hydroxy-20-deoxyguanosine (8-OHdG) levels and caspase-3 activities besides the histological features of the tissues were examined. The experimental data showed that Keto group, significantly increased the level of TOS, 8-OHdG and caspase-3 activation, while decreased level of TAS in tissue samples. On the other hand, because thymol exhibits strong antioxidant properties, Thymol treatment significantly decreased the level of TOS, 8-OHdG and caspase-3 activation, and ameliorated the pancreas histopathological changes induced by Keto. We found that thymol administration nearly eliminated Keto induced pancreatic damage.