ANTI-INFLAMMATORY EFFECTS OF NESFATIN-1 ON ACETIC ACID-INDUCED GASTRIC ULCER IN RATS: INVOLVEMENT OF CYCLO-OXYGENASE PATHWAY


Kolgazi M., Ozdemir-Kumral Z. N. , Cantali-Ozturk C., Demirci E. K. , Yuksel M., Sirvanci S. , ...Daha Fazla

JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, cilt.68, ss.765-777, 2017 (SCI İndekslerine Giren Dergi) identifier

  • Cilt numarası: 68 Konu: 5
  • Basım Tarihi: 2017
  • Dergi Adı: JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY
  • Sayfa Sayıları: ss.765-777

Özet

In order to elucidate the contribution of cycloxygenase (COX) enzymes in the anti-oxidant and anti-inflammatory mechanisms of nesfatin-1, which improves the healing process of chronic gastric ulcers, either acetic acid (80%; ulcer groups; n = 40) or saline (control groups; n = 40) was applied to the serosal surface of male Sprague Dawley rats' stomachs for 1 min. Both the control and ulcer groups were treated daily with either i.p. saline or nesfatin-1 (0.3 mu g/kg; for 3 days). Nesfatin-1-treatment was preceded with i.p. saline, COX-2 inhibitor NS-398 (2 mg/kg), COX-1 inhibitor ketorolac (3 mg/kg) or non-selective COX inhibitor indomethacin (5 mg/kg) for 3 days. The rats were decapitated at the end of the third day, and their trunk blood was collected for the measurements of tumor necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1 beta) and IL-10 using ELISA. The induction of ulcers resulted in increased macroscopic scores, along with elevated gastric malondialdehyde, luminol- and lucigenin-enhanced chemiluminescence levels and myeloperoxidase activity. On the other hand, nesfatin-1 treatment abolished these elevations. Depleted glutathione, superoxide dismutase and catalase activity levels in the saline-treated ulcer group were preserved in the nesfatin-1-treated ulcer group. Increased levels of serum TNF-alpha, IL-1 beta, IL-10 in the saline-treated ulcer group, as compared to control group, were significantly decreased in the nesfatin- 1 -treated ulcer group. The inhibition of COX-1, and/or COX-2 reversed most of the alterations induced with nesfatin-1, but COX-2-blockade was consistently more effective to abolish all nesfatin- 1-induced changes. Our results suggest that nesfatin-1 ameliorates ulcer-induced inflammatory response through the modulation of oxidant-antioxidant balance. As selective pharmacological inhibition of COX-1 or COX-2 suppresses the antioxidant/anti-inflammatory effects of nesfatin-1, it appears that nesfatin-1 decreases inflammatory mediators and neutrophil migration by a COX-dependent mechanism, especially by a COX-2- dependent mechanism, during the ulcer healing stage.