The protective effects of omega 3 fatty acids and sesame oil against cyclosporine A-induced nephrotoxicity


Erol A. Y. G., Avci G., Sevimli A., Ulutas E., Ozdemir M.

DRUG AND CHEMICAL TOXICOLOGY, cilt.36, sa.2, ss.241-248, 2013 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 36 Sayı: 2
  • Basım Tarihi: 2013
  • Doi Numarası: 10.3109/01480545.2012.710627
  • Dergi Adı: DRUG AND CHEMICAL TOXICOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.241-248
  • Anahtar Kelimeler: Apoptosis, histopathology, kidney, OXIDATIVE-STRESS, RENAL INJURY, ANGIOTENSIN-II, CELL-DEATH, MATRIX PROTEINS, NITRIC-OXIDE, APOPTOSIS, MECHANISMS, ACID, NEPHROPATHY
  • Yozgat Bozok Üniversitesi Adresli: Hayır

Özet

Cyclosporine A (CsA) is a drug used in autoimmune disorders and organ transplantations. Omega 3 fatty acids (O-3) and sesame oil (SO) have antioxidant properties. We aimed to investigate and compare the protective effects of O-3 and SO against CsA-induced nephrotoxicity. Seven groups of male Wistar albino rats were included in the study. In group 1 (control), saline was administered, and in group 2, CsA (subcutaneously) was administered. In group 3, CsA+SO (orally; p.o.) was given; in group 4, CsA+O-3 (p.o.) was given; and in group 5, CsA+SO+O-3 was given. In group 6, SO was administered, and in group 7, O-3 was administered. After 15 days of treatment, kidneys were excised. Histopathological evaluation, apoptotic cell count, and renal/hepatic function tests were performed. In group 2, vacuolar degeneration and necrosis of tubular cells as well as hemorrhagic foci were observed; the apoptotic cell number was higher than in the control (P < 0.001). In groups 3, 4, and 5, tubular scores and apoptotic cell count were lower than in group 2 (P < 0.01 and P <0.001, respectively). In groups 6 and 7, healthy renal histology and a few apoptotic cells were determined. In groups 2, 3,4, and 5, blood urea nitrogen was higher and albumin was lower than in the control (P < 0.001). Liver enzymes were unchanged. O-3/SO showed similar protective effects against CsA-induced nephrotoxicity, as revealed by a remarkable decrease in histopathological changes and apoptotic cell count. However, impaired renal function tests were not improved with O3/SO treatment. SO and O-3 can be used as chemoprotectants against CsA.