Effect of verapamil on responses to endothelin-1 in aortic rings from streptozotocin-induced diabetic rats.

Murat N., Kalkan Ş., Gidener S.

Pharmacological research, cilt.40, sa.1, ss.37-40, 1999 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 40 Sayı: 1
  • Basım Tarihi: 1999
  • Doi Numarası: 10.1006/phrs.1998.0485
  • Dergi Adı: Pharmacological research
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.37-40
  • Anahtar Kelimeler: diabetes mellitus, endothelin-1, verapamil, rat, aorta, SMOOTH-MUSCLE CELLS, CALCIUM-ANTAGONISTS, CHANNEL, INSULIN, SECRETION, MELLITUS, GLUCOSE
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

In this study, we investigated the constrictor responsiveness to endothelin-l (ET-1, 10-30 nM) of aortic rings (under 1 g resting tension in Krebs-Bicarbonate solution) from 8-weeks streptozotocin (STZ, 65 mg kg(-1), i.p)-induced diabetic rats and vehicle-treated control rats. The maximum ET-1-induced contraction of the aorta in diabetic rats was increased by 150%, but the EC50 of ET-1 remained unchanged. Although in both groups, verapamil reduced the constrictor responses to ET-1 (diabetic group P < 0.001, control group P < 0.05), there were not any significant differences between PD2 values. These results suggest that verapamil inhibits ET-1-induced Ca2+ entry through the L-type channel and this effect did not change in diabetes mellitus. (C) 1999 Academic Press.