Nigella sativa seed decreases endothelial dysfunction in streptozotocin-induced diabetic rat aorta
(ندگان)پدیدآور
Abbasnezhad, AbbasaliNiazmand, SaeedMahmoudabady, MaryamSoukhtanloo, MohammadRezaee, Seyed AbdolrahimMousavi, Seyed Mojtabaنوع مدرک
TextOriginal Research Article
زبان مدرک
Englishچکیده
Objective: Diabetes is an important risk factor for cardiovascular events. The great percent of morbidity in patients with diabetes is due to endothelial dysfunction. The present study investigated the effects of hydroalcholic extract of Nigella sativa (N. sativa) on contractile and dilatation response of isolated aorta in streptozotocin (STZ)-induced diabetic rat. Materials and Methods: Rats were divided into six experimental groups (control, untreated STZ-diabetic, and N. sativa hydroalcholic extract or metformin-treated diabetic rats). Treated rats received N. sativa extract (100, 200, and 400 mg/kg) or metformin (300 mg/kg) by gavage, daily for 6 weeks. Isolated rat thoracic rings were mounted in an organ bath system then contractile and dilatation responses induced by phenylephrine (PE), acetylcholine (ACh), potassium chloride (KCl), and sodium nitroprusside (SNP) were evaluated in different situations. Results: The lower concentrations of N. sativa seed extract (DE 100 and DE 200) and metformin significantly reduced the contractile responses to higher concentrations of PE (10-6 - 10-5 M) compared to diabetic group (pThe relaxation response to Ach 10-8M, was increased in DE 200 and metformin groups compared to diabetic group (p-7 - 10-5Mwere significantly higher in all treated groups compared to diabetic group (pConclusion: Chronic administration of N. sativa seed extract has a significant hypoglycemic effect and improves aortic reactivity to vasoconstrictor and vasodilator agents in STZ-induced diabetic rats.
کلید واژگان
Diabetes MellitusNigella Sativa
Endothelial dysfunction
Isolated aorta
Rat
Physiology
شماره نشریه
1تاریخ نشر
2016-01-011394-10-11
ناشر
Mashhad University of Medical Sciencesسازمان پدید آورنده
Department of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, IranCardiovascular Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
Department of Biochemistry, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
Department of Immunology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
Department of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
شاپا
2228-79302228-7949




