Literature DB >> 30223051

Nigella sativa L. seed regulated eNOS, VCAM-1 and LOX-1 genes expression and improved vasoreactivity in aorta of diabetic rat.

Abbasali Abbasnezhad1, Saeed Niazmand2, Maryam Mahmoudabady3, Seyed Abdolrahim Rezaee4, Mohmmad Soukhtanloo5, Razieh Mosallanejad6, Parichehr Hayatdavoudi7.   

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE: Nigella sativa L. seed has been widely used in traditional medicine for the treatment of diabetes. The major reason for vascular complications in diabetic patients is endothelial dysfunction. However, the impact of N. sativa seed on endothelial dysfunction in diabetes remains unclear. AIM OF THE STUDY: This study was conducted to evaluate the effect of the hydroalcoholic extract of N. sativa seed on eNOS, VCAM-1, and LOX-1 genes expression and the vasoreactivity of aortic rings to acetylcholine (Ach) in streptozotocin (STZ)-induced diabetic rat.
MATERIALS AND METHODS: Treated rats received N. sativa seed extract (100, 200, and 400 mg/kg) daily by gavage for 6 weeks. The fasting blood glucose and lipids were measured and atherogenic index of plasma (AIP) was calculated. The endothelium-dependent vasoreactivity responses of isolated aortic rings were evaluated in the presence of cumulative concentrations of Ach (10-8-10-5 M). eNOS, VCAM-1, and LOX-1 genes expression in aortic tissue was assessed by using real time polymerase chain reaction (PCR).
RESULTS: Male diabetic Wistar rats treated with N. sativa seed extract for six weeks reduced serum glucose and lipids and improved AIP. The vasorelaxant responses of aortic rings to Ach were markedly improved. N. sativa seed significantly increased eNOS in mRNA expression level and function, while it decreased VCAM-1 and LOX-1 expressions in vascular cells of aortic tissue which assessed only in mRNA level.
CONCLUSIONS: The results of this study showed that N. sativa seed more likely, has antidiabetic and antihyperlipidemic properties and improved vasoreactivity, endothelial dysfunction, and vascular inflammation in diabetic rats' aorta.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Acetylcholine chloride (PubChem CID: 6060); Calcium chloride (PubChem CID: 5284359); Magnesium sulfate (PubChem CID: 24083); Phenylephrine hydrochloride (PubChem CID: 5284443); Potassium chloride (PubChem CID: 4873); Sodium bicarbonate (PubChem CID: 516892); Sodium chloride (PubChem CID: 5234); Streptozocin (PubChem CID: 29327)

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Year:  2018        PMID: 30223051     DOI: 10.1016/j.jep.2018.09.021

Source DB:  PubMed          Journal:  J Ethnopharmacol        ISSN: 0378-8741            Impact factor:   4.360


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