The effect of dioxidovanadium complex (V) on hepatic function in streptozotocin-induced diabetic rats

Sibiya, S; Msibi, B; Khathi, A; Sibiya, N; Booysen, I; Ngubane, P

HERO ID

6308101

Reference Type

Journal Article

Year

2019

Language

English

PMID

31491333

HERO ID 6308101
In Press No
Year 2019
Title The effect of dioxidovanadium complex (V) on hepatic function in streptozotocin-induced diabetic rats
Authors Sibiya, S; Msibi, B; Khathi, A; Sibiya, N; Booysen, I; Ngubane, P
Journal Canadian Journal of Physiology and Pharmacology
Volume 97
Issue 12
Page Numbers 1169-1175
Abstract Diabetics are susceptible to hepatic dysfunction risks due to hyperglycaemia and insulin therapy. Conventional diabetes treatments improve glycaemic control; however, hepatic hazards associated with these agents remains a challenge. Accordingly, this study sought to investigate the effect of a dioxidovanadium complex (V) on the hepatic function in streptozotocin-induced diabetic rats. Sprague-Dawley rats (240-250 g) were divided into 4 groups (n = 6): nondiabetic control, diabetic control, insulin-treated, and vanadium complex groups. The dioxidovanadium (10, 20, and 40 mg/kg) was administered twice every 2nd day for 5 weeks and blood glucose concentration was monitored weekly. At the end of the experimental period, all the experimental groups were sacrificed, and then the lipid profile, liver superoxide dismutase, glutathione peroxidase and malondialdehyde, plasma alanine aminotransferase and aspartate aminotransferase, and C-reactive protein (CRP) concentration were measured. The administration of dioxidovanadium significantly alleviated hyperglycaemia with concomitant attenuation in oxidative stress as evidenced by reduced malondialdehyde concentrations. Furthermore, vanadium complex abolished diabetes-induced dyslipidaemia. Lastly, vanadium complex administration attenuated the increase in alanine aminotransferase, aspartate aminotransferase, and plasma C-reactive protein. These findings suggest that this metallo-compound (dioxidovanadium) may ameliorate liver dysfunction often observed in diabetes.
Doi 10.1139/cjpp-2019-0369
Pmid 31491333
Wosid WOS:000497746400008
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword hyperglycaemia; oxidative stress; liver dysfunction; C-reactive protein; liver function marker enzymes