Methanolic extract of African mistletoe (Viscum album) improves carbohydrate metabolism and hyperlipidemia in streptozotocin-induced diabetic rats

被引:35
作者
Adaramoye, Oluwatosin [1 ,5 ]
Amanlou, Massoud [2 ]
Habibi-Rezaei, Mehran [3 ]
Pasalar, Parvin [4 ]
Moosavi-Movahedi, Ali [5 ]
机构
[1] Univ Ibadan, Dept Biochem, Coll Med, Ibadan, Nigeria
[2] Univ Tehran, Tehran Univ Med Sci, Fac Pharm, Dept Med Chem, Tehran 14174, Iran
[3] Univ Tehran, Coll Sci, Sch Biol, Tehran 14174, Iran
[4] Univ Tehran Med Sci, Fac Med, Dept Clin Biochem, Tehran, Iran
[5] Univ Tehran, IBB, Tehran 14174, Iran
基金
美国国家科学基金会;
关键词
Hypoglycemic; African mistletoe; Diabetes; Streptozotocin; COLORIMETRIC METHOD; SERUM; ANTIOXIDANTS; TOXICITY; SEEDS;
D O I
10.1016/S1995-7645(12)60073-X
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective: To justify the use of African mistletoe (AM) Viscum album (V. album) in folkoric medicine to treat diabetes. Methods: In one experiment, the fasting blood glucose (FBG) levels of diabetic rats were monitored for 4 h. Diabetic rats were treated with AM at doses of 50 mg/kg (AM1) and 100 mg/kg (AM2), glibenclamide (GB) (positive control) and saline solution (SS). In another experiment, diabetic rats were treated with AM2, GB and SS daily for 3 weeks. Results: AM1 and AM2 elicited significant (P<0.05) hypoglycaemic effects within 4 h of extract administration. AM1 and AM2 decreased the FBG by 41% and 49%, respectively, at 2 h. AM2 was found to lower FBG by 51%, relative to baseline, which was comparable to GB at 3 h. In the second experiment, AM2 and GB significantly (P<0.05) decreased the FBG by 34% and 51%, respectively. This was followed by marked decrease in levels of HbA1C in AM2- and GB- treated diabetic rats. AM2 significantly (P<0.05) decreased the STZ-induced increase in levels of serum triglyceride, urea, lactate dehydrogenase, alpha -amylase and low-density lipoprotein-cholesterol. Furthermore, diabetic rats treated with AM2 had significantly (P<0.05) elevated high-density lipoprotein-cholesterol. In contrast, STZ administration produced insignificant (P<0.05) effect on the levels of serum creatinine and total bilirubin. Conclusions: Extract of African mistletoe has anti-diabetic and anti-hyperlipidemic effects in STZ-diabetic rats. AM may find clinical application in the amelioration of diabetes-induced lipid disorders.
引用
收藏
页码:427 / 433
页数:7
相关论文
共 41 条
[1]   Hypoglycaemic and hypolipidaemic effects of fractions from kolaviron, a biflavonoid complex from Garcinia Kola in streptozotocin-induced diabetes mellitus rats [J].
Adaramoye, OA ;
Adeyemi, EO .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2006, 58 (01) :121-128
[2]   Hypoglycemic activity of Buchholzia coriacea (Capparaceae) seeds in streptozotocin-induced diabetic rats and mice [J].
Adisa, Rahmat A. ;
Choudhary, Mohammed I. ;
Olorunsogo, Olufunso O. .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2011, 63 (7-8) :619-625
[3]   The Toxic Effects of Nickel Chloride on Liver, Erythropoiesis, and Development in Wistar albino Preimplanted Rats Can Be Reversed with Selenium Pretreatment [J].
Adjroud, Ounassa .
ENVIRONMENTAL TOXICOLOGY, 2013, 28 (05) :290-298
[4]  
Akhtar N, 2011, ACTA POL PHARM, V68, P919
[5]   Effect of antioxidants and ACE inhibition on chemical modification of proteins and progression of nephropathy in the streptozotocin diabetic rat [J].
Alderson, NL ;
Chachich, ME ;
Frizzell, N ;
Canning, P ;
Metz, TO ;
Januszewski, AS ;
Youssef, NN ;
Stitt, AW ;
Baynes, JW ;
Thorpe, SR .
DIABETOLOGIA, 2004, 47 (08) :1385-1395
[6]  
[Anonymous], 1886, physiol. Chem., DOI DOI 10.1515/BCHM1.1886.10.5.391
[7]  
Asvadi I, 2011, EUR REV MED PHARMACO, V15, P1003
[8]   Consensus meeting on reporting glycated haemoglobin and estimated average glucose in the UK: report to the National Director for Diabetes, Department of Health [J].
Barth, Julian H. ;
Marshall, Sally M. ;
Watson, Ian D. .
ANNALS OF CLINICAL BIOCHEMISTRY, 2008, 45 :343-344
[9]   Liver Enzymes: Interaction Analysis of Smoking with Alcohol Consumption or BMI, Comparing AST and ALT to γ-GT [J].
Breitling, Lutz P. ;
Arndt, Volker ;
Drath, Christoph ;
Brenner, Hermann .
PLOS ONE, 2011, 6 (11)
[10]  
Chaulya NC, 2011, ACTA POL PHARM, V68, P989