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RESEARCH PRODUCT

Ajuga ivaaqueous extract improves reverse cholesterol transport in streptozotocin-induced diabetic rat

Malika BouchenakDouja Taleb-senouciMarie Aleth Lacaille-dubois

subject

Malemedicine.medical_specialtyApolipoprotein Bmedicine.medical_treatmentIntraperitoneal injectionPharmaceutical ScienceAjugaAjugaDiabetes Mellitus ExperimentalPhosphatidylcholine-Sterol O-AcyltransferaseInternal medicineDiabetes mellitusLecithinsmedicineAnimalsRats WistarPhospholipidsTriglyceridesPharmacologyApolipoprotein A-IbiologyPlant ExtractsChemistryCholesterol HDLReverse cholesterol transportBiological TransportStreptozotocinbiology.organism_classificationmedicine.diseaseRatsCholesterolEndocrinologyAcyltransferaseDietary Supplementsbiology.proteinlipids (amino acids peptides and proteins)Cholesterol EstersPhytotherapymedicine.drugLipoprotein

description

AbstractObjectivesThe aim of this study was to determine the effects of Ajuga iva aqueous extract on lecithin : cholesterol acyltransferase (LCAT) activity and amount and composition of high-density lipoprotein (HDL)2 and (HDL)3, in streptozotocin (STZ)-induced diabetic rats.MethodsDiabetes was induced in male Wistar rats by intraperitoneal injection of STZ (60 mg/kg body weight). Diabetic rats (n = 12) were divided into two groups. The diabetic control group (D) received a 20% casein diet and the diabetic treated group received the same diet supplemented with A. iva aqueous extract (0.5 g/100 g diet) (DAi), for 4 weeks.Key findingsTotal cholesterol and HDL3-C were respectively decreased by 32% and 55% in the DAi group compared with the D group, whereas HDL2-C was increased by 30%. The amounts of HDL2 and HDL3, which were the sum of apolipoproteins, unesterified cholesterol (UC), cholesteryl esters (CEs), triacylglycerols (TGs) and phospholipids (PLs), showed no significant difference. A. iva treatment increased LCAT by 33% and its cofactor-activator, apolipoprotein A-I, by 58%. HDL3-PL (enzyme substrate) and HDL3-UC (acyl group acceptor) were respectively decreased by 70% and 57%, whereas HDL2-CE (product of LCAT reaction) was enhanced by 30%.ConclusionsIn STZ-induced diabetic rats, A. iva improves reverse cholesterol transport by enhancing LCAT activity, leading to anti-atherogenic effects.

https://doi.org/10.1111/j.2042-7158.2012.01501.x