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J Pharm Pharmacol ; 72(12): 1812-1821, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32880967

ABSTRACT

AIM: The present study aimed mainly to demonstrate the effect of the antihistamine azelastine (AZ) and Angiotensin receptor blocker ( ARB), represented by losartan (LOS) either alone or in combined form on certain metabolic aspects, endothelial dysfunction and platelets activation markers in diabetic hyperlipidemic rat model. METHODS: Rats were randomly classified to five groups: One group fed normal chow diet (NC). Four groups received alloxan and CCT-diet. One group received no treatment (DHC while the other three groups received AZ, LOS and their combination form, respectively for 8 weeks. Serum and tissue samples were collected for biochemical and histological evaluations. RESULTS: DHC rats demonstrated significant hyperglycaemia, dyslipidemia, disturbances in endothelial and platelet activation markers. AZ or LOS administration demonstrated hypoglycaemic and hypolipidemic effects. VCAM-1 and sE-selectin (Endothelial function markers) along with CD63 (Platelet activation marker) showed significant decrease as compared to control group. AZ administration exerted little prominent effects than that of LOS, while their combination demonstrated remarkable changes compared to monotherapy. Histopathological findings were in agreement to certain extent with the biomarkers results. CONCLUSIONS: Both drug categories may be expressed as suitable therapeutic tools for atherosclerotic complications either alone or along with other hypolipidemic drugs.


Subject(s)
Angiotensin II Type 1 Receptor Blockers/pharmacology , Blood Platelets/drug effects , Diabetes Mellitus, Experimental/drug therapy , Endothelial Cells/drug effects , Histamine H1 Antagonists, Non-Sedating/pharmacology , Hyperlipidemias/drug therapy , Hypolipidemic Agents/pharmacology , Losartan/pharmacology , Phthalazines/pharmacology , Platelet Activation/drug effects , Alloxan , Animals , Atherosclerosis/etiology , Atherosclerosis/metabolism , Atherosclerosis/prevention & control , Blood Platelets/metabolism , Diabetes Mellitus, Experimental/blood , Diabetes Mellitus, Experimental/chemically induced , Drug Therapy, Combination , Endothelial Cells/metabolism , Hyperlipidemias/blood , Hyperlipidemias/chemically induced , Male , Rats
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