2 results match your criteria: "Department of Preclinical and Clinical Pharmacology with Toxicology[Affiliation]"
Pril (Makedon Akad Nauk Umet Odd Med Nauki)
March 2016
Department of Preclinical and Clinical Pharmacology with Toxicology, Medical Faculty, Vodnjanska b.b., Skopje, R. Macedonia.
This study was initiated to refine and characterize a nongenetic experimental model of type 2 diabetes mellitus and to follow up various metabolic parameters up to six weeks after diabetes induction. Male Wistar rats were divided into 4 groups: CON group--consumed standard rat chow and served as control; HFD group--consumed high-fat diet (45% calories as fat); STZ group-was injected once intraperitoneally with streptozotocin (35 mg/kg) on day 14, and DM-2 group--consumed high-fat diet and was injected with streptozotocin. The metabolic parameters were measured one week after streptozotocin injection (week 3) and at the end of the study (week 9).
View Article and Find Full Text PDFPril (Makedon Akad Nauk Umet Odd Med Nauki)
April 2016
Department of Preclinical and Clinical Pharmacology with Toxicology, Medical Faculty, Skopje, R. Macedonia.
Diabetic nephropathy (DN) is one of the most common causes of terminal stadium damage to the kidneys. The angiotensin-converting enzyme (ACE) represents a significant risk factor for the progression of DN. ACE inhibitors are medications of particular interest knowing the role of angiotensin II in the development of DN.
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