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Georgian Med News ; (271): 55-61, 2017 Oct.
Article in English | MEDLINE | ID: mdl-29099702

ABSTRACT

Purpose - to improve antihypertensive therapy on the basis of studying the antioxidant properties of an angiotensin-converting enzyme (ACE) inhibitor (fosinopril sodium) and a diuretic (hydrochlorothiazide), their impact on endothelial dysfunction and pro-inflammatory cytokines activity in hypertensive patients with overweight and obesity. A combination of fosinopril sodium 20 mg/day and hydrochlorothiazid 12.5 mg/day was prescribed to 54 patients with essential hypertension of 1-3 grades, 30 to 65 years old . The control group included 10 healthy subjects matched for age and sex. During the course of combined antihypertensive therapy we observed a significant decrease of i-NOS activity, reduce of TNF-α type I of its soluble receptor (sTNF-αRI), and 8-iso-PgF2α in the patients. Activity of e-NOS, superoxide dismutase and catalase, in contrast, were increased in patients with hypertension and concomitant obesity. Thus, the improvement of endothelial function, a significant decrease autoimmune activation due to lower tension of oxidative stress in the examined patients optimizes use of a combination of fosinopril sodium and hydrochlorothiazid for differentiated therapy in hypertensive patients with obesity.


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Antihypertensive Agents/therapeutic use , Diuretics/therapeutic use , Essential Hypertension/drug therapy , Fosinopril/therapeutic use , Hydrochlorothiazide/therapeutic use , Overweight/complications , Adult , Aged , Case-Control Studies , Dinoprost/analogs & derivatives , Dinoprost/blood , Drug Therapy, Combination , Endothelium, Vascular/drug effects , Endothelium, Vascular/physiopathology , Essential Hypertension/complications , Essential Hypertension/physiopathology , Female , Humans , Male , Middle Aged , Nitric Oxide Synthase Type II/blood , Obesity/complications , Obesity/physiopathology , Overweight/physiopathology , Receptors, Tumor Necrosis Factor, Type I/blood , Tumor Necrosis Factor-alpha/metabolism
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