Блокаторы рецепторов АТ1 (БРА) являются в настоящее время одним из основных классов антигипертензивных препаратов для лечения артериальной гипертензии. Телмисартан – структурно уникальный бифункциональный БРА, который в среднетерапевтических дозах частично активирует PPARγ-рецепторы, ответственные за регуляцию липидного и углеводного обмена. За счет второго механизма действия телмисартан способен уменьшить величину глюкозы, инсулина и триглицеридов в плазме крови. В отличие от I поколения и пероральных антиантидиабетических препаратов, лекарства, которые могут одновременно блокировать рецепторы к ангиотензину II и активировать PPARγ-рецепторы, могут обеспечить уникальную возможность лечения сердечно-сосудистых заболеваний и предотвращения сахарного диабета типа 2.
Ключевые слова: телмисартан, второе поколение БРА, предотвращение сахарного диабета.
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The angiotensin II receptor blockers (ARB) is one of basic antihypertensive drugs for treatment of arterial hypertension at first stages of the disease. The telmisartan a structurally unique bifunctional ARB, can function as a partial agonist of PPARγ involved in carbohydrate and lipid metabolism; and reduce glucose, insulin, and triglyceride levels. In contrast to first generation ARB and antidiabetic agents, drugs that can simultaneously block the angiotensin II receptor and activate PPARγ have the potential to provide unique opportunities for the treatment of cardiovascular disease and prevention diabetes.
Key words: telmisartan, second generation of the ARB, diabetes prevention.
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Авторы
И.Е.Чазова, Л.Г.Ратова
ФГУ Российский кардиологический научно-производственный комплекс Минздравсоцразвития
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I.E.Chazova, L.G.Ratova
FS1 Russian cardiology scientific and production complex, Moscow