[Effects of сramizol on expression of the ApoA1 gene in rats with experimental hyperlipidemia]

Autor: Petr Dmitriyevich Shabanov, A.V. Lizunov, E. R. Bychkov, A. A. Lebedev, S. V. Orlov, I.V. Okunevich, L. B. Piotrovskiy
Rok vydání: 2019
Předmět:
Zdroj: Biomeditsinskaia khimiia. 65(5)
ISSN: 2310-6972
Popis: An imidazole derivative cramizol, has lipid-lowering and anti-atherogenic effects. Cramizol reduces blood levels of cholesterol and triglycerides, and also reduces the atherogenic index in animals with acute hyperlipidemia induced by Triton WR-1339. Cramizol and the lipid-lowering drug fenofibrate exhibited similar effectiveness as hypolipidemic agents. Cramizol also restores the expression of theiApoa1/igene in rats with experimentally induced hyperlipidemia to normal values. This may be a basis of its hypolipidemic and anti-atherogenic action.Proizvodnoe imidazola kramizol obladaet tsitoprotektornym, gipolipidemicheskim i antiaterogennym deĭstviem. Na modeli ostroĭ giperlipidemii, indutsirovannoĭ detergentom tritonom WR-1339, étot preparat snizhaet soderzhanie kholesterina i triglitseridov v krovi, a takzhe znachitel'no umen'shaet kholesterinovyĭ indeks aterogennosti. Po vyrazhennosti gipolipidemicheskogo deĭstviia kramizol sootvetstvuet étalonnomu gipolipidemicheskomu preparatu fenofibratu. Kramizol takzhe vosstanavlivaet do normal'nykh znacheniĭ ékspressiiu genaiApoa1/iv pecheni u krys s éksperimental'no indutsirovannoĭ ostroĭ giperlipidemieĭ, chto, vozmozhno, iavliaetsia osnovoĭ ego gipolipidemicheskogo i antiaterogennogo deĭstviia.
Databáze: OpenAIRE