РОЛЬ K+ - КАНАЛОВ В ВАЗОРЕЛАКСАНТНОМ ДЕЙСТВИИ АЛКАЛОИДОВ 1-О-БЕНЗОИЛНАПЕЛЛИНА И 6 – О – БЕНЗОИЛГЕТЕРАТИЗИНА НА АОРТЫ КРЫСЫ

Есимбетов, А.Т., Кунисов, Б., Зарипов, А.А., Бакиева, M., Усманов, П.Б., Султанходжаев, М.

Ilim ha’m ja’miyet · 2020-yil

Annotatsiya

In our investigation the relaxant effect of the alkaloids 1-O-benzoylnapelline and 6-O-benzoylgeteratizine on the rat aorta was studied. These alkaloids effectively relax the aortic contraction induced by KCI (30 mM). It would be concluded that the glibenclamide significantly reduces the relaxing effect of alkaloids on the basis of it, and can be assumed that the activation of ATP-dependently potassium channels which is involved in the mechanism of action. In contrast to glibenclamide, the effects of TEA, BaCl2 and 4-aminopyridine on relaxation caused by 1-O-benzoylnapelline and 6-O-benzoylheteratisine were less pronounced and did not significantly affect this process. This indicates that these alkaloids do not significantly affect the activity of Kca, K+V, and KIR channels of rat aortic smooth muscle cells.

Maqola ma’lumotlari
MualliflarЕсимбетов, А.Т., Кунисов, Б., Зарипов, А.А., Бакиева, M., Усманов, П.Б., Султанходжаев, М.
JurnalIlim ha’m ja’miyet
Nashr sanasi2020-07-01
Son2-1
Betlar32-34
TilRus

Kalit so‘zlar

дитерпен алкалоид, каламуш аортаси, силлиқ мускул, К+-канал, глибенкламид, дитерпеноидный алкалоид, аорта крысы, гладкие мышцы, К+-канал, глибенкламид, diterpenoid alkaloid, rat aorta, smooth muscles, K+ -channel, glibenclamide

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