Poster presentation
221
CHARACTERISTICS OF THE RELAXING ACTION OF 5-(4-
AMINOPHENYL)-1,3,4-OXADIAZOL-2(3H)-THIONE
Yu.T. Mirzaeva
1
, D.S. Ismailova
2
, P.B. Usmanov
1
, B.J. Elmuradov
2
,
О.А Тursunova.
3
1) Institute of Biophysics and Biochemistry at the National University of Uzbekistan,
Tashkent, Uzbekistan
2) S.Yu. Yunusov Institute of the Chemistry of Plant Substances Academy of sciences of
the Republic of Uzbekistan
3) Andijan State University, Andijan, Uzbekistan
*e-mail: ymirzayeva@mail.ru
We have found that oxadiazole – D-111 exhibited marked vasorelaxant activity and
significantly inhibited the contraction of rat aortic rings induced by KCl and
phenylephrine (PE) study the effect of oxadiazole – D-111 action 5-(4-aminophenyl)-
1,3,4-oxadiazol-2(3H)-thione (D-111)) on the contractile activity of rat aortic smooth
muscle cells (SMC). It is shown that the synthetic compound triazole-D-111 has a
relaxing effect.
In
this regard, we carried out studies on the effect of oxadiazole -D-111 on the
contractile activity of SMC of the rat aorta to establish the dependence of the relaxant
activity of oxadiazole D-111 on its structure. The studies were carried out on the
isolated preparations of the rat aorta, the contractile activity of the aorta was assessed in
the isometric mode using a tension sensor (FT.03, Grass, USA) and a camera base. The
experimental chamber was perfused with oxygenated carbogen (95% O
2
, 5% CO
2
) in
the Krebs solution at a constant temperature of 37˚C.
The relaxant effect of this triazole was dose-dependent,
and with an increase in its
concentration, the suppression degree of the contractions of aortic preparations induced
by hyperpotassium solutions increased markedly. To further clarify the mechanism of
action of oxadiazole, experiments were performed on the dependence of the relaxant
effect of D-111 on the concentration (50-250 µM) of Ca
2+
ions in the incubation
medium. In particular, in the presence of 250μM D-111, the addition of 2.5 mM CaCl2
to the calcium-free solution caused a contraction
of the aorta preparation, which was
69,9±4,1% less than the contraction recorded in the absence of the oxadiazole. In these
experiments, an increase in the concentration of CaCl
2
(0,5 mM- 2.5 mM) in the
incubation medium was accompanied by a stepwise increase in the force of contraction
of the aorta due to
the penetration of Ca
2+
ions through the L-type Ca
2+
channels.
The results of these experiments convincingly indicate that the relaxant effect of the
test compound oxadiazole D-111 under conditions of KCl-induced contracture is
associated with the suppression of the transport of Ca
2+
ions
from the extracellular
medium to the SMC cytoplasm through voltage-dependent Ca
2+
channels of the
plasmalemma.
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