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EFFECTS OF DRACOCEPHALUM DIVERSIFOLIUM EXTRACT AND N-1 POLYPHENOL ON CALCIUM ION INFLUX IN AORTIC SMOOTH MUSCLE

Alikhon Khasanov*Department of Anatomy and Physiology, Namangan State University, Namangan Region, UzbekistanShoxista MelievaInstitute of the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Tashkent, UzbekistanShahlo IsmailovaDepartment of Anatomy and Physiology, Namangan State University, Namangan Region, UzbekistanKamila EshbakovaInstitute of the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Tashkent, UzbekistanAzizbek AbdullayevA.S. Sadykov Institute of Bioorganic Chemistry of the Science Academy of Uzbekistan, Tashkent, UzbekistanIzzatullo AbdullaevA.S. Sadykov Institute of Bioorganic Chemistry of the Science Academy of Uzbekistan, Tashkent, UzbekistanKuvonchoy TojiboevaNational University of Uzbekistan, Toshkent, UzbekistanSirojiddin OmonturdievA.S. Sadykov Institute of Bioorganic Chemistry of the Science Academy of Uzbekistan, Tashkent, UzbekistanMuxtorjon MamajanovDepartment of Anatomy and Physiology, Namangan State University, Namangan Region, UzbekistanUlugbek GayibovA.S. Sadykov Institute of Bioorganic Chemistry of the Science Academy of Uzbekistan, Tashkent, Uzbekistan
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This study investigated the effects of the ethyl acetate extract of Dracocephalum diversifolium and its main component, N-1 polyphenol, on rat aortic smooth muscle. The aim was to elucidate the vasorelaxant properties of these compounds and their interaction mechanisms with voltage-dependent Ca²⁺ channels (VDCCs). Experiments were conducted in vitro on aortic rings isolated from male Wistar rats. Aortic contractions were recorded using an isometric transducer, and depolarization was induced by 50 mM KCl solution. Dracocephalum diversifolium extract (10–130 µg/ml) and N-1 polyphenol (5–30 µM) significantly reduced aortic contraction in a concentration-dependent manner. The IC₅₀ values of the extract and N-1 polyphenol were 54.8 µg/ml and 20 µM, respectively. In Ca²⁺-free Krebs solution, KCl failed to induce contraction, whereas the addition of Ca²⁺ ions (0–2.5 mM) restored contractile responses. Under these conditions, the presence of the extract or N-1 polyphenol significantly attenuated Ca²⁺-dependent contractions compared to control. These results indicate that both compounds induce vasorelaxation by inhibiting VDCC activity and limiting Ca²⁺ influx. The findings suggest that Dracocephalum diversifolium extract and N-1 polyphenol may serve as natural Ca²⁺ channel blockers and potential antihypertensive agents.

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