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    Please use this identifier to cite or link to this item: https://ir.fy.edu.tw:8080/ir/handle/987654321/9509

    Title: Effects of 1-pyrrolidinylmethyl-2-naphthol on contractile force and ionic current in cardiac and vascular smooth myocytes.
    Authors: Ai Yu Shen;Sheng Nan Wu.
    Contributors: 輔英科技大學 物理治療系
    Keywords: Pyrrolidine derivatives;Antihypertensive agent;Ionic channel;Calcium ion;Sodium ion;Biological activity;Mechanism of action;Cell culture;In vitro;Myocyte;Thoracic aorta;Animal;Rat;Left atrium;Isolated organ;Electrophysiology;Aminophenols;Rodentia;Mammalia;Vertebrata
    Date: 1998-03-01
    Issue Date: 2010-11-10 09:42:38 (UTC+8)
    Abstract: Ionic mechanisms of the cardiovascular actions of 1 -pyrrolidinylmethyl-2-naphthol hydrochloride (TPY-β) were examined. Intravenous infusion of TPY-β produced hypotension and bradycardia in a dose-dependent manner. TPY-β (30 μM) produced biphasic change in contractile force in isolated rat atria, i.e., an initial decrease and a gradual increase. In electrophysiological studies of rat ventricular myocytes, TPY-β dose-dependently suppressed the amplitude of L-type Ca2+ inward current (ICa,L), but it did not modify the time constants for ICa,L inactivation and the overall shape of the current-voltage relationship of ICa,L. The EC50 value for TPY-β-mediated inhibition of ICa,L is 10.6± 1.0 μM. TPY-β (50 μM) mildly suppressed the amplitude of Na+ current. TPY-β (50 μM) effectively suppressed the amplitude of transient outward current (ITO). The time course for inactivation of ITO was changed to a biexponential process after the application of TPY-β. TPY-β (50 μM) also mildly suppressed the amplitude of inwardly rectifying current. In addition, the effect of TPY-β on Ba2+ inward current (IBa) was examined in A7r5 vascular smooth muscle cells. TPY-β dose-dependently inhibited IBa. The EC50 value for the inhibitory effect of TPY-β is 3.4 ± 0.6 μM. The results indicate that the suppressive effects of TPY-β involve a direct depressant action on heart cells and vascular smooth muscle cells. Thus, direct inhibition of voltage-dependent L-type Ca2+ channel is involved in the TPY-β-mediated vasodilatory action. In addition, the inhibitory effect of TPY-β on cardiac contractility through the blockade of L-type Ca2+ channels can be prevented by TPY-β-mediated inhibition of ITO.
    Relation: Drug Dev. Res. 44(2-3),87-96
    Appears in Collections:[物理治療系] 期刊論文

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