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Biomedical subjects

S Yagi

Publications and source records attributed to S Yagi.

362 records · Page 21Linked to original sources

[Effect of chronic cardiac pacing on cross-bridge activation rate in the human left ventricle].

Our active cross-bridge model has theoretically established that the cross-bridge activation rate constant of the left ventricular myocardium (Ka), which may correspond to the rate constant for the binding of Ca2+ with troponin C, can be approximately expressed as a simple formula: Ka = 3/electromechanical systole (sec-1). To determine whether this constant has the potential to be used as a clinical index of cardiac adrenergic tone, we investigated the chronic effect of cardiac pacing on the value of Ka in 15 subjects with a pacemaker in full pacing rhythm. The value of Ka (7.10 +/- 0.50 vs 6.62 +/- 0.39 sec-1, p < 0.05) and that of Ka corrected for heart rate (Kac) (7.63 +/- 0.50 vs 6.60 +/- 0.41 sec-1, p < 0.01) were both decreased significantly at one month or more after permanent pacemaker implantation. Another eight subjects were investigated to evaluate the effect on Kac of acute left bundle branch block due to intermittent right ventricular pacing. Intermittent pacing did not cause a significant change of the Kac value (7.46 +/- 0.43 vs 7.29 +/- 0.39 sec-1). The decrease of Kac during chronic cardiac pacing might reflect reduced cardiac adrenergic activity, since acute left bundle branch block due to intermittent right ventricular pacing did not affect this parameter.

Adult↗

[Effect of vesnarinone on the myocardial force-length relationship in the in situ canine left ventricle].

The left ventricular (LV) end-systolic force-diameter (Fes-Des) relationship was used to examine the effect of a new positive inotropic agent (vesnarinone) on the contractility of the beta-blocked canine left ventricle. Seven adult mongrel dogs were implanted with ultrasonic crystals to measure the LV diameter and a micromanometer to measure LV pressure. Beta-adrenergic and vagal blockades were induced with intravenous propranolol (2 mg/kg) and atropine (0.2 mg/kg), respectively, and preload was decreased by inferior vena caval occlusion. The slope (Ec) and extrapolated diameter intercept (Do) of the LV Fes-Des relationship were derived from the end-systolic data obtained in the control, beta-blocked state, after sulfolane infusion, and after infusion of vesnarinone (3 mg/kg) dissolved in sulfolane. Ec was used as a new index of LV myocardial contractility. After vesarinone infusion, the LV Fes-Des relationship seemed to be nearly linear, and its Ec value was significantly increased by 18% (68.4 +/- 15.4 vs 80.4 +/- 21.8 g/cm, p < 0.05) without changes in heart rate, whereas Do did not change (1.74 +/- 0.44 vs. 1.70 +/- 0.42 cm). These results indicate that vesnarinone significantly enhances myocardial contractility in the beta-blocked canine left ventricle.

Animals↗