| Autor: |
Takada, Toyokazu, Miyawaki, Nobuaki, Kageyama, Masaaki, Matsuno, Kiyoshi, Ishida, Naruhiro, Yamauchi, Hideyasu, Iso, Tadashi |
| Zdroj: |
Journal of Cardiovascular Pharmacology; December 1991, Vol. 18 Issue: 6 p855-862, 8p |
| Abstrakt: |
The antihypertensive effect of SD-3211. a structurally novel type of nondihydropyridine calcium antagonist, was assessed using several types of experimental hypertensive rats. Oral administration of SD-3211 (10. 20, and 30 mg/kg) to conscious spontaneously hypertensive rats (SHR). deoxycorticosterone acetate-salt hypertensive rats (DHR) and 2-kidney, 1-clip renal hypertensive rats (RHR) resulted in a dose-dependent decrease in systolic blood pressure (SBP). The hypotensive effect of SD-3211 in these hypertensive rats was more pronounced than in normotensive rats (NR). The potencies of SD-3211 for the hypotensive effect in the hypertensive rats and NR were 5–7 times greater than that of diltiazem but 2–3 times less than that of nicardipine. Furthermore, SD-3211 showed longer-lasting hypotensive action than diltiazem and nicardipine, at the respective equihypotensive dose. During the course of hypotension. SD-3211 did not exert any influence on heart rate (HR) in any type of hypertensive rats or NR, in contrast to the appearance of tachycardia with nicardipine in SHR, DHR, and NR and of bradycardia with diltiazem in DHR. At doses of 10 and 30 mg/kg, the hypotensive doses; SD-3211 elicited a dose dependent natriuresis but no kaliuresisin SHR. In the chronic study using SHR. SD-3211 at 10 mg/kg/day showed an antihypertensive effect during anadministration period of 12 consecutive weeks. These results allow us to conclude that SD-3211 has a potent and long-lasting hypotensive action with little cardiac effect. |
| Databáze: |
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