Moran A, Martín E, Velasco C, Martín M L, San Roman L, Caballero E, Puebla P, Medarde M, San Feliciano A
Departmento de Fisiología y Farmacología, Facultad de Farmacia, Universidad de Salamanca, Spain.
J Pharm Pharmacol. 1997 Apr;49(4):421-5. doi: 10.1111/j.2042-7158.1997.tb06817.x.
The antihypertensive activity of eighteen 'oxazolo[3,2-a]pyridine, thiazolo[3,2-a]pyridine and pyrido[2,1-b]oxazine derivatives has been evaluated in conscious spontaneously hypertensive rats (SHRs), and compared with that of nifedipine, used as reference. At a dose of 50 mg kg-1 (i.p.) eleven compounds resulted in a significant reduction in mean arterial blood pressure; four of the eleven were particularly effective, resulting in significant hypotension more than 6 h after administration and an effect that was still apparent after 24 h. The hypotension induced by nifedipine gradually decreased, disappearing 6-8 h after administration. The long-lasting activity shown by these compounds is, in general, not accompanied by reflex tachycardia. Intraperitoneal administration of two oxazolo[3,2-a]pyridine derivatives and two pyrido[2,1-b]oxazine derivatives resulted in potent and long-lasting antihypertensive action in SHRs. Further studies on the mechanism of action of these derivatives might help the determination of better structure-activity correlations and the design, synthesis and evaluation of better antihypertensive agents.
已在清醒的自发性高血压大鼠(SHRs)中评估了18种恶唑并[3,2-a]吡啶、噻唑并[3,2-a]吡啶和吡啶并[2,1-b]恶嗪衍生物的降压活性,并与用作对照的硝苯地平进行了比较。在50mg/kg(腹腔注射)的剂量下,11种化合物可使平均动脉血压显著降低;其中4种尤为有效,给药后6小时以上导致显著低血压,且24小时后仍有明显效果。硝苯地平引起的低血压逐渐降低,给药后6-8小时消失。这些化合物表现出的长效活性通常不伴有反射性心动过速。腹腔注射两种恶唑并[3,2-a]吡啶衍生物和两种吡啶并[2,1-b]恶嗪衍生物在SHRs中产生了强效且持久的降压作用。对这些衍生物作用机制的进一步研究可能有助于确定更好的构效关系,并有助于设计、合成和评估更好的抗高血压药物。