Weselcouch E O, Demusz C D
Cardiovascular Pharmacology Department, Bristol-Myers Squibb Co., Wallingford, CT 06492.
J Pharmacol Methods. 1990 Jul;23(4):255-64. doi: 10.1016/0160-5402(90)90054-o.
In this article a new model of peripheral occlusive arterial disease is described. The lower hindlimb of an anesthetized ferret was fixed to a holder, the distal end of the Achilles tendon attached to an isometric force transducer, and a passive preload of 100 g was applied to the muscle preparation. The hindlimb was stimulated to contract isometrically via supramaximal electrical stimulation of the sciatic nerve. During the initial period, when femoral blood pressure equaled aortic blood pressure, net contractile force peaked within 1 or 2 min (372 +/- 24g, n = 20) and gradually declined to about 85% of peak over 20 min. Following 60 min of ischemia (induced by partial occlusion of the abdominal aorta), when blood pressure in the contralateral femoral artery was about 45 mm Hg, the 15-min area under the force-time curve (AUC) was 33.2 +/- 2.5% (n = 4) of the initial value. To validate the utility of this model in the search for treatment of peripheral vascular diseases, two drugs were tested. Pentoxifylline, which is clinically effective, attenuated the loss of function observed during ischemia in a dose-related manner, but nifedipine, which is without clinical benefit, had no effect at a dose that was extremely hypotensive. Because femoral perfusion pressure was controlled, systemic hemodynamic effects of test compounds are minimized as potential mechanisms of action, simplifying the evaluation of novel pharmacotherapy for treatment of ischemic diseases.
本文描述了一种外周闭塞性动脉疾病的新模型。将一只麻醉后的雪貂的后肢固定在一个支架上,跟腱远端连接到一个等长力传感器,并对肌肉制剂施加100克的被动预负荷。通过坐骨神经的超强电刺激来刺激后肢进行等长收缩。在初始阶段,当股动脉血压等于主动脉血压时,净收缩力在1或2分钟内达到峰值(372±24克,n = 20),并在20分钟内逐渐下降至峰值的约85%。在60分钟缺血(由腹主动脉部分闭塞诱导)后,当对侧股动脉血压约为45毫米汞柱时,力-时间曲线下15分钟的面积(AUC)为初始值的33.2±2.5%(n = 4)。为了验证该模型在寻找外周血管疾病治疗方法中的实用性,测试了两种药物。临床上有效的己酮可可碱以剂量相关的方式减轻了缺血期间观察到的功能丧失,但临床上无益处的硝苯地平在一个导致极度低血压的剂量下没有效果。由于股动脉灌注压力得到控制,测试化合物的全身血流动力学效应作为潜在作用机制被最小化,从而简化了对缺血性疾病新型药物治疗的评估。