Blumental H P, Ryan J R, McMahon F G
Eur J Clin Pharmacol. 1975 Aug 14;8(6):409-14. doi: 10.1007/BF00562314.
PR-G-138-C1, a new antihypertensive agent with vasodilating properties, was studied in ten patients with moderate to severe hypertension. The patients were admitted to a metabolic ward and followed on a 2 gm salt diet. Placebo was given daily until blood pressure and weight were stabilized. A dose titration was then started with increasing single daily doses of 3, 5, 8, and 10 mg of PR-G-138-C1 orally. The dose at which the mean arterial pressure was reduced by 15 mm Hg was continued for a total of seven days. PR-G-138-C1 lowered sitting mean arterial pressures significantly in all subjects (133.8+/-15.1 leads to 116.0+/-12.4 mm Hg, p less than 0.001). The antihypertensive effect was first noted 30 minutes following drug administration and persisted for as long as six hours with a peak effect at one hour. All patients had a significant increase in sitting pulse rate (80.4+/-9.11 leads to 90.0+/-6.91/min, p less than 0.002). Blood pressure reduction and increase in pulse rate were dose related. The most common side effects noted were headaches in eight out of ten patients and postural dizziness in seven out of ten patients. There were no signs of fluid retention (weight gain or edema). Electrocardiogram and other laboratory parameters remained essentially unchanged.
PR - G - 138 - C1是一种具有血管舒张特性的新型抗高血压药物,对10例中重度高血压患者进行了研究。患者入住代谢病房,采用2克盐饮食并接受随访。在血压和体重稳定之前,每天给予安慰剂。然后开始剂量滴定,口服PR - G - 138 - C1,每日单次剂量递增,分别为3毫克、5毫克、8毫克和10毫克。将平均动脉压降低15毫米汞柱的剂量持续服用7天。PR - G - 138 - C1使所有受试者的坐位平均动脉压显著降低(从133.8±15.1降至116.0±12.4毫米汞柱,p<0.001)。给药后30分钟首次观察到降压效果,持续长达6小时,1小时时达到峰值效应。所有患者的坐位脉搏率均显著增加(从80.4±9.11升至90.0±6.91次/分钟,p<0.002)。血压降低和脉搏率增加与剂量相关。最常见的副作用是10名患者中有8名出现头痛,10名患者中有7名出现体位性头晕。没有液体潴留(体重增加或水肿)的迹象。心电图和其他实验室参数基本保持不变。