Silas J H, Lennard M S, Tucker G T, Smith A J, Malcolm S L, Marten T R
Br Med J. 1977 Feb 12;1(6058):422-5. doi: 10.1136/bmj.1.6058.422.
The relation between dose, systemic availability, and response to oral debrisoquine was studied in 13 hypertensive patients receiving no other treatment. In 11 who received the same daily dose (40 mg) the fall in mean standing systolic blood pressure varied between 0-3 and 44-4 mm Hg. There was a ninefold difference in the daily urinary excretion and pre-dose plasma concentration of unchanged drug but an inverse correlation between daily urinary excretion of debrisoquine and its 4-hydroxy metabolite (r= -0-86), suggesting that a low recovery of debrisoquine occurs because of extensive metabolism. There was a significant correlation between the fall in standing systolic blood pressure and the mean daily urinary excretion (r= +0-82) and pre-dose plasma concentration (r= +0-82) of unchanged debrisoquine. In contrast, there was a significant inverse correlation between the urinary recovery of the metabolite and the fall in blood pressure (r= -0-82). The availability of debrisoquine is the major determinant of response to this drug. In the absence of side effects a poor response may be an indication to increase the daily dose rather than add another hypotensive agent.
在13名未接受其他治疗的高血压患者中研究了剂量、全身可用性与口服异喹胍反应之间的关系。在11名接受相同日剂量(40毫克)的患者中,平均站立收缩压的下降幅度在0 - 3至44 - 4毫米汞柱之间。未变化药物的每日尿排泄量和给药前血浆浓度存在九倍差异,但异喹胍的每日尿排泄量与其4 - 羟基代谢物之间呈负相关(r = -0 - 86),这表明异喹胍回收率低是由于广泛代谢所致。站立收缩压的下降与未变化异喹胍的平均每日尿排泄量(r = +0 - 82)和给药前血浆浓度(r = +0 - 82)之间存在显著相关性。相反,代谢物的尿回收率与血压下降之间存在显著负相关(r = -0 - 82)。异喹胍的可用性是对该药物反应的主要决定因素。在没有副作用的情况下,反应不佳可能表明应增加日剂量而非添加另一种降压药。