Kunka R L, Mattocks A M
J Pharm Sci. 1979 Mar;68(3):347-9. doi: 10.1002/jps.2600680324.
Acetazolamide concentration values derived from a nonlinear model system were related to two pharmacological responses in the rabbit. Kidney response was measured by monitoring urine flow and sodium elimination. Ocular response was followed using an applanation tonometer. Maximum urine flow and sodium elimination occurring immediately after injection correlated with log dose. Urine flow dropped below control values along with a rise in osmolality, suggesting the involvement of antidiuretic hormone. Sodium elimination was correlated with plasma levels. Urine pH is thought to be involved in reducing accessibility of drug to carbonic anhydrase in the kidney. Maximum ocular response also was correlated with log dose. Ocular response was related to a protein fraction, which is believed to be mainly carbonic anhydrase. However, the duration of ocular response was related to the red blood cell protein fraction. Thus, drug activity could conceivably be regulated by monitoring a tissue that is not the site of action and can be sampled readily.
从非线性模型系统得出的乙酰唑胺浓度值与家兔的两种药理反应相关。肾脏反应通过监测尿流量和钠排泄来测量。眼部反应使用压平眼压计进行跟踪。注射后立即出现的最大尿流量和钠排泄与对数剂量相关。随着渗透压升高,尿流量降至对照值以下,提示抗利尿激素参与其中。钠排泄与血浆水平相关。尿液pH值被认为与降低药物在肾脏中对碳酸酐酶的可及性有关。最大眼部反应也与对数剂量相关。眼部反应与一种蛋白质组分有关,该蛋白质组分被认为主要是碳酸酐酶。然而,眼部反应的持续时间与红细胞蛋白质组分有关。因此,可以想象,通过监测一个并非作用部位且易于取样的组织,药物活性能够得到调节。