Koopmans S J, van der Wee-Pals L, Löwik C W, Papapoulos S E
Department of Endocrinology and Metabolic Diseases, University Hospital, Leiden, The Netherlands.
J Bone Miner Res. 1994 Feb;9(2):241-6. doi: 10.1002/jbmr.5650090213.
Bisphosphonates are drugs that suppress osteoclast-mediated bone resorption and are used with increasing frequency in the treatment of skeletal disorders. Therapeutic regimens are largely based on pharmacodynamic information because of difficulties in obtaining and interpreting pharmacokinetic data. We describe here the application of a permanently cannulated rat model, previously used in other areas of endocrine research, to the simultaneous study of pharmacokinetic and pharmacodynamic properties of the newly developed bisphosphonate EB-1053 [1-hydroxy-3-(1-pyrrolidinyl)propylidene-1,1-bisphosphonate]. Two groups of five rats each received daily intravenous injections of [14C]EB-1053 (0.025 and 0.1 mg/day, respectively); a third group (n = 7) received only normal saline injections and served as control. Treatment was given for at least 20 days. A fourth group (n = 3) received IV injections of the bisphosphonate on three separate occasions. Following IV administration, EB-1053 was rapidly cleared from the circulation. Urinary excretion of radioactivity reached about 55% of the daily administered dose within 48 h and remained at this level during the whole treatment period, indicating continuing retention of the bisphosphonate. Bone resorption, assessed biochemically as the hydroxyproline to creatinine ratio in urine, was suppressed effectively with both doses used. Suppression reached a maximum around day 4 and remained at the same level until the end of treatment. Accumulation of the bisphosphonate in the skeleton was therefore not associated with a cumulative effect on bone resorption. This strongly suggests that in treatment planning a distinction should be made between surface-bound and hence biologically active bisphosphonate from the drug which is incorporated in bone during bone turnover.(ABSTRACT TRUNCATED AT 250 WORDS)
双膦酸盐类药物可抑制破骨细胞介导的骨吸收,在骨骼疾病治疗中的应用日益广泛。由于获取和解释药代动力学数据存在困难,治疗方案很大程度上基于药效学信息。我们在此描述了一种永久插管大鼠模型的应用,该模型先前用于内分泌研究的其他领域,用于同时研究新开发的双膦酸盐EB - 1053[1 - 羟基 - 3 - (1 - 吡咯烷基)亚丙基 - 1,1 - 双膦酸盐]的药代动力学和药效学特性。两组各五只大鼠每天分别静脉注射[14C]EB - 1053(分别为0.025和0.1毫克/天);第三组(n = 7)仅注射生理盐水作为对照。治疗至少持续20天。第四组(n = 3)在三个不同时间点静脉注射双膦酸盐。静脉给药后,EB - 1053迅速从循环中清除。48小时内放射性物质的尿排泄量达到每日给药剂量的约55%,并在整个治疗期间保持在该水平,表明双膦酸盐持续潴留。以尿中羟脯氨酸与肌酐比值进行生化评估的骨吸收,在使用的两种剂量下均得到有效抑制。抑制作用在第4天左右达到最大,并在治疗结束前保持在同一水平。因此,双膦酸盐在骨骼中的蓄积与对骨吸收的累积效应无关。这强烈表明,在治疗方案制定中,应区分表面结合的、因此具有生物活性的双膦酸盐与在骨转换过程中掺入骨中的药物。(摘要截短于250字)