Bergholm A M, Henning C, Holm S E
Eur J Clin Microbiol. 1984 Apr;3(2):126-30. doi: 10.1007/BF02014329.
The properties of tissue cage fluid in a steel net tissue cage model in rabbits were compared to those of serum by determination of the protein profile, the cell contents, and the pharmacokinetics of 125I albumin, 3H sucrose and 3H fusidic acid. The dominating serum proteins demonstrated by crossed immunoelectrophoresis were also detected in tissue cage fluid but at lower levels and at various ratios. The cell pattern gradually changed from an initial dominance of polymorphonuclear cells to lymphocytes during the five weeks following the subcutaneous implantation of the cages. The distribution of the highly protein-bound fusidic acid was markedly slower and the maximal tissue cage fluid level significantly lower than that of sucrose. Equilibrium of 125I albumin between serum and tissue cage fluid was slowly achieved during the following two weeks. The advantages and disadvantages of tissue cage models for studies of drug pharmacokinetics are discussed. The properties of tissue cage fluid and the possibility of repeated sampling make the model suitable for studies of experimental local infections. The influence of therapeutic agents and the host's response to the infectious process may also be elucidated.
通过测定蛋白质谱、细胞成分以及125I白蛋白、3H蔗糖和3H夫西地酸的药代动力学,将兔钢网组织笼模型中组织笼液的性质与血清的性质进行了比较。交叉免疫电泳显示的主要血清蛋白在组织笼液中也能检测到,但水平较低且比例各异。在皮下植入笼子后的五周内,细胞模式从最初多形核细胞占主导逐渐转变为淋巴细胞占主导。与蔗糖相比,高度蛋白结合的夫西地酸的分布明显较慢,组织笼液中的最大水平显著较低。血清和组织笼液之间的125I白蛋白平衡在接下来的两周内缓慢实现。讨论了组织笼模型在药物药代动力学研究中的优缺点。组织笼液的性质和重复采样的可能性使该模型适用于实验性局部感染的研究。治疗剂的影响以及宿主对感染过程的反应也可能得到阐明。