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他莫昔芬及其代谢产物在稳态治疗期间在大鼠和人体组织中的分布。

Distribution of tamoxifen and its metabolites in rat and human tissues during steady-state treatment.

作者信息

Lien E A, Solheim E, Ueland P M

机构信息

Department of Pharmacology and Toxicology, University of Bergen, Norway.

出版信息

Cancer Res. 1991 Sep 15;51(18):4837-44.

PMID:1893376
Abstract

A procedure for the extraction of tamoxifen and metabolites from various rat and human tissues was developed and verified. With this method, we determined the drug and metabolite concentrations during one dosing interval in various tissues (brain, fat, liver, heart, lung, kidney, uterus, and testes) of rats given tamoxifen once daily for 3 or 14 days, and in various normal and malignant tissues obtained during surgery or at autopsy from patients with breast cancer treated with tamoxifen. In the rat, the concentrations of tamoxifen and metabolites in most tissues were 8- to 70-fold higher than in serum. The highest levels were observed in lung and liver; substantial amounts were also recovered from kidney and fat. Fluctuations of metabolites and tamoxifen content in most tissues were observed during one dosing interval, corresponding to a ratio of 4:8 between Cmax and Cmin, except in fat and testicular tissues, where the drug concentrations were relatively stable. In addition to tamoxifen, N-desmethyltamoxifen, followed by 4-hydroxytamoxifen, 4-hydroxy-N-desmethyltamoxifen, and N-desdimethyltamoxifen, were abundant in most tissues. In contrast, adipose tissue contained only small amounts of these metabolites. The concentrations of tamoxifen and metabolites found in human normal and malignant tissues confirmed and extended the conclusions made in the experiments with rats. In humans, levels were 10- to 60-fold higher in tissues than in serum, and relatively high concentrations were detected in liver and lung. Additionally, pancreas, pancreatic tumor, and brain metastases from breast cancer and primary breast cancer retained large amounts of drug. Again, the amounts of demethylated and hydroxylated metabolites were high in most tissues, except in fat. Tamoxifen and some metabolites were also present in specimens of skin and bone tissue. In one patient, significant amounts of drugs could be detected in lung, heart, ovary, and intestinal wall 14 months after withdrawal of tamoxifen, demonstrating efficient retention and slow washout of these compounds in human tissue.

摘要

我们开发并验证了一种从各种大鼠和人体组织中提取他莫昔芬及其代谢物的方法。采用该方法,我们测定了每日给药一次、连续给药3天或14天的大鼠各组织(脑、脂肪、肝、心、肺、肾、子宫和睾丸)在一个给药间隔期内的药物和代谢物浓度,以及接受他莫昔芬治疗的乳腺癌患者手术或尸检时获取的各种正常和恶性组织中的药物和代谢物浓度。在大鼠中,大多数组织中的他莫昔芬及其代谢物浓度比血清中的高8至70倍。肺和肝中的浓度最高;肾和脂肪中也能回收大量药物。除脂肪和睾丸组织中药物浓度相对稳定外,在一个给药间隔期内,大多数组织中的代谢物和他莫昔芬含量都有波动,Cmax与Cmin之比为4:8。除他莫昔芬外,N-去甲基他莫昔芬含量在大多数组织中也很丰富,其次是4-羟基他莫昔芬、4-羟基-N-去甲基他莫昔芬和N-去二甲基他莫昔芬。相比之下,脂肪组织中这些代谢物的含量很少。在人体正常和恶性组织中发现的他莫昔芬及其代谢物浓度证实并扩展了在大鼠实验中得出的结论。在人体中,组织中的浓度比血清中的高10至60倍,肝和肺中的浓度相对较高。此外,胰腺、胰腺肿瘤、乳腺癌脑转移瘤和原发性乳腺癌中保留了大量药物。同样,除脂肪外,大多数组织中去甲基化和羟基化代谢物的含量也很高。他莫昔芬和一些代谢物也存在于皮肤和骨组织标本中。在一名患者中,停用他莫昔芬14个月后,在肺、心、卵巢和肠壁中仍能检测到大量药物,表明这些化合物在人体组织中保留效率高且清除缓慢。

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