Moorghen M, Ince P, Finney K J, Watson A J, Harris A L
Department of Pathology, University of Newcastle upon Tyne, United Kingdom.
In Vitro Cell Dev Biol. 1991 Nov;27A(11):873-7. doi: 10.1007/BF02630990.
The in-vitro effects of hydroxyurea 5-FU and 5-FUdR have been extensively studied in experimental systems employing cell-line techniques. In this study we investigated the effects of these drugs on the levels of incorporation of labeled nucleosides into DNA in explants of intact rat colonic mucosa maintained in organ culture. The effects of the nucleoside transport inhibitors nitrobenzylthioinosine (NBMPR) and dipyridamole--which are modulators of antimetabolite cytotoxicity--on the incorporation of tritiated thymidine ([3H]TdR) into DNA were also studied. The incorporation of tritiated TdR into DNA was reduced by hydroxyurea but was not altered by either 5-FU or 5-FUdR. The levels of tritiated deoxyuridine were reduced by 5-FU and 5-FUdR in separate experiments; this is in keeping with thymidylate synthase inhibition. NBMPR and dipyridamole also reduced 3H-TdR incorporation into DNA. These results can be explained in terms of the known mechanisms of action of these drugs. This experimental model is therefore useful in assessing the effects of antimetabolites and nucleoside transport inhibitors in intact colonic mucosa.
在采用细胞系技术的实验系统中,对羟基脲、5-氟尿嘧啶(5-FU)和5-氟脱氧尿苷(5-FUdR)的体外效应进行了广泛研究。在本研究中,我们调查了这些药物对维持在器官培养中的完整大鼠结肠黏膜外植体中标记核苷掺入DNA水平的影响。还研究了核苷转运抑制剂硝基苄硫肌苷(NBMPR)和双嘧达莫(它们是抗代谢物细胞毒性的调节剂)对氚标记胸腺嘧啶核苷([3H]TdR)掺入DNA的影响。羟基脲可降低[3H]TdR掺入DNA的水平,但5-FU或5-FUdR对其无影响。在单独的实验中,5-FU和5-FUdR降低了氚标记脱氧尿苷的水平;这与胸苷酸合成酶抑制作用一致。NBMPR和双嘧达莫也降低了3H-TdR掺入DNA的水平。这些结果可以根据这些药物已知的作用机制来解释。因此,该实验模型有助于评估抗代谢物和核苷转运抑制剂对完整结肠黏膜的影响。