Tamura S, Matsumoto Y
J Toxicol Sci. 1981 Feb;6(1):19-16. doi: 10.2131/jts.6.19.
In this study, an effect of single administration of organic thio-compounds on the combined use with uridine diphosphate glucuronic acid was investigated. In the single administration of organic thio-compounds to Wistar strain rats, the synthesis of glucuronide was slightly accelerated by glutathione or methionine, but it was not so much as in the single administration of UDPGA. The glucuronyltransferase activity was accelerated, when either taurine or methionine was administered in combination with UDPGA. None of these organic thio-compounds used in this study showed more significant inhibitory action of beta-glucuronidase activity than UDPGA in the single administration. It was perceived, however that the inhibitory action of beta-glucuronidase activity was much accelerated, when UDPGA was administered in combination either with taurine or methionine. In the administration of organic thio-compounds to Gunn strain rats, cysteine was detected to be the compound which accelerated the synthesis of glucuronide. It was also noted that no organic thio-compounds used in this study affected as influence on beta-glucuronidase activity.
在本研究中,对有机硫化合物单次给药与尿苷二磷酸葡萄糖醛酸联合使用的效果进行了研究。在向Wistar品系大鼠单次给药有机硫化合物时,谷胱甘肽或蛋氨酸可使葡萄糖醛酸苷的合成略有加速,但不如单次给药尿苷二磷酸葡萄糖醛酸(UDPGA)时加速明显。当牛磺酸或蛋氨酸与UDPGA联合给药时,葡萄糖醛酸基转移酶活性会加速。在本研究中使用的这些有机硫化合物,在单次给药时,均未表现出比UDPGA更显著的β-葡萄糖醛酸酶活性抑制作用。然而,可以察觉到,当UDPGA与牛磺酸或蛋氨酸联合给药时,β-葡萄糖醛酸酶活性的抑制作用会大大加速。在向Gunn品系大鼠给药有机硫化合物时,检测到半胱氨酸是加速葡萄糖醛酸苷合成的化合物。还注意到,本研究中使用的有机硫化合物均未对β-葡萄糖醛酸酶活性产生影响。