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尿苷诱导的小鼠和大鼠体温过低与血浆及组织中尿苷及其代谢产物水平的关系

Uridine-induced hypothermia in mice and rats in relation to plasma and tissue levels of uridine and its metabolites.

作者信息

Peters G J, van Groeningen C J, Laurensse E J, Lankelma J, Leyva A, Pinedo H M

机构信息

Department of Oncology, Free University Hospital, Amsterdam, The Netherlands.

出版信息

Cancer Chemother Pharmacol. 1987;20(2):101-8. doi: 10.1007/BF00253962.

Abstract

Administration of high-dose uridine or cytidine (3500 mg/kg) resulted in severe hypothermia of 6-10 degrees C in mice. This effect of uridine was observed in three different mouse strains, C57B1/6, Balb/c, and Swiss. A high-dose of uridine also caused hypothermia in Wistar rats. Co-infusion of uridine with benzylacyclouridine, an inhibitor of uridine phosphorylase, partially prevented uridine-mediated hypothermia in mice. A low dose of uridine (100 mg/kg) resulted in a slight increase in temperature. Plasma pharmacokinetics of uridine (at 3500 mg/kg) were studied in two mouse strains, C57B1/6 and Balb/c, and those of cytidine only in C57B1/6 mice. Peak plasma concentrations of uridine in both strains after uridine administration were about 20 mM (at 30-60 min). The peak plasma concentration of cytidine in C57B1/6 mice after cytidine administration was about 12 mM and that of uridine, 1.3 mM. The mean residence time for uridine was about 105 min. The area under the plasma concentration-time curve for uridine was about 50 mmol h/l, and that for cytidine, about 25 mmol h/l. In various tissues of C57B1/6 mice the levels of uridine, uracil and total uracil and cytosine nucleotide pools were determined before and 2 h after uridine administration. Uridine levels increased about 53-fold in liver, about 70-fold in a colon tumor, and only about 7-fold in brain, while the corresponding uracil levels increased about 9-fold, 4-fold and 11-fold, respectively. Total uracil nucleotide pools increased about 8-fold, 3.2-fold and 1.6-fold, respectively. Cytosine nucleotide pools did not increase in the brain. In conclusion, high-dose uridine administration caused severe hypothermia. Plasma levels of uridine and uracil were enhanced to a considerably higher extent than the levels in the tissues. The hypothermia might be related to breakdown products of uridine, since inhibition of uridine breakdown partially prevented hypothermia and since in brain uracil nucleotide levels were only slightly increased after uridine administration, while those of uracil were more markedly increased than in other tissues.

摘要

给小鼠注射高剂量的尿苷或胞苷(3500毫克/千克)会导致体温严重降低6至10摄氏度。在三种不同的小鼠品系C57B1/6、Balb/c和瑞士小鼠中均观察到了尿苷的这种作用。高剂量的尿苷也会使Wistar大鼠体温降低。将尿苷与尿苷磷酸化酶抑制剂苄基阿糖胞苷共同输注,可部分预防小鼠中尿苷介导的体温降低。低剂量的尿苷(100毫克/千克)会使体温略有升高。在两种小鼠品系C57B1/6和Balb/c中研究了尿苷(3500毫克/千克)的血浆药代动力学,而仅在C57B1/6小鼠中研究了胞苷的血浆药代动力学。给药后,两种品系小鼠中尿苷的血浆峰值浓度约为20毫摩尔(在30 - 60分钟时)。胞苷给药后,C57B / 6小鼠中胞苷的血浆峰值浓度约为12毫摩尔,尿苷的血浆峰值浓度为1.3毫摩尔。尿苷的平均驻留时间约为105分钟。尿苷的血浆浓度 - 时间曲线下面积约为50毫摩尔·小时/升,胞苷的约为25毫摩尔·小时/升。在C57B1/6小鼠的各种组织中,在注射尿苷前和注射后2小时测定了尿苷、尿嘧啶以及总尿嘧啶和胞嘧啶核苷酸池的水平。尿苷水平在肝脏中增加了约53倍,在结肠肿瘤中增加了约70倍,而在脑中仅增加了约7倍,而相应的尿嘧啶水平分别增加了约9倍、4倍和11倍。总尿嘧啶核苷酸池分别增加了约8倍、3.2倍和1.6倍。脑中胞嘧啶核苷酸池未增加。总之,高剂量注射尿苷会导致严重体温降低。尿苷和尿嘧啶的血浆水平升高幅度明显高于组织中的水平。体温降低可能与尿苷的分解产物有关,因为抑制尿苷分解可部分预防体温降低,并且因为在脑中,尿苷给药后尿嘧啶核苷酸水平仅略有增加,而尿嘧啶水平的增加比其他组织更明显。

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