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低剂量3-去氮尿苷和1-β-D-阿拉伯呋喃糖基胞嘧啶治疗的小鼠中药物序列依赖性毒性和小肠粘膜损伤

Drug sequence-dependent toxicity and small bowel mucosal injury in mice treated with low doses of 3-deazauridine and 1-beta-D-arabinofuranosylcytosine.

作者信息

Paterson A R, Jakobs E S, Lauzon G J, Weinstein W M

出版信息

Cancer Res. 1979 Jun;39(6 Pt 1):2216-9.

PMID:445420
Abstract

The toxicity to mice of combinations of 1-beta-D-arabinofuranosylcytosine and 3-deazauridine was investigated. The drugs were administered daily i.p. on Days 1 to 5, each drug at 10 mg/kg body weight; these dosages are small fractions of the dosages at which 10% of the treated animals died when either drug was administered alone on the foregoing schedule. This drug combination was severely toxic when 3-deazauridine was administered 2 to 8 hr prior to 1-beta-D-arabinofuranosylcytosine; most mice treated in this way died within 3 days of the last treatment. Histological examination showed that severe damage to the small bowel mucosa resulted from treatment with the drugs in the above, lethal sequence. In contrast, treatments with this drug combination at the same dosages were tolerated when the two agents were administered simultaneously or when 1-beta-D-arabinofuranosylcytosine preceded 3-deazauridine. Under the latter conditions, small bowel mucosal injury was much less severe. Female mice were more sensitive to the toxic treatment regimen than were male mice and were protected against the latter when either the 3-deazauridine or the 1-beta-D-arabinofuranosylcytosine component was preceded by treatment with nitrobenzylthioinosine (100 mg/kg), a potent inhibitor of nucleoside transport.

摘要

研究了1-β-D-阿拉伯呋喃糖基胞嘧啶与3-去氮尿苷联合用药对小鼠的毒性。在第1至5天每天腹腔注射给药,每种药物剂量为10mg/kg体重;这些剂量只是按上述给药方案单独使用任一种药物时使10%受试动物死亡剂量的一小部分。当在注射1-β-D-阿拉伯呋喃糖基胞嘧啶前2至8小时给予3-去氮尿苷时,这种药物组合具有严重毒性;以这种方式给药的大多数小鼠在最后一次给药后3天内死亡。组织学检查表明,上述致死给药顺序的药物治疗导致小肠黏膜严重损伤。相比之下,当两种药物同时给药或1-β-D-阿拉伯呋喃糖基胞嘧啶先于3-去氮尿苷给药时,相同剂量的这种药物组合可被耐受。在后一种情况下,小肠黏膜损伤要轻得多。雌性小鼠对这种毒性治疗方案比雄性小鼠更敏感,并且当3-去氮尿苷或1-β-D-阿拉伯呋喃糖基胞嘧啶成分之前先用硝基苄硫基肌苷(100mg/kg)治疗时,雌性小鼠可受到保护,硝基苄硫基肌苷是一种有效的核苷转运抑制剂。

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