试图通过谷胱甘肽耗竭调节Balb/c小鼠的二硫抗肿瘤活性。

R K Coshan-Gauthier, D L Kirkpatrick
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引用次数: 1

摘要

我们研究了巯基亚砜(BSO)介导的谷胱甘肽(GSH)耗损对6-TG和6-MP四种二硫衍生物产生的Balb/c小鼠抗肿瘤活性的影响。初步研究表明,注射BSO (5 mmol/kg) 14小时后,肿瘤GSH水平最大限度地减少,而正常组织GSH水平已恢复到接近对照水平。比较两组动物在14小时前分别给药和不给药的肿瘤生长延迟和生长速率。单独使用BSO处理与对照相比没有延迟或生长速度差异。在存在和不存在BSO的情况下给药的化合物II或III也没有产生与对照相比的延迟或生长速率差异。单独添加化合物1 (10 mg/kg)可延迟5.2 d,生长速度显著低于对照(p = 0.05)。与BSO联合使用,效果未增强。复方IV (50 mg/kg)在2个单独的试验中(3.1天和4.8天)也产生延迟,并且每次的生长速度都明显低于对照组(p = 0.05)。BSO的存在没有显著降低生长速率。两次静脉注射,间隔4天,产生的延迟(4.9天)与单次注射相似。它产生了2种治疗方法,毒性也更大,导致3人死亡。与单独给药相比,静脉注射联合BSO预处理的延迟时间更长(16.0 d),生长速率也显著延长(p = 0.05)。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Attempted modulation of disulfide antitumor activity in Balb/c mice through glutathione depletion.

We investigated the effects of buthionine sulfoximine (BSO)-mediated glutathione (GSH) depletion on the antitumor activity in Balb/c mice produced by four disulfide derivatives of 6-TG and 6-MP. Initial studies indicated that 14 h after BSO (5 mmol/kg) injections, tumor GSH levels were maximally depleted, while normal tissue GSH levels had returned to near control levels. Tumor growth delays and growth rates were compared for groups of animals receiving disulfides I-IV with and without BSO administration 14 h previous. Treatments with BSO alone produced no delay or growth rate differences from the control. Compounds II or III administered in the presence and absence of BSO also produced no delay or growth rate differences from control. Compound I (10 mg/kg) alone showed a delay of 5.2 days and a growth rate significantly slower than that of control (p = 0.05). In combination with BSO the effects were not enhanced. Compound IV (50 mg/kg) also produced delays in 2 separate trials (3.1 and 4.8 days) and significantly slower growth rates on each occasion compared to the control (p = 0.05). The growth rates were not significantly lowered in the presence of BSO. Administration of two doses of IV, 4 days apart, produced a delay (4.9 days) similar to that seen with a single dose. It produced 2 cures and was also more toxic, causing 3 deaths. Two doses of IV in combination with BSO pretreatment had a greater delay (16.0 days) and a significantly longer growth rate (p = 0.05) than two doses of IV alone.(ABSTRACT TRUNCATED AT 250 WORDS)

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