Holsapple M P, Tucker A N, McNerney P J, White K L
J Pharmacol Exp Ther. 1984 May;229(2):493-500.
Female B6C3F1 mice were given i.p. injections with 1.5, 3.0 and 5.0 mg/kg N-nitrosodimethylamine (DMN) daily for 14 days and evaluated on day 15. The day 4 immunoglobulin M (peak day) antibody response to sheep red blood cells (sRBC) was inhibited by 20, 53 and 81%, respectively. The day 5 immunoglobulin G (peak day) antibody response to sRBC was only inhibited significantly (60%) at the highest dose. Recovery studies indicated that the IgM antibody response was still significantly inhibited (48%) 30 days after the completion of the exposure to 5 mg/kg of DMN. The peak response (day 3) to 100 micrograms of the B-cell mitogen, lipopolysaccharide, was inhibited by 15, 26 and 32%, respectively, indicating that a portion of the suppression of the antibody response by DMN may be due to an effect on the ability of the lymphocytes to proliferate. Concentrations of DMN up to 100 mM added directly to untreated spleen cell suspensions had no effect on the in vitro antibody responses to lipopolysaccharide and sRBC. Preincubating DMN (100 mM) with either phenobarbital-induced or 3-methylcholanthrene-induced liver proteins (postmitochondrial supernatant from a 9000 X g liver homogenate) was still ineffective. The activation of DMN by either preparation was verified by measuring formaldehyde production, which reflects demethylation. In contrast to the results with DMN added directly to untreated spleen cell suspensions, the most sensitive indicator of suppression by DMN was the in vitro antibody responses to lipopolysaccharide and sRBC by spleen cell suspensions from DMN-treated mice.(ABSTRACT TRUNCATED AT 250 WORDS)
雌性B6C3F1小鼠每天腹腔注射1.5、3.0和5.0毫克/千克的N-亚硝基二甲胺(DMN),持续14天,并在第15天进行评估。对绵羊红细胞(sRBC)的第4天免疫球蛋白M(峰值日)抗体反应分别被抑制了20%、53%和81%。对sRBC的第5天免疫球蛋白G(峰值日)抗体反应仅在最高剂量时被显著抑制(60%)。恢复研究表明,在接触5毫克/千克DMN结束后30天,IgM抗体反应仍被显著抑制(48%)。对100微克B细胞有丝分裂原脂多糖的峰值反应(第3天)分别被抑制了15%、26%和32%,这表明DMN对抗体反应的部分抑制可能是由于对淋巴细胞增殖能力的影响。直接添加到未处理的脾细胞悬液中的高达100毫摩尔的DMN浓度对脂多糖和sRBC的体外抗体反应没有影响。将DMN(100毫摩尔)与苯巴比妥诱导或3-甲基胆蒽诱导的肝蛋白(9000×g肝匀浆的线粒体后上清液)预孵育仍然无效。通过测量反映去甲基化的甲醛生成来验证两种制剂对DMN的激活。与直接添加到未处理的脾细胞悬液中的DMN结果相反,DMN抑制的最敏感指标是来自DMN处理小鼠的脾细胞悬液对脂多糖和sRBC的体外抗体反应。(摘要截短于250字)