首页> 外文期刊>Teratogenesis, carcinogenesis, and mutagenesis >Suppressive effects of two bioresponse modifiers, Krestin and Levamisole, on 5‐azacytidine‐induced digital defects in rats
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Suppressive effects of two bioresponse modifiers, Krestin and Levamisole, on 5‐azacytidine‐induced digital defects in rats

机译:两种生物反应调节剂 Krestin 和左旋咪唑对 5-氮杂胞苷诱导的大鼠手指缺陷的抑制作用

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AbstractThe effects of two bioresponse modifiers, krestin (PSK) and levamisole hydrochloride (levamisole), on 5‐azacytidine (5‐AC)‐induced syndactyly, brachydactyly, and ectrodac‐tyly were investigated. Both PSK and levamisole suppressed 5‐AC‐induced digital malformations in the rat. The effect of PSK was significant when given 24 h before to 1 h after 5‐AC treatment, and levamisole when given 12 h before to 3 h after treatment. Both agents showed an immune‐stimulating effect and have been used as cancer chemotherapeutic drugs. However, as the contribution of fetal or maternal immune functions or the alleviation action is unknown, further investigations are required to clarif
机译:摘要 研究了克雷司汀(PSK)和盐酸左旋咪唑(levamisole)两种生物反应调节剂对5-氮杂胞苷(5-AC)诱导的并指、短指和外指的影响。PSK和左旋咪唑均抑制了5-AC诱导的大鼠指畸形。PSK在5-AC治疗前24小时至5-AC治疗后1小时给药时效果显著,左旋咪唑在治疗前12小时至治疗后3小时给药时效果显著。这两种药物都显示出免疫刺激作用,并已被用作癌症化疗药物。然而,由于胎儿或母体免疫功能的贡献或缓解作用尚不清楚,因此需要进一步检查以澄清

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