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高剂量多克隆药物特异性抗体Fab片段的毒性。

Toxicity of high doses of polyclonal drug-specific antibody Fab fragments.

作者信息

Keyler D E, Shelver W L, Landon J, Sidki A, Pentel P R

机构信息

Department of Medicine, Hennepin County Medical Center, University of Minnesota Medical School, Minneapolis 55415.

出版信息

Int J Immunopharmacol. 1994 Dec;16(12):1027-34. doi: 10.1016/0192-0561(94)90082-5.

Abstract

Drug-specific antibody Fab fragments have been used as a treatment for acute drug overdose. For some drugs, the required Fab dose may be very high (up to several g/kg) and may have adverse effects of its own. The current study evaluated the potential toxicity of an affinity purified sheep polyclonal Fab (TFab) directed at the two antidepressants desipramine (DMI) and nortriptyline. TFab 4 g/kg was administered to anesthetized rats i.v. over 10, 25 or 60 min, with or without a toxic dose of DMI. This high dose of TFab, which is in excess of that needed to reduce DMI toxicity, was used in order to exaggerate any adverse effects. In the absence of DMI, TFab produced minimal changes in the electrocardiographic QRS duration, systolic blood pressure and heart rate compared with control animals and was well tolerated. In the presence of DMI, groups receiving TFab as a 10 or 25 min infusion showed a therapeutic effect (lessening of DMI toxicity) over the first 60 min compared with the control group, but one of six animals in each of the TFab groups died prior to the end of the 180 min experiment. No control animals died, but progressive QRS prolongation and decreasing blood pressure toward the end of the experiment suggested that DMI toxicity was increasing over time. These data suggest that, when administered alone, very high doses of rapidly infused TFab are well tolerated. When administered with DMI, TFab is effective in initially reducing DMI toxicity. However, this dose of TFab may later aggravate DMI toxicity and/or the effects of prolonged anesthesia.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

药物特异性抗体Fab片段已被用于治疗急性药物过量。对于某些药物,所需的Fab剂量可能非常高(高达数克/千克),且其本身可能会产生不良反应。本研究评估了一种针对两种抗抑郁药地昔帕明(DMI)和去甲替林的亲和纯化羊多克隆Fab(TFab)的潜在毒性。将4克/千克的TFab静脉注射给麻醉大鼠,注射时间为10、25或60分钟,同时给予或不给予毒性剂量的DMI。使用这个高于降低DMI毒性所需剂量的高剂量TFab,是为了夸大任何不良反应。在没有DMI的情况下,与对照动物相比,TFab对心电图QRS波时限、收缩压和心率产生的变化极小,且耐受性良好。在有DMI的情况下,与对照组相比,接受10或25分钟输注TFab的组在最初60分钟内显示出治疗效果(DMI毒性减轻),但每个TFab组中有六分之一的动物在180分钟实验结束前死亡。没有对照动物死亡,但在实验接近尾声时,QRS波逐渐延长和血压下降表明DMI毒性随时间增加。这些数据表明,单独给药时,快速输注的高剂量TFab耐受性良好。与DMI一起给药时,TFab最初能有效降低DMI毒性。然而,这个剂量的TFab后来可能会加重DMI毒性和/或延长麻醉的影响。(摘要截短为250字)

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