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甲基苯丙胺和地西泮抑制卵清蛋白致敏的BALB/c小鼠中抗原特异性细胞因子表达和抗体产生。

Methamphetamine and diazepam suppress antigen-specific cytokine expression and antibody production in ovalbumin-sensitized BALB/c mice.

作者信息

Wey Shiaw-Pyng, Wu Hsin-Ying, Chang Fang-Chia, Jan Tong-Rong

机构信息

Department of Medical Imaging and Radiological Sciences, Chang Gung University, Taoyuan, Taiwan, ROC.

出版信息

Toxicol Lett. 2008 Oct 1;181(3):157-62. doi: 10.1016/j.toxlet.2008.07.015. Epub 2008 Jul 29.

Abstract

Methamphetamine is a widely abused psychostimulant. Abusing methamphetamine causes various adverse effects, such as immune dysfunction. The present study investigated the effect of diazepam, a central depressant, on methamphetamine-induced immunosuppression. BALB/c mice were daily administered with diazepam and methamphetamine (5mg/kg of each), either alone or in combination, for 5 consecutive days followed by sensitization with ovalbumin (OVA). Two days later the same dosing and sensitization regimen was repeated once. The production of serum anti-OVA antibodies, and the cellularity and functional activities of splenocytes were measured 7 days post the 2nd OVA sensitization. The results demonstrated that methamphetamine and/or diazepam significantly attenuated the production of OVA-specific IgM, IgG(1) and IgG(2a). Concordantly, splenocytes of mice administered with diazepam and/or methamphetamine produced less IL-4 and IFN-gamma upon ex vivo re-stimulation with OVA, as compared to the vehicle-treated control. In contrast, the cellularity and metabolic activity of splenocytes were not altered by the drug treatment. These results indicated that the central depressant diazepam did not affect methamphetamine-mediated immunosuppression. Rather, both drugs markedly suppressed antigen-specific antibody production and T-cell reactivity.

摘要

甲基苯丙胺是一种广泛滥用的精神兴奋剂。滥用甲基苯丙胺会导致各种不良反应,如免疫功能障碍。本研究调查了中枢抑制剂地西泮对甲基苯丙胺诱导的免疫抑制的影响。将BALB/c小鼠每天单独或联合给予地西泮和甲基苯丙胺(各5mg/kg),连续5天,随后用卵清蛋白(OVA)致敏。两天后,重复相同的给药和致敏方案一次。在第二次OVA致敏后7天,测量血清抗OVA抗体的产生以及脾细胞的细胞数量和功能活性。结果表明,甲基苯丙胺和/或地西泮显著减弱了OVA特异性IgM、IgG(1)和IgG(2a)的产生。与此一致的是,与载体处理的对照组相比,用OVA体外再刺激时,给予地西泮和/或甲基苯丙胺的小鼠的脾细胞产生的IL-4和IFN-γ较少。相反,药物处理并未改变脾细胞的细胞数量和代谢活性。这些结果表明,中枢抑制剂地西泮不会影响甲基苯丙胺介导的免疫抑制。相反,两种药物均显著抑制抗原特异性抗体的产生和T细胞反应性。

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