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白细胞介素-2对DBA/2小鼠各种实验性癫痫模型的影响。

Effects of interleukin-2 on various models of experimental epilepsy in DBA/2 mice.

作者信息

De Sarro G, Rotiroti D, Audino M G, Gratteri S, Nisticó G

机构信息

Department of Experimental and Clinical Medicine, Faculty of Medicine, University of Reggio Calabria, Catanzaro.

出版信息

Neuroimmunomodulation. 1994 Nov-Dec;1(6):361-9. doi: 10.1159/000097189.

Abstract

The effects of interleukin-2 (IL-2) on various models of experimental epilepsy were studied after intracerebroventricular administration in DBA/2 mice, a strain genetically susceptible to sound-induced seizures. Convulsions were induced by physical stimulus (sound of 109 dB. 12-16 kHz) or by chemical compounds (bicuculline, cephazolin or kainate). The present study demonstrated that human recombinant IL-2 (hr-IL-2) and mouse recombinant IL-2 (mr-IL-2) not only did not antagonize audiogenic seizures in DBA/2 mice but increased the incidence of seizures after the highest doses studied. In addition, hr-IL-2 and mr-IL-2 dose dependently facilitated sound-induced seizures at subthreshold sound exposure (83 dB). Pretreatment with monoclonal rat-antimouse IL-2 antibodies significantly affected the changes of occurrence of audiogenic seizures in DBA/2 mice induced by mr-IL-2. In addition, pretreatment with anti-IL-2 receptor monoclonal antibodies (anti-Tac) was able to completely antagonize or reduce the effects of IL-2 on audiogenic seizures. The effects of mr-IL-2 were also studied in two different models of epilepsy: the bicuculline and cephazolin models, due to impairment of GABAergic transmission, and the kainate model, due to an increase in excitatory amino acid transmission. In all models, mr-IL-2 demonstrated to facilitate the seizures induced by these chemoconvulsants. Since the proconvulsant properties of IL-2 were antagonized by specific monoclonal antibodies, we suggest that some epileptic phenomena may be linked to stimulation of IL-2 receptors.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在对声音诱发癫痫遗传易感的DBA/2小鼠脑室内注射白细胞介素-2(IL-2)后,研究了其对各种实验性癫痫模型的影响。通过物理刺激(109分贝、12 - 16千赫的声音)或化合物(荷包牡丹碱、头孢唑林或海藻酸)诱发惊厥。本研究表明,人重组IL-2(hr-IL-2)和小鼠重组IL-2(mr-IL-2)不仅不能拮抗DBA/2小鼠的听源性惊厥,反而在研究的最高剂量后增加了惊厥的发生率。此外,hr-IL-2和mr-IL-2在阈下声音暴露(83分贝)时剂量依赖性地促进声音诱发的惊厥。用单克隆大鼠抗小鼠IL-2抗体预处理显著影响了mr-IL-2诱导的DBA/2小鼠听源性惊厥发生的变化。此外,用抗IL-2受体单克隆抗体(抗Tac)预处理能够完全拮抗或降低IL-2对听源性惊厥的影响。还在两种不同的癫痫模型中研究了mr-IL-2的作用:由于GABA能传递受损的荷包牡丹碱和头孢唑林模型,以及由于兴奋性氨基酸传递增加的海藻酸模型。在所有模型中,mr-IL-2均显示促进这些化学惊厥剂诱发的惊厥。由于IL-2的促惊厥特性被特异性单克隆抗体拮抗,我们认为某些癫痫现象可能与IL-2受体的刺激有关。(摘要截短至250字)

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