Zalcman S S
Department of Psychiatry and Rutgers/UMDNJ Integrative Neuroscience Program, UMD-New Jersey Medical School, Medical Science Building, E-503, 185 S. Orange Ave., Newark, NJ 07103-2714, USA.
Brain Res. 2001 Apr 27;899(1-2):1-9. doi: 10.1016/s0006-8993(01)02090-x.
Interleukin (IL)-2 is a cytokine that influences exploratory behavior and central dopamine activity in rodents, and induces schizophrenic-like behavior and cognitive deficits in humans. We presently report that a single i.p. injection of murine IL-2 (0.05-0.80 microg/mouse) induced significant increases in novelty-induced locomotion and exploration in BALB/c mice. These measures were not significantly altered in mice that were pre-exposed to the test cage prior to cytokine injection. The IL-2-induced behavioral changes were not further augmented by repeated intermittent injections (five daily i.p. injections; 0.4 microg/mouse), however. Nonetheless, during the treatment period, activity scores of IL-2-treated mice significantly exceeded those of mice receiving saline; hence, repeated injections of IL-2 induced a persistent behavioral activation. IL-2 treatment also increased sensitivity to the behavior-stimulating effects of GBR 12909, a highly selective dopamine uptake inhibitor. This effect was a very long-lasting one since the dopamine agonist was administered 6 weeks after cessation of IL-2 treatment. The latter finding indicates that IL-2 interacts with the mesolimbic dopamine system, changing its sensitivity to seemingly different substances. Based on these data, and those of Zalcman and colleagues (S. Zalcman, I. Savina, R.A. Wise, Interleukin-6 increases sensitivity to the locomotor-stimulating effects of amphetamine in rats, Brain Res. 847 (1999) 276-283), it is suggested that cytokines can influence the development of behavioral abnormalities that are characteristic of aberrant mesolimbic dopamine activity via sensitization-like processes.
白细胞介素(IL)-2是一种细胞因子,可影响啮齿动物的探索行为和中枢多巴胺活性,并在人类中诱发精神分裂症样行为和认知缺陷。我们目前报告,单次腹腔注射小鼠IL-2(0.05 - 0.80微克/小鼠)可显著增加BALB/c小鼠的新奇诱导运动和探索行为。在细胞因子注射前预先暴露于测试笼的小鼠中,这些指标没有显著变化。然而,重复间歇性注射(每日腹腔注射五次;0.4微克/小鼠)并没有进一步增强IL-2诱导的行为变化。尽管如此,在治疗期间,IL-2处理小鼠的活动得分显著超过接受生理盐水的小鼠;因此,重复注射IL-2可诱导持续的行为激活。IL-2处理还增加了对GBR 12909(一种高度选择性多巴胺摄取抑制剂)行为刺激作用的敏感性。由于多巴胺激动剂在IL-2治疗停止6周后给药,这种作用持续时间非常长。后一发现表明IL-2与中脑边缘多巴胺系统相互作用,改变其对看似不同物质的敏感性。基于这些数据以及Zalcman及其同事的数据(S. Zalcman,I. Savina,R.A. Wise,白细胞介素-6增加大鼠对苯丙胺运动刺激作用的敏感性,《脑研究》847(1999)276 - 283),提示细胞因子可通过类似致敏的过程影响中脑边缘多巴胺活性异常所特有的行为异常的发展。