Swiergiel Artur H, Dunn Adrian J
Department of Pharmacology, Toxicology and Neuroscience, Louisiana State University Health Sciences Center, Shreveport, P.O. Box 33932, Louisiana, USA.
Pharmacol Biochem Behav. 2007 Apr;86(4):651-9. doi: 10.1016/j.pbb.2007.02.010. Epub 2007 Feb 16.
It has been postulated that infections, inflammatory processes and resulting cytokines may be causative factors in emotional disorders, including depression and anxiety. Support for this possibility has been sought in studies of animal behavior following administration of interleukin-1 (IL-1) and lipopolysaccharide (LPS). However, such treatments induce a variety of behavioral responses, collectively known as sickness behavior, some of which could affect the performance in tests used to assess anxiety and depression. Thus the effects of peripheral administration of IL-1beta and LPS on the behavior of mice were studied in the elevated plus-maze (EPM) and the open field (OF). Mouse IL-1beta (30, 100, 300, and 1000 ng) was injected intraperitoneally 30 or 60 min, and LPS (0.5, 1 and 5 microg) 120 min before the tests. IL-1beta and LPS induced dose-dependent decreases in open arm entries and the time spent on the open arms in the EPM, effects considered to reflect anxiety-like behavior. However, entries to all arms were also reduced in a dose-dependent manner, indicating a decrease in general activity. In the OF, IL-1beta and LPS decreased the number of line crossings in the center of the field, that can also be considered to reflect anxiety-like behavior. However, this effect was accompanied by a similar decrease in line crossings in the periphery, as well as in rears and climbs. Thus the doses of IL-1beta and LPS necessary to induce these effects also decreased locomotor activity in the EPM and OF. Therefore, the behavioral responses induced by IL-1beta and LPS in the EPM and the OF considered to reflect anxiety must be interpreted in the light of this reduction in overall activity. Thus the results do not provide unequivocal support for the suggestion that LPS or IL-1 mediate anxiety. Nevertheless, because infections, endotoxins, and the ensuing cytokines cause alterations in CNS norepinephrine and serotonin, they may contribute to emotionality, and perhaps to anxiety.
据推测,感染、炎症过程以及由此产生的细胞因子可能是包括抑郁症和焦虑症在内的情绪障碍的致病因素。人们通过对白介素-1(IL-1)和脂多糖(LPS)给药后动物行为的研究来探寻这种可能性的证据。然而,此类处理会引发多种行为反应,统称为疾病行为,其中一些可能会影响用于评估焦虑和抑郁的测试表现。因此,我们在高架十字迷宫(EPM)和旷场实验(OF)中研究了腹腔注射IL-1β和LPS对小鼠行为的影响。在测试前30或60分钟腹腔注射小鼠IL-1β(30、100、300和1000纳克),在测试前120分钟注射LPS(0.5、1和5微克)。IL-1β和LPS使EPM中进入开放臂的次数和在开放臂上停留的时间呈剂量依赖性减少,这些效应被认为反映了类似焦虑的行为。然而,进入所有臂的次数也呈剂量依赖性减少,表明总体活动减少。在旷场实验中,IL-1β和LPS减少了场地中央的穿线次数,这也可被认为反映了类似焦虑的行为。然而,这种效应伴随着周边穿线次数以及站立和攀爬次数的类似减少。因此,诱导这些效应所需的IL-1β和LPS剂量也降低了EPM和旷场实验中的运动活性。因此,必须根据整体活动的这种减少来解释IL-1β和LPS在EPM和旷场实验中诱导的被认为反映焦虑的行为反应。因此,这些结果并未为LPS或IL-1介导焦虑这一观点提供明确支持。尽管如此,由于感染、内毒素以及随之产生的细胞因子会导致中枢神经系统去甲肾上腺素和血清素的改变,它们可能会影响情绪,甚至可能导致焦虑。