Dunn Adrian J
Department of Pharmacology, Toxicology and Neuroscience, Louisiana State University Health Sciences Center, 1501 Kings Highway, P.O. Box 33932, Shreveport, LA 71130-3932, USA.
Clin Neurosci Res. 2006 Aug;6(1-2):52-68. doi: 10.1016/j.cnr.2006.04.002.
Administration of cytokines to animals can elicit many effects on the brain, particularly neuroendocrine and behavioral effects. Cytokine administration also alters neurotransmission, which may underlie these effects. The most well studied effect is the activation of the hypothalamo-pituitary-adrenocortical (HPA) axis, especially that by interleukin-1 (IL-1). Peripheral and central administration of IL-1 also induces norepinephrine (NE) release in the brain, most markedly in the hypothalamus. Small changes in brain dopamine (DA) are occasionally observed, but these effects are not regionally selective. IL-1 also increases brain concentrations of tryptophan, and the metabolism of serotonin (5-HT) throughout the brain in a regionally nonselective manner. Increases of tryptophan and 5-HT, but not NE, are also elicited by IL-6, which also activates the HPA axis, although it is much less potent in these respects than IL-1. IL-2 has modest effects on DA, NE and 5-HT. Like IL-6, tumor necrosis factor-α (TNFα) activates the HPA axis, but affects NE and tryptophan only at high doses. The interferons (IFN's) induce fever and HPA axis activation in man, but such effects are weak or absent in rodents. The reported effects of IFN's on brain catecholamines and serotonin have been very varied. However, interferon-γ, and to a lesser extent, interferon-α, have profound effects on the catabolism of tryptophan, effectively reducing its concentration in plasma, and may thus limit brain 5-HT synthesis.Administration of endotoxin (LPS) elicits responses similar to those of IL-1. Bacterial and viral infections induce HPA activation, and also increase brain NE and 5-HT metabolism and brain tryptophan. Typically, there is also behavioral depression. These effects are strikingly similar to those of IL-1, suggesting that IL-1 secretion, which accompanies many infections, may mediate these responses. Studies with IL-1 antagonists, support this possibility, although in most cases the antagonism is incomplete, suggesting the existence of multiple mechanisms. Because LPS is known to stimulate the secretion of IL-1, IL-6 and TNFα, it seems likely that these cytokines mediate at least some of the responses, but studies with antagonists indicate that there are multiple mechanisms. The neurochemical responses to cytokines are likely to underlie the endocrine and behavioral responses. The NE response to IL-1 appears to be instrumental in the HPA activation, but other mechanisms exist. Neither the noradrenergic nor the serotonergic systems appear to be involved in the major behavioral responses. The significance of the serotonin response is unknown.
给动物注射细胞因子可对大脑产生多种影响,尤其是神经内分泌和行为方面的影响。细胞因子的注射还会改变神经传递,这可能是这些影响的基础。研究得最充分的影响是下丘脑 - 垂体 - 肾上腺皮质(HPA)轴的激活,尤其是白细胞介素 -1(IL -1)所引起的激活。外周和中枢注射IL -1也会诱导大脑中去甲肾上腺素(NE)的释放,在下丘脑中最为明显。偶尔会观察到大脑多巴胺(DA)有微小变化,但这些影响没有区域选择性。IL -1还会增加大脑中色氨酸的浓度,并以区域非选择性的方式促进全脑血清素(5 - HT)的代谢。IL -6也会引起色氨酸和5 - HT的增加,但不会引起NE的增加,它也会激活HPA轴,尽管在这些方面其效力远低于IL -1。IL -2对DA、NE和5 - HT有适度影响。与IL -6一样,肿瘤坏死因子 -α(TNFα)会激活HPA轴,但仅在高剂量时才会影响NE和色氨酸。干扰素(IFN)在人类中会诱导发热和HPA轴激活,但在啮齿动物中这种影响较弱或不存在。关于IFN对大脑儿茶酚胺和血清素的报道影响差异很大。然而,干扰素 -γ以及程度稍轻的干扰素 -α,对色氨酸的分解代谢有深远影响,有效降低其血浆浓度,因此可能会限制大脑5 - HT的合成。注射内毒素(LPS)会引发与IL -1类似的反应。细菌和病毒感染会诱导HPA激活,还会增加大脑NE和5 - HT的代谢以及大脑色氨酸含量。通常还会出现行为抑郁。这些影响与IL -1的影响惊人地相似,表明许多感染时伴随的IL -1分泌可能介导了这些反应。使用IL -1拮抗剂的研究支持了这种可能性,尽管在大多数情况下拮抗作用并不完全,这表明存在多种机制。由于已知LPS会刺激IL -1、IL -6和TNFα的分泌,这些细胞因子似乎很可能介导了至少部分反应,但使用拮抗剂的研究表明存在多种机制。对细胞因子的神经化学反应可能是内分泌和行为反应的基础。对IL -1的NE反应似乎在HPA激活中起作用,但其他机制也存在。去甲肾上腺素能和血清素能系统似乎都不参与主要的行为反应。血清素反应的意义尚不清楚。