Urbach-Ross Daniella, Crowell Beth, Kusnecov Alexander W
Joint Graduate Program in Toxicology, Rutgers University, Piscataway, NJ, United States.
J Neuroimmunol. 2008 May 30;196(1-2):49-59. doi: 10.1016/j.jneuroim.2008.02.006. Epub 2008 Apr 14.
Staphylococcal enterotoxin A (SEA) is a superantigen that stimulates T cells and induces the production of multiple cytokines. Previous studies have shown that SEA augments gustatory neophobia and activates the hypothalamic-pituitary-adrenal (HPA) axis. This study aimed to determine if the cytokine response, behavioral effects, and HPA axis activation persisted after repeated SEA treatment. Male C57BL/6J mice were given 1-4 intraperitoneal injections of 5 microg SEA, after which food intake, corticosterone, or peripheral cytokines were measured. In a series of experiments, it was found that secondary exposure to SEA two or three days after priming increased corticosterone, but attenuated splenic TNFalpha, while augmenting IL-1beta, IL-2, and IFNgamma. The anorexic response was intact after secondary exposure, but absent after a third injection, which was still able to elevate corticosterone. It is unlikely that IL-1 mediated the persistent effects on corticosterone, since this was increased in groups lacking corticosterone elevations. Similarly, TNFalpha was only modestly elevated under repeated SEA conditions that elevated plasma corticosterone. This attenuation appeared to be inversely related to the levels of IL-10, the production of which incrementally rose with each successive injection. In conclusion, repeated exposure to SEA activates the HPA axis and alters behavior. However, there may be dissociation between the behavioral and endocrine effects of SEA with increased SEA exposure. Furthermore, it is possible that while TNFalpha was previously shown to be important in response to acute SEA-induced HPA axis activation, further exposure to SEA elicits other cytokines that may exert neuromodulatory effects through sensitization and/or synergistic mechanisms.
葡萄球菌肠毒素A(SEA)是一种超抗原,可刺激T细胞并诱导多种细胞因子的产生。先前的研究表明,SEA会加剧味觉性新恐惧症并激活下丘脑-垂体-肾上腺(HPA)轴。本研究旨在确定重复SEA治疗后细胞因子反应、行为影响和HPA轴激活是否持续存在。给雄性C57BL/6J小鼠腹腔注射1至4次5微克SEA,之后测量食物摄入量、皮质酮或外周细胞因子。在一系列实验中发现,初次注射后两到三天再次接触SEA会增加皮质酮,但会减弱脾脏肿瘤坏死因子α(TNFα),同时增加白细胞介素-1β(IL-1β)、白细胞介素-2和干扰素γ(IFNγ)。再次接触后厌食反应依然存在,但第三次注射后则消失,而第三次注射仍能升高皮质酮。IL-1不太可能介导对皮质酮的持续影响,因为在皮质酮未升高的组中其水平也升高了。同样,在重复SEA处理使血浆皮质酮升高的情况下,TNFα仅适度升高。这种减弱似乎与IL-10的水平呈负相关,IL-10的产生随着每次连续注射而逐渐增加。总之,重复接触SEA会激活HPA轴并改变行为。然而,随着SEA接触增加,SEA的行为和内分泌效应之间可能存在分离。此外,虽然先前已证明TNFα在急性SEA诱导的HPA轴激活反应中很重要,但进一步接触SEA会引发其他细胞因子,这些细胞因子可能通过致敏和/或协同机制发挥神经调节作用。