Roberts H C, Hardie L J, Chappell L H, Mercer J G
Rowett Research Institute, Bucksburn, Aberdeen, UK.
Parasitology. 1999 Jan;118 ( Pt 1):117-23. doi: 10.1017/s0031182098003503.
The nematode parasite, Nippostrongylus brasiliensis, induces a biphasic anorexia in its rat host. The mechanisms, underlying this anorexia and its possible advantages to the host or parasite are unknown. We have investigated the effect of acute (12-24 h) and chronic (2-17 days) infections on plasma concentrations of leptin, insulin and corticosterone, and on hypothalamic expression of neuropeptide Y, galanin and corticotrophin-releasing factor genes. Plasma leptin was elevated in infected rats relative to uninfected ad libitum-fed controls and pair-fed controls in 12 h infections initiated at dark onset and in infections of 2 days' duration. At other times prior to parasite expulsion, plasma leptin in infected and pair-fed rats was lower than that of uninfected ad libitum-fed controls, reflecting the existing state of negative energy balance. Elevated plasma leptin concentrations in infected rats at day 2 post-infection were accompanied by reduced neuropeptide Y gene expression in the hypothalamic arcuate nucleus compared with both ad libitum control and pair-fed animals, and by lowered corticotrophin-releasing factor gene expression in the paraventricular nucleus relative to pair-feds. Twelve hour infections were characterized by a substantial increase in plasma corticosterone that was independent of reduced food intake, and in 12 h infections initiated at dark onset, where plasma leptin was elevated, there was also increased plasma insulin concentration in infected rats. In longer infections, differences between the groups in plasma insulin and corticosterone concentration were only observed at day 4 post-infection. In summary, perturbations to leptin, insulin and corticosterone signals early in infection may have a causative role and might feed back onto hypothalamic gene expression, whereas subsequent changes in these parameters are more likely to be secondary to negative energy balance.
巴西日圆线虫这种线虫寄生虫会在其大鼠宿主中引发双相厌食症。这种厌食症背后的机制以及它对宿主或寄生虫可能存在的优势尚不清楚。我们研究了急性(12 - 24小时)和慢性(2 - 17天)感染对瘦素、胰岛素和皮质酮血浆浓度,以及对神经肽Y、甘丙肽和促肾上腺皮质激素释放因子基因在下丘脑表达的影响。与未感染的自由采食对照组和配对喂食对照组相比,在黑暗开始时开始的12小时感染以及持续2天的感染中,感染大鼠的血浆瘦素升高。在寄生虫排出之前的其他时间,感染和配对喂食大鼠的血浆瘦素低于未感染的自由采食对照组,这反映了现有的负能量平衡状态。与自由采食对照组和配对喂食动物相比,感染后第2天感染大鼠血浆瘦素浓度升高,同时下丘脑弓状核中神经肽Y基因表达降低,相对于配对喂食组,室旁核中促肾上腺皮质激素释放因子基因表达降低。12小时感染的特征是血浆皮质酮大幅增加,这与食物摄入量减少无关,并且在黑暗开始时开始的12小时感染中,血浆瘦素升高,感染大鼠的血浆胰岛素浓度也增加。在更长时间的感染中,仅在感染后第4天观察到各组之间血浆胰岛素和皮质酮浓度的差异。总之,感染早期瘦素、胰岛素和皮质酮信号的扰动可能具有因果作用,并可能反馈到下丘脑基因表达上,而这些参数随后的变化更可能是负能量平衡的继发结果。