Swiergiel A H, Smagin G N, Dunn A J
Department of Pharmacology and Therapeutics, Louisiana State University Medical Center, Shreveport 71103, USA.
Pharmacol Biochem Behav. 1997 May-Jun;57(1-2):389-96. doi: 10.1016/s0091-3057(96)00335-8.
The effects of infection of mice with influenza virus on ingestive behavior were assessed by both 22-h intake of food pellets, and intake of sweetened milk in a 30-minute access period. Infection with a lethal dose of virus resulted in losses in body weight as well as a reduction in food pellet intake. By contrast, infection with a sublethal dose of virus decreased body weight and food pellet intake to a lesser extent, but did not alter milk intake. Acute intraperitoneal injection of endotoxin (LPS, 0.3-5 micrograms), interleukin-1 alpha (IL-1 alpha, 50-100 ng) or IL-1 beta (100 ng) reduced milk intake, suggesting that the reduction of ingestive behavior may be associated with immune activation in general, and IL-1 in particular Pretreatment of the mice with the cyclooxygenase inhibitor, indomethacin (10 mg/kg SC) substantially attenuated, but did not completely reverse, the reduction in milk intake by LPS and IL-1. However, chronic treatment with indomethacin failed to alter the body weight or the intake of sweetened milk in influenza-infected mice, although there was some attenuation of the reduction in food intake. These results suggest that although IL-1 may play a role in the anorexia caused by influenza virus infection, it is not the only factor involved.
通过测量小鼠22小时内的食丸摄入量以及在30分钟进食期内的甜牛奶摄入量,评估感染流感病毒对小鼠摄食行为的影响。感染致死剂量的病毒会导致体重减轻以及食丸摄入量减少。相比之下,感染亚致死剂量的病毒会使体重和食丸摄入量下降幅度较小,但不会改变牛奶摄入量。急性腹腔注射内毒素(LPS,0.3 - 5微克)、白细胞介素-1α(IL-1α,50 - 100纳克)或IL-1β(100纳克)会减少牛奶摄入量,这表明摄食行为的减少可能总体上与免疫激活有关,特别是与IL-1有关。用环氧化酶抑制剂吲哚美辛(10毫克/千克,皮下注射)对小鼠进行预处理,可显著减轻但不能完全逆转LPS和IL-1引起的牛奶摄入量减少。然而长期用吲哚美辛治疗并不能改变流感感染小鼠的体重或甜牛奶摄入量,尽管食物摄入量减少有一定程度的减轻。这些结果表明,虽然IL-1可能在流感病毒感染引起的厌食中起作用,但它不是唯一涉及的因素。