Wong Tracie, Hildebrandt Marie A, Thrasher Seana M, Appleton Judith A, Ahima Rexford S, Wu Gary D
Division of Gastroenterology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Gastroenterology. 2007 Dec;133(6):1979-88. doi: 10.1053/j.gastro.2007.09.006. Epub 2007 Sep 14.
BACKGROUND & AIMS: Diet-induced obesity results from increased ingestion of energy-dense food and sedentary lifestyle in genetically susceptible individuals. An environmental factor that may have shaped our energy homeostasis throughout evolution is parasitic nematode infection.
To test the hypothesis that a metabolically "thrifty phenotype" is advantageous during intestinal nematode infection, we compared the responses to Heligmosomoides polygyrus infection between 2 mouse strains: obesity-prone C57Bl/6J vs obesity-resistant SWR/J. Metabolic phenotyping was performed using indirect calorimetry, dual energy x-ray absorptiometry, and magnetic resonance imaging scanning. Gene expression was assessed by quantitative reverse-transcription polymerase chain reaction and immunohistochemistry.
Body weight was maintained in both strains during nematode infection via different mechanisms. There was no apparent change in energy expenditure between the strains; however, SWR/J mice exhibited a marked hyperphagia (calorie intake 60% higher than C57Bl/6J) to maintain body weight. The importance of hyperphagia was confirmed by severe weight loss in a group of infected SWR/J mice whose food intake was restricted to that of naïve mice. Furthermore, SWR/J mice expelled nematodes more rapidly than C57Bl/6J mice, an effect related to a T helper cell 2 immune response.
C57Bl/6J mice are more energy efficient during parasitic nematode infection, which may explain their ability to tolerate the infection. SWR/J mice, on the other hand, require an increase in food intake to maintain energy stores during nematode infection. In addition, a strong T helper cell 2-mediated immune response that facilitates a prompt clearance of nematode infection in SWR/J mice may have evolved to conserve energy in this strain.
在遗传易感性个体中,饮食诱导的肥胖是由于摄入高热量食物增加和久坐不动的生活方式所致。在整个进化过程中,可能塑造我们能量平衡的一个环境因素是寄生线虫感染。
为了验证代谢“节俭表型”在肠道线虫感染期间具有优势这一假设,我们比较了两种小鼠品系对多房棘球绦虫感染的反应:易肥胖的C57Bl/6J小鼠与抗肥胖的SWR/J小鼠。使用间接量热法、双能X线吸收法和磁共振成像扫描进行代谢表型分析。通过定量逆转录聚合酶链反应和免疫组织化学评估基因表达。
在感染线虫期间,两种品系的体重均通过不同机制得以维持。品系间能量消耗无明显变化;然而,SWR/J小鼠表现出明显的食欲亢进(热量摄入比C57Bl/6J小鼠高60%)以维持体重。一组食物摄入量限制在未感染小鼠水平的感染SWR/J小鼠出现严重体重减轻,证实了食欲亢进的重要性。此外,SWR/J小鼠排出线虫的速度比C57Bl/6J小鼠更快,这一效应与辅助性T细胞2免疫反应有关。
C57Bl/6J小鼠在寄生线虫感染期间能量利用效率更高,这可能解释了它们耐受感染的能力。另一方面,SWR/J小鼠在感染线虫期间需要增加食物摄入量以维持能量储备。此外,SWR/J小鼠中促进线虫感染迅速清除的强大辅助性T细胞2介导的免疫反应可能已经进化,以在该品系中保存能量。