Olivé A P, Dudley M, Harari Y, Dudley A, Castro G A, Lifschitz C H
Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
J Pediatr Gastroenterol Nutr. 1999 Mar;28(3):276-81. doi: 10.1097/00005176-199903000-00012.
Fish oil has been recommended as a source of omega-3 fatty acids for preterm infants and for therapy of some inflammatory diseases.
Because fish oil supplementation could downregulate the host's immune response, we studied the gut inflammatory response to an enteric infection in 72 rats assigned to three dietary groups with differing fatty acid profile: 1) fish oil, rich in eicosapentaenoic and docosahexaenoic acid; 2) olive oil, containing 71% monounsaturated fat; and 3) rat chow, containing 57% saturated fat. One half (n = 36) of the rats were infected with Trichinella spiralis larvae; the other half served as controls. The inflammatory response to initial infection (study 1), and type I hypersensitivity response to a subsequent parasite-derived antigenic challenge (study 2) were assessed. Jejunal inflammatory cell infiltrate, mean villus height, disaccharidase levels, changes in short-circuit current in response to glucose absorption, and chloride secretagogues (study 1) were measured 9 days after infection. Short-circuit current changes induced by chloride secretion were measured when the proximal jejunum was challenged with T. spiralis-derived antigen 40 days after infection (study 2).
In study 1, jejunal tissue from infected animals had more eosinophilic infiltrate, lower disaccharidase levels, and less glucose absorptive and chloride secretory capacity than tissue from noninfected animals. In study 2, the jejunum of infected animals showed an antigen-induced chloride secretory response, whereas no response was obtained from jejunal tissue from noninfected animals. Type of diet did not affect the response in either study.
Under the conditions of this experiment, fish oil supplementation did not interfere with the local intestinal inflammatory response after T. spiralis infection.
鱼油已被推荐作为早产婴儿omega-3脂肪酸的来源以及某些炎症性疾病的治疗手段。
由于补充鱼油可能会下调宿主的免疫反应,我们研究了72只大鼠对肠道感染的肠道炎症反应,这些大鼠被分为三个脂肪酸组成不同的饮食组:1)富含二十碳五烯酸和二十二碳六烯酸的鱼油组;2)含71%单不饱和脂肪的橄榄油组;3)含57%饱和脂肪的大鼠饲料组。一半(n = 36)的大鼠感染旋毛虫幼虫;另一半作为对照。评估了对初次感染的炎症反应(研究1)以及对随后寄生虫衍生抗原攻击的I型超敏反应(研究2)。在感染后9天测量空肠炎症细胞浸润、平均绒毛高度、双糖酶水平、葡萄糖吸收时短路电流的变化以及氯化物促分泌剂(研究1)。在感染后40天用旋毛虫衍生抗原攻击空肠近端时,测量氯化物分泌引起的短路电流变化(研究2)。
在研究1中,感染动物的空肠组织比未感染动物的组织有更多嗜酸性粒细胞浸润、更低的双糖酶水平以及更低的葡萄糖吸收和氯化物分泌能力。在研究2中,感染动物的空肠显示出抗原诱导的氯化物分泌反应,而未感染动物的空肠组织未获得反应。饮食类型在两项研究中均未影响反应。
在本实验条件下,补充鱼油不会干扰旋毛虫感染后局部肠道炎症反应。