Pierre Joseph F, Heneghan Aaron F, Feliciano Rodrigo P, Shanmuganayagam Dhanansayan, Krueger Christian G, Reed Jess D, Kudsk Kenneth A
Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
JPEN J Parenter Enteral Nutr. 2014 Jan;38(1):107-14. doi: 10.1177/0148607112473654. Epub 2013 Jan 28.
Elemental enteral nutrition (EEN) decreases gut-associated lymphoid tissue (GALT) function, including fewer Peyer's patch lymphocytes and lower levels of the tissue T helper 2 (Th2) cytokines and mucosal transport protein polymeric immunoglobulin receptor (pIgR), leading to lower luminal secretory immunoglobulin A (sIgA) levels. Since we recently demonstrated that cranberry proanthocyanidins (PACs) maintain the Th2 cytokine interleukin (IL)-4 when added to EEN, we hypothesized the addition of PACs to EEN would normalize other GALT parameters and maintain luminal levels of sIgA.
Institute of Cancer Research mice were randomized (12/group) to receive chow, EEN, or EEN + PACs (100 mg/kg body weight) for 5 days, starting 2 days after intragastric cannulation. Ileum tissue was collected to measure IL-4 by enzyme-linked immunosorbent assay, pIgR by Western blot, and phosphorylated STAT-6 by microarray. Intestinal wash fluid was collected to measure sIgA by Western blot.
Compared with chow, EEN significantly decreased tissue IL-4, phosphorylated STAT-6, and pIgR. The addition of PACs to EEN prevented these alterations. Compared with chow, EEN resulted in significantly lower levels of luminal sIgA. The addition of PACs to EEN increased luminal sIgA levels compared with EEN alone.
This study suggests the addition of PACs to EEN may support GALT function and maintain intestinal sIgA levels compared with EEN administration alone.
要素肠内营养(EEN)会降低肠道相关淋巴组织(GALT)的功能,包括派尔集合淋巴结淋巴细胞数量减少、组织辅助性T细胞2(Th2)细胞因子水平降低以及黏膜转运蛋白多聚免疫球蛋白受体(pIgR)水平降低,从而导致肠腔分泌型免疫球蛋白A(sIgA)水平降低。由于我们最近证明,蔓越莓原花青素(PACs)添加到EEN中时可维持Th2细胞因子白细胞介素(IL)-4水平,因此我们推测,在EEN中添加PACs可使其他GALT参数恢复正常,并维持肠腔sIgA水平。
将癌症研究所的小鼠(每组12只)随机分组,在胃内插管2天后开始,分别给予普通饲料、EEN或EEN + PACs(100 mg/kg体重),持续5天。收集回肠组织,通过酶联免疫吸附测定法测量IL-4水平,通过蛋白质印迹法测量pIgR水平,通过微阵列测量磷酸化信号转导和转录激活因子6(STAT-6)。收集肠道冲洗液,通过蛋白质印迹法测量sIgA。
与普通饲料组相比,EEN显著降低了组织IL-4、磷酸化STAT-6和pIgR水平。在EEN中添加PACs可防止这些改变。与普通饲料组相比,EEN导致肠腔sIgA水平显著降低。与单独使用EEN相比,在EEN中添加PACs可提高肠腔sIgA水平。
本研究表明,与单独给予EEN相比,在EEN中添加PACs可能有助于维持GALT功能并保持肠道sIgA水平。