Negative Effects of a High-Fat Diet on Intestinal Permeability: A Review

被引:508
作者
Rohr, Michael W. [1 ]
Narasimhulu, Chandrakala A. [1 ]
Rudeski-Rohr, Trina A. [1 ]
Parthasarathy, Sampath [1 ]
机构
[1] Univ Cent Florida, Coll Med, Burnett Sch Biomed Sci, Orlando, FL 32816 USA
关键词
high-fat diet; intestinal permeability; gut barrier; tight junction; inflammatory bowel disease; inflammation; bile acids; superficial unstirred mucus layer; shedding-proliferation axis; gut microbiota; INFLAMMATORY-BOWEL-DISEASE; TIGHT JUNCTION PERMEABILITY; BARRIER FUNCTION; INDUCED OBESITY; OXIDATIVE STRESS; GUT MICROBIOTA; URSODEOXYCHOLIC ACID; INSULIN-RESISTANCE; IL-1-BETA-INDUCED INCREASE; AKKERMANSIA-MUCINIPHILA;
D O I
10.1093/advances/nmz061
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The intestinal tract is the largest barrier between a person and the environment. In this role, the intestinal tract is responsible not only for absorbing essential dietary nutrients, but also for protecting the host from a variety of ingested toxins and microbes. The intestinal barrier system is composed of a mucus layer, intestinal epithelial cells (IECs), tight junctions (TJs), immune cells, and a gut microbiota, which are all susceptible to external factors such as dietary fats. When components of this barrier system are disrupted, intestinal permeability to luminal contents increases, which is implicated in intestinal pathologies such as inflammatory bowel disease, necrotizing enterocolitis, and celiac disease. Currently, there is mounting evidence that consumption of excess dietary fats can enhance intestinal permeability differentially. For example, dietary fat modulates the expression and distribution of TJs, stimulates a shift to barrier-disrupting hydrophobic bile acids, and even induces IEC oxidative stress and apoptosis. In addition, a high-fat diet (HFD) enhances intestinal permeability directly by stimulating proinflammatory signaling cascades and indirectly via increasing barrier-disrupting cytokines [TNF alpha, interleukin (IL) 1B, IL6, and interferon gamma (IFN gamma)] and decreasing barrier-forming cytokines (IL10, IL17, and IL22). Finally, an HFD negatively modulates the intestinal mucus composition and enriches the gut microflora with barrier-disrupting species. Although further research is necessary to understand the precise role HFDs play in intestinal permeability, current data suggest a stronger link between diet and intestinal disease than was first thought to exist. Therefore, this review seeks to highlight the various ways an HFD disrupts the gut barrier system and its many implications in human health.
引用
收藏
页码:77 / 91
页数:15
相关论文
共 167 条
  • [81] Reciprocal modulation of toll-like receptor-4 signaling pathways involving MyD88 and phosphatidylinositol 3-kinase/AKT by saturated and polyunsaturated fatty acids
    Lee, JY
    Ye, JP
    Gao, ZG
    Youn, HS
    Lee, WH
    Zhao, L
    Sizemore, N
    Hwang, DH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (39) : 37041 - 37051
  • [82] Bile Acid Malabsorption in Inflammatory Bowel Disease: Assessment by Serum Markers
    Lenicek, Martin
    Duricova, Dana
    Komarek, Viktor
    Gabrysova, Bronislava
    Lukas, Milan
    Smerhovsky, Zdenek
    Vitek, Libor
    [J]. INFLAMMATORY BOWEL DISEASES, 2011, 17 (06) : 1322 - 1327
  • [83] Microbial ecology - Human gut microbes associated with obesity
    Ley, Ruth E.
    Turnbaugh, Peter J.
    Klein, Samuel
    Gordon, Jeffrey I.
    [J]. NATURE, 2006, 444 (7122) : 1022 - 1023
  • [84] Direct anodic hydrochloric acid and cathodic caustic production during water electrolysis
    Lin, Hui-Wen
    Cejudo-Marin, Rocio
    Jeremiasse, Adriaan W.
    Rabaey, Korneel
    Yuan, Zhiguo
    Pikaar, Ilje
    [J]. SCIENTIFIC REPORTS, 2016, 6
  • [85] Protective Effects of Bifidobacterium on Intestinal Barrier Function in LPS-Induced Enterocyte Barrier Injury of Caco-2 Monolayers and in a Rat NEC Model
    Ling, Xiang
    Peng Linglong
    Du Weixia
    Hong, Wei
    [J]. PLOS ONE, 2016, 11 (08):
  • [86] Increased epithelial gaps in the small intestines of patients with inflammatory bowel disease: density matters
    Liu, Julia J.
    Wong, Karen
    Thiesen, Aducio L.
    Mah, Stephanie J.
    Dieleman, Levinus A.
    Claggett, Brian
    Saltzman, John R.
    Fedorak, Richard N.
    [J]. GASTROINTESTINAL ENDOSCOPY, 2011, 73 (06) : 1174 - 1180
  • [87] Interleukin-10 Enhances the Intestinal Epithelial Barrier in the Presence of Corticosteroids through p38 MAPK Activity in Caco-2 Monolayers: A Possible Mechanism for Steroid Responsiveness in Ulcerative Colitis
    Loren, Violeta
    Cabre, Eduard
    Ojanguren, Isabel
    Domenech, Eugeni
    Pedrosa, Elisabet
    Garcia-Jaraquemada, Arce
    Manosa, Miriam
    Manye, Josep
    [J]. PLOS ONE, 2015, 10 (06):
  • [88] High Beta-Palmitate Fat Controls the Intestinal Inflammatory Response and Limits Intestinal Damage in Mucin Muc2 Deficient Mice
    Lu, Peng
    Bar-Yoseph, Fabiana
    Levi, Liora
    Lifshitz, Yael
    Witte-Bouma, Janneke
    de Bruijn, Adrianus C. J. M.
    Korteland-van Male, Anita M.
    van Goudoever, Johannes B.
    Renes, Ingrid B.
    [J]. PLOS ONE, 2013, 8 (06):
  • [89] Regulation of Obesity-Related Insulin Resistance with Gut Anti-inflammatory Agents
    Luck, Helen
    Tsai, Sue
    Chung, Jason
    Clemente-Casares, Xavier
    Ghazarian, Magar
    Revelo, Xavier S.
    Lei, Helena
    Luk, Cynthia T.
    Shi, Sally Yu
    Surendra, Anuradha
    Copeland, Julia K.
    Ahn, Jennifer
    Prescott, David
    Rasmussen, Brittany A.
    Chng, Melissa Hui Yen
    Engleman, Edgar G.
    Girardin, Stephen E.
    Lam, Tony K. T.
    Croitoru, Kenneth
    Dunn, Shannon
    Philpott, Dana J.
    Guttman, David S.
    Woo, Minna
    Winer, Shawn
    Winer, Daniel A.
    [J]. CELL METABOLISM, 2015, 21 (04) : 527 - 542
  • [90] Role of STAT6 and mast cells in IL-4-and IL-13-induced alterations in murine intestinal epithelial cell function
    Madden, KB
    Whitman, L
    Sullivan, C
    Gause, WC
    Urban, JF
    Katona, IM
    Finkelman, FD
    Shea-Donohue, T
    [J]. JOURNAL OF IMMUNOLOGY, 2002, 169 (08) : 4417 - 4422