Physiological concentrations of short-chain fatty acids immediately suppress colonic epithelial permeability

被引:293
作者
Suzuki, Takuya [1 ]
Yoshida, Shoko [1 ]
Hara, Hiroshi [1 ]
机构
[1] Hokkaido Univ, Grad Sch Agr, Div Appl Biosci, Sapporo, Hokkaido, Japan
关键词
SCFA; barrier function; tight junction; caecum; T84; cells; Caco-2;
D O I
10.1017/S0007114508888733
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
Colonic fermentation products, SCFA, have various effects on colonic functions. Here, we found that physiological concentrations of SCFA immediately promote epithelial barrier function in the large intestine. Solutions of mixed and individual SCFA were applied to the caecal walls mounted on Ussing-type chambers. Transepithelial electrical resistance (TER) increased rapidly and reached a peak 35% higher than that in the control specimen within 10 min post application of the SCFA mixture (80 acetate, 40 propionate, 20 butyrate (mmol/l)). The Lucifer yellow permeability, a paracellular transport market, was dose-dependently reduced by the mixed SCFA, acetate and propionate solutions. Inhibition of monocarboxylate transporter-1 did not influence the increase in TER with acetate; however, lowering the pH (from 7.5 to 5.5) clearly enhanced the effect of acetate. Non-metabolizable, bromo and chloro derivatives of SCFA also increased TER. These results suggest that passive diffusion of SCFA is dominant and the metabolism of SCFA is not required for the promotive effect of SCFA on barrier function. We also observed that individual SCFA dose-dependently increased TER in T84 and Caco-2 cells, which indicates that SCFA directly stimulate epithelial cells. Depletion of membrane cholesterol and inhibitors of phosphatidylinositol-3 kinase and Gq protein attenuated the acetate-mediated promotive effect. Finally, we found that the mucosal application of the SCFA mixture dose-dependently Suppressed [(3)H] mannitol transport from the caecal lumen to the mesenteric blood in the anaesthetized rats. We conclude that physiological concentrations of SCFA immediately enhance barrier function of the colonic epithelium through cholesterol-rich microdomain in the plasma membrane.
引用
收藏
页码:297 / 305
页数:9
相关论文
共 42 条
[1]   Mechanism of butyrate-induced vasorelaxation of rat mesenteric resistance artery [J].
Aaronson, PI ;
McKinnon, W ;
Poston, L .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 117 (02) :365-371
[2]   Promotive effects of non-digestible disaccharides on rat mineral absorption depend on the type of saccharide [J].
Asvarujanon, P ;
Ishizuka, S ;
Hara, H .
NUTRITION, 2005, 21 (10) :1025-1035
[3]   The orphan G protein-coupled receptors GPR41 and GPR43 are activated by propionate and other short chain carboxylic acids [J].
Brown, AJ ;
Goldsworthy, SM ;
Barnes, AA ;
Eilert, MM ;
Tcheang, L ;
Daniels, D ;
Muir, AI ;
Wigglesworth, MJ ;
Kinghorn, I ;
Fraser, NJ ;
Pike, NB ;
Strum, JC ;
Steplewski, KM ;
Murdock, PR ;
Holder, JC ;
Marshall, FH ;
Szekeres, PG ;
Wilson, S ;
Ignar, DM ;
Foord, SM ;
Wise, A ;
Dowell, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (13) :11312-11319
[4]   Structure and function of sphingolipid- and cholesterol-rich membrane rafts [J].
Brown, DA ;
London, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) :17221-17224
[5]   Nonionic diffusion of short-chain fatty acids across rat colon [J].
Charney, AN ;
Micic, L ;
Egnor, RW .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 274 (03) :G518-G524
[6]   Valproic acid and butyrate induce apoptosis in human cancer cells through inhibition of gene expression of Akt/protein kinase B [J].
Chen, Jihong ;
Ghazawi, Feras M. ;
Bakkar, Wafae ;
Li, Qiao .
MOLECULAR CANCER, 2006, 5 (1)
[7]   KINETIC-STUDIES ON THE METABOLISM OF SHORT-CHAIN FATTY-ACIDS AND GLUCOSE BY ISOLATED RAT COLONOCYTES [J].
CLAUSEN, MR ;
MORTENSEN, PB .
GASTROENTEROLOGY, 1994, 106 (02) :423-432
[8]   KINETIC-STUDIES ON COLONOCYTE METABOLISM OF SHORT-CHAIN FATTY-ACIDS AND GLUCOSE IN ULCERATIVE-COLITIS [J].
CLAUSEN, MR ;
MORTENSEN, PB .
GUT, 1995, 37 (05) :684-689
[9]   The relationship between the effects of short-chain fatty acids on intestinal motility in vitro and GPR43 receptor activation [J].
Dass, N. B. ;
John, A. K. ;
Bassil, A. K. ;
Crumbley, C. W. ;
Shehee, W. R. ;
Maurio, F. P. ;
Moore, G. B. T. ;
Taylor, C. M. ;
Sanger, G. J. .
NEUROGASTROENTEROLOGY AND MOTILITY, 2007, 19 (01) :66-74
[10]  
DUNCAN DB, 1955, BIOMETRICS, V11, P42