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抗性淀粉结肠内酵解对大鼠肠道健康的影响 被引量:24

Effects of resistant starch fermentation on physiological changes of colon in rats
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摘要 目的:探讨不同浓度抗性淀粉(RS),特别在高蛋白饲养模式下,对实验大鼠肠道功能、肠内短链脂肪酸和有害及酵解产物等健康指标的影响. 方法:57只健康♂SD大鼠根据体重随机分成5组,分别给予含有0%,6%和12%RS的基础饲料,或含有6%和12% RS的高蛋白饲料(36%酪蛋白,HP)喂养.实验3 wk进行肠道转运时间(GTT)的观察实验;5 wk连续收集3 d粪便; 7 wk处死大鼠,取盲肠进行形态学和组织学观察,并对盲肠内容物中的短链脂肪酸(SCFA)、氨、酚含量以及肠道pH进行测定. 结果:和0%RS组大鼠相比,12%RS组大鼠GTT明显缩短(601±49 min vs 700±58 min,P<0.001),粪便量、盲肠壁及盲肠内容物质量显著增加(分别为1.04±0.22 g vs 0.37±0.12 g,1.12±0.14 g vs 0.73±0.13 g,P<0.001; 4.78±1.44 g vs 3.00±1.12 g,P=0.004<0.01);盲肠内SCFA增加2-3倍(35.5±11.4μmol/g vs13.9±6.7μmol/g, P=0.003<0.01);粪氨、盲肠内氨及酚浓度下降(0.26±0.13 mg/g vs 0.59±0.15 mg/g.0.35±0.13 mg/g vs 0.63±0.13 mg/g,2.03±0.42 mg/g vs 3.15±0.55 mg/g, P<0.001);盲肠和粪便pH值减低(6.26±0.36 vs 7.46±0.28, 5.67±0.31 vs 7.24±0.31,P<0.001),且粪便pH值显著低于盲肠pH值(P<0.001),提示RS使远端结肠发酵增加. 6%RS组粪氨、盲肠酚及肠道pH值亦有中度下降(P<0.05). 以上各指标与RS摄入量存在明显的剂量反应关系(P<0.01). 和相应等剂量RS组相比,HP+12%RS组大鼠GTT延长(659±47 min,P=0.009<0.01),粪便量减少(0.80±0.29 g,P=0.005<0.01),盲肠内容物SCFA降低(24.6±13.6μmol/g,P=0.043<0.0 5);HP+6RS%组和HP+12RS% 组盲肠内酚浓度增加(分别为3.20±0.49 mg/g,2.71±0.55 mg/g,P<0.001),且肠道pH升高.但随着RS摄入的增加,这一现象有所缓解,HP+12%RS组粪便水分,盲肠SCFA、氨、酚浓度及pH值均与HP+6%组有显著差异(P<0.05).RS和酪蛋白对粪便于质量和盲肠pH值有显著交互作用(P<0.01).组织病理切片未显示实验期间RS喂养大鼠盲肠壁细胞出现异常变化. 结论:RS有助于维持肠道健康相关指标,适量摄取可改善高酪蛋白饮食引起的肠道功能改变,起到酸化肠道,促进肠内有益产物SCFA生成,降低有毒代谢产物酚的作用. AIM: To evaluate the effects of resistant starch (RS) fermentation on colon health-related indexes, including bowel functions, luminal short-chain fatty acid production and toxic compounds excretion. METHODS: Fifty-seven healthy male SD rats were randomly divided into 5 groups based on body weight, and given basal diets with 0%, 6% and 12% RS, or high-protein diets (36% casein, HP) with 6% or 12% RS, respectively. After fed for 3 wk, gut transit time (GTT) for rats in each group was examined; at 5 wk three day feces samples were collected and their contents were assessed; at 7 wk all rats were killed. The morphological and histo logical characteristics of caecum were observed and the caecal function was evaluated by determination of the weight of caecal wall and caecal digesta, detection of caecal short chain fatty acid (SCFA), ammonia, phenol concentration and pH value. RESULTS: In comparison with those in rats fed with 0% RS diet, shortened GTT was significantly shortened (601± 49 min vs 700±58 min, P<0.001), stool bulk was increased with more moisture (1.04±0.22 g vs 0.37±0.12 g, P <0.001), and weight of caecal wall and caecal digesta was also increased (1.12±0.14 g vs 0.73±0.13 g,P<0.001; 4.78±1.44 g vs 3.00±1.12 g, P= 0.004<0.01) in rats fed with 12% RS diet; the concentration of SCFA in caecum was two- to three-fold enhanced by 12% RS (35.5±11.4 μmol/g vs 13.9±6.7 μmol/g, P =0.003<0.01), while the concentration of ammonia in both feces and caecum and phenol in caecum decreased (0.26±0.13 mg/g 1/50.59± 0.15 mg/g, 0.35±0.13 mg/g vs 0.63±0.13 mg/g, 2.03± 0.42 mg/g vs 3.15±0.55 mg/g, P<0.001, respectively); caecal and fecal pH value dropped significantly (6.26± 0.36 vs 7.46±0.28; 5.67±0.31 vs 7.24±0.31, P<0.001), and the variation of pH in feces was greater than that in caecum (P<0.001), suggesting extended fermentation in distal colon. Rats in 6% RS group had similar but intermediate variances in fecal ammonia, caecal phenol and intestinal pH value (P<0.05). All indexes mentioned above were dose-dependent (P <0.01). For rats fed with HP, GTT was prolonged. Fecal bulk and caecal SCFA level dropped in HP+12% RS group (659 ±47 min, P= 0.009 <0.01; 0.80±0.29 g, P= 0.005<0.01, 24.6±13.6 μmol/g P= 0.043<0.05), compared with 12% RS group. The concentrations of caecal phenol in HP+6% RS and HP+12% RS group were 3.20±0.49 mg/g and 2.71±0.55 mg/g respectively, significantly higher than that in 6% and 12% RS groups (P<0.001); fecal and caecal pH value elevated as well. However, as RS intake increased (12%), these negative changes above were attenuated (P<0.05). There was a significant interaction between RS and casein on fecal dry matter and caecal pH value (P<0.01). Histologi cal observation showed no abnormal changes in caecum tissues of rats fed with RS. CONCLUSION: RS is beneficial to sustain intestinal health related indexes and has potential protective effects on bowel functions. Adequate RS intake could attenuate the negative effects of high casein on colon by improving bowel habit, acidifying intestinal tract, promoting SCFA production and decreasing intestinal inner noxious phenol.
出处 《世界华人消化杂志》 CAS 2004年第11期2618-2622,共5页 World Chinese Journal of Digestology
基金 国家自然科学基金资助项目 No.30070657~~
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  • 1Englyst HN, Kingman SM, Cummings JH. Classification and measurement of nutritionally important starch fractions. Eur J Clin Nutr 1992;46(Suppl 2):$33-50
  • 2FAO. Carbohydrates in Human Nutrition. FAO Food and Nutrition Paper 66, Rome: FAO 1998:1-5
  • 3Champ M. Determination of resistant starch in foods and food products: interlaboratory study. Eur J Clin Nutr 1992;46(Suppl 2):S51-62
  • 4Topping DL, Illman RJ, Clarke JM, Trimble RP, Jackson KA,Marsono Y. Dietary fat and fiber alter large bowel and portal venous volatile fatty acids and plasma cholesterol but not biliary steroids in pigs. J Nutr 1993;123:133-143
  • 5Birkett AM, Jones GP, Muir JG. Simple high-performance liquid chromatographic analysis of phenol and p-cresol in urine and feces. J Chromatogr B Biomed Appl 1995;674:187-191
  • 6Satia-Abouta J, Galanko JA, Potter JD, Ammerman A, Martin CF, Sandler RS, North carolina colen cancer study. Associations of total energy and macronutrients with colon cancer risk in African Americans and Whites: results from the North Carolina colon cancer study, Am J Epidemiol 2003;158:951-962
  • 7Chiu BC, Ji BT, Dai Q, Gridley G, McLaughlin JK, Gao YT,Fraumeni JF Jr, Chow WH, Dietary factors and risk of colon cancer in Shanghai, China. Cancer Epidemiol Biomarkers Prev 2003;12:201-208
  • 8Favero A, Parpinel M, Montella M, Energy sources and risk of cancer of the breast and colon-rectum in Italy. Adv Exp Med Biol 1999;472:51-55
  • 9Cai J, Chen Y, Murphy TJ, Jones DP, Sartorelli AC, Role of caspase activation in butyrate-induced terminal differentiation of HT29 colon carcinoma cells, Arch Biochem Biophys 2004;424:119-127
  • 10李可洲,李宁,黎介寿,鲍扬,李幼生.短链脂肪酸对大鼠移植小肠形态及功能的作用研究[J].世界华人消化杂志,2002,10(6):720-722. 被引量:65

二级参考文献58

  • 1[18]Kato Y, Yu D, Schwartz MZ. Glucagonlike peptide-2 enhances small intestinal absorptive function and mucosal mass in vivo. J Pediatr Surg 1999;34:18-20
  • 2[1]Soin AS, Friend PJ, Richard JK, Russel PS. A modification to improve technical success rate of small bowel transplantation in rats. Transpl Proc 1996; 28: 2722
  • 3[2]Cummings JH, Branch WJ. Fermentation and the production of short chain fatty acids in the human large intestine. In: Vahouny GB, Kritchevsky D, eds.Dietary fiber. Basic and clinical aspects. New York Plenum 1986:131-152
  • 4[3]Koruda MJ, Rolandelli RH, Bliss DZ. Parenteral nutrition supplemented with short-chain fatty acids: effect on the small-bowel mucosa in normal rats. Am J Clin Nutr 1990;51:685-689
  • 5[4]Frankel WI, Zhang W, Singh A. Mediation of the trophic effects of shortchain fatty acids on the rat jejunum and colon. Gastroenterology 1994; 106:375-380
  • 6[5]LeLeiko NS, Walsh MJ. The role of glutamine, short-chain fatty acids, and nucleotides in intestinal adaptation to gastrointestinal disease. Pediatr Clin North Am 1996;43:451-470
  • 7[6]Thompson JS, Quigly EM, Palmer JM. Luminal short-chain fatty acids and postresection intestinal adaptation. J Parenter Enteral Nutr 1996;20:338-343
  • 8[7]Tappenden KA, Thomson ABR, Wild GE, Mcbumey MI. Short-chain fatty acid-supplemented total parenteral nutrition enhances functional adaptation to intestinal resection in rats. Gastroenterology 1997; 112: 792-802
  • 9[8]Tappenden KA, Drozdowski LA, Thomson ABR, Wild GE. Short-chain fatty acid-supplemented total parenteral nutrition alters intestinal struture, glucose transporter 2 (GLUT2) mRNA and protein, and proglucagon mRNA abbundance in nomrmal rats. J Clin Nutr 1998; 68: 118-125
  • 10[9]Waston AJM, Lear PA, Montgomery A. Water, electrolyte, glucose, and glycine absorption in rat small intestinal transplants. Gastroenterology 1988;94:863

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