Fasting Enhances p-Cresol Production in the Rat Intestinal Tract
p-Cresol is a metabolite of aromatic amino acid metabolism produced by intestinal microflora, and its formation is influenced by intestinal conditions. Fasting drastically changes intestinal conditions. However, the effect of fasting on p-cresol production is unclear. In this study, serum and cecal...
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Published in | Experimental Animals Vol. 56; no. 4; pp. 301 - 307 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Japanese Association for Laboratory Animal Science
01.07.2007
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ISSN | 1341-1357 1881-7122 |
DOI | 10.1538/expanim.56.301 |
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Abstract | p-Cresol is a metabolite of aromatic amino acid metabolism produced by intestinal microflora, and its formation is influenced by intestinal conditions. Fasting drastically changes intestinal conditions. However, the effect of fasting on p-cresol production is unclear. In this study, serum and cecal p-cresol levels were determined in non-fasted rats and in rats fasting for either 12 or 18 h. Serum p-cresol increased significantly with 12-h fasting (3.44 ± 2.15 nmol/ml; P<0.05) and 18-h fasting (5.40 ± 2.20; P<0.001) as compared to the level in the non-fasted rats (1.02 ± 0.50). Cecal p-cresol levels of the 12-h fasted (272.6 ± 313.2 nmol/cecum) and 18-h fasted rats (436.6 ± 190.8; P<0.01) were higher than those in non-fasted rats (27.1 ± 21.9). The total cecal protein in content did not change with 18-h fasting. However, the cecal protein concentration increased significantly with fasting (P<0.001), and correlated closely with total cecal p-cresol contents (P<0.001). These results indicate that fasting enhances p-cresol production in the rat cecum, resulting in accumulation of serum p-cresol. We presume that the increase in p-cresol produced by fasting is related to the enhancement of bacterial nitrogen metabolism via an increased concentration of endogenous protein in the cecum. |
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AbstractList | p-Cresol is a metabolite of aromatic amino acid metabolism produced by intestinal microflora, and its formation is influenced by intestinal conditions. Fasting drastically changes intestinal conditions. However, the effect of fasting on p-cresol production is unclear. In this study, serum and cecal p-cresol levels were determined in non-fasted rats and in rats fasting for either 12 or 18 h. Serum p-cresol increased significantly with 12-h fasting (3.44 +/- 2.15 nmol/ml; P<0.05) and 18-h fasting (5.40 +/- 2.20; P<0.001) as compared to the level in the non-fasted rats (1.02 +/- 0.50). Cecal p-cresol levels of the 12-h fasted (272.6 +/- 313.2 nmol/cecum) and 18-h fasted rats (436.6 +/- 190.8; P<0.01) were higher than those in non-fasted rats (27.1 +/- 21.9). The total cecal protein in content did not change with 18-h fasting. However, the cecal protein concentration increased significantly with fasting (P<0.001), and correlated closely with total cecal p-cresol contents (P<0.001). These results indicate that fasting enhances p-cresol production in the rat cecum, resulting in accumulation of serum p-cresol. We presume that the increase in p-cresol produced by fasting is related to the enhancement of bacterial nitrogen metabolism via an increased concentration of endogenous protein in the cecum.p-Cresol is a metabolite of aromatic amino acid metabolism produced by intestinal microflora, and its formation is influenced by intestinal conditions. Fasting drastically changes intestinal conditions. However, the effect of fasting on p-cresol production is unclear. In this study, serum and cecal p-cresol levels were determined in non-fasted rats and in rats fasting for either 12 or 18 h. Serum p-cresol increased significantly with 12-h fasting (3.44 +/- 2.15 nmol/ml; P<0.05) and 18-h fasting (5.40 +/- 2.20; P<0.001) as compared to the level in the non-fasted rats (1.02 +/- 0.50). Cecal p-cresol levels of the 12-h fasted (272.6 +/- 313.2 nmol/cecum) and 18-h fasted rats (436.6 +/- 190.8; P<0.01) were higher than those in non-fasted rats (27.1 +/- 21.9). The total cecal protein in content did not change with 18-h fasting. However, the cecal protein concentration increased significantly with fasting (P<0.001), and correlated closely with total cecal p-cresol contents (P<0.001). These results indicate that fasting enhances p-cresol production in the rat cecum, resulting in accumulation of serum p-cresol. We presume that the increase in p-cresol produced by fasting is related to the enhancement of bacterial nitrogen metabolism via an increased concentration of endogenous protein in the cecum. p-Cresol is a metabolite of aromatic amino acid metabolism produced by intestinal microflora, and its formation is influenced by intestinal conditions. Fasting drastically changes intestinal conditions. However, the effect of fasting on p-cresol production is unclear. In this study, serum and cecal p-cresol levels were determined in non-fasted rats and in rats fasting for either 12 or 18 h. Serum p-cresol increased significantly with 12-h fasting (3.44 +/- 2.15 nmol/ml; P<0.05) and 18-h fasting (5.40 +/- 2.20; P<0.001) as compared to the level in the non-fasted rats (1.02 +/- 0.50). Cecal p-cresol levels of the 12-h fasted (272.6 +/- 313.2 nmol/cecum) and 18-h fasted rats (436.6 +/- 190.8; P<0.01) were higher than those in non-fasted rats (27.1 +/- 21.9). The total cecal protein in content did not change with 18-h fasting. However, the cecal protein concentration increased significantly with fasting (P<0.001), and correlated closely with total cecal p-cresol contents (P<0.001). These results indicate that fasting enhances p-cresol production in the rat cecum, resulting in accumulation of serum p-cresol. We presume that the increase in p-cresol produced by fasting is related to the enhancement of bacterial nitrogen metabolism via an increased concentration of endogenous protein in the cecum. p-Cresol is a metabolite of aromatic amino acid metabolism produced by intestinal microflora, and its formation is influenced by intestinal conditions. Fasting drastically changes intestinal conditions. However, the effect of fasting on p-cresol production is unclear. In this study, serum and cecal p-cresol levels were determined in non-fasted rats and in rats fasting for either 12 or 18 h. Serum p-cresol increased significantly with 12-h fasting (3.44 ± 2.15 nmol/ml; P<0.05) and 18-h fasting (5.40 ± 2.20; P<0.001) as compared to the level in the non-fasted rats (1.02 ± 0.50). Cecal p-cresol levels of the 12-h fasted (272.6 ± 313.2 nmol/cecum) and 18-h fasted rats (436.6 ± 190.8; P<0.01) were higher than those in non-fasted rats (27.1 ± 21.9). The total cecal protein in content did not change with 18-h fasting. However, the cecal protein concentration increased significantly with fasting (P<0.001), and correlated closely with total cecal p-cresol contents (P<0.001). These results indicate that fasting enhances p-cresol production in the rat cecum, resulting in accumulation of serum p-cresol. We presume that the increase in p-cresol produced by fasting is related to the enhancement of bacterial nitrogen metabolism via an increased concentration of endogenous protein in the cecum. |
Author | KAWAKAMI, Koji KOJIMA, Kenji MAKINO, Ikuyo ONOUE, Masaharu KATO, Ikuo |
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Cites_doi | 10.1016/S0021-9673(01)84102-9 10.1046/j.1365-2036.1998.00377.x 10.1093/jn/98.2.217 10.1016/0278-6915(91)90141-S 10.1093/ajcn/29.12.1448 10.1111/j.1365-2672.1996.tb04331.x 10.1113/jphysiol.1978.sp012156 10.1016/0003-2697(85)90442-7 10.1093/ajcn/32.10.2094 10.1046/j.1523-1755.2002.t01-1-00651.x 10.1016/B978-0-12-545680-7.50007-4 10.1136/gut.29.6.809 10.12938/bifidus.25.39 10.1038/ki.1995.64 10.1016/0009-8981(81)90299-0 10.1093/ndt/14.12.2813 10.1053/gast.1996.v111.pm8698202 10.1093/jn/116.9.1694 |
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References | 4. Chacko, A. and Cummings, J.H. 1988. Nitrogen losses from the human small bowel: obligatory losses and the effect of physical form of food. Gut 29: 809-815. 7. Curtius, H.C., Mettler, M., and Ettlinger, L. 1976. Study of the intestinal tyrosine metabolism using stable isotopes and gas chromatography-mass spectrometry. J. Chromatogra. 126: 569-580. 19. Tohyama, K. and Kobayashi, Y. 1993. Suppression of intestinal putrefactive fermentation by Bifidobacterium breve. Bifidus (J. Intest. Microbiol.) 6: 151-160 (in Japanese). 3. Boutwell, R.K. and Bosch, D.K. 1959. The tumor-promoting action of phenol and related compounds for mouse skin. Cancer Res. 19: 413-424. 9. Evenepoel, P., Claus, D., Geypens, B., Maes, B., Hiele, M., Rutgeerts, P., and Ghoos, Y. 1998. Evidence for impaired assimilation and increased colonic fermentation of protein, related to gastric acid suppression therapy. Aliment. Pharmacol. Ther. 12: 1011-1019. 14. Niwa, T., Maeda, K., Ohki, T., Saito, A., and Kobayashi, K. 1981. A gas chromatographic-mass spectrometric analysis for phenols in uremic serum. Clin. Chim. Acta 110: 51-57. 23. Ward, F.W. and Coates, M.E. 1987. Gastrointestinal pH measurement in rats: influence of the microbial flora, diet and fasting. Lab. Anim. 21: 216-222. 22. Visek, W.J. 1972. Effects of urea hydrolysis on cell life-span and metabolism. Fed. Proc. 31: 1178-1193. 2. Bone, E., Tamm, A., and Hill, M. 1976. The production of urinary phenols by gut bacteria and their possible role in the causation of large bowel cancer. Am. J. Clin. Nutr. 29: 1448-1454. 13. Matsumoto, K., Takada, T., Shimizu, K., Kado, Y., Kawakami, K., Makino, I., Yamaoka, Y., Hirano, K., Nishimura, A., Kajimoto, O., and Nomoto, K. 2006. The effects of a probiotic milk product containing Lactobacillus casei strain Shirota on the defecation frequency and the intestinal microflora of sub-optimal health state volunteers: a randomized placebo-controlled cross-over study. Biosci. Microflora 25: 39-48. 16. Smith, E.A. and Macfarlane, G.T. 1996. Enumeration of human colonic bacteria producing phenolic and indolic compounds: effects of pH, carbohydrate availability and retention time on dissimilatory aromatic amino acid metabolism. J. Appl. Bacteriol. 81: 288-302. 5. Cummings, J.H., Hill, M.J., Bone, E.S., Branch, W.J., and Jenkins, D.J. 1979. The effect of meat protein and dietary fiber on colonic function and metabolism. II. Bacterial metabolites in feces and urine. Am. J. Clin. Nutr. 32: 2094-2101. 6. Curtis, K.J., Kim, Y.S., Perdomo, J.M., Silk, D.B., and Whitehead, J.S. 1978. Protein digestion and absorption in the rat. J. Physiol. 274: 409-419. 10. Fujiwara, S., Hirota, T., Nakazato, H., Mizutani, T., and Mitsuoka, T. 1991. Effect of Konjac mannan on intestinal microbial metabolism in mice bearing human flora and in conventional F344 rats. Food Chem. Toxicol. 29: 601-606. 17. Smith, P.K., Krohn, R.I., Hermanson, G.T., Mallia, A.K., Gartner, F.H., Provenzano, M.D., Fujimoto, E.K., Goeke, N.M., Olson, B.J., and Klenk, D.C. 1985. Measurement of protein using bicinchoninic acid. Anal. Biochem. 150: 76-85. 21. Vanholder, R., De Smet, R., Waterloos, M.A., Van Landschoot, N., Vogeleere, P., Hoste, E., and Ringoir, S. 1995. Mechanisms of uremic inhibition of phagocyte reactive species production: characterization of the role of p-cresol. Kidney Int. 47: 510-517. 8. Dou, L., Cerini, C., Brunet, P., Guilianelli, C., Moal, V., Grau, G., De Smet, R., Vanholder, R., Sampol, J., and Berland, Y. 2002. p-Cresol, a uremic toxin, decreases endothelial cell response to inflammatory cytokines. Kidney Int. 62:1999-2009. 12. Kotal, P., Vitek, L., and Fevery, J. 1996. Fasting-related hyperbilirubinemia in rats: the effect of decreased intestinal motility. Gastroenterology 111: 217-223. 1. Bakke, O.M. 1969. Urinary simple phenols in rats fed diets containing different amounts of casein and 10% tyrosine. J. Nutr. 98: 217-221. 15. Niwa, T. 1993. Phenol and p-cresol accumulated in uremic serum measured by HPLC with fluorescence detection. Clin. Chem. 39: 108-111. 18. Tanimoto, Y. 1988. Biochemistry of Blood and Urine in Experimental Animals, Soft Science Inc., Tokyo (in Japanese). 20. Vanholder, R., De Smet, R., and Lesaffer, G. 1999. p-Cresol: a toxin revealing many neglected but relevant aspects of uraemic toxicity. Nephrol. Dial. Transplant. 14: 2813-2815. 11. Illman, R.J., Topping, D.L., and Trimble, R.P. 1986. Effects of food restriction and starvation-refeeding on volatile fatty acid concentrations in the rat. J. Nutr. 116: 1694-1700. 22 12 23 14 15 MATSUMOTO KAZUMASA (13) 2006; 25 17 18 19 1 2 3 4 (11) 1986; 116 5 6 7 8 9 (16) 1996; 81 20 10 21 |
References_xml | – reference: 16. Smith, E.A. and Macfarlane, G.T. 1996. Enumeration of human colonic bacteria producing phenolic and indolic compounds: effects of pH, carbohydrate availability and retention time on dissimilatory aromatic amino acid metabolism. J. Appl. Bacteriol. 81: 288-302. – reference: 23. Ward, F.W. and Coates, M.E. 1987. Gastrointestinal pH measurement in rats: influence of the microbial flora, diet and fasting. Lab. Anim. 21: 216-222. – reference: 6. Curtis, K.J., Kim, Y.S., Perdomo, J.M., Silk, D.B., and Whitehead, J.S. 1978. Protein digestion and absorption in the rat. J. Physiol. 274: 409-419. – reference: 14. Niwa, T., Maeda, K., Ohki, T., Saito, A., and Kobayashi, K. 1981. A gas chromatographic-mass spectrometric analysis for phenols in uremic serum. Clin. Chim. Acta 110: 51-57. – reference: 18. Tanimoto, Y. 1988. Biochemistry of Blood and Urine in Experimental Animals, Soft Science Inc., Tokyo (in Japanese). – reference: 1. Bakke, O.M. 1969. Urinary simple phenols in rats fed diets containing different amounts of casein and 10% tyrosine. J. Nutr. 98: 217-221. – reference: 3. Boutwell, R.K. and Bosch, D.K. 1959. The tumor-promoting action of phenol and related compounds for mouse skin. Cancer Res. 19: 413-424. – reference: 10. Fujiwara, S., Hirota, T., Nakazato, H., Mizutani, T., and Mitsuoka, T. 1991. Effect of Konjac mannan on intestinal microbial metabolism in mice bearing human flora and in conventional F344 rats. Food Chem. Toxicol. 29: 601-606. – reference: 20. Vanholder, R., De Smet, R., and Lesaffer, G. 1999. p-Cresol: a toxin revealing many neglected but relevant aspects of uraemic toxicity. Nephrol. Dial. Transplant. 14: 2813-2815. – reference: 7. Curtius, H.C., Mettler, M., and Ettlinger, L. 1976. Study of the intestinal tyrosine metabolism using stable isotopes and gas chromatography-mass spectrometry. J. Chromatogra. 126: 569-580. – reference: 9. Evenepoel, P., Claus, D., Geypens, B., Maes, B., Hiele, M., Rutgeerts, P., and Ghoos, Y. 1998. Evidence for impaired assimilation and increased colonic fermentation of protein, related to gastric acid suppression therapy. Aliment. Pharmacol. Ther. 12: 1011-1019. – reference: 22. Visek, W.J. 1972. Effects of urea hydrolysis on cell life-span and metabolism. Fed. Proc. 31: 1178-1193. – reference: 2. Bone, E., Tamm, A., and Hill, M. 1976. The production of urinary phenols by gut bacteria and their possible role in the causation of large bowel cancer. Am. J. Clin. Nutr. 29: 1448-1454. – reference: 19. Tohyama, K. and Kobayashi, Y. 1993. Suppression of intestinal putrefactive fermentation by Bifidobacterium breve. Bifidus (J. Intest. Microbiol.) 6: 151-160 (in Japanese). – reference: 8. Dou, L., Cerini, C., Brunet, P., Guilianelli, C., Moal, V., Grau, G., De Smet, R., Vanholder, R., Sampol, J., and Berland, Y. 2002. p-Cresol, a uremic toxin, decreases endothelial cell response to inflammatory cytokines. Kidney Int. 62:1999-2009. – reference: 12. Kotal, P., Vitek, L., and Fevery, J. 1996. Fasting-related hyperbilirubinemia in rats: the effect of decreased intestinal motility. Gastroenterology 111: 217-223. – reference: 5. Cummings, J.H., Hill, M.J., Bone, E.S., Branch, W.J., and Jenkins, D.J. 1979. The effect of meat protein and dietary fiber on colonic function and metabolism. II. Bacterial metabolites in feces and urine. Am. J. Clin. Nutr. 32: 2094-2101. – reference: 13. Matsumoto, K., Takada, T., Shimizu, K., Kado, Y., Kawakami, K., Makino, I., Yamaoka, Y., Hirano, K., Nishimura, A., Kajimoto, O., and Nomoto, K. 2006. The effects of a probiotic milk product containing Lactobacillus casei strain Shirota on the defecation frequency and the intestinal microflora of sub-optimal health state volunteers: a randomized placebo-controlled cross-over study. Biosci. Microflora 25: 39-48. – reference: 21. Vanholder, R., De Smet, R., Waterloos, M.A., Van Landschoot, N., Vogeleere, P., Hoste, E., and Ringoir, S. 1995. Mechanisms of uremic inhibition of phagocyte reactive species production: characterization of the role of p-cresol. Kidney Int. 47: 510-517. – reference: 17. Smith, P.K., Krohn, R.I., Hermanson, G.T., Mallia, A.K., Gartner, F.H., Provenzano, M.D., Fujimoto, E.K., Goeke, N.M., Olson, B.J., and Klenk, D.C. 1985. Measurement of protein using bicinchoninic acid. Anal. Biochem. 150: 76-85. – reference: 4. Chacko, A. and Cummings, J.H. 1988. Nitrogen losses from the human small bowel: obligatory losses and the effect of physical form of food. Gut 29: 809-815. – reference: 11. Illman, R.J., Topping, D.L., and Trimble, R.P. 1986. Effects of food restriction and starvation-refeeding on volatile fatty acid concentrations in the rat. J. Nutr. 116: 1694-1700. – reference: 15. Niwa, T. 1993. Phenol and p-cresol accumulated in uremic serum measured by HPLC with fluorescence detection. Clin. Chem. 39: 108-111. – ident: 7 doi: 10.1016/S0021-9673(01)84102-9 – ident: 3 – ident: 9 doi: 10.1046/j.1365-2036.1998.00377.x – ident: 18 – ident: 1 doi: 10.1093/jn/98.2.217 – ident: 10 doi: 10.1016/0278-6915(91)90141-S – ident: 2 doi: 10.1093/ajcn/29.12.1448 – volume: 81 start-page: 288 issn: 0021-8847 issue: 3 year: 1996 ident: 16 doi: 10.1111/j.1365-2672.1996.tb04331.x – ident: 6 doi: 10.1113/jphysiol.1978.sp012156 – ident: 17 doi: 10.1016/0003-2697(85)90442-7 – ident: 19 – ident: 5 doi: 10.1093/ajcn/32.10.2094 – ident: 8 doi: 10.1046/j.1523-1755.2002.t01-1-00651.x – ident: 15 doi: 10.1016/B978-0-12-545680-7.50007-4 – ident: 4 doi: 10.1136/gut.29.6.809 – volume: 25 start-page: 39 issn: 1342-1441 issue: 2 year: 2006 ident: 13 doi: 10.12938/bifidus.25.39 – ident: 21 doi: 10.1038/ki.1995.64 – ident: 14 doi: 10.1016/0009-8981(81)90299-0 – ident: 20 doi: 10.1093/ndt/14.12.2813 – ident: 12 doi: 10.1053/gast.1996.v111.pm8698202 – volume: 116 start-page: 1694 issn: 0022-3166 issue: 9 year: 1986 ident: 11 doi: 10.1093/jn/116.9.1694 – ident: 22 – ident: 23 |
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Title | Fasting Enhances p-Cresol Production in the Rat Intestinal Tract |
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ispartofPNX | Experimental Animals, 2007, Vol.56(4), pp.301-307 |
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