Abstract
Patients with short bowel syndrome require long term parenteral nutrition support. However, after massive intestinal resection the intestine undergoes adaptation and nutritional autonomy may be obtained. Given that the complications of parenteral nutrition may be life threatening or result in treatment failure and the need for intestinal transplantation, a more attractive option is to wean patients off nutrition support by optimising the adaptive process. The article examines the evidence that after extensive small bowel resection adaptation occurs in humans and focuses on the factors that influence adaptation and the strategies that have been used to optimise this process. The review is based on an English language Medline search with secondary references obtained from key articles. There is evidence that adaptation occurs in humans. Adaptation is a complex process that results in response to nutrient and non-nutrient stimuli. Successful and reproducible strategies to improve adaptation remain elusive despite an abundance of experimental data. Nevertheless given the low patient survival and quality of life associated with other treatments for irreversible intestinal failure it is imperative that clinical research continues into the optimisation of the adaptation.
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- Alavi K., Kato Y., Yu D., Schwartz M. Z. Enteral glutamine does not enhance the effects of hepatocyte growth factor in short bowel syndrome. J Pediatr Surg. 1998 Nov;33(11):1666–1669. doi: 10.1016/s0022-3468(98)90605-4. [DOI] [PubMed] [Google Scholar]
- Alavi K., Prasad R., Lundgren K., Schwartz M. Z. Interleukin-11 enhances small intestine absorptive function and mucosal mass after intestinal adaptation. J Pediatr Surg. 2000 Feb;35(2):371–374. doi: 10.1016/s0022-3468(00)90043-5. [DOI] [PubMed] [Google Scholar]
- Alavi Karim, Schwartz Marshall Z., Prasad Rajeev, O'connor Darlise, Funanage Vicky. Leptin: a new growth factor for the small intestine. J Pediatr Surg. 2002 Mar;37(3):327–330. doi: 10.1053/jpsu.2002.30805. [DOI] [PubMed] [Google Scholar]
- Alpers David H. How adaptable is the intestine in patients with short-bowel syndrome? Am J Clin Nutr. 2002 May;75(5):787–788. doi: 10.1093/ajcn/75.5.787. [DOI] [PubMed] [Google Scholar]
- Andorsky D. J., Lund D. P., Lillehei C. W., Jaksic T., Dicanzio J., Richardson D. S., Collier S. B., Lo C., Duggan C. Nutritional and other postoperative management of neonates with short bowel syndrome correlates with clinical outcomes. J Pediatr. 2001 Jul;139(1):27–33. doi: 10.1067/mpd.2001.114481. [DOI] [PubMed] [Google Scholar]
- Bakker H., Bozzetti F., Staun M., Leon-Sanz M., Hebuterne X., Pertkiewicz M., Shaffer J., Thul P. Home parenteral nutrition in adults: a european multicentre survey in 1997. ESPEN-Home Artificial Nutrition Working Group. Clin Nutr. 1999 Jun;18(3):135–140. doi: 10.1054/clnu.1999.0021. [DOI] [PubMed] [Google Scholar]
- Benedetti E., Baum C., Cicalese L., Brown M., Raofi V., Massad M. G., Abcarian H. Progressive functional adaptation of segmental bowel graft from living related donor. Transplantation. 2001 Feb 27;71(4):569–571. doi: 10.1097/00007890-200102270-00014. [DOI] [PubMed] [Google Scholar]
- Benhamou P. H., Canarelli J. P., Leroy C., De Boissieu D., Dupont C. Stimulation by recombinant human growth hormone of growth and development of remaining bowel after subtotal ileojejunectomy in rats. J Pediatr Gastroenterol Nutr. 1994 May;18(4):446–452. doi: 10.1097/00005176-199405000-00007. [DOI] [PubMed] [Google Scholar]
- Bjerknes M., Cheng H. Modulation of specific intestinal epithelial progenitors by enteric neurons. Proc Natl Acad Sci U S A. 2001 Sep 25;98(22):12497–12502. doi: 10.1073/pnas.211278098. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Buchman A. L., Moukarzel A. A., Ament M. E., Eckhert C., Bhuta S., Mestecky J., Hollander D. Effects of total parenteral nutrition on intestinal morphology and function in humans. Transplant Proc. 1994 Jun;26(3):1457–1457. [PubMed] [Google Scholar]
- Buchman Alan L., Scolapio James, Fryer Jon. AGA technical review on short bowel syndrome and intestinal transplantation. Gastroenterology. 2003 Apr;124(4):1111–1134. doi: 10.1016/s0016-5085(03)70064-x. [DOI] [PubMed] [Google Scholar]
- Byrne T. A., Cox S., Karimbakas M., Veglia L. M., Bennett H. M., Lautz D. B., Robinson M. K., Wilmore D. W. Bowel rehabilitation: an alternative to long-term parenteral nutrition and intestinal transplantation for some patients with short bowel syndrome. Transplant Proc. 2002 May;34(3):887–890. doi: 10.1016/s0041-1345(02)02654-4. [DOI] [PubMed] [Google Scholar]
- Byrne T. A., Morrissey T. B., Nattakom T. V., Ziegler T. R., Wilmore D. W. Growth hormone, glutamine, and a modified diet enhance nutrient absorption in patients with severe short bowel syndrome. JPEN J Parenter Enteral Nutr. 1995 Jul-Aug;19(4):296–302. doi: 10.1177/0148607195019004296. [DOI] [PubMed] [Google Scholar]
- Byrne T. A., Persinger R. L., Young L. S., Ziegler T. R., Wilmore D. W. A new treatment for patients with short-bowel syndrome. Growth hormone, glutamine, and a modified diet. Ann Surg. 1995 Sep;222(3):243–255. doi: 10.1097/00000658-199509000-00003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carbonnel F., Cosnes J., Chevret S., Beaugerie L., Ngô Y., Malafosse M., Parc R., Le Quintrec Y., Gendre J. P. The role of anatomic factors in nutritional autonomy after extensive small bowel resection. JPEN J Parenter Enteral Nutr. 1996 Jul-Aug;20(4):275–280. doi: 10.1177/0148607196020004275. [DOI] [PubMed] [Google Scholar]
- Chan J. M., Stampfer M. J., Giovannucci E., Gann P. H., Ma J., Wilkinson P., Hennekens C. H., Pollak M. Plasma insulin-like growth factor-I and prostate cancer risk: a prospective study. Science. 1998 Jan 23;279(5350):563–566. doi: 10.1126/science.279.5350.563. [DOI] [PubMed] [Google Scholar]
- Chance W. T., Foley-Nelson T., Thomas I., Balasubramaniam A. Prevention of parenteral nutrition-induced gut hypoplasia by coinfusion of glucagon-like peptide-2. Am J Physiol. 1997 Aug;273(2 Pt 1):G559–G563. doi: 10.1152/ajpgi.1997.273.2.G559. [DOI] [PubMed] [Google Scholar]
- Chen M., Yang Y., Braunstein E., Georgeson K. E., Harmon C. M. Gut expression and regulation of FAT/CD36: possible role in fatty acid transport in rat enterocytes. Am J Physiol Endocrinol Metab. 2001 Nov;281(5):E916–E923. doi: 10.1152/ajpendo.2001.281.5.E916. [DOI] [PubMed] [Google Scholar]
- Cheng H., Leblond C. P. Origin, differentiation and renewal of the four main epithelial cell types in the mouse small intestine. V. Unitarian Theory of the origin of the four epithelial cell types. Am J Anat. 1974 Dec;141(4):537–561. doi: 10.1002/aja.1001410407. [DOI] [PubMed] [Google Scholar]
- Cicalese L., Baum C., Brown M., Sileri P., Smith D., Abcarian H., Benedetti E. Segmental small bowel transplant from adult living-related donors. Transplant Proc. 2001 Feb-Mar;33(1-2):1553–1553. doi: 10.1016/s0041-1345(00)02590-2. [DOI] [PubMed] [Google Scholar]
- Cosnes J., Evard D., Beaugerie L., Gendre J. P., Le Quintrec Y. Improvement in protein absorption with a small-peptide-based diet in patients with high jejunostomy. Nutrition. 1992 Nov-Dec;8(6):406–411. [PubMed] [Google Scholar]
- Czernichow B., Nsi-Emvo E., Galluser M., Gossé F., Raul F. Enteral supplementation with ornithine alpha ketoglutarate improves the early adaptive response to resection. Gut. 1997 Jan;40(1):67–72. doi: 10.1136/gut.40.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dahly Elizabeth M., Gillingham Melanie B., Guo Ziwen, Murali Sangita G., Nelson David W., Holst Jens J., Ney Denise M. Role of luminal nutrients and endogenous GLP-2 in intestinal adaptation to mid-small bowel resection. Am J Physiol Gastrointest Liver Physiol. 2002 Dec 27;284(4):G670–G682. doi: 10.1152/ajpgi.00293.2002. [DOI] [PubMed] [Google Scholar]
- Dahly Elizabeth M., Guo Ziwen, Ney Denise M. Alterations in enterocyte proliferation and apoptosis accompany TPN-induced mucosal hypoplasia and IGF-I-induced hyperplasia in rats. J Nutr. 2002 Jul;132(7):2010–2014. doi: 10.1093/jn/132.7.2010. [DOI] [PubMed] [Google Scholar]
- Deutz N. E., Dejong C. H., Athanasas G., Soeters P. B. Partial enterectomy in the rat does not diminish muscle glutamine production. Metabolism. 1992 Dec;41(12):1343–1350. doi: 10.1016/0026-0495(92)90106-k. [DOI] [PubMed] [Google Scholar]
- Drucker D. J., DeForest L., Brubaker P. L. Intestinal response to growth factors administered alone or in combination with human [Gly2]glucagon-like peptide 2. Am J Physiol. 1997 Dec;273(6 Pt 1):G1252–G1262. doi: 10.1152/ajpgi.1997.273.6.G1252. [DOI] [PubMed] [Google Scholar]
- Drucker D. J., Erlich P., Asa S. L., Brubaker P. L. Induction of intestinal epithelial proliferation by glucagon-like peptide 2. Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7911–7916. doi: 10.1073/pnas.93.15.7911. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Du X., Williams D. A. Interleukin-11: review of molecular, cell biology, and clinical use. Blood. 1997 Jun 1;89(11):3897–3908. [PubMed] [Google Scholar]
- Ellis P. D., Hadfield K. M., Pascall J. C., Brown K. D. Heparin-binding epidermal-growth-factor-like growth factor gene expression is induced by scrape-wounding epithelial cell monolayers: involvement of mitogen-activated protein kinase cascades. Biochem J. 2001 Feb 15;354(Pt 1):99–106. doi: 10.1042/0264-6021:3540099. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Erwin C. R., Helmrath M. A., Shin C. E., Falcone R. A., Jr, Stern L. E., Warner B. W. Intestinal overexpression of EGF in transgenic mice enhances adaptation after small bowel resection. Am J Physiol. 1999 Sep;277(3 Pt 1):G533–G540. doi: 10.1152/ajpgi.1999.277.3.G533. [DOI] [PubMed] [Google Scholar]
- Evers B. M., Izukura M., Townsend C. M., Jr, Uchida T., Thompson J. C. Neurotensin prevents intestinal mucosal hypoplasia in rats fed an elemental diet. Dig Dis Sci. 1992 Mar;37(3):426–431. doi: 10.1007/BF01307738. [DOI] [PubMed] [Google Scholar]
- Fiore N. F., Ledniczky G., Liu Q., Orazi A., Du X., Williams D. A., Grosfeld J. L. Comparison of interleukin-11 and epidermal growth factor on residual small intestine after massive small bowel resection. J Pediatr Surg. 1998 Jan;33(1):24–29. doi: 10.1016/s0022-3468(98)90354-2. [DOI] [PubMed] [Google Scholar]
- Fürstenberger Gregor, Senn Hans-Jörg. Insulin-like growth factors and cancer. Lancet Oncol. 2002 May;3(5):298–302. doi: 10.1016/s1470-2045(02)00731-3. [DOI] [PubMed] [Google Scholar]
- Gibson Rachel J., Keefe Dorothy M. K., Thompson Fiona M., Clarke Julie M., Goland Gary J., Cummins Adrian G. Effect of interleukin-11 on ameliorating intestinal damage after methotrexate treatment of breast cancer in rats. Dig Dis Sci. 2002 Dec;47(12):2751–2757. doi: 10.1023/a:1021061306913. [DOI] [PubMed] [Google Scholar]
- Gorard David A. Enteral nutrition in Crohn's disease: fat in the formula. Eur J Gastroenterol Hepatol. 2003 Feb;15(2):115–118. doi: 10.1097/00042737-200302000-00002. [DOI] [PubMed] [Google Scholar]
- Gouttebel M. C., Astre C., Briand D., Saint-Aubert B., Girardot P. M., Joyeux H. Influence of N-acetylglutamine or glutamine infusion on plasma amino acid concentrations during the early phase of small-bowel adaptation in the dog. JPEN J Parenter Enteral Nutr. 1992 Mar-Apr;16(2):117–121. doi: 10.1177/0148607192016002117. [DOI] [PubMed] [Google Scholar]
- Gouttebel M. C., Saint Aubert B., Colette C., Astre C., Monnier L. H., Joyeux H. Intestinal adaptation in patients with short bowel syndrome. Measurement by calcium absorption. Dig Dis Sci. 1989 May;34(5):709–715. doi: 10.1007/BF01540342. [DOI] [PubMed] [Google Scholar]
- Gruessner R. W., Sharp H. L. Living-related intestinal transplantation: first report of a standardized surgical technique. Transplantation. 1997 Dec 15;64(11):1605–1607. doi: 10.1097/00007890-199712150-00019. [DOI] [PubMed] [Google Scholar]
- Gu Y., Wu Z. H., Xie J. X., Jin D. Y., Zhuo H. C. Effects of growth hormone (rhGH) and glutamine supplemented parenteral nutrition on intestinal adaptation in short bowel rats. Clin Nutr. 2001 Apr;20(2):159–166. doi: 10.1054/clnu.2000.0379. [DOI] [PubMed] [Google Scholar]
- Hajri Tahar, Abumrad Nada A. Fatty acid transport across membranes: relevance to nutrition and metabolic pathology. Annu Rev Nutr. 2002 Apr 4;22:383–415. doi: 10.1146/annurev.nutr.22.020402.130846. [DOI] [PubMed] [Google Scholar]
- Hamilton J. A. Fatty acid transport: difficult or easy? J Lipid Res. 1998 Mar;39(3):467–481. [PubMed] [Google Scholar]
- Hankinson S. E., Willett W. C., Colditz G. A., Hunter D. J., Michaud D. S., Deroo B., Rosner B., Speizer F. E., Pollak M. Circulating concentrations of insulin-like growth factor-I and risk of breast cancer. Lancet. 1998 May 9;351(9113):1393–1396. doi: 10.1016/S0140-6736(97)10384-1. [DOI] [PubMed] [Google Scholar]
- Hanson W. R., Osborne J. W., Sharp J. G. Compensation by the residual intestine after intestinal resection in the rat. I. Influence of amount of tissue removed. Gastroenterology. 1977 Apr;72(4 Pt 1):692–700. [PubMed] [Google Scholar]
- Hart M. H., Grandjean C. J., Park J. H., Erdman S. H., Vanderhoof J. A. Essential fatty acid deficiency and postresection mucosal adaptation in the rat. Gastroenterology. 1988 Mar;94(3):682–687. doi: 10.1016/0016-5085(88)90239-9. [DOI] [PubMed] [Google Scholar]
- Helmrath M. A., Shin C. E., Fox J. W., Erwin C. R., Warner B. W. Adaptation after small bowel resection is attenuated by sialoadenectomy: the role for endogenous epidermal growth factor. Surgery. 1998 Nov;124(5):848–854. [PubMed] [Google Scholar]
- Higashiyama S., Abraham J. A., Miller J., Fiddes J. C., Klagsbrun M. A heparin-binding growth factor secreted by macrophage-like cells that is related to EGF. Science. 1991 Feb 22;251(4996):936–939. doi: 10.1126/science.1840698. [DOI] [PubMed] [Google Scholar]
- Hines O. J., Bilchik A. J., Zinner M. J., Skotzko M. J., Moser A. J., McFadden D. W., Ashley S. W. Adaptation of the Na+/glucose cotransporter following intestinal resection. J Surg Res. 1994 Jul;57(1):22–27. doi: 10.1006/jsre.1994.1103. [DOI] [PubMed] [Google Scholar]
- Holst J. J. Enteroglucagon. Annu Rev Physiol. 1997;59:257–271. doi: 10.1146/annurev.physiol.59.1.257. [DOI] [PubMed] [Google Scholar]
- Howarth G. S., Shoubridge C. A. Enhancement of intestinal growth and repair by growth factors. Curr Opin Pharmacol. 2001 Dec;1(6):568–574. doi: 10.1016/s1471-4892(01)00098-4. [DOI] [PubMed] [Google Scholar]
- Iwamoto R., Mekada E. Heparin-binding EGF-like growth factor: a juxtacrine growth factor. Cytokine Growth Factor Rev. 2000 Dec;11(4):335–344. doi: 10.1016/s1359-6101(00)00013-7. [DOI] [PubMed] [Google Scholar]
- Izukura M., Evers B. M., Parekh D., Yoshinaga K., Uchida T., Townsend C. M., Jr, Thompson J. C. Neurotensin augments intestinal regeneration after small bowel resection in rats. Ann Surg. 1992 May;215(5):520–527. doi: 10.1097/00000658-199205000-00015. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jao W., Sileri P., Holaysan J., Morini S., Chejfec G., Rastellini C., Benedetti E., Cicalese L. Morphologic adaptation following segmental living related intestinal transplantation. Transplant Proc. 2002 May;34(3):924–924. doi: 10.1016/s0041-1345(02)02672-6. [DOI] [PubMed] [Google Scholar]
- Jasleen Jasleen, Ashley Stanley W., Shimoda Naoshi, Zinner Michael J., Whang Edward E. Glucagon-like peptide 2 stimulates intestinal epithelial proliferation in vitro. Dig Dis Sci. 2002 May;47(5):1135–1140. doi: 10.1023/a:1015062712767. [DOI] [PubMed] [Google Scholar]
- Jeppesen P. B., Hartmann B., Hansen B. S., Thulesen J., Holst J. J., Mortensen P. B. Impaired meal stimulated glucagon-like peptide 2 response in ileal resected short bowel patients with intestinal failure. Gut. 1999 Oct;45(4):559–563. doi: 10.1136/gut.45.4.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jeppesen P. B., Hartmann B., Thulesen J., Graff J., Lohmann J., Hansen B. S., Tofteng F., Poulsen S. S., Madsen J. L., Holst J. J. Glucagon-like peptide 2 improves nutrient absorption and nutritional status in short-bowel patients with no colon. Gastroenterology. 2001 Mar;120(4):806–815. doi: 10.1053/gast.2001.22555. [DOI] [PubMed] [Google Scholar]
- Jeppesen P. B., Hartmann B., Thulesen J., Hansen B. S., Holst J. J., Poulsen S. S., Mortensen P. B. Elevated plasma glucagon-like peptide 1 and 2 concentrations in ileum resected short bowel patients with a preserved colon. Gut. 2000 Sep;47(3):370–376. doi: 10.1136/gut.47.3.370. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson W. F., DiPalma C. R., Ziegler T. R., Scully S., Farrell C. L. Keratinocyte growth factor enhances early gut adaptation in a rat model of short bowel syndrome. Vet Surg. 2000 Jan-Feb;29(1):17–27. doi: 10.1111/j.1532-950x.2000.00017.x. [DOI] [PubMed] [Google Scholar]
- Kato Y., Yu D., Schwartz M. Z. Enhancement of intestinal adaptation by hepatocyte growth factor. J Pediatr Surg. 1998 Feb;33(2):235–239. doi: 10.1016/s0022-3468(98)90438-9. [DOI] [PubMed] [Google Scholar]
- Kato Y., Yu D., Schwartz M. Z. Hepatocyte growth factor up-regulates SGLT1 and GLUT5 gene expression after massive small bowel resection. J Pediatr Surg. 1998 Jan;33(1):13–15. doi: 10.1016/s0022-3468(98)90351-7. [DOI] [PubMed] [Google Scholar]
- Kellett M., Potten C. S., Rew D. A. A comparison of in vivo cell proliferation measurements in the intestine of mouse and man. Epithelial Cell Biol. 1992 Oct;1(4):147–155. [PubMed] [Google Scholar]
- Klimberg V. S., Souba W. W., Salloum R. M., Holley D. T., Hautamaki R. D., Dolson D. J., Copeland E. M., 3rd Intestinal glutamine metabolism after massive small bowel resection. Am J Surg. 1990 Jan;159(1):27–33. doi: 10.1016/s0002-9610(05)80603-8. [DOI] [PubMed] [Google Scholar]
- Kollman-Bauerly K. A., Thomas D. L., Adrian T. E., Lien E. L., Vanderhoof J. A. The role of eicosanoids in the process of adaptation following massive bowel resection in the rat. JPEN J Parenter Enteral Nutr. 2001 Sep-Oct;25(5):275–281. doi: 10.1177/0148607101025005275. [DOI] [PubMed] [Google Scholar]
- Koruda M. J., Rolandelli R. H., Settle R. G., Saul S. H., Rombeau J. L. Harry M. Vars award. The effect of a pectin-supplemented elemental diet on intestinal adaptation to massive small bowel resection. JPEN J Parenter Enteral Nutr. 1986 Jul-Aug;10(4):343–350. doi: 10.1177/0148607186010004343. [DOI] [PubMed] [Google Scholar]
- Kuemmerle John F., Zhou Huiping. Insulin-like growth factor-binding protein-5 (IGFBP-5) stimulates growth and IGF-I secretion in human intestinal smooth muscle by Ras-dependent activation of p38 MAP kinase and Erk1/2 pathways. J Biol Chem. 2002 Mar 28;277(23):20563–20571. doi: 10.1074/jbc.M200885200. [DOI] [PubMed] [Google Scholar]
- Lostao M. P., Urdaneta E., Martínez-Ansó E., Barber A., Martínez J. A. Presence of leptin receptors in rat small intestine and leptin effect on sugar absorption. FEBS Lett. 1998 Feb 27;423(3):302–306. doi: 10.1016/s0014-5793(98)00110-0. [DOI] [PubMed] [Google Scholar]
- Lukanova A., Toniolo P., Akhmedkhanov A., Biessy C., Haley N. J., Shore R. E., Riboli E., Rinaldi S., Kaaks R. A prospective study of insulin-like growth factor-I, IGF-binding proteins-1, -2 and -3 and lung cancer risk in women. Int J Cancer. 2001 Jun 15;92(6):888–892. doi: 10.1002/ijc.1265. [DOI] [PubMed] [Google Scholar]
- Lund P. K. Molecular basis of intestinal adaptation: the role of the insulin-like growth factor system. Ann N Y Acad Sci. 1998 Nov 17;859:18–36. doi: 10.1111/j.1749-6632.1998.tb11108.x. [DOI] [PubMed] [Google Scholar]
- Ma J., Pollak M. N., Giovannucci E., Chan J. M., Tao Y., Hennekens C. H., Stampfer M. J. Prospective study of colorectal cancer risk in men and plasma levels of insulin-like growth factor (IGF)-I and IGF-binding protein-3. J Natl Cancer Inst. 1999 Apr 7;91(7):620–625. doi: 10.1093/jnci/91.7.620. [DOI] [PubMed] [Google Scholar]
- Malden L. T., Novak U., Burgess A. W. Expression of transforming growth factor alpha messenger RNA in the normal and neoplastic gastro-intestinal tract. Int J Cancer. 1989 Mar 15;43(3):380–384. doi: 10.1002/ijc.2910430305. [DOI] [PubMed] [Google Scholar]
- McIntyre P. B., Fitchew M., Lennard-Jones J. E. Patients with a high jejunostomy do not need a special diet. Gastroenterology. 1986 Jul;91(1):25–33. doi: 10.1016/0016-5085(86)90434-8. [DOI] [PubMed] [Google Scholar]
- Messing B., Crenn P., Beau P., Boutron-Ruault M. C., Rambaud J. C., Matuchansky C. Long-term survival and parenteral nutrition dependence in adult patients with the short bowel syndrome. Gastroenterology. 1999 Nov;117(5):1043–1050. doi: 10.1016/s0016-5085(99)70388-4. [DOI] [PubMed] [Google Scholar]
- Michail S., Mohammadpour H., Park J. H., Vanderhoof J. A. Effect of glutamine-supplemented elemental diet on mucosal adaptation following bowel resection in rats. J Pediatr Gastroenterol Nutr. 1995 Nov;21(4):394–398. doi: 10.1097/00005176-199511000-00005. [DOI] [PubMed] [Google Scholar]
- Mulligan Claire, Rochford Justin, Denyer Gareth, Stephens Richard, Yeo Giles, Freeman Thomas, Siddle Kenneth, O'Rahilly Stephen. Microarray analysis of insulin and insulin-like growth factor-1 (IGF-1) receptor signaling reveals the selective up-regulation of the mitogen heparin-binding EGF-like growth factor by IGF-1. J Biol Chem. 2002 Sep 3;277(45):42480–42487. doi: 10.1074/jbc.M206206200. [DOI] [PubMed] [Google Scholar]
- Murphy M. S. Growth factors and the gastrointestinal tract. Nutrition. 1998 Oct;14(10):771–774. doi: 10.1016/s0899-9007(98)00081-1. [DOI] [PubMed] [Google Scholar]
- Nelson L. M., Russell R. I., Lee F. D. Elemental diet composition and the structure and function of rat small intestine: comparison of the effects of two diets on morphology and in vivo absorption of water. JPEN J Parenter Enteral Nutr. 1981 May-Jun;5(3):204–206. doi: 10.1177/0148607181005003204. [DOI] [PubMed] [Google Scholar]
- Nightingale J. M., Lennard-Jones J. E., Gertner D. J., Wood S. R., Bartram C. I. Colonic preservation reduces need for parenteral therapy, increases incidence of renal stones, but does not change high prevalence of gall stones in patients with a short bowel. Gut. 1992 Nov;33(11):1493–1497. doi: 10.1136/gut.33.11.1493. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nordgaard I., Hansen B. S., Mortensen P. B. Colon as a digestive organ in patients with short bowel. Lancet. 1994 Feb 12;343(8894):373–376. doi: 10.1016/s0140-6736(94)91220-3. [DOI] [PubMed] [Google Scholar]
- Nordskog B. K., Phan C. T., Nutting D. F., Tso P. An examination of the factors affecting intestinal lymphatic transport of dietary lipids. Adv Drug Deliv Rev. 2001 Aug 23;50(1-2):21–44. doi: 10.1016/s0169-409x(01)00147-8. [DOI] [PubMed] [Google Scholar]
- Nygaard K. Resection of the small intestine in rats. 3. Morphological changes in the intestinal tract. Acta Chir Scand. 1967;133(3):233–248. [PubMed] [Google Scholar]
- O'Brien David P., Nelson Lindsey A., Williams Jodi L., Kemp Christopher J., Erwin Christopher R., Warner Brad W. Selective inhibition of the epidermal growth factor receptor impairs intestinal adaptation after small bowel resection. J Surg Res. 2002 Jun 1;105(1):25–30. doi: 10.1006/jsre.2002.6440. [DOI] [PubMed] [Google Scholar]
- Orazi A., Du X., Yang Z., Kashai M., Williams D. A. Interleukin-11 prevents apoptosis and accelerates recovery of small intestinal mucosa in mice treated with combined chemotherapy and radiation. Lab Invest. 1996 Jul;75(1):33–42. [PubMed] [Google Scholar]
- Park J. H., Grandjean C. J., Hart M. H., Baylor J. M., Vanderhoof J. A. Effects of dietary linoleic acid on mucosal adaptation after small bowel resection. Digestion. 1989;44(2):57–65. doi: 10.1159/000199893. [DOI] [PubMed] [Google Scholar]
- Pearson P. Y., O'Connor D. M., Schwartz M. Z. Novel effect of leptin on small intestine adaptation. J Surg Res. 2001 May 15;97(2):192–195. doi: 10.1006/jsre.2001.6153. [DOI] [PubMed] [Google Scholar]
- Peterson C. A., Carey H. V., Hinton P. L., Lo H. C., Ney D. M. GH elevates serum IGF-I levels but does not alter mucosal atrophy in parenterally fed rats. Am J Physiol. 1997 May;272(5 Pt 1):G1100–G1108. doi: 10.1152/ajpgi.1997.272.5.G1100. [DOI] [PubMed] [Google Scholar]
- Peterson C. A., Gillingham M. B., Mohapatra N. K., Dahly E. M., Adamo M. L., Carey H. V., Lund P. K., Ney D. M. Enterotrophic effect of insulin-like growth factor-I but not growth hormone and localized expression of insulin-like growth factor-I, insulin-like growth factor binding protein-3 and -5 mRNAs in jejunum of parenterally fed rats. JPEN J Parenter Enteral Nutr. 2000 Sep-Oct;24(5):288–295. doi: 10.1177/0148607100024005288. [DOI] [PubMed] [Google Scholar]
- Ponder B. A., Schmidt G. H., Wilkinson M. M., Wood M. J., Monk M., Reid A. Derivation of mouse intestinal crypts from single progenitor cells. Nature. 1985 Feb 21;313(6004):689–691. doi: 10.1038/313689a0. [DOI] [PubMed] [Google Scholar]
- Potten C. S. The significance of spontaneous and induced apoptosis in the gastrointestinal tract of mice. Cancer Metastasis Rev. 1992 Sep;11(2):179–195. doi: 10.1007/BF00048063. [DOI] [PubMed] [Google Scholar]
- Richards D. M., Deeks J. J., Sheldon T. A., Shaffer J. L. Home parenteral nutrition: a systematic review. Health Technol Assess. 1997;1(1):i-iii, 1-59. [PubMed] [Google Scholar]
- Richards D. M., Irving M. H. Assessing the quality of life of patients with intestinal failure on home parenteral nutrition. Gut. 1997 Feb;40(2):218–222. doi: 10.1136/gut.40.2.218. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roberts John P., Brown Robert S., Jr, Edwards Erick B., Farmer Douglas G., Freeman Richard B., Jr, Wiesner Russell H., Merion Robert M. Liver and intestine transplantation. Am J Transplant. 2003;3 (Suppl 4):78–90. doi: 10.1034/j.1600-6143.3.s4.8.x. [DOI] [PubMed] [Google Scholar]
- Rubin D. C., Swietlicki E. A., Wang J. L., Dodson B. D., Levin M. S. Enterocytic gene expression in intestinal adaptation: evidence for a specific cellular response. Am J Physiol. 1996 Jan;270(1 Pt 1):G143–G152. doi: 10.1152/ajpgi.1996.270.1.G143. [DOI] [PubMed] [Google Scholar]
- Ryan J., Costigan D. C. Determination of the histological distribution of insulin like growth factor 1 receptors in the rat gut. Gut. 1993 Dec;34(12):1693–1697. doi: 10.1136/gut.34.12.1693. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scolapio J. S., Camilleri M., Fleming C. R., Oenning L. V., Burton D. D., Sebo T. J., Batts K. P., Kelly D. G. Effect of growth hormone, glutamine, and diet on adaptation in short-bowel syndrome: a randomized, controlled study. Gastroenterology. 1997 Oct;113(4):1074–1081. doi: 10.1053/gast.1997.v113.pm9322500. [DOI] [PubMed] [Google Scholar]
- Scolapio J. S. Effect of growth hormone, glutamine, and diet on body composition in short bowel syndrome: a randomized, controlled study. JPEN J Parenter Enteral Nutr. 1999 Nov-Dec;23(6):309–313. doi: 10.1177/0148607199023006309. [DOI] [PubMed] [Google Scholar]
- Scolapio James S. Tales from the crypt. Gastroenterology. 2003 Feb;124(2):561–564. doi: 10.1053/gast.2003.50071. [DOI] [PubMed] [Google Scholar]
- Scott R. B., Kirk D., MacNaughton W. K., Meddings J. B. GLP-2 augments the adaptive response to massive intestinal resection in rat. Am J Physiol. 1998 Nov;275(5 Pt 1):G911–G921. doi: 10.1152/ajpgi.1998.275.5.G911. [DOI] [PubMed] [Google Scholar]
- Seguy David, Vahedi Kouroche, Kapel Nathalie, Souberbielle Jean-Claude, Messing Bernard. Low-dose growth hormone in adult home parenteral nutrition-dependent short bowel syndrome patients: a positive study. Gastroenterology. 2003 Feb;124(2):293–302. doi: 10.1053/gast.2003.50057. [DOI] [PubMed] [Google Scholar]
- Shin C. E., Helmrath M. A., Falcone R. A., Jr, Fox J. W., Duane K. R., Erwin C. R., Warner B. W. Epidermal growth factor augments adaptation following small bowel resection: optimal dosage, route, and timing of administration. J Surg Res. 1998 Jun;77(1):11–16. doi: 10.1006/jsre.1998.5336. [DOI] [PubMed] [Google Scholar]
- Shulman D. I., Hu C. S., Duckett G., Lavallee-Grey M. Effects of short-term growth hormone therapy in rats undergoing 75% small intestinal resection. J Pediatr Gastroenterol Nutr. 1992 Jan;14(1):3–11. doi: 10.1097/00005176-199201000-00002. [DOI] [PubMed] [Google Scholar]
- Sondheimer J. M., Cadnapaphornchai M., Sontag M., Zerbe G. O. Predicting the duration of dependence on parenteral nutrition after neonatal intestinal resection. J Pediatr. 1998 Jan;132(1):80–84. doi: 10.1016/s0022-3476(98)70489-5. [DOI] [PubMed] [Google Scholar]
- Stahl Andreas. A current review of fatty acid transport proteins (SLC27). Pflugers Arch. 2003 Jul 11;447(5):722–727. doi: 10.1007/s00424-003-1106-z. [DOI] [PubMed] [Google Scholar]
- Sukhotnik I., Gork A. S., Chen M., Drongowski R. A., Coran A. G., Harmon C. M. Effect of low fat diet on lipid absorption and fatty-acid transport following bowel resection. Pediatr Surg Int. 2001 May;17(4):259–264. doi: 10.1007/s003830100590. [DOI] [PubMed] [Google Scholar]
- Sukhotnik Igor, Lerner Aaron, Sabo Edmund, Krausz Michael M., Siplovich Leonardo, Coran Arnold G., Mogilner Jorge, Shiloni Eitan. Effects of enteral arginine supplementation on the structural intestinal adaptation in a rat model of short bowel syndrome. Dig Dis Sci. 2003 Jul;48(7):1346–1351. doi: 10.1023/a:1024167428092. [DOI] [PubMed] [Google Scholar]
- Sukhotnik Igor, Shiloni Eitan, Krausz Michael M., Yakirevich Evgeny, Sabo Edmund, Mogilner Jorge, Coran Arnold G., Harmon Carroll M. Low-fat diet impairs postresection intestinal adaptation in a rat model of short bowel syndrome. J Pediatr Surg. 2003 Aug;38(8):1182–1187. doi: 10.1016/s0022-3468(03)00264-1. [DOI] [PubMed] [Google Scholar]
- Sukhotnik Igor, Yakirevich Evgeny, Coran Arnold G., Siplovich Leonardo, Krausz Michael, Hirsh Mark, Sabo Edmund, Shiloni Eitan. Effect of transforming growth factor-alpha on intestinal adaptation in a rat model of short bowel syndrome. J Surg Res. 2002 Dec;108(2):235–242. doi: 10.1006/jsre.2002.6556. [DOI] [PubMed] [Google Scholar]
- Sweetser D. A., Hauft S. M., Hoppe P. C., Birkenmeier E. H., Gordon J. I. Transgenic mice containing intestinal fatty acid-binding protein-human growth hormone fusion genes exhibit correct regional and cell-specific expression of the reporter gene in their small intestine. Proc Natl Acad Sci U S A. 1988 Dec;85(24):9611–9615. doi: 10.1073/pnas.85.24.9611. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Szkudlarek J., Jeppesen P. B., Mortensen P. B. Effect of high dose growth hormone with glutamine and no change in diet on intestinal absorption in short bowel patients: a randomised, double blind, crossover, placebo controlled study. Gut. 2000 Aug;47(2):199–205. doi: 10.1136/gut.47.2.199. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tamada H., Nezu R., Matsuo Y., Imamura I., Takagi Y., Okada A. Alanyl glutamine-enriched total parenteral nutrition restores intestinal adaptation after either proximal or distal massive resection in rats. JPEN J Parenter Enteral Nutr. 1993 May-Jun;17(3):236–242. doi: 10.1177/0148607193017003236. [DOI] [PubMed] [Google Scholar]
- Tavakkolizadeh Ali, Whang Edward E. Understanding and augmenting human intestinal adaptation: a call for more clinical research. JPEN J Parenter Enteral Nutr. 2002 Jul-Aug;26(4):251–255. doi: 10.1177/0148607102026004251. [DOI] [PubMed] [Google Scholar]
- Thiesen A., Wild G. E., Tappenden K. A., Agellon L. B., Drozdowski L., Keelan M., Thomson B. K. A., McBurney M. I., Clandinin M. T., Thomson A. B. R. Intestinal resection- and steroid-associated alterations in gene expression were not accompanied by changes in lipid uptake. Digestion. 2002;66(2):112–120. doi: 10.1159/000065590. [DOI] [PubMed] [Google Scholar]
- Thiesen Aducio L., Tappenden Kelly A., McBurney Mike I., Clandinin M. Thomas, Keelan Monika, Thomson Ben K., Wild Gary E., Thomson Alan B. Dietary lipids alter the effect of steroids on the transport of glucose after intestinal resection: Part I. Phenotypic changes and expression of transporters. J Pediatr Surg. 2003 Feb;38(2):150–160. doi: 10.1053/jpsu.2003.50034. [DOI] [PubMed] [Google Scholar]
- Vanderhoof J. A., Blackwood D. J., Mohammadpour H., Park J. H. Effects of oral supplementation of glutamine on small intestinal mucosal mass following resection. J Am Coll Nutr. 1992 Apr;11(2):223–227. [PubMed] [Google Scholar]
- Vanderhoof J. A., Grandjean C. J., Baylor J. M., Baily J., Euler A. R. Morphological and functional effects of 16,16-dimethyl-prostaglandin-E2 on mucosal adaptation after massive distal small bowel resection in the rat. Gut. 1988 Jun;29(6):802–808. doi: 10.1136/gut.29.6.802. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vanderhoof J. A., Park J. H., Herrington M. K., Adrian T. E. Effects of dietary menhaden oil on mucosal adaptation after small bowel resection in rats. Gastroenterology. 1994 Jan;106(1):94–99. doi: 10.1016/s0016-5085(94)94589-6. [DOI] [PubMed] [Google Scholar]
- Welters C. F., Dejong C. H., Deutz N. E., Heineman E. Intestinal function and metabolism in the early adaptive phase after massive small bowel resection in the rat. J Pediatr Surg. 2001 Dec;36(12):1746–1751. doi: 10.1053/jpsu.2001.28813. [DOI] [PubMed] [Google Scholar]
- Welters Carlo F. M., Dejong Cornelius H. C., Deutz Nicolaas E. P., Heineman Erik. Intestinal adaptation in short bowel syndrome. ANZ J Surg. 2002 Mar;72(3):229–236. doi: 10.1046/j.1445-2197.2002.02357.x. [DOI] [PubMed] [Google Scholar]
- Wheeler E. E., Challacombe D. N. The trophic action of growth hormone, insulin-like growth factor-I, and insulin on human duodenal mucosa cultured in vitro. Gut. 1997 Jan;40(1):57–60. doi: 10.1136/gut.40.1.57. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wildhaber Barbara E., Yang Hua, Teitelbaum Daniel H. Total parenteral nutrition-induced apoptosis in mouse intestinal epithelium: modulation by keratinocyte growth factor. J Surg Res. 2003 Jun 15;112(2):144–151. doi: 10.1016/s0022-4804(03)00160-4. [DOI] [PubMed] [Google Scholar]
- Williamson R. C. Intestinal adaptation (first of two parts). Structural, functional and cytokinetic changes. N Engl J Med. 1978 Jun 22;298(25):1393–1402. doi: 10.1056/NEJM197806222982505. [DOI] [PubMed] [Google Scholar]
- Williamson R. C. Intestinal adaptation (second of two parts). Mechanisms of control. N Engl J Med. 1978 Jun 29;298(26):1444–1450. doi: 10.1056/NEJM197806292982604. [DOI] [PubMed] [Google Scholar]
- Windmueller H. G., Spaeth A. E. Identification of ketone bodies and glutamine as the major respiratory fuels in vivo for postabsorptive rat small intestine. J Biol Chem. 1978 Jan 10;253(1):69–76. [PubMed] [Google Scholar]
- Wirén M. E., Permert J., Skullman S. P., Wang F., Larsson J. No differences in mucosal adaptive growth one week after intestinal resection in rats given enteral glutamine supplementation or deprived of glutamine. Eur J Surg. 1996 Jun;162(6):489–498. [PubMed] [Google Scholar]
- Wong W. M., Wright N. A. Cell proliferation in gastrointestinal mucosa. J Clin Pathol. 1999 May;52(5):321–333. doi: 10.1136/jcp.52.5.321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wu G. Intestinal mucosal amino acid catabolism. J Nutr. 1998 Aug;128(8):1249–1252. doi: 10.1093/jn/128.8.1249. [DOI] [PubMed] [Google Scholar]
- Xia Guliang, Martin Abigail E., Michalsky Marc P., Besner Gail E. Heparin-binding EGF-like growth factor preserves crypt cell proliferation and decreases bacterial translocation after intestinal ischemia/reperfusion injury. J Pediatr Surg. 2002 Jul;37(7):1081–1087. doi: 10.1053/jpsu.2002.33881. [DOI] [PubMed] [Google Scholar]
- Yagi M., Sakamoto K., Inoue T., Fukushima W., Muraoka K., Ii T., Iyobe T., Iwasa K., Hashimoto T., Shimizu K. Effect of a glutamine-enriched elemental diet on regeneration of the small bowel mucosa following isotransplantation of small intestine. Transplant Proc. 1994 Aug;26(4):2297–2298. [PubMed] [Google Scholar]
- Yang Hua, Antony Paul A., Wildhaber Barbara E., Teitelbaum Daniel H. Intestinal intraepithelial lymphocyte gamma delta-T cell-derived keratinocyte growth factor modulates epithelial growth in the mouse. J Immunol. 2004 Apr 1;172(7):4151–4158. doi: 10.4049/jimmunol.172.7.4151. [DOI] [PubMed] [Google Scholar]
- Yang Hua, Wildhaber Barbara E., Teitelbaum Daniel H. 2003 Harry M. Vars Research Award. Keratinocyte growth factor improves epithelial function after massive small bowel resection. JPEN J Parenter Enteral Nutr. 2003 May-Jun;27(3):198–207. doi: 10.1177/0148607103027003198. [DOI] [PubMed] [Google Scholar]
- Yusta B., Huang L., Munroe D., Wolff G., Fantaske R., Sharma S., Demchyshyn L., Asa S. L., Drucker D. J. Enteroendocrine localization of GLP-2 receptor expression in humans and rodents. Gastroenterology. 2000 Sep;119(3):744–755. doi: 10.1053/gast.2000.16489. [DOI] [PubMed] [Google Scholar]
- Zhang D. L., Jiang Z. W., Jiang J., Cao B., Li J. S. D-lactic acidosis secondary to short bowel syndrome. Postgrad Med J. 2003 Feb;79(928):110–112. doi: 10.1136/pmj.79.928.110. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhou X., Li Y. X., Li N., Li J. S. Effect of bowel rehabilitative therapy on structural adaptation of remnant small intestine: animal experiment. World J Gastroenterol. 2001 Feb;7(1):66–73. doi: 10.3748/wjg.v7.i1.66. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ziegler T. R., Mantell M. P., Chow J. C., Rombeau J. L., Smith R. J. Gut adaptation and the insulin-like growth factor system: regulation by glutamine and IGF-I administration. Am J Physiol. 1996 Nov;271(5 Pt 1):G866–G875. doi: 10.1152/ajpgi.1996.271.5.G866. [DOI] [PubMed] [Google Scholar]
- Ziegler Thomas R., Fernández-Estívariz Concepción, Gu Li H., Bazargan Niloofar, Umeakunne Kay, Wallace Timothy M., Diaz Emma E., Rosado Kathia E., Pascal Robert R., Galloway John R. Distribution of the H+/peptide transporter PepT1 in human intestine: up-regulated expression in the colonic mucosa of patients with short-bowel syndrome. Am J Clin Nutr. 2002 May;75(5):922–930. doi: 10.1093/ajcn/75.5.922. [DOI] [PubMed] [Google Scholar]
- de Miguel E., Gómez de Segura I. A., Bonet H., Rodríguez Montes J. A., Mata A. Trophic effects of neurotensin in massive bowel resection in the rat. Dig Dis Sci. 1994 Jan;39(1):59–64. doi: 10.1007/BF02090061. [DOI] [PubMed] [Google Scholar]
- van der Hulst R. R., van Kreel B. K., von Meyenfeldt M. F., Brummer R. J., Arends J. W., Deutz N. E., Soeters P. B. Glutamine and the preservation of gut integrity. Lancet. 1993 May 29;341(8857):1363–1365. doi: 10.1016/0140-6736(93)90939-e. [DOI] [PubMed] [Google Scholar]