Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/14333
標題: 三價鉻離子對小鼠手術傷口癒合之影響
The effects of trivalent chromium on healing of surgical wound in mice
作者: 謝侑達
Hsieh, Yu-Ta
關鍵字: 鉻離子;chromium;傷口癒合;小鼠;類固醇;類胰島素生長因子;wound healing;mice;dexamethasone;IGF-1
出版社: 獸醫學系暨研究所
引用: 1. Anderson RA. Stress effects on chromium nutrition of humans and farm animals, in Lyons TP, ed. Biotechnology in the Feed Industry. Proceedings of Alltech’s Tenth symposium. Nottingham, UK, University Press, 267-274, 1994. 2. Anderson RA. Nutritional factors influencing the glucose/insulin system : Chromium. J Am Col Nutr 16: 404-410, 1997. 3. Anderson RA. Recent advances in the clinical and biochemical manifestations of chromium deficiency in human and animal nutrition. J Trace Elem Med Biol 11: 241-250, 1998. 4. Anderson RA. Chromium in the prevention and control of diabetes. Diabetes & Metabolism 26: 22-27, 2000. 5. Anderson RA. Chromium in human nutrition. Nutr Rev 46(7): 271-272, 1988. 6. Anderson RA, Bryden NA, Polansky MM, Deuster PA. Exercise effects on chromium excretion of trained and untrained men comsuming a constant diet. J Appl Physiol 64: 249-252, 1988. 7. Anderson RA, Kozlowski AS. Chromium intake, absorption and excretion of subjects consuming self-selected diets. Am J Clin Nutr 41: 571-577, 1985. 8. Anderson RA, Polansky MM, Bryden NA, Roginski EE, Patterson KY, Reamer DC. Effects of exercise (running) on serum glucose, insulin, glucagon and chromium excretion. Diabetes 32: 212-216, 1982. 9. Anderson RA, Polansky MM, Bryden NA, Roginski EE, Patterson KY, Reamer DC. Effect of exercise (running) on serum glucose, insulin, glucagon, and chromium excretion. Diabetes. 31(3): 212-216, 1982. 10. Ando Y, Jensen PJ. Epidermal growth factor and insulin-like growth factor I enhance keratinocyte migration. J Invest Dermatol 100: 633-639, 1993. 11. Baldi A, Bontempo V, Dell''Orto V. Effects of dietary chromium yeast in weaning-stressed piglets. Can J Anim Sci 79: 369-374, 1999. 12. Barreca A, De Luca M, Del Monte P, Bondanza S, Damonte G, Cariola G, Di Marco E, Giordano G, Cancedda R, Minuto F. In vitro paracrine regulation of human keratinocyte growth by fibroblast-derived insulin-like growth factors. J Cell Physiol 151(2): 262-268, 1992. 13. Baxter RC. Insulin-like growth factor (IGF)-binding proteins: interactions with IGFs and intrinsic bioactivities. Am J Physiol Endocrinol Metabol Gastrointest Physiol 278: 967-976, 2000. 14. Beck LS, DeGuzman L, Lee WP, Xu Y, Siegel MW, Amento EP. One systemic administration of transforming growth factor-β1 reverses age or glucocorticoid impaired wound healing. J Clin Invest 92: 2841-2849, 1993. 15. Beer HD, Fassler R, Werner S. Glucocorticoid-regulated gene expression during cutaneous wound repair. Vitam Horm 59: 217-239, 2000. 16. Bitar MS. Insulin-like growth factor I reverses diabetes induced wound healing impairment in rats. Horm Metab Res 29: 383-386, 1997. 17. Blakytny R, Jude EB, Martin Gibson J, Boulton AJ, Ferguson MW. Lack of insulin-like growth factor 1 (IGF1) in the basal keratinocyte layer of diabetic skin and diabetic foot ulcers. J Pathol 190: 589-594, 2000. 18. Bonefeld K, Moller S. Insulin-like growth factor-1 and the liver. Liver Int 31(7): 911-999, 2011. 19. Borgs P, Mallard BA. Immune-endocrine interactions in agricultural species: chromium and its effect on health and performance. Domest Anim Endocrinol 15: 431-438, 1998. 20. Boucek RJ. Factors affecting wound healing. Symposium on wound healing. Otolaryngol Clin North Am 17(2): 243-264, 1984. 21. Braiman-Wiksman L, Solomonik I, Spira R, Tennenbaum T. Novel insights into wound healing sequence of events. Toxicol Pathol 35(6): 767-779, 2007. 22. Broughton G II, Janis JE, Attinger CE. The basic science of wound healing. Plast Reconstr Surg 117: 12-34, 2006. 23. Bunker W, Lawson MD, Delves HT. The uptake and excretion of chromium by the elderly. Am J Clin Nutr 39: 799-802, 1984. 24. Burton JL. Supplemental chromium: its benefits to the bovine immune system. Anim Feed Sci Technol 53: 117-133, 1995. 25. Carroll PV. Treatment with growth hormone and insulin-like growth factor-I in critical illness. Best Pract Res Cl En 15(4): 435-451, 2001. 26. Chang X, Mowat DN. Supplemental chromium for stressed and growing feeder calves. J Anim Sci 70: 559-565, 1992. 27. Chedid M, Hoyle JR, Csaky KG, Rubin JS. Glucocorticoids inhibit keratinocyte growth factor production in primary dermal fibroblasts. Endocrinology 137: 2232-2237, 1996. 28. Chen NSC, Tsai A, Duer IA. Effects of chelating agents on chromium absorption in rats. J Nutr 103: 1182-1186, 1973. 29. Chen TD. Prednisolone altered chromium distribution in diet-induced obesity mice. Master thesis, NCHU, DVM. Taiwan. May, 2005. 30. Chiquetti Junior A, Rodrigues MA, Delfino VD. An experimental model for the study of drug effects on cutaneous healing. Acta Cir Bras 22(4): 317-321, 2007. 31. Clark RAF, Gallin JI, Fauci AS. Effect of in vivo prednisone on in vitro eosinophil and neutrophil adherence and chemotaxis. Blood 53: 633-641, 1979. 32. Demling RH. The role of anabolic hormones for wound healing in catabolic states. J Burns Wounds. 17: 4:e2, 2005. 33. Ducros V. Chromium metabolism. Biol Trace Elem Res 32: 65-77, 1992. 34. Dunaiski V, Belford DA. Contribution of circulating IGF-1 to wound repair in GH-treated rats. Growth Horm IGF Res 12: 381-387, 2002. 35. Eaglstein WH, Falanga V. Chronic wounds. Surg Clin North Am 77: 689-700, 1997. 36. Edwards JC, Dunphy JE. Wound healing. Injury and abnormal repair. N Engl J Med 259: 275-285, 1958. 37. Ehrlich HP, Hunt TK. Effects of cortisone and vitamine A on wound healing. Ann Surg 167: 324-328, 1968. 38. Ehrlich HP, Tarver H, Hunt TK. Effect of vitamin A and glucocorticoids upon inflammation and collagen synthesis. Ann Surg 177: 222-227, 1973. 39. Elijah IE, Branski LK, Finnerty CC, Herndon DN. The GH/IGF-1 system in critical illness. Best Pract Res Clin Endocrinol Metab 25(5): 759-767, 2011. 40. Enoch S, John D. Basic science of wound healing. Surgery 23(2): 37-42, 2008. 41. Evans GW, Bowman TD. Chromium picolinate increased membrane fluidity and rate of insulin internalization. J Inorg Biochem 46: 243-250, 1992. 42. Evans GW, Bowman TD. Chromium picolinate increases membrane fluidity and rate of insulin internalization. J Inorg Biochem 48: 243-250, 1992. 43. Evock-Clover CM, Polansky MM, Anderson RA, Steele NC. Dietary chromium supplementation with or without somatotropin treatment alters serum hormones and metabolites in growing pigs without affecting growth performance. J Nutr 123: 1504-1512, 1993. 44. Fanciulli G, Delitala A, Delitala G. Growth hormone, menopause and ageing: no definite evidence for ‘rejuvenation’ with growth hormone. Hum Reprod Update 15: 341-358, 2009. 45. Fauci AS, Dale DC, Balow JE. Glucocorticoid therapy: mechanisms of action and clinical considerations. Ann Intern Med 84: 304-315, 1976. 46. Froesch ER, Schmid C, Schwander J, Zapf J. Actions of insulin-like growth factors. Annu Rev Physiol 47: 443-467, 1985. 47. Gal P, Kilik R, Mokry M, Vidinsky B, Vasilenko T, Mozes S, Bobrov N, Tomori Z, Bober J, Lenhardt L. Simple method of open skin wound healing model in corticosteroid-treated and diabetic rats: standardization of semi-quantitative and quantitative histological assessments. Vet Med 53: 652-659, 2008. 48. Gartner MH, Benson JD, Caldwell MD. Insulin-like growth factors I and II expression in the healing wound. J Surg Res 52: 389-394, 1992. 49. Ghahary A, Shen YJ, Wang R, Scott PG, Tredget EE. Expression and localization of insulin-like growth factor-1 in normal and post-burn hypertrophic scar tissue in human. Mol Cell Biochem 183: 1-9, 1998. 50. Giordano R, Bonelli L, Marinazzo E, Ghigo E, Arvat E. Growth hormone treatment in human ageing: benefits and risks. Hormones 7: 133-139, 2008. 51. Goforth P, Gudas CJ. Effects of steroids on wound healing: a review of the literature. J Foot Surg 19: 22-28, 1980. 52. Gorski J, Gannon F. Current models of steroid hormone action: a critique. Ann Rev Physiol 38: 425-450, 1976. 53. Green H, Morikawa M, Nixon T. A dual effector theory of growth-hormone action. Differentiation 29: 195-198, 1985. 54. Grewal RS, Gupta SC, Singhal GM, Gupta SN. Wound healing in relation to insulin. Int Surg 57(3): 229-232, 1972. 55. Grose R, Werner S, Kessler D, Tuckermann J, Huggel K, Durka S, Reichardt HM, Werner S. A role for endogenous glucocorticoids in wound repair. EMBO Rep 3: 575-582, 2002. 56. Guo S, DiPietro LA. Factors affecting wound healing. J Dent Res 89(3): 219–229, 2010. 57. Haase I, Evans R, Pofahl R, Watt FM. Regulation of keratinocyte shape, migration and wound epithelialization by IGF-1- and EGF dependent signalling pathways. J Cell Sci 116: 3227-3238, 2003. 58. Haber RS, Weinstein SP. Role of glucose transporters in glucocorticoid-induced insulin resistance. GLUT4 isoform in rat skeletal muscle is not decreased by dexamethasone. Diabetes 41: 728-735, 1992. 59. Habif TP. Clinical Dermatology. A color guide to diagnosis and therapy. 3rd ed. St Louis, Mosby, 46, 1996. 60. Hori Y, Hu DE, Yasui K, Smither RL, Gresham GA, Fan TP. Differential effects of angiostatic steroids and dexamethasone on angiogenesis and cytokine levels in rat sponge implants. Br J Pharmacol 118: 1584-1591, 1996. 61. Jacob R, Barrett E, Plewe G, Fagin KD, Sherwin RS. Acute effects of insulin-like growth factor I on glucose and amino acid metabolism in the awake fasted rat. comparison with insulin. J Clin Invest 83: 1717-1723, 1989. 62. Jeejeebhoy KN, Chu RC, Marliss EB, Greenberg GR, Bruce-Robertson A. Chromium deficiency, glucose intolerance and neuropathy reversed by chromium supplementation in a patient receiving longterm total parenteral nutrition. Am J Clin Nutr 30: 531-538, 1977. 63. Jeschke MG, Schubert T, Krickhahn M, Polykandriotis E, Klein D, Perez-Polo JR, Przkora R, Herndon DN. Interaction of exogenous liposomal insulin-like growth factor-I cDNA gene transfer with growth factors on collagen expression in acute wounds. Wound Repair Regen 13(3): 269-277, 2005. 64. Jones JI, Clemmons DR. Insulin-like growth factors and their binding proteins: biological actions. Endocr Rev 16: 3-34, 1995. 65. Jorgensen PH, Oxlund H. Growth hormone increases the biomechanical strength and collagen deposition rate during the early phase of skin wound healing. Wound Repair Regen 4: 40-47, 1996. 66. Jyung RW, Mustoe JA, Busby WH, Clemmons DR. Increased woundbreaking strength induced by insulin-like growth factor I in combination with insulin-like growth factor binding protein-1. Surgery 115: 233-239, 1994. 67. Kawahara RS, Deng ZW, Deuel TF. Glucocorticoids inhibit the transcriptional induction of JE, a platelet-derived growth factor-inducible gene. J Biol Chem 266(20): 13261-13266, 1991. 68. Kegley EB, Spears JW, Brown TT. Effect of shipping and chromium supplementation on performance, immune response, and disease resistance of steers. J Anim Sci 75: 1956-1964, 1997. 69. Kim BG, Lindemann MD, Cromwell GL. The effects of dietary chromium(III) picolinate on growth performance, blood measurements, and respiratory rate in pigs kept in high and low ambient temperature. J Anim Sci 87: 1695-1704, 1999. 70. Kim BG, Adams JM, Jackson BA, Lindemann MD. effects of chromium(III) picolinate on cortisol and DHEAs secretion in H295R human adrenocortical cells. Biol Trace Elem Res 133(2):171-180, 2009. 71. Kim DS, Kim TW, Park IK, Kang JS, Om AS. Effects of chromium picolinate supplementation on insulin sensitivity, serum lipids, and body weight in dexamethasone-treated rats. Metabolism 51(5): 589-594, 2002. 72. Koob T, Jeffrey TT, Eisen AZ. Regulation of human skin collagenase activity by hydrocortisone and dexamethasone in organ culture. Biochem Biophys Res Commum 61: 1083-1088, 1974. 73. Kozlovsky AS, Moser PB, Reiser S, Anderson RA. Effects of diets high in simple sugars on urinary chromium losses. Metabolism 35: 515-518, 1986. 74. Kritsch KR, Murali S, Adamo ML, Ney DM. Dexamethasone decreases serum and liver IGF-I and maintains liver IGF-I mRNA in parenterally fed rats. Am J Physiol Regul Integr Comp Physiol 282(2): 28-36, 2002. 75. Lawrence RT, Salter JM, Best CH. The effect of insulin on nitrogen retention in the hypophysectomized rat. Br Med J 2: 437-439, 1954. 76. Lee SW, Kim SH, Kim JY, Lee Y. The effect of growth hormone on fibroblast proliferation and keratinoctye migration. J Plast Reconstr Aesthet Surg 63(4): 364-369, 2010. 77. Lefavi RG, Wilson GD, Keith RE. Lipid-lowering effect of a dietary chromium (III)-nicotinic acid complex in male athletes. Nutr Res 13: 239-249, 1993. 78. Lengyel AM. Novel mechanisms of growth hormone regulation: growth hormone-releasing peptides and ghrelin. Braz J Med Biol Res 39: 1003-1011, 2006. 79. LeRoith D. Insulin-like growth factors. New Engl J Med 336: 633-640, 1997. 80. LeRoith D, Clemmons D, Nissley P, Rechler MM. Insulin-like growth factor I in health and disease. Ann Intern Med 116: 854-862, 1992. 81. Leroith D, Yakar S. Mechanisms of disease: metabolic effects of growth hormone and insulin-like growth factor 1. Nat Clin Pract Endocrinol Metab 3: 302-310, 2007. 82. Lindemann MD. Chromium and swine nutrition. J Trace Elem Exp Med 12: 149-161, 1999. 83. Liu Y, Petreaca M, Yao M, Martins-Green M. Cell and molecular mechanisms of keratinocyte function stimulated by insulin during wound healing. BMC Cell Biol 10: 1, 2009. 84. Losada F, Garcia-Luna PP, Gomez-Cia T, Garrido M, Pereira JL, Marin F, Astorga R. Effects of human recombinant growth hormone on donor-site healing in burned adults. World J Surg 26: 2-8, 2002. 85. Luo J, Murphy LJ. Dexamethasone inhibits growth hormone induction of insulin-like growth factor–I (IGF-I) messenger ribonucleic acid (mRNA) in hypophysectomized rats and reduces IGF-1, mRNA abundance in the intact rat. Endocrinology 125: 165-171, 1989. 86. Mccarty MF, Glucosamine for wound healing. Medical Hypotheses 47: 273-275, 1996. 87. Mertz W. Chromium in human nutrition: a review. J Nutr 123: 626-633, 1993. 88. Mertz W. Chromium occurrence and function in biological systems. Physiol Rev 49: 163-239, 1969 89. Mertz W. Chromium: history and nutritional importance. Biol Trace Elem Res 32: 3-8, 1992. 90. Meyer NA, Barrow RE, Herndon DN. Combined insulin-like growth factor-1 and growth hormone improves weight loss and wound healing in burned rats. J Trauma 41(6): 1008-1012, 1996. 91. Misra P, Nickoloff BJ, Morhenn VB, Hintz RL, Rosenfeld RG. Characterization of insulin-like growth factor-I/somatomedin-C receptors on human keratinocyte monolayers. J Invest Dermatol 87(2): 264-267, 1986. 92. Moonsie-Shageer S, Mowat DN. Effects of level of supplemental chromium on performance, serum constituents, and immune status of stressed feeder calves. J Anim Sci 71: 232-238, 1993. 93. Moore PK, Hoult JRS. Antiinflammatory steroids induce tissue prostaglandin synthetase activity and enhance prostaglandin breakdown. Nature 288: 269-270, 1980. 94. Mowat DN. Organic chromium: a new nutrient for stressed animals. In: Lyons P, Jacques KA, ed. Proceedings of Alltech’s 10th Annual Symposium, Biotechnology in the Feed Industry. Nottingham University Press, 275-282, 1994. 95. Mowat DN, Chang X, Yang WZ. Chelated chromium for stressed feeder calves. J Anim Sci 73: 49-55, 1993. 96. Mueller RV, Hunt TK, Tokunaga A, Spencer M. The effect of insulin-like growth factor I on wound healing variables and macrophages in rats. Arch Surg 129: 262-265, 1994. 97. Mueller RV, Spencer EM, Sommer A, Maack CA, Suh D, Hunt TK. The role of IGF-I and IGFBP-3 in wound healing. In: Spencer EM (ed.). Modern Concepts of Insulin-Like Growth Factors, Elsevier, New York, NY, 185-192, 1991. 98. Norris DA, Capin L, Weston WL. The effect of epicutaneous glucocorticoids on human monocyte and neutrophil migration in vivo. J Invest Dermatol 78: 386-390, 1982. 99. O''Dell SD, Day IN. Molecules in focus. Insulin-like growth factor II (IGF-II). Int J Biochem Cell Biol 30: 767-771, 1998. 100. Okada S, Susuki M, Ohba H. Enhancement of ribonucleic acid synthesis by chromium (III) in mouse liver. J Inorg Biochem 19: 95-103, 1983. 101. Oxlund H, Fogdestam I, Viidik A. The influence of cortisol on wound healing of the skin and distant connective tissue response. Surg Gynecol Obstet 148(6): 876-880, 1979. 102. Pagan JD, Jackson SG, Duren SE. The effect of chromium supplementation on metabolic response to exercise in thoroughbred horses. In: Lyons P, Jacques KA, ed. Proceedings of Alltech’s 11th Annual Symposium, Biotechnology in the Feed Industry, Nottingham University Press, UK, 249-256, 1995. 103. Pechova A, Podhorsky A, Lokajova E. Metabolic effects of chromium supplementation in dairy cows in the peripartal period. Acta Vet Hung 71: 9-18, 2002. 104. Pell JM, Bates PC. Differential actions of growth hormone and insulin-like growth factor-1 on tissue protein metabolism in dwarf mice. Endocrinology 130: 1942-1950, 1992. 105. Peng Z, Qiao W, Wang Z, Dai Q, He J, Guo C, Xu J, Zhou A. Chromium improves protein deposition through regulating the mRNA levels of IGF1-R, and Ub in rat skeletal muscle cell. Biol Trace Elem Res 137(2): 226-234, 2010. 106. Pierre EJ, Perez-Polo JR, Mitchell AT, Matin S, Foyt HL, Herndon DN. Insulin-like growth factor-1 liposomal gene transfer and systemic growth hormone stimulate wound healing. J Burn Care Rehabil 18: 287-291, 1997. 107. Pollard GV, Richardson CR, Kamezos TP. Effects of supplemental organic chromium on growth, feed efficiency and carcass characteristics of feedlot steers. Anim Feed Sci Technol 98: 121-128, 2002. 108. Ponec M, de Haas C, Bachra BN, Polano MK. Effects of glucocorticoids on primary human skin fibroblasts. I: Inhibition of proliferation of culture of primary human skin and mouse L929 fibroblasts. Arch Dermatol Res 259: 117-123, 1977. 109. Rabinowitz MB, Gonick HC, Levin SR, Davidson MB. Clinical trial of chromium and yeast supplements on carbohydrate and lipid metabolism in diabetic men. Biol Trace Elem Res 5: 449-466, 1983. 110. Rasmussen LH, Garbarsch C, Schuppan D, Moe D, Horslev-Pedersen K, Gottrup F, Steenfos H. Influence of human growth hormone on granulation tissue formation, collagen deposition, and the aminoterminal propeptide of collagen type III in wound chambers in rats. Wound Rep Regen 2: 31-36, 1994. 111. Reed BR, Clark RAF. Cutaneous tissue repair: practical implications of current knowledge. J Am Acad Dermatol 13: 919-941, 1985. 112. Riales R, Albrink JM. Effect of chromium chloride supplementation on glucose tolerance and serum lipids including high density lipoprotein of adult men. Am J Clin Nutr 34: 2670-2678, 1981. 113. Robertson JG, Walton PE, Dunshea F, Dunaiski V, Ballard FJ. Growth hormone but not insulin-like growth factor-I improves wound strength in pigs. Wound Rep Regen 5: 168-174, 1997. 114. Robson MC. The role of growth factors in the healing of chronic wounds. Wound Repair Regen 5: 7-12, 1997. 115. Robson MC, Burns BF, Phillips LG. Wound repair: principles and applications. In: Ruberg RL, Smith DJ, ed. Plastic surgery: a core curriculum. St. Louis, 3-30, 1994. 116. Robson MC, Hill DP, Woodske ME, Steed DL. Wound healing trajectories as predictors of effectiveness of therapeutic agents. Arch Surg 135: 773-777, 2000. 117. Roginski EE, Mertz W. Effects of chromium(III) supplementation on glucose and amino acid metabolism in rats fed a low protein diet. J Nutr 97: 525-530, 1969. 118. Salmela K. Comparison of the effects of methylprednisolone and hydrocortisone on granulation tissue. Scand J Plast Reconstr Surg 15: 87-91, 1981. 119. Scott CD, Martin JL, Baxter RC. Production of insulin-like growth factor-I and its binding protein by adult rat hepatocytes in primary culture. Endocrinology 116: 1094-1101, 1985. 120. Seaborn CD, Cheng N, Adeleye B, Owens F, Stoecker BJ. Chromium and chronic ascorbic acid depletion effects on tissue ascorbate, manganese and C14 retention from C14-ascorbate in guinea pigs. Biol Trace Elem Res 41:279-294, 1994. 121. Singer AJ, Clark RA. Cutaneous wound healing. N Engl J Med 341(10): 738-746, 1999. 122. Smith RG, Jiang H, Sun Y. Developments in ghrelin biology and potential clinical relevance. Trends Endocrinol Metab 16: 436-442, 2005. 123. Spears JW, van Heugten E. Immune response and growth of stressed weanling pigs fed diets supplemented with organic or inorganic forms of chromium. J Anim Sci 75: 409-416, 1997. 124. Spies M, Nesic O, Barrow RE, Perez-Polo JR, Herndon DN. Liposomal IGF-1 gene transfer modulates pro- and anti-inflammatory cytokine mRNA expression in the burn wound. Gene Ther 8(18): 1409-1415, 2001. 125. Steenfos H, Spencer EM, Hunt TK. Insulin-like growth factor 1 has a major role in wound healing. Surg Forum 40: 68-70, 1989. 126. Steenfos HH. Growth factors and wound healing. Scand J Plast Reconstr Surg Hand Surg 28(2): 95-105, 1994. 127. Steenfos HH, Jansson JO. Growth hormone stimulates granulation tissue formation and insulin-like growth factor-I gene expression in wound chambers in the rat. J Endocrino 132(2): 293-298, 1992. 128. Straus DS. Growth-stimulatory actions of insulin in vitro and in vivo. Endocr Rev 5: 356-569, 1984. 129. Suh DY, Hunt TK, Spencer EM. Insulin-like growth factor-I reverses the impairment of wound healing induced by corticosteroids in rats. Endocrinology 131: 2399-2403, 1992. 130. Sureshbabu A, Okajima H, Yamanaka D, Shastri S, Tonner E, Rae C, Szymanowska M, Shand JH, Takahashi S, Beattie J, Allan GJ, Flint DJ. IGFBP-5 induces epithelial and fibroblast responses consistent with the fibrotic response. Biochem Soc Trans 37: 882-825, 2009. 131. Tavakkol A, Elder JT, Griffiths CE, Cooper KD, Talwar H, Fisher GJ, Keane KM, Foltin SK, Voorhees JJ. Expression of growth hormone receptor, insulin-like growth factor 1 (IGF-1) and IGF-1 receptor mRNA and proteins in human skin. J Invest Dermatol 99(3): 343-349, 1992. 132. Thompson EB, Lippman ME. Mechanism of action of glucocorticoids. Metabolism 23: 159-202, 1974. 133. Thorey IS, Hinz B, Hoeflich A, Kaesler S, Bugnon P, Elmlinger M, Wanke R, Wolf E, Werner S. Transgenic mice reveal novel activities of growth hormone in wound repair, angiogenesis, and myofibroblast differentiation. J Biol Chem 18: 26674-26684, 2004. 134. Todorović V, Pesko P, Micev M, Bjelović M, Budec M, Mićić M, Brasanac D, Ilić-Stojanović O. Insulin-like growth factor-1 in wound healing of rat skin. Regul Pept 150: 7-13, 2008. 135. Vincent JB. Recent developments in the biochemistry of chromium (III). Biol Trace Elem Res 99: 1-16, 2004. 136. Vincent JB. The biochemistry of chromium. J Nutr 130: 715-718, 2000. 137. Wang HS, Chard T. IGFs and IGF binding proteins in the regulation of human ovarian and endometrial function. J Endocrinol 161: 1-13, 1999. 138. Wang JM, Hayashi T, Zhang WR, Li F, Iwai M, Abe K. Reduction of ischemic damage by application of insulin-like growth factor-1 in rat brain after transient ischemia. Acta Med 55(1): 25-30, 2001. 139. Wang MQ, Xu ZR, Li WF, Jiang ZG. Effect of chromium nanocomposite supplementation on growth hormone pulsatile secretion and mRNA expression in finishing pigs. J Anim Physiol Anim Nutr 93: 520-525, 2009. 140. Wang MQ, Xu ZR, Li WF, Jiang ZG. Effects of chromium nanocomposite supplementation on blood metabolites, endocrine parameters and immune traits in finishing pigs. Anim Feed Sci Technol 139: 69-80, 2007. 141. Ward TL, Southern, LL, Anderson RA. Effect of dietary chromium source on growth, carcass characteristics, and plasma metabolite and hormone concentrations in growing-finishing pigs. J Anim Sci 73: 189, 1995. 142. Werner S, Grose R. Regulation of wound healing by growth factors and cytokines. Physiol Rev 83: 835-870, 2003. 143. Wicke C, Halliday B, Allen D, Roche NS, Scheuenstuhl H, Spencer MM, Roberts AB, Hunt TK. Effects of steroids and retinoids on wound healing. Arch Surg 135(11): 1265-1270, 2000. 144. Wild T, Rahbarnia A, Kellner M, Sobotka L, Eberlein T. Basics in nutrition and wound healing. Nutrition 26(9): 862-866, 2010. 145. Yamamoto KR, Albers BM. Steroid receptors: elements for modulation of eukaryotic transcription. Annu Rev Biochem 45: 721-746, 1976. 146. Yang WZ, Mowat DN, Subiyatno A. Effects of chromium supplementation on early lactation performance of Holstein cows. J Anim Sci 76: 221-230, 1996. 147. Yao F, Visovatti S, Johnson CS, Chen M, Slama J, Wenger A, Eriksson E. Age and growth factors in porcine full-thickness wound healing. Wound Repair Regen 9(5): 371-377, 2001. 148. Yoshida A, Araki T, Omata T, Yamaguchi I, Matsuda K, Kurimoto T, Tagashira E. Basal studies on the model of circular excisional wounds made on the dorsal skin of rats treated with hydrocortisone. Nippon Yakurigaku Zasshi 98: 369-377, 1991. 149. Yoshimoto H, Ishihara H, Ohtsuru A, Akino K, Murakami R, Kuroda H, Namba H, Ito M, Fujii T, Yamashita S. Overexpression of insulin-like growth factor-1 (IGF-I) receptor and the invasiveness of cultured keloid fibroblasts. Am J Pathol 154: 883-889, 1999. 150. Zha L, Zeng J, Sun S, Deng H, Luo H, Li W. Chromium(III) nanoparticles affect hormone and immune responses in heat-stressed rats. Biol Trace Elem Res 129(1-3): 157-169, 2009. 151. Zha LY, Wang MQ, Xu ZR, Gu LY. Efficacy of chromium(III) supplementation on growth, body composition, serum parameters, and tissue chromium in rats. Biol Trace Elem Res 119: 42-50, 2007. 152. Zapf J, Froesch ER. Insulin-like growth factors/somatomedins: structure, secretion, biological actions and physiological role. Horm Res 24: 121-130, 1986.
摘要: 
本實驗為研究三價鉻離子對於小鼠傷口癒合的影響。傷口癒合為一個複雜進行的連續過程,期間有許多細胞及生長因子參與其中。最近的研究發現三價鉻離子對於傷口癒合過程中增殖期的重要生長素─類胰島素生長因子 (Insulin-likie growth factor 1, IGF-1)有增強的作用。根據研究,我們假設鉻離子在體內荷爾蒙上可增加IGF-1的表現及減低類固醇 (Cortisol)的濃度,進而幫助傷口癒合的過程。本實驗使用96隻雄性C57BL/6J小鼠,分成4組,每組24隻並分別給予不同的藥物。第一組灌食生理食鹽水作為控制組,第二及第三組分別灌食三氯化鉻(CrCl3)及類固醇 (Dexamethasone);第四組則同時給予相同劑量之三氯化鉻及類固醇。經過一週的藥物給予後,所有動物皆於背上切創一道傷口,術後每天持續灌食口服藥物直到犧牲日。於術後第7、14、21及28日每組犧牲6隻小鼠。測量傷口大小並採集皮膚傷口做組織學判讀,臟器組織收集做鉻離子濃度分析,血清檢體做IGF-1濃度分析。傷口測量的結果發現類固醇顯著延遲了傷口癒合,而鉻離子卻加速了傷口癒合。組織切片結果中發現類固醇顯著延遲了炎症反應、再上皮化、肉芽組織生成、血管新生以及膠原纖維沉積;然而鉻離子則有反轉類固醇所造成之不良影響的現象。血清分析結果發現類固醇顯著減少IGF-1的濃度,但可由添加鉻離子而反轉。綜合以上結果,鉻離子可經由調節體內內分泌如IGF-1的表現而加速傷口癒合,當動物面臨緊迫或給予類固醇治療時,此效果可更加顯著。

This study was conducted to investigate the effects of trivalent chromium (Cr3+) on wound healing in mice. Wound healing is a complex event involving many cells and growth factors. Recent study revealed that expression of insulin-like growth factor 1 (IGF-1), one of the key growth factors in proliferative cascade can be enhanced by Cr3+. Based on studies, we postulated that Cr could be of helpful on wound healing by increasing the level of IGF-1 and decreasing the level of serum cortisol on hormone to accelerate the wound healing process. A total of 96 male C57BL6/J mice were randomly assigned to four groups (n=24/group). The first group was treated with normal saline as control, the second and third groups were treated for chromium chloride (CrCl3) and dexamethasone (Dex), respectively. The combination of CrCl3 and Dex were applied to the fourth group. All animals underwent surgical incision on their dorsal region after one week of treatment, the regimen of treatment were continued until the day of sacrifice. Six mice of each group were sacrificed on day 7, 14, 21 and 28 after surgery. Skin wound area were measured and collected for histology evaluation, tissue of organs were collected for Cr concentration analysis, serum concentrations of IGF-I were determined as well. The measurement revealed the delayed healing in Dex-treated group, and an accelerated healing was observed in both CrCl3-treated groups. In histology, the delayed inflammation process, reepithelization, granulation tissue formation as well as collagen deposition were observed in Dex-treated groups. However, reversed detrimental effects of Dex were observed in CrCl3-treated groups. The concentrations of IGF-1 in Dex-treated groups revealed significant decrement compared to other groups, but Cr reversed this effect. Taken up together, Cr accelerated wound healing in surgical wound model in mice through the regulation of hormone concentrations such as IGF-1, the effects could be more prominent when animal is under stress or treated by exogenous glucocorticoids.
URI: http://hdl.handle.net/11455/14333
其他識別: U0005-0408201215215900
Appears in Collections:獸醫學系所

Files in This Item:
File Description SizeFormat Existing users please Login
nchu-101-7098038004-1.pdf2.65 MBAdobe PDFThis file is only available in the university internal network   
Show full item record
 

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.