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葡萄糖是自然界分布最廣且最為重要的一種單糖。葡萄糖是一種多羥基醛。水溶液旋光向右,故亦稱「右旋糖」。葡萄糖在生物學領域具有重要地位,是活細胞的能量來源和新陳代謝中間產物。葡萄糖增生注射療(Dextrose  Prolotherapy)藉由多種機制啟動修復,包含葡萄糖直接的反應滲透壓(osmotic)誘發反應發炎生長效應(inflammatory growth effect)。葡萄糖增生注射治的濃度如果在10%以上,會造成細胞處於滲透壓梯度變化下。這樣的滲透壓變化會讓注射區域的細胞失去水分,進而開啟生長因子流入(influx)細胞與患部修復連鎖反應(wound-healing cascade)
 

葡萄糖水是非常理想的增生劑,原因是()葡糖糖是屬於水溶性、(二)葡萄糖是人體正常血液中的化學物質,因此安全性佳即便打在身體多個區域或是使用較大劑量,都相對安全。葡萄糖增生注射治的最終結果,可使新生的膠原蛋白(collagen)積累在受傷韌帶與肌腱上。人體正常的細胞中,葡萄糖含量僅有 0.1%。增加葡萄糖的濃度可以促進細胞蛋白質的合成、DNA的合成、細胞體積(cell volume)的增加與細胞增生 (cell proliferation)

正常人類細胞處於0.5%的葡萄糖濃度環境下,便會誘發細胞增生,並刺激多種生長因子的產,例如血小板生長因子(platelet-derived growth factor, PDGF)轉化生長因子β (transforming growth factor-beta, TGF-β)、表皮細胞生長因子(epidermal growth factor, EGF), 鹼性纖維母細胞生長因子(basic fibroblast growth factor,  bFGF), 類胰島素生長因子(insulin-like growth factor, IGF-1), 結締組織生長因子(connective tissue growth factor, CTGF)。這些生長因子與肌腱、韌帶、軟組織的修復、健康狀態與生長有關。

許多研究指出,葡萄糖注射到動物與人類的組織中,會刺激韌帶增厚、肌腱肥大(tendon hypertrophy)、增加細胞外間質成分(extracellular matrix)、纖維母細胞增(fibroblastic proliferation)、修復關節軟骨缺損(articular cartilage defects)。葡萄糖增生注射被證實,在不同的葡萄糖濃度下,可以誘發修復反應,保護收受傷的軟骨組織,且產生發炎性(inflammatory)與非發炎性(noninflammatoryru)的生化效應。

 

By Ross H, et al. Evidence-Based Use of Dextrose Prolotherapy for Musculoskeletal Pain: A Scientific Literature Review. Journal of Prolotherapy. 2011;3(4):765-789.

http://www.journalofprolotherapy.com/pdfs/issue_12/issue_12_03_evidence_based_prolo.pdf

 normal cellular growth                    Growth factors of cellular growth  


 

 

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參考文獻

 

  1. Jensen K, et al. Response of knee ligaments to Prolotherapy in a rat injury model. American Journal of Sports Medicine. 2008;36:1347-1357.
  2. Jensen K, et al. Early inflammatory response of knee ligaments to Prolotherapy in a rat model. Journal of Orthopedic Research. 2008;26:816-823.
  3. Reeves K, et al. Evidenced-based regenerative injection (Prolotherapy) in sports medicine. In Seidenberg P, Beutler A (eds.) The Sports Medicine Resource Manual. 2008; Saunders Publishing, Philadelphia PA, Chapter 50.
  4. Natarajan R, et al. Vascular smooth muscle cells exhibit increased growth in response to elevated glucose. Biochemistry and Biophysic Research and Communication. 1992;186:552-560.
  5. McGinn S, et al. High glucose and endothelial cell growth: novel effects independent of autocrine TGF-beta 1 and hyperosmolality. American Journal of Phyiology and Cell Physiology. 2003;234:C1374-C1386.
  6. Berl T, et al. Multiple mitogen-activated protein kinases are regulated by hyperosmolality in mouse IMCD cells. American Journal of Physiology. 1997;272:305-311.
  7. Caruccio L, et al. The heat-shock transcription factor HSF1 is rapidly activated by either hyper- or hypo-osmotic stress in mammalian cells. Journal of Biochemistry. 1997;327:341-347.
  8. Di Paloa S, et al. High glucose concentration induces the overexpression of transforming growth factor-beta through the activation of a platelet-derived growth factor loop in human mesangial cells. American Journal of Pathology. 1996;149:2095-2106.
  9. Oh J, et al. Sequential effects of high glucose on mesangial cell transforming growth factor-beta 1 and fibronectin synthesis. Kidney International. 1998;54:1872-1878.
  10. Murphy M, et al. Suppression subtractive hybridization identifies high glucose levels as a stimulus for expression of connective tissue growth factor and other genes in human mesangial cells. Journal of Biology and Chemistry. 1999;274:5830-5834.
  11. Fukuda K, et al. High concentration of glucose increases mitogenic responsiveness to heparin-binding epidermal growth factor-like growth factor in rat vascular smooth muscle cells. Arteriosclerosis Thombosis and Vasculature Biology. 1997;17:1962-1968.
  12. Ohgi S, et al. Glucose modulates growth of gingival fibroblasts and periodontal ligament cells: correlation with expression of basic fibroblast growth factor. Journal of Periodontal Research. 1996;31:579-588.
  13. Pugliese G, et al. Increased activity of the insulin-like growth factor system in mesangial cells cultured in high glucose conditions. Relation to glucose-enhanced extracellular matrix production. Diabetologia. 1996;39:775-784.
  14. Reeves K. Prolotherapy: injection of growth factors or growth factor production stimulants to growth normal cells or tissue. In Waldman SD (ed): Pain Management. Philadelphia, Elsevier, 2006; 1106-1127.
  15. Martinez-Zapata M, et al. Efficacy and safety of autologous plasma rich in platelets for tissue regeneration: a systematic review. Transfusion. 2009;49:44-56.
  16. Creaney L, et al. Growth factor delivery methods of sports injuries: the state of play. British Journal of Sports Medicine. 2008;42:314-320.
  17. Sanchez M, et al. Platelet-rich therapies in treatment of orthopaedic sport injuries. Sports Medicine. 2009;39:345-354. Tabata Y. Tissue regeneration based on growth factor release. Tissue Engineering. 2003;9:S5-15.
  18. Jensen K, et al. Early inflammatory response of knee ligaments to Prolotherapy in a rat model. Journal of Orthopaedic Research. 2008;26:816-823.
  19. Jensen K, et al. Response of knee ligaments to Prolotherapy in a rat injury model. American Journal of Sports Medicine. 2008;36:1347-1357.
  20. Kim H, et al. The effects of anti-inflammatory drugs on histologic findings of the experimental Prolotherapy model. Journal of the Korean Academy of Rehabilitation Medicine. 2006;30:378-384.
  21. Ahn K, et al. The effect of the Prolotherapy on the injured Achilles tendon in a rat model. Journal of the Korean Academy of Rehabilitation Medicine. 2002;26:332-336.
  22. Oh S, et al. Dextrose-induced subsynovial connective tissue fibrosis in the rabbit carpal tunnel: a protential model to study carpal tunnel syndrome. Hand. 2008;3:34-40.
  23. Kim H, et al. Comparison of histological changes in accordance with the level of dextrose-concentration in experimental Prolotherapy model. Journal of Korean Academy of Rehabilitation Medicine. 2003;27:935-940.
  24. Kim S, et al. The effects of hyperosmolar dextrose and autologous serum injection in the experimental articular defect of rabbit. Journal of the Korean Acdemy of Rehabilitation Medicine. 2006;30:173-178.
  25. Park Y, et al. Intra-articular injection of a nutritive mixture solution protects articular cartilage from osteoarthritic progression induced by anterior cruciate ligament transaction in mature rabbits: a randomized controlled trial. Arthritis Research and Therapy. 2007;9:R8.
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