Herndon D N, Hawkins H K, Nguyen T T, Pierre E, Cox R, Barrow R E
Department of Surgery, University of Texas Medical Branch, Glaveston, USA.
Ann Surg. 1995 Jun;221(6):649-56; discussion 656-9. doi: 10.1097/00000658-199506000-00004.
Human growth hormone is an anabolic agent that attenuates injury-induced catabolism and stimulates protein synthesis. Recombinant human growth hormone (rhGH) administered therapeutically to patients with massive burns has been shown to increase the rate of skin graft donor site healing. It has been postulated that growth hormone affects wound healing and tissue repair by stimulating the production of insulin-like growth factor-1 (IGF-1) by the liver to increase circulating IGF-1 concentrations. The mechanism by which it improves wound healing, however, remains in question. The authors hypothesize that rhGH up-regulates IGF-1 receptors and IGF-1 levels both systemically and locally in the wound site to stimulate cell mitosis and increase synthesis of laminin, collagen types IV and VII, and cytokeratin. This hypothesis was tested in nine patients with burns covering > 40% of total body surface area.
The authors assessed the efficacy of rhGH in promoting several major building materials in the donor site of patients with massive burns.
Ten massively burned patients with full-thickness burns covering more than 40% of total body surface area were participants in a placebo-controlled prospective study to determine the efficacy of 0.2 mg/kg/day rhGH on donor site wound healing and to identify some of the major components involved in wound healing and its integrity.
Donor sites in burn patients receiving rhGH showed an increased coverage by the basal lamina of 26% for placebo to 68% coverage of the dermal-epidermal junction. Insulin-like growth factor-1 receptors and laminin, types IV and VII collagen, and cytokeratin-14 all increased significantly. Healing times of the donor sites were significantly decreased compared with patients receiving placebo.
Results indicate that growth hormone or its secondary mediators may directly stimulate the cells of the epidermis and dermis during wound healing to produce the structural proteins and other components needed to rebuild the junctional structures.
人生长激素是一种合成代谢剂,可减轻损伤诱导的分解代谢并刺激蛋白质合成。对大面积烧伤患者进行治疗性给予重组人生长激素(rhGH)已显示可提高皮肤移植供区的愈合速度。据推测,生长激素通过刺激肝脏产生胰岛素样生长因子-1(IGF-1)以增加循环中IGF-1的浓度来影响伤口愈合和组织修复。然而,其改善伤口愈合的机制仍存在疑问。作者推测,rhGH可上调全身及伤口局部的IGF-1受体和IGF-1水平,以刺激细胞有丝分裂并增加层粘连蛋白、IV型和VII型胶原蛋白以及细胞角蛋白的合成。该假设在9名烧伤面积超过全身表面积40%的患者中进行了验证。
作者评估了rhGH在促进大面积烧伤患者供区几种主要结构成分生成方面的疗效。
10名大面积全层烧伤且烧伤面积超过全身表面积40%的患者参与了一项安慰剂对照前瞻性研究,以确定每日0.2mg/kg的rhGH对供区伤口愈合的疗效,并确定参与伤口愈合及其完整性的一些主要成分。
接受rhGH治疗的烧伤患者供区基底膜覆盖面积从安慰剂组的26%增加至真皮-表皮交界处覆盖面积的68%。胰岛素样生长因子-1受体、层粘连蛋白、IV型和VII型胶原蛋白以及细胞角蛋白-14均显著增加。与接受安慰剂的患者相比,供区愈合时间显著缩短。
结果表明,生长激素或其二级介质可能在伤口愈合过程中直接刺激表皮和真皮细胞,以产生重建连接结构所需的结构蛋白和其他成分。