Liapaki Ioannis, Anagnostoulis Stavros, Karayiannakis Anastasios, Korkolis Dimitris, Labropoulou Maria, Matarasso Alan, Simopoulos Constantinos
Department of Plastic and Reconstructive Surgery, Hellenic Anticancer Institute, Saint Savvas Hospital, Athens, Greece.
Acta Cir Bras. 2008 Mar-Apr;23(2):118-24. doi: 10.1590/s0102-86502008000200002.
Leptin is a potent direct angiogenic factor that stimulates endothelial cell migration and activation in vitro and angiogenesis in vivo. In addition, leptin has been discussed to play an important role in angiogenesis, as it promotes the formation of new blood vessels.
The effect of exogenously administered leptin on the healing process of a full tissue burn wound model.
Sixty-three Sprague-Dawley male rats were used. Full tissue burn wound was created by electrocautery. The width of the pin was 0.3 cm; its length was 2 cm and was used at the "cut" modulation. Rats were divided into seven groups of nine animals each. Burn wounds were injected with murine recombinant leptin and the rats were sacrificed 3, 7 and 9 days after surgery. Every group had obtained three animals for the three different days of sacrifice. Three different leptin doses of 250 pg/ml, 500 pg/ml and 1000 pg/ml were used in different animal groups (A, B and C). For every one of the three leptin doses used, another animal group was evaluated by using the combined injection of leptin and antileptin (A1, B1, and C1), in order to study the inhibitory effect to the leptin factor. Nine rats were served as controls. These were injected with 0.3 ml water for injection solution and sacrificed at the same time intervals. After sacrifice of the animals, the skin was grossly determined by its appearance, colour and texture. Full thickness burn wounds were dissected for histological examination. A qualitative analysis of angiogenesis in the burn wound was conducted following a standard hematoxylin and eosin stain. The wound tissue samples from each experimental group underwent immunohistochemical evaluation of microvessel density by endothelial cell staining with mouse anti-rat CD 34 monoclonal antibody.
The most impressive growth of new blood vessels appeared seven and nine days after treatment with the highest leptin doses. There were no significant differences in microvessel density between the seventh and the ninth postoperative day among different groups treated with leptin. All wounds from the control group, as well as those from animal groups treated with the combined injection of leptin and antileptin did not develop any new vessels.
Exogenous administration of recombinant leptin increases early tissue angiogenesis in the burn wound level of an experimental animal model.
瘦素是一种有效的直接血管生成因子,在体外可刺激内皮细胞迁移和活化,在体内可促进血管生成。此外,由于瘦素能促进新血管的形成,因此人们认为它在血管生成中发挥着重要作用。
研究外源性给予瘦素对全层组织烧伤创面模型愈合过程的影响。
选用63只雄性Sprague-Dawley大鼠。采用电灼法造成全层组织烧伤创面。针的宽度为0.3 cm;长度为2 cm,用于“切割”调节。将大鼠分为7组,每组9只。烧伤创面注射小鼠重组瘦素,术后3天、7天和9天处死大鼠。每组在三个不同的处死日各取3只动物。不同动物组(A、B和C组)分别使用250 pg/ml、500 pg/ml和1000 pg/ml三种不同剂量的瘦素。对于所使用的三种瘦素剂量中的每一种剂量,另一个动物组通过联合注射瘦素和抗瘦素(A1、B1和C1组)进行评估,以研究对瘦素因子的抑制作用。9只大鼠作为对照。给它们注射0.3 ml注射用水溶液,并在相同的时间间隔处死。处死动物后,通过外观、颜色和质地对皮肤进行大体观察。解剖全层烧伤创面进行组织学检查。在标准苏木精和伊红染色后,对烧伤创面的血管生成进行定性分析。用小鼠抗大鼠CD 34单克隆抗体对各实验组的伤口组织样本进行内皮细胞染色,以评估微血管密度。
在给予最高剂量瘦素治疗后7天和9天,新血管生长最为显著。不同剂量瘦素治疗组术后第7天和第9天的微血管密度无显著差异。对照组以及联合注射瘦素和抗瘦素的动物组的所有伤口均未形成任何新血管。
在实验动物模型的烧伤创面水平,外源性给予重组瘦素可增加早期组织血管生成。