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I型糖尿病患者足部皮肤对组织损伤的微血管反应及毛细血管超微结构

Microvascular response to tissue injury and capillary ultrastructure in the foot skin of type I diabetic patients.

作者信息

Rayman G, Malik R A, Sharma A K, Day J L

机构信息

Diabetes Centre, Ipswich Hospital, Suffolk, U.K.

出版信息

Clin Sci (Lond). 1995 Nov;89(5):467-74. doi: 10.1042/cs0890467.

DOI:10.1042/cs0890467
PMID:8549060
Abstract
  1. Microvascular blood flow responses to injury and capillary ultrastructure were assessed by laser Doppler flowmetry and detailed light and electron microscopy respectively in skin biopsied from 28 patients with insulin-dependent diabetes and 17 control subjects. 2. The hyperaemic response induced by biopsy (P < 0.001) and heating to 44 degrees C (P < 0.001) was significantly lower in the diabetic patients and showed progressive impairment with the severity of complications (P < 0.001). 3. Skin capillary basement membrane thickness was significantly increased in the diabetic patients (P < 0.001) and also increased with the severity of complications (P < 0.002). Both the luminal area (P < 0.001) and the endothelial cell outer perimeter (P < 0.002), measures of luminal and capillary size, respectively, were significantly reduced in all diabetic patients. 4. Basement membrane thickness was related significantly to the impaired hyperaemic response to both biopsy (P < 0.01) and thermal injury (P < 0.01). 5. Our findings support the hypothesis that structural abnormalities, which are characterized by an early reduction in capillary size and later thickening of basement membrane, form an important mechanism for the impaired hyperaemic response in diabetic patients.
摘要
  1. 分别通过激光多普勒血流仪以及详细的光学和电子显微镜检查,对28例胰岛素依赖型糖尿病患者和17名对照者的皮肤活检样本进行检测,评估微血管对损伤的血流反应和毛细血管超微结构。2. 糖尿病患者活检(P < 0.001)和加热至44摄氏度(P < 0.001)所诱导的充血反应显著降低,且随着并发症严重程度加重而逐渐受损(P < 0.001)。3. 糖尿病患者皮肤毛细血管基底膜厚度显著增加(P < 0.001),且也随着并发症严重程度增加(P < 0.002)。所有糖尿病患者的管腔面积(P < 0.001)和内皮细胞外周长度(P < 0.002)(分别为管腔和毛细血管大小的测量指标)均显著减小。4. 基底膜厚度与活检(P < 0.01)和热损伤(P < 0.01)时充血反应受损显著相关。5. 我们的研究结果支持以下假说:以毛细血管大小早期减小和随后基底膜增厚为特征的结构异常,是糖尿病患者充血反应受损的重要机制。

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