Caetano Guilherme F, Fronza Marcio, Leite Marcel N, Gomes Ary, Frade Marco Andrey Cipriani
a Division of Dermatology, Department of Internal Medicine, Ribeirão Preto School of Medicine , University of São Paulo (USP) , Ribeirão Preto , SP , Brazil.
b Department of Pharmacy , University of Vila Velha , Vila Velha , Espirito Santo , Brazil.
Pharm Biol. 2016 Nov;54(11):2555-2559. doi: 10.3109/13880209.2016.1170861. Epub 2016 May 14.
The quantification of total collagen is of major importance in a wide range of research areas, including the study of cutaneous wound healing and new drugs trials.
The total collagen content in skin biopsies was compared by biochemical hydroxyproline assay and by two computer-aided histomorphometric analyses of histological sections.
Two methods were used to evaluate collagen formation: the hydroxyproline assay, as the gold standard and histomorphometric image analysis of the filled areas by corresponding stained collagen fibres, using picrosirius and Gomori's trichrome staining. The image analyses were determined by digital densitometry recognition using computer-aided ImageJ software. One-way ANOVA, simple linear regression and ANCOVA were applied for the statistical analysis and correlation.
In a simple linear regression analysis carried out on the 14th day period after the induction of skin injury, three techniques, picrosirius red (F = 33.57, p = 0.00), Gomori's trichrome (F = 81.61, p = 0.00) and hydroxyproline content (F = 16.85, p = 0.00) were able to detect collagen production. After scale adjustment, there were no significant differences among either the slopes (F = 1.17, p = 0.32) or the intercepts (F = 0.69, p = 0.51) of the estimated regression lines. It seems that a highly significant correlation exists between the histomorphometrical analysis and hydroxyproline assay.
The morphometric analysis proved to be adequate and can be used as a simple, rapid, low-cost technology for evaluating total collagen in cutaneous wound specimens, compared with the gold standard hydroxyproline assay.
在包括皮肤伤口愈合研究和新药试验在内的广泛研究领域中,总胶原蛋白的定量分析至关重要。
通过生化羟脯氨酸测定法以及对组织切片进行两种计算机辅助组织形态计量分析,比较皮肤活检中的总胶原蛋白含量。
采用两种方法评估胶原蛋白形成:羟脯氨酸测定法作为金标准,以及使用天狼星红和戈莫里三色染色对相应染色的胶原纤维填充区域进行组织形态计量图像分析。图像分析通过使用计算机辅助ImageJ软件的数字密度测定识别来确定。应用单因素方差分析、简单线性回归和协方差分析进行统计分析和相关性分析。
在皮肤损伤诱导后第14天进行的简单线性回归分析中,三种技术,即天狼星红(F = 33.57,p = 0.00)、戈莫里三色染色(F = 81.61,p = 0.00)和羟脯氨酸含量(F = 16.85,p = 0.00)能够检测到胶原蛋白的产生。在进行尺度调整后,估计回归线的斜率(F = 1.17,p = 0.32)或截距(F = 0.69,p = 0.51)之间均无显著差异。组织形态计量分析与羟脯氨酸测定法之间似乎存在高度显著的相关性。
与金标准羟脯氨酸测定法相比,形态计量分析被证明是足够的,并且可以作为一种简单、快速、低成本的技术用于评估皮肤伤口标本中的总胶原蛋白。