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使用偏光显微镜和数字图像分析对纤维化病变的年龄进行定量评估。

Quantitative assessment of the age of fibrotic lesions using polarized light microscopy and digital image analysis.

作者信息

Pickering J G, Boughner D R

机构信息

Department of Medicine (Cardiology), University of Western Ontario, London, Canada.

出版信息

Am J Pathol. 1991 May;138(5):1225-31.

Abstract

Reliable histologic methods for gauging the maturity of fibrotic lesions are limited, making interventions in the healing process difficult to assess. As collagen ages there is enhanced birefringence due to increased molecular and fibrillar organization. The purpose of this study was to develop a microscopal technique to quantify this process and to determine its ability to distinguish scars of varying ages. Fibrosis in the rat gracilis muscle was studied 5 to 63 days after superficial injury. Sections were stained with picrosirius red and illuminated with monochromatic, polarized light. The microscope fields were digitized using a computer-video system yielding an image in which noncollagenous material was dark (gray level 0) and collagen was depicted by grey levels 1 to 255. In the fibrosis model used, the collagen area fraction plateaued at 80% by day 21. The median collagen grey level increased progressively as the scar aged. It is concluded that this histologic, nondestructive technique can reliably quantify age-related optical properties of fibrotic collagen and that this could be used to determine the maturity of fibrotic lesions.

摘要

用于评估纤维化病变成熟度的可靠组织学方法有限,这使得对愈合过程的干预难以评估。随着胶原蛋白老化,由于分子和纤维组织增加,双折射增强。本研究的目的是开发一种显微镜技术来量化这一过程,并确定其区分不同年龄瘢痕的能力。在大鼠股薄肌浅表损伤后5至63天研究纤维化情况。切片用苦味酸天狼星红染色,并用单色偏振光照射。使用计算机视频系统对显微镜视野进行数字化处理,得到一幅图像,其中非胶原物质呈黑色(灰度级0),胶原由灰度级1至255表示。在所使用的纤维化模型中,到第21天胶原面积分数稳定在80%。随着瘢痕老化,胶原灰度中位数逐渐增加。得出的结论是,这种组织学的、非破坏性技术能够可靠地量化纤维化胶原与年龄相关的光学特性,并且可用于确定纤维化病变的成熟度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba41/1886024/950723082df9/amjpathol00101-0166-a.jpg

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