Studies on Hematoxylin Stains

2012

ISRN Rheumatology

Objective. Articular cartilage shows changes with age that are considered to be the most important factors in the development and progression of osteoarthritis. The studies on age changes in articular cartilage have been traditionally based on individual observations but this approach is limited by its subjectivity and bias, yielding considerable variability. So the present study was conducted to observe various age related changes in morphology of femoral articular cartilage using computerized morphometric analysis. Design. The articular cartilage specimens were divided into two groups according to age: group 1 (n = 16) below 40 years (16–40 years) and group 2 (n = 12) above 40 years (41–86 years) of age. 5 μm thick paraffin sections were stained with H&E and analyzed using Image Pro Express image analysis software for quantitative analysis of articular cartilage. Various parameters, that is, total thickness of the cartilage, area of lacunae in each zone, area of subchondral cavities, and number of chondrocytes per 10,000 μm2 area in each zone were measured. Results. Significant difference with age was found in the total thickness and area of lacunae in zone 3. Conclusions. Not much difference is observed in articular cartilage morphology with age. So ageing is not the only risk factor in development of osteoarthritis.

Section: Methodsmentioning

confidence: 99%

Computerized Morphometric Analysis of Human Femoral Articular Cartilage

Goyal

2012

ISRN Rheumatology

“…The H&E staining 9 and PAS staining 10 were done by regular protocol. Immunohistochemistry was done by the standard avidin-biotin-peroxidase complex technique.…”

Section: Methodsmentioning

confidence: 99%

Age-Related Changes in the Chorioretinal Junction: An Immunohistochemical Study

Saini

Arora

et al. 2017

J Histochem Cytochem.

The chorioretinal junction comprises the retinal pigment epithelium, Bruch's membrane (BM), and adjacent choroidal capillaries. Its significance lies in its ability to support the retina mechanically and metabolically. The aim of this cross-sectional study was to record the senescent changes affecting all the constituents of the chorioretinal junction in 40 histological specimens across the whole spectrum of the adult age range. This study included light microscopy, with hematoxylin and eosin and PAS stains, and fluorescent microscopy. Immunohistochemistry was done using antibodies against neurofilament, synaptophysin, S-100, and collagen IV. The descriptive microanatomy was corroborated by morphometry. The amount of melanin and lipofuscin granule and drusens were noted. The ratio of thickness of BM to capillary diameter reduced from 1:6 or less in the 2nd decade to 1:3 in the 10th decade. Complete hyalinization of intercapillary pillars was seen in the 10th decade. The accumulation of lipofuscin with age was documented with the diminution in the size of epithelial cells. The subepithelial accumulation of drusen was first noted in the specimen from the late 60s. We have described all senescent changes in the chorioretinal junction chronologically. Similar changes are found in a more pronounced form in age-related macular degeneration. These data might serve as a reference baseline for clinicians and pathologists.

“…The specimens were divided into 2 groups. [7] to confirm the histological structure of the articular cartilage and to study the various features for morphometry.…”

Section: Methodsmentioning

confidence: 99%

A Study of Changes in Morphology of Osteoarthritic Articular Cartilage Using Computerized Image Analysis

Goyal

2013

Journal of Histology

Histological studies on articular cartilage have been traditionally based on individual observations but this approach is limited by its subjectivity and bias, yielding considerable variability. So the present study was conducted to observe the various changes in the morphology of osteoarthritic femoral articular cartilage using computerized image analysis. The cartilage specimens were divided into two groups: group 1 (n=23) (46–81 years) consisted of OA specimens. Group 2 (n=12) (41–86 years) consisted of non-OA specimens. A 5 μm thick paraffin sections were stained with H&E staining and analyzed using Image-Pro Express image analysis software for quantitative analysis of articular cartilage. Various parameters, namely, total thickness of the cartilage, area of lacunae in each zone, area of subchondral cavities, and number of chondrocytes per 10,000 μm2area in each zone, were measured. Microscopic appearance of OA cartilage was much different as compared to control. Various changes seen were different in all specimens and they were not related to age. Lacunar size in all four zones was found to differ significantly in the OA (group 1) and control (group 2) (P<0.05). The results suggest that OA should be considered as a specific process and not simply as an inevitable feature of ageing.