Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:3.2.1.36 (hyaluronidase)
 4,606 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Rabbit aortic changes were investigated after different sclerogenic diets. A subintimal chondroitin sulfate layer was characterized by toluidine blue metachromatic staining at pH 1--3, CEC value expressed in MgCl2 concentration: 0.4M, hyaluronidase sensitivity. This layer becomes disorganized during plaque formation and partly disaappears. A long-lasting sclerogenic diet, as well as a diet containing several sclerogenic factors, produced an increase of frequency and extension of the media necrosis, calcification, and chondroid metaplasia of the aortic wall. In these lesions, an increase of mucopolysaccharide secretion of modified smooth muscle cells was observed.
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PMID:Histological investigation of aortic wall in experimental sclerosis of rabbits. 14 19

Proteoglycans were studied in articular cartilage of human femoral condyles. On the basis of the histochemical data obtained by means of light microscopy (AB + CEC MgCl2; pre-incubation with hyaluronidase or with chondroitinase ABC), the proteoglycan concentration as well as the keratan sulfate-chondroitin sulfate ratio seemed to increase proportionally to the articular cartilage depth. AB-proteoglycan particles of various shapes (filament-like or leaf-like) and sizes (10 nm or 16-18 nm), depending on the articular cartilage depth and on the histochemical conditions (as above), were visualized in thin sections. Similar heterogeneity of elongated non-collagen particles was shown in replicas of fresh freeze-fractured and deep-etched specimens. An interpretation of the distribution and nature of articular cartilage proteoglycans was made by comparing the obtained morphological findings.
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PMID:Heterogeneity of proteoglycan particles in thin sections and replicas of human articular cartilage. 624 53

The brains of 6 rats aged 12 months (adult) and 6 rats aged 24 months (aged) were embedded in paraffin following steady state perfusion with fixation solution. Glycosaminoglycans (GAGs) were demonstrated by histochemical methods using the Alcian blue CEC method in combination with the Feulgen reaction and testis hyaluronidase. Cell nuclei revealed different patterns of GAGs in different layers of the brain cortex and in different cell types. In neuronal cell nuclei of layer 2, no GAGs are found and this may be the case also in certain types of pyramidal cells. There was a reduction of the blue staining components of the chromatin network by hyaluronidase, and also a reduction of the electronmicroscopic contrast by this enzyme in pilot study using a specimen of one animal. The enzyme effects were found to be more marked or even exclusively present in the group of aged animals. Thus, the contents of chrondroitin sulfates or hyluronate which are substrates of the enzyme may be increased either relatively or absolutely in cell nuclei of aged brains whereas GAGs resistant to the enzyme may be reduced in activity. Since GAGs are known to influence DNA activity, the variations demonstrated may be assumed to be of significance for the aging process in postmitotic cells.
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PMID:Age-related histochemical staining patterns of glycosaminoglycans in cell nuclei of different regions of the rat brain: a pilot study. 1537 11