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Biomedical subjects

J Krajícková

Publications and source records attributed to J Krajícková.

14 recordsLinked to original sources
PubMed2006

[Polymorphisms of adiponectin and resistin genes in patients with obesity and anorexia nervosa].

BACKGROUND: Adiponectin and resistin are hormones that may represent a link between obesity and insulin resistance. Genes for these hormones are new candidate genes of insulin resistance and type 2 diabetes mellitus. The aim of our study was to determine the frequency of single nucleotide polymorphisms 45T > G and 276T > G of adiponectin gene and 62G > A and -180C > G of resistin gene in patients with obesity, anorexia nervosa and in lean women and to study the influence of particular genotypes on serum concentrations of these hormones. METHODS AND RESULTS: Serum adiponectin, resistin, TNF-alfa and insulin levels were measured in 51 patients with obesity, 17 with anorexia nervosa and 17 lean women. DNA analysis was carried out by means of polymerase chain reaction (PCR) with restriction analysis of PCR product (RFLP). Adiponectin levels were lowest in obese women and highest in anorexia nervosa patients. Resistin concentrations were lowest in anorexia nervosa and highest in obese patients. Genotype analysis within respective groups showed no differences in assessed parameters when comparing different adiponectin and resistin polymorphisms. The only difference detected was significantly higher BMI in G/G genotype relative to T allele carries in 276 position of ADP gene in control group (23.48 +/- 0.85 vs. 19,7 +/- 0.95, p < 0.05). In anorexia nervosa patients, frequency of G allele in RETN -180 polymorphism was significantly higher relative to control group (p < 0.05). CONCLUSIONS: Polymorphisms 45T > G a 276T > G of ADP gene and 62G>A and -180C > G RETN gene did not influence serum ADP and RETN concentrations. BMI was influenced by T allele presence in 276 position of ADP gene in control group only. Anorexia nervosa patients had higher frequency of G allele of RETN -180 polymorphism compared to healthy women.

Adiponectin↗
PubMed1995

Age-dependent changes in proteoglycan biosynthesis in human intervertebral discs.

Proteoglycans from annulus fibrosus and nucleus pulposus of human intervertebral disc were investigated by electrophoresis in a composite agarose-polyacrylamide gel and immunohistochemically using various monoclonal antibodies against components of extracellular matrix. There were at least five different populations of proteoglycans in both annulus fibrosus and nucleus pulposus. Proteoglycans represented by individual electrophoretic bands differed from each other in hydrodynamic size but all of them contained epitopes present in keratan sulphate. Chondroitin sulphate could be detected in populations with molecular weight above 200,000 daltons. We could postulate that the cleavage of proteoglycan chains starts at the C-terminal end. This is supported by the finding that the globular region G2 on the protein core was detected in the same populations as keratan sulphate. We could confirm these results using tissue cultures of nucleus pulposus, inner and external part of annulus fibrosus. Of interest is the finding that there is de novo synthesis of globular domain G1 only in structures of intervertebral disc from a 16-year-old male and not in the tissue of a 69-year-old male. This might contribute to an explanation of decreased aggregation of proteoglycans during the aging process.

Adolescent↗
PubMed1991

[Indicators of articular cartilage degeneration in synovial fluid].

Detection of proteoglycans in biological fluids is a perspective method for the evaluation of the degree of catabolic processes in articular cartilage. The demand of accuracy and specificity of detection of substructures of the degradation products of the cartilaginous matrix, with the perspective of routine large scale examinations, restricts available possible methods practically only to the use of immunochemical methods. In the present investigation in the inhibitory ELISA test polyclonal antibodies with a double specificity in relation to basic structures of the cartilage--proteoglycans--were used. The highest concentrations of degradation products of proteoglycans in punctates of synovial fluid were found in diseases where the clinical picture is dominated by repeated attacks of the joints with longer remission periods, and where the attack is stimulated, usually by stimuli of an intermittent systemic or exogenous character (gout, reactive arthritis incl. Reiter's syndrome, Lyme disease).

Antigen-Antibody Reactions↗
PubMed1990

[Changes in proteoglycans in human articular cartilage in relation to age].

The authors investigated in articular cartilage the presence and amount of the free fragment of the protein nucleus of the proteoglycan monomer containing the area of the bond with hyaluronic acid (HABR) and the presence of the small dermatan sulfate proteoglycan in relation to age. The articular cartilage of older subjects contains a much higher ratio of the protein fragment with functional HABR, as compared with young adult tissue. The more ready extractability of this fragment suggests an impaired bond between the proteoglycan monomer and hyaluronic acid. The ratio of the small dermatan sulfate proteoglycan is significantly reduced in the articular cartilage of older subjects. In the articular cartilage of a very old person (87 years) this proteoglycan was not detected or its content is at the borderline of detection of the methods used.

Adult↗
PubMed1990

[The effect of nonsteroidal antirheumatic agents on articular cartilage].

The authors submit a review on the influence of non-steroid anti-rheumatic drugs on the articular cartilage. First they review the general literature and then discuss the effect of different NSA on cartilage, taking into account their classification into six groups with regard to their chemical composition. Experience is based practically only on laboratory and experimental work and the results therefore cannot be mechanically applied in clinical medicine. However, NSA which do not have a negative impact on the cartilage of experimental animals are probably also safer in clinical practice. In this country the following NSA are available: diclofenac, piroxicam and thia profenic acid.

Animals↗
PubMed1990

[Levels of large proteoglycan aggregate binding proteins and the level of small proteoglycans in healthy human articular cartilage and in osteoarthrosis].

The investigation was focused on the electronmicroscopic localization of one structure of the aggregate of the large proteoglycan--binding proteins and the small dermatan sulphate proteoglycan, using specific antibodies prepared against these structures and the complex colloid gold--protein A. The authors investigated the incidence and distribution of these structures in the intercellular area of ultrathin sections of the sound and arthritic human articular cartilage. In the arthritic cartilage, consistent with biochemical findings, the authors detected a loss of the binding protein or its disappearance and conversely an increase of the small dermatan sulphate proteoglycan.

Carrier Proteins↗
PubMed1989

[Degenerative changes in intervertebral disks].

A histotopographic study of lumbar spine was made in 27 deceased of the age of 2 to 85 years lacking of any spinal clinical symptomatology. Regressive changes were found in all the intervertebral disks except in infants. A central necrosis was present in 26 cases and pericentral striped necrosis in 19 cases. Other disks showed consequences of necrosis--vascularization, scarring, regenerative proliferation of chondrocytes, ganglion type cavities. A concept of disk lesion as a trigger of further spinal lesions was supported by frequent regressive changes of the disks. Schmorl's (internal) nodes were found in 35 cases, quite often in young persons without clinical symptomatology. The amount of glycosaminoglycans during the disk regression was detected by Safranin O-Fast Green stain with ambiguous results. A hypothetical spontaneous vanishing of the nucleus pulposus in accordance with the age was a topic of discussion. Protrusions of the disks into the spinal canal were not found. Initial osteophytes at ventral margins of vertebral bodies were identified in 49 cases, at dorsal margins in only 3 cases.

Adolescent↗
PubMed1988

Urinary proteoglycan degradation product excretion in patients with rheumatoid arthritis and osteoarthritis.

The excretion of sugar components of glycosaminoglycans in the urine was investigated in 19 healthy controls, 27 patients with rheumatoid arthritis, and 24 with osteoarthritis. Both groups of patients excreted significantly more glucosamine, galactosamine, and mannose than the controls. The total uronic acid excretion, also, was higher in the two groups than in the healthy subjects. The possibility of using this method for the long term follow up of rheumatoid arthritis and osteoarthritis and the response to treatment is discussed.

Arthritis, Rheumatoid↗
PubMed1987

Effect of tolfenamic acid on the metabolism of the main connective tissue components in rats.

Tolfenamic acid (Clotam) has been used in the therapy of rheumatic diseases for some years. Regarding its chemical structure it belongs to the group of fenamates. The effect of tolfenamic acid on the synthesis of collagen and proteoglycans in granulation tissue, skin or cartilage of rat weanlings was tested and compared with the action of mefenamic acid. According to the results obtained, tolfenamic acid is a potent inhibitor of collagen as well as proteoglycan syntheses. The concentrations of the constituents of proteoglycans, i.e. protein core, link protein as well as glycosaminoglycans were decreased in the tissue after treatment with tolfenamic acid. In comparison with mefenamic acid, if the same doses were used (50 mg and 100 mg/kg of body weight/day in in vivo experiments and 10 mg/g wet tissue in in vitro experiments), tolfenamic acid exhibits more distinct inhibitory effect. A general inhibitory effect of tolfenamic acid on proteosynthesis is suggested.

Animals↗