Search PubMed⌕ Search

Biomedical subjects

T Papp

Publications and source records attributed to T Papp.

At least 37 records · Page 2Linked to original sources

An in vitro study of the biomechanical effects of flexible stabilization on the lumbar spine.

STUDY DESIGN: Lumbar motion segments were tested in vitro to examine biomechanical changes after posterior fixation by a flexible device. OBJECTIVES: To assess changes in load distribution and conformation of vertebral structures after a flexible stabilization. This should provide the foundations for a scientific understanding of the immediate effects of this surgical procedure. METHODS: Hooks were placed over the proximal spinous process and the distal laminas of a motion segment and connected by a polyester braid. Tension applied to the braid then generated a compression of the posterior elements. The force between the articular facets, the displacement of the posterior anulus fibrosus of the intervertebral disc, and the change in the relative position of the adjacent vertebrae were measured as the applied tension was increased. RESULTS: Facet joint force, disc bulge, and vertebral angulation increased with applied tension until a position of "locking" was achieved, apparently when the bony margin of the superior half of the facet joint contacted the inferior pars interarticularis. A tension of between 50 to 100 N in the braid was required for this. Facet joint force was less than 40% of this, and disc bulge was only 0.15 mm. The extension of the motion segment was between 2 degrees and 8 degrees. CONCLUSIONS: The results suggest that if such a system is applied surgically, stabilization is produced by compaction of the bony margins of the facet joints. Only a relatively small proportion of the posteriorly applied load is carried by the facet joints themselves, and little angulatory change is expected with minimal disc bulge.

Aged↗

DNA amplification polymorphisms of Mucor piriformis.

Mucor piriformis can cause postharvest decay in various fruits and vegetables stored at low temperatures. Thirty isolates of this fungus, collected from infected fruit, were subjected to random amplified polymorphic DNA (RAPD) analysis. Seven different 10-bp primers were used to determine the type and extent of intraspecific genetic polymorphisms. Nineteen composite amplification types were identified, indicating a higher degree of variability than found in previous isoenzyme studies. Numerical analysis with the UPGMA technique revealed three clusters, which correlated with the mating competency of the isolates or their place of origin. These results demonstrate that RAPD analysis can identify isolates and subspecific populations of M. piriformis.

DNA Primers↗

Lack of p53 mutations and loss of heterozygosity in non-cultured human melanocytic lesions.

In this study we analysed snap-frozen surgical resections of 16 superficial spreading melanomas, 13 nodular malignant melanomas, 2 lentigo maligna melanomas, 1 dysplastic nevus, 1 congenital nevus and 5 normal nevi from 38 patients for point mutations in the human p53 gene at exons 5-8 by polymerase chain reaction/single-strand conformation polymorphism as well as for loss of heterozygosity of p53 by restriction-fragment-length polymorphism/polymerase chain reaction in order to determine whether p53 aberrations are associated with melanoma subtypes. In addition, we analysed six melanoma cell lines for point mutations in p53. Our results revealed the absence of point mutations and loss of heterozygosity in all fresh resected lesions. However, a TAC (Tyr) to TGC (Cys) transition at codon 163 in exon 5 was found in one cell line.

Base Sequence↗

Analysis of ras mutations in human melanocytic lesions: activation of the ras gene seems to be associated with the nodular type of human malignant melanoma.

We have analyzed the Ha-ras, Ki-ras and N-ras gene for point mutations at codons 12, 13 and 61 via restriction fragment length polymorphism/polymerase chain reaction analysis and subsequent direct sequencing in non-cultured fresh-frozen tissues of 16 superficial spreading melanomas (SSM), 13 nodular malignant melanomas (NMM), 2 lentigo malignant melanomas (LMM), 1 dysplastic nevus, 1 congenital nevus and 5 normal nevi from 38 patients. Mutations were found in 4 melanoma samples, all belonging to the nodular malignant type. Three of them were mutated in N-ras and one in the Ha-ras gene. Mutation in N-ras was also detected in the congenital nevus. All mutations were exclusively located at the first two base pairs of codon 61. No Ki-ras mutation was detected in any lesion. No mutation could be found in SSM and LMM in addition to dysplastic and normal nevi. The frequency of ras mutation in NMM was 31%, whereas in SSM it was 0%. Our study suggests (a) an association between ras mutations (mainly N-ras) and the NMM as a subgroup of human melanoma; (b) that activation of Ki-ras is not involved in the pathogenesis of melanoma. The role of UV radiation in point mutations of ras genes in human melanoma is discussed.

Base Sequence↗

Mineral fibers induce apoptosis in Syrian hamster embryo fibroblasts.

It is known that asbestos and other mineral fibers induce lung cancer and mesothelioma. However, the primary mechanisms of fiber-induced carcinogenesis still remain to be elucidated. Previous studies, including our own, have shown that asbestos causes specific mitotic disturbances, micronucleus formation and typical changes in chromatin structure resembling those of apoptosis. This effect has been considered as programmed cell death removing damaged or pre-cancerous cells. We investigated the induction of apoptosis by asbestos (amosite, crocidolite, chrysotile) and ceramic fibers. The typical ladder pattern of DNA fragments was identified by means of gel electrophoresis, the intracellular calcium concentration was measured and flow cytometry analyses were carried out to determine the percentage of apoptotic cells. The different fibers showed different potencies for the induction of apoptosis in Syrian hamster embryo (SHE) cells. Depending on the type of fiber applied 3-33% of cells underwent apoptosis. Chrysotile proved to be the most potent inducer of apoptosis compared to the other fibers. In addition, an increase intracellular calcium level was observed in apoptotic SHE cells. Chrysotile induced apoptosis after a considerably longer exposure time (66-72 h) than cisplatin (24 h). In view of these findings we hypothesize that chrysotile induces apoptosis resulting from long-term changes in intracellular regulation pathways.

Animals↗

Trefoil configuration and developmental stenosis of the lumbar vertebral canal.

The midsagittal and interpedicular diameters and the trefoil shape of lumbar vertebrae of known age at death were measured in skeletons from a population aged between 1 and 70 years. All the trefoil configurations were at L5 with the exception of one at L4. The overall prevalence was 25%, but this shape was not generally apparent until adulthood. The midsagittal diameter in the trefoil canals was found to be significantly smaller than that in the unaffected canals. This did not change significantly after six years of age indicating that the cause of the trefoil configuration is probably present early in life. The trefoil shape was no more common in the spines of the elderly subjects. Our findings indicate that the trefoil configuration of the lumbar vertebral canal has a developmental origin and is not a consequence of degenerative processes.

Adult↗

The growth of the lumbar vertebral canal.

STUDY DESIGN: This study examines the growth and development of the lumbar spinal canal with emphasis on early life. OBJECTIVE: Changes in dimensions of the canal were investigated throughout life. SUMMARY OF BACKGROUND DATA: Seven hundred and fifteen lumbar vertebrae were examined from the Spitalfield Collection of Skeletons at the Natural History Museum, London. METHODS: Unmagnified silhouette pictures were taken of the canals with a specially designed photographic box. Computerized image analysis provided the accurate measurements. RESULTS: Regarding the midsagittal diameter and the cross-sectional area, the cranial four lumbar vertebrae were already fully matured in infants. At L5 there was significant increase up to 4 years of age when the midsagittal diameter was even larger than in the adult. The interpedicular diameter significantly increased at L1 until 10 years of age, at the other levels until adulthood, as did the perimeter at L4 and L5 until 14 years of age. The shape of the canal was assessed by measuring the circularity, the 'trefoilness' and the situation of the centroid. The first measurement significantly decreased with age, the trefoilness increased until adulthood, and the centroid of the canal approached the vertebral body. In spines with spina bifida occulta, the lumbar canal was significantly larger proximal to the lesion than in the unaffected spines. CONCLUSION: The lumbar spinal canal exhausts its growth potential by infancy as regards the midsagittal diameter and the cross-sectional area. Thus, in the case of delayed development, it is not capable of catch-up growth.

Adolescent↗

Changes of the lumbar spinal canal proximal to spina bifida occulta. An archaeologic study with clinical significance.

STUDY DESIGN: This archaeologic study, based on four populations, examines the incidence of spina bifida occulta in the lumbar spine and the size of the vertebral canal proximal to the lesion. OBJECTIVES: To ascertain any significant change in the dimensions of the lumbar spinal canal of skeletons with spina bifida occulta. The incidence of the lesion also was compared in the separate genetic groups. METHODS: Central canals of 1760 lumbar vertebrae were examined. Silhouette, unmagnified pictures of the vertebral canals were measured by computerized image analysis. RESULTS: The mid-sagittal diameter at L4 and L5 and the cross-sectional area at L5 were found to be significantly larger proximal to the lesion compared with the unaffected spines. The overall incidence was 18%. CONCLUSIONS: The capacity of the lumbar canal is greater proximal to spina bifida occulta. Therefore, delayed closure of the neural arch at a single segment has morphologic significance to the more proximal spine.

Adolescent↗

Cytogenetic changes in primary, immortalized and malignant mammalian cells.

Some chromosomes in transformed rat cells and somatic cell hybrids fail to display the presence of kinetochore proteins as detected by antikinetochore antibodies. Such chromosomes (K- chromosomes) may constitute a novel mechanism for the genesis of aneuploidy. We have analyzed primary, immortalized and malignant mammalian cells for the presence of kinetochore proteins and micronuclei. Our results suggest a correlation of the K- chromosome and micronucleus frequency with the variability in chromosome number. Upon in situ hybridization with the minor satellite and alpha satellite sequences some K- chromosomes showed a signal. This indicates that the observed lack of kinetochores is not necessarily due to a lack of centromeric DNA. We conclude that dislocated K- chromosomes may become incorporated into micronuclei which are prone to loss. Such events would be associated with the generation of aneuploidy.

3T3 Cells↗