ABSTRACT
INTRODUCTION: The flexible derotator is one of the therapeutic resources used to combat primary and secondary abnormalities in walking cerebral palsy children. It was developed to reduce abnormal femoral and tibial torsions and lessen the latter's negative functional impact. OBJECTIVE: To determine the effect of wearing a flexible derotator on anatomic and functional parameters in walking cerebral palsy children. METHODS: We performed a retrospective study of walking cerebral palsy children by gathering data on bone-related parameters (femoral and tibial torsion) and functional parameters (distance and speed gait, and the energy expenditure index (EEI)). Fifteen walking cerebral palsy children were treated with the flexible derotator for one year and 15 untreated walking cerebral palsy children were included as controls. The two groups were compared in terms of the various parameters' change over time between the initial examination (the last examination prior to the start of the study or prior to use of the flexible derotator) and the final examination (after one year of follow-up). RESULTS: Right femoral anteversion and right and left external tibial torsion improved. There was a significant increase in distance and speed gait and a decrease in the EEI in walking cerebral palsy children. CONCLUSION: Our retrospective study revealed a significant improvement in functional parameters in children with cerebral palsy, as a result of wearing the flexible derotator for at least 6 hours a day for a year. Bone parameters only improved slightly. Use of the flexible derotator could improve these children's quality of life.
Subject(s)
Cerebral Palsy/rehabilitation , Femur/physiopathology , Gait Disorders, Neurologic/rehabilitation , Orthotic Devices , Tibia/physiopathology , Anthropometry , Biomechanical Phenomena , Child , Equipment Design , Gait Disorders, Neurologic/physiopathology , Humans , Quality of Life , Retrospective Studies , Torsion, Mechanical , WalkingABSTRACT
In order to have a model for studying the possible implications of 2-ethylhexyl-phthalate and dialysate on connective tissue, we evaluated their direct effects on the air pouch lining tissue and on fibroblast cultures. Air pouches were formed on the backs of 60 ten-week-old Wistar rats by subcutaneous injections of 10 ml sterile air. On the tenth day 2 ml sterile air, or 2 ml 5 microg/L or 2 ml 10 microg/L 2-ethylhexyl-phthalate in olive oil, or 2 ml olive oil alone, or 2 ml 5 mg/ml or 12 mg/ml lyophilized dialysate were injected into the air pouches. After sampling at seven or twenty-one days, the rats were killed. The biochemical data showed an increase in sulphated glycosaminoglycans with 2-ethylhexyl-phthalate and dialysate. Electron microscopy findings revealed cellular alterations such as vacuolation and cell remnants with 2-ethylhexyl-phthalate, while the cells of the air pouches treated with dialysate showed regular organelles with increased and dilated cisternae of rough endoplasmic reticulum. Moreover, an increase in collagen fibres surrounding the damaged zones was noticed in 2-ethylhexyl-phthalate and dialysate treated rats. The glycosaminoglycan modifications and collagen fibre increase seem to suggest that the morphological changes, with the features of fibrosis, could be the result of 2-ethylhexyl-phthalate and dialysate action on connective tissue. Moreover, the air pouch technique can be considered a good model for studying the direct effects of 2-ethylhexyl-phthalate and other substances, such as uremic toxins, on connective tissue.
Subject(s)
Connective Tissue/drug effects , Diethylhexyl Phthalate/pharmacology , Fibroblasts/drug effects , Renal Dialysis , Animals , Cells, Cultured , Microscopy, Electron , Models, Animal , Rats , Rats, WistarABSTRACT
Implanting an expander in the subcutaneous layer causes gradual expansion and provides additional tissue for reconstruction of tissular defects. The force applied remodels the connective tissue and modifies dermis contractibility in additional tissue. Other authors confirm that parameters such as mitosis and hyaluronan influence the system in the tissue regeneration processes. We studied histochemical and morphological variations of tissue expanders before and 6 months after transplant. Our histochemical data do not show any changes in dermis glycosaminoglycans of the expanded and transplant-expanded skin when compared to controls. Morphological data demonstrate reorganization of connective fibers and disappearance of the papillar layer. The latter is not yet formed in the expanded skin 6 months after transplant. This suggests that a long time is required for biological reconstruction of epidermal-dermal interactions after transplant.
Subject(s)
Extracellular Matrix/pathology , Extracellular Matrix/ultrastructure , Tissue Expansion Devices/adverse effects , Adolescent , Child , Child, Preschool , Histocytochemistry , Humans , Infant , Microscopy, Electron , Surgical FlapsABSTRACT
Cyclopentenone prostaglandins PGA1 and PGJ2 induce growth arrest at the G1/S interphase of the cell cycle in tumour cell lines. Notably, PGE, the precursor molecule of PGA, downregulates the interleukin (IL)-2-dependent proliferation of lymphocytes. Therefore the IL-2/IL-2 receptor system and relative signal transduction is a possible target of the antiproliferative effect of PGA/PGJ. In the present study the PGA1/PGJ2-dependent growth inhibition of IL-2-stimulated primary human cord blood mononuclear cells (CBMCs) was found to be mediated by interference with the IL-2 proliferative signal. Both prostaglandins (PGs) inhibited the synthesis of total RNA and protein in IL-2 stimulated cells. PGA1 and even more PGJ2 downregulated the expression of IL-2 receptor alpha (CD25 phenotype). IL-2 partly reversed this effect. Moreover, suppression of IL-2-stimulated cells was not the result of PG-mediated activation of apoptosis. On the contrary, PGs reduced both apoptosis and the high expression of c-Jun detectable in CBMCs spontaneously. Cyclin A/Cdk2 complexes regulate G1/S transition during the cell cycle. In IL-2-stimulated cells, the levels of Cdk2 were found to be lower in PG-treated cells than those detected in controls. In conclusion, cyclopentenone PGs inhibit CBMCs spontaneous or IL-2-dependent proliferation in part by interfering with the IL-2 pathway.
Subject(s)
Antineoplastic Agents/pharmacology , Fetal Blood , Interleukin-2/antagonists & inhibitors , Leukocytes, Mononuclear , Prostaglandin D2/analogs & derivatives , Prostaglandins A/pharmacology , Apoptosis/drug effects , Cell Division/drug effects , Cells, Cultured , DNA Fragmentation/drug effects , Down-Regulation , Female , Humans , Immunoblotting , In Vitro Techniques , Interleukin-2/pharmacology , Pregnancy , Prostaglandin D2/pharmacology , Protein Biosynthesis , RNA/biosynthesis , Recombinant Proteins/antagonists & inhibitors , Recombinant Proteins/pharmacology , Uridine/metabolismABSTRACT
Fumonisin B1 is hepatotoxic in all species, but nephrotoxicity has only been reported in rats. It is a specific inhibitor of sphinganine N-acyltransferase. Our objective was to determine the target organs for fumonisin toxicosis in the rabbit. We administered fumonisin B1 ( > 95% pure) intravenously to adult rabbits and examined selected clinical, biochemical, and histological parameters for up to 5 days. In a pilot study, rabbits were given fumonisin B1 at 1, 0.5, 0.3, 0.15, or 0 mg/kg daily for 4 or 5 days and then euthanized. Additional rabbits were given a single dose of fumonisin B1 at 1 mg/kg and euthanized on day 2 or 4. In the formal time-course study, rabbits were given a single dose of fumonisin B1 at 0 or 1.25 mg/kg and euthanized on days 1, 3, or 5. Rabbits given multiple doses of fumonisin B1 were lethargic and anorectic, and had decreased urine production. Liver- and renal-associated clinical chemistry parameters were elevated. Renal lesions consisted of severe proximal tubular necrosis. Liver lesions were variable and consisted of mild necrosis, hepatocyte vacuolation, and bile stasis. The sphinganine-to-sphingosine ratio, in both target and nontarget tissues, was markedly elevated in treated rabbits. A single dose of fumonisin B1 induced renal but not hepatic injury. Therefore, the target organs for fumonisin B1 toxicity in rabbits are kidney and liver, with the kidney being more sensitive.
Subject(s)
Carcinogens, Environmental/toxicity , Fumonisins , Kidney Tubules, Proximal/drug effects , Liver/drug effects , Mycotoxins/toxicity , Animals , Bile Ducts/drug effects , Bile Ducts/pathology , Biomarkers/blood , Carcinogens, Environmental/administration & dosage , Carcinogens, Environmental/pharmacokinetics , Dose-Response Relationship, Drug , Enzyme Inhibitors/metabolism , Female , Injections, Intravenous , Liver/cytology , Male , Mycotoxins/administration & dosage , Mycotoxins/pharmacokinetics , Necrosis/chemically induced , Pilot Projects , Rabbits , Sphingosine/analogs & derivatives , Sphingosine/metabolismABSTRACT
Central neurons and peripheral nervous structures, e.g. cutaneous free endings, perifollicular nets, Meissners corpuscles and intramuscular fibres, were studied using various impregnation methods. The confocal scanning laser microscopes (CSLMs) used were equipped with different laser sources, in order to evaluate their limitations and advantages with these techniques and to contribute to a better understanding of the general morphology of the nervous system. When staining with silver sections with clouds of tiny silver granules which are beyond the resolution power of the conventional light microscope but which show a high reflectivity with the CSLM are obtained. Golgi-Cox mercuric impregnation, however, provides specimens which are precipitate-free, thus ensuring the reliability of information obtained. It does, however, have the disadvantage of being applicable only to the central nervous system. In all cases it is an advantage for the instrument to be fitted with different lasers (e.g. Ar and He-Ne), so as to optimize the images of samples impregnated with different methods. Notwithstanding the possibility that artefacts may distort the geometry of the sample and reduce the resolution, the images presented in this paper show that with careful selection of optical sectioning distances, the use of a suitable stack of sections and, if necessary, the aid of false electronic colours and of partial or complete rotation, it is possible to achieve a more precise interpretation of the morphology and organization of complex structures, such as those of the nervous system.
Subject(s)
Mechanoreceptors/ultrastructure , Nerve Endings/ultrastructure , Nerve Fibers/ultrastructure , Nerve Net/ultrastructure , Neurons/ultrastructure , Animals , Central Nervous System/ultrastructure , Humans , Microscopy, Confocal/instrumentation , Microscopy, Confocal/methods , Peripheral Nervous System/ultrastructure , RatsABSTRACT
The ultrastructure and organization of free nerve fibers occurring in dermal papillae containing Meissner's corpuscles were studied in the fingertips of the Green Monkey (Cercopithecus aethiops L.). The course of the thin unmyelinated fibers leads in the vicinity of Meissner's corpuscles in the connective tissue of its sheaths, between the epidermis and the peripheral fibroblast layer; they never come into contact with the nervous component of the receptor. Consequently, neither a "pericorpuscular reticulum" nor an "apparatus of Timofeew" is formed. The presence of thin axons containing dense-cored vesicles is evident, but they are not autonomous fibers, as indicated by the negative results of the Falck-Hillarp test for catecholamines. The nerve fibers occasionally seem to bear a close resemblance to the "open" and "plain" endings described by other authors in papillae devoid of corpuscles. Despite failure for close mutual contact to be established between the Meissner's corpuscle and the unmyelinated fibers ramifying in the connective tissue surrounding it, the hypothesis that the two may cooperate to form a "multimodal sensory package" is not without interest.
Subject(s)
Chlorocebus aethiops/anatomy & histology , Nerve Fibers/ultrastructure , Pressoreceptors/ultrastructure , Animals , Schwann Cells/ultrastructureABSTRACT
By removing epidermis with EDTA and a subsequent enzymatic digestion of dermis, eccrine sweat glands of rat fingertips were exposed and examined by scanning electron microscopy (SEM). Different protocols were tested to remove as much connective tissue as possible, while minimizing damage to other structures, and to expose the epithelial surface of secretory tubules in order to display vascular and nervous networks. SEM observations gave detailed information on the relationship between epithelial secretory cells and myoepithelial cells, as well as on the vascular and nervous networks which surround the glomeruli of glands.
Subject(s)
Eccrine Glands/ultrastructure , Forelimb/anatomy & histology , Sweat Glands/ultrastructure , Animals , Microscopy, Electron, Scanning , Rats , Rats, Inbred StrainsABSTRACT
Light-microscope findings and pathological ultrastructural changes in sural nerve biopsies from two patients affected by hypothyroidism, one with overt signs of peripheral neuropathy, the other asymptomatic, were studied. In both patients the endoneural vessels showed clear pathological changes similar to those of other metabolic neuropathies, but more marked in the symptomatic patient. It is proposed that the changes observed in the nerve fibers in hypothyroid neuropathy are secondary to changes in the endothelial cells and in the vessel wall.