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  • 1
    Electronic Resource
    Electronic Resource
    Induction of the morphologic changes of both acute and chronic experimental myasthenia by monoclonal antibody directed against acetylcholine receptor (1984)
    Springer
    Acta neuropathologica 63 (1984), S. 131-143 
    Details
    ISSN: 1432-0533
    Keywords: Anti-acetylcholine receptor antibody ; Experimental autoimmune myasthenia gravis ; Monoclonal antibody ; Myasthenia gravis ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary To investigate pathogenic mechanisms in experimental autoimmune myasthenia gravis (EAMG) and myasthenia gravis (MG), we studied the acute and chronic effects in rats of injection of rat monoclonal antibodies (MCABs) directed against the acetylcholine receptor (AChR). Animals were severely weak 12 h after a single injection, at which time macrophages were found invading endplate regions of muscle and cholinesterase-stained regions were separted from the underlying muscle fibers. Ultrastructural studies showed findings identical to the acute phase of EAMG: degenerating postsynaptic membranes and invasion and phagocytosis of endplate regions by macrophages. Animals receiving sublethal doses of MCAB recovered clinically by 4–5 days after injection. Recovery was accompanied by a progressive decrease in the number of macrophages associated with endplates and reapposition to the myofibers of the cholinesterasestained regions. Animals injected once, or repeatedly over several months, remained clinically and electromyographically normal after recovery from the initial episode of weakness, but their endplate ultrastructure was highly simplified with blunted or absent synaptic folds and shallow or absent secondary synaptic clefts. These studies demonstrate that anti-AChR MCABs can induce the changes of both acute and chronic EAMG. There is good correlation between the inflammatory changes and the acute clinical disease but poor correlation between morphological and clinical parameters in the chronic syndrome. The latter observation suggests that severe ultrastructural changes, similar to those seen in chronic EAMG and MG, cannot account, at least in rats, for the clinical and electrophysiologic abnormalities of MG.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00697195
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    A comparative study between cosolvent and cononsolvent ternary polymer systems through the preferential adsorption coefficient (1993)
    Springer
    Colloid & polymer science 271 (1993), S. 30-37 
    Details
    ISSN: 1435-1536
    Keywords: Ternary polymeric systems ; preferential adsorption coefficient ; cosolvent ; cononsolvent ; ternary interactions ; excess free energy ; intensity light scattering
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Sorption equilibrium of polystyrene and poly (dimethyl siloxane) in mixed solvents has been monitored by means of the preferential adsorption coefficient experimentally determined from intensity light scattering measurements. The pairs of solvents used to dissolve each polymer sample have been selected for the purpose to perform cosolvent and cononsolvent ternary polymer systems. Flory-Huggins formalism including ternary interactions has been used to predict the sorption equilibrium for the cosolvent system and, for the first time, for cononsolvent ones. Moreover, the proportionality between binary and ternary interactions, recognized by Pouchly, is also corroborated for both ternary polymer systems. From a thermodynamic standpoint, the sorption equilibrium has been described by approaching the behavior of the “bulk solvent” to the binary liquid mixture through the excess Gibbs free energy.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00652300
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    Paper (German National Licenses)
    Fulltext
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