267 research outputs found
Development of Postural Muscles and Their Innervation
Control of posture is a prerequisite for efficient motor performance. Posture depends on muscles capable of enduring contractions, whereas movements often require quick, forceful muscle actions. To serve these different goals, muscles contain fibers that meet these different tasks. Muscles with strong postural functions mainly consist of slow muscle fibers with a great resistance against fatigue. Flexor muscles in the leg and arm muscles are mainly composed of fast muscle fibers producing relatively large forces that are rapidly fatigable. Development of the neuromuscular system continues after birth. We discuss in the human baby and in animal experiments changes in muscle fiber properties, regression from polyneural into mononeural innervation, and developmental changes in the motoneurons of postural muscles during that period. The regression of poly-neural innervation in postural muscles and the development of dendrite bundles of their motoneurons seem to be linked to the transition from the immature into the adult-like patterns of moving and postural control
Stability of Biaxial Nematic Phase for Systems with Variable Molecular Shape Anisotropy
We study the influence of fluctuations in molecular shape on the stability of
the biaxial nematic phase by generalizing the mean field model of Mulder and
Ruijgrok [Physica A {\bf 113}, 145 (1982)]. We limit ourselves to the case when
the molecular shape anisotropy, represented by the alignment tensor, is a
random variable of an annealed type. A prototype of such behavior can be found
in lyotropic systems - a mixture of potassium laurate, 1-decanol, and ,
where distribution of the micellar shape adjusts to actual equilibrium
conditions. Further examples of materials with the biaxial nematic phase, where
molecular shape is subject to fluctuations, are thermotropic materials composed
of flexible trimeric- or tetrapod-like molecular units. Our calculations show
that the Gaussian equilibrium distribution of the variables describing
molecular shape (dispersion force) anisotropy gives rise to new classes of the
phase diagrams, absent in the original model. Depending on properties of the
shape fluctuations, the stability of the biaxial nematic phase can be either
enhanced or depressed, relative to the uniaxial nematic phases. In the former
case the splitting of the Landau point into two triple points with a direct
phase transition line from isotropic to biaxial phase is observed.Comment: 18 pages containing 6 figure
Cerebellar Development and Plasticity: Perspectives for Motor Coordination Strategies, for Motor Skills, and for Therapy
The role of the mammalian cerebellum ranges from motor coordination, sensory-motor integration, motor learning, and timing to nonmotor functions such as cognition. In terms of motor function, the development of the cerebellum is of particular interest because animal studies show that the development of the cerebellar cortical circuitry closely parallels motor coordination. Ultrastructural analysis of the morphological development of the cerebellar circuitry, coupled with the temporal and spatial identification of the neurochemical substrates expressed during development, will help to elucidate their roles in the establishment of the cerebellar circuitry and hence motor activity. Furthermore, the convenience of a number of naturally occurring mouse mutations has allowed a functional dissection of the various cellular elements that make up the cerebellar circuitry. This understanding will also help in the approach to possible therapies of pathologies arising during development because tile cerebellum is especially prone to such perturbation because of its late development
Corticotropin-releasing factor receptor types 1 and 2 are differentially expressed in pre- and post-synaptic elements in the post-natal developing rat cerebellum
Corticotropin-releasing factor (CRF)-like proteins act via two G-protein-coupled receptors (CRF-R1 and CRF-R2) playing important neuromodulatory roles in stress responses and synaptic plasticity. The cerebellar expression of corticotropin-releasing factor-like ligands has been well documented, but their receptor localization has not. This is the first combination of a light microscopic and ultrastructural study to localize corticotropin-releasing factor receptors immunohistologically in the developing rat cerebellum. Both CRF-R1 and CRF-R2 were expressed in climbing fibres from early stages (post-natal day 3) to the adult, but CRF-R2 immmunoreactivity was only prominent throughout the molecular layer in the posterior cerebellar lobules. CRF-R1 immunoreactivity was concentrated in apical regions of Purkinje cell somata and later in primary dendrites exhibiting a diffuse cytoplasmic appearance. In Purkinje cells, CRF-R1 immunoreactivity was never membrane bound post-synaptically in dendritic spines while CRF-R2 immunoreactivity was found on plasmic membranes of Purkinje cells from post-natal day 15 onwards. We conclude that the localization of these receptors in cerebellar afferents implies their pre-synaptic control of the release of corticotropin-releasing factor-like ligands, impacting on the sensory information being transmitted from afferents. Furthermore, the fact that CRF-R2 is membrane bound at synapses, while CRF-R1 is not, suggests that ligands couple to CRF-R2 via synaptic transmission and to CRF-R1 via volume transmission. Finally, the distinct expression profiles of receptors along structural domains of Purkinje cells suggest that the role for these receptors is to modulate afferent inputs
Evolution of interfaces and expansion in width
Interfaces in a model with a single, real nonconserved order parameter and
purely dissipative evolution equation are considered. We show that a systematic
perturbative approach, called the expansion in width and developed for curved
domain walls, can be generalized to the interfaces. Procedure for calculating
curvature corrections is described. We also derive formulas for local velocity
and local surface tension of the interface. As an example, evolution of
spherical interfaces is discussed, including an estimate of critical size of
small droplets.Comment: Discussion of stability of the interface is added, and the numerical
estimates of width and velocity of the interface in the liquid crystal
example are corrected. 25 pages, Latex2
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