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1.
Acta Neuropathol ; 121(3): 291-312, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21136068

ABSTRACT

The endoneurial microenvironment, delimited by the endothelium of endoneurial vessels and a multi-layered ensheathing perineurium, is a specialized milieu intérieur within which axons, associated Schwann cells and other resident cells of peripheral nerves function. The endothelium and perineurium restricts as well as regulates exchange of material between the endoneurial microenvironment and the surrounding extracellular space and thus is more appropriately described as a blood-nerve interface (BNI) rather than a blood-nerve barrier (BNB). Input to and output from the endoneurial microenvironment occurs via blood-nerve exchange and convective endoneurial fluid flow driven by a proximo-distal hydrostatic pressure gradient. The independent regulation of the endothelial and perineurial components of the BNI during development, aging and in response to trauma is consistent with homeostatic regulation of the endoneurial microenvironment. Pathophysiological alterations of the endoneurium in experimental allergic neuritis (EAN), and diabetic and lead neuropathy are considered to be perturbations of endoneurial homeostasis. The interactions of Schwann cells, axons, macrophages, and mast cells via cell-cell and cell-matrix signaling regulate the permeability of this interface. A greater knowledge of the dynamic nature of tight junctions and the factors that induce and/or modulate these key elements of the BNI will increase our understanding of peripheral nerve disorders as well as stimulate the development of therapeutic strategies to treat these disorders.


Subject(s)
Aging/physiology , Homeostasis/physiology , Peripheral Nerves/physiology , Animals , Blood Vessels/physiology , Humans , Lead Poisoning/physiopathology , Peripheral Nervous System Diseases/physiopathology , Trauma, Nervous System/physiopathology
2.
Methods Mol Biol ; 686: 149-73, 2011.
Article in English | MEDLINE | ID: mdl-21082370

ABSTRACT

The blood-nerve barrier (BNB) defines the physiological space within which the axons, Schwann cells, and other associated cells of a peripheral nerve function. The BNB consists of the endoneurial microvessels within the nerve fascicle and the investing perineurium. The restricted permeability of these two barriers protects the endoneurial microenvironment from drastic concentration changes in the vascular and other extracellular spaces. It is postulated that endoneurial homeostatic mechanisms regulate the milieu intérieur of peripheral axons and associated Schwann cells. These mechanisms are discussed in relation to nerve development, Wallerian degeneration and nerve regeneration, and lead neuropathy. Finally, the putative factors responsible for the cellular and molecular control of BNB permeability are discussed. Given the dynamic nature of the regulation of the permeability of the perineurium and endoneurial capillaries, it is suggested that the term blood-nerve interface (BNI) better reflects the functional significance of these structures in the maintenance of homeostasis within the endoneurial microenvironment.


Subject(s)
Blood-Nerve Barrier/cytology , Blood-Nerve Barrier/physiology , Animals , Humans , Peripheral Nerves/blood supply , Peripheral Nerves/metabolism , Peripheral Nerves/ultrastructure
3.
Exp Neurol ; 203(2): 293-301, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17125767

ABSTRACT

Pyridoxine (vitamin B6) intoxicated rodents develop a peripheral neuropathy characterized by sensory nerve conduction deficits associated with disturbances of nerve fiber geometry and axonal atrophy. To investigate the possibility that glucagon-like peptide-1 (7-36)-amide (GLP-1) receptor agonism may influence axonal structure and function through neuroprotection neurotrophic support, effects of GLP-1 and its long acting analog, Exendin-4 (Ex4) treatment on pyridoxine-induced peripheral neuropathy were examined in rats using behavioral and morphometric techniques. GLP-1 is an endogenous insulinotropic peptide secreted from the gut in response to the presence of food. GLP-1 receptors (GLP-1R) are coupled to the cAMP second messenger pathway, and are expressed widely throughout neural tissues of humans and rodents. Recent studies have established that GLP-1 and Ex4, have multiple synergistic effects on glucose-dependent insulin secretion pathways of pancreatic beta-cells and on neural plasticity. Data reported here suggest that clinically relevant doses of GLP-1 and Ex4 may offer some protection against the sensory peripheral neuropathy induced by pyridoxine. Our findings suggest a potential role for these peptides in the treatment of neuropathies, including that associated with type II diabetes mellitus.


Subject(s)
Glucagon-Like Peptide 1/physiology , Neurons, Afferent , Neuroprotective Agents , Peptides/therapeutic use , Peripheral Nervous System Diseases/prevention & control , Pyridoxine , Receptors, Glucagon/agonists , Venoms/therapeutic use , Vitamins , Amino Acid Sequence , Animals , Behavior, Animal/drug effects , Blood Glucose/metabolism , Body Weight/drug effects , Exenatide , Ganglia, Spinal/pathology , Glucagon-Like Peptide-1 Receptor , Male , Molecular Sequence Data , Muscle Tonus/physiology , Nerve Degeneration/chemically induced , Nerve Degeneration/pathology , Peripheral Nervous System Diseases/chemically induced , Postural Balance/drug effects , Rats , Rats, Sprague-Dawley , Sciatic Nerve/pathology
4.
Biol Cybern ; 93(6): 410-25, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16320080

ABSTRACT

The previous companion paper describes the initial (seed) schema architecture that gives rise to the observed prey-catching behavior. In this second paper in the series we describe the fundamental adaptive processes required during learning after lesioning. Following bilateral transections of the hypoglossal nerve, anurans lunge toward mealworms with no accompanying tongue or jaw movement. Nevertheless anurans with permanent hypoglossal transections eventually learn to catch their prey by first learning to open their mouth again and then lunging their body further and increasing their head angle. In this paper we present a new learning framework, called schema-based learning (SBL). SBL emphasizes the importance of the current existent structure (schemas), that defines a functioning system, for the incremental and autonomous construction of ever more complex structure to achieve ever more complex levels of functioning. We may rephrase this statement into the language of Schema Theory (Arbib 1992, for a comprehensive review) as the learning of new schemas based on the stock of current schemas. SBL emphasizes a fundamental principle of organization called coherence maximization, that deals with the maximization of congruence between the results of an interaction (external or internal) and the expectations generated for that interaction. A central hypothesis consists of the existence of a hierarchy of predictive internal models (predictive schemas) all over the control center-brain-of the agent. Hence, we will include predictive models in the perceptual, sensorimotor, and motor components of the autonomous agent architecture. We will then show that predictive models are fundamental for structural learning. In particular we will show how a system can learn a new structural component (augment the overall network topology) after being lesioned in order to recover (or even improve) its original functionality. Learning after lesioning is a special case of structural learning but clearly shows that solutions cannot be known/hardwired a priori since it cannot be known, in advance, which substructure is going to break down.


Subject(s)
Anura/physiology , Hypoglossal Nerve Diseases/physiopathology , Learning/physiology , Motor Skills/physiology , Predatory Behavior/physiology , Animals , Behavior, Animal , Feedback , Models, Neurological , Motor Activity
5.
Biol Cybern ; 93(6): 391-409, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16292659

ABSTRACT

A motor action often involves the coordination of several motor synergies and requires flexible adjustment of the ongoing execution based on feedback signals. To elucidate the neural mechanisms underlying the construction and selection of motor synergies, we study prey-capture in anurans. Experimental data demonstrate the intricate interaction between different motor synergies, including the interplay of their afferent feedback signals (Weerasuriya 1991; Anderson and Nishikawa 1996). Such data provide insights for the general issues concerning two-way information flow between sensory centers, motor circuits and periphery in motor coordination. We show how different afferent feedback signals about the status of the different components of the motor apparatus play a critical role in motor control as well as in learning. This paper, along with its companion paper, extend the model by Liaw et al. (1994) by integrating a number of different motor pattern generators, different types of afferent feedback, as well as the corresponding control structure within an adaptive framework we call Schema-Based Learning. We develop a model of the different MPGs involved in prey-catching as a vehicle to investigate the following questions: What are the characteristic features of the activity of a single muscle? How can these features be controlled by the premotor circuit? What are the strategies employed to generate and synchronize motor synergies? What is the role of afferent feedback in shaping the activity of a MPG? How can several MPGs share the same underlying circuitry and yet give rise to different motor patterns under different input conditions? In the companion paper we also extend the model by incorporating learning components that give rise to more flexible, adaptable and robust behaviors. To show these aspects we incorporate studies on experiments on lesions and the learning processes that allow the animal to recover its proper functioning.


Subject(s)
Adaptation, Biological/physiology , Anura/anatomy & histology , Learning/physiology , Perception/physiology , Predatory Behavior/physiology , Action Potentials/physiology , Afferent Pathways/cytology , Afferent Pathways/physiology , Animals , Anura/physiology , Behavior, Animal , Denervation/methods , Feedback/physiology , Hypoglossal Nerve/physiology , Hypoglossal Nerve Injuries , Models, Neurological , Motor Activity , Neural Networks, Computer , Neurons/physiology , Physical Stimulation/methods , Psychomotor Performance/physiology
6.
Exp Neurol ; 190(1): 133-44, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15473987

ABSTRACT

Excess ingestion of pyridoxine (vitamin B6) causes a severe sensory neuropathy in humans. The mechanism of action has not been fully elucidated, and studies of pyridoxine neuropathy in experimental animals have yielded disparate results. Pyridoxine intoxication appears to produce a neuropathy characterized by necrosis of dorsal root ganglion (DRG) sensory neurons and degeneration of peripheral and central sensory projections, with large diameter neurons being particularly affected. The major determinants affecting the severity of the pyridoxine neuropathy appear to be duration and dose of pyridoxine administration, differential neuronal vulnerability, and species susceptibility. The present study used design-based stereological techniques in conjunction with electrophysiological measures to quantify the morphological and physiological changes that occur in the DRG and the distal myelinated axons of the sciatic nerve following pyridoxine intoxication. This combined stereological and electrophysiological method demonstrates a general approach that could be used for assessing the correlation between pathophysiological and functional parameters in animal models of toxic neuropathy.


Subject(s)
Neurodegenerative Diseases/chemically induced , Neurodegenerative Diseases/pathology , Pyridoxine/toxicity , Sensation Disorders/chemically induced , Sensation Disorders/pathology , Animals , Cell Count/statistics & numerical data , Cell Size/drug effects , Disease Models, Animal , Disease Progression , Electrophysiology , Ganglia, Spinal/pathology , H-Reflex/drug effects , Male , Motor Neurons/drug effects , Motor Neurons/pathology , Nerve Fibers, Myelinated/drug effects , Nerve Fibers, Myelinated/pathology , Neural Conduction/drug effects , Neurodegenerative Diseases/physiopathology , Psychomotor Performance/drug effects , Rats , Rats, Sprague-Dawley , Sciatic Nerve/drug effects , Sciatic Nerve/pathology , Sensation Disorders/physiopathology
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