Disorders of the peripheral nervous systems, including trauma and peripheral neuropathies, create a disconnection between the central nervous system and its peripheral targets (i.e.-sensory receptors and muscle). Recovery from these disorders requires both regeneration of the peripheral nerve and reinnervation of targets. In patients with peripheral nerve disorders, this recovery is rarely complete, resulting in residual weakness, sensory dysfunction, and balance problems. The long term objectives of this program are to 1) advance our understanding of the constraints to full sensory and motor recovery after peripheral nervous system injury and disease, and 2) to develop strategies for enhancing recovery in peripheral nervous system disorders though scientifically- based interventions in biological processes. To achieve these goals we have formed a team of scientists and clinician-scientists to focus experimental attention on specific cellular and systems-level mechanisms that determine the responses to, and recovery from the effects of peripheral nerve injury and disease in experimental animals. There are 5 projects within this Program. The proposal begins where the biological problem begins, with the cellular mechanisms that underlie axonal degeneration. Two projects focus on the interactions between motor neurons and muscle, and two projects address the mechanisms and behavioral consequences of the poor recovery of sensory feedback in reinnervated muscles. Project 1 examines axonal degeneration in two models of nerve injury. Project 1 examines axonal degeneration in two models of nerve injury, axotomy and exposure to neurotoxins. This project will focus on the roles of calcium and proteases in these models. Project 2 tests the dependency of sensory afferent functions, including sensory transduction and central synaptic transmission, on reconnection with sensory receptor organs in muscle. This will be done by directly examining the physiology and morphology of individual regenerated sensory afferents. Project 3 asks whether altering the conditions or reinnervation of muscle fiber changes the properties of the reinnervating motoneurons. Project 4 examines the role of muscle activity in regulating synaptic transmission. Denervation-induced changes in muscle gene expression will be manipulate to test the effects on recovery. In Project 5, the manner in which abnormalities of proprioceptive pathways result in loss of coordination will be studied during locomotion and targeted reaching.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS040405-04
Application #
6644852
Study Section
Special Emphasis Panel (ZNS1-SRB-W (01))
Program Officer
Kleitman, Naomi
Project Start
2000-07-01
Project End
2005-06-30
Budget Start
2003-07-01
Budget End
2004-06-30
Support Year
4
Fiscal Year
2003
Total Cost
$1,345,293
Indirect Cost
Name
Emory University
Department
Physiology
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Livingston, Beven P; Nichols, T Richard (2014) Effects of reinnervation of the triceps brachii on joint kinematics and electromyographic patterns of the feline forelimb during level and upslope walking. Cells Tissues Organs 199:405-22
Livingston, Beven P; Nichols, T Richard (2014) Effects of reinnervation of the biarticular shoulder-elbow muscles on joint kinematics and electromyographic patterns of the feline forelimb during downslope walking. Cells Tissues Organs 199:423-40
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Haftel, Valerie K; Bichler, Edyta K; Nichols, T Richard et al. (2004) Movement reduces the dynamic response of muscle spindle afferents and motoneuron synaptic potentials in rat. J Neurophysiol 91:2164-71
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Wang, Xueyong; Engisch, Kathrin L; Li, Yingjie et al. (2004) Decreased synaptic activity shifts the calcium dependence of release at the mammalian neuromuscular junction in vivo. J Neurosci 24:10687-92

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