Skeletal Muscle Contraction Using Functional Electrical Stimulation Reduces Effects of Unloading on Bone Resorption Independently from the Central Nervous System: Studies in a Rat Model of Complete Spinal Cord Transection

2011 ◽  
pp. P1-219-P1-219
Author(s):  
Weiping Qin ◽  
Lauren Collier ◽  
Yuanzhen Peng ◽  
Yong Wu ◽  
Li Sun ◽  
...  
1946 ◽  
Vol 23 (2) ◽  
pp. 162-176 ◽  
Author(s):  
H. W. LISSMANN

Some of the more striking effects of de-afferentation in the spinal dogfish are diagrammatically represented in Fig. 13. 1. The persistent locomotory rhythm of a spinal dogfish depends upon afferent excitation. If all afferent excitation is cut off by severance of all dorsal roots, the rhythm is abolished (Fig. 13, 1). 2. The rhythm clearly emerges when about half the number of all the dorsal roots is transected, irrespective whether the anterior or the posterior half of the animal be de-afferentated (Fig. 13, 2 and 3), or whether complete unilateral de-afferentation is executed (Fig. 13, 4). 3. Extensively de-afferentated preparations may exhibit swimming movements after exteroceptive stimulation. These swimming movements do not persist. 4. Preparations de-afferentated except for the tail exhibit after exteroceptive stimulation a static reflex posture. 5. The de-afferentated musculature takes part in both tonic and rhythmic responses as long as it is connected through the spinal cord with normally innervated musculature. 6. In response to electrical stimulation applied to the cord of a spinal dogfish two distinct types of rhythmic response have been evoked. 7. No rhythmic responses have bee obtained through electrical stimulation of the spinal cord in completely de-afferentated preparations. 8. No evidence has been found in support of the view that the swimming rhythm emanates through a spontaneous, automatic activity from the central nervous system.


2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Katherine N. Gibson-Corley ◽  
Oliver Flouty ◽  
Hiroyuki Oya ◽  
George T. Gillies ◽  
Matthew A. Howard

Spinal cord stimulation has been utilized for decades in the treatment of numerous conditions such as failed back surgery and phantom limb syndromes, arachnoiditis, cancer pain, and others. The placement of the stimulating electrode array was originally subdural but, to minimize surgical complexity and reduce the risk of certain postsurgical complications, it became exclusively epidural eventually. Here we review the relevant clinical and experimental pathologic findings, including spinal cord compression, infection, hematoma formation, cerebrospinal fluid leakage, chronic fibrosis, and stimulation-induced neurotoxicity, associated with the early approaches to subdural electrical stimulation of the central nervous system, and the spinal cord in particular. These findings may help optimize the safety and efficacy of a new approach to subdural spinal cord stimulation now under development.


Author(s):  
Rahman Davoodi ◽  
Gerald E. Loeb

Movement disabilities due to spinal cord injury (SCI) are usually incomplete, leaving the patients with partially functioning movement system. As a result, functional electrical stimulation (FES) systems for restoration of movement to the paralyzed limbs must operate in parallel with the residual voluntary movements of the patient. In the resulting man-machine system, the central nervous system (CNS) controls the residual voluntary movements while the FES system controls the paralyzed muscles of the same limbs. Clearly, these two control systems must work in synchrony to benefit the patient. In this chapter we will discuss different methods for cooperative control of man-machine FES systems and use a clinical FES system to demonstrate the successful application of these strategies.


2018 ◽  
Vol 23 (1) ◽  
pp. 10-13
Author(s):  
James B. Talmage ◽  
Jay Blaisdell

Abstract Injuries that affect the central nervous system (CNS) can be catastrophic because they involve the brain or spinal cord, and determining the underlying clinical cause of impairment is essential in using the AMA Guides to the Evaluation of Permanent Impairment (AMA Guides), in part because the AMA Guides addresses neurological impairment in several chapters. Unlike the musculoskeletal chapters, Chapter 13, The Central and Peripheral Nervous System, does not use grades, grade modifiers, and a net adjustment formula; rather the chapter uses an approach that is similar to that in prior editions of the AMA Guides. The following steps can be used to perform a CNS rating: 1) evaluate all four major categories of cerebral impairment, and choose the one that is most severe; 2) rate the single most severe cerebral impairment of the four major categories; 3) rate all other impairments that are due to neurogenic problems; and 4) combine the rating of the single most severe category of cerebral impairment with the ratings of all other impairments. Because some neurological dysfunctions are rated elsewhere in the AMA Guides, Sixth Edition, the evaluator may consult Table 13-1 to verify the appropriate chapter to use.


1963 ◽  
Vol 44 (3) ◽  
pp. 475-480 ◽  
Author(s):  
R. Grinberg

ABSTRACT Radiologically thyroidectomized female Swiss mice were injected intraperitoneally with 131I-labeled thyroxine (T4*), and were studied at time intervals of 30 minutes and 4, 28, 48 and 72 hours after injection, 10 mice for each time interval. The organs of the central nervous system and the pituitary glands were chromatographed, and likewise serum from the same animal. The chromatographic studies revealed a compound with the same mobility as 131I-labeled triiodothyronine in the organs of the CNS and in the pituitary gland, but this compound was not present in the serum. In most of the chromatographic studies, the peaks for I, T4 and T3 coincided with those for the standards. In several instances, however, such an exact coincidence was lacking. A tentative explanation for the presence of T3* in the pituitary gland following the injection of T4* is a deiodinating system in the pituitary gland or else the capacity of the pituitary gland to concentrate T3* formed in other organs. The presence of T3* is apparently a characteristic of most of the CNS (brain, midbrain, medulla and spinal cord); but in the case of the optic nerve, the compound is not present under the conditions of this study.


1985 ◽  
Vol 55 ◽  
Author(s):  
F. Terry Hambrecht

ABSTRACTNeural prostheses which are commercially available include cochlear implants for treating certain forms of deafness and urinary bladder evacuation prostheses for individuals with spinal cord disorders. In the future we can anticipate improvements in bioelectrodes and biomaterials which should permit more sophisticated devices such as visual prostheses for the blind and auditory prostheses for the deaf based on microstimulation of the central nervous system.


1908 ◽  
Vol 54 (226) ◽  
pp. 560-561
Author(s):  
David Orr ◽  
R. G. Rows

At a quarterly meeting of this Association held last year at Nottingham, we showed the results of our experiments with toxins upon the spinal cord and brain of rabbits. Our main conclusion was, that the central nervous system could be infected by toxins passing up along the lymph channels of the perineural sheath. The method we employed in our experiments consisted in placing a celloidin capsule filled with a broth culture of an organism under the sciatic nerve or under the skin of the cheek; and we invariably found a resulting degeneration in the spinal cord or brain, according to the situation of the capsule. These lesions we found to be identical in morphological type and anatomical distribution with those found in the cord of early tabes dorsalis and in the brain and cord of general paralysis of the insane. The conclusion suggested by our work was that these two diseases, if toxic, were most probably infections of lymphogenous origin.


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