Physiology of Spinal Cord, Nerve Root and Peripheral Nerve Compression

1956 ◽  
Vol 185 (1) ◽  
pp. 217-229 ◽  
Author(s):  
Samuel Gelfan ◽  
I. M. Tarlov

The reversible conduction block produced by maintained mechanical pressure around small segments of spinal cord, nerve root or peripheral nerve (dog) is due to mechanical deformation of the neuronal tissue and not to lack of O2. The compressed segment, although ischemic, is not anoxic; O2 from adjacent nonischemic tissue reaches it, presumably by diffusion. The entire pattern of modification of neuronal responses by compression and the postdecompression recovery pattern are distinctly different from the patterns observed during anoxia and recovery from the latter, indicating the difference in mechanisms by which mechanical deformation and O2 lack block conduction. The largest fibers in dorsal columns, roots and peripheral nerves are most susceptible to pressure and the smallest ones are relatively most resistant. Secondary neurons are less vulnerable than the primary afferent ones to light and moderate, but suprasystolic, circumferential spinal cord pressure. All components of the composite spinal cord potential are blocked at about the same time by larger compressive forces. Anoxia, on the other hand, always inactivates secondary neurons before dorsal column fibers and blocks smaller A fibers in peripheral nerves before the larger ones. The latency for complete blocking in each neuronal structure is specific and irreducible in the case of anoxia, whereas in compression it varies over a wide range, depending upon the magnitude of the compressive force.

Author(s):  
Alexander Scarborough ◽  
Robert J MacFarlane ◽  
Michail Klontzas ◽  
Rui Zhou ◽  
Mohammad Waseem

The upper limb consists of four major parts: a girdle formed by the clavicle and scapula, the arm, the forearm and the hand. Peripheral nerve lesions of the upper limb are divided into lesions of the brachial plexus or the nerves arising from it. Lesions of the nerves arising from the brachial plexus are further divided into upper (proximal) or lower (distal) lesions based on their location. Peripheral nerves in the forearm can be compressed in various locations and by a wide range of pathologies. A thorough understanding of the anatomy and clinical presentations of these compression neuropathies can lead to prompt diagnosis and management, preventing possible permanent damage. This article discusses the aetiology, anatomy, clinical presentation and surgical management of compressive neuropathies of the upper limb.


1984 ◽  
Vol 21 (4) ◽  
pp. 384-393 ◽  
Author(s):  
J. Beech

Data were collected from 37 horses with a neurologic disability and compared to a group of 34 normal horses. Affected horses had neuroaxonal dystrophy, gliosis, vacuoles, and sometimes pigment localized to the accessory cuneate nuclei with minimal or no changes in the spinal cord and no changes in the proximal peripheral nerves. The focal nature of the change and usual absence of significant light microscopic spinal cord or peripheral nerve changes are different than previously described equine neuropathologic conditions.


1980 ◽  
Vol 58 (2) ◽  
pp. 227-229 ◽  
Author(s):  
I. Bishai ◽  
F. Coceani

Catabolism of prostaglandin (PG) E2 was studied in homogenates of spinal cord and spinal nerve roots of the cat. Spinal roots enzymatically converted PGE2 to a product (metabolite I) with the chromatographic mobility of 15-keto-PGE2. Little metabolic degradation occurred in the spinal cord; however, incubation of PGE2 with combined spinal cord and nerve root tissue yielded a second metabolite (metabolite II) in addition to metabolite I. Metabolite II was identified as 15-keto-13,14-dihydro-PGE2. These results prove that spinal nerve roots, unlike the spinal cord, contain 15-hydroxyprostaglandin dehydrogenase (15-PGDH) which is the major and rate-limiting enzyme in the inactivation of prostaglandins. The location and functional significance of 15-PGDH in peripheral nerves remain to be elucidated.


Neurosurgery ◽  
1982 ◽  
Vol 11 (4) ◽  
pp. 482-485 ◽  
Author(s):  
H. Lueders ◽  
J. Hahn ◽  
A. Gurd ◽  
A. Gurd ◽  
S. Tsuji ◽  
...  

Abstract Spinal cord and subcortical brain stem evoked potentials had an amplitude at least 2 times higher when the cauda equina rather than bilateral peripheral nerves was stimulated. Cauda equina stimulation is indicated when potentials to peripheral nerve stimulation are absent or are too low in amplitude to permit reliable surgical monitoring. The technique is essentially without risks, but should be performed with a small lumbar puncture needle (21 to 22 gauge), and is contraindicated in patients with general infections, increased cerebrospinal fluid pressure, or a hemorrhagic tendency (thrombocytopenia or anticoagulant therapy).


Spine ◽  
1988 ◽  
Vol 13 (11) ◽  
pp. 1278-1283 ◽  
Author(s):  
KEISUKE TAKAHASHI ◽  
SUSUMU NOMURA ◽  
KATSURO TOMITA ◽  
TADAMI MATSUMOTO

1978 ◽  
Vol 49 (4) ◽  
pp. 551-557 ◽  
Author(s):  
Joseph F. Cusick ◽  
Joel Myklebust ◽  
Sanford J. Larson ◽  
Anthony Sances

✓ Summated responses evoked by peripheral nerve stimulation were recorded from electrodes located in the epidural and subdural spaces anterior and posterior to the monkey spinal cord. Segmental microsurgical resection of the dorsal columns both at the thoracic and cervical levels resulted in total obliteration of the response recorded rostral to these lesions. Isolated segmental dorsal column preservation did not significantly alter response latency or wave form recorded at the rostral electrodes. Bilateral cervical dorsolateral column resection also resulted in no discernible alterations of these responses. These data indicate that spinal evoked potentials recorded from levels rostral to their root entry zones arise almost exclusively from the dorsal columns.


1953 ◽  
Vol 36 (5) ◽  
pp. 643-657 ◽  
Author(s):  
Donald O. Rudin ◽  
George Eisenman

A method is evolved whereby the after-potential sequence intrinsic to longitudinal dorsal column myelinated fibers may be studied in isolation from those events occurring in intact spinal cord subjected to an afferent volley. The recovery sequence intrinsic to dorsal column fibers, after refractoriness is over, is characterized by supernormality approximately four to five times greater than that seen in peripheral nerve. This supemormality averages 15.7 ± 4 per cent (current calibration) at peak and decays exponentially with a half-time of 7.5 msecs. It is not followed by subnormality unless conditioning is repeated more than three times at frequencies greater than 100/sec. Characterization of the recovery curve of dorsal column fibers permits by exclusion, the allocation of the origin of DRV to structures more centrally located. DCV (the dorsal column counterpart of DRV) is seen to exist equally developed in active and passive dorsal column fibers.


2020 ◽  
Vol 4 (4) ◽  
Author(s):  
Mary P Galea ◽  
◽  
Natasha van Zyl ◽  
Aurora Messina ◽  

Spinal cord injury (SCI) leads to an immediate loss of sensory and motor function below the level of injury mostly affecting people in the prime of life. In addition to the primary injury there is accumulating neurophysiological and histological evidence of dysfunction in the peripheral nerves, not related to direct damage from the primary injury, which exacerbates muscle wasting, and contributes to further functional loss and poor recovery. Among the potential contributing factors are systemic inflammation, and motor neuron and myelin abnormalities that result from a lack of neural traffic. The reversibility of these factors, and prevention strategies and possible therapies that may be of benefit to the peripheral nerves in spinal cord injury require further investigation. Preventing or reversing peripheral nerve dysfunction after SCI is essential to maintain this critical component of the nervous system in readiness for the application of other emerging interventions focused on spinal cord repair.


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