scholarly journals AFTER-POTENTIAL OF SPINAL AXONS IN VIVO

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.

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):  
Marco Morsch ◽  
Rowan Radford ◽  
Albert Lee ◽  
Emily K. Don ◽  
Andrew P. Badrock ◽  
...  

Neuroscience ◽  
2016 ◽  
Vol 316 ◽  
pp. 13-25 ◽  
Author(s):  
K.E. Farrell ◽  
M.M. Rank ◽  
S. Keely ◽  
A.M. Brichta ◽  
B.A. Graham ◽  
...  

Author(s):  
Xiaoming Chen ◽  
Garrett W. Astary ◽  
Thomas H. Mareci ◽  
Malisa Sarntinoranont

Biotransport in nervous tissues is complicated by the existence of neural fibers. These axonal fibers result in inhomogeneous and anisotropic extracellular transport, which complicates the prediction of local drug delivery such as convection-enhanced delivery [1]. Previous studies by our group [4] have shown that by using diffusion tensor imaging (DTI) [2, 3], anisotropic transport in rat spinal cord can be modeled using computational models, and consequently extracellular flows which influence drug transport can be well predicted. In previous studies, DTI-based models used data from an excised and fixed rat spinal cord. In the current study, we extend our DTI study to in vivo measures, and report the in vivo characterization of transport anisotropy in rat spinal cord. The MR imaging method is presented and the DTI data is discussed.


NeuroImage ◽  
2003 ◽  
Vol 18 (4) ◽  
pp. 1010
Author(s):  
Shinichi Sasaki ◽  
Itaru Yazawa ◽  
Naohisa Miyakawa ◽  
Hiraku Mochida ◽  
Kenichi Shinomiya ◽  
...  

NeuroImage ◽  
2002 ◽  
Vol 17 (3) ◽  
pp. 1240-1255 ◽  
Author(s):  
Shinichi Sasaki ◽  
Itaru Yazawa ◽  
Naohisa Miyakawa ◽  
Hiraku Mochida ◽  
Kenichi Shinomiya ◽  
...  

2018 ◽  
Vol 31 (4) ◽  
pp. e3894 ◽  
Author(s):  
Samantha By ◽  
Junzhong Xu ◽  
Bailey A. Box ◽  
Francesca R. Bagnato ◽  
Seth A. Smith

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Rachael L. Bosma ◽  
Patrick W. Stroman

The aim of this study was to characterizein vivomeasurements of diffusion along the length of the entire healthy spinal cord and to compare DTI indices, including fractional anisotropy (FA) and mean diffusivity (MD), between cord regions. The objective is to determine whether or not there are significant differences in DTI indices along the cord that must be considered for future applications of characterizing the effects of injury or disease. A cardiac gated, single-shot EPI sequence was used to acquire diffusion-weighted images of the cervical, thoracic, and lumbar regions of the spinal cord in nine neurologically intact subjects (19 to 22 years). For each cord section, FA versus MD values were plotted, and a k-means clustering method was applied to partition the data according to tissue properties. FA and MD values from both white matter (averageFA=0.69, averageMD=0.93×10−3 mm2/s) and grey matter (averageFA=0.44, averageMD=1.8×10−3 mm2/s) were relatively consistent along the length of the cord.


2014 ◽  
Vol 32 (3) ◽  
pp. 250-258 ◽  
Author(s):  
Piotr Kozlowski ◽  
Paulina Rosicka ◽  
Jie Liu ◽  
Andrew C. Yung ◽  
Wolfram Tetzlaff

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