JN Watch the video to see how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 68: 1951-1966, 1992;
0022-3077/92 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Palecek, J.
Right arrow Articles by Willis, W. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Palecek, J.
Right arrow Articles by Willis, W. D.

Journal of Neurophysiology, Vol 68, Issue 6 1951-1966, Copyright © 1992 by APS


ARTICLES

Responses of spinothalamic tract neurons to mechanical and thermal stimuli in an experimental model of peripheral neuropathy in primates

J. Palecek, P. M. Dougherty, S. H. Kim, V. Paleckova, H. Lekan, J. M. Chung, S. M. Carlton and W. D. Willis
Department of Anatomy and Neurosciences, University of Texas Medical Branch, Galveston 77555-0843.

1. An experimental peripheral neuropathy (EPN) was induced in three monkeys (Macaca fascicularis) by ligation of spinal nerve L7. Behavioral responses to innocuous mechanical stimuli were tested before and after the surgery. Two weeks after the nerve ligation, the activity of spinothalamic tract (STT) neurons was recorded on both sides of the spinal cord with the animal under general anesthesia. Responses of the STT neurons to the following stimuli applied to the skin were recorded: graded mechanical stimuli (brush, press, pinch and squeeze), von Frey filaments of different bending forces (0.077-19.05 g), 5-s heat stimuli ranging from 39 to 53 degrees C, and 15 s cold stimuli (32-8 degrees C). 2. Innocuous mechanical stimulation of the foot did not evoke hindlimb withdrawal in the animals before surgery. Within 24-48 h after nerve ligation, the animals showed hindlimb withdrawal to the same innocuous stimuli. This behavior was more pronounced on the side of the ligation than on the sham-operated side and more frequent during the second week after the surgery. 3. Responses of 51 STT neurons recorded on the side of the ligation (EPN all group) were compared with responses of 33 STT cells recorded on the sham-operated side (control group) and with records from STT neurons in unoperated animals obtained earlier (reference group). Neurons from the EPN all group were divided into two sets according to their rostrocaudal location (EPN R, rostral to L6/7 border, n = 40; EPN C, caudal to L6/7 border, n = 11). 4. Neurons from the EPN all and EPN R groups had significantly higher background frequencies than those from the control and reference groups. Innocuous brush stimuli evoked mean discharge frequencies of approximately 35 Hz in EPN R neurons and only approximately 15 Hz in both control and reference groups. Increased responsiveness of EPN R neurons to innocuous stimuli was also demonstrated by lower thresholds and higher discharge frequencies to von Frey filament stimulation and by discriminative analysis of the responses evoked by graded mechanical stimuli. 5. The responses of the EPN R neurons to heat stimulation of the skin showed decreased thresholds and increased responses to suprathreshold stimuli, resulting in a significant leftward shift of the stimulus-response curve compared with both reference and control groups. The neurons from the control group showed responses comparable to reference group values. 6. Neurons from the reference group tested with the cooling stimuli showed no evoked response above background.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
K. Saito, S. Hitomi, I. Suzuki, Y. Masuda, J. Kitagawa, Y. Tsuboi, M. Kondo, B. J. Sessle, and K. Iwata
Modulation of Trigeminal Spinal Subnucleus Caudalis Neuronal Activity Following Regeneration of Transected Inferior Alveolar Nerve in Rats
J Neurophysiol, May 1, 2008; 99(5): 2251 - 2263.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. D. Carlson, J. J. Maire, M. E. Martenson, and M. M. Heinricher
Sensitization of Pain-Modulating Neurons in the Rostral Ventromedial Medulla after Peripheral Nerve Injury
J. Neurosci., November 28, 2007; 27(48): 13222 - 13231.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. Liu and J. M. Walker
Effects of a Cannabinoid Agonist on Spinal Nociceptive Neurons in a Rodent Model of Neuropathic Pain
J Neurophysiol, December 1, 2006; 96(6): 2984 - 2994.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. Andrew and A. D. Craig
Responses of Spinothalamic Lamina I Neurons to Maintained Noxious Mechanical Stimulation in the Cat
J Neurophysiol, April 1, 2002; 87(4): 1889 - 1901.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
K. Iwata, T. Imai, Y. Tsuboi, A. Tashiro, A. Ogawa, T. Morimoto, Y. Masuda, Y. Tachibana, and J. Hu
Alteration of Medullary Dorsal Horn Neuronal Activity Following Inferior Alveolar Nerve Transection in Rats
J Neurophysiol, December 1, 2001; 86(6): 2868 - 2877.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
R. Baron, Y. Baron, E. Disbrow, and T. P. L. Roberts
Brain processing of capsaicin-induced secondary hyperalgesia: A functional MRI study
Neurology, August 1, 1999; 53(3): 548 - 548.
[Abstract] [Full Text]


Home page
J. Appl. Physiol.Home page
G. Zacharová, H. Knotkova-Urbancova, and P. Hnik
Nociceptive atrophy of the rat soleus muscle induced by bone fracture: a morphometric study
J Appl Physiol, February 1, 1997; 82(2): 552 - 557.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online