Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
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
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
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by De Riu, P. L.
Right arrow Articles by Madeddu, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by De Riu, P. L.
Right arrow Articles by Madeddu, G.

Stroke, Vol 20, 253-258, Copyright © 1989 by American Heart Association


ARTICLES

Beta-endorphin in experimental canine spinal ischemia

PL De Riu, V Petruzzi, G Palmieri, C Gentili, F Melis, MA Caria, GB Azzena, AR Casu, G Marras and G Madeddu
Department of Neurological Rehabilitation, University of Turin, Italy.

Plasma and cerebrospinal fluid beta-endorphin concentrations were radioimmunologically assayed in dogs subjected to spinal cord ischemia induced by infrarenal aortic ligature and in control sham-operated dogs. Plasma beta-endorphin levels rose significantly following surgery in control dogs but were unaffected by spinal ischemia. On the other hand, a significant increase in cerebrospinal fluid beta-endorphin concentration occurred after spinal ischemia, while surgical stress had no significant effect. Thus, the origins of plasma and cerebrospinal fluid beta-endorphin may be different, with the former secreted from the hypophysis and the latter from nervous tissue. Observed changes in cerebrospinal fluid beta-endorphin concentration could be related to the ischemic lesion of nervous tissue while the changes in plasma levels may reflect general stressing factors such as the surgery in our experiments.


This article has been cited by other articles:


Home page
Asian Cardiovasc. Thorac. Ann.Home page
Y. Fujisawa, K. Morishita, J. Fukada, N. Kawaharada, Y. Hachiro, and T. Abe
Treatment Methods for Spinal Cord Injury Caused by Acute Type B Aortic Dissection
Asian Cardiovasc Thorac Ann, December 1, 2006; 14(6): e106 - e107.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
M. Kakinohana, S. Nakamura, T. Fuchigami, K. J. Davison, M. Marsala, and K. Sugahara
Mu and delta, but not kappa, opioid agonists induce spastic paraparesis after a short period of spinal cord ischaemia in rats
Br. J. Anaesth., January 1, 2006; 96(1): 88 - 94.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
M. Kakinohana, T. Fuchigami, S. Nakamura, T. Sasara, T. Kawabata, and K. Sugahara
Intrathecal Administration of Morphine, but Not Small Dose, Induced Spastic Paraparesis After a Noninjurious Interval of Aortic Occlusion in Rats
Anesth. Analg., March 1, 2003; 96(3): 769 - 775.
[Abstract] [Full Text] [PDF]