Cell body reorganization in the spinal cord after elective surgery to treat palmar sweating

The amount of compensatory sweating depends on the patient, the damage that the white rami communicans incurs, and the amount of cell body reorganization in the spinal cord after surgery.

Other potential complications include inadequate resection of the ganglia, gustatory sweating, pneumothorax, cardiac dysfunction, post-operative pain, and finally Horner’s syndrome secondary to resection of the stellate ganglion.
www.ubcmj.com/pdf/ubcmj_2_1_2010_24-29.pdf

After severing the cervical sympathetic trunk, the cells of the cervical sympathetic ganglion undergo transneuronic degeneration
After severing the sympathetic trunk, the cells of its origin undergo complete disintegration within a year.

http://onlinelibrary.wiley.com/doi/10.1111/j.1439-0442.1967.tb00255.x/abstract

Spinal cord infarction occurring during thoraco-lumbar sympathectomy
J Neurol Neurosurg Psychiatry 1963;26:418-421 doi:10.1136/jnnp.26.5.418

Saturday, July 28, 2012

When sympathectomized rats were injected with the same carcinogen, 24 out of 38 developed tumors

"Lesions od the sympathetic nervous system have been shown to increase the incidence, induction, and take and growth, of tumors. In neurally intact rats which were infected with a known carcinogen, only 1 out of 30 developed a tumor. When sympathectomized (intentional sympathetic nerve interference) rats were injected with the same carcinogen, 24 out of 38 developed tumors. These results confirm that sympathetic block enhances tumor implantation."
"Clearly the autonomic nervous system in exquisitely sensitive to information from all parts of the nervous system and may affect many aspects of the immune response."
"Since immune response is initiated by the nervous system, this appears to be a likely place to look for the cause of disease."
Edward E. Cremata, Neural control of immunity, January/February, 1982 The Digest of Chiropractic Economics
1. Couhard, R. and P. Hein, Cancers de types divers provoqucs par lesion du sympathique, CR. Acad. Sci,  2434-2437, 1957.
2. Couhard, R. and F. Heitz, Production de tumeurs malìgncs consecutivas a des lesions des fibres sympaxhiqucs du neri sciatique chez le cobaye. CR. Amd. Scl", 244: 4-09-411, 1957. 
3. Nayar, KK., Arthur, E. and Ballís,  M4, Th: transmission of tumours induced in cockroaches by nerve severance, Experienria, 27: 183, 1971. 
4. Champy, C.. Lesions neum-sympathìques precedam la canccrixation dans Patlaque de Porganìsmc par les substances cancerîgenes, C.R. Acad. Sci, 248: 3665-1666; 1959. 
 www.usapr.org/paperpdfs/75.pdf

we observed significant increase in net survival rate in non sympathectomised rates in comparison to sympathectomised
Chemical sympathectomy was performed by double intraperitoneal administration of 6-hydroxydopamine (6OHDA) 100mg/1 kg. 6OHDA is a neurotoxin used for selective ablation of dopaminergic and noradrenergic neurons. YA cells AH-130 which typically grow as free cells in ascites were injected intraperitoneally in amount of 20 - 25 mil/2 ml.
               
                Four groups of Wistar rats (AnLab, Prague) weighing 150 - 175g were used in the experiment. An absolute control group (8 rats), and a control sympathectomised group (8 rats), a group injected with YA cells (16 rats) and the last group was sympathectomised and injected with YA cells (16 rats).
               
                After a week of acclimatization of rats to conditions of animal room, sympathectomy was performed. One week later, YA cells were applied. The incidence and growth of ascites, and mortality were monitored.

Results
                Graph 1 shows the survival rate in both sympathectomised and non sympathectomised rats after the administration of YA cells. The graph shows an overall shorter survival rate of sympathectomised rats. In both groups there is a steep decrease in survival after 15 days, causing the median survival rate (18 days) of both groups to overlap. On the other hand the net survival rate is increased in non sympathectomised rates by 6 days
References:
1.        Ewa Chelmicka – Szorc, Barry G. W. Arnason. Effect of 6-Hydroxydopamine on Tumor Growth. CANCER RESEARCH 1976, 36, 2382-2384.
2.        Boris Mravec, Neurobiológia chorôb periférnych tkanív, Bratislava, SAP 2008, 220 s.,  ISBN 978-80-8095-030-9
3.        Raju B, Haug SR, Ibrahim SO, Heyeraas KJ. Sympathectomy decreases size and invasiveness of tongue cancer in rats. Neuroscience. 2007;149(3):715-25.
4.        Mravec B ,Gidron Y,Hulin I. Neurobiology of cancer: Interactions between nervous, endocrine
and immune systems as a base for monitoring and modulating the tumorigenesis by the brain. Seminars in Cancer Biology 18 (2008) 150–163.
5.        Paul G. Green,Wilfrid Janig, Jon D. Levinel. Negative Feedback Neuroendocrine Control of Inflammatory Response in the Rat is Dependent on the Sympathetic Postganglionic Neuron. The Journal of Neuroscience, 1997, 17(8):3234 –3238
6.      Aparna A. Bhanushali , R. Raghunathan , Rajiv D. Kalraiya , Narendra G. Mehta. Cancer-related anemia in a rat model: α2-macroglobulin from Yoshida sarcoma shortens erythrocyte survival. European Journal of Haematology 2002. 68(1),42 - 48


The effect of sympathectomy on the growth of intraperitoneally administered Yoshida ascitic cells in rats
El-Hassoun Olia, Coauthors: Zuzana Valašková, Ivan Hulín
Supervisor: Boris Mravec
Institute of Pathophysiology, LF UK Bratislava
http://svoc.fmed.uniba.sk/abstrakty/48/36.html