What’s in the News

The above paragraph comes directly from our friends at Pets over Paralysis. Pictures of many of their clients are included in this story.

For many years Pets over Paralysis has supported the work of the Center for Paralysis Research. We greatly value partners like this. Naturally Injured Paraplegic dogs have been test vehicles for dog and human treatments for over 20 years at the CPR, thus helping both dogs and their owners and the advancement of human and veterinary medicine. Dr. Borgens, the Director of the CPR and Mari Hulman George Professor of Neurology, holds professional appointments in both the School of Veterinary Medicine and the Weldon School of Biomedical Engineering. The combined use of both of these areas of scholarship has been instrumental in developing three therapies for Spinal Cord injury. Pets Over Paralysis, which is organized by Veterinarian Dr. Deirdre Henson and the Paumanok Veterinary Hospital, is an example of veterinary medical specialism understanding this relationship and supporting it.

In a very recent article in the prestigious British medical journal “Lancet”, the use of Fampridine (time release 4 – aminopyridine or 4 AP) was heralded as a breakthrough producing a “new era” in the treatment of MS ( citation ) This is because in addition to slowing the progression of the disease, Fampridine also recovers some important functions for afflicted patients such as better walking. The history of this new therapy began with former CPR faculty member Andrew Blight who knew the potassium channel blocker 4 AP could induce some behavioral changes in rats with spinal cord injuries. Dr. B and veterinary surgeon James Toombs understood the fundamental importance of this view and the three colleagues organized a direct test of 4 AP on paraplegic dogs brought to the clinic by their owners. The very first dog treated by injection of 4 AP reversed some behavioral loss within 15 minutes of the injection  – and then lost these gains within 2 hours as the effect of the drug wore off.

At that time, Dr. B served on the Executive Council of the American Spinal Cord Society and arranged with the help of President Charles Carson, the first human trials in Canada with another council member, Robert Hansebout, then Chairman of Neurosurgery at McMaster University Medical School, Hamilton, Ontario.  Dr Blight simultaneously arranged human testing with Dr. Keith Hayes at Western Ontario University Medical School in London, Ontario.  The rest is history. Dr. B predicted publically that this new approach towards therapy would lead to “taking a pill for paraplegia” – sometimes ridiculed by the so called “experts”. He turned out to be spot–on in the end. 

The US and world-wide Patent for 4 AP’s use in CNS injury and Disease is owned by Purdue University which licensed it out to companies for commercialization. The inventor’s were Blight and company at the Center for Paralysis Research. More discussion of this can be found throughout this Website.
We consider Fampridine the first “penicillin” which has great promise – but also great drawbacks. The chemical derivatives of 4 AP have been developed by CPR scientist Steven Byrn, Dan Smith, Riyi Shi, and Dr. B. All are the “inventors” of a new generation of drugs that will have less side effects and more extended use in patients than the parent compound. Purdue University licensed the US Patent on the derivatives to Neurometrix Corporation in Waltham Massachutes for Commercialization. As a group we are very proud of these achievements.


Over the years, there have been some reports of the deaths of patients due to tumor formation undergoing stem cell therapies. In the past, it was unknown if the tumors arose spontaneously (likely due to the weak immune system of the patient), or due to uncontrolled development of the implanted or injected stem cells. Associated Press Medical Writer Lauren Neergaard reported on Feb. 17, 2009, the first documented case of
the death of an Israeli child associated with a slow growing brain and spinal cord tumors after fetal stem cell “therapy” in Moscow. In this case, extensive genetic testing at Tel Aviv University showed the tumors to be derived from the fetal human neural stem cells injected into the boy. The child had a rare and fatal genetic disease, and like the families of spinal cord and brain injured patients, the parents were desperate for a “cure” traveling to Russia for this unproven treatment.  

Increasingly, desperate spinal trauma patients are going out of the US for stem cell therapies offered in China and Portugal in particular. Another related therapy, injections of a type of the patients own blood cells – but experimentally altered in the laboratory before reinjection into the spinal cord ( called “Procord”) has been abandoned in Israel.
The CPR’s position on this issue is that it is far too soon to be experimenting with humans using these largely unproven and unstable therapies. As quoted by Ms Neergaard, Professor John Gearhart, a stem cell specialist at the University of Pennsylvania, says “Patients, Please Beware …..  cells are not drugs. They can misbehave in so many different ways it just is going to take a good deal of time”  …. to prove they are worthwhile and safe. Dr. B, as a trained Developmental Biologist, concurs.

He feels that Human stem cell therapy is more driven by fad, popularity, and desperation for a “regenerative” therapy for disease and trauma to the Central Nervous System…. than by sound basic science.  While these notions hold great promises, we are not at a justified place in Human Medicine to warrant human use. For the “non-scientist” reading this essay, they should look into an Obstetrics and Gynecology Textbook or website detailing “Ovarian Cysts”. There are sources in even the adult human where cells can be found that have the capability to grown and mature into many different kinds of cells and tissues of the body…. one of these are cells of the Ovary. In women that produce an ovarian cyst (some as large as grapefruits), surgical removal of the cyst is sometimes enlightening to this discussion. Inside the cyst, it is not rare to find well developed parts of the body, including skin complete with hair and hair follicles, teeth, and eyes. The lesson is clear, when the normal controls of cell and tissue development fail – many unforeseen things can happen. Tumors are only one possibility for unwanted and dangerous consequences of a therapy that counts on implanted or injected cells to behave themselves, and to form only one necessary and desired type of cell. The same can be said for “genetically engineered” cells for implantation. This is another very promising area of research – but many years away from safe use in human patients.  


Dr. B’s former Doctoral Student, Dr. Andrew Koob, Has just published a fine new book on the biology of Glia. Andy’s Ph.D work was on Brain Injury, he pursued this as a postdoc at Dartmouth Medical school, and later at UCSD. He is now doing research in Munich Germany. All this while his interest in the role of Glia cells in disease and injury has grown by “leaps and bounds”....... So……….he has put some of his thinking to paper.

Go to Amazon.com, and check out “The Root of Thought” by Andrew Koob.



Dr. Andrew Blight, Dr. Jim Tooms, and Dr. B began a journy together in the early 1990’s to produce a therepy for chronic spinal cord injury where an injured person could “take a pill” for paraplegia. Dr. Blight devoted most of his career to the development of the drug 4-AP (time released for called frampradine) He and his company (Acorda Therapeutics) have succeeded in moving the work of the CPR to a commercially available treatment for multiple sclirosis, and chronic spinal cord injury.

Functional Recovery of movement and sensation, is based on 4-AP’s ability to restore nerve inpulse conduction in damaged nerve fibers that do not work but are still intact. In particular, the drug can counter the functional loss assosiated with the loss of nerve fiber’s insulation. (Myelin) This is why Multiple Sclirosis and spinal cord injury are both able to be treated with frampadine.
The idea that one could take an oral medication and recover some function after CNS damage or disease was very controversial. Now it is established fact. Medications for multple sclirosis may slow down the progression of the disease – but not restore walking or other useful functions. 4-AP can do both.

The original invention of 4-AP by Purdue University and you can learn more about this by clicking ****. Dr. Steven Byne, Dr. B, Dr. Dan Smith, Dr. Riyi Shi, have developed the next generation of this drug which will active at lower concentrations and have less side effects. Clinical testing in dogs is being conducted by Natasha Olby at the North Carolina State University at Raligh.
Indeed we are proud of this accmplishment and indeed 4-AP indicative of a “New Era” of treatment.