Prolozone is a technique that combines the principles of neural therapy, Prolotherapy, and ozone therapy. It involves injecting combinations of procaine, anti-inflammatory medications, homeopathics, vitamins, minerals, proliferatives, and ozone/oxygen gas into degenerated or injured joints, and into areas of pain. This article reviews the nature of what medical grade ozone is, how it works in biological systems, and how it can be used to regenerate joints and other damaged tissues, and to alleviate pain. Three case studies are presented.
Journal of Prolotherapy. 2011;3(2):630-638.
Prolozone is a technique that marries concepts from neural therapy, Prolotherapy, and ozone therapy. It involves injecting various combinations of procaine, anti-inflammatory medications/homeopathics, vitamins, minerals, proliferatives, and a mixture of ozone/oxygen gas into degenerated or injured joints, and into areas of pain. The result of this combination is nothing short of remarkable in that damaged tissues can be regenerated, and otherwise untreatable pain can be permanently cured. The purpose of this article is to provide insight into what Prolozone is, and how it works. Let’s start with ozone.
OZONE = TRIATOMIC OXYGEN
Oxygen is an atom that cannot exist in a stabilized form as a single atom. This is because it does not have enough electrons to balance it out. So in order to provide stability, two oxygen atoms bond together in close proximity and share electrons. This molecule, called O2, is what is generally referred to when the word “oxygen” is used. O2 is the stable form of oxygen that exists in the atmosphere.
When an energetic force, such as electricity (lightening) or ultra-violet light (solar exposure), is imposed upon a molecule of O2, the two oxygen atoms are temporarily split apart into single oxygen atoms. Then, in a matter of nanoseconds these highly unstable oxygen atoms will pair up again and reform back into O2 molecules. But a small percentage of them will unite in a ménage-a-trio known as ozone. Thus, ozone, referred to as O3, is a gaseous molecule which consists of three oxygen atoms all sharing the same electrons.
This is exactly what happens in a corona discharge ozone generator. Oxygen (O2) molecules go into the generator and are exposed to an electric spark. What emerges from the other end is a mixture of oxygen and ozone. The parameters of the generator can be set to produce a given amount of ozone in that mixture. In clinical circumstances the concentration of ozone in the final gas mixture is between 1-3%. In the therapeutic sections of this article I will be using the word “ozone” to refer to this mixture of ozone and oxygen.
Ozone is a relatively unstable molecule. This is because there just are not enough electrons to go around to keep three oxygen atoms stabilized. There are enough for two atoms, but not three. This instability is exactly why ozone is so powerful—because it is driven to give off the extra oxygen atom so that it can be reduced to the stable O2 form. This of course requires getting electrons, and the best place for a single oxygen atom to get an electron in a cellular environment is from the double bonds found in lipids and amino acids. The reaction looks like this:
O3 + -C=C- → -C-O3-C- → -CO-CO2→ -C=O + -C-O2
The resulting peroxides (- C-O2) are short chained, and can easily penetrate cellular membranes. There, they will exert their oxidizing effect on NADH by accepting its electrons, and thereby oxidizing it to NAD. The importance of this reaction will be discussed later. However, this is not the only reaction that can occur with ozone. As I mentioned above, it can also react with itself to be converted back into oxygen. In a matter of only minutes, ozone molecules can react with each other to form the more stable O2 molecule:
O3 + O3 → 3O2
This process is referred to as dismutation. It does not happen when ozone is injected into tissue, but it does happen when ozone is kept in a syringe. It has been found that in a glass container at room temperature ozone will dismutate at a rate of 50% every 45 minutes. In a plastic container it will dismutate even faster, at the rate of 50% every 30 minutes. This is important to know because once ozone has been generated for a medical application; it must be used rather quickly. It can’t be stored and used later. As you can see, this fact somewhat limits the usefulness of ozone. I just can’t give my patient a bottle of ozone to take home with him, because within hours it will all have dismutated back into O2.
An important precaution to note here is that, with the exception of ozone generators that are strictly used for air or water purification, in no case should ozone destined to be used for medical applications ever be made from room air! The reason is that room air contains 80% nitrogen, and when this nitrogen passes through the energy chamber, it is converted to nitrous oxide and nitric oxide, both of which are toxic in even small doses. So it is imperative that only high quality pure oxygen be used to generate the ozone used for medical purposes.
Before I delve into the next section, I need to define the term oxygen utilization. Oxygen utilization quite simply refers to how efficiently a cell or cells are converting oxygen to energy. Decreased oxygen utilization therefore refers to a condition in which oxygen is being less efficiently converted into energy.
When a molecule of oxygen reaches a cell (specifically the mitochondria of the cell) there are two possible ways that it can be metabolized. One, in aerobic metabolism it can interact with either glucose or fatty acids to produce energy. Or two, it will be converted into free radical molecules. In a state of decreased oxygen utilization, more of it will be directed towards free radical production, and less towards energy production. This of course leads to a lethal one-two punch to the cell. It has less energy to maintain itself, and it is being increasingly burdened with free radical injury. Decreased oxygen utilization is at the root of all chronic disease, and I believe is also the fundamental cause of chronic pain and tissue degeneration.
In 1983 I went to a four day training seminar in Germany on the use of ozone in medicine. One of the things that I learned was that ozone was very effective when injected into rheumatic joints. Inflammation decreased, swelling decreased, and most importantly pain decreased. How and why all this was happening was not explained, but the procedure had been done for years, and several clinical studies had verified the effect.
As so often happens after we learn something, shortly after the seminar I had a patient with rheumatoid arthritis show up at the clinic with severe inflammation and pain in both of her knees. After explaining to her what I had learned, she consented, and I injected both of her knees with ozone gas. The result was dramatic. Within two days 75% of the pain and inflammation was gone. But this case is only the beginning of the story.
The following week a neighbor of this patient came to the clinic asking to have her right knee injected with “the same thing you gave Mary.” Only this patient did not have an inflammatory condition. She had an osteoarthritic knee that she had been suffering with for several years. I explained to her that treating an inflamed joint was very much different from treating a degenerated joint, and although Mary had a good result, I did not know if the treatment would be helpful in her particular case. I told her that as far as I knew, no one had reported any success in treating degenerative conditions with ozone.
Then she asked, “Well will it make me any worse? I can hardly walk as it is. They already want me to have a total knee replacement. What harm could it do to try?” I had to admit that she had a good point, so I consented to the proposal.
She called me up one week later and told me that she was 20% better, and would I please give her another injection. We continued the treatments for a total of seven times, at which point she was so functional that she saw no need for further treatments. She remained that way for months, and only needed to return 2-3 times each year for a “booster.” Soon, she told several other people about her success, and I began using the treatment on a host of other patients.
One of those patients, after her third injection, asked me a question. “Doctor, these injections really hurt a lot. Why don’t you use any Novacaine?” It’s true. When ozone is injected into tissue, especially in the higher concentrations that I was using at the time, it causes intense pain for the first few minutes while it is exerting its oxidizing effects. After 3-4 minutes, the pain is almost completely gone, but those first few minutes can be rough.
In addition to its pain blocking effects, as any student of neural therapy knows, procaine (the generic form of Novacaine) also stabilizes and restores damaged membrane potentials. This effect often results in curing chronic pain with nothing more than simply injecting procaine into the damaged area. For both of these reasons, the next time I injected this patient I pre-injected the knee with buffered procaine. The result was just as good as what I had been seeing when using only ozone, perhaps even better, and now I had a much happier patient. I continued to use this combination.
Then I thought since I was already pre-injecting the area with procaine, what else might I put into the mix that might make the results even better? I reasoned that ozone was exerting its healing effect through the process of improving oxygen utilization, so I added various nutrients that play important roles in the utilization of oxygen. This included magnesium, niacin, methycobalamin, folic acid, and pyridoxine. I also experimented with using sea salts. Soon, I discovered a combination of ingredients that was easy to administer, inexpensive, and definitely improved my results. But I was not finished.
I also knew that many of the patients I was treating were suffering not only from pain stemming from degeneration, but also pain from inflammation. The two were often combined. This became very obvious to me after treating several cases in which the patients had been previously treated with injectable corticosteroids. The previous use of steroids not only did not interfere with ozone therapy, in some cases it actually seemed to help the process along. So I made a homeopathic dilution of methylprednisolone, and began adding it to the pre-injection mixture. To this I also added an anti-inflammatory homeopathic combination called Traumeel™. My results continued to improve. But something else also occurred to me.
All along, I had been wondering if these injections of ozone weren’t simply another version of Prolotherapy. After all, ozone is an irritating substance, and it hurt. Perhaps it was working in the same way that a proliferative solution worked. But proliferative solutions require inflammation in order to be effective, and I was now discovering that ozone injections worked even in the face of anti-inflammation therapy. So just to further check this out, I started using allopathic doses of methylprednisolone in the pre-injection. I also experimented with using oral prednisone in combination with the ozone treatments. What I discovered was that the effects of ozone therapy, unlike those from proliferative agents, was not interfered with by anti-inflammatory medications. Indeed, they seemed to be synergistic.
This simple observation caused me to theorize that ozone therapy was working along a principle that was different from the way that Prolotherapy works. I will explain what I think this principle is in the next section. But if that is the case, if they are both working from two different principles, might it not be reasonable to expect that there may be some synergistic effect from combining ozone with Prolotherapy? So that’s what I did. I developed a protocol wherein when I initially began treating a patient I used an anti-inflammatory mixture for the first 2-3 times. Then, when inflammation was no longer part of the clinical picture, I started adding in various proliferative agents. The one that I have the best results with is sodium morrhuate.
HOW DOES PROLOZONE WORK?
If Prolozone is not working simply as another form of Prolotherapy, how is it working? The answer to this question came to me one day as I was talking with a friend and colleague David Edwards, MD. Dave is a cardiologist, and the conversation was about myocardial hibernation. Myocardial hibernation is a term used to describe the condition in which there is a localized decrease in cardiac function due to localized ischemia. Restoration of normal coronary flow (e.g., by coronary bypass, chelation therapy, etc.) will restore normal function in the affected region. In other words, it is a localized area of tissue that is trapped in a state of reduced oxygen utilization. Restore oxygen utilization, and the tissue will function normally again.
This same principle also applies to cases of cerebral infarct. Between the area of dead brain tissue and healthy tissue, there is a localized penumbra of brain tissue that is trapped in a state of decreased oxygen utilization. This tissue is not dead, but it is non functional. Restoring oxygen utilization to these cells with hyperbaric oxygen will often result in significant clinical improvement. I believe that Prolozone works by improving oxygen utilization in a localized area of damaged connective tissue, allowing it to heal, and to restore full function.
WHAT CAUSES CHRONIC PAIN?
We damage our connective tissues all the time. This is normal. In fact, it is controlled damage that is at the very heart of why exercise is so beneficial. When the tissue is damaged, stem cells and blast cells are called to the area of injury. Growth factors are stimulated, and very soon the damage is repaired. You sprain your ankle, and then it heals. You break your neck, and then it heals. That is, unless it doesn’t.
Why is it that some injuries never heal, and go on to become areas of chronic pain and dysfunction? What happened to the healing mechanisms that always worked before? I think it’s the same process as myocardial hibernation and cerebral penumbra of injury. I believe that these localized areas fail to heal because of a localized decrease in oxygen utilization. Reverse this, and an area of chronic pain will become normal again. Reverse this, and an area of chronic degeneration will begin to regenerate exactly as it was supposed to in the first place.
Here’s another question. Why does chronic pain and degeneration only occur in joints and ligaments instead of other tissues? And why do people heal so much more reliably when they are young than when they become older? The answer in both cases has to do with decreased oxygen utilization.
Ligaments and joints are notoriously known as areas of decreased oxygen tension. The oxygen tension in a healthy ligament is often only 1/10th that of the tissue only several millimeters away from it. The same is true for joints. These areas are setups for developing a situation that involves a localized area of decreased oxygen utilization.
But as we grow older, does our circulation improve, or does it decrease? Of course it decreases. So the natural decrease in oxygen utilization that is seen in the healthy ligaments and joints of the young become even further compromised with aging. So here’s the scenario for chronic pain and tissue degeneration that seems to correlate well with what I have clinically seen from using Prolozone in thousands of patients over these past 20 years.
There is a naturally occurring decrease in circulation to ligaments and joints. This condition is further compromised with aging. The result is a naturally occurring localized decrease in oxygen utilization in these tissues. Then along comes a trauma. The trauma produces edema and inflammation causing a further localized decrease in oxygen utilization. This decrease in oxygen utilization produces a localized increase in lactic acid production, free radical damage, and necrosis which serves as the foundation for sensory irritation and injury, all of which causes chronic pain.
Both the initial trauma and the ensuing edema and inflammation result in a decrease in circulation. This compromises the delivery of oxygen and important nutrients to the localized area of damage, and decreases oxygen utilization even more. The trauma also compromises cell membrane potential, which both causes decreased oxygen utilization, and in turn is caused by decreased oxygen utilization. So, even though stem cells and blast cells are there, and growth factors are being released, healing does not occur. None of these mechanisms can be effective because of a lack of adequate oxygen utilization. Thus, a vicious cycle, which I dub “The Circle of Chronic Pain” results: decreased oxygen utilization leads to a decrease in cell membrane potential and an increase in free radical damage, which leads to tissue damage and increased inflammation and edema, which perpetuates the trauma, which leads to a further decrease in oxygen utilization. All of which adds up to chronic pain and degeneration. Break that cycle, and the cells and tissues can begin to do what they usually do so well—heal themselves. That is precisely what Prolozone does.
Each component of Prolozone has a specific biological purpose. Procaine acts to re-establish cellular membrane potentials. Anti-inflammatory agents decrease edema and swelling. The inclusion of vitamins and minerals provides necessary substrates for oxygen utilization that in damaged tissues are often deficient. And finally, oxygen utilization is directly stimulated by ozone.
How does ozone stimulate oxygen utilization? The answer to this question is beyond the scope of this article, but is answered in my book, The Principles and Applications of Ozone Therapy – A Practical Guideline For Physicians, which can be purchased from Amazon.com. The short answer is that is does it by oxidizing NADH to NAD.
As oxygen utilization decreases, in this case from trauma, the ratio of NAD to NADH decreases. A decrease in the cells’ NAD/NADH ratio results in a slowdown of all cellular function including protein synthesis, cellular division, growth factor function, membrane potential maintenance, etc. As previously mentioned, ozone reacts with the double bonds in lipids and amino acids and creates peroxides that are able to oxidize NADH to NAD, and thereby correct the declining NAD/NADH ratio. And by doing this, cellular function is stimulated to return to business as usual, and oxygen utilization is returned to normal. The net result is that the tissues get what they need to heal—energy. And as they heal, the circulation to the area is re-established, pain is cured, and the treatment is complete.
OTHER LOCALIZED EFFECTS OF OZONE
As a powerful oxidizing agent, ozone also has several other effects that are important for tissue repair and regeneration. One is by stimulating growth factor production and release. One paper published in 1996 examined the critical role that protein tyrosine phosphorylation events play in proliferation and differentiation. The authors determined that oxidizing agents “stimulate growth response events in vascular smooth muscle cells,” and also “stimulate tyrosine phosphorylation of several proteins including epidermal growth factor receptor.” The stimulation of growth factors, especially endothelial factors are important for tissue regeneration to occur.
But ozone therapy can do more than just stimulate growth factor production and release. It also activates the membrane receptors through which growth factors exert their effects. For example, a paper published in the Journal of Biological Chemistry established a novel role for the mitochondrion as a proximal target specific to oxidant induced signaling and growth factor transactivation.
And finally, there is evidence that ozone therapy can mediate the effects of the various growth factors. A recent 2005 paper entitled, “NAD(P)H Oxidase 4 Mediates Transforming Growth Factor-ß1–Induced Differentiation of Cardiac Fibroblasts Into Myofibroblasts,” describes how oxidized nicotinamide adenine dinucleotide (NAD) induces circulating fibroblasts into repairing damaged cardiac tissue. NAD activity is enhanced by ozone therapy because it increases the NAD/NADH ratio.
IT’S A GAS!
One last note about the effect of injecting a gas. Unlike injecting a liquid, which will just pool in the area of injection, gases expand when injected, and dissect along areas of inflammation. This fact is exploited in the Prolozone technique by injecting large volumes (10-30cc) of gas into each treated area. The effect is that very large areas, and difficult to reach areas are treated with only one injection. This decreases the number of injections needed to treat a given area, and also greatly decreases the chance of missing the area of primary involvement. I call it, “Target practicing with a shot gun.”
WHAT A PROLOZONE PATIENT CAN EXPECT
The first thing that most patients notice after a Prolozone treatment is an almost immediate 50-80% decrease in pain. This is in part due to the effect of the procaine. But ozone itself has a significant ability to directly relieve pain. A 2009 article published in the European Journal of Pharmacology demonstrated that a single subcutaneous injection of ozone prevents allodynia and decreases the over-expression of pro-inflammatory caspases in the orbito-frontal cortex of neuropathic mice, immediately eliminating any signs of pain. Lamberto Re, a medical doctor and soccer team physician in Verona, Italy routinely injects the acutely injured areas of his players with ozone alone. He does not use procaine. And he reports a marked decrease in pain as well as an improved rate of healing.
Next, chronic areas of degeneration such as in osteoarthritic knees, hips, and ankles will regenerate. Although more research is needed to fully document this effect, some physicians have already taken pre and post treatment x-rays that have shown an increase in cartilage thickness in knees treated with Prolozone. And fortunately, other than a rarely occurring and temporary increase in pain in the area injected, no significant side effects from Prolozone have ever been demonstrated. Other than the possibility of an allergy to one of the liquid components, there are no contraindications to its use.
CONDITIONS THAT RESPOND
The primary criterion for selecting a patient for Prolozone is pain. If it hurts, Prolozone should be tried. I have had cases in which the chief complaint was instability, and the patient had no complaints of pain. A classic example would be a recurring dislocating shoulder. Whereas Prolozone has worked well in many of these cases, my experience is that it should be combined with classical Prolotherapy for best results.
The following is a list of conditions that have been found to be very responsive to Prolozone: chronic neck and back pain from any cause, rotator cuff injuries, degenerative and arthritic hips, knees, and ankles, degenerated discs, plantar fasciitis, carpal tunnel syndrome, TMJ, sciatica, heel spurs, neuromas, tennis elbow, sinus infections, pelvic disorders, dental infections, post-op pain, non-union fractures, painful scars, and sports injuries—basically anything that hurts. (See Table 1.)
|Conditions responsive to Prolozone:|
• Carpal tunnel syndrome
• Chronic back pain
• Chronic neck pain
• Degenerated discs
• Degenerative & arthritic ankles
• Degenerative & arthritic hips
• Degenerative & arthritic knees
• Dental infections
• Heel spurs
• Non-union fractures
• Painful scars
• Pelvic disorders
• Plantar fasciitis
• Post-op pain
• Rotator cuff injuries
• Sinus infections
• Sports injuries
• Tennis elbow
While clinical trials using the exact technique involved in Prolozone have not been published, there have been several papers published in the international literature lauding the use of ozone injections in various pain syndromes. A list of these articles is provided at the end of this article.
ADVANTAGES OF PROLOZONE
I am a big fan of classical Prolotherapy and neural therapy. These are the techniques that I originally learned years ago, and they are very effective. They set the stage for the development of the various Prolozone techniques. However, at this point, simply because Prolozone is so effective, I virtually never use these other modalities as they are classically used. Additionally, Prolozone offers some advantages over classical proliferative therapy.
First and foremost, ozone directly stimulates the down regulated oxygen utilization in damaged areas of the body that is at the heart of why these areas don’t heal. Prolotherapy does not have this action. Secondly, Prolotherapy is typically very painful, with the pain from the therapy often persisting for days to weeks after a treatment. In contrast, patients receiving Prolozone feel immediate improvement, with very little or no pain at all during or after the treatments.
Prolotherapy requires many injections, whereas Prolozone only requires a few. This means that Prolozone is faster, and typically much less expensive.
Because Prolozone involves the injection of a gas in large volumes which expands into a large area of surrounding tissue, it is not as critical to pinpoint each Prolozone injection as it is when using proliferatives. Thus, it is easier to master.
Since Prolozone does not work as a proliferative, the use of anti-inflammatory medications is not contraindicated, and can in fact be synergistic.
Prolozone is especially effective when used intra-articularly. It can stimulate the regeneration of damaged cartilage in knees, shoulders, ankles, and hips.
CASE EXAMPLE #1
Mary Anne is a 48 year old master ICU nurse. 10 years prior to her visit she injured her back in a lifting accident. After a year of failed conservative management, she had a lumbar spinal fusion involving the placement of several metal plates. Her pain continued, and was managed with narcotics. Several years later for no apparent reason her neck began to hurt, and she developed right arm neuropathy. Her neck was then fused, and metal plates placed there as well. Shortly after, she was forced to stop nursing.
Previous to my seeing her, she had had neural therapy, classical Prolotherapy, acupuncture, and various physical therapy techniques. All of these modalities had failed to offer anything but temporary relief. On her first visit she presented as a woman addicted to narcotics, with chronic and severe pain in her neck, down her right arm, in her lower back, and down both legs. She also was developing increasing weakness in her right hand. She was only able to ambulate into the treatment room with assistance.
She was treated with Prolozone injections to her neck and lower back every two weeks for three months. The treatments took about 10 minutes. At this point the weakness in the hand had disappeared, and her pains had diminished to the point that she had cut her medication dose in half. Her treatments were decreased to three week intervals, and after three more months her pain had reduced to a fraction of what it had been, and she was off all medication.
This was obviously an extreme case, but she is a great example of what Prolozone can do. Most cases of chronic back or neck pain resolve in 4-6 treatments. This patient went on to have several relapses of her pain, primarily because she had to make frequent flights across the country. It was not until a full year of therapy, with treatments being performed at six week intervals that she became completely functional with minimal pain. It has now been almost one year since her last treatment and she continues to do well.
Joe is a 66 year old retired metal worker who presented with bilateral knee pain. His x-rays showed bilateral medial compartment bone on bone. He had been advised by orthopedic surgeons to have bilateral replacements. He was very limited in his activities, could no longer play golf, and walked with a slow, shuffling gait. He took NSAIDs daily.
Joe was treated with intra-articular Prolozone every two weeks for three sessions. At that point he was no longer requiring medication, and was able to perform activities that he previously could not do. The treatments were stretched out to every 3 weeks and then every 4 weeks, and ultimately every 6 weeks until he was completely asymptomatic and playing golf again. He had a total of eight treatments.
I have seen many cases just like Joe’s. About 85% of the time they have the same kind of result. I have never had a patient go to knee surgery in fifteen years of using Prolozone. Figure 1 is an x-ray of another patient (not Joe) taken in August. Figure 2 was taken the following February after eight Prolozone treatments. I wish I had more x-rays like this, but I don’t routinely take post therapy x-rays. These were done by a colleague trained in the Prolozone technique.
Randy is a 67 year old retired plumber. I was treating his wife for a rotator cuff injury, when on her third visit he told me the following. “Doc, my wife is doing so well that I thought maybe you can help me too. Nobody else can. About 12 years ago I was wrenching a pipe when the wrench slipped and the back of my right hand was slammed hard against a piece of metal. Nothing was broken, but I have had severe pain which limits the use of my wrist ever since then. I more or less just ignore it, but I am unable to do certain things like reach over and pick up a bag because of the pain.”
Randy’s examination revealed pain on stressing the wrist, and tenderness over the affected area on the dorsum of the wrist. It took me all of five minutes to infiltrate the area with Prolozone. When Randy returned with his wife four weeks later, he happily reported that the pain was completely gone. It has now been 1½ years since that first injection, and he remains asymptomatic.
What? A chronic pain that goes away with only one inexpensive five minute treatment? Sounds like an exaggeration. But I have seen this kind of thing happening so often that I am convinced that ozone has properties for alleviating chronic pain which are unique, and still not fully understood. But don’t believe me. Call up any one of the doctors using Prolozone. They will tell you they see the same kind of remarkable results.
JOIN THE AMERICAN ACADEMY OF OZONOTHERAPY
I have been training doctors in the Prolozone technique for over fifteen years. Of course the ones who learn the fastest are the ones who are already versed in classical Prolotherapy, and/or are used to injecting tissue. Because of their understanding of anatomy, orthopedists, osteopaths, and chiropractors are particularly quick learners. But anyone can do this therapy. It is a very forgiving modality. Remember, it’s like target practice with a shotgun. It’s hard to miss the bull’s eye.
This January, 2011, The American Academy of Ozonotherapy (AAO) was formed. The AAO is an academy of health professionals dedicated to establishing standards for the art and science of Ozonotherapy, educating the public and other health professionals about the many uses of Ozonotherapy in medicine, and promoting research in Ozonotherapy. Our goal is to enhance the health and well being of people through this safe, inexpensive, and effective therapy. You can learn more about the AAO at www.aaot.us.
For information on Prolozone training and joining the AAO, please contact me at email@example.com.
1 Rao GN. Protein tyrosine phosphorylation events play determinant roles in cellular processes such as proliferation and differentiation. Oncogene. 1996 Aug 15;13(4):713-9.
4 Bonetti M, et al. Intraforaminal O(2)-O(3) versus periradicular steroidal infiltrations in lower back pain: randomized controlled study. Am J Neuroradiol.2005 May; 26(5):996-1000.CONCLUSION: Oxygen-ozone treatment was highly effective in relieving acute and chronic lower back pain and sciatica. The gas mixture can be administered as a first treatment to replace epidural steroids.
5 Al-Jaziri AA, et al. Painkilling effect of ozone-oxygen injection on spine and joint osteoarthritis. Saudi Med J.2008 Apr;29(4):553-7.CONCLUSION: This study validates the painkilling effect of ozone-oxygen injection on osteoarthritis of the joints and spine. Its long term effect on pain advocates the likelihood of some histological changes as mechanism of its action.
6 Fuccio C, et al. A single subcutaneous injection of ozone prevents allodynia and decreases the over-expression of pro-inflammatory caspases in the orbito-frontal cortex of neuropathic mice. Eur J Pharmacol.2009 Jan 28;603(1-3):42-9.CONCLUSION: These preliminary data show that peripheral neuropathy induced over-expression of pro-inflammatory/pro-apoptotic caspases in the orbito-frontal cortex and that ozone, by mechanisms that are as yet unknown, can regulate the expression of the genes that play a pivotal role in the onset and maintenance of allodynia.
7 Paoloni M, et al. Intramuscular oxygen-ozone therapy in the treatment of acute back pain with lumbar disc herniation-a multicenter, randomized, double-blind, clinical trial of active and simulated lumbar paravertebral injection. Spine.2009;34(13):1337–1344.CONCLUSION: Ozone vs placebo – 61% vs 33% pain free.
8 Bonetti M, et al. Intraforaminal O(2)-O(3) versus periradicular steroidal infiltrations in lower back pain: randomized controlled study. AJNR Am JNeuroradiol. 2005 May;26(5):996-1000.CONCLUSION: Ozone more effective than steroids – 8.6 vs 21.4% poor outcomes.
9 Fifth International Symposium on the Applications of Ozone, April 2007, Havana, Cuba.CONCLUSION: We conclude that intra-articular ozone is an effective therapy in the treatment of grade III knee osteoarthritis resistant to treatment with NSAIDs.“Ozone Shot as Effective as Surgery for Herniated Discs” As reported in CyberRounds, by Neil Wagner online at www.cyberrounds.com.A Toronto team examined the results of 12 previous studies involving over 8,000 patients of ozone treatment of herniated discs. The studies showed ozone therapy to be just as effective as surgery but with a shorter recovery time and a much lower risk of complications.