Guest guest Posted April 21, 2004 Report Share Posted April 21, 2004 Hi Jan & All, .. Colleagues, have you any scientific references on, or personal clinical experiences of, electrostimulation or electro-AP): (a) accelerating malignancy? and/or (b) accelerating it FASTER than other forms of stimulation (AP needling, point injection, etc)? Jan, many thanks for your reply re the risk of electrostimulation or electro-AP in cancer cases. You raise interesting questions. I take the liberty of passing my question, and your reply (see below), to other AP Lists Best regards, Phil >>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>> Jan wrote: > Based on available medical literature, there seem to be some good > reasons not to use electro-AP (electrical current generally) in the > area affected by a malignant neoplasia. > 1. A recent experimental study in humans suggests that local > electro-AP [EA] increases significantly the metabolic rate ---> a > risk of the re-activation of the neoplasia? > 2. Local mechanical stimulation (vibration, contractions) might, > theoretically, contribute to the disintegration of malignant cells > from the core of the tumour into the lymphatic/vascular network > ---> a risk of the dissemination? > 3. Studies on human bone cancer (Honore et al, Neuroscience, 2000) > reported an increased expression of dynorphin (a peptide that > contributes to hyperalgesia) in the corresponding spinal segments. > This is an interesting report. We tend to assume that endogenous > opioids have only analgesic properties, and that their release is > always desirable. Indeed, there seem to be exceptions to the rule. > It is well established that EA is efficacious in stimulating the > release of endogenous opioids. There are some indications in earlier > medical literature suggesting that patients receiving morphine had > more/earlier metastases from lung cancers than non-treated > patients. A fact or an accidental finding? Indeed, the drug and the > endogenous opioids operate via the same receptor sites. Just some > " food for thought " . > The dog discussed by Karen suffers from pain. Due to spondylosis? > Due to the neoplasia or its medical treatment? The dog also has an > unidentified neurological problem. Some lymphomas are associated > with alimentary lymphatic proliferation. Theoretically, EA at BL23 > (lumbar aortic lymphonodes) could affect this locally. Similarly, > AP/EA at BL40-Weizhong (popliteal lymph node) might affect > generalized lymphoma. Indeed, nothing is cast in stone, and the > use of EA at distant body areas might be quite a safe procedure in > localized neoplasia. TENS has been used in terminally-ill cancer > patients to suppress associated neoplastic pain symptomatically. > Are Thoresen has been popularizing his original approach to AP > treatment of neoplasia for many years. It would be nice if Are > could enlighten us on details of his findings in animals. ... Jan > >>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>> Best regards, Email: < WORK : Teagasc Research Management, Sandymount Ave., Dublin 4, Ireland Mobile: 353-; [in the Republic: 0] HOME : 1 Esker Lawns, Lucan, Dublin, Ireland Tel : 353-; [in the Republic: 0] WWW : http://homepage.eircom.net/~progers/searchap.htm Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.