Millimeter wave‐induced suppression of B16 F10 melanoma growth in mice: Involvement of endogenous opioids

Millimeter wave treatment (MMWT) is widely used in Eastern European countries, but is virtually unknown in Western medicine. Among reported MMWT effects is suppression of tumor growth. The main aim of the present "blind" and dosimetrically controlled experiments was to evaluate quantitatively the ability of MMWT to influence tumor growth and to assess whether endogenous opioids are involved. The murine experimental model of B16 F10 melanoma subcutaneous growth was used. MMWT characteristics were: frequency, 61.22 GHz; average incident power density, 13.3 x 10(-3) W/cm2; single exposure duration, 15 min; and exposure area, nose. Naloxone (1 mg/kg, intraperitoneally, 30 min prior to MMWT) was used as a nonspecific blocker of opioid receptors. Five daily MMW exposures, if applied starting at the fifth day following B16 melanoma cell injection, suppressed subcutaneous tumor growth. Pretreatment with naloxone completely abolished the MMWT-induced suppression of melanoma growth. The same course of 5 MMW treatments, if started on day 1 or day 10 following tumor inoculations, was ineffective. We concluded that MMWT has an anticancer therapeutic potential and that endogenous opioids are involved in MMWT-induced suppression of melanoma growth in mice. However, appropriate indications and contraindications have to be developed experimentally before recommending MMWT for clinical usage.

[1]  Alexis Agelan,et al.  Effect of millimeter waves on cyclophosphamide induced suppression of the immune system , 2002, Bioelectromagnetics.

[2]  J. Sheridan,et al.  Stress‐Induced Neuroendocrine Modulation of Viral Pathogenesis and Immunity a , 1998, Annals of the New York Academy of Sciences.

[3]  M. Ziskin,et al.  Effect of millimeter waves on cyclophosphamide induced suppression of T cell functions , 2003, Bioelectromagnetics.

[4]  J. Trapani,et al.  A fresh look at tumor immunosurveillance and immunotherapy , 2001, Nature Immunology.

[5]  N. Korpan,et al.  Clinical effects of continuous microwave for postoperative septic wound treatment: a double-blind controlled trial. , 1995, American journal of surgery.

[6]  E.P. Khizhnyak,et al.  Heating patterns in biological tissue phantoms caused by millimeter wave electromagnetic irradiation , 1994, IEEE Transactions on Biomedical Engineering.

[7]  T. Usichenko,et al.  Treatment of chronic pain with millimetre wave therapy (MWT) in patients with diffuse connective tissue diseases: a pilot case series study , 2003, European journal of pain.

[8]  M. Palkovits,et al.  Stressor specificity of central neuroendocrine responses: implications for stress-related disorders. , 2001, Endocrine reviews.

[9]  J. Kowalski Immunomodulatory action of class μ, δ- and κ-opioid receptor agonists in mice , 1998, Neuropeptides.

[10]  Bakkar Khalid,et al.  EFFECTS OF NALOXONE, GLYCYRRHIZIC ACID, DEXAMETHASONE AND DEOXYCORTICOSTERONE IN REPETITIVE STRESS , 1999, Clinical and experimental pharmacology & physiology.

[11]  A Cowan,et al.  Peripheral neural system involvement in hypoalgesic effect of electromagnetic millimeter waves. , 2001, Life sciences.

[12]  D. Carr,et al.  Exogenous and endogenous opioids as biological response modifiers. , 1995, Immunopharmacology.

[13]  Sabita Roy,et al.  Effects of opioids on the immune system , 1996, Neurochemical Research.

[14]  A. Pakhomov,et al.  Low-intensity millimeter waves as a novel therapeutic modality , 1999, Digest of Technical Papers. 12th IEEE International Pulsed Power Conference. (Cat. No.99CH36358).

[15]  Y. Akyel,et al.  Current state and implications of research on biological effects of millimeter waves: a review of the literature. , 1998, Bioelectromagnetics.

[16]  P. Gold,et al.  Multiple feedback mechanisms activating corticotropin-releasing hormone system in the brain during stress , 2002, Pharmacology Biochemistry and Behavior.

[17]  A Cowan,et al.  Suppression of pain sensation caused by millimeter waves: a double-blinded, cross-over, prospective human volunteer study. , 1999, Anesthesia and analgesia.

[18]  V A Polunin,et al.  Resonance effect of millimeter waves in the power range from 10(-19) to 3 x 10(-3) W/cm2 on Escherichia coli cells at different concentrations. , 1996, Bioelectromagnetics.

[19]  E. Castanas,et al.  Somatostatin and Opioid Receptors in Mammary Tissue , 2002 .

[20]  A Cowan,et al.  Pain relief caused by millimeter waves in mice: results of cold water tail flick tests. , 2000, International journal of radiation biology.

[21]  J. Bidlack Detection and Function of Opioid Receptors on Cells from the Immune System , 2000, Clinical Diagnostic Laboratory Immunology.

[22]  G. D. Gamaro,et al.  The Effects of Acute and Repeated Restraint Stress on the Nociceptive Response in Rats , 1998, Physiology & Behavior.

[23]  M C Ziskin,et al.  Medical application of millimetre waves. , 1998, QJM : monthly journal of the Association of Physicians.

[24]  Steven A. Rosenberg,et al.  Progress in human tumour immunology and immunotherapy , 2001, Nature.

[25]  A Cowan,et al.  Hypoalgesic effect of millimeter waves in mice: dependence on the site of exposure. , 2000, Life sciences.