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1.
Integr Cancer Ther ; 15(1): 69-79, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26209468

ABSTRACT

UNLABELLED: Naturopathic oncology is a relatively new and emerging field capable of providing professional integrative or alternative services to cancer patients. Foundational research is critical to identify topics in the clinical and research development of naturopathic oncology for future growth of the field. STUDY DESIGN: This study implements a modified Delphi protocol to develop expert consensus regarding ethics, philosophy, and research development in naturopathic oncology. METHODS: The modified protocol implements a nomination process to select a panel of 8 physicians and to assist in question formulation. The protocol includes an in-person discussion of 6 questions with multiple iterations to maintain the concept of the Delphi methodology as well as a postdiscussion consensus survey. RESULTS: The protocol identified, ranked, and established consensus for numerous themes per question. Underlying key topics include integration with conventional medicine, evidence-based medicine, patient education, patient safety, and additional training requirements for naturopathic oncologists. CONCLUSIONS: The systematic nomination and questioning of a panel of experts provides a foundational and educational resource to assist in clarification of clinical ethics, philosophy, and research development in the emerging field of naturopathic oncology.


Subject(s)
Medical Oncology/methods , Naturopathy/methods , Neoplasms/drug therapy , Neoplasms/therapy , Adult , Aged , Consensus , Female , Humans , Male , Middle Aged , Physicians , Surveys and Questionnaires
3.
Altern Med Rev ; 15(2): 147-51, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20806999

ABSTRACT

Most treatments for methicillin-resistant Staphylococcus aureus (MRSA) focus on agents to eliminate the bacterium. Since MRSA infection is not universal, susceptibility factors are possible. Immune resistance could be lowered in such individuals; therefore, locating immune-inhibiting or immune-enhancing factors might decrease susceptibility. Such seemed to be the case in a 48-year-old female who presented with recurring MRSA despite multiple rounds of a variety of antibiotics. When the patient encountered an intensely stressful situation an outbreak of MRSA occurred. The patient had additional underlying health issues that suppressed her immune system and made her more susceptible to stress. Gluten allergy and hypothyroidism were discovered and alleviated but did not end the MRSA outbreaks. Implementation of a popular treatment from the 1930s, intravenous dilute hydrochloric acid (for immune stimulation), prevented most MRSA outbreaks when administered frequently. This case provides anecdotal support for the proposition that immune enhancement is a viable approach to forestall or clear recurring MRSA.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Hydrochloric Acid/administration & dosage , Methicillin-Resistant Staphylococcus aureus/drug effects , Staphylococcal Infections/drug therapy , Female , Humans , Immunity/drug effects , Middle Aged , Staphylococcal Infections/physiopathology
4.
Altern Med Rev ; 15(1): 33-47, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20359267

ABSTRACT

Eucalyptus oil (EO) and its major component, 1,8-cineole, have antimicrobial effects against many bacteria, including Mycobacterium tuberculosis and methicillin-resistant Staphylococcus aureus (MRSA), viruses, and fungi (including Candida). Surprisingly for an antimicrobial substance, there are also immune-stimulatory, anti-inflammatory, antioxidant, analgesic, and spasmolytic effects. Of the white blood cells, monocytes and macrophages are most affected, especially with increased phagocytic activity. Application by either vapor inhalation or oral route provides benefit for both purulent and non-purulent respiratory problems, such as bronchitis, asthma, and chronic obstructive pulmonary disease (COPD). There is a long history of folk usage with a good safety record. More recently, the biochemical details behind these effects have been clarified. Although other plant oils may be more microbiologically active, the safety of moderate doses of EO and its broad-spectrum antimicrobial action make it an attractive alternative to pharmaceuticals. EO has also been shown to offset the myelotoxicity of one chemotherapy agent. Whether this is a general attribute that does not decrease the benefit of chemotherapy remains to be determined. This article also provides instruction on how to assemble inexpensive devices for vapor inhalation.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/pharmacology , Immunity/drug effects , Oils, Volatile/administration & dosage , Oils, Volatile/pharmacology , Administration, Inhalation , Asthma/drug therapy , Bronchitis/drug therapy , Eucalyptus , Eucalyptus Oil , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Humans , Lymphocyte Activation/drug effects , Monoterpenes/administration & dosage , Monoterpenes/pharmacology , Pulmonary Disease, Chronic Obstructive/drug therapy
5.
Altern Med Rev ; 15(4): 345-51, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21194250

ABSTRACT

The oxidizing anticancer system of vitamin C and vitamin K3 (VC:VK3, producing hydrogen peroxide via superoxide) was combined individually with melatonin, curcumin, quercetin, or cholecalciferol (VD3) to determine interactions. Substrates were LNCaP and PC-3 prostate cancer cell lines. Three of the tested antioxidants displayed differences in cell line cytotoxicity. Melatonin combined with VC:VK3 quenched the oxidizing effect, while VC:VK3 applied 24 hours after melatonin showed no quenching. With increasing curcumin concentrations, an apparent combined effect of VC:VK3 and curcumin occurred in LNCaP cells, but not PC-3 cells. Quercetin alone was cytotoxic on both cell lines, but demonstrated an additional 50-percent cytotoxicity on PC-3 cells when combined with VC:VK3. VD3 was effective against both cell lines, with more effect on PC-3. This effect was negated on LNCaP cells with the addition of VC:VK3. In conclusion, a natural antioxidant can enhance or decrease the cytotoxicity of an oxidizing anticancer system in vitro, but generalizations about antioxidants cannot be made.


Subject(s)
Antineoplastic Agents/pharmacology , Antioxidants/pharmacology , Ascorbic Acid/pharmacology , Cytotoxins/pharmacology , Prostatic Neoplasms/drug therapy , Vitamin K 3/pharmacology , Cell Cycle/drug effects , Cholecalciferol/pharmacology , Curcumin/pharmacology , Drug Interactions , Drug Therapy, Combination , Humans , Male , Melatonin/pharmacology , Oxidative Stress/drug effects , Quercetin/pharmacology , Tumor Cells, Cultured
7.
Altern Med Rev ; 10(1): 24-35, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15771560

ABSTRACT

This article covers in vitro, in vivo, and human data on the positive effect of vitamin K2 on osteoporosis. Data is available on vitamin K2 for osteoporosis caused by a number of conditions, including postmenopausal osteoporosis, Parkinson's disease, biliary cirrhosis, stroke, and drug-induced osteoporosis. The activity of vitamin K2 involves both an increase in the bone-building process and a separate decrease in the bone-loss process. Vitamin K2 exerts a more powerful influence on bone than vitamin K1, and should be considered for prevention or treatment in those conditions known to contribute to osteoporosis.


Subject(s)
Osteoporosis/drug therapy , Vitamin K 2/therapeutic use , Animals , Bone Diseases, Metabolic/etiology , Bone Diseases, Metabolic/prevention & control , Disease Models, Animal , Humans , Osteoporosis/prevention & control , Vitamin K 2/metabolism
8.
Altern Med Rev ; 8(3): 303-18, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12946240

ABSTRACT

Vitamin K, an essential nutrient often associated with the clotting cascade, has been the focus of considerable research demonstrating an anticancer potential. Much of this research has focused on vitamin K3, although vitamins K2 and K1 have also been shown to have anticancer effects. Early studies of vitamin K3 employed an oxidative model to explain the anticancer effects seen in both in vitro and in vivo studies; however, this model does not adequately address the action of vitamins K1 and K2. Recent research has demonstrated the anticancer action of vitamin K may act at the level of tyrosine kinases and phosphatases, modulating various transcription factors such as Myc and Fos. Tyrosine kinases associated with cyclins have also been shown to be affected by vitamin K, which can lead to cell cycle arrest and cell death.


Subject(s)
Anticarcinogenic Agents/therapeutic use , Neoplasms/prevention & control , Vitamin K/therapeutic use , Animals , Cell Cycle/drug effects , Humans , Mice , Rats , Transcription Factors/drug effects , Vitamin K/physiology , Vitamin K 1/therapeutic use , Vitamin K 2/therapeutic use , Vitamin K 3/therapeutic use
9.
Altern Med Rev ; 8(1): 55-8, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12611561

ABSTRACT

The use of three herbal/nutritional products over a period of two months normalized blood urea nitrogen (BUN), serum creatinine, and creatinine clearance in a case of early functional kidney impairment. Although previous use of intravenous EDTA resolved Raynaud's syndrome symptoms, it provided little improvement to abnormal creatinine clearance.


Subject(s)
Chelation Therapy/methods , Phytotherapy/methods , Renal Insufficiency/therapy , Aged , Aged, 80 and over , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Blood Urea Nitrogen , Bromelains/therapeutic use , Chitin/therapeutic use , Creatinine/metabolism , Drugs, Chinese Herbal/therapeutic use , Edetic Acid/therapeutic use , Humans , Male , Medicine, Ayurvedic , Plant Preparations/therapeutic use , Raynaud Disease/therapy , Renal Insufficiency/metabolism
10.
Altern Med Rev ; 7(3): 218-35, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12126463

ABSTRACT

The data on the standards for chromium requirements and the safety of various chromium compounds and doses are reviewed. The 350-fold difference between the acceptable daily intake and the calculated reference dose for humans of 70 mg per day seems without precedent with respect to other nutritional minerals. Previous claims of mutagenic effects of chromium are of questionable relevance. While studies have found DNA fragmentation (clastogenic effects) by chromium picolinate, anecdotal reports of high-dose chromium picolinate toxicity are few and ambiguous. The beneficial effects of chromium on serum glucose and lipids and insulin resistance occur even in the healthy. Serum glucose can be improved by chromium supplementation in both types 1 and 2 diabetes, and the effect appears dose dependent. Relative absorption of various chromium compounds is summarized and the mechanism of low molecular weight chromium binding substance (LMWCr) in up-regulating the insulin effect eight-fold is discussed. There is evidence of hormonal effects of supplemental chromium besides the effect on insulin. Chromium supplementation does result in tissue retention, especially in the kidney, although no pathogenic effect has been demonstrated despite considerable study.


Subject(s)
Chromium , Adult , Blood Glucose/drug effects , Chromium/administration & dosage , Chromium/adverse effects , Chromium/pharmacology , Chromium Compounds/administration & dosage , Chromium Compounds/adverse effects , Chromium Compounds/pharmacology , Diabetes Mellitus, Type 2/drug therapy , Dietary Supplements , Dose-Response Relationship, Drug , Female , Glucose/metabolism , Humans , Male , Middle Aged , Nutritional Requirements , Randomized Controlled Trials as Topic
11.
Altern Med Rev ; 7(2): 94-111, 2002 Apr.
Article in English | MEDLINE | ID: mdl-11991790

ABSTRACT

A growing body of evidence has demonstrated a link between various disturbances in mitochondrial functioning and type 2 diabetes. This review focuses on a range of mitochondrial factors important in the pathogenesis of this disease. The mitochondrion is an integral part of the insulin system found in the islet cells of the pancreas. Because of the systemic complexity of mitochondrial functioning in terms of tissue and energetic thresholds, details of structure and function are reviewed. The expression of type 2 diabetes can be ascribed to a number of qualitative or quantitative changes in the mitochondria. Qualitative changes refer to genetic disturbances in mitochondrial DNA (mtDNA). Heteroplasmic as well as homoplasmic mutations of mtDNA can lead to the development of a number of genetic disorders that express the phenotype of type 2 diabetes. Quantitative decreases in mtDNA copy number have also been linked to the pathogenesis of diabetes. The study of the relationship of mtDNA to type 2 diabetes has revealed the influence of the mitochondria on nuclear-encoded glucose transporters and the influence of nuclear encoded uncoupling proteins on the mitochondria. This basic research into the pathogenesis of diabetes has led to the awareness of natural therapeutics (such as coenzyme Q10) that increase mitochondrial functioning and avoidance of trans-fatty acids that decrease mitochondrial functioning.


Subject(s)
DNA, Mitochondrial/genetics , Diabetes Mellitus, Type 2/etiology , Diabetes Mellitus, Type 2/therapy , Mitochondria/physiology , Ubiquinone/analogs & derivatives , Ubiquinone/therapeutic use , Adenosine Triphosphate/metabolism , Animals , Carrier Proteins/physiology , Coenzymes , Dietary Fats/adverse effects , Glucose/metabolism , Humans , Insulin/metabolism , Ion Channels , Membrane Proteins/physiology , Mitochondrial Proteins , Mutation , Rats , Uncoupling Protein 1
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