Category Archives: RESEARCH, STUDIES, DOCUMENTATION
Cytochrome P450 testing covered by Health policies
10% of Caucasians are “non metabolizers”. This means that they cannot metabolize more than 50% of today’s drugs such as adderall, and other SSRIS. It is suspected that the heinous trend of school shootings and suicides are caused by non metabolizers who are given psychiatric drugs without first being tested for their ability to metabolize them. Because this test is not standard of care hospitals and doctors who destroy lives by giving counter indicated medication can not be successfully sued. There is a movement to make this test standard of care but it is being thwarted by the invested pharmacuetical companies who would stand to lose billions of dollars if the public knew.
Description:
The cytochrome p450 (CYP450) family is involved in the metabolism of a significant proportion of currently administered drugs, and genetic variants in cytochrome p450 are associated with altered metabolism of many drugs. It is proposed that genetic testing for cytochrome p450 variants may assist in selecting and dosing drugs that are impacted by these genetic variants.
Drug efficacy and toxicity vary substantially between individuals. Because drugs and doses are typically adjusted to meet individual requirements as needed by using trial and error, clinical consequences may include a prolonged time to optimal therapy and serious adverse events.
Various factors may influence the variability of drug effects, including age, liver function, concomitant diseases, nutrition, smoking, and drug-drug interactions. Inherited (germline) DNA sequence variation (polymorphisms) in genes coding for drug metabolizing enzymes, drug receptors, drug transporters, and molecules involved signal transduction pathways also may have major effects on the activity of those molecules and also on the efficacy and toxicity of the drug.
Pharmacogenomics is the study of how an individual’s genetic inheritance affects the body’s response to drugs. It may be possible to predict therapeutic failures or severe adverse drug reactions in individual patients by testing for important DNA polymorphisms (genotyping) in genes related to the metabolic pathway (pharmacokinetics) or single transduction pathway (pharmacodynamics) of the drug. Potentially, test results could be used to optimize drug choice and/or dose for more effective therapy, avoid serious adverse effects and decrease medical costs.
Some CYP450 enzyme genes are highly polymorphic, resulting in some enzyme variants that have variable metabolic capacities among individuals, and some with little to no impact on activity.
Individuals with a lack of function activity in these enzymes (CYP2C19, CYP2D6, CYP2C9, etc.) can be classified according to how fast they metabolize medications:
- Poor metabolizers (PMs): lack active enzyme gene alleles, they will process a certain drug more slowly than normal because of the missing enzyme(s), the medication can build up in their system which can increase the likelihood that it will cause side effects. The individual might still be able to benefit from the medication, but at lower dosages.
- Intermediate metabolizers (IMs): have one active and one inactive enzyme gene allele, these individuals have a reduced enzyme function in processing drugs, they may not process some medications as well as a normal metabolizer would. This can increase risk of side effects and drug interactions.
- Normal metabolizers (extensive metabolizers Ems): these individuals have 2 copies (alleles) of the most common (wild type) DNA sequence of a particular CYP450 enzyme gene resulting in an active molecule and are termed extensive metabolizers. Medications are processed normally, these individuals are more likely to benefit from treatment and have fewer side effects than people who don’t process the same medication(s) as well.
- Ultra-rapid metabolizers (UMs): individuals with more than 2 alleles of an active enzyme gene, which cause the medications to leave the body too quickly and often before they have had a chance to work properly. These individuals will likely need a higher than usual dose of medications.
US patents on Cannibas
Patents Related To The Dietary And Medicinal Study And Use Of Cannabis
US Patent 6,630,507 (pdf-120KB)
“Cannabinoids as Antioxidants and Neuroprotectants” Assigned to the United States of America, it provides guidelines for relevant medical conditions and dosage schedules for CBD. Review LOG notes on the use of vaporization to separate CBD from THC
Medicinal Acidic Cannabinoids / US 7,807,711 B2 (pdf-120KB)
Invention relates to an acidic cannabinoid, the method for extracting and preparing.
Pharmaceutical Compositions For The Treatment Of Chronic Obstructive Pulmonary Disease US 2009 / 0197941 A1 Aug. 6, 2009 (pdf-132KB)
Discusses the preferred ratio of CBD to THC being 1:1
Anti-nausea And Anti-vomiting Activity Of Cannabidiol Compounds / US 2003 0225156 A1 Dec. 4, 2003 (pdf-64KB)
Inventor: Raphael Mechoulam. The applied dose can be adjusted based on the relative bioavailability and potency of the administered compound. Adjusting the dose to achieve maximal efficacy…
Combination Of Cannabinoids For The Treatment Of Peripheral Neuropathic Pain US 2010/0035978 A1 Feb 11, 2010 (pdf-1.5MB)
This patent identifies “the ratio of CBD:THC by weight is between 10:1 to 1:10.”
US Patent 6,410,588 B1 (pdf-1.5MB)
Feldmann, et al. “Use of Cannabinoids as Anti-inflammatory Agents”
US 2007/0099987 A1 (pdf-1.4MB)
Weiss, et al. “Treating or Preventing Diabetes with Cannabidiol”
US Patent 6,946,150 B27 (pdf-2.7MB)
Brian Whittle. “Pharmaceutical Formulation.” Using a pump action spray to administer cannabinoids via the mucosal surfaces
Dr. Obukhanych, pHD, Immunology: Open letter to Legislators
Harvard Trained Immunologist Demolishes California Legislation That Terminates Vaccine Exemptions
In summary: 1) due to the properties of modern vaccines, non-vaccinated individuals pose no greater risk of transmission of polio, diphtheria, pertussis, and numerous non-type b H. influenzae strains than vaccinated individuals do, non-vaccinated individuals pose virtually no danger of transmission of hepatitis B in a school setting, and tetanus is not transmissible at all; 2) there is a significantly elevated risk of emergency room visits after childhood vaccination appointments attesting that vaccination is not risk-free; 3) outbreaks of measles cannot be entirely prevented even if we had nearly perfect vaccination compliance; and 4) an effective method of preventing measles and other viral diseases in vaccine-ineligible infants and the immunocompromised, immunoglobulin, is available for those who may be exposed to these diseases.
Taken together, these four facts make it clear that discrimination in a public school setting against children who are not vaccinated for reasons of conscience is completely unwarranted as the vaccine status of conscientious objectors poses no undue public health risk. Read letter from Dr. Obukhanych, PHD, Immunology
SOTN Editor note: When the California Senate refuses to consider authoritative scientific evidence which categorically proves the dangerous vaccine side effects on the schoolchildren, something is very wrong. Such conduct by the Senate constitutes criminal action that endangers the lives and welfare of children. Their official behavior must be acknowledged for what it is — CRIMINAL — and prosecuted to the fullest extent of the law.
Mitochondrial Iatrogenic (medication induced) Damage – Dr. Gary Kohls, MD
Dr Kohls is a retired physician who practiced holistic mental health care for the last decade of his career. Virtually all of his patients exhibited iatrogenic (prescription drug-related) syndromes such as are mentioned in the article above. In retrospect, those patients were actually manifesting iatrogenic mitochondrial diseases.
“Mitochondrial damage is now understood to play a role in a wide range of seemingly unrelated disorders such as schizophrenia, diabetes, Parkinson’s disease, chronic fatigue syndrome, and nonalcoholic steatohepatitis. Recently it has become known that iatrogenic (physician or treatment-caused) mitochondrial damage explains many adverse reactions from medications. All classes of psychotropic drugs have been documented to damage mitochondria, as have statin medications, analgesics such as acetaminophen, and many others.”— John Neustadt, MD and Steven Pieczenik, MD
1) Aluminum-induced Defective Mitochondrial Metabolism Perturbs Cytoskeletal Dynamics in Human Astrocytoma Cells.
2) Thimerosal-Derived Ethylmercury Is a Mitochondrial Toxin in Human Astrocytes
3) Medication-induced Mitochondrial Damage and Disease
Acquired Conditions in which Mitochondrial Dysfunction has been Implicated (as of 2007)
Diabetes
Huntington’s disease
Cancer including hepatitis-C virus-associated hepatocarcinogenesis
Alzheimer disease
Parkinson’s disease
Bipolar disorder
Schizophrenia
Aging and senescence
Anxiety disorders
Nonalcoholic steatohepatitis (NASH – late stage of nonalcoholic fatty infiltration of the liver)
Cardiovascular disease, including atherosclerosis
Sarcopenia (muscle-wasting disease, mainly of the elderly)
Exercise intolerance
Fatigue, including chronic fatigue syndrome, fibromyalgia, and myofascial pain
<<snip>>
Medications Documented to Induce Mitochondrial Damage (as of 2007)
http://psychrights.org/research/Digest/NLPs/DrugsCauseMitochondrialDamage.PDF
Alcoholism medications Ex: Antabuse
Alzheimer’s dementia drugs Ex: Tacrine (Cognex), Galantamine
Analgesics (for pain) and anti-inflammatory drugs, Ex: Aspirin, acetaminophen (Tylenol), indomethacin, Naproxen
Anesthetics Ex: lidocaine, propofol (also general anesthetics like halothane. isoflurane, sevoflurane)
Angina medications Ex: amiodarone
Antiarrhythmic (regulates heartbeat) Ex: amiodarone (also beta blockers)
Antibiotics Ex: tetracycline (also chloramphenicol, Cipro)
Antidepressants Ex: amitriptyline, citalopram (Celexa), fluoxetine (Prozac, Symbyax, Sarafem)
Antipsychotics Ex: chlorpromazine, fluphenazine, haloperidol, risperidone, quetiapine, clozapine, olanzapine
Anxiety medications Ex:(Every benzodiazepine), including alprazolam (Xanax), diazepam (valium)
Barbiturates Ex: amobarbital, phenobarbital, pentobarbital, , propofol, secobarbital
Cholesterol-lowering medications Ex: All statins – atorvastatin, fluvastatin, lovastatin, pravastatin, rosuvastatin (Crestor), simvastatin, cholestyramine, clofibrate (Atromid-S)
Cancer (chemotherapy) medications Ex: Mitomycin C, profiromycin, adriamycin
Diabetes medications Ex: metformin, Glucophage, troglitazone, rosiglitazone, buformin
HIV/AIDS medications Ex: (AZT, zidovudine)
Epilepsy/Seizure medications Ex: valproic acid (Depakene, depakote, divalproex sodium)
Mood stabilizers Ex: lithium
Parkinson’s disease medications
Vaccine Ingredients Ex: Mercury, aluminum, ethylene glycol
Dr. Russell Blaylock-Neurosurgeon “The Central Mechanism by which Vaccines Induce Autism
New: Vaccine patches to facilitate vaccination goals
What if a vaccine could be delivered by simply applying a patch? That’s Mark Prausnitz’s goal: creating a nickel-sized bandage-like device covered with 100 microscopic needles that would puncture the skin, then dissolve to get the vaccine into the body.
First up for a patch trial? The measles vaccine. Putting the vaccine in a patch eliminates the need for a medical professional and a refrigerator. “It would enable us to get the vaccine to a lot more people,” says Prausnitz. Read more…






