The Institute for BioFunctional Psychology

 

 

Detoxification, Neurotransmitter Balancing, Nutritional Restoration and Stress Reduction to Prepare Your BRAIN for the PsychoSpiritual Journey

Why Zebras Ain’t Nuts[1]

Neurotransmitters of Past and Future

Anger, Trauma and Fear, and the “Power of Now[2]

Copyright Charles Gant  MD, PhD © June, 2008

 

The Problem

  Our human brain provides us with amazing tool for survival and technology building. It permits us to observe, with astounding clarity, causal relationships between antecedent events and those of the future, culminating in forecasting faculties which are at the root of knowledge acquisition and the scientific age. Anthropologists estimate that the human brain is over 6 times as large as it “should be” compared to our mammal cousins[3] (see graph at end).  The term for this “braininess index” is called the EQ or Encephalization Quotient, which is calculated based on body mass and brain size. In other words, both a tiny shrew and an enormous elephant both have EQs of approximately 1, which is expected for just about all mammals.  The graph below fills in the time between Homo Sapiens (including Neanderthalis) and our distant mammal cousins by plotting the EQs versus the log of time. Fossil evidence clearly suggests that our hominid ancestors gradually increased their EQs over the last 10 to 20 million years.

  The enormous human brain is not only a powerful tool. It is capable of astonishing genius and creativity. Gifted humans have used this tool to compose symphonies, invent microcomputers, comprehend the implications of a 15 billion-year-old cosmos and write poetry and literature.  But like most powerful tools, the human brain must be used with discretion, because if it is applied to tasks beyond its design features, untoward consequences can result.  In the United States and probably elsewhere[4], over 25% of the population (over 75 million people in the USA), suffer from a DSM IV[5] diagnosable mental disorder.  Is there a relationship between a misuse of our large, powerful brains and the apparent unique human propensity to misuse this tool and suffer from mental disorders? 

  Our mammalian cousins and all animal and non-human species have Encephalization Quotients which are only a fraction of ours and they seem far less vulnerable to mental illnesses and addictions than human beings.  Perhaps they may be spared the consequences of mental disorders because their nervous systems are not as capable of analyzing, memorizing, and ruminating over causal relationships of antecedent events, to those of the future with great clarity and imaginative embellishment.  If so, such misapplication of our powerful tool, our human brain, may be a critical way of understanding why humans have an apparent greater vulnerability to developing mental disorders and to incurring psychological suffering. 

  From a psychological perspective, the down side of our amazing tool for genius, creativity and survival and technology building, may be that we can't seem to easily turn the tool off when it has completed its tasks and is no longer required.  Thus, big brains can be double-edged swords, with a negative potential of being obsessional[6], perpetually replaying the fears of the future and the traumas and resentments of the past, and an apparent vulnerability to compulsively[7] act on them.  This tool can then turn into a weapon of self-destruction, like a chain saw with all the safety features removed.  Perhaps this is an important causal factor behind the suffering of over 25% of Americans, those who have a diagnosable mental disorder. Their (our) powerful tool, the human brain, may have no obvious “off switch,” and like a chain saw, it may have the potential to cut the human psyche into “dissociative” fragments.

  How could our powerful and most precious tool also be our undoing?  Perhaps some answers may be discovered in an historical context - not in the infinitesimal span of recorded human history such as racial or ethnic histories - but far beyond this into deeper “roots,” our mammalian and pre-mammalian ancestry[8]. We have inherited an ancient “paleomammalian” emotional brain[9] and a reptilian brain from which the “fight-or-flight response[10],” also called the fright, fight or flight response, a hyperarousal or the acute stress response, is generated.  We share this evolutionary baggage with our mammal cousins.  Specifically, the locus ceruleus, located within the dorsal wall of the rostral pons in the lateral floor of the fourth ventricle is the principal site for synthesis of norepinephrine, the primary neurotransmitter which invokes the fight (anger) and flight (fear) response.  It was designed into our brains as a crisis survival tool and it has genetically been passed down through the ages to us. 

  Being primitive, the fight or flight part of our nervous system is rather “stupid.” It appears to be somewhat incapable of distinguishing between a real event happening “in the now” from a fictional or fantasized, past-future event invented or embellished by our recently-evolved, and far more creative cerebral cortex.  The ancient fight- or flight-generating locus ceruleus can be activated by thoughts and pictures about the past and future “as if” such events were actually happening.  It seems to be incapable of distinguishing an actual crisis in the present from an imaginary crisis which happened in the past or might happen in the future.  Thus, a perceived, “life-threatening” event caused by a harsh letter from an Internal Revenue Service agent can provoke a reaction from the locus ceruleus “as if” a true perilous event were actually happening.  Or, by simply imagining a financial crisis, even though it was not actually occurring, cascading signaling to the locus ceruleus could provoke its norepinephrine surge generating a fight or flight response “as if” ones survival were threatened.

  Our creative, huge brains allow imagination, which is capable of perpetually inventing, replaying and embellishing a past or a future crisis, real or imaginary. This explains in part our apparent far greater capacity for being and acting neurotic[11] or even psychotic, than any of our mammalian cousins.  Zebras, lacking a human’s creative memory or foresight, are less capable of such imaginary embellishments.  In other words, Zebras would be less likely to carry grudges about a lion’s assault for years on end (resentment) or suffer interminable panic attacks about fantasized impending attacks.  Zebras deal with fight or flight, a response that should last 15 to 30 minutes, and as a consequence they are a meal for a predator or not.  Our animals cousins live more in the present or “the now.”  But like our mammalian relatives, we have inherited their/our “paleomammalian” fight or flight nervous system which is designed to fight with anger to defend against an immediate threat from an immediate “past” (e.g., a competitor is observed stealing our food), or run in fear from an immediate threat due to an immediate “future” possibility (e.g., a predator shows up intending to convert us into a meal).  Our large digital[12], “neomammalian” brains are plunked on top of the older analogue[13] paleomammalian, emotional brain, perhaps cursing us with an amazing ability to run and rerun memories of old traumas and dream up creative, perpetual ruminations about awful outcomes, driving our older, emotional, autonomic nervous system into “chronic stress” or so-called “burnout.”

  For instance, if a zebra[14] is confronted by a lion, it has roughly 15 to 30 minutes to either angrily fight off a threatening young lion by giving it a good kick or two, or fearfully run away.  That’s the extent of it - the Zebra gets away or it is dinner for the lion.  Zebra’s don’t carry around the burden of huge, human, cerebral cortices, which have enormous memory capacity, imagination and extraordinary foresight, so they do not have the required intellectual hardware to spend several years replaying old traumas or fantasizing far more terrible encounters, over and over, stressing their old, emotional brain 18 hours a day with imagery that is not even happening.  Zebras don’t have the “marbles” to run a continuous “trauma drama,” so they don’t need medication, alcohol or drugs to anesthetize the replay of the past or the anxious fantasies of awful, possible futures. For Zebras, emotional stress is over in 15-30 minutes one way or the other, and that’s it.

 

The Solution

  If our big brained condition is an important factor in causing human emotional suffering, how do we deal with it?  Is it possible to use our prodigious memory, imagination and foresight appropriately and then turn it off?  If we can put a simple tool like a hammer back in the toolbox when we are finished with it, why does it seem so problematic to put our main tool, the human brain, away when we have completed the tasks that it was needed for? 

  The main question is pointedly, are safety features built into our powerful and useful tool, our brains, which can prevent the “chain saw” injuries derived from an apparent inability to turn it off when we are done with it?  Mainstream, modern psychiatry and medicine would answer this question with a definitive no.  From this position, that no inherent safety mechanisms or “off switches” are built into the human brain, the only remaining recourse, if the brain is running out of control, is to selectively injure it with surgery[15] (cutting), electroconvulsive therapy or ECT[16] (burning) or psychopharmacological medication (poisoning).  This “cut, burn and poison” approach, espoused by most conventional medial and psychiatric practitioners, may be a valid, last resort option for those suffering from a hopelessly malfunctioning, overactive brain which is perpetually replaying its past traumas or projecting its future fears.  However, an enormous body of information derived from highly divergent areas of investigation, both scientific and experiential, strongly suggests that “off switches” do indeed exist and can be readily accessed for most adults.    

  In fact, structures in the brain and other neurotransmitters systems besides norepinephrine have been found through various lines of research to be designed to activate “the safety features on the chain saw,” and many peer-reviewed, mainstream psychiatry, published studies[17] are now widely available to support this notion.  Subjects engaged in various psychospiritual practices, which have been shown since ancient times to assist in the extrication from the pain and suffering derived from a preoccupation with ones past (resentments and PTSD) and future (fear/anxiety), have been shown under controlled laboratory testing to possess structures and chemistry built into the very structure and physiology of the human brain, which indeed appear to be designed to keep us in the “now.”  Since for millions of years we have profited from the survival benefit of increasingly enlarging brains, permitting us to make tools for killing and capable of ever-improving methods of defense and warfare, having he neurological hardware to subdue aggression could arguably be a survival benefit also.  And if we do have safety features built into our brain which can prevent “chain saw” injuries, then it would behoove us to make the information about enhancing them widely available as first resort interventions for chronic stress and resultant mental disorders.  Thus the potentially dangerous “cut, burn and poison” strategies of conventional medicine and psychiatry should be reserved as last resort options for those who can’t, won’t or choose not to apply safer, first resort options. 

  These “safety features” appear to be somewhat dormant in most people, and various psychotherapies, spiritual practices, prayer, contemplative and meditation “techniques,” in one way or another, attempt to activate them.  Resentments or traumas from past experiences or fear of potentially awful outcomes, when perpetually replayed like a broken record, generates chronic stress “as if” these events were actually happening in the present, and pushes the “fight or flight response” to remain active far beyond the 15 to 30 minutes it was designed to be operating.  I am postulating that this is one primary mechanism and perhaps the main one, in the generation of the symptoms of most mental disorders.  Various psychospiritual practices have been shown in the studies referenced above to awaken innate mechanisms in the brain which extricate the mind from an obsession with the suffering derived from a preoccupation with an illusory past and future and bring its focus into the stress-reducing, reality of the “here and now.”     

  Like it or not we are living a series of “now moments,” but our large brains, designed to process past and future events in lurid detail, unfortunately have a tendency to over-process such information as if by doing so we can control and somehow change the unchangeable past.  We also project imagery about fantasized futures which could be awful and terrible (AKA “awfulizing and catastrophizing”), as if by doing so we can totally control the future and avoid all mistakes. If we were gods or God, perhaps we could time travel and change the past, or perfectionistically predict and avoid all future problems. But this belief in one’s deity-like powers, also know as Hubris (Godly arrogance - common theme in Greek tragedy plays), poses enormous challenges in the human experience.  Such tragedies are played out every day in the lives of most human beings to some extent, and excessively in over 25% of Americans who would quality symptomatically for a DSM IV diagnosis.

   The more we deny the “actuality” of the present and instead preoccupy ourselves with the imaginary past and future, as if by doing so we can improve our survival, the more we tend to suffer.  The more we stay in “The Now” and simply deal with our mortal, fallible lives one day at a time, or even one moment at a time, the less mental suffering we seem to incur. Actually this improves our survival, because the norepinephrine-driven chronic fight or flight is at the root of a wide array of medical disorders, including hypertension, heart arrhythmias, and many other disorders.  We do indeed have an innate but often dormant capacity which is built into the structure and chemistry of our brains which is designed to help us “let go” of the past and future, and “surrender to,” “turn over” and accept that the present moment has just about everything we need to survive.  This seems to be a simple, basic fact of human existence.

  Modern psychology and psychiatry have devised various strategies to deal with this human angst derived from having big brains.  Many psychotherapeutic methods are helpful in guiding people back to the reality of their lives where emotional pain lessens, away from a rehashing of a past which is over, and away from a future which we have little control of, and back to the here and now which we can do something about.

  Unfortunately, another ever-more-popular method promoted by psychiatry and the mental health fields, perhaps stemming from a denial or ignorance that most individuals already possess perfectly operational equipment to solve psychic pain, has been to invent diagnostic labels and diseases for the symptoms which come from a preoccupation with the past and future trauma-dramas, and then to anesthetize the brain with drugs to numb the emotional pain.  But such an approach, by anaesthetizing many regions of the brain, also lessens the ability to “awaken” the very innate brain structures and physiologies which are designed to extricate us from emotion pain, and brain imagery studies even suggest that the frontal lobes, the area most involved with awareness, seems to be the most vulnerable to such chemical manipulation. As fear of the future and/or resentment/PTSD of the past becomes progressively numbed by psychotropic drugs, and/or the origin of the pain, the inexhaustible human memory or foresight which replays the “trauma-drama movie” becomes anaesthetized, the naïve user of psychotropic drugs appreciates a lessening of emotional pain. Many are tricked into assuming that something beneficial has happened, and this is the mechanism which leads many into addiction to alcohol, illicit substances and prescription drugs.

  But unbeknownst to drug users, they simultaneously become increasingly incapable of activating the dormant, hard-wired resources in the brain which could have helped to bring them back to the “now” and which could have been their ultimate salvation.  Active addicts move farther and farther away from “living one day at a time,” a famous AA saying.  And as an increasing percentage of humanity appears to have become mesmerized by this psychopharmacological trap, and as their intellectual capacity to even understand the deception is also “dumbed down,” their attempts to benefit from authentically healing psychospiritual interventions are thwarted, and they are driven into the conclusion that drugs are their only answer for “hopeless” mental suffering. 

  As discussed above, the rationale for prescribing psychotropic drugs, is a false assumption that most individuals don’t have the neurological equipment to come to terms with their existential dilemmas and to extricate themselves from the suffering derived from a preoccupation with an illusory past or future.  We no longer hear or read much about so-called “existential psychiatry,” the radical notion that human beings exist freely now and have the capacity to choose what to do now with their lives today, however alone or emotionally distraught we find ourselves to be. Therefore, the only option available for humans who are incapable of “seizing the day” is to anaesthetize themselves with psychotropic chemicals, which numb the painful, unresolved memories or the awfulizing fantasies, as well as the consequent autonomic, emotional responses, especially fear, anger, boredom and PTSD symptoms.  This is certainly a valid approach for individuals who are brain damaged by severe trauma or dementia, or for those who may be hopelessly enmeshed in severe mental illnesses, in which case their entire life is cast as a replay of past and future scenarios and they do not seem to have the capacity to bring themselves back to reality, the present moment. 

  But those who have such severe problems are a relatively small portion of humanity, and to anaesthetize the brains of human beings with drugs who are playing with “full decks” on a mass scale as is now being done, mostly for drug profits, is in my opinion counterproductive and appalling.  The very structures of the brain, especially the dormant frontal lobes, which must be activated in order to fully extricate oneself from the pain-laden past and future, and to appreciate the “Power of Now[18],” are especially vulnerable to damage from psychotropic drugs.  This catch 22, or psychic double bind, damned if you do take drugs, damned if you don’t (because authentically, healing psychotherapy or meditation training is generally not offered as a treatment option), is the dilemma now faced by 10s of millions of Americans, and many more throughout the world.

  Let’s reconsider a possible solution from a bio/psycho/social/spiritual[19] perspective.  If an awakening of dormant structures in the human brain, designed to extricate us from the delusions of our past and future, is indeed possible, it behooves us to make use of them in ourselves and to share our experiences with others so that they too can benefit.  Many excellent self-help methods are available in this regard, and understandably they discourage psychopharmacology[20] and drug addiction.  However, the vast majority of such self-help methods promote only psychosocial and psychospiritual methods of extrication from the suffering of a preoccupation with the past and future.  Few methodologies address the biological and molecular dimensions of this problem, even though the “accepted standard of care” in psychiatry and modern medicine is molecular or psychopharmacological. 

  For instance, Dr. Peter Breggin[21] and many other authors, attempting to expose the fraud of psychiatry and the menace of psychopharmacology, essentially deny that there is any physical or biological answer at all.  Their position, while laudatory, takes a position that amassed scientific evidence about a molecular basis for brain function somehow does not exist!  They essentially deny that the brain is a physical organ, which like all organs of the body are dependent on proper nutrients, are potentially injured by a wide array of toxins and are regulated by optimal hormone and neurotransmitter functioning.  Somehow, nutritional restoration, detoxification and neurotransmitter balancing are seen to have nothing to do with the health and function of the brain.

  Nutritional restoration, detoxification and neurotransmitter balancing have not only been proven by amassed scientific studies to be a predominant issue in the health and function of the brain, they also have direct relevance to the whole issue of extrication from emotional pain stemming from the big-brained, human’s tendency to be preoccupied with an imaginary past and future. At least eight primary neurotransmitter systems (see table at end of article) are key players in this regard, and they are absolutely critical physiological components to the awakening process of the dormant brain physiology which has been shown to be activated by psychospiritual interventions (see above references). In various ways, they downregulate the excessive norepinephrine associated with chronic stress.  These eight neurotransmitters play critical roles in helping to extricate the mind from an illusory, painful past and future.  Optimal functioning of these neurotransmitter systems thus provides us with important therapeutic options as indicated in the table below. 

  The neurotransmitter systems are dopamine, serotonin, GABA, endocannabinoids, histidine, taurine, acetylcholine and enkephalins.  Conversely, deficiencies in these neurotransmitters, induced by psychotropic drugs (illicit, prescribed or recreational), nutritional deficiencies, toxicities, genetic vulnerabilities or other factors, will tend to thwart the downregulation of noradrenaline which can keep the mind “stuck” in the imaginary fight (past anger) and flight (future fear) response.  The benefits of psychospiritual interventions can also be thwarted by deficiencies in the fight- or flight-calming neurotransmitters. These eight neurotransmitters seem to be designed to ameliorate emotional pain (coping) by either playing an inhibitory role to lessen the impact of a preoccupation with the past or future, or to augment an experience of the “here and now” by enhancing joy and pleasure (for bonding) reward pathways.  The table below charts these neurotransmitter systems, their neuronal and temporal effects, the symptoms or disorders related to their deficiencies, and the nutritional interventions.

  Other neurotransmitter/hormonal systems, such as glutamate, glycine, aspartate and cortisol can modify the fight or flight norepinephrine stress effects, and both pharmaceutical and nutraceutical interventions have been devised to address them.  Glutamate excess and cortisol deficiency can both mimic the symptoms of a GABA deficiency, and in fact glutamate (excitatory) is converted into GABA (inhibitory) requiring the cofactor B6.  Noradrenaline stimulates ACTH which increases cortisol secretion by the adrenals and chronic stress can lead to imbalanced cortisol levels.

 

Business Concerns

  The alcohol, tobacco, illicit and pharmacological drug industries are enormously profitable because they have successfully hoodwinked both healthcare consumers and providers into a false premise, that toxic substances are beneficial because they temporarily alleviate emotional pain.  Drugs accomplish this by anaesthetizing the brain’s cognitive and emotional centers which are preoccupied with a past and future, thus artificially and temporarily alleviating the symptoms of chronic stress.  Most seasoned psychotherapists, meditation teachers and authentic healers have observed that such users and abusers of drugs are relatively incapable of benefiting from the psychospiritual interventions which they provide.   

  In a free enterprise economic system, maintaining illness while simultaneously controlling symptoms is profitable, especially when consumers can be duped into believing that anaesthetizing pain and stress is tantamount to healing.  Can the truth about human suffering be heard above the TV advertisements and peer pressure? Is it possible to capitalize on the truth and provide authentic healing for the number one disability in the world, mental disorders?  Certainly, information technology (IT) has undermined the attempts to hide such truth from consumers, and if economically successful ventures dedicated to providing the truth about human suffering on a widespread level are to be discovered, IT is likely to be at its core.  Such strategies would focus on two very different markets, healthcare professionals and healthcare consumers.    



[1] This article borrows some of the basic logic from in the bestseller, “Why Zebras don’t get Ulcers” by Robert M. Sapolsky.

[2] The Power of Now: A Guide to Spiritual Enlightenment is a book by spiritual author Eckhart Tolle. It was first published in 1999. It has been on the New York Times Best Seller list and has grown in popularity since Oprah Winfrey recommended it for her book club. It has been subsequently translated in 33 languages. The book is a spiritually focused self help book that is of no specific religious denomination. The book begins with Eckhart recalling his initial transformative experience in 1980. The book covers topics including personal and collective forms of the ego and the emotional "pain body".

 The book teaches that, while our use of time has a practical aspect, most people are lost in time and are only peripherally aware of the present moment, or the "Now".[3] In doing so, we make the present moment a means to an end for future fulfillment, and we become what Tolle calls unconscious. In this unconscious mind-state, we are easily controlled, live in fear, and manifest other egoic behaviors. He explains that to the ego, this future is going to save us (retirement, graduation, job promotion, etc), and that it will inevitably kill us. This paradox of how we view time adds to our anxieties and fears.

[3] From The Ancestor’s Tale (2004) by Richard Dawkins, Houghton Mifflin Co., NY, p. 84.

 

[4] I suppose.

[5] Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision, also known as DSM-IV-TR, is a manual published by the American Psychiatric Association (APA) that includes all currently recognized mental health disorders. The coding system utilized by the DSM-IV is designed to correspond with codes from the International Classification of Diseases, commonly referred to as the ICD.

[6] An obsession is a persistent disturbing preoccupation with an often unreasonable idea or feeling.

[7] A compulsion is a seemingly irresistible impulse to perform an irrational act.

[8] For those who, on theological grounds, deny that we evolved from more primitive life-forms, I would ask, “Why would God be such a trickster and fake DNA, fossil, radioactive dating and other evidence?”

[9] Actually, it’s the older segment of the paleomammalian brain which is responsible for the “fight of flight response.”  The newer parts of the “old-mammal” brain include structures involved with tenderness, carressiveness and play, as anyone who loves their pets can observe.  See the triune brain, a model proposed by Dr. Paul D. MacLean, which explains the function of traces of evolution existing in the structure of the human brain, and is supported by many thousands of scientific references. In this model, the brain is broken down into three separate brains that have their own special intelligence, subjectivity, sense of time and space, and memory. The triune brain consists of the R-complex (reptilian), the paleomammalian limbic system, and the neomammalian neocortex.

[10] Gleitman, Henry; Alan J. Fridlund, Daniel Reisberg (2004). Psychology, 6, NY: Norton.

[11] Neurosis, also known as psychoneurosis or neurotic disorder, is a "catch all" term that refers to any mental imbalance that causes distress, but, unlike a psychosis or some personality disorders, does not prevent or affect rational thought.

[12] A digital system uses discrete (that is, discontinuous) values to represent information for input, processing, transmission, storage, etc. By contrast, non-digital, or analog, system uses a continuous range of values to represent information.  For example, a CD uses digital technology and the older plastic records used an analogue technology.  The neomammalian brain is analogously digital, using “on-off” rapid fire neurotransmitters such as GABA and glutamate, with mechanisms of action a hundred times faster than the older paleomammalian brain, which uses “sloshy” slow neurotransmitters.  One can appreciate the difference in meditation, by observing the rapid digital nature of thought, versus the slower to emerge and often very slow to fall away nature of emotions.

[13] Ibid.

[15] Actually the proper term is psychosurgery, a subset of neurosurgery (surgery of the brain) intended to modulate the performance of the brain, and thus effect changes in cognition, with the intent to treat or alleviate severe mental illness. It was originally thought that by severing the nerves that give power to ideas you would achieve the desirable result of a loss of affect and an emotional flattening which would diminish creativity and imagination; the idea being that those are the human characteristics that are disturbed. Historically, the procedure typically considered psychosurgery, prefrontal leukotomy is now almost universally shunned as inappropriate, due in part to the emergence of less-invasive or less-objectionable methods of treatment such as psychiatric medication [poisoning] and modified electroconvulsive therapy [burning]. In modern neurosurgery however, more minimally invasive techniques like gamma knife irradiation and foremost deep brain stimulation have arisen as novel tools for psychosurgery.

[16] Electroconvulsive therapy (ECT), also known as electroshock, is a controversial psychiatric treatment in which seizures are electrically induced in anesthetized patients for therapeutic effect. Today, ECT is most often used as a treatment for severe major depression which has not responded to other treatment, and is also used in the treatment of mania (often in bipolar disorder), catatonia, schizophrenia and other disorders. It was first introduced in the 1930s and gained widespread use as a form of treatment in the 1940s and 50s; today, an estimated 1 million people worldwide receive ECT every year, usually in a course of 6-12 treatments administered 2 or 3 times a week. Electroconvulsive therapy can differ in its application in three ways; electrode placement, length of time that the stimulus is given, and the property of the stimulus. The variance of these three forms of application have significant differences in both adverse side effects and positive outcomes.

[17] 1)  Richard J. Davidson, Katherine M. Putnam, Christine L. Larson, Dysfunction in the Neural Circuitry of Emotion Regulation--A Possible Prelude to Violence, Science, vol. 289, July 28, 2000, 591-594.

2)  Jacqueline Borg, Bengt Andrée,  Henrik Soderstrom, Lars Farde. The Serotonin System & Spiritual Experiences. Am J Psychiatry 160:1965-1969, Nov 2003.

3)  Chadi Calarge, et. al. Visualizing How One Brain Understands Another: A PET Study of Theory of Mind (TOM). Am J Psychiatry 160:1954-1964, November 2003.

4)  Davidson, R, et. al., Alterations in Brain and Immune Function Produced by Mindfulness Meditation, Psychosomatic Medicine, 65:564-570 (2003).

 

[18] The Power of Now: A Guide to Spiritual Enlightenment is a book by spiritual author Eckhart Tolle. It was first published in 1999. It has been on the New York Times Best Seller list and has grown in popularity since Oprah Winfrey recommended it for her book club. It has been subsequently translated in 33 languages. The book is a spiritually focused self help book that is of no specific religious denomination. The book begins with Eckhart recalling his initial transformative experience in 1980. The book covers topics including personal and collective forms of the ego and the emotional "pain body".

 The book teaches that, while our use of time has a practical aspect, most people are lost in time and are only peripherally aware of the present moment, or the "Now".[3] In doing so, we make the present moment a means to an end for future fulfillment, and we become what Tolle calls unconscious. In this unconscious mind-state, we are easily controlled, live in fear, and manifest other egoic behaviors. He explains that to the ego, this future is going to save us (retirement, graduation, job promotion, etc), and that it will inevitably kill us. This paradox of how we view time adds to our anxieties and fears.

[19] The biopsychosocial (BPS) model is a general model or approach that posits that biological, psychological (which entails thoughts, emotions, and behaviors), love and social factors (abbreviated "BPS") all play a significant role in human functioning in the context of disease or illness.  The "model" was theorized by psychiatrist George Engel at the University of Rochester, and putatively discussed in a 1977 article in Science (Engel, George L. "The need for a new medical model" 196:129–136, 1977). The general BPS model has guided formulation and testing of models within many professional fields.

[20] For instance, see the works of Peter R. Breggin, M.D., an American psychiatrist, best known as a leader of the reform movement in the field of psychiatry, psychology and mental health. In his many books, including Brain-Disabling Treatments in Psychiatry (2008), he advocates replacing psychiatry's reliance on drugs and electroshock with a humanistic, caring reliance on psychotherapy, education and broader human services. Professor of Psychology Bertram Karon of Michigan State University has called Dr. Breggin "the conscience of American Psychiatry."  Dr. Breggin is a critic of biological psychiatry and psychiatric medication, and the author of books such as Toxic Psychiatry, Talking Back to Prozac, Talking Back to Ritalin, The Ritalin Fact Book, and The Heart of Being Helpful. His most recent book, the second edition of Brain-Disabling Treatments in Psychiatry, presents extensive research on subjects such as the brain-disabling principle of psychiatric treatment, medication spellbinding, the adverse effects of drugs and electroshock (ECT), the hazards of diagnosing and medicating children, the psychopharmaceutical complex, and guidelines for psychotherapy and counseling.

[21] Ibid.

 

Neurotransmitter Family

Neuronal effects & source neurons

Temporal effects

Deficiency symptoms or disorders

Toximolecular,

pharmaceutical

analogue

Orthomolecular

(nutraceutical)

interventions

 

 

1)  Serotonin

 

Inhibitory

Raphe Nuclei

Inhibits NE release.

The Past

Mitigate anger  towards others -resentments & self-guilt/regret

Anxious, irritable depression, terminal insomnia, inability to “let go” of anger and resentment,

 

SSRIs (selective serotonin reuptake inhibitors)

Tryptophan or 5HTP, B3, B6, folic acid, iron, B12, biopterin, methionine, B5

 

 

2)  GABA

Inhibitory, Synthesized in Cerebral Cortex neurons. Inhibits NE effects.

The Future

Mitigate fear, worry and anxiety about the future

GAD, panic disorder, obsessive worry, awfulizing, catastrophizing, initial insomnia

 

Benzodiazepines, sedatives, sleeping pills, “downers,”

Glutamine, AKG, B6, B3, magnesium

GABA (a bioidentical hormone)

 

 

 

3)  Endorphins and Enkephalins

Inhibitory.  Widely distributed sources in brain stem and limbic regions of the brain, Inhibits NE release

The Past and Future Mitigate traumatic memories stored in body and brain, and worry of recurrence

PTSD symptoms hypervigalance, insomnia, muscle pain, hyperventilation, agitation, tachycardia, fever, dilated pupils, tremors, fasiculations,

 

Opioids (buprenorphine, methadone, morphine, demerol, oxycodone, heroin)

DLPA (enkephalinase inhibitor), leucine, methionine, glycine, d-phenylalanine, and tyrosine (enkephalin synthesis)

 

4)  Endocannabinoids

anandamide (AEA, arachidonoyl ethanolamide),

 2-AG[1], 2-AGE[2], NADA[3], OAE[4]

Postsynaptic neurons throughout CNS use retrograde signaling to inhibit presynaptic neurons (including noradrenaline)

The Past and Future

All stream of consciousness (past & future) inhibited

irritability, anger, depressed mood, headaches, restlessness, lack of appetite, and cravings

Marijuana (THC, Dronabinol, Marinol), Nabilone (Cesamet), Sativex synthetic cannabinoids, Rimonabant (Acomplia,antagonist)

Lecithin (purified, or granular - supplies phosphatidyl ethanolamine), borage oil, organic butter

 

 

 

5)  Acetylcholine

Inhibitory of norepinephrine and dopamine.

Basal optic nucleus of Meynert and medial septal nucleus

The Present

Inhibit dopamine’s potential for unrestrained delusional, paranoid content

By enhancing “reality based” memory, consciousness is “grounded” in the Now, the mundane bare essence of experience

Aricept and other Alzheimer drugs which inhibit acetylcholin-          esterase, same mechanism as  nerve gases, pesticides

Lecithin, purified, or granular - supplies phosphatidyl choline – precursor for acetylcholine

 

 

6)  Dopamine

Excitatory, Substantia Nigra.  “Steals” tyrosine precursor to downregulate NE synthesis

The Present

Enhance joy & pleasure of The NOW, especially the mundane

Anhedonic depression, RDS (reward deficiency syndrome), self-pity, boredom, risk-taking behaviors

Amphetamine-like drugs (stimulants), methamphetamine, Ritalin, Adderall, Concerta

Tyrosine, Phenylalanine, B3, B6, folic acid, iron, biopterin, B12, methionine, copper, vit. C

 

 

 

7)  Taurine

Inhibitory, widely distributed in CNS probably secreted by microglia as neuromodulator.  Effects similar to GABA.  Transports magnesium across cell membranes.  Inhibits NE effects.

 

 

The Future

Mitigate fear, worry and anxiety about the future

GAD, panic disorder, obsessive worry, awfulizing, catastrophizing, initial insomnia.

Also magnesium deficiency symptoms, arrhythmias, headaches, muscle cramps, PMS

 

 

Benzodiazepines, sedatives, sleeping pills, “downers,” Muscle relaxants

Exists in diet and can be supplemented or as magnesium taurate, synthesized from methionine and cysteine requiring B6.  Sulfur amino acid

 

 

8)  Histamine

Alertness. Wake-sleep cycles.  Oppose NE release

Tuberomammillary nuclei.

The Present

Alertness.  But excess causes insomnia,  pituitary dysreg.

 

Fatigue, inattentiveness, arthralgias

 

Antihistamines if high histamine

Histidine & B6 to synthesize if low, SAMe (? histamine N-methyltransferase) if  histamine is high



[1] 2-AG is an abbreviation for the endocannabinoid 2-arachidonoyl glycerol

[2] 2-AGE is an abbreviation for the endocannabinoid 2-arachidonyl glyceryl ether (noladin ether)

[3] NADA is an abbreviation for the endocannabinoid N-arachidonoyl-dopamine

[4] OAE is an abbreviation for the endocannabinoid O-arachidonoyl-ethanolamine (Virodhamine)

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