The Psychedelic Brain
Psychoactive drugs have gained widespread popularity over the years. Growing acceptance has occurred amongst the young with in the urban and suburban societies. In fact, colleges and high schools appear to be breeding grounds for this growing substance abuse. The most popular of such drugs is marijuana as it is regarded as the least harmful and least costly of the psychoactive drugs. Therefore, this lack of cost restriction for marijuana implies easier access amongst the lower class in comparison to other stronger hallucinogens such as lysergic acid diethylamide. This widespread popularity is evident by the observation that millions of Americans have once tried marijuana. While other drugs do not maintain the same pervasive reputation, their usage remains pertinent. For example, Dr. Timothy Leary claims that there were one hundred thousand regular LSD users, one single experience. It is hypothesized that the increase in interest and usage of the internet and World Wide Web along with a heightened rave and trance culture based in an interest of exploring the conscious and unconscious mind has greatly contributed to this problematic drug growth. As a result, the effects of such drugs have become of increasing concern for such chemicals are foreign to the body and produce detrimental effects.
The nervous system in particular is greatly impacted by psychoactive drugs. In turn, such boasts drastic implications as the nervous system is responsible for relaying messages back and forth within the body. This complex system consists of the central nervous system and the peripheral nervous systems, the central nervous system is the larger of the two and is comprised of the brain and spinal cord. The main function of the central nervous system is to receive information from the body and send out instructions, whereas the peripheral nervous system sends messages from the brain to the remai nder of the body both indicative of the input/output mechanism. Therefore, as the brain is related to behavior, such is implicative of the relationship between the central nervous system and brain and behavior.
One such mechanism which affects behavior is drugs. Specifically, psychoactive drugs, chemicals that act in the central nervous system, infringe upon the function of the brain. These brain complications include ones related to perception, consciousness, thought, emotions, mood, and behavior. Clearly, psychoactive drugs induce differing effects on the body depending upon classification. These drugs are commonly subdivided into four categories: antipsychotics, depressants, stimulants and hallucinogens, of which hallucinogens are further divided into psychedelics, dissociatives, and deliriants. Deliriants are defined as substances which cause a temporary state of mental confusion and fluctuating consciousness by anxiety, disorientation, hallucinations, delusions and incoherent speech. Dissociatives are drugs which reduce, or block, signals to the conscious mind from other parts of the brain, typically, but not necessarily, limited to the physical senses. Lastly, psychedelics are psychoactive drugs whose primary action is to alter the thought processes of the brain. Thus, many of the widely used illegal drugs can be placed into one of the three categories. For example, phenylcyclohexylpiperidine, ketamine, dextromethorphan, nitrous oxide, salvia divinorum, and muscimol are all dissociatives. In comparison, deadly nightshade, mandrake, henbane, antihistamine diphenhydramine, antiemetic dimenhydrinate, and datura are known as deliriants.
Such varying drug classifications withi n the hallucinogenic psychoactive drugs infer differences amongst their individual effects. Primarily, deliriants are considered true hallucinogens th nonexistent people. Therefore, the hallucinogenic quality of deliriants initiates immediate effects such as sleepwalking, for the abuser is unable to recall their experience after taking the substance. Deliriants such as diphenhydramine exhibit direct effects on the central nervous system as they are classified as anticholinergic agents, and thus reduce the affects of ac etylcholine in the nervous system. An example of acetylcholine function lies in synaptic plasticity. Common central nervous system malfunctioning includes agitation, respiratory depression, short-term memory loss, incoherent speech, photophobia, unusual sensitivity to stimuli, inability to sustain a train of thought, etc. An overdose of a deliriant causes additional side effects including dehydration and mydriasis, while the most severe outcome of this drug is death due to its high level of toxicity.
Similarly, while deliriants appear to lead to a loss of consciousness , dissociatives induce conscious dreaming, more commonly known as lucid dreaming, elicit states of mind due to sensory deprivation. Dissociatives also play a unique role as a central nervous system depressant lowering ones heart rate and/or respiration and oxygen intake, ultimately causing death. Specific long term use of dissociatives, such as ketamine and phenylcyclohexylpiperidine, has even been claimed to induce Olneys lesions known as NMDA Receptor Antagonist Neurotoxicity, a form of brain damage. Such damage pertains to the vacuoles in the posterior cingulated cortex and retrosplenial cortex of the brain and causes an increase in microglia and heat-shock protein 70 concentrations. Other damages to the brain include hypertension, a toxic acute brain syndrome manifested by disorientation of consciousness and convulsions. Thus, overdosing on deliriants and dissociatives is extremely caustic, while overdosing on psychedelics is extremely rare due to the non-toxicity quality of these drugs.
Common psychedelic hallucinogens include lysergic acid diethylamide (LSD), psilocybin, mescaline, dimethyltryptamine, 4-methyl-2,5-dimethoxyamphetamine, San Pedro cactus, peyote, and even cannabis. Their effects are extremely dependent upon the actual drug, the dosage, and the environment as they disable filters of the mind. Such effects range from distortions of a single sense such as auditory hallucinations, to effects on cognition, to empathogenic emotional and social effects. However, one common property, especially amongst perception-altering psychedelics, is the ability to act on the 5HT-2A receptor, a serotonin receptor of the brain.
Lysergic acid diethylamide is a primal example of a psychedelic drug associated with serotonin activity in the brain. The specific effects of LSD usage include impaired intellectual ability, lowered IQ, an inability to concentrate, breakdown of ego functioning, and feelings characterized by emptiness, loneliness an d isolation. Such is also characteristic of schizophrenia, and thus has alluded to similarities between LSD and the mental disorder, ultimately proposing the hypothesis that LSD has the ability to cause schizophrenia. With such, the relationship between LSD and the brain is essential in understanding the chemical's mechanisms. Specifically, the drug is often considered to inhibit the production of serotonin in brain cells - a monoamine neurotransmitter synthesized in serotonergic neurons in the central nervous system associated with perception and memory. Further evidence supporting such a relationship includes the data that illustrates that drugs which stimulate serotonin production directly impede on the effects of the psychedelic. Therefore, it can be hypothesized that LSD interacts with the 5-hydroxytryptamine (serotonin) receptors in the brain, ultimately lowering the concentrations of brain serotonin. Research indicated that lysergic acid diethylamine reduced the turnover rate of brain 5-hydroxytryptamine in rats rate of discharge of raphe nuclei neurons located in the area of reticular formation containing most of the serotonergic cell bodies. In addition, LSD antagonizes the potentiating action of reserpine, which is the chemical typically involved with releasing large amounts of serotonin. Therefore, it is evident that lysergic acid diethylamine essentially lowers the levels of serotonin in the brain through various functions.
Overall, hallucinogenic drugs are directly involved with the central nervous system, directly involved with the input and output system. Therefore, the psychoactive drugs' relationship with neurons in turn indicates their ability to induce permanent damage. It has even been shown that psychedelic substances cause chromosome breakage, which not only affects the user, but ultimately affects and unborn child. In order to preserve a healthy brain, a healthy nervous system and healthy children, psychoactive drugs need to be avoided. However, ceasing usage of the drugs d oes not include halting research regarding the numerous drugs. The relationship that exists between substances and the brain including the neurons of the nervous system, can be advantageously exploited. If we are able to better understand the mechanisms behind these drugs and their hallucinogenic effects, their effect on the brain, advancements could be made. As such, could gain the ability to understand the role of the unconscious, and more importantly, better our understanding of neuronal functioning, which in turn could lead to various cures and promote health.
Bibliography
[ed. note: Bibliography/ End Notes was damaged in backup /restore operation. Will be re-built.]
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I HOPE ALEX READS THIS! really
I HOPE ALEX READS THIS!
I quote all of you wonderful people for truth.
I was going to pick it apart further, there are a few areas, but that's basically good enough.
It's really too vague, contrived, and flat out pseudoscience, , BS and rehashing of words, for me to waste my time picking apart further. there would have to be some truth there, you might as well toss this whole article. I intend no offense to you Alex.
your communication also could use some improvement, you build up with all these words, but they are not in a commonly used context. it's even worse when the logic is fallacious and misplaced.
You'd be better off studying mystical experiences, in which you don't have this bias. however you may have another bias, or several. we all have our subjectivities, to the supposed objectivity.
"Other damages to the brain
"Other damages to the brain include hypertension, a toxic acute brain syndrome manifested by disorientation of consciousness and convulsions."
hypertension - "a. elevation of the blood pressure, esp. the diastolic pressure.
b. an arterial disease characterized by this condition" (Dictionary.com)
Here, you take the liberty of creating your own "toxic acute brain syndromes;" in reality, hypertension is simply raised blood pressure. This does result (usually insignificantly, except in the case of overdose) from MDMA usage, but the opposite actually results from Cannabis use (the blood pressure is lowered). The picture is more obscure in the case of your true psychedelics - LSD, Psilocin, and Mescaline, etc. - but there is no way that any increase in blood pressure from use of these drugs amounts to any brain damage...(as far as I am aware, the only brain damage that could be done would be caused by a stroke!) Hypertension = a "toxic acute brain sydrome"? Come on, this is offensive!
Also, you misidentify your drug pharmacology: "Common psychedelic hallucinogens include lysergic acid diethylamide (LSD), psilocybin, mescaline, dimethyltryptamine, 4-methyl-2,5-dimethoxyamphetamine, San Pedro cactus, peyote, and even cannabis...However, one common property, especially amongst perception-altering psychedelics, is the ability to act on the 5HT-2A receptor, a serotonin receptor of the brain." You may not be aware, but MDMA's action on the brain is very different and incomparable to both cannabis or the true psychedelics mentioned above. MDMA results in a massive release of serotonin into the synapses, while at the same time, it acts as a SSRI (serotonin reuptake inhibitor). As far as I know (and I am quite sure), MDMA has no specific effects on the 5-HT2a receptor, which is consequently why MDMA produces no actual visuals or hallucinations in the same sense that LSD, Psilo., or Mescal. do. You should also research the pharmacology of THC (cannabis) because it certainly doesn't produce its effects through the 5-HT2a receptor.
All in all, I found this article to be quite offensive. As anonymous above said, it seemed clearly biased towards the anti-drug side. It's factual validity is highly disputable in many places, and it is absolutely incorrect in others.
Amen to that
After extensive readings of authors such as Stanislav Grof and John C. Lily (amongst many others) I can also back up what anonymous said above. The original article is biased and fraught with supercilious statements which indicate a rather ill considered and unbalanced view of entheogens.
Please take the time to consider the inreasingly available literature on the topic from credible scientists and anthropological academics alike who have backed up the more holistic view of psychoactive substances using cross-cultural and cross-temporal evidence.
Thanks
Your article is fraught with
The psychotomimmetic model of LSD and mescaline "Model Schizophrenia" was abandoned in the late 1950s when researchers like Humphry Osmond, Abraham Hoffer and Sidney Cohen discovered the importance of Set and Setting when using hallucinogens. The idea proper hallucinogens mimic schizophrenia was the result of researchers putting subjects in sterile white rooms and telling them they were going to be temporarily insane, thus shaping expectation and setting.
The idea that LSD can cause schizophrenia has also been debunked knowledge that many people who became schizophrenic after LSD use already had a heritable liklihood of the disease or exhibited symptoms. The concensus today is that LSD can trigger latent schizophrenia in persons who were most likely going to develop it anyway.
As for your comments about chromosome breakage and LSD, these claims have been discredited since the late 1960s. http://www.sciencemag.org/cgi/content/abstract/172/3982/431
Additionally, no researcher has ever produced concrete evidence of organic brain damage as the result of hallucinogen use. In the 50s and 60s LSD was administered to tens of thousands of people without a single record brain or nervous system damage. In fact recently Dr. John Halpern of the Harvard School of medicine showed that Native Americans who had consumed peyote more than 100 times showed no cognitive deficits, and were in fact, better psychologically adjusted than non-peyote users.http://www.researchmatters.harvard.edu/story.php?article_id=966
Lastly I have to add, if it wasn't obvious by the lack of factual accountability in your article your extreme and unscientific bias against hallucinogens is patently obvious when you state only the negative effects and then generalize them as if they were typical. This is like saying the effects of Prozac are nausea, dizziness, decreased sex drive and drowsiness. Why would anyone take it? You write "The specific effects of LSD usage include impaired intellectual ability, lowered IQ, an inability to concentrate, breakdown of ego functioning, and feelings characterized by emptiness, loneliness an d isolation" Are you speaking of accute effects, long term effects? If LSD is so horrible, you would have to question why anyone would be motivated to take it all? If hallucinogen use is a frightening epidemic as you say, you might want to question what the appeal of these drugs are.
Many people will also tell you than specific effects of LSD usage include self-trancedence, insight, heightened positive attitude, existential adjustment, higher levels empathy, better aesthetic appreciation and increased intellectual ability. Indeed, to evaluate the meaning of hallucinogen use in our society you might want to investigate if the drugs actually are having a detrimental effect, or perhaps if they are having a positive influence. I can say this, one is much more apt to get into a fight at bar than at a rave, and more likely to get a hug or backrub at a rave than a bar.
Indeed, there is a renewel of legitimate research into using hallucinogens and MDMA in medicinal and psychiatric context. I would suggest to take a look here or do a search of peer reviewed journals. www.maps.org
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