Tag Archives: THC

schizophrenia

Cannabidiol may treat psychosis while tetrahydrocannabinol can induce schizophrenia in those susceptible  

Virginia Thornley, M.D., Neurologist, Epileptologist

@VThornleyMD

May 6, 2018

Introduction

There is a well-known correlation of use of cannabis whether it is medical or recreational to the onset of schizophrenia. It unclear if this could be to a direct correlation and disinhibition of the genetic component or the behavior of using it is a prodrome leading up to schizophrenia. This review seeks to elucidate the mechanisms in the correlation of the use of cannabis and onset of schizophrenia.

Mechanisms related to the underlying genetic composition

Schizophrenia may be linked when some of the normal pathways become disrupted with an introduction of THC.  There are 4 genes that were described after a lifetime use of cannabis including KCNT2 which were THC responsive, NCAM1 and CADM2 are significant in functioning in post-synapse. With THC in the system, there are more post-synaptic density genes (1).

Mechanisms related to other neurotransmitter pathways influenced by cannabinoids

In one study, because of the alarming rate of potent synthetic cannabis used recreationally which was found to leave long-lasting schizophrenia disorder in recreational users, this has accelerated research into the pathophysiology. Because cannabinoids work on the CB1 receptor, it is likely that it plays a modulatory role on the other neurotransmitters that can give rise to schizophrenia including dopaminergic, glutamatergic and serotonergic pathways. These pathways are well-established as playing a role in a pro-psychotic state. High efficacy synthetic cannabinoids which are manufactured for recreational purposes are highly more potent compared to natural organic cannabinoids and there is an alarming increase in the correlation of schizophrenia in these users (2).

In one study it is thought to be due to the hypofunctioning of the glutamate system which is directly affected by THC. Exposure to tetrahydrocannabinol appears to reduce the activity at the level of the glutamate receptor as well as deregulate genes for synaptic function(1).

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Susceptibility is related to the development of schizophrenia

In one animal model, the set-up tried to mimic a more real state seen where not all adolescents exposed to synthetic cannabinoids react by developing schizophrenia, there are some studies where all animals develop schizophrenia with exposure. In this animal model, they provided a model that resembles the human model more closely and found that exposure to synthetic cannabinoids in schizophrenia-prone animals caused hyperfunctioning of dopaminergic pathways compared to the control group who were not susceptible at the same dosages. There may be underlying genetic or environmental factors that cause certain individuals to become more prone (2).

THC can cause anxiety and behavioral disorders but can be prevented with CBD

In one animal study, it was found in a rat study that THC can induce anxiety and behavioral disorders. With THC  administration object recognition was impaired in adolescent rates. The studies support effect on the developing brain in relation to cognitive impairment in the animal model. In addition, when rats were exposed to THC there was increased marble burying behavior which in scientific research is thought to signify anxiety or obsessive-compulsive type behavior usually ameliorated with serotonin reuptake inhibitors or benzodiazepines(4).

It was found, however, that a combination of CBD and THC or cannabidiol alone was administered, these behaviors were not produced or produced only minimally. The thought is that CBD is an allosteric competitive inhibitor at the CB1 receptor so that one sees less of the toxic undesirable effects of THC if administered alone (4).

Cannabinoids have a similar profile to atypical anti-psychotics and may be a possible adjunctive treatment in the treatment of psychotic events (5).

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In summary

There is historical evidence that exposure to THC can give rise to schizophrenia in those individuals that are susceptible accounting for the fact that it does not happen to everybody exposed to it. This is related to its influence on serotonergic, dopaminergic and glutamate pathways. THC can induce anxiety, repetitive behaviors which are ameliorated by CBD. CBD may be a useful adjunctive treatment for psychotic disorders. However, the elucidated mechanisms are based on scientific research based on animal models which may not translate into humans.

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References

  1. Guennewig, et al, “THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorder,” Transl. Psychiatry, 2018, Apr., 8(1):89.
  2. Fantegrossi, et al, “Pro-psychotic effects of synthetic cannabinoids: interactions with central dopamine, serotonin and glutamate systems, Drug Metab. Review, 2018, Jan, 50(1)
  3. Aguilar, et al, “Adolescent synthetic cannabinoid exposure produces enduring changes in dopamine neuron activity in the rodent model of schizophrenia,” Int. J. Neurpsychopharmacol., 2018, Apr., 31 (4):393-403.
  4. Murphy, et al, “Chronic adolescent delta9-tetrahydrocannabinol treatment of male mice leads to long-term cognitive behavioral dysfunction which is prevented by concurrent cannabidiol treatment,” Cannabis Cannabinoid Res., 2017, 2(1):235-246.
  5. Deiana, et al, “Medical use of cannabis: a new light for schizophrenia?” Drug Test Analysis, 2013, Jan., (5)1:46-51
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ADHD

Medical marijuana: effect in pediatric patients with ADHD, long-term cognitive effects in children and review of literature

Virginia Thornley, M.D.,  Neurologist, Epileptologist
May 2, 2018

Introduction
With the advent of a wide use of cannabinoids in neurological disease compared to previous times, attention hyperactivity deficit disorder has arisen as one of the possible disorders where patients may benefit. Because it starts in childhood, questions arise whether it may be applied to the pediatric patients with ADHD. If so, what are the long-term consequences on the developing brain?

Effect of cannabis in ADHD and on the brain
There is a paucity of literature on cannabis use in children with ADHD, most have been on adults.  There are some recent clinical trials and its use in adult patients with ADHD.  In a recent study on ADHD in adults, 30 patients were studied, 15 were in the placebo-controlled group and 15 were given Sativex oromucosal spray (combination CBD:THC). There was no statistical difference in cognitive performance although the score patterns on those on Sativex were higher. There was some improvement in attention. There was a significant improvement in emotional lability and hyperactivity (p=0.3). This implies that cannabinoids may play a role in adult ADHD (1).

In a study of 579 young adult patients with an early history of ADHD of which 129 had to be excluded, it was found that the dorsal attention network found in the parietal region was stronger in those with ADHD. The right fronto-parietal and right inferior frontal region connections were weaker in the ADHD group. The left prefrontal dorsal connections and the right prefrontal cortex connections in ADHD were reduced (2).

One of the key components of ADHD in children is motor dysregulation and weakened connections in the somatosensory region. The stronger connections in ADHD in the frontal-opercular regions suggests compensatory adaptations to maintain normal cognition.  There are stronger right parietal region connections in patients with ADHD possibly suggesting maladaptive mechanisms. When patients with ADHD and cannabis use were studied it appeared that there were neuroadaptive processes. In those who used cannabis, there were stronger intrinsic connections with a superior delayed recall.  There were stronger connections in the left fusiform gyrus that correlated with a) less cognitive interference, these are emotional thoughts or personality traits that can intrude and affect tasks at hand and b) better response inhibition performance, this is the ability to ignore distractions. This is consistent with other studies showing an increased task activation response (2).

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Effect of cannabis on the fetus
Tetrahydrocannabinol is lipophilic and crosses the blood-brain barrier. It can get stored in the fatty stores which are likely the reason it may have a long-lasting effect.  Cannabinoids have been found to cross the placenta and affect the fetus. It may result in hyperactivity and impulsivity in babies with cannabinoid exposure in utero (3). There was a greater incidence of inattention and delinquency in prenatal exposure to cannabis.

Effect of medical marijuana in early cerebral development
It was found that in adolescents who used cannabis, there is a reduction in the IQ by the age of 38. It was found that cannabinoid receptors influence axonal migrations as well as subcortical projections within the cerebrum. This affects synaptic connections during childhood and adolescence(4).

The adolescent brain is still not fully matured and likely still subject to neuronal plasticity and changes. It may be affected by substances. One study showed that the frontal lobe is vulnerable to cannabis in adolescents who used it heavily and that cannabis use may impact working memory (5).

During adolescence, when cannabis is initiated it may affect the neuronal circuitry developing in the immature brain. The richest regions in the brain with cannabinoid receptors are the prefrontal cortex, medial temporal lobes, striatum, white matter connections, and cerebellum. When cannabis is introduced during this neurocritically important time of development, these regions can become dysfunctional although some functional studies have shown altered, weakened, strengthened or combination of changes (2).

Some of the most common adverse effects
At high doses in chronic users, it was found to induce anxiety, panic attacks. It can increase blood pressure. However, clinically, it may control seizures

Discussion
There is a paucity of literature on the effects of medical marijuana on the pediatric population. It has been mostly studied in adult patients. It is difficult to correlate the results of beneficial effects on adults on children since the pediatric brain is still developing. In adult patients with ADHD, apparently exposure to cannabis results in a superior delayed recall, there were fewer thought intrusions when completing tasks and better able to ignore distractions.

When exposed in utero, there was a greater risk of developing inattention, hyperactivity, and impulsivity in children who were exposed before conception. There was a greater tendency towards delinquency. In addition, adolescents who had been chronically exposed to cannabis may have had their working memory impacted. The adolescent period is significant from a neurological standpoint in brain development. There were mixed reports on connections being strengthened, weakened or a combination of the two being reported.

It is difficult to correlate the data of chronic medical cannabis exposure of adolescents in a patient who will use it for its medicinal value since the route, amount and administration and frequency will be completely and distinctly different. In addition, most of the adolescent data has been derived from those who had used it recreationally usually by smoking it heavily, there may be a synthetic component which may be detrimental and it is not clear what other substances may have been added.

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In summary
In short, there is not enough scientific and clinical data to support the use of medical cannabis in pediatric patients. Most of the data is derived from animal studies or studies in adults where there are medical benefits. In the pediatric brain even while studies showed abnormal memory in chronic use it was studied in a very different population of heavy recreational users. Therefore, it is not clear if adult findings can translate into similar pediatric success and the same dysfunctional development of chronic heavy abusers would correlate with similar findings in pediatric patients using it for distinctly different reasons and dosing and administrations. If there is some adverse effect on the pediatric brain, it is unclear if the risks outweigh the benefits in a developing brain of the pediatric population. It may be used anecdotally in some practices with some benefits. Large clinical trials are needed to support this.

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Reference

1.  Cooper, et al, “Cannabinoid in attention-deficit/hyperactivity disorder: a randomized controlled trial,” Eur. Neuropsychopharmacol., 2017, Aug., 27 (8):795-808
2.  Kelly, et al, “Distinct effects of childhood ADHD and cannabis use on brain functional architecture in young adults, Neuroimage Clin., 2017, 13:188-200.
3.   Goldschimd, et al, “Effects of prenatal marijuana exposure on child behavior problems at age 10,” Neurotoxicol. Teratol., 2000, May-Jun., 22(3):325-326.
4.  Scott, et al, “Medical marijuana: a review of the science and implications for developmental-behavioral pediatric practice,” J. Dev. Behav. Ped., 2016, Feb., 36 (2):115-123.
5.  Jager, et al, “Cannabis use and memory brain function in adolescent boys: a cross-sectional multicenter fMRI study,” J. Am. Acad. Child Adolesc. Psychiatry, 2010, Jun., 49(6):561-572.

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medical marijuana

Cannabinoids: the other side of the coin, side effects, drug-drug interaction and possible problems of cannabidiol and tetrahydrocannabinol

Virginia Thornley, M.D., Board-Certified Neurologist, Epileptologist

@VThornleyMD

April 6, 2018

 

Introduction

Medical marijuana seems like the shining breakthrough drug the shining pill in armor, the magic pill that seems to cure everything. However, there are always two sides to every coin. One must still proceed with caution. The phytocannabinoids, cannabidiol, and tetrahydrocannabinol exert their effects through the endocannabinoid pathway, the CB1 receptor is most abundantly found in the nervous system. Cannabidiol which has no euphoria acts weakly with the CB1 receptor almost as a reverse agonist blocking the THC from exerting its effect offsetting potent side effects of tetrahydrocannabinol.

The medical benefits are overwhelmingly numerous including ameliorating seizures, spasms from multiple sclerosis, peripheral neuropathy in HIV patients, chronic debilitating pain, post-traumatic stress disorder symptoms and other associated diseases. Despite the stigma of using it, the delay in clinical trials and marked hesitation of the medical community, medical marijuana has landed and there is no going back. Yet even with its numerous health benefits, it is always prudent to take a step back and examine any flaws as with any other new kid on the block or any new agent that comes along even though it’s been around for thousands of years.

Is marijuana safe for medical use? The take on medical marijuana by the FDA

So far from the FDA official website, the FDA does not recognize medical marijuana coming from the botanical plant with any medical indication. The FDA does not recognize it to be safe or beneficial for any type of disease or condition. The FDA will facilitate any companies interested in bringing quality products including science-based research. The full take of the FDA on marijuana can be found here https://www.fda.gov/NewsEvents/PublicHealthFocus/ucm421168.htm#use

Long-term effects on the brain

Perusing the scientific literature, it is difficult to find any long-term damage to the brain. There was a report in a heavy marijuana user where there was damage to the corpus callosum, possibly worse with young users (1). This is a small study of 11 heavy marijuana users with 11 age-matched cohorts. Diffusion tensor imaging was used. Previous reports alluded towards poor cognition with heavy marijuana use. This study is aligned with that. It was suggested that there may be increased diffusibility within the white matter tracts of the corpus callosum. Young age is thought to make the corpus more susceptible to white matter damage. The only caveat is this is with heavy use and the substance found in recreational marijuana is going to be a different form compared to medical marijuana extracted from the marijuana plant used for medicinal purposes. It is not clear if this report would carry over to medical marijuana users where the preparation of the product is much different(1).

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Effect on schizophrenia spectrum diseases

In a large study of 171 patients, it was found that with heavy use of cannabis, the age of onset of schizophrenia spectrum disorders seems to occur earlier (6). This is one of the reasons why in some dispensaries, it is not sold to patients with a history of schizophrenia. There are some anecdotal reports of some patients having a paranoia with medical marijuana that is reversible once taken off.

Effect on the heart, reports of myocardial infarcts and ST elevations

While the literature suggests low toxicity and most side effects are related to cognition and gastrointestinal problems, there are several cannabis-associated myocardial infarcts in the literature. The dispensaries in the state of Florida use a previous history of a previous myocardial infarct as a contraindication in using medical marijuana. These were synthetic drugs used recreationally. There was one case report where a heavy user suffered from an ST elevation and subsequent myocardial infarct after becoming toxic to marijuana used recreationally.  In one study, synthetic cannabis was used, the myocardial happened to a young patient where an atheromatous plaque was excluded as the source. Etiology and mechanism are unclear why infarcts should occur. It is quite possible that because it works on the 5HT receptor for anxiety which can cause vasoconstriction, this may be one mechanism. Other studies are needed to elucidate the mechanism of action.

Drug-drug interactions

Because medical marijuana is used as an adjunctive agent for epilepsy, perhaps off-label since it has not been approved through FDA as an anti-epileptic agent yet, it was found that medical marijuana used in conjunction with Clobazam (Onfi) tended to elevate Onfi at higher levels.

In one small clinical study, in 13 patients, 9 had an increase of about 60 in the Clobazam level and by 300 in Norclobazam level. There was, however, a tremendous reduction of seizures by >50% but Onfi (Clobazam and Norclobazam levels) should be monitored (3) on a routine basis to avoid any untoward toxicity.

Other milder symptoms

In one large study on Lennox-Gastaut syndrome where cannabidiol was titrated to a 20mg/kg over a course of 14 weeks, mild to moderate symptoms were noted including pyrexia, sedation, dizziness, and diarrhea. However, the titration rate was very rapid and the patents who were 50kg were quickly at 1000mg within 14 weeks which does not usually happen in the real world. Medications are usually increased over a longer period of time in slower increments.

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In summary

While everybody is touting the horn of medical marijuana it is always prudent to stand back and ensure there are no possible risk factors for adverse side effects. The most serious and common seen in the literature appear to be related to schizophrenia spectrum disorders and cannabis associated myocardial infarct. The only caveat is that the literature is peppered with these reports, however, the quality of the recreational drugs are vastly different from medical marijuana which tends to be organic and all natural extracted from the plant in licensed medical dispensaries. The extraction of the medical components is vastly different from the smoked synthetic version of tetrahydrocannabinol. So, is difficult to know if these reports would actually corroborate with use in medical marijuana. The ones with side effects were heavy users of recreational smoked types of marijuana, it is unclear if it was synthetic or organic. As the popularity of medical marijuana progresses, more information will be available regarding the side effect profile.

References

  1. Arnone, et al, “Corpus callosum damage in heavy use: preliminary evidence from diffusion tensor tractography and tract-based spatial statistics,” Neuroimage, 2008, Jul., 1, 41 (3): 1067-74.  “J Addict Med. 2017 Sep/Oct;11(5):405-407. doi: 10.1097/ADM.0000000000000326.
  2. Volpon, et al, “Multiple cerebral infarcts in a young patient associated with marijuana use, ” Journ. Addic. Med, 2017, Sep./Oct., 11(5):405-407.
  3. Geffrey, Drug-drug interaction between clobazam and cannabidiol in children with refractory epilepsy,” Epilepsia, 2015, Aug., 58 (8):1246-1251.
  4. Stewart, et al, “Obstructive sleep apnea due to laryngospasm links ictal to postictal events in SUDEP cases and offers practical biomarkers for review of past cases and prevention of new ones,” Epilepsia, 2017, Jun., 58(6): e87-90
  5. https://www.fda.gov/NewsEvents/PublicHealthFocus/ucm421168.htm#use
  6. Shahzade, et al, “Patterns in adolescent cannabis use predict the onset and symptom structure of schizophrenia-spectrum disorder,” Schizophrenia Research, 2018, Feb., 2 pii S090-9964 doi:10. 1016/j. schres. 2018.01.008 (Epub ahead of print)
  7. Orsini, et al, “Prolonged cardiac arrest complicating massive ST-segment elevation myocardial infarct associated with myocardial consumption,” J. Community Hosp. Intern. Med. Perspect, 2016, Sep., 7. 6 (4):31695
  8. Thiele, et al, “Cannabidiol in patients with seizures from Lennox-Gastaut Syndrome (GWPCARE4): a randomized, double-blind placebo-controlled phase 3 trial,” Lancet, 2018, Jan., 390 (10125):1085-1096

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Post-Traumatic Stress Disorder

Post-traumatic stress disorder and traumatic brain injury among military veterans and use of non-intoxicating medical marijuana as a treatment

 

Virginia Thornley, M.D., Neurologist, Epileptologist

@VThornleyMD

March 28, 2018

Introduction

Post-traumatic stress disorder occurs due to a single or a sequence of traumatic events which causes a great deal of anxiety when exposed to situations similar to the event. Flashbacks and nightmares may occur. In military veterans returning from the Iraqi or war in Afghanistan and even to this day in Vietnam War veterans, emotional disruption is noticeable. It is difficult to know if this is related to blast injury or is a symptom of post-traumatic stress disorder.

PTSD correlated with mild traumatic brain injury

In a retrospective study reviewing medical records of 27,169 military personnel of the U.S. Army Special Operations Command (USASOC), 2831 met criteria of mild traumatic brain injury using the Immediate post-concussion assessment cognitive test, PTSD checklist, and the post-concussion symptom scale. Of these, 28% exhibited symptoms of post-traumatic stress disorder. Military veterans of blunt, blast or a combination injury had a higher percent of meeting criteria for post-traumatic stress disorder than those without mild traumatic brain injury. Those with blast/combination injury had a higher percent of post-traumatic stress disorder and performed worse with visual memory and time for reacting compared the cohort without any blunt or mild traumatic brain injury.  Repetitive exposure to blast-type injuries may have a lingering effect (2). This study found a  high degree of PTSD symptoms in those with blast, blunt and combination injury compared to the cohort without it.

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In a study, disrupted emotional responses correlate with PTSD rather than blast-related traumatic brain injury

Another study tried to dissect whether the emotional responses of war veterans are due to PTSD or due to the mild brain injury itself.  In one study of 123 military veterans from the war in Iraq and Afghanistan, affective evaluations and psychological assessments were made in response to pleasant, neutral, unpleasant and war-related images.  Those with emotional disruption due to PTSD rated pleasant images as unpleasant and had increased physiological responses towards combat-related images. Symptoms of post-traumatic stress disorder included increased skin conductance responses, greater corrugator muscle electromyography responses, and reduced heart decelerations. There were no effects noted in veterans with mild traumatic brain injury.  This points towards the emotional disruption seen in military veterans as related with post-traumatic stress disorder rather than due to the mild traumatic brain injury itself. This study may help guide treatment as military veterans transition to civilian life (1).

Medical marijuana and mechanism of action, a non-intoxicating solution when cannabidiol is used alone or in conjunction with low dose tetrahydrocannabinol

Cannabidiol is a non-intoxicating endocannabinoid that works within the endocannabinoid system found naturally in our systems. It has only a weak affinity to the CB1 receptor which is found abundantly within the neurological system.  CB1 receptors are found to be increased in response to cerebral cell damage and seem to work as a repair mechanism for neural systems that are not functioning. Tetrahydrocannabinol at low concentrations has medical properties without the intoxication of high dose THC. THC should be used in combination with CBD to offset the possible side effects such as hyperactivity.

There are increasing studies showing the value of medical marijuana, especially in the central nervous system especially given the large abundance of the CB1 receptor within the nervous system. The receptors are found to be upregulated in the face of disease suggesting a cell repair role or a response to the abnormalities within the brain, For example, in patient with seizures, the CB1 receptor is found to be increased in the temporal lobe within the dentate gyrus compared to other cells almost as a response to the aberrant system within the cortex. The receptors are found to be increased in patients with Parkinson’s disease.

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Medical Marijuana as a solution for symptoms of cognitive impairment in war veterans

In one study, 24 patients were enrolled in a study for executive function and were registered medical marijuana users. After 3 months, 11 patients returned and using the Stroop Color Word Test, were found to have a higher level of executive function and increased speed completing tasks without being inaccurate. Patients reported less insomnia, less depression, better attention, less impulsivity and a better quality of life. There was less use of pharmacologic use and less use of opioid agents by 42% in conjunction with medical marijuana. Larger clinical randomized controlled clinical studies are needed.

Medical marijuana seems to be an excellent agent in those affected by traumatic brain injury.

Medical Marijuana as a solution for and PTSD symptom in war veterans

Cannabidiol works at the level of the 5HT1 receptor causing patients to feel less anxious and may be used in post-traumatic stress disorder. In addition, it has been found to have a role in modulating memory and instead of the learned fear response and may help with PTSD by modulating the conditioned response to a stimulus that normally begets anxiety and fearfulness. In other words, instead of the heart rate increasing or having flashbacks when a war scene is on TV, medical marijuana can exert its effect by modulating behavior by changing the learned response by not responding the same way and being calm in face of a previously anxiety-inciting war scene(4).

In conclusion

In summary, PTSD and traumatic brain injury are real problems faced by war veterans returning with blast injury, blunt-injury or combination type combat-related injuries. Medical marijuana may be an excellent non-intoxicating solution when cannabidiol is taken or combined with low dose tetrahydrocannabinol which can help with depression, anxiety and help modulate responses to post-traumatic stress disorder. Medical marijuana can help with executive function and attention and may be beneficial in treating war veterans suffering from mild traumatic brain injury.

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References

  1. Marquardt, et al, “Symptoms of Post-traumatic stress rather than mild traumatic brain injury best account for altered emotional responses in military veterans,” J. Trauma Stress, 2018, Feb., 31 (1):114-124.
  2. Kontos, et al, “Residual effects of combat-related mild traumatic brain injury, “J. Neurotrauma, 2013, Apr., 15, 30 (8):680-6.
  3. Gruber, et al, “Splendor in the Grass? A pilot study assessing the impact of medical marijuana on executive function,” Front. Pharmacology, 2016,. Oct., 13 (7):355.
  4. Uhernik, et al, “Learning and memory are modulated by cannabidiol when administered during trace fear-conditioning,” Neurobiology of Learned Memory, 2018, Feb., 9, 149:58-76. doi: 10.1016/j.nlm.2018.02.009 (Epub ahead of print)
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chronic pain

Medical Marijuana: a non-intoxicating pain-relieving solution to the opioid epidemic?

Virginia Thornley, M.D., Neurologist, Epileptologist

March 24, 2018

Introduction

Any news outlet you peruse is bound to have mention of the current opioid crisis looming on the horizon. Opioids are commonly prescribed as the last resort for patients with chronic pain who have failed conventional medications, interventional measures such as epidural injections or surgery, non-pharmacologic measures such as physical therapy and even Eastern techniques such as acupuncture. With tolerance a common problem and patients needing higher and higher dosages for pain control because of the properties of opioids, it is little wonder that chronic pain control is difficult to maintain.

The hot topic of debate in many states is the recognition of medical marijuana as a legitimate medication for chronic ailments. However, because of the stigma it has incurred being well-known for its psychoactive properties and widely seen in pop culture in movies with kingpins smoking it for recreation, the medicinal values are often overshadowed and lack of side effects in low doses is easily overlooked.

Not your stereotypical patient and not your direct referral

Patients and even physicians likely have a preconceived notion of who seeks medical marijuana. While chronic pain is top of the list, often times, it is discovered by the hard-working carpenter who discovered it online and found a small scientific article on non-pharmacologic treatments trying to come off sedating pain-relieving medications. It will be the former business owner who lived an enjoyable life being active dancing or the woman afflicted with an autoimmune disorder and has failed every medication under the sun. Many times patients come in not because they want to feel good but because it is their last resort and they’ve exhausted every treatment option known to mankind. They dislike the side effects of the strong painkillers such as opioids and just want the pain to stop and live a normal life. It is amazing how indirectly patients hear about the wonders of medical marijuana, it will usually be a neighbor who swears by it, or somebody’s friend who mentions it out of the blue.  Oftentimes, it is by word of mouth since the few physicians interested in recommending it are very reluctant to advertise with good reason.

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Mechanisms of cannabidiol and tetrahydrocannabinol

Medical marijuana has been used since B.C. period for thousands of years as a medication. It was incorporated into the pharmacopeia of American medicine in the 1850’s until it was banned in the 1930’s. It regained popularity and notoriety as a recreational substance. However, more and more patients are turning towards this now alternative medication after years of frustration towards the ineffectiveness and adverse effects of conventional medications.  The endocannabinoid pathway is found inherently in the system and is responsible for the runner’s high that people get after a vigorous run or after exercising and gives the sense of well-being. The CB1 receptor is found most abundantly in the central nervous system which is likely why many neurological conditions are found to benefit from its use. The CB2 receptor is most commonly found in the immune system. As more research is pursued, there are CB receptors found diffusely throughout many organ systems.  Cannabidiol weakly interacts with the CB1 receptor. It takes at least 100 times cannabidiol to attain the same intoxication one gets with tetrahydrocannabinol, the substance which is more popular and found in the marijuana joints people smoke to obtain euphoria. THC at low concentrations is effective in treating many different medical conditions. It must be used in conjunction with CBD so that side effects are offset. Cannabidiol has no intoxication while low doses of THC does not give euphoria one associates with this drug. There is no tolerance.

Scientific evidence cannabidiol and tetrahydrocannabinol work in chronic pain and other medical diseases

In animal studies, it is well known to reduce seizures by inhibiting the excitation within the hippocampus of the brain where seizures are commonly propagated (http://www.pnas.org/content/early/2017/09/26/1711351114).There are many clinical trials in humans attesting its efficacy at controlling seizures effectively.  CB1 receptors appear to be increased in many neurological disorders which implies it is a compensatory mechanism for diseases. In Parkinson’s disease, there are increased CB1 receptors which may help with the reduced dopamine commonly found in Parkinson’s disease. 9tetrahydrocannabinol was found to lower intraocular pressure in glaucoma in rabbits (https://www.ncbi.nlm.nih.gov/pubmed/6329602). Sativex is a combination of THC:CBD which reduces spasms in patients with multiple sclerosis and has been available in Europe for several years now with very little side effects http://jnnp.bmj.com/content/87/9/944. There is extensive evidence in both animal and human models that it works in chronic pain (https://www.ncbi.nlm.nih.gov/pubmed/26830780). Many diseases are being evaluated for mechanisms on which CBD and THC may exert its effects. It has been found to have anti-oxidant and anti-inflammatory properties which are important mechanisms by which many diseases cause pathology. In cancer cell cultures, it has been found to reduce proliferation of tumor cells in urologic cancer and reduce the pro-inflammatory states that are necessary for metastatic conditions (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434502/).CBD interacts with the 5HT1 receptor where many anti-depressants and anxiolytic medications exert their effects, making CBD an effective anxiolytic. It works to stimulate appetite and is commonly used by patients with cancer for anorexia and end-stage cancer pain.

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In conclusion

In summary, cannabidiol and tetrahydrocannabinol are effective medications in treating pain from many chronic illnesses and is not reserved for patients with terminal illness. Despite the reticence of physicians, Congress and even patients, there is overwhelming evidence that cannabidiol and tetrahydrocannabinol are effective in many different diseases, although in some conditions there’s a long way to go from preclinical data to human trials.  It is fairly clear in many disease states, medical marijuana is significantly effective. There is no tolerance and may be an effective treatment for patients with chronic pain. CBD by itself has no euphoric properties and low concentrations of THC do not give intoxicating psychoactive effects. These are 2 alternatives that may provide relief and solution to the growing epidemic of the opioid crisis.

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