Wednesday, October 8, 2014

Chapter 4: Cannabinoid Effects on Anxiety-Related Behaviors and Hypothalamic Neurotransmitters


Now that we have determined what exactly medical marijuana is, what it does, and how it could be possible to relate it to psychological disorders, I would like to introduce an article proving how cannabinoids affect behavior and the neurotransmitters of the brain. Cristina Arévalo, Rosario De Miguel, and Rafael Hernández-Tristán published an article, titled Cannabinoid Effects on Anxiety-Related Behaviors and Hypothalamic Neurotransmitters, in 2001. Like most psychological studies, this experiment was tested on rats. They treated the animals with CP 55,940 (a cannabinoid agonist) and SR 141716A (a cannabinoid antagonist). An agonist is defined as a chemical substance capable of activating a receptor to induce a full or partial pharmacological response. On the other hand, an antagonist is defined as a drug that counteracts the effects of another drug. The chemical structure of ∆9-tetrahydrocannabinol compared to both, CP 55,940 and SR 141716A, can be dictated below:

  • “CP 55940 is a cannabinoid which mimics the effects of naturally occurring THC (one of the psychoactive compounds found in marijuana). It is currently used to study the endocannabinoid system. CP 55940 is considered a full agonist at both CB1 and CB2 receptors. Application of [3H] CP 55940 can be found in: binding to cannabinoid-1 receptors associated with schizophrenia and cannabis use in neuroscience, inhibition by phthalate esters in vitro in neurochemistry, actions of benzophenanthridine alkaloids, piperonyl butoxide and (S)-methoprene in pharmacology, etc."
  • “SR141716A is a selective antagonist for CB1 cannabinoid receptors. It has been used as an anorectic anti-obesity drug. It is an inverse agonist for the cannabinoid receptor CB1. Its main avenue of effect is reduction in appetite; it has also been studied in smoking cessation and short-term memory improvement.”

Arévalo, De Miguel, and Hernández-Tristán used both of these drug treatments on rats, individually and simultaneously, to test the effects on brain stimulation through hypothalamic neurotransmitters. They compare CP 55,940 to the active ingredients of ∆9-THC and the similar affects of both.  THC is said to be the leading cannabinoid from marijuana that can cause psychoactive effects on the brain. Evidentially, the research of this study determined that “CP 55,940 increased hypothalamic dopamine and serotonin levels” which could be “involved in the activation of the hypothalamic-pituitary-adrenal axis” in the brain, particular to cannabinoids (Arévalo, et al. 123). SR 141716A “induced a reduction in exploratory parameters and an increase in anxiety-like responses” (123). This article proves that all three examples of cannabinoids given, cause psychoactive effects and can lead to a change in behavior and cause anxiety. While determining these factors, the researchers studied numerous behavioral characteristics of the rats while providing them with the treatments of drug(s).


The reason why I chose this article to talk about is because of its’ relation to THC. As noted before, THC causes psychoactive effects; so why would we turn to marijuana for treating psychological disorders if it can cause anxiety? Well, medical cannabis has specific ratios of cannabinoids in order to treat specific disorders. Marijuana high in THC content is not recommended for people suffering from psychological disorders because it can cause anxiety and motor inhibition. However, cannabinoids like CBD, CBC, CBN, CBG and THCV all exhibit crucial roles as anti-psychotics. These cannabinoids would have higher content ratios if being patients are being treated for psychological purposes.



Sources:
http://ac.els-cdn.com/S0091305701005780/1-s2.0-S0091305701005780-main.pdf?_tid=97e3eac8-4f1e-11e4-93d0-00000aacb35f&acdnat=1412795534_f9189ed7405c60a1fe57a2d078254b05