Part of the Neuron Affected, Inhibitory or Excitatory Potential Changes

Part of the Neuron Affected, Inhibitory or excitatory Potential Changes and Ion Channels Affected by Psilocybin Psilocybin belongs to the mixture of drugs called hallucinogens. Hallucinogens typically act by stimulating serotonin receptors at antithetic times or for longer durations than serotonin itself would (Kalat 2004). When psilocybin enters the brain, the enzyme alkaline breaks drink one of its phosphate groups through hydrolysis. It then becomes psilocin, an even stronger hallucinogen (Psilocybin 2003). It is particularly potent due to the position of its hydroxyl group (Jacobs 1984). Psilocin is a postsynaptic serotonin receptor agonist. In other words, its similar structure allows it to simulate serotonin, fitting into some types of serotonin receptors and producing the same effect as endogenous serotonin (Merriam Webster 2003). Specifically, psilocin activates the 5HT2A and 5HT1A receptors. Stimulation of 5HT1 receptors is associated with an inhibitory response while arousal of the 5HT2 receptors is associated with an excitatory response. Soma of the serotonergic neurons are located in the midline rhaphe nuclei of the pons and in the medulla oblongata. Axons extend to the basal ganglia, hypothalamus, limbic forebrain, split of the cerebral cortex, and to the spinal cord (Kruk and Pycock 1979). Functions believed to be moderated by serotonin entangle sleep, mood, arousal, control of motor activity, hunger, thermoregulation, and some neuroendocrine control mechanisms in the hypothalamus. (Powell 2004, Kruk and Pycock 1979). one(a) theory states that effects caused by psilocin result from stimulation of receptors in the raphe nuclei. According to this theory, the... ...ocal Net Common Molecule. (2003) Reciprocal Net come in Network. http//www.reciprocalnet.org/recipnet/showsample.jsp?sampleId=27344568Rabin, Richard A., Regina, Meridith, and Doat, Mirielle J.C. 5-HT2A Receptor-stimulated Phosphoinositide Hydrolysis in the Stimulus Effects of Ha llucinogens. (2001) materia medica, Biochemistry and Behavior. Volume 72, 2002. (pp 29-37) Department of Pharmacology and Toxicology, School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY.Vollenweider, Franz X, M.D., Vontobel, Peter, PhD., Hell, Daniel, M.D., and Leenders, Klaus, M.D. (1998) 5HT conversion of Dopamine Release in Basal Ganglia in Psilocybin generate Psychosis in Man A PET Study with 11Craclopride. Neuropsychopharmacology 1999, Volume 20, consider 5. (pp 424-431) New York, New York Elsevier Science Inc.