Anxiety suppression: Difference between revisions
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'''Anxiety suppression''' (also known as '''anxiolysis'''<ref> | '''Anxiety suppression''' (also known as '''anxiolysis''' or '''minimal sedation''')<ref>National Cancer Institute. (2016). NCI dictionary of cancer terms. https://www.cancer.gov/publications/dictionaries/cancer-terms/def/anxiolysis</ref> is a partial to complete suppression of a person’s ability to feel anxiety, general unease, and negative feelings of both psychological and physiological tension.<ref>Gordon, J. A. (2002). Anxiolytic drug targets: beyond the usual suspects. The Journal of clinical investigation, 110(7), 915-917. https://dx.doi.org/10.1172%2FJCI16846</ref> The experience of this effect may decrease anxiety-related behaviours such as restlessness, muscular tension,<ref>Tyrer, P. (1988). Prescribing psychotropic drugs in general practice. British medical journal (Clinical research ed.), 296(6622), 588. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2545227/</ref> rumination, and panic attacks. This typically results in feelings of extreme calmness and relaxation. | ||
Anxiety suppression is often accompanied by other coinciding effects such as [[disinhibition]] and [[sedation]]. It is most commonly induced under the influence of [[dosage#common|moderate]] [[dosage|dosages]] of [[anxiolytic]] compounds which primarily include [[GABAergic]] [[depressant|depressants]],<ref>Lydiard, R. B. (2003). The role of GABA in anxiety disorders. The Journal of clinical psychiatry, 64, 21-27. https://www.ncbi.nlm.nih.gov/pubmed/12662130</ref><ref>Nuss, P. (2015). Anxiety disorders and GABA neurotransmission: a disturbance of modulation. Neuropsychiatric disease and treatment, 11, 165. https://dx.doi.org/10.2147%2FNDT.S58841</ref> such as [[benzodiazepine|benzodiazepines]],<ref>Shader, R. I., & Greenblatt, D. J. (1993). Use of benzodiazepines in anxiety disorders. New England Journal of Medicine, 328(19), 1398-1405. https://doi.org/10.1056/NEJM199305133281907</ref> [[alcohol]],<ref> | Anxiety suppression is often accompanied by other coinciding effects such as [[disinhibition]] and [[sedation]]. It is most commonly induced under the influence of [[dosage#common|moderate]] [[dosage|dosages]] of [[anxiolytic]] compounds which primarily include [[GABAergic]] [[depressant|depressants]],<ref>Lydiard, R. B. (2003). The role of GABA in anxiety disorders. The Journal of clinical psychiatry, 64, 21-27. https://www.ncbi.nlm.nih.gov/pubmed/12662130</ref><ref>Nuss, P. (2015). Anxiety disorders and GABA neurotransmission: a disturbance of modulation. Neuropsychiatric disease and treatment, 11, 165. https://dx.doi.org/10.2147%2FNDT.S58841</ref> such as [[benzodiazepine|benzodiazepines]],<ref>Shader, R. I., & Greenblatt, D. J. (1993). Use of benzodiazepines in anxiety disorders. New England Journal of Medicine, 328(19), 1398-1405. https://doi.org/10.1056/NEJM199305133281907</ref> [[alcohol]],<ref>Smith, J. P., & Randall, C. L. (2012). Anxiety and alcohol use disorders: comorbidity and treatment considerations. Alcohol research: current reviews. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3860396/</ref> [[GHB]],<ref>Schmidt-Mutter, C., Pain, L., Sandner, G., Gobaille, S., & Maitre, M. (1998). The anxiolytic effect of γ-hydroxybutyrate in the elevated plus maze is reversed by the benzodiazepine receptor antagonist, flumazenil. European journal of pharmacology, 342(1), 21-27. https://doi.org/10.1016/S0014-2999(97)01503-3</ref> and [[gabapentinoid|gabapentinoids]]<ref>Pollack, M. H., Matthews, J., & Scott, E. L. (1998). Gabapentin as a potential treatment for anxiety disorders. American Journal of Psychiatry, 155(7), 992-993. (9) https://doi.org/10.1176/ajp.155.7.992</ref>. However, it can also occur to a lesser extent under the influence of a large variety of other pharmacological classes which include but are not limited to [[opioid|opioids]], [[dissociative|dissociatives]],<ref>Irwin, S. A., & Iglewicz, A. (2010). Oral ketamine for the rapid treatment of depression and anxiety in patients receiving hospice care. Journal of palliative medicine, 13(7), 903-908. https://doi.org/10.1089/jpm.2010.9808</ref> and [[SSRI|SSRIs]]<ref>Evans, B. J., & Burrows, G. D. (Eds.). (1998). Hypnosis in Australia. 82-3. Australian Journal of Clinical and Experimental Hypnosis. http://hc.rediris.es/pub/bscw.cgi/d4501310/Evans-Hypnosis_Australia.pdf#page=96</ref>. | ||
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===Psychoactive substances=== | ===Psychoactive substances=== |