Abstract
Arachidonic acid (AA)-derived lipid mediators are called eicosanoids. Eicosanoids have emerged as key regulators of a wide variety of physiological responses and pathological processes, and control important cellular processes. AA can be converted into biologically active compounds by metabolism by cyclooxygenases (COX). Beneficial effect of COX-2 inhibitor celecoxib add-on therapy has been reported in early stage of schizophrenia. Moreover, add-on treatment of celecoxib attenuated refractory depression and bipolar depression. Further, the COX/prostaglandin E pathway play an important role in synaptic plasticity and may be included in pathophysiology in autism spectrum disorders (ASD). In this regard, plasma transferrin, which is an iron mediator related to eicosanoid signaling, may be related to social impairment of ASD. COX-2 is typically induced by inflammatory stimuli in the majority of tissues, and the only isoform responsible for propagating the inflammatory response. Thus, COX-2 inhibitors considered as the best target for Alzheimer’s disease.
Keywords: Alzheimer’s disease, arachidonic acid, autism spectrum disorder, cyclooxygenases-1 inhibitors, cyclooxygenases-2 inhibitors, depression, eicosanoids, schizophrenia.
Graphical Abstract
Current Neuropharmacology
Title:Eicosanoids Derived From Arachidonic Acid and Their Family Prostaglandins and Cyclooxygenase in Psychiatric Disorders
Volume: 13 Issue: 6
Author(s): Kunio Yui, George Imataka, Hiroyuki Nakamura, Naoki Ohara and Yukiko Naito
Affiliation:
Keywords: Alzheimer’s disease, arachidonic acid, autism spectrum disorder, cyclooxygenases-1 inhibitors, cyclooxygenases-2 inhibitors, depression, eicosanoids, schizophrenia.
Abstract: Arachidonic acid (AA)-derived lipid mediators are called eicosanoids. Eicosanoids have emerged as key regulators of a wide variety of physiological responses and pathological processes, and control important cellular processes. AA can be converted into biologically active compounds by metabolism by cyclooxygenases (COX). Beneficial effect of COX-2 inhibitor celecoxib add-on therapy has been reported in early stage of schizophrenia. Moreover, add-on treatment of celecoxib attenuated refractory depression and bipolar depression. Further, the COX/prostaglandin E pathway play an important role in synaptic plasticity and may be included in pathophysiology in autism spectrum disorders (ASD). In this regard, plasma transferrin, which is an iron mediator related to eicosanoid signaling, may be related to social impairment of ASD. COX-2 is typically induced by inflammatory stimuli in the majority of tissues, and the only isoform responsible for propagating the inflammatory response. Thus, COX-2 inhibitors considered as the best target for Alzheimer’s disease.
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Cite this article as:
Yui Kunio, Imataka George, Nakamura Hiroyuki, Ohara Naoki and Naito Yukiko, Eicosanoids Derived From Arachidonic Acid and Their Family Prostaglandins and Cyclooxygenase in Psychiatric Disorders, Current Neuropharmacology 2015; 13 (6) . https://dx.doi.org/10.2174/1570159X13666151102103305
DOI https://dx.doi.org/10.2174/1570159X13666151102103305 |
Print ISSN 1570-159X |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6190 |
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