van Kammen D P, Yao J K, Goetz K
Highland Drive Veterans Administration Hospital, Pittsburgh, Pennsylvania 15206.
Ann N Y Acad Sci. 1989;559:411-23. doi: 10.1111/j.1749-6632.1989.tb22626.x.
Psychotic disorders, particularly schizophrenia, are associated with clinical phenomena that can be explained by disturbances in polyunsaturated fatty acid and prostaglandin metabolism. Previous studies of PUFA, PG synthesis, PGE1 receptor activity and aggregation responses in platelets, and clinical treatment trials suggest a role for PGE in the pathophysiology of schizophrenia. Since a decrease in PGE1 activity can be associated with an increase of dopamine release, a deficiency of PGE1 is consistent with the dopamine hypothesis of schizophrenia. State-of-the-art assay and clinical trial methodology should clarify the role of PUFA metabolism in schizophrenia.
精神障碍,尤其是精神分裂症,与一些临床现象相关,这些现象可以用多不饱和脂肪酸和前列腺素代谢紊乱来解释。先前关于多不饱和脂肪酸(PUFA)、前列腺素(PG)合成、血小板中前列腺素E1(PGE1)受体活性和聚集反应的研究以及临床治疗试验表明,PGE在精神分裂症的病理生理学中发挥作用。由于PGE1活性降低可能与多巴胺释放增加有关,PGE1缺乏与精神分裂症的多巴胺假说相符。先进的检测方法和临床试验方法应能阐明PUFA代谢在精神分裂症中的作用。