期刊論文
學年 | 94 |
---|---|
學期 | 2 |
出版(發表)日期 | 2006-02-01 |
作品名稱 | D-Alanine Added to Antipsychotics for the Treatment of Schizophrenia |
作品名稱(其他語言) | |
著者 | Tsai, Guochuan E.; Yang, Pinchen; 張玉坤; Chang, Yue-cune; Chong, Mian-yoon |
單位 | 淡江大學數學學系 |
出版者 | Elsevier |
著錄名稱、卷期、頁數 | Biological Psychiatry 59(3), pp.230-234 |
摘要 | Background Hypofunction of the N-methyl-d-aspartate (NMDA) subtype glutamate receptor had been implicated in the pathophysiology of schizophrenia. Treatment with D-serine, glycine, endogenous full agonists of the glycine site of the NMDA receptor (NMDA-glycine site), D-cycloserine, a partial agonist, or sarcosine, a glycine transporter-1 inhibitor, improves the symptoms of schizophrenia. D-alanine is another endogenous agonist of the NMDA-glycine site that might have beneficial effects on schizophrenia. Methods Thirty-two schizophrenic patients enrolled in a 6-week double-blind, placebo-controlled trial of D-alanine (100 mg/kg/day), which was added to their stable antipsychotic regimens. Measures of clinical efficacy and side effects were determined every other week. Results Patint who received D-alanine treatment revealed significant reductions in their Clinical Global Impression Scale and Positive and Negative Syndrome Scale (PANSS) total scores. The Scale for the Assessment of Negative Symptoms and PANSS subscores of positive and cognitive symptoms were improved. D-alanine was well tolerated, and no significant side effect was noted. Conclusions The significant improvement with the D-alanine further supports the hypothesis of hypofunction of NMDA neurotransmission in schizophrenia and strengthens the proof of the principle that NMDA-enhancing treatment is a promising approach for the pharmacotherapy of schizophrenia. |
關鍵字 | N-methyl-D-aspartate;glutamate;schizophrenia;treatment-resistant |
語言 | en |
ISSN | 0006-3223 |
期刊性質 | 國內 |
收錄於 | |
產學合作 | |
通訊作者 | |
審稿制度 | 否 |
國別 | TWN |
公開徵稿 | |
出版型式 | ,電子版 |
相關連結 |
機構典藏連結 ( http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/41651 ) |