Sandyk R
Department of Psychiatry, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 1046.
Int J Neurosci. 1990 Jun;52(3-4):233-8. doi: 10.3109/00207459009000525.
Several clinical studies have suggested that patients with affective disorders, are at high risk for developing tardive dyskinesia (TD). An intriguing aspect of the relationship between TD and affective disorders involves mood dependent alterations in severity of TD. In most reported cases, depressive episodes are associated with exacerbation of TD, while manic episodes are accompanied by attenuation of TD. Current neurochemical hypotheses of TD do not explain adequately the relations of TD to depression or the mood dependent variations in the severity of TD. I propose that alterations in the secretory activity of pineal melatonin during manic and depressive episodes may explain better both the higher risk of TD in patients with affective disorders and the mood-dependent fluctuations in severity of TD. Consideration of pineal melatonin functions may further our understanding of the pathophysiology of TD in patients with affective disorders.
多项临床研究表明,情感障碍患者发生迟发性运动障碍(TD)的风险很高。TD与情感障碍之间关系的一个有趣方面涉及TD严重程度的情绪依赖性改变。在大多数报道的病例中,抑郁发作与TD加重相关,而躁狂发作则伴有TD减轻。目前关于TD的神经化学假说并不能充分解释TD与抑郁症的关系或TD严重程度的情绪依赖性变化。我认为,在躁狂和抑郁发作期间松果体褪黑素分泌活动的改变可能更好地解释情感障碍患者发生TD的较高风险以及TD严重程度的情绪依赖性波动。考虑松果体褪黑素的功能可能会增进我们对情感障碍患者TD病理生理学的理解。