Rehfeld J F
Department of Clinical Biochemistry (KB 3011), University of Copenhagen, Rigshospitalet, DK-2100, Copenhagen, Denmark.
Regul Pept. 2000 Sep 25;93(1-3):79-83. doi: 10.1016/s0167-0115(00)00179-8.
The serendipitously discovered panicogenic effect of the cholecystokinin fragment, the C-terminal tetrapeptide amide (CCK-4), has suggested that the widespread network of CCK neurons and corresponding CCK-B receptors in the brain are in some way involved in pathogenesis panic disorders in man. Two decades of research have now established that exogenous CCK-4 in a reproducible, dose-dependent and sensitive manner indeed evokes panic attacks in both healthy subjects and at even lower doses in anxiety patients. But several questions about the molecular mechanisms by which endogenous CCK peptides may precipitate panic attacks remain to be answered. This review focuses on three immediate questions. (1) Does endogenous CCK-4 exist? (2) Is the panicogenic effect mediated only through CCK-B receptors? (3) Are measurements of CCK peptides in cerebrospinal fluid of use in elucidating the pathogenesis and/or diagnosis? This review concludes that the answers to these questions may further the understanding of panic disorder substantially, and hence contribute to improved diagnosis and therapy of the disease.
胆囊收缩素片段C末端四肽酰胺(CCK-4)意外发现的致惊恐效应表明,大脑中广泛分布的胆囊收缩素神经元网络及相应的CCK-B受体在某种程度上参与了人类惊恐障碍的发病机制。二十年的研究现已证实,外源性CCK-4确实能以可重复、剂量依赖性且敏感的方式在健康受试者中诱发惊恐发作,而在焦虑症患者中,更低剂量就能诱发。但关于内源性胆囊收缩素肽引发惊恐发作的分子机制仍有几个问题有待解答。本综述聚焦于三个紧迫问题。(1)内源性CCK-4是否存在?(2)致惊恐效应是否仅通过CCK-B受体介导?(3)脑脊液中胆囊收缩素肽的测量对于阐明发病机制和/或诊断是否有用?本综述得出结论,这些问题的答案可能会极大地增进对惊恐障碍的理解,从而有助于改善该疾病的诊断和治疗。