Brambilla F, Bellodi L, Perna G, Garberi A, Panerai A, Sacerdote P
Centro di Psiconeuroendocrinologia, Ospedale Psichiatrico Pini, Milan, Italy.
Am J Psychiatry. 1993 Jul;150(7):1111-3. doi: 10.1176/ajp.150.7.1111.
Since cholecystokinin (CCK) is known to be anxiogenic in experimental animals and to induce panic attacks in humans, lymphocyte CCK-8 concentrations were measured in 15 patients with panic disorder and 15 age- and sex-matched healthy subjects. The patients' levels were measured again after a 30-day course of alprazolam therapy, 1.5 mg/day. The CCK-8 concentrations were significantly lower in the patients than in the control subjects and did not change after alprazolam therapy. There was no correlation between the peptide values and levels of anxiety or frequency and severity of panic attacks.
由于已知胆囊收缩素(CCK)在实验动物中具有致焦虑作用,并可诱发人类恐慌症发作,因此对15名恐慌症患者和15名年龄及性别匹配的健康受试者的淋巴细胞CCK-8浓度进行了测量。在接受为期30天、每日1.5毫克阿普唑仑治疗后,再次测量了患者的CCK-8浓度。患者的CCK-8浓度显著低于对照组,且在阿普唑仑治疗后未发生变化。肽值与焦虑水平或恐慌症发作频率及严重程度之间无相关性。