Bradwejn J, Koszycki D, Couëtoux du Tertre A, van Megen H, den Boer J, Westenberg H
Department of Psychiatry, McGill University, Montreal, Quebec.
Arch Gen Psychiatry. 1994 Jun;51(6):486-93. doi: 10.1001/archpsyc.1994.03950060050005.
We investigated whether the selective brain cholecystokinin (CCKB) receptor antagonist, L-365,260, could antagonize the panicogenic effects of CCK-tetrapeptide (CCK-4) in patients with panic disorder.
The study employed a double-blind, placebo-controlled, two-period crossover design. Patients (N = 29) received a single oral dose of L-365,260 (10 or 50 mg) or placebo 90 minutes prior to injection of CCK-4. After a 1-week washout period, patients received a different dose of L-365,260 or placebo according to a balanced incomplete block design.
The 50-mg dose of L-365,260 was superior to placebo in reducing the number (P < .01) and sum intensity (P < .001) of symptoms induced with CCK-4. Panic attack frequency following CCK-4 injection was 88% for patients receiving placebo, 33% for those receiving the 10-mg dose, and 0% for those receiving the 50-mg dose. The difference between the effects of the 50-mg dose and placebo was statistically significant (P = .002). Increases in heart rate following CCK-4 injection were markedly reduced with both the 50-mg (P < .0001) and 10-mg (P < .01) doses compared with placebo.
These data suggest that CCKB receptors are an important site of action of exogenous CCK-4. It will be important to determine in future studies the efficacy of CCKB receptor antagonists as antipanic agents.
我们研究了选择性脑胆囊收缩素(CCKB)受体拮抗剂L-365,260是否能拮抗惊恐障碍患者中胆囊收缩素四肽(CCK-4)的致惊恐作用。
该研究采用双盲、安慰剂对照、两阶段交叉设计。患者(N = 29)在注射CCK-4前90分钟口服单剂量的L-365,260(10或50毫克)或安慰剂。经过1周的洗脱期后,患者根据平衡不完全区组设计接受不同剂量的L-365,260或安慰剂。
50毫克剂量的L-365,260在减少CCK-4诱发的症状数量(P <.01)和症状总强度(P <.001)方面优于安慰剂。接受安慰剂的患者在注射CCK-4后的惊恐发作频率为88%,接受10毫克剂量的患者为33%,接受50毫克剂量的患者为0%。50毫克剂量与安慰剂的效果差异具有统计学意义(P =.002)。与安慰剂相比,50毫克(P <.0001)和10毫克(P <.01)剂量均显著降低了CCK-4注射后心率的增加。
这些数据表明CCKB受体是外源性CCK-4的重要作用位点。在未来的研究中确定CCKB受体拮抗剂作为抗惊恐药物的疗效将很重要。