Eser Daniela, Schüle Cornelius, Baghai Thomas, Floesser Anette, Krebs-Brown Axel, Enunwa Michaela, de la Motte Stephan, Engel Rolf, Kucher Klaus, Rupprecht Rainer
Department of Psychiatry and Psychotherapy, Ludwig-Maximilian-University, Nussbaumstr. 7, 80336 Munich, Germany.
Psychopharmacology (Berl). 2007 Jul;192(4):479-87. doi: 10.1007/s00213-007-0738-7. Epub 2007 Feb 23.
Experimental panic induction with cholecystokinin-tetrapeptide (CCK-4) has been established as a model to study the pathophysiology of panic disorder and might serve as a tool to asses the antipanic potential of novel anxiolytic compounds. However, assessment of CCK-4-induced panic does not follow consistent rules.
To provide a basis for the use of the CCK-4 model in proof-of-concept studies, we investigated CCK-4-induced panic according to different criteria in 85 healthy volunteers who underwent a CCK-4 bolus injection.
We assessed panicker/non-panicker ratios according to different panic criteria and explored whether differences in cardiovascular and neuroendocrine responses to CCK-4 paralleled subjective panic responses. Subjective panic responses were measured with the Acute Panic Inventory (API) and the Panic Symptom Scale (PSS). Heart rate, blood pressure, adrenocorticotropic hormone (ACTH) and cortisol were assessed concomitantly.
The API-derived panic rate was 10.6% higher than that derived from the PSS. CCK-4 induced an increase in heart rate, systolic blood pressure and ACTH/cortisol plasma levels, which did not differ between panickers and non-panickers.
The panic criterion applied appears to be of major importance for the panic rate achieved, whereas CCK-4-induced cardiovascular and hormonal alterations are not valuable as an objective "read out". The CCK-4 challenge might serve as a useful model to study putative anxiolytic effects of novel compounds during the early phase of drug development if the challenge procedure is carried out according to strictly comparable conditions.
用胆囊收缩素四肽(CCK-4)进行实验性惊恐诱导已被确立为研究惊恐障碍病理生理学的模型,并且可能作为评估新型抗焦虑化合物抗惊恐潜力的工具。然而,CCK-4诱导的惊恐评估并未遵循一致的规则。
为在概念验证研究中使用CCK-4模型提供依据,我们在85名接受CCK-4推注的健康志愿者中,根据不同标准研究了CCK-4诱导的惊恐。
我们根据不同的惊恐标准评估惊恐者/非惊恐者比例,并探讨对CCK-4的心血管和神经内分泌反应差异是否与主观惊恐反应平行。用急性惊恐量表(API)和惊恐症状量表(PSS)测量主观惊恐反应。同时评估心率、血压、促肾上腺皮质激素(ACTH)和皮质醇。
API得出的惊恐率比PSS得出的高10.6%。CCK-4导致心率、收缩压以及ACTH/皮质醇血浆水平升高,惊恐者和非惊恐者之间无差异。
所应用的惊恐标准对于所达到的惊恐率似乎至关重要,而CCK-4诱导的心血管和激素变化作为客观“指标”并无价值。如果按照严格可比的条件进行激发程序,CCK-4激发可能作为一个有用的模型,用于在药物研发早期研究新型化合物假定的抗焦虑作用。