Department of Psychiatry, Columbia University, and New York State Psychiatric Institute, New York, NY, USA.
Psychol Med. 2011 Feb;41(2):385-93. doi: 10.1017/S0033291710000838. Epub 2010 May 6.
The expanded suffocation false alarm theory (SFA) hypothesizes that dysfunction in endogenous opioidergic regulation increases sensitivity to CO2, separation distress and panic attacks. In panic disorder (PD) patients, both spontaneous clinical panics and lactate-induced panics markedly increase tidal volume (TV), whereas normals have a lesser effect, possibly due to their intact endogenous opioid system. We hypothesized that impairing the opioidergic system by naloxone could make normal controls parallel PD patients' response when lactate challenged. Whether actual separations and losses during childhood (childhood parental loss, CPL) affected naloxone-induced respiratory contrasts was explored. Subjective panic-like symptoms were analyzed although pilot work indicated that the subjective aspect of anxious panic was not well modeled by this specific protocol.
Randomized cross-over sequences of intravenous naloxone (2 mg/kg) followed by lactate (10 mg/kg), or saline followed by lactate, were given to 25 volunteers. Respiratory physiology was objectively recorded by the LifeShirt. Subjective symptomatology was also recorded.
Impairment of the endogenous opioid system by naloxone accentuates TV and symptomatic response to lactate. This interaction is substantially lessened by CPL.
Opioidergic dysregulation may underlie respiratory pathophysiology and suffocation sensitivity in PD. Comparing specific anti-panic medications with ineffective anti-panic agents (e.g. propranolol) can test the specificity of the naloxone+lactate model. A screen for putative anti-panic agents and a new pharmacotherapeutic approach are suggested. Heuristically, the experimental unveiling of the endogenous opioid system impairing effects of CPL and separation in normal adults opens a new experimental, investigatory area.
扩展窒息性假警报理论(SFA)假设内源性阿片能调节功能障碍会增加对 CO2、分离痛苦和惊恐发作的敏感性。在惊恐障碍(PD)患者中,自发性临床惊恐发作和乳酸引起的惊恐发作都会显著增加潮气量(TV),而正常人的影响较小,这可能是由于他们完整的内源性阿片系统。我们假设通过纳洛酮损害阿片能系统可以使正常对照者在乳酸挑战时与 PD 患者的反应相平行。在探讨童年时期(父母丧失,CPL)实际分离和丧失是否会影响纳洛酮引起的呼吸对比时,我们考虑了这一点。尽管初步研究表明,这种特定方案并不能很好地模拟焦虑性惊恐的主观方面,但仍分析了主观惊恐样症状。
对 25 名志愿者进行静脉内纳洛酮(2mg/kg)继以乳酸(10mg/kg)或生理盐水继以乳酸的随机交叉试验序列。生命衬衫客观记录呼吸生理学。还记录了主观症状学。
纳洛酮对内源性阿片能系统的损害加重了 TV 和对乳酸的症状反应。CPL 大大减轻了这种相互作用。
阿片能调节障碍可能是 PD 呼吸病理生理学和窒息敏感性的基础。将特定的抗惊恐药物与无效的抗惊恐药物(如普萘洛尔)进行比较可以检验纳洛酮+乳酸模型的特异性。建议进行潜在抗惊恐药物的筛选和新的药物治疗方法。从启发式的角度来看,实验揭示了内源性阿片能系统在正常成年人中对 CPL 和分离的损害作用,开辟了一个新的实验和研究领域。