Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY, USA.
Brain Res. 2011 Jun 17;1396:54-9. doi: 10.1016/j.brainres.2011.04.042. Epub 2011 Apr 28.
The false-suffocation hypothesis of panic disorder (Klein, 1993) suggested δ-opioid receptors as a possible source of the respiratory dysfunction manifested in panic attacks occurring in panic disorder (Preter and Klein, 2008). This study sought to determine if a lack of δ-opioid receptors in a mouse model affects respiratory response to elevated CO₂, and whether the response is modulated by benzodiazepines, which are widely used to treat panic disorder. In a whole-body plethysmograph, respiratory responses to 5% CO₂ were compared between δ-opioid receptor knockout mice and wild-type mice after saline, diazepam (1mg/kg), and alprazolam (0.3mg/kg) injections. The results show that lack of δ-opioid receptors does not affect normal response to elevated CO₂, but does prevent benzodiazepines from modulating that response. Thus, in the presence of benzodiazepine agonists, respiratory responses to elevated CO₂ were enhanced in δ-opioid receptor knockout mice compared to wild-type mice. This suggests an interplay between benzodiazepine receptors and δ-opioid receptors in regulating the respiratory effects of elevated CO₂, which might be related to CO₂ induced panic.
惊恐障碍的虚假窒息假说(Klein,1993 年)认为 δ-阿片受体可能是惊恐发作中呼吸功能障碍的来源,惊恐发作发生在惊恐障碍中(Preter 和 Klein,2008 年)。本研究旨在确定在小鼠模型中缺乏 δ-阿片受体是否会影响对高浓度二氧化碳的呼吸反应,以及苯二氮䓬类药物(广泛用于治疗惊恐障碍)是否会调节这种反应。在全身 plethysmograph 中,在给予生理盐水、地西泮(1mg/kg)和阿普唑仑(0.3mg/kg)后,比较 δ-阿片受体敲除小鼠和野生型小鼠对 5%二氧化碳的呼吸反应。结果表明,缺乏 δ-阿片受体不会影响对高浓度二氧化碳的正常反应,但会阻止苯二氮䓬类药物调节这种反应。因此,在苯二氮䓬类激动剂存在的情况下,与野生型小鼠相比,δ-阿片受体敲除小鼠对高浓度二氧化碳的呼吸反应增强。这表明苯二氮䓬类受体和 δ-阿片受体在调节高浓度二氧化碳的呼吸效应方面存在相互作用,这可能与二氧化碳引起的惊恐有关。