4.5 Article

Orexin 1 receptors are a novel target to modulate panic responses and the panic brain network

期刊

PHYSIOLOGY & BEHAVIOR
卷 107, 期 5, 页码 733-742

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.physbeh.2012.04.016

关键词

Hypothalamus; Orexin; Hypocretin; Panic; Anxiety; GABA; FG-7142; Benzodiazepine; Amygdala; Periaqueductal gray; Rostroventrolateral medulla; Bed nucleus of the stria terminalus; BNST

资金

  1. Indiana CTSI Project Development Team Pilot Grant [RR025761]
  2. Indiana CTSI [UL1 RR025761]
  3. NIH Student LRP
  4. NARSAD Young Investigator Award
  5. [R01 MH52619]
  6. [R01 MH065702]

向作者/读者索取更多资源

Background: Although the hypothalamic orexin system is known to regulate appetitive behaviors and promote wakefulness and arousal (Sakurai, 2007 [561), this system may also be important in adaptive and pathological anxiety/stress responses (Suzuki et al., 2005 141). In a recent study, we demonstrated that CSF orexin levels were significantly higher in patients experiencing panic attacks compared to non-panicking depressed subjects (Johnson et al., 2010 191). Furthermore, genetically silencing orexin synthesis or blocking orexin 1 receptors attenuated lactate-induced panic in an animal model of panic disorder. Therefore, in the present study, we tested if orexin (ORX) modulates panic responses and brain pathways activated by two different panicogenic drugs. Methods: We conducted a series of pharmacological, behavioral, physiological and immunohistochemical experiments to study the modulation by the orexinergic inputs of anxiety behaviors, autonomic responses, and activation of brain pathways elicited by systemic injections of anxiogenic/panicogenic drugs in rats. Results: We show that systemic injections of two different anxiogenic/panicogenic drugs (FG-7142, an inverse agonist at the benzodiazepine site of the GABA(A) receptor, and caffeine, a nonselective competitive adenosine receptor antagonist) increased c-Fos induction in a specific subset of orexin neurons located in the dorsomedial/perifornical (DMH/PeF) but not the lateral hypothalamus. Pretreating rats with an orexin 1 receptor antagonist attenuated the FG-7142-induced anxiety-like behaviors, increased heart rate, and neuronal activation in key panic pathways, including subregions of the central nucleus of the amygdala, bed nucleus of the stria terminalis, periaqueductal gray and in the rostroventrolateral medulla. Conclusion: Overall, the data here suggest that the ORX neurons in the DMH/PeF region are critical to eliciting coordinated panic responses and that ORX1 receptor antagonists constitute a potential novel treatment strategy for panic and related anxiety disorders. The neural pathways through which ORX1 receptor antagonists attenuate panic responses involve the extended amygdala, periaqueductal gray, and medullary autonomic centers. (C) 2012 Elsevier Inc. All rights reserved.

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