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胆囊收缩素-2受体调节大鼠背外侧导水管周围灰质电刺激诱发的僵住和逃避行为。

Cholecystokinin-2 receptors modulate freezing and escape behaviors evoked by the electrical stimulation of the rat dorsolateral periaqueductal gray.

作者信息

Bertoglio Leandro José, de Bortoli Valquiria Camin, Zangrossi Hélio

机构信息

Departamento de Farmacologia, CCB, UFSC, Florianópolis, SC, 88049-900, Brazil.

出版信息

Brain Res. 2007 Jul 2;1156:133-8. doi: 10.1016/j.brainres.2007.04.038. Epub 2007 Apr 21.

DOI:10.1016/j.brainres.2007.04.038
PMID:17498673
Abstract

Systemic injection of the cholecystokinin type 2 (CCK(2)) receptor agonist CCK-4 evokes panic attacks in humans and facilitates the expression of a panic-related defensive behavior, escape, in rats. Given the prominent role attributed to the dorsal periaqueductal gray (dPAG) in the pathophysiology of panic, this midbrain area has been assumed to be one of the key regions mediating these effects of CCK-4. However, only a few studies have directly investigated the role of dPAG CCK(2) receptors in the regulation of panic-related behaviors. Even more disappointingly, the results of these investigations have been far from conclusive. In the present study we further addressed this issue by evaluating the effect of the intra-dorsolateral periaqueductal gray (dlPAG) injection of CCK-4 on two panic-related defensive behaviors, freezing and escape, evoked in male Wistar rats by the electrical stimulation of the dlPAG. The effects of CCK-4 (0.005-0.5 microg/0.2 microl) were compared to those caused by the local microinjection of the CCK(2) receptor antagonist LY225910 (0.001-1.0 microg/0.2 microl). The results showed that whereas CCK-4 facilitated the expression of both freezing and escape behaviors, LY225910 had the opposite effect. Pretreatment with an ineffective dose of LY225910 prevented the panicogenic-like effect of CCK-4. These results strengthen the view that CCK(2) receptors located in the dlPAG are involved in the regulation of panic-related behaviors and may mediate the effect of CCK-4 on panic.

摘要

全身注射2型胆囊收缩素(CCK(2))受体激动剂CCK-4可诱发人类恐慌发作,并促进大鼠表现出与恐慌相关的防御行为——逃跑。鉴于中脑导水管周围灰质背侧(dPAG)在恐慌病理生理学中具有重要作用,该脑区被认为是介导CCK-4这些效应的关键区域之一。然而,只有少数研究直接探究了dPAG中CCK(2)受体在调控恐慌相关行为中的作用。更令人失望的是,这些研究结果远未得出定论。在本研究中,我们通过评估向背外侧中脑导水管周围灰质(dlPAG)注射CCK-4对雄性Wistar大鼠因电刺激dlPAG诱发的两种恐慌相关防御行为——僵住和逃跑的影响,进一步探讨了这一问题。将CCK-4(0.005 - 0.5微克/0.2微升)的作用与局部微量注射CCK(2)受体拮抗剂LY225910(0.001 - 1.0微克/0.2微升)所产生的作用进行了比较。结果显示,CCK-4促进了僵住和逃跑行为的表现,而LY225910则产生相反的效果。用无效剂量的LY225910进行预处理可预防CCK-4的致恐慌样效应。这些结果强化了这样一种观点,即位于dlPAG的CCK(2)受体参与调控恐慌相关行为,并可能介导CCK-4对恐慌的影响。

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