Sahuque Lacey L, Kullberg Erika F, Mcgeehan Andrew J, Kinder Jennifer R, Hicks Megan P, Blanton Mary G, Janak Patricia H, Olive M Foster
Ernest Gallo Clinic and Research Center, Department of Neurology, University of California at San Francisco, Emeryville, CA 94608, USA.
Psychopharmacology (Berl). 2006 May;186(1):122-32. doi: 10.1007/s00213-006-0362-y. Epub 2006 Mar 28.
Corticotropin-releasing factor (CRF) produces anxiety-like and aversive effects when infused directly into the various regions of the brain, including the bed nucleus of the stria terminalis (BNST). However, the CRF receptor subtypes within the BNST mediating these phenomena have not been established.
We used selective CRF receptor antagonists to determine the receptor subtypes involved in the anxiogenic-like and aversive effects CRF in the BNST.
Male Long-Evans rats were bilaterally infused with CRF (0.2 or 1.0 nmol) either alone or in combination with the CRF1 receptor antagonist CP154,526 or the CRF2 receptor antagonist anti-sauvagine 30 (AS30) before behavioral testing in the elevated plus maze or place conditioning paradigms.
Intra-BNST administration of CRF produced a dose-dependent reduction in open arm entries and open arm time in the elevated plus maze, indicating an anxiogenic-like effect. These effects were inhibited by co-infusion of CP154,526 but not of AS30, indicating that the anxiogenic-like effects of CRF in the BNST are mediated by CRF1 receptors. Place conditioning with intra-BNST administration of CRF produced a dose-dependent aversion to the CRF-paired environment that was prevented by co-infusion of either CP154,526 or AS30, indicating that both CRF receptor subtypes mediate the aversive effects of this peptide. Intra-BNST infusions of the CRF receptor antagonists alone produced no effects in either behavioral paradigm.
CRF1 receptors in the BNST mediate the anxiogenic-like effects of CRF in this region, whereas both CRF1 and CRF2 receptor subtypes mediate the conditioned aversive effects of this peptide within the BNST.
促肾上腺皮质激素释放因子(CRF)直接注入包括终纹床核(BNST)在内的大脑各个区域时,会产生类似焦虑和厌恶的效应。然而,介导这些现象的BNST内的CRF受体亚型尚未明确。
我们使用选择性CRF受体拮抗剂来确定参与BNST中CRF产生类似焦虑和厌恶效应的受体亚型。
在高架十字迷宫或位置条件反射范式的行为测试前,对雄性Long-Evans大鼠双侧注射CRF(0.2或1.0 nmol),单独注射或与CRF1受体拮抗剂CP154,526或CRF2受体拮抗剂抗蛙皮素30(AS30)联合注射。
BNST内注射CRF在高架十字迷宫中使进入开放臂的次数和在开放臂停留的时间呈剂量依赖性减少,表明产生了类似焦虑的效应。这些效应被CP154,526共同注射所抑制,但未被AS30抑制,表明BNST中CRF的类似焦虑效应由CRF1受体介导。BNST内注射CRF进行位置条件反射产生了对CRF配对环境的剂量依赖性厌恶,而CP154,526或AS30共同注射可预防这种厌恶,表明两种CRF受体亚型均介导该肽的厌恶效应。单独BNST内注射CRF受体拮抗剂在两种行为范式中均未产生影响。
BNST中的CRF1受体介导该区域中CRF的类似焦虑效应,而CRF1和CRF2受体亚型均介导BNST内该肽的条件性厌恶效应。