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终纹床核中的促肾上腺皮质激素释放因子1(CRF1)和促肾上腺皮质激素释放因子2(CRF2)受体调节大鼠对急性束缚应激的心血管反应。

CRF1 and CRF2 receptors in the bed nucleus of the stria terminalis modulate the cardiovascular responses to acute restraint stress in rats.

作者信息

Oliveira Leandro A, Almeida Jeferson, Benini Ricardo, Crestani Carlos C

机构信息

Laboratory of Pharmacology, School of Pharmaceutical Sciences, Univ. Estadual Paulista - UNESP, Araraquara, SP, Brazil; Joint UFSCar-UNESP Graduate Program in Physiological Sciences, São Carlos, SP, Brazil.

Laboratory of Pharmacology, School of Pharmaceutical Sciences, Univ. Estadual Paulista - UNESP, Araraquara, SP, Brazil.

出版信息

Pharmacol Res. 2015 May-Jun;95-96:53-62. doi: 10.1016/j.phrs.2015.03.012. Epub 2015 Mar 28.

Abstract

The corticotropin-releasing factor (CRF) is involved in behavioral and physiological responses to emotional stress through its action in several limbic structures, including the bed nucleus of the stria terminalis (BNST). Nevertheless, the role of CRF1 and CRF2 receptors in the BNST in cardiovascular adjustments during aversive threat is unknown. Therefore, in the present study we investigated the involvement of CRF receptors within the BNST in cardiovascular responses evoked by acute restraint stress in rats. For this, we evaluated the effects of bilateral treatment of the BNST with selective agonists and antagonists of either CRF1 or CRF2 receptors in the arterial pressure and heart rate increase and the decrease in tail skin temperature induced by restraint stress. Microinjection of the selective CRF1 receptor antagonist CP376395 into the BNST reduced the pressor and tachycardiac responses caused by restraint. Conversely, BNST treatment with the selective CRF1 receptor agonist CRF increased restraint-evoked arterial pressure and HR responses and reduced the fall in tail skin temperature response. All effects of CRF were inhibited by local BNST pretreatment with CP376395. The selective CRF2 receptor antagonist antisalvagine-30 reduced the arterial pressure increase and the fall in tail skin temperature. The selective CRF2 receptor agonist urocortin-3 increased restraint-evoked pressor and tachycardiac responses and reduced the drop in cutaneous temperature. All effects of urocortin-3 were abolished by local BNST pretreatment with antisalvagine-30. These findings indicate an involvement of both CRF1 and CRF2 receptors in the BNST in cardiovascular adjustments during emotional stress.

摘要

促肾上腺皮质激素释放因子(CRF)通过其在包括终纹床核(BNST)在内的多个边缘结构中的作用,参与对情绪应激的行为和生理反应。然而,在厌恶威胁期间,BNST中CRF1和CRF2受体在心血管调节中的作用尚不清楚。因此,在本研究中,我们调查了BNST内的CRF受体在大鼠急性束缚应激诱发的心血管反应中的作用。为此,我们评估了用CRF1或CRF2受体的选择性激动剂和拮抗剂对BNST进行双侧处理对束缚应激引起的动脉压升高、心率加快以及尾部皮肤温度降低的影响。向BNST微量注射选择性CRF1受体拮抗剂CP376395可降低束缚引起的升压和心动过速反应。相反,用选择性CRF1受体激动剂CRF处理BNST可增加束缚诱发的动脉压和心率反应,并减少尾部皮肤温度反应的下降。CRF的所有作用均被BNST局部预处理CP376395所抑制。选择性CRF2受体拮抗剂抗salvagine-30可降低动脉压升高和尾部皮肤温度下降。选择性CRF2受体激动剂urocortin-3可增加束缚诱发的升压和心动过速反应,并减少皮肤温度下降。urocortin-3的所有作用均被BNST局部预处理抗salvagine-30所消除。这些发现表明,在情绪应激期间,BNST中的CRF1和CRF2受体均参与心血管调节。

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