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胆囊收缩素(B)激动剂对大鼠修饰行为的相反作用:胆囊收缩素(B)两个亚位点的进一步证据

Opposite effects of CCK(B) agonists in grooming behaviour in rats: further evidence for two CCK(B) subsites.

作者信息

Ladurelle N, Sebret A, Garbay C, Roques B P, Daugé V

机构信息

Département de Pharmacochimie Moléculaire et Structurale, U 266 INSERM, URA D 1500 CNRS, Faculté des Sciences Pharmaceutiques et Biologiques, Paris, France.

出版信息

Br J Pharmacol. 1998 Jul;124(6):1091-8. doi: 10.1038/sj.bjp.0701933.

Abstract
  1. The hypothesis of the existence of two CCK(B) receptor subsites, CCK(B1) and CCK(B2) corresponding probably to different coupling states of CCK(B) receptors, was studied by measuring grooming behaviour in rats. 2. The B1 receptor agonist, BC197 (300 microg kg(-1), i.p.) produced a 45-50% decrease in grooming activity, which was prevented by both the CCK(B) receptor antagonists CI-988 (20 microg kg(-1) i.p.) and L-365,260 (200 microg kg(-1), i.p.). 3. In contrast, 3, 10 and 30 microg kg(-1), i.p., of the potent B2 receptor agonist, BC264, enhanced grooming (150-190%). This effect was prevented by previous injection of 75 microg kg(-1) of L-365,260 while higher doses (200 microg kg(-1), i.p.) produced only a partial antagonism. Moreover, CI-988 (20 microg kg(-1), i.p.), showed an opposite effect in potentiating the responses induced by BC264. However, 200 microg kg(-1) of CI-988 tended to suppress the increase of grooming induced by BC264. 4. The effects of BC264 were prevented by the D1 receptor (SCH 23390) and D2 receptor (sulpiride) antagonists, while those of BC197 were only antagonized by sulpiride, emphasizing the existence of a link between peptidergic (CCK) and dopaminergic systems. 5. This study brings additional evidence for the existence of the two CCK(B) receptor subsites and suggests that particular attention should be focused on the selectivity of CCK(B) receptor agonists, notably to explain the fact that some compounds such as Boc-CCK4 induce anxiogenic-like effects while others, including BC264, are devoid of these effects.
摘要
  1. 通过测量大鼠的梳理行为,研究了存在两种CCK(B)受体亚位点CCK(B1)和CCK(B2)的假说,这两个亚位点可能对应于CCK(B)受体的不同偶联状态。2. B1受体激动剂BC197(300微克/千克,腹腔注射)使梳理活动减少45 - 50%,CCK(B)受体拮抗剂CI - 988(20微克/千克,腹腔注射)和L - 365,260(200微克/千克,腹腔注射)均可阻断该作用。3. 相比之下,强效B2受体激动剂BC264腹腔注射3、10和30微克/千克可增强梳理行为(增强150 - 190%)。预先注射75微克/千克的L - 365,260可阻断该作用,而更高剂量(200微克/千克,腹腔注射)仅产生部分拮抗作用。此外,CI - 988(20微克/千克,腹腔注射)在增强BC264诱导的反应中表现出相反的作用。然而,200微克/千克的CI - 988倾向于抑制BC264诱导的梳理行为增加。4. BC264的作用可被D1受体拮抗剂(SCH 23390)和D2受体拮抗剂(舒必利)阻断,而BC197的作用仅被舒必利拮抗,这强调了肽能(CCK)系统和多巴胺能系统之间存在联系。5. 本研究为两种CCK(B)受体亚位点的存在提供了额外证据,并表明应特别关注CCK(B)受体激动剂的选择性,尤其是要解释某些化合物如Boc - CCK4会诱导焦虑样效应而其他化合物(包括BC264)则无此效应这一事实。

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