Hernandez-Gómez A M, Aguilar-Roblero R, Pérez de la Mora M
Department of Biophysics, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, México, DF México.
Amino Acids. 2002;23(1-3):283-90. doi: 10.1007/s00726-001-0139-x.
Evidence from several laboratories indicates that the anxiogenic effects of cholecystokinin (CCK) are mediated by CCKB receptors. However, it has been reported that CCKA receptors have been found in brain and CCKA antagonists have anxiolytic properties. The aim of this work was to study whether CCKA receptors are also involved in the modulation of anxiety. Anxiogenic effects were observed in the elevated plus maze in rats when pure CCKB receptor agonists (CCK-4 and CCK-8 non-sulfated) or CCK-8S, a CCKB/CCKA agonist, were injected into the lateral ventricle. In contrast, CCK-33, a CCKA agonist or CCK-(1-21) and CCK-(26-29) were ineffective. Furthermore, the anxiogenic effects of CCK-8S were prevented by blocking CCKB but not CCKA receptors. Finally, CCK-33 injected into the postero-medial nucleus accumbens failed to affect the anxiety level of the rats. These results indicate that CCKA receptors are not involved in anxiety, as measured by the paradigms used in this work.
多个实验室提供的证据表明,胆囊收缩素(CCK)的致焦虑作用是由CCKB受体介导的。然而,据报道,在大脑中发现了CCKA受体,并且CCKA拮抗剂具有抗焦虑特性。这项研究的目的是探究CCKA受体是否也参与焦虑调节。当将纯CCKB受体激动剂(CCK-4和非硫酸化的CCK-8)或CCK-8S(一种CCKB/CCKA激动剂)注入大鼠侧脑室时,在高架十字迷宫实验中观察到了致焦虑作用。相比之下,CCKA激动剂CCK-33或CCK-(1-21)和CCK-(26-29)则没有效果。此外,通过阻断CCKB受体而非CCKA受体可预防CCK-8S的致焦虑作用。最后,向伏隔核后内侧核注射CCK-33未能影响大鼠的焦虑水平。这些结果表明,按照本研究中使用的实验范式来衡量,CCKA受体不参与焦虑调节。