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Somatostatin receptors in the ventral pallidum/substantia innominata modulate rat locomotor activity.

机译:腹侧苍白球/无症状的生长抑素受体调节大鼠的自发活动。

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RATIONAL: Somatostatin and its receptors (sst(1) and sst(2)) have been localized in brain nuclei implicated in motor control, such as the nucleus accumbens, ventral pallidum (VP) and substantia innominata (SI). OBJECTIVES: The objective of the study is to investigate the effect of somatostatin and selective sst(1) and sst(2) analogs infused in the VP/SI on the locomotor activity of the rat. METHODS: Somatostatin (15, 30, 60, 120 and 240 ng/0.5 microl/side), CH275 (sst(1) analog; 60, 180, 240 and 480 ng/0.5 microl/side), MK678 (sst(2) analog; 120, 240 and 480 ng/0.5 microl/side), L-809,087 (sst(4) agonist, 240 ng/0.5 microl/side) or saline (vehicle) were infused bilaterally in the VP/SI of the rat and locomotor activity measured for 60 min. The effect of SRA-880 (sst(1) antagonist) and CYN-154806 (sst(2) antagonist) on somatostatin-, CH275- and MK678-mediated locomotor activity was also ascertained. RESULTS: Somatostatin decreased locomotor activity in the first 30 min after its infusion in the VP/SI and in a dose-dependent manner. The sst(1) and sst(2) antagonists, SRA-880 and CYN-154806, respectively, reversed the somatostatin effect. The sst(1) and sst(2) agonists CH275 and MK678, respectively, mimicked somatostatin's actions, while the selective sst(4) agonist L-809,087 had no effect. Moreover, SRA-880 and CYN-154806 reversed the respective agonist action on locomotor activity. CONCLUSION: The present study provides functional evidence for the presence of sst(1) and sst(2) receptors in the VP/SI and their implication in motor control. The mechanism via which somatostatin and agonists mediate the attenuation of locomotor activity is presently being investigated.
机译:合理:生长抑素及其受体(sst(1)和sst(2))已定位于牵涉运动控制的脑核中,例如伏隔核,腹侧苍白球(VP)和无名状实体(SI)。目的:本研究的目的是研究在VP / SI中注入生长抑素和选择性sst(1)和sst(2)类似物对大鼠运动能力的影响。方法:生长抑素(15、30、60、120和240 ng / 0.5微升/边),CH275(sst(1)类似物; 60、180、240和480 ng / 0.5微升/边),MK678(sst(2)类似物;将120、240和480 ng / 0.5微升/边),L-809,087(sst(4)激动剂,240 ng / 0.5微升/边)或生理盐水(车辆)分别注入大鼠的VP / SI和测量60分钟的运动活动。还确定了SRA-880(sst(1)拮抗剂)和CYN-154806(sst(2)拮抗剂)对生长抑素,CH275和MK678介导的运动活性的影响。结果:生长抑素在注入VP / SI后的前30分钟内以剂量依赖性方式降低了运动活性。 sst(1)和sst(2)拮抗剂SRA-880和CYN-154806分别逆转了生长抑素的作用。 sst(1)和sst(2)激动剂CH275和MK678分别模仿生长抑素的作用,而选择性sst(4)激动剂L-809,087没有作用。此外,SRA-880和CYN-154806逆转了各自对运动活性的激动剂作用。结论:本研究为功能性证据表明VP / SI中sst(1)和sst(2)受体的存在及其在运动控制中的意义。目前正在研究生长抑素和激动剂介导运动活性减弱的机制。

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