Li M S, Peng Y L, Jiang J H, Xue H X, Wang P, Zhang P J, Han R W, Chang M, Wang R
Institute of Biochemistry and Molecular Biology, School of Life Sciences, Key Laboratory of Preclinical Study for New Drugs of Gansu Province, Lanzhou University, Lanzhou 730000, China.
Institute of Biochemistry and Molecular Biology, School of Life Sciences, Key Laboratory of Preclinical Study for New Drugs of Gansu Province, Lanzhou University, Lanzhou 730000, China.
Peptides. 2015 Sep;71:196-201. doi: 10.1016/j.peptides.2015.07.024. Epub 2015 Jul 31.
Neuropeptide S (NPS), the endogenous ligand of NPS receptor (NPSR), was reported to be involved in the regulation of arousal, anxiety, locomotion, learning and memory. The basal ganglia play a crucial role in regulating of locomotion-related behavior. Here, we found that NPSR protein of mouse was distributed in the substantia nigra (SN) and globus pallidus (LGP) by immunohistochemical analysis. However, less is known about the direct locomotion-related effects of NPS in both SN and LGP. Therefore, we investigated the role of NPS in locomotion processes, using the open field test. The results showed that NPS infused into the SN (0.03, 0.1, 1nmol) or LGP (0.01, 0.03, 0.1nmol) dose-dependently increased the locomotor activity in mice. SHA 68 (50mg/kg), an antagonist of NPSR, blocked the locomotor stimulant effect of NPS in both nuleus. Meanwhile, these effects of NPS were also counteracted by the CRF1 receptor antagonist antalarmin (30mg/kg, i.p.). In addition, we found that the expression of c-Fos was significantly increased after NPS was delivered into SN. In conclusion, these results indicate that NPS-NPSR system may regulate locomotion together with the CRF1 system in SN.
神经肽S(NPS)是NPS受体(NPSR)的内源性配体,据报道其参与觉醒、焦虑、运动、学习和记忆的调节。基底神经节在调节与运动相关的行为中起关键作用。在此,我们通过免疫组织化学分析发现小鼠的NPSR蛋白分布于黑质(SN)和苍白球(LGP)。然而,关于NPS在SN和LGP中对运动的直接影响知之甚少。因此,我们使用旷场试验研究了NPS在运动过程中的作用。结果显示,向SN(0.03、0.1、1nmol)或LGP(0.01、0.03、0.1nmol)注入NPS可剂量依赖性地增加小鼠的运动活性。NPSR拮抗剂SHA 68(50mg/kg)可阻断NPS在两个核团中的运动刺激作用。同时,NPS的这些作用也被促肾上腺皮质激素释放因子1(CRF1)受体拮抗剂安他拉明(30mg/kg,腹腔注射)抵消。此外,我们发现向SN注入NPS后c-Fos的表达显著增加。总之,这些结果表明NPS-NPSR系统可能与SN中的CRF1系统共同调节运动。