College of Pharmacy, Xinxiang Medical University, Xixiang, Henan, China.
Peptides. 2011 Oct;32(10):2104-7. doi: 10.1016/j.peptides.2011.08.021. Epub 2011 Aug 30.
Our previous studies have demonstrated that oxytocin (OXT) in the central nervous system plays a role in pain modulation. Many studies have found that caudate nucleus (CdN) enriches OXT and OXT receptors by the methods of historadioautograph and gene expression. The communication was designed to investigate OXT effect in the rat CdN on pain modulation. The results showed that (1) intra-CdN microinjection of OXT receptor antagonist, desGly-NH(2), d(CH(2))(5)[D-Tyr(2), Thr-sup-4]OVT decreased the pain threshold, whereas the local administration of OXT increased the pain threshold in a dose-dependent manner; (2) OXT receptor antagonist can attenuate the analgesic role induced intra-CdN administration of OXT; and (3) pain stimulation could increase OXT concentration in the CdN perfusion liquid. The data suggested that OXT in the CdN was involved in this pain process via OXT receptors.
我们之前的研究表明,中枢神经系统中的催产素(OXT)在疼痛调节中发挥作用。许多研究发现,尾状核(CdN)通过放射自显影和基因表达的方法丰富了 OXT 和 OXT 受体。本研究旨在探讨大鼠 CdN 中 OXT 对疼痛调节的影响。结果表明:(1)OXT 受体拮抗剂 desGly-NH(2),d(CH(2))(5)[D-Tyr(2),Thr-sup-4]OVT 经尾状核内微注射可降低痛阈,而 OXT 则以剂量依赖性方式增加痛阈;(2)OXT 受体拮抗剂可减弱尾状核内 OXT 引起的镇痛作用;(3)疼痛刺激可增加尾状核灌流液中的 OXT 浓度。数据表明,CdN 中的 OXT 通过 OXT 受体参与了这一疼痛过程。