Roy Nisa, Ogawa Satoshi, Tsuda Sachiko, Parhar Ishwar S
Jeffrey Cheah School of Medicine & Health Sciences, Monash University Malaysia, Subang Jaya, Malaysia.
Graduate School of Science and Engineering, Saitama University, Saitama, Japan.
Front Neurosci. 2024 Dec 5;18:1461148. doi: 10.3389/fnins.2024.1461148. eCollection 2024.
G protein-coupled receptor 139 (GPR139), a highly conserved orphan receptor, is predominantly expressed in the habenula of vertebrate species. Habenula is an ancient epithalamic structure, which is critical to comprehending adaptive behaviors in vertebrates. We have previously demonstrated the role of GPR139 agonists in fear-associated decision-making processes in zebrafish. However, how GPR139 signaling in the habenula modulates such adaptive behavioral responses remains unsolved. Fish centrally administered with a synthetic antagonist for human GPR139 (NCRW0005-F05) exhibited significant suppression of odorant cue (alarm substance, AS)-induced fear learning in the conditioned place avoidance paradigm. On the other hand, co-treatment with a GPR139 antagonist and a synthetic agonist for human GPR139 (JNJ-63533054) interrupted the fear conditioning process by significantly reducing locomotion during post-conditioning. Calcium imaging of acute brain slices showed a significant increase in peak amplitude of calcium transients in the habenula upon bath application of either a GPR139 antagonist or agonist. Furthermore, KCl-evoked calcium transients were reduced by the GPR139 antagonist and co-treatment of the GPR139 antagonist-agonist. These results suggest that the GPR139 antagonist did not block the inhibitory action of the GPR139 agonist in the decision-making process during the fear-retrieval phase; however, solitarily, it functions in governing the fear consolidation process via activation of the ventral habenula neurons in zebrafish.
G蛋白偶联受体139(GPR139)是一种高度保守的孤儿受体,主要在脊椎动物的缰核中表达。缰核是一个古老的上丘脑结构,对理解脊椎动物的适应性行为至关重要。我们之前已经证明了GPR139激动剂在斑马鱼恐惧相关决策过程中的作用。然而,缰核中的GPR139信号如何调节这种适应性行为反应仍未得到解决。向鱼中枢注射人GPR139的合成拮抗剂(NCRW0005-F05)后,在条件性位置回避范式中,气味线索(警报物质,AS)诱导的恐惧学习受到显著抑制。另一方面,在条件化后,将GPR139拮抗剂与人GPR139的合成激动剂(JNJ-63533054)联合处理,通过显著减少运动中断了恐惧条件化过程。急性脑片的钙成像显示,在浴槽中应用GPR139拮抗剂或激动剂后,缰核中钙瞬变的峰值幅度显著增加。此外,GPR139拮抗剂以及GPR139拮抗剂-激动剂联合处理均可降低氯化钾诱发的钙瞬变。这些结果表明,在恐惧恢复阶段的决策过程中,GPR139拮抗剂并未阻断GPR139激动剂的抑制作用;然而,单独使用时,它通过激活斑马鱼腹侧缰核神经元来调控恐惧巩固过程。