Kow Teck Fong, Mok Siew Ying, Tang Pek Yee, Chong Lor Huai, Ogawa Satoshi
Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Bandar Sunway, Selangor Darul Ehsan, Malaysia.
Department of Mechatronics and Biomedical Engineering, Universiti Tunku Abdul Rahman, Kajang, Selangor, Malaysia.
FASEB J. 2025 May 31;39(10):e70656. doi: 10.1096/fj.202500594R.
GPR139, an orphan G-protein coupled receptor predominantly expressed in the habenula, has recently been implicated in understanding neurobehavior and neuropsychiatric disorders. Surrogate agonists for human GPR139 have shown the potential to alleviate cognitive impairment associated with schizophrenia in rodent models and human clinical trials. Yet, the effect of GPR139 agonists on the neurophysiological properties of the habenula remains elusive. We examined the effect of GPR139 agonists (JNJ-63533054 and TAK-041) on short-term startle habituation of 6-day post-fertilization (dpf) larval zebrafish (Danio rerio) in an automated solenoid setup and on reversing the pharmacologically impaired startle habituation. GPR139 agonists enhanced startle habituation at the lowest tested concentrations, whereas moderate and highest concentrations delayed startle habituation. Furthermore, GPR139 agonists reversed the non-competitive N-methyl-d-aspartate (NMDA) receptor antagonist MK-801-induced startle habituation impairment. Using exponential decay curve fit analysis, we found that the lowest concentration of GPR139 agonists performed better than moderate and highest concentrations in reversing the MK-801-induced impairment of startle habituation. Using in vivo GCaMP calcium imaging and phosphorylated extracellular-signal-regulated kinase (pERK) as a proxy for neural activity, we found that GPR139 agonists exerted effects on the habenula activities at the habituated state but not during the spontaneous state (without startle habituation paradigm), suggesting the GPR139 agonists-evoked neural activation in the habenula is sensory stimuli-dependent. Moreover, both GPR139 agonists differently reduced MK-801-induced hyperexcitability of the habenula at both spontaneous and habituated states. Taken together, we showed that GPR139 agonists reverse startle habituation impairment caused by MK-801 via the normalization of hyperexcitability of zebrafish habenula.
GPR139是一种主要在缰核中表达的孤儿G蛋白偶联受体,最近被认为与理解神经行为和神经精神疾病有关。人GPR139的替代激动剂已显示出在啮齿动物模型和人体临床试验中减轻与精神分裂症相关的认知障碍的潜力。然而,GPR139激动剂对缰核神经生理特性的影响仍然不清楚。我们在自动螺线管装置中研究了GPR139激动剂(JNJ-63533054和TAK-041)对受精后6天(dpf)幼虫斑马鱼(Danio rerio)短期惊吓习惯化的影响,以及对药理学诱导的惊吓习惯化受损的逆转作用。GPR139激动剂在最低测试浓度下增强了惊吓习惯化,而中等和最高浓度则延迟了惊吓习惯化。此外,GPR139激动剂逆转了非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂MK-801诱导的惊吓习惯化损伤。使用指数衰减曲线拟合分析,我们发现GPR139激动剂的最低浓度在逆转MK-801诱导的惊吓习惯化损伤方面比中等和最高浓度表现更好。使用体内GCaMP钙成像和磷酸化细胞外信号调节激酶(pERK)作为神经活动的指标,我们发现GPR139激动剂在习惯化状态下对缰核活动有影响,但在自发状态下(无惊吓习惯化范式)没有影响,这表明GPR139激动剂诱发的缰核神经激活是感觉刺激依赖性的。此外,两种GPR1激动剂在自发和习惯化状态下均不同程度地降低了MK-801诱导的缰核过度兴奋性。综上所述,我们表明GPR139激动剂通过使斑马鱼缰核过度兴奋性正常化来逆转由MK-801引起的惊吓习惯化损伤。