Department of Anaesthesiology and Pain Management, Maastricht University Medical Center(+), Maastricht, the Netherlands; School for Mental Health and Neuroscience (MHeNs), Faculty of Health, Medicine and Life Sciences, University of Maastricht, Maastricht, the Netherlands.
School for Mental Health and Neuroscience (MHeNs), Faculty of Health, Medicine and Life Sciences, University of Maastricht, Maastricht, the Netherlands; Department of Genetics and Cell Biology, Clinical Genomics Unit, Maastricht University, Maastricht, the Netherlands.
Eur J Pharmacol. 2021 Dec 5;912:174517. doi: 10.1016/j.ejphar.2021.174517. Epub 2021 Sep 20.
Dopamine (DA) is an important modulator in nociception and analgesia. Spinal DA receptors are involved in descending modulation of the nociceptive transmission. Genetic variations within DA neurotransmission have been associated with altered pain sensitivity and development of chronic pain syndromes. The variant rs6277 in dopamine receptor 2 a (drd2a) has been associated with a decreased D receptor availability and increased nociception. The aim of this study is to further characterize the role of DA neurotransmission in nociception and the anti-nociceptive function of drd2a. The phenotype caused by rs6277 was modelled in zebrafish larvae using morpholino's and the effect on nociception was tested using a validated behavioural assay. The anti-nociceptive role of drd2a was tested using pharmacological intervention of D agonist Quinpirole. The experiments demonstrate that a decrease in drd2a expression results in a pro-nociceptive behavioural phenotype (P = 0.016) after a heat stimulus. Furthermore, agonism of drd2a with agonist Quinpirole (0.2 μM) results in dose-dependent anti-nociception (P = 0.035) after a heat stimulus. From these results it is concluded that the dopamine receptor drd2a is involved in anti-nociceptive behaviour in zebrafish. The model allows further screening and testing of genetic variation and treatment involved in nociception.
多巴胺(DA)是痛觉和镇痛的重要调节剂。脊髓 DA 受体参与伤害性传递的下行调制。DA 神经递质内的遗传变异与疼痛敏感性改变和慢性疼痛综合征的发展有关。多巴胺受体 2a(drd2a)中的变体 rs6277 与 D 受体可用性降低和伤害感受增加有关。本研究的目的是进一步表征 DA 神经递质在伤害感受中的作用以及 drd2a 的抗伤害感受功能。使用 morpholino 在斑马鱼幼虫中模拟 rs6277 引起的表型,并使用经过验证的行为测定法测试对伤害感受的影响。使用 D 激动剂 Quinpirole 进行药理学干预来测试 drd2a 的抗伤害感受作用。实验表明,热刺激后,drd2a 表达减少会导致伤害感受增加的行为表型(P=0.016)。此外,用激动剂 Quinpirole(0.2 μM)激动 drd2a 会导致热刺激后的剂量依赖性抗伤害感受(P=0.035)。从这些结果可以得出结论,多巴胺受体 drd2a 参与了斑马鱼的抗伤害感受行为。该模型允许进一步筛选和测试与伤害感受相关的遗传变异和治疗方法。