Department of Anatomy & Physiology, University of Melbourne, Melbourne, VIC, Australia.
School of Biomedical Sciences, University of Queensland, Brisbane, QLD, Australia.
J Physiol. 2023 Dec;601(23):5195-5211. doi: 10.1113/JP285217. Epub 2023 Sep 29.
Agonists of dopamine D2 receptors (D2R), 5-hydroxytryptamine (5-HT, serotonin) receptors (5-HTR) and ghrelin receptors (GHSR) activate neurons in the lumbosacral defecation centre, and act as 'colokinetics', leading to increased propulsive colonic motility, in vivo. In the present study, we investigated which neurons in the lumbosacral defecation centre express the receptors and whether dopamine, serotonin and ghrelin receptor agonists act on the same lumbosacral preganglionic neurons (PGNs). We used whole cell electrophysiology to record responses from neurons in the lumbosacral defecation centre, following colokinetic application, and investigated their expression profiles and the chemistries of their neural inputs. Fluorescence in situ hybridisation revealed Drd2, Ghsr and Htr2C transcripts were colocalised in lumbosacral PGNs of mice, and immunohistochemistry showed that these neurons have closely associated tyrosine hydroxylase and 5-HT boutons. Previous studies showed that they do not receive ghrelin inputs. Whole cell electrophysiology in adult mice spinal cord revealed that dopamine, serotonin, α-methylserotonin and capromorelin each caused inward, excitatory currents in overlapping populations of lumbosacral PGNs. Furthermore, dopamine caused increased frequency of both IPSCs and EPSCs in a cohort of D2R neurons. Tetrodotoxin blocked the IPSCs and EPSCs, revealing a post-synaptic excitatory action of dopamine. In lumbosacral PGNs of postnatal day 7-14 rats, only dopamine's postsynaptic effects were observed. Furthermore, inward, excitatory currents evoked by dopamine were reduced by the GHSR antagonist, YIL781. We conclude that lumbosacral PGNs are the site where the action of endogenous ligands of D2R and 5-HT2R converge, and that GHSR act as a cis-modulator of D2R expressed by the same neurons. KEY POINTS: Dopamine, 5-hydroxytryptamine (5-HT, serotonin) and ghrelin (GHSR) receptor agonists increase colorectal motility and have been postulated to act at receptors on parasympathetic preganglionic neurons (PGNs) in the lumbosacral spinal cord. We aimed to determine which neurons in the lumbosacral spinal cord express dopamine, serotonin and GHSR receptors, their neural inputs, and whether agonists at these receptors excite them. We show that dopamine, serotonin and ghrelin receptor transcripts are contained in the same PGNs and that these neurons have closely associated tyrosine hydroxylase and serotonin boutons. Whole cell electrophysiology revealed that dopamine, serotonin and GHSR receptor agonists induce an inward excitatory current in overlapping populations of lumbosacral PGNs. Dopamine-induced excitation was reversed by GHSR antagonism. The present study demonstrates that lumbosacral PGNs are the site at which actions of endogenous ligands of dopamine D2 receptors and 5-HT type 2 receptors converge. Ghrelin receptors are functional, but their role appears to be as modulators of dopamine effects at D2 receptors.
多巴胺 D2 受体(D2R)、5-羟色胺(5-HT,血清素)受体(5-HTR)和生长激素释放肽受体(GHSR)激动剂激活腰骶排便中枢的神经元,并作为“结肠动力学激动剂”,导致体内推进性结肠运动增加。在本研究中,我们研究了腰骶排便中枢的哪些神经元表达这些受体,以及多巴胺、5-HT 和 ghrelin 受体激动剂是否作用于相同的腰骶节前神经元(PGNs)。我们使用全细胞膜片钳记录腰骶排便中枢神经元的反应,观察结肠动力学激动剂的作用,并研究它们的表达谱和神经输入的化学性质。荧光原位杂交显示,Drd2、Ghsr 和 Htr2C 转录本在小鼠腰骶 PGNs 中存在共定位,免疫组织化学显示这些神经元具有密切相关的酪氨酸羟化酶和 5-HT 末梢。先前的研究表明,它们不接受 ghrelin 的输入。成年小鼠脊髓的全细胞膜片钳电生理学研究表明,多巴胺、5-HT、α-甲基 5-HT 和卡普莫瑞林在重叠的腰骶 PGN 群体中均引起内向、兴奋性电流。此外,多巴胺导致一群 D2R 神经元中 IPSC 和 EPSC 的频率增加。河豚毒素阻断 IPSC 和 EPSC,表明多巴胺具有突触后兴奋性作用。在出生后 7-14 天大鼠的腰骶 PGNs 中,仅观察到多巴胺的突触后效应。此外,多巴胺引起的内向兴奋性电流被 GHSR 拮抗剂 YIL781 减少。我们得出结论,腰骶 PGNs 是 D2R 和 5-HT2R 内源性配体作用的部位,而 GHSR 作为同一神经元表达的 D2R 的顺式调节剂发挥作用。关键点:多巴胺、5-羟色胺(5-HT,血清素)和 ghrelin(GHSR)受体激动剂增加结直肠蠕动,并被假定作用于腰骶脊髓中的副交感节前神经元(PGNs)上的受体。我们旨在确定腰骶脊髓中的哪些神经元表达多巴胺、5-HT 和 GHSR 受体,它们的神经输入,以及这些受体的激动剂是否兴奋它们。我们表明,多巴胺、5-HT 和 ghrelin 受体转录本包含在相同的 PGNs 中,并且这些神经元具有密切相关的酪氨酸羟化酶和 5-HT 末梢。全细胞膜片钳电生理学显示,多巴胺、5-HT 和 GHSR 受体激动剂在重叠的腰骶 PGN 群体中诱导内向兴奋性电流。多巴胺诱导的兴奋被 GHSR 拮抗剂逆转。本研究表明,腰骶 PGNs 是多巴胺 D2 受体和 5-HT 型 2 受体内源性配体作用的部位。生长激素释放肽受体具有功能,但它们的作用似乎是作为多巴胺对 D2 受体作用的调节剂。