Serotonin enhances depolarizing spontaneous fluctuations, excitability, and ongoing activity in isolated rat DRG neurons via 5-HT4 receptors and cAMP-dependent mechanisms. (15th February 2021)

• Record Type: Journal Article
• Authors: Lopez, Elia R.; Carbajal, Anibal Garza; Tian, Jin Bin; Bavencoffe, Alexis; Zhu, Michael X.; Dessauer, Carmen W.; Walters, Edgar T.
• Is Part Of: Neuropharmacology. Volume 184(2021)
• Publication Date: 2021-02-15
• Subjects: Nociceptor -- Ongoing pain -- Serotonin -- 5-HT4 receptor -- cAMP -- Hyperexcitability; Neuropsychopharmacology -- Periodicals; Autonomic Agents -- Periodicals; Neuropsychopharmacologie -- Périodiques; Neuropsychopharmacology; Periodicals; Electronic journals; 615.78
• DOI: 10.1016/j.neuropharm.2020.108408
• Languages: English
• ISSNs: 0028-3908

Abstract

Abstract: Ongoing activity in nociceptors, a driver of spontaneous pain, can be generated in dorsal root ganglion neurons in the absence of sensory generator potentials if one or more of three neurophysiological alterations occur – prolonged depolarization of resting membrane potential (RMP), hyperpolarization of action potential (AP) threshold, and/or increased amplitude of depolarizing spontaneous fluctuations of membrane potential (DSFs) to bridge the gap between RMP and AP threshold. Previous work showed that acute, sustained exposure to serotonin (5-HT) hyperpolarized AP threshold and potentiated DSFs, leading to ongoing activity if a separate source of maintained depolarization was present. Cellular signaling pathways that increase DSF amplitude and promote ongoing activity acutely in nociceptors are not known for any neuromodulator. Here, isolated DRG neurons from male rats were used to define the pathway by which low concentrations of 5-HT enhance DSFs, hyperpolarize AP threshold, and promote ongoing activity. A selective 5-HT4 receptor antagonist blocked these 5-HT-induced hyperexcitable effects, while a selective 5-HT4 agonist mimicked the effects of 5-HT. Inhibition of cAMP effectors, protein kinase A (PKA) and exchange protein activated by cAMP (EPAC), attenuated 5-HT's hyperexcitable effects, but a blocker of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels had no significant effect. 5-HT4 -dependent PKA activation was specific to DRG neurons that bind isolectin B4 (a nonpeptidergic nociceptor marker). 5-HT's effects on AP threshold, DSFs, and ongoing activity were mimicked by a cAMP analog. Sustained exposure to 5-HT promotes ongoing activity in nonpeptidergic nociceptors through the Gs -coupled 5-HT4 receptor and downstream cAMP signaling involving both PKA and EPAC. Graphical abstract: Image 1 Highlights: Sustained exposure to 5-HT induces nociceptor hyperexcitability via 5-HT4 receptors. The hyperexcitable effects promote ongoing activity during modest depolarization. A major effect is enhancement of irregular, depolarizing spontaneous fluctuations. cAMP, PKA, and EPAC mediate hyperexcitable effects that promote ongoing activity.