Electrophysiological properties of brain-natriuretic peptide- and gastrin-releasing peptide-responsive dorsal horn neurons in spinal itch transmission. (3rd August 2016)

• Record Type: Journal Article
• Authors: Kusube, Fumiya; Tominaga, Mitsutoshi; Kawasaki, Hiroaki; Yamakura, Fumiyuki; Naito, Hisashi; Ogawa, Hideoki; Tomooka, Yasuhiro; Takamori, Kenji
• Is Part Of: Neuroscience letters. Volume 627(2016)
• Page Start: 51
• Page End: 60
• Publication Date: 2016-08-03
• Subjects: BNP B-type natriuretic peptide -- CQ chloroquine -- DRG dorsal root ganglia -- GRP gastrin-releasing peptide -- GRPR gastrin-releasing peptide receptor -- i.d. intradermal -- i.t. intrathecal -- Npra B-type natriuretic peptide receptor -- NS nociceptive-specific -- WDR wide dynamic range; BNP -- Dorsal horn -- GRP -- In vivo electrophysiology -- Itch; Neurology -- Periodicals; Neurology -- Periodicals; Research -- Periodicals; Neurologie -- Périodiques; Neuroanatomie -- Périodiques; Neuropharmacologie -- Périodiques; Neurophysiologie -- Périodiques; Neurology; Periodicals; Electronic journals; 617.48
• DOI: 10.1016/j.neulet.2016.05.051
• Languages: English
• ISSNs: 0304-3940

Abstract

Highlights: The BNP-Npra and GRP-GRPR signaling pathways of spinal itch transmission differ. Spinal BNP may contribute little directly to histaminergic itch. Multiple neurotransmitters are involved in spinal itch transmission. Abstract: Spinal itch transmission has been reported to be mediated by at least two neuronal populations in spinal dorsal horn, neurons expressing brain-natriuretic peptide (BNP) receptor (Npra) and gastrin-releasing peptide (GRP) receptor (GRPR). Although Npra-expressing neurons were shown to be upstream of GRPR- expressing neurons in spinal itch transmission, the roles of BNP and GRP in the spinal neurotransmission of histamine-dependent and −independent itch remains unclear. Using in vivo electrophysiology and behavior analysis, this study examined the responses of chloroquine (histamine-independent pruritogen)-responsive and histamine-responsive dorsal horn neurons to spinal applications of BNP and GRP. Electrophysiologically, 9.5% of chloroquine-responsive neurons responded to BNP, 33.3% to GRP, and 4.8% to both, indicating that almost half of chloroquine-responsive neurons were unresponsive to both BNP and GRP. In contrast, histamine-responsive neurons did not respond to spinal BNP application, whereas 30% responded to spinal GRP application, indicating that 70% of histamine-responsive neurons were unresponsive to both BNP and GRP. Behavioral analyses showed differences in the time-course and frequency of scratching responses evoked by intrathecal BNP and GRP. These findings provide evidence that most BNP-Npra and GRP-GRPR signaling involve different pathways of spinal itch transmission, and that multiple neurotransmitters, in addition to BNP and GRP, are involved in spinal itch transmission. The electrophysiological results also suggest that spinal BNP contributes little to histaminergic itch directly.