Participation of mu-opioid, GABA(B), and NK1 receptors of major pain control medullary areas in pathways targeting the rat spinal cord: Implications for descending modulation of nociceptive transmission

• Tipo: Artigo em Revista Científica Internacional
• Data: 2008

Autores

Pinto, M (Autor) Outra; Sousa, M (Autor) Outra; Deolinda Lima (Autor) FMUP; Isaura Tavares (Autor) FMUP

Revista

Título: Journal of Comparative Neurology

Vol. 510

Páginas: 175-187

ISSN: 0021-9967

Editora: Wiley-Blackwell

Indexação

ISI Web of Knowledge - 42 Citações

Scopus - 44 Citações

Outras Informações

ID Authenticus: P-003-W82

DOI: 10.1002/cne.21793

Abstract (EN): Several brain areas modulate pain transmission through direct projections to the spinal cord. The descending modulation is exerted by neurotransmitters acting both at spinally projecting neurons and at interneurons that target the projection neurons. We analyzed the expression of mu-opioid (MOR), gamma-aminobutyric acid GABA(B), and NK1 receptors in spinally projecting neurons of major medullary pain control areas of the rat: rostroventromedial medulla (RVM), dorsal reticular nucleus (DRt), nucleus of the solitary tract, ventral reticular nucleus, and lateralmost part of the caudal ventrolateral medulla. The retrograde tracer cholera toxin subunit B (CTb) was injected into the spinal dorsal horn, and medullary sections were processed by double immunocytochemistry for CTb and each receptor. The RVM contained the majority of double-labeled 2neurons followed by the DRt. In general, high percentages of MOR- and NK1-expressing neurons were retrogradely labeled, whereas GABA, receptors were mainly expressed in neurons that were not labeled from the cord. The results suggest that MOR and NK1 receptors play an important role in direct and indirect control of descending modulation. The co-localization of MOR and GABA, in DRt neurons also demonstrated by the present study suggests that the pronociceptive effects of this nucleus may be controlled by local opoidergic and GABAergic inhibition of the pronociception increased during chronic pain. J. Comp. Neurol. 510:175-187, 2008. (c) 2008 Wiley-Liss, Inc.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 13