The effects of cobalt protoporphyrin IX and tricarbonyldichlororuthenium (II) dimer treatments and its interaction with nitric oxide in the locus coeruleus of mice with peripheral inflammation

Patricia Moreno, Rafael Alves Cazuza, Joyce Gomes-Mendes, Andrés Felipe Díaz, Sara Polo, Sergi Leánez, Christie Ramos Andrade Leite-Panissi, Olga Pol

Research output: Contribution to journalArticleResearch

5 Citations (Scopus)

Abstract

© 2019 by the authors. Licensee MDPI, Basel, Switzerland. Heme oxygenase 1 (HO-1) and carbon monoxide were shown to normalize oxidative stress and inflammatory reactions induced by neuropathic pain in the central nervous system, but their effects in the locus coeruleus (LC) of animals with peripheral inflammation and their interaction with nitric oxide are unknown. In wild-type (WT) and knockout mice for neuronal (NOS1-KO) or inducible (NOS2-KO) nitric oxide synthases with inflammatory pain induced by complete Freund’s adjuvant (CFA), we assessed: 1) antinociceptive actions of cobalt protoporphyrin IX (CoPP), an HO-1 inducer; 2) effects of CoPP and tricarbonyldichlororuthenium(II)dimer (CORM-2), a carbon monoxide-liberating compound, on the expression of HO-1, NOS1, NOS2, CD11b/c, GFAP,and mitogen-activated protein kinases (MAPK)in the LC. CoPP reduced inflammatory pain in different time-dependent manners in WT and KO mice. Peripheral inflammation activated astroglia in the LC of all genotypes and increased the levels of NOS1 and phosphorylated extracellular signal-regulated kinase 1/2 (p-ERK 1/2) in WT mice. CoPP and CORM-2 enhanced HO-1 and inhibited astroglial activationin all genotypes. Both treatments blocked NOS1 overexpression,and CoPP normalized ERK 1/2 activation. This study reveals an interaction between HO-1 and NOS1/NOS2 during peripheral inflammation andshows that CoPP and CORM-2 improved HO-1 expression and modulated the inflammatory and/or plasticity changes caused by peripheral inflammation in the LC.
Original languageEnglish
Article number2211
Number of pages14
JournalInternational Journal of Molecular Sciences
Volume20
Issue number9
DOIs
Publication statusPublished - 5 May 2019

Keywords

  • Analgesia
  • Animals
  • Biomarkers
  • CARBON-MONOXIDE
  • Carbon monoxide
  • EXPRESSION
  • GLIAL ACTIVATION
  • Heme oxygenase 1
  • Inflammation/etiology
  • Inflammatory pain
  • Locus coeruleus
  • MAP-KINASE
  • MONOXIDE-RELEASING MOLECULE
  • MOUSE MODEL
  • Male
  • Mice
  • Mice, Knockout
  • NEUROPATHIC PAIN
  • Nitric Oxide Synthase Type I/genetics
  • Nitric Oxide Synthase Type II/genetics
  • Nitric Oxide/metabolism
  • Nitric oxide
  • OXYGENASE 1 INDUCER
  • Organometallic Compounds/chemistry
  • PATHWAYS
  • Protoporphyrins/chemistry
  • RECEPTORS
  • analgesia
  • carbon monoxide
  • heme oxygenase 1
  • inflammatory pain
  • locus coeruleus
  • nitric oxide

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