Corticotropin-releasing hormone deficiency results in impaired analgesic response during CFA-induced inflammation.

CRH Cytokine Glucocorticoid Inflammation Pain

Journal

Hormones (Athens, Greece)
ISSN: 2520-8721
Titre abrégé: Hormones (Athens)
Pays: Switzerland
ID NLM: 101142469

Informations de publication

Date de publication:
14 May 2024
Historique:
received: 10 11 2023
accepted: 25 04 2024
medline: 14 5 2024
pubmed: 14 5 2024
entrez: 13 5 2024
Statut: aheadofprint

Résumé

Corticotropin-releasing hormone (CRH) plays an important role in relief of pain by releasing analgesia-associated molecules in several inflammatory states. During inflammation, peripheral CRH acts on cells of the immune system to stimulate the local expression of proopiomelanocortin (POMC) and the production of β-endorphin, which in turn binds to opioid receptors on sensory neurons to produce antinociception. In the present study, we further investigated the role of endogenous CRH in inflammatory pain by determining the effects of Crh-deficiency on this process. For this purpose, we used Crh-deficient (Crh-/-) mice and their wildtype (Crh + / +) littermates in the CFA (Complete Freund's Adjuvant)-induced inflammatory pain model. Pain thresholds were evaluated with the Hargreaves apparatus. Our experiments showed that Crh deficiency led to increased pain response, which was associated with decreased POMC mRNA levels in locally inflamed paws of these mice. Furthermore, Crh-/- mice had higher paw edema than Crh + / + mice. Histological evaluation of inflamed paw tissues revealed increased inflammatory response in Crh-/- mice. Protein levels of proinflammatory cytokines, such as IL-6, TNF-α, and IL-1β, were higher in inflamed tissue of Crh-/- mice compared to wildtype mice. Corticosterone replacement increased the pain threshold of Crh-/- mice, restored their paw volume to the levels of wildtype mice, and significantly reduced their proinflammatory cytokine levels. Furthermore, glucocorticoid administration significantly increased POMC mRNA expression in the inflamed paw. Our data suggest that genetic deficiency of CRH is associated with increased pain. This effect is likely attributable to the accompanying glucocorticoid insufficiency and is in part mediated by opioids expressed locally.

Identifiants

pubmed: 38740711
doi: 10.1007/s42000-024-00565-8
pii: 10.1007/s42000-024-00565-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s).

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Auteurs

Efthymia Karagianni (E)

Department of Clinical Chemistry, School of Medicine, University of Crete, Heraklion, Greece.

Olga Rassouli (O)

Department of Clinical Chemistry, School of Medicine, University of Crete, Heraklion, Greece.

Smaragda Poulaki (S)

Department of Clinical Chemistry, School of Medicine, University of Crete, Heraklion, Greece.

Eirini Dermitzaki (E)

Department of Clinical Chemistry, School of Medicine, University of Crete, Heraklion, Greece.

George Liapakis (G)

Department of Pharmacology, School of Medicine, University of Crete, Heraklion, Greece.

Andrew N Margioris (AN)

Department of Clinical Chemistry, School of Medicine, University of Crete, Heraklion, Greece.

Maria Venihaki (M)

Department of Clinical Chemistry, School of Medicine, University of Crete, Heraklion, Greece. venycham@uoc.gr.

Classifications MeSH