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CRF 2 mediates the increased noradrenergic activity in the hypothalamic paraventricular nucleus and the negative state of morphine withdrawal in rats
Author(s) -
NavarroZaragoza Javier,
Núñez Cristina,
RuizMedina Jessica,
Laorden M Luisa,
Valverde Olga,
Milanés M Victoria
Publication year - 2011
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.2010.01090.x
Subject(s) - endocrinology , medicine , hypothalamus , (+) naloxone , kindling , morphine , chemistry , corticosterone , physical dependence , stimulation , antagonist , receptor , hormone
BACKGROUND AND PURPOSE Recent evidence suggests that corticotropin‐releasing factor (CRF) receptor signalling is involved in modulating the negative symptoms of opiate withdrawal. In this study, a series of experiments were performed to further characterize the role of CRF‐type 2 receptor (CRF 2 ) signalling in opiate withdrawal‐induced physical signs of dependence, hypothalamus‐pituitary‐adrenal (HPA) axis activation, enhanced noradrenaline (NA) turnover in the hypothalamic paraventricular nucleus (PVN) and tyrosine hydroxylase (TH) phosphorylation (activation), as well as CRF 2 expression in the nucleus of the solitary tract‐A 2 noradrenergic cell group (NTS‐A 2 ). EXPERIMENTAL APPROACH The contribution of CRF 2 signalling in opiate withdrawal was assessed by i.c.v. infusion of the selective CRF 2 antagonist, antisauvagine‐30 (AS‐30). Rats were implanted with two morphine (or placebo) pellets. Six days later, rats were pretreated with AS‐30 or saline 10 min before naloxone and the physical signs of abstinence, the HPA axis activity, NA turnover, TH activation and CRF 2 expression were measured using immunoblotting, RIA, HPLC and immunohistochemistry. KEY RESULTS Rats pretreated with AS‐30 showed decreased levels of somatic signs of naloxone‐induced opiate withdrawal, but the corticosterone response was not modified. AS‐30 attenuated the increased production of the NA metabolite, 3‐methoxy‐4‐hydroxyphenylglycol, as well as the enhanced NA turnover observed in morphine‐withdrawn rats. Finally, AS‐30 antagonized the TH phosphorylation at Serine40 induced by morphine withdrawal. CONCLUSIONS AND IMPLICATIONS These results suggest that physical signs of opiate withdrawal, TH activation and stimulation of noradrenergic pathways innervating the PVN are modulated by CRF 2 signalling. Furthermore, they indicate a marginal role for the HPA axis in CRF 2 ‐mediation of opiate withdrawal.