Bicuculline, a GABAA-receptor antagonist, blocked HPA axis activation induced by ghrelin under an acute stress

• Published in: Behavioural brain research 2017-03, Vol.320, p.464-472
• Main Authors: Gastón, M.S., Cid, M.P., Salvatierra, N.A.
• Format: Article
• Language: English
• Subjects: Adrenocorticotropic hormone; Anxiety-like behavior; Corticosterone; GABAA receptor; Ghrelin
• ISSN: 0166-4328; 1872-7549
• DOI: 10.1016/j.bbr.2016.10.035

•Central administration of ghrelin in chicks induced anxiogenic like effect.•Ghrelin significantly increased plasma ACTH and corticosterone level.•Bicuculline methiodide blocks the behavioral and physiological effect of ghrelin.•Ghrelin, GABAAR and HPA axis interacts a complex way to regulate anxiogenic response. Ghrelin is a peptide of 28 amino acids with a homology between species, which acts on the central nervous system to regulate different actions, including the control of growth hormone secretion and metabolic regulation. It has been suggested that central ghrelin is a mediator of behavior linked to stress responses and induces anxiety in rodents and birds. Previously, we observed that the anxiogenic-like behavior induced by ghrelin injected into the intermediate medial mesopallium (IMM) of the forebrain was blocked by bicuculline (a GABAA receptor competitive antagonist) but not by diazepam (a GABAA receptor allosteric agonist) in neonatal meat-type chicks (Cobb). Numerous studies have indicated that hypothalamic–pituitary–adrenal (HPA) axis activation mediates the response to stress in mammals and birds. However, it is still unclear whether this effect of ghrelin is associated with HPA activation. Therefore, we investigated whether anxiety behavior induced by intra-IMM ghrelin and mediated through GABAA receptors could be associated with HPA axis activation in the neonatal chick. In the present study, in an Open Field test, intraperitoneal bicuculline methiodide blocked anxiogenic-like behavior as well as the increase in plasma ACTH and corticosterone levels induced by ghrelin (30pmol) in neonatal chicks. Moreover, we showed for the first time that a competitive antagonist of GABAA receptor suppressed the HPA axis activation induced by an anxiogenic dose of ghrelin. These results show that the anxiogenic ghrelin action involves the activation of the HPA axis, with a complex functional interaction with the GABAA receptor.