Glutamate and N‐Methyl‐D‐Aspartate Stimulate Rat Hypothalamic Corticotropin‐Releasing Factor Secretion in vitro

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Abstract
It is known that in vivo excitatory amino acids (EAA) stimulate the hypothalamo‐pituitary‐adrenal axis. However their site of action is not fully understood. We investigated the possibility of a direct action of EAA on the secretion of the major adrenocorticotropin hormone (ACTH) secretagogue: corticotropin‐releasing factor (CRF) from incubated rat hypothalamic slices. N‐methyl‐D‐aspartic acid (NMDA) or L‐glutamate (1×10−7 to 1×10−3 M) stimulated in a dose‐dependent fashion CRF release. The maximal effect was obtained at a concentration of 1×10−4 M for both drugs. The IC50 was 1.3×10−5 M and 3.3×10−5 M for NMDA and L‐glutamate, respectively. Incubation with 2.5×10−4 M D‐2‐amino‐5‐phosphonovalerate (a NMDA receptor antagonist) or 2‐amino‐4‐phosphonobutyrate (a metabotropic receptor antagonist) was without significant effect on basal CRF secretion and completely blocked the increase in CRF release induced by 5×10−5 M NMDA or L‐glutamate, respectively. Incubation with 1×10−4 M kainate or 0.5×10−4 M AMPA did not change basal CRF secretion. Incubation with 2×10−4 M γ‐D‐glutamylglycine (a specific antagonist of kainate and AMPA receptor) had no effect under basal conditions or during exposure to kainate or AMPA. Our data demonstrate that EAA could stimulate directly CRF secretion, by an action through NMDA and metabotropic receptors, but not kainate or AMPA receptors. These findings may be relevant to the regulation of the hypothalamo‐pituitary adrenal axis, both under basal conditions and during exposure to stress.

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