GAMMA-AMINOBUTYRIC-ACID TYPE-A BENZODIAZEPINE RECEPTORS REGULATE RAT RETINA NEUROSTEROIDOGENESIS

It has been previously shown that retinal ganglion cells have the abil ity to synthesize steroids including neuroactive steroids such as preg nenolone sulfate. Since ganglion cells possess GABA(A)/benzodiazepine (BZ) receptors and neurosteroids modulate retinal GABA(A) receptor fun ction, we investigated the role of these receptors in isolated rat ret ina neurosteroidogenesis. Ligands for central-type BZ receptors stimul ated retinal pregnenolone synthesis. Clonazeparn was the most potent l igand examined acting at nanomolar concentrations. Moreover, the effec tive steroidogenesis stimulatory dose (ED(50)) for these ligands and t he K-i to inhibit [H-3]flunitrazepam binding showed a coefficient of c orrelation of r = 0.87, suggesting the involvement of the central-type BZ receptors in this event. Ro 5-4864, which preferentially binds to peripheral-type BZ receptors, was less efficacious and potent whereas PK 11195 did not affect the basal pregnenolone formation and did not a ntagonize the Ro 5-4864 stimulated steroid synthesis. The GABAergic ag onist muscimol, stimulated neurosteroid synthesis and this effect was reversed by the GABAergic antagonists bicuculline and picrotoxinin. In addition, these antagonists decreased basal pregnenolone formation, s uggesting a tonic GABAergic control of the steroidogenic pathway, and reduced clonazepam-stimulated steroidogenesis. These results, together with the reported ability of neurosteroids to modulate GABA(A) recept or function, suggest a novel regulatory mechanism to control the inhib itory transmission.