The a, receptor is an intracellular molecule that shares no homology with any mammalian proteins. sigma(1) receptors normally localize at the endoplasmic reticulum and regulate a variety of signal transductions including intracellular Ca2+ dynamics and neurotrophic factor signaling. In the brain, sigma(1) receptors are known to regulate the activity of diverse ion channels via protein-protein interactions. Accumulated evidences strongly indicate that the activation/upregulation of sigma(1) receptors promotes the neuronal differentiation as well as a robust antiapoptotic action. In animals, sigma(1) receptor agonists exhibit an antidepressant-like action. Furthermore, the agonists enhanced neuronal survival eventhough they were administered several hours after a brain ischemia. Thus, primary clinical targets of sigma(1) receptor ligands are proposed to include stroke, neurodegenerative disorders and depression. Ligands for the sigma(1) receptor may constitute a new class of therapeutic drugs targeting an endoplasmic reticular protein.