Our understanding of the cellular and molecular mechanisms underlying adult neurogenesis in response to diseases of the CNS is incomplete. Decreased neurogenesis in the adult hippocampus in response to stressors is well established in rodent and nonhuman primate models of depression. Recently, increased neurogenesis has been linked to the actions of certain antidepressants, including tranylcypromine (TCP) in the treatment of depression. The goldfish (Carassius auratus) has the ability to grow its body and brain throughout its life and is an ideal model for studying adult neurogenesis. The hypothesis was that alterations in adult goldfish proliferation zones can be used to determine antidepressant effects on proliferation. Three specific aims were used to test this hypothesis: 1) To produce an atlas of the goldfish brain based on cresyl violet stained sections. 2) To construct an atlas of proliferation zones in the goldfish brain. 3) To study the influence of the antidepressant tranylcypromine on progenitor cell proliferation zones in the telencephalon, optic tectum, and cerebellum of adult goldfish. Proliferation zones were identified using BrdU and H3 immunohistochemistry and mapped using the brain atlas. Proliferation zones were associated with periventricular surfaces in the telencephalon, diencephalon, optic tectal lobes, cerebellum, and hindbrain. The presence of proliferation zones within the hindbrain was one region that differed from other teleosts.