GHRELIN is an endogenous ligand of GH secretagogue receptor (GHS-R) 1a. It is a unique GH-releasing 28-aminoacid n-octanoilated peptide that is mainly synthesized and released from the stomach [1]. In addition to its major effects on GH release and energy homeostasis [2,3], ghrelin also has diverse peripheral effects [4]. Furthermore, several lines of evidence indicated that ghrelin acts in the central nervous system to control neuronal functions and subsequently alter many brain functions [5]. We have reported that ghrelin stimulates the proliferation of newborn cells in the hippocampus of adult mice and systemic administration of anti-ghrelin antiserum reduces the proliferation of hippocampal progenitor cells in the subgranu- Abstract. Neurogenesis occurs in the adult hippocampus and is enhanced by dietary restriction (DR), and neurogenesis enhancement is paralleled by circulating ghrelin level enhancement. We have previously reported that ghrelin modulates adult neurogenesis in the hippocampus. In order to investigate the possible role of ghrelin in DR-induced hippocampal neurogenesis in adult mice, ghrelin knockout (GKO) mice and wild-type (WT) mice were maintained for 3 months on DR or ad libitum (AL) diets. Protein levels of ghrelin in the stomach and the hippocampus were increased by DR in WT mice. One day after BrdU administration, the number of BrdU-labeled cells in the hippocampal dentate gyrus was decreased in GKO mice maintained on the AL diet. DR failed to alter the proliferation of progenitor cells in both WT and GKO mice. Four weeks after BrdU injection, the number of surviving cells in the dentate gyrus was decreased in AL-fed GKO mice. DR increased survival of newborn cells in WT mice, but not in GKO mice. Levels of brain-derived neurotrophic factor protein in the hippocampus were similar between WT and GKO mice, and were increased by DR both in WT and GKO mice. These results suggest that elevated levels of ghrelin during DR may have an important role in the enhancement of neurogenesis induced by DR.Key words: Ghrelin, Adult neurogenesis, Hippocampus, Dietary restriction lar zone (SGZ) [6]. Additionally, in our recent report [7], we found that mice with targeted disruption of the ghrelin gene showed a decreased number of progenitor cells in the dentate gyrus (DG) of the hippocampus, while ghrelin replacement restored progenitor cell numbers to those of wild-type (WT) controls. Proliferative effect of ghrelin on hippocampal progenitor cells seems to be mediated through the activation of its receptor because GHS-R1a antagonist completely blocked the effect of ghrelin in vitro [8]. Collectively, these findings suggest that ghrelin may play an important role in adult hippocampal neurogenesis.It is now well documented that dietary restriction (DR) gives beneficial effects like increasing life span, delaying the onset of age-associated diseases, and reducing oxidative stress and damage [9]. Previous data suggest that DR increases adult hippocampal neurogenesis by increasing the survival of neural stem...