7. Conclusions and future directions
Neurogenesis in the hippocampus represents a form of morphological and functional plasticity in the mammalian adult brain. Activity-dependent regulation of neurogenesis and experiencedependent participation of adult born DGCs in information processing imply the contribution of adult born DGCs in hippocampus-dependentfunctions. Neurogenesis ablation and IEG labeling methods consistently suggest the involvement of adult born DGCs in learning and memory. Reduction of hippocampal neurogenesis is always accompanied with cognitive decline in diseases such as depression, AD and PD. Improvement of hippocampal neurogenesis induced by exercise benefits some but not all hippocampus-dependent functions. The precise mechanisms of exercise-induced neurogenesis are largely unclear. However, physical exercise may regulate the overall dynamic balance in the neurogenic niche through increasing proliferation of astrocytes and enhancing the secretion of some transmitters, growth factors or neurotrophic factors. The non-invasive imaging techniques have been developed for monitoring hippocampal neurogenesis in humans [24,25], despite their validity and precision await further testing. These techniques pave the ways for us to investigate the functions of hippocampal neurogenesis in living persons under various physiological or pathological conditions, which will hopefully lead to novel diagnoses and therapies for neurological disorders.