A reduced rate of neurogenesis occurs in the adult brain of patients with neurological diseases, with the
rate of new neuron proliferation not sufficient to replace neuron loss. Neurogenesis can be induced by
several factors, including basic fibroblast growth factor, epidermal growth factor, and brain-derived neurotrophic
factor.
Neurogenesis determination is a valuable parameter for determining disease progression and monitoring
various treatments. Currently, neurogenesis detection is possible by invasive methods, such as
bromodeoxyuridine (BrdU) cell labeling and immunohistological analysis of immature neuron markers.
However, these are not compatible with alive model examination. Neurogenesis detection by noninvasive
methods, such as radiolabeling of specific antibodies and scintigraphy imaging, could shed light on
immature neuronal markers.
We propose that brain scintigraphy after radiolabeling of a specific antibody of an immature neuronal
marker is a useful new modality for neurogenesis detection and that it would aid the management of
neurological diseases