59 In such non-neural systems, 5-HT has been a potent mitogen.60,61 Figure 1. A) Putative model of the serotonergic (5-HT) machinery in adult neural stem cells. Tryptophan hydroxylases (TPH) produces 5-HT, which controls its own metabolism mainly via 5-HT1Aand 5HT2C receptors. B) TPH inactivation leads to less 5-HT production … In the brain, 5-HT is among the most widely distributed neurotransmitters. All serotonergic fibers originate in the brain stem raphe
nuclei. By way of extensive synaptic connections of the serotonergic fibers, 5-HT contributes to many physiologic functions such as endocrine and circadian rhythms, food intake, sleep, reproductive Inhibitors,research,lifescience,medical activity, and motor function, as well as cognition, mood, and anxiety.62 In the brain we VE-821 currently know of 16 different cloned receptor
types and subtypes, but it can be expected that their number will grow even further in the near future. In contrast to the multitude Inhibitors,research,lifescience,medical of 5-1 IT receptors, there is only a single 5-HT transporter (5-HTT) responsible for the reuptake of 5-HT into serotonergic neurons after its release into the synaptic cleft. As our own studies have shown, 5 -I ITT does not have a large impact on neurogenesis.63 A possible role for 5-HT as Inhibitors,research,lifescience,medical direct mediator of granule cell generation is currently discussed, since elevated 5-HT levels in the hippocampus increase the rate of proliferation of granule cell Inhibitors,research,lifescience,medical precursors.64 Epidermal growth factor (EGF) is believed to exert an essential function on the generation and maintenance of neural stem cells.
It is therefore not surprising that in non-neural systems, EGF and 5-HT can augment the rate of cell proliferation in a synergistic manner.65 BDNF again seems involved in mediating the effects of 5-HT. Thus, chronic administration of 5-IIT-selective reuptake inhibitors, Inhibitors,research,lifescience,medical clinically used as antidepressants, leads to upregulation of BDNF niRNA.56 As already mentioned above, 5-HT exerts its action through a large family of receptors in the periphery and throughout the CNS.62 A possible role for the 5-IIT1A receptor in the modulation of anxiety and depression, as well as in the mode of action of anxiolytic and antidepressant drugs, has been suspected for many years.66 5IIT1A receptors operate both as somatodendritic autoreceptors and postsynaptic receptors. Research regarding 5-HT1A receptor has shown67 found that the effect of antidepressants upregulating extracellular serotonin levels worked via the 5-HT1A receptor subtype, thus opening a link between our in vitro system, neurogenesis, and clinical relevance in terms of affective disorders. Althogh the serotonin hypothesis of depression68 is very attractive in this regard, it should not be omitted here that there are additional compelling findings dealing with other neurotransmitting systems, eg, supporting cholinergic mechanisms.