Developmental Changes in Serotonergic Modulation of GABAergic Synaptic Transmission and Postsynaptic GABAA Receptor Composition in the Cerebellar Nuclei

• Published in: Cerebellum (London, England) England), 2018-06, Vol.17 (3), p.346-358
• Main Authors: Saitow, Fumihito, Nagano, Masatoshi, Suzuki, Hidenori
• Format: Article
• Language: English
• Subjects: Biomedical and Life Sciences; Biomedicine; Brain slice preparation; Calcium (extracellular); Cerebellum; Fibers; Inhibitory postsynaptic potentials; Neurobiology; Neurology; Neurosciences; Original Paper; Purkinje cells; Raphe nuclei; Rodents; Serotonin; Synapses; Synaptic transmission; Synaptogenesis; γ-Aminobutyric acid A receptors
• ISSN: 1473-4222; 1473-4230
• DOI: 10.1007/s12311-018-0922-9

Outputs from the cerebellar nuclei (CN) are important for generating and controlling movement. The activity of CN neurons is controlled not only by excitatory inputs from mossy and climbing fibers and by γ-aminobutyric acid (GABA)-based inhibitory transmission from Purkinje cells in the cerebellar cortex but is also modulated by inputs from other brain regions, including serotonergic fibers that originate in the dorsal raphe nuclei. We examined the modulatory effects of serotonin (5-HT) on GABAergic synapses during development, using rat cerebellar slices. As previously reported, 5-HT presynaptically decreased the amplitudes of stimulation-evoked inhibitory postsynaptic currents (IPSCs) in CN neurons, with this effect being stronger in slices from younger animals (postnatal days [P] 11–13) than in slices from older animals (P19–21). GABA release probabilities accordingly exhibited significant decreases from P11–13 to P19–21. Although there was a strong correlation between the GABA release probability and the magnitude of 5-HT-induced inhibition, manipulating the release probability by changing extracellular Ca 2+ concentrations failed to control the extent of 5-HT-induced inhibition. We also found that the IPSCs exhibited slower kinetics at P11–13 than at P19–21. Pharmacological and molecular biological tests revealed that IPSC kinetics were largely determined by the prevalence of α 1 subunits within GABA A receptors. In summary, pre- and postsynaptic developmental changes in serotonergic modulation and GABAergic synaptic transmission occur during the second to third postnatal weeks and may significantly contribute to the formation of normal adult cerebellar function.