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Glutamate-evoked currents in acutely dissociated neurons from the rat medial preoptic nucleus
Umeå University, Faculty of Medicine, Department of Integrative Medical Biology (IMB).
1997 (English)In: Brain Research, ISSN 0006-8993, E-ISSN 1872-6240, Vol. 759, no 2, 270-276 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
1997. Vol. 759, no 2, 270-276 p.
URN: urn:nbn:se:umu:diva-2612OAI: diva2:140825
Available from: 2007-10-04 Created: 2007-10-04 Last updated: 2010-06-24Bibliographically approved
In thesis
1. GABA-, glycine- and glutamate-induced currents in rat medial preoptic neurons: functional interactions and modulation by capsaicin
Open this publication in new window or tab >>GABA-, glycine- and glutamate-induced currents in rat medial preoptic neurons: functional interactions and modulation by capsaicin
2007 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

The medial preoptic nucleus (MPN) of the hypothalamus plays a major role in many functions involved in maintaining bodily homeostasis, such as thermoregulation and osmoregulation, as well as in the control of complex behaviours, e.g. sexual behaviour. A fundamental basis for the control and execution of these functions is the synaptic communication between neurons of the MPN. However, the functional properties of the synapses involved are largely unknown. The present thesis is a study of ligand-gated ion channels involved in the pre- and post-synaptic aspects of neuronal communication in the MPN of rat. The aim was to clarify synaptic properties in the MPN, to identify the major channel types involved and to obtain a better understanding of their functional properties.

By fast application of agonists to isolated neurons, it was first demonstrated that all neurons responded to glutamate with currents mediated by α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, and a majority of neurons also with currents mediated by N-Methyl-D-aspartate (NMDA) receptors. All neurons also responded to γ-aminobutyric acid (GABA) and glycine with currents mediated by GABAA receptors and glycine receptors, respectively. These findings show that fast-acting excitatory and inhibitory amino-acid transmitters are most likely important for communication between hypothalamic neurons.

Application of agonists to isolated neurons revealed cross-talk, detected as an apparent cross-desensitization, between the responses to GABA and those to glycine. Parallel analysis of current and conductance, using gramicidin-perforated patches to avoid perturbing intracellular chloride concentration, showed that the cross-talk was not dependent on a direct interaction between the receptors as previously suggested, but was a consequence of the change in the intracellular chloride concentration during receptor activation. Strengthened by a computer model, the analysis also showed that the current decay in the presence of GABA or glycine was mainly due to a change in the chloride driving force and that receptor desensitization played a minor role only.

The role of thermo-sensitive transient receptor potential TRPV1 channels in the regulation of glutamate- and GABA-mediated transmission was studied in the slice preparation, where much of the synaptic connections between neurons are preserved. It was shown that application of the TRPV1 agonist capsaicin increased the frequency of excitatory AMPA receptor- mediated as well as inhibitory GABAA receptor-mediated postsynaptic currents. This effect was partly presynaptic and demonstrates that TRP channels play a role in regulating synaptic transmission in the MPN. The results imply that such mechanisms may possibly contribute to the thermoregulation by MPN neurons.

Place, publisher, year, edition, pages
Umeå: Integrativ medicinsk biologi, 2007. 31 p.
Umeå University medical dissertations, ISSN 0346-6612 ; 1122
medial preoptic nucleus, synaptic transmission, glutamate, GABA, glycine, TRPV1
National Category
urn:nbn:se:umu:diva-1383 (URN)978-91-7264-408-3 (ISBN)
Public defence
2007-10-26, BiA201, Biologihuset, Umeå universitet, Umeå, 13:00 (English)
Available from: 2007-10-04 Created: 2007-10-04 Last updated: 2009-05-26Bibliographically approved

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