Source:http://linkedlifedata.com/resource/pubmed/id/18082329
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2008-1-14
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pubmed:abstractText |
Anatomical and neurochemical studies indicated that the globus pallidus receives serotonergic innervation from raphe nuclei but the membrane effects of 5-HT on globus pallidus neurons are not entirely clear. We address this question by applying whole-cell patch-clamp recordings on globus pallidus neurons in immature rat brain slices. Under current-clamp recording, 5-HT depolarized globus pallidus neurons and increased their firing rate, an action blocked by both 5-HT(4) and 5-HT(7) receptor antagonists and attributable to an increase in cation conductance(s). Further experiments indicated that 5-HT enhanced the hyperpolarization-activated inward conductance which is blocked by 5-HT(7) receptor antagonist. To determine if 5-HT exerts any presynaptic effects on GABAergic and glutamatergic inputs, the actions of 5-HT on synaptic currents were studied. At 10 microM, 5-HT increased the frequency of spontaneous inhibitory postsynaptic currents (sIPSCs) but had no effect on both the frequency and amplitude of miniature inhibitory postsynaptic currents (mIPSCs). However, 5-HT at a higher concentration (50 microM) decreased the frequency but not the amplitude of the mIPSCs, indicating an inhibition of GABA release from the presynaptic terminals. This effect was sensitive to 5-HT(1B) receptor antagonist. In addition to the presynaptic effects on GABAergic neurotransmission, 5-HT at 50 microM had no consistent effects on glutamatergic neurotransmission, significantly increased the frequency of miniature excitatory postsynaptic currents (mEPSCs) in 4 of 11 neurons and decreased the frequency of mEPSCs in 3 of 11 neurons. In conclusion, we found that 5-HT could modulate the excitability of globus pallidus neurons by both pre- and post-synaptic mechanisms. In view of the extensive innervation by globus pallidus neurons on other basal ganglia nuclei, this action of 5-HT originated from the raphe may have a profound effect on the operation of the entire basal ganglia network.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cations,
http://linkedlifedata.com/resource/pubmed/chemical/Ion Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Pindolol,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Presynaptic,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Serotonin, 5-HT4,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/cyanopindolol,
http://linkedlifedata.com/resource/pubmed/chemical/serotonin 7 receptor
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0306-4522
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
24
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pubmed:volume |
151
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
439-51
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pubmed:meshHeading |
pubmed-meshheading:18082329-Animals,
pubmed-meshheading:18082329-Cations,
pubmed-meshheading:18082329-Electrophysiology,
pubmed-meshheading:18082329-Excitatory Postsynaptic Potentials,
pubmed-meshheading:18082329-Globus Pallidus,
pubmed-meshheading:18082329-Ion Channels,
pubmed-meshheading:18082329-Male,
pubmed-meshheading:18082329-Neurons,
pubmed-meshheading:18082329-Patch-Clamp Techniques,
pubmed-meshheading:18082329-Pindolol,
pubmed-meshheading:18082329-Rats,
pubmed-meshheading:18082329-Rats, Sprague-Dawley,
pubmed-meshheading:18082329-Receptors, Presynaptic,
pubmed-meshheading:18082329-Receptors, Serotonin,
pubmed-meshheading:18082329-Receptors, Serotonin, 5-HT4,
pubmed-meshheading:18082329-Serotonin,
pubmed-meshheading:18082329-Serotonin Antagonists,
pubmed-meshheading:18082329-Synapses,
pubmed-meshheading:18082329-Synaptic Transmission
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pubmed:year |
2008
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pubmed:articleTitle |
5-HT excites globus pallidus neurons by multiple receptor mechanisms.
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pubmed:affiliation |
Department of Physiology, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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