TY - JOUR
T1 - Thalamic ryanodine receptors are involved in controlling the tonic firing of thalamocortical neurons and inflammatory pain signal processing
AU - Cheong, Eunji
AU - Kim, Chanki
AU - Choi, B. Jiwon
AU - Sun, Minjeong
AU - Shin, Hee Sup
PY - 2011/1/26
Y1 - 2011/1/26
N2 - Ryanodine receptors (RyRs) are highly conductive intracellular Ca 2+ release channels which are widely expressed in the CNS. They rapidly increase the intracellular Ca2+ concentrations in neuronal cells in response to Ca2+ influx through voltage-gated Ca 2+ channels. A previous study reported that RyRs were expressed in thalamocortical (TC) neurons, but their physiological function has remained elusive. Here, we show that the activation of RyRs in TC neurons in mice decreases their tonic firing rate while blocking them induces the opposite response. Furthermore, activation of RyRs in ventroposteriomedial/ ventroposteriolateral nuclei reduces the behavioral responses to inflammatory pain and blocking them increases the responses. This study highlights the importance of the intracellular Ca2+ release via RyRs in controlling the excitability of TC neurons and in inflammatory pain signal processing in the thalamus.
AB - Ryanodine receptors (RyRs) are highly conductive intracellular Ca 2+ release channels which are widely expressed in the CNS. They rapidly increase the intracellular Ca2+ concentrations in neuronal cells in response to Ca2+ influx through voltage-gated Ca 2+ channels. A previous study reported that RyRs were expressed in thalamocortical (TC) neurons, but their physiological function has remained elusive. Here, we show that the activation of RyRs in TC neurons in mice decreases their tonic firing rate while blocking them induces the opposite response. Furthermore, activation of RyRs in ventroposteriomedial/ ventroposteriolateral nuclei reduces the behavioral responses to inflammatory pain and blocking them increases the responses. This study highlights the importance of the intracellular Ca2+ release via RyRs in controlling the excitability of TC neurons and in inflammatory pain signal processing in the thalamus.
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U2 - 10.1523/JNEUROSCI.3203-10.2011
DO - 10.1523/JNEUROSCI.3203-10.2011
M3 - Article
C2 - 21273406
AN - SCOPUS:79251553117
SN - 0270-6474
VL - 31
SP - 1213
EP - 1218
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 4
ER -