TY - JOUR
T1 - Risperidone reduces mRNA expression levels of Sulfonylurea Receptor 1 and TASK1 in PC12 cells
AU - Ota, Miyuki
AU - Nakashima, Akira
AU - Kaneko, Yoko S.
AU - Mori, Keiji
AU - Takami, Goro
AU - Ota, Akira
N1 - Funding Information:
The authors wish to acknowledge Janssen Pharmaceutica for supplying risperidone. This study was supported by grants-in-aid from Fujita Health University, Japan, to Akira Ota.
PY - 2007/2/2
Y1 - 2007/2/2
N2 - Electrophysiological and immunohistochemical studies have demonstrated that glucose-sensing neurons in the hypothalamus contain both ATP-sensitive K+ (KATP) and tandem-pore K+ (TASK1 and TASK3) channels and that glucose-induced depolarization or hyperpolarization of these neurons function as an important link between glucose-excited or glucose-inhibited neurons and feeding behavior. Medication with atypical antipsychotics increases the appetite of schizophrenic patients and thus causes increases in body weight. Therefore, the present study investigates mRNA expression levels of the genes encoding the components of these K+ channel subsets in PC12 cells cultured with risperidone (an atypical antipsychotic) and in the hypothalami of rats subcutaneously injected for 21 consecutive days with 0.1 or 0.01 mg/kg/day of risperidone. The mRNA expression levels of various genes were not obviously altered in rat hypothalami. However, the mRNA expression levels for sulfonylurea receptor 1, a component affording nucleotide-binding folds to KATP channels, and TASK1 were down-regulated in PC12 cells cultured with 50 μM risperidone for 24 h, but the amount of intracellular ATP in these cells was not affected by the drug. Collectively, these results indicate that the amplitude of the current through these K+ channels in PC12 cells might be modulated as a pharmacological effect of risperidone.
AB - Electrophysiological and immunohistochemical studies have demonstrated that glucose-sensing neurons in the hypothalamus contain both ATP-sensitive K+ (KATP) and tandem-pore K+ (TASK1 and TASK3) channels and that glucose-induced depolarization or hyperpolarization of these neurons function as an important link between glucose-excited or glucose-inhibited neurons and feeding behavior. Medication with atypical antipsychotics increases the appetite of schizophrenic patients and thus causes increases in body weight. Therefore, the present study investigates mRNA expression levels of the genes encoding the components of these K+ channel subsets in PC12 cells cultured with risperidone (an atypical antipsychotic) and in the hypothalami of rats subcutaneously injected for 21 consecutive days with 0.1 or 0.01 mg/kg/day of risperidone. The mRNA expression levels of various genes were not obviously altered in rat hypothalami. However, the mRNA expression levels for sulfonylurea receptor 1, a component affording nucleotide-binding folds to KATP channels, and TASK1 were down-regulated in PC12 cells cultured with 50 μM risperidone for 24 h, but the amount of intracellular ATP in these cells was not affected by the drug. Collectively, these results indicate that the amplitude of the current through these K+ channels in PC12 cells might be modulated as a pharmacological effect of risperidone.
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U2 - 10.1016/j.neulet.2006.11.018
DO - 10.1016/j.neulet.2006.11.018
M3 - Article
C2 - 17174476
AN - SCOPUS:33846223527
SN - 0304-3940
VL - 412
SP - 254
EP - 258
JO - Neuroscience Letters
JF - Neuroscience Letters
IS - 3
ER -