Nucleotide sequence analysis of the binding site on the inositol 1,4,5-trisphosphate type-1 receptor in bipolar disorder - a negative study

被引:1
作者
Fujimaki, K
Morinobu, S [1 ]
Takahashi, J
Yamawaki, S
Kato, N
Kanno, M
Okuyama, N
Kawakatsu, S
Otani, K
Kusumi, I
Koyama, T
机构
[1] Hiroshima Univ, Sch Med, Dept Psychiat & Neurosci, Hiroshima, Japan
[2] Shiga Univ Med Sci, Dept Psychiat, Otsu, Shiga 52021, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Neuropsychiat, Tokyo, Japan
[4] Yamagata Univ, Sch Med, Dept Neuropsychiat, Yamagata, Japan
[5] Hokkaido Univ, Sch Med, Dept Psychiat, Sapporo, Hokkaido 060, Japan
关键词
bipolar disorder; inositol 1,4,5-trisphosphate receptor; calcium; calcineurin; FKBP-12;
D O I
10.1016/S0165-0327(00)00273-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Pharmacological studies of bipolar disorder suggest that dysfunction of calcium mobilization via phosphatidylinositol-mediated transduction may be involved in its pathogenesis. The present study tests the hypothesis that dysfunction of calcium mobilization in bipolar disorder is due to the mutation of the nucleotide sequence in the FKBP12 binding site on the inositol 1,4,5-trisphosphate type-1 receptor (IP(3)R1). Nucleotide sequence analysis of the FKBP12 binding site on IP(3)R1 was performed using reverse transcription-polymerase chain reaction and DNA sequencing. The nucleotide sequence in this region was preserved in all subjects. This finding suggests that IP(3)R1 dysfunction through the FKBP12 binding site is not involved in the pathogenesis of bipolar disorder. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:139 / 143
页数:5
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