期刊
EUROPEAN JOURNAL OF PHARMACOLOGY
卷 651, 期 1-3, 页码 137-145出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2010.11.013
关键词
L-type voltage-dependent calcium channel; alpha 1C subunit (Ca(v)1.2); Morphine; Place preference; Trafficking; Vps34
资金
- Ministry of Education, Culture, Sports, Science, and Technology of Japan
- Kawasaki Medical University
In the present study, we investigated the role of Vps34, a kinase classified into PI 3-kinase class Ill, in the brain of mouse after repeated in vivo treatment with morphine. The intracerebroventricular ( Icy.) administration of nifedipine caused a dose-dependent inhibition of morphine-induced place preference. The protein levels of Vps34 in the frontal cortex including the cingulate cortex and the limbic forebrain including the nucleus accumbens significantly increased in morphine-induced place preference. I.c.v, administration of PI 3-kinase inhibitors such as wortmannin and LY294002 inhibited morphine-induced place preference in a dose-dependent manner. Ca(v)1.2 protein level of L-type voltage-dependent calcium channels significantly increased in the frontal cortex and the limbic forebrain of the morphine psychologically dependent mice, which was significantly inhibited by PI 3-kinase inhibitors. Similar changes in the expression of Ca(v)1.2 and Vps34 proteins are found in the primary culture of cerebral cortical neurons during short-term exposure to morphine. Under such conditions, facilitated translocation of Ca(v)1.2 to the plasma membrane remarkably increased by the treatment of the cultured neurons with morphine when measuring protein level of Ca(v)1.2, and such changes in Ca(v)1.2 were also suppressed by PI 3-kinase inhibitors. These findings indicate a critical role of Vps34 in the up-regulation of Ca(v)1.2 in the neuronal plasma membrane and the development of morphine-induced place preference. (c) 2010 Elsevier B.V. All rights reserved.
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