| Budget Amount *help |
¥3,800,000 (Direct Cost: ¥3,800,000)
Fiscal Year 2000: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1999: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1998: ¥1,600,000 (Direct Cost: ¥1,600,000)
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| Research Abstract |
Although central sigma receptors has been proposed to play roles for various neurological and psychiatric functions, those mechanisms is not well understood. Cloning of cDNA of sigma receptor type 1 of human and guinea-pig have been reported, however, that of rat was not yet. Based on homologous sequence search of amino acids between human and guinea pig, I produced degenerated primer sets encoding 30-37th and 166-173 amino acids of sigma receptor type 1. Using the primer set, I have cloned a cDNA of rat sigma receptor type 1 from rat brain cDNA library using PCR technique. The rat cDNA sequence of sigma receptor type 1 showed 90% and 87% homology to that of human and guinea pig, respectively.
From the sequence of the rat cDNA of sigma receptor type 1, three kinds of 45mer antisense oligonucleotides complementary to cording region, 3' and 5' untranslated region were produced, and in situ hybridization was performed using rat brain. However, any probe showed a significant signals in rat
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brain. Neither northern blotting from whole rat brain showed signals. These results indicated that expression of sigma receptor type 1 mRNA should be very low. To examine protein levels of rat sigma receptors, an autoradiography study was performed using rat brain. So far, there was no suitable and enough strong ligands for sigma receptor autoradiography. However, I found that [^3H]YM-09151-2, usually used as D2 dopamine receptors, is a potent ligand for sigma receptors under Na^+ free condition with no binding to D2 receptors. Using this ligand and the condition, the autoradiography showed that sigma receptors are rich in cortex, hippocampus and red nucleus, whereas those intensity was quite less than that in guinea pig brain. The results indicated that not only mRNA and also protein expression of sigma receptor in rat is quite less than that of guinea pig brain. Behavioral sensitization was an animal model for human psychoses. Rats received intermittent methamphetamine injection developed sensitization. In sensitized brain to methamphetamine showed increased binding of sigma receptors in prefrontal cortex, hippocampus, substantia nigra and cerebellum. The two former brain region showed a sustained increase of sigma receptor binding at least 3 weeks after discontinuation of methamphetamine treatment.
As to human methamphctamine-induced psychosis, I examined two kinds of polymorphisms in promoter regions in the sigma receptor type 1 gene compared with normal controls. It was revealed that there was no significant difference in genotypic or allelic distribution between the patients with methamphetamine-induced psychoses and normal controls. This finding showed that sigma receptor gene polymorphisms did not confer susceptibility to methamphetamine-precipitated psychoses. Less
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