| Project/Area Number |
09470023
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
General pharmacology
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| Research Institution | Fukui Medical University |
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Principal Investigator |
MURAMATSU Ikunobu Fukui Medical University, School of Medicine, Professor, 医学部, 教授 (10111965)
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| Co-Investigator(Kenkyū-buntansha) |
SUZUKI Fumiko Fukui Medical University, School of Medicine, Assistant Professor, 医学部, 助手 (80291376)
TANIGUCHI Takanobu Fukui Medical University, School of Medicine, Associate Professor, 医学部, 助教授 (60217130)
ZHU Jun Fukui Medical University, School of Medicine, Assistant Professor (90303370)
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| Project Period (FY) |
1997 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥11,700,000 (Direct Cost: ¥11,700,000)
Fiscal Year 1998: ¥4,100,000 (Direct Cost: ¥4,100,000)
Fiscal Year 1997: ¥7,600,000 (Direct Cost: ¥7,600,000)
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| Keywords | alpha_1 adrenoceptor / molecular cloning / splice variants / cytosensor / 組織分布 |
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| Research Abstract |
alpha_1 Adrenoceptor plays important physiological roles in blood pressure, lipid metabolism, urinary tissues and central nervous system. In the present research project. we carried out molecular biological and classical pharmacological studies in order to clarify alpha_1 adrenoceptor functions.
1 . Molecular cloning of rabbit alpha_1 adrenoceptor subtypes : We screened rabbit liver cDNA library and identified alpha_<1a> alpha_<1b> and alpha_<1d> subtypes. Rabbit alpha_<1b> and alpha_<1d> subtypes showed high homology and the same pharmacological characters to those of other species reported previously. However, three splice variants were identified in rabbit alpha_<1b> adrenoceptor, which had uniqe sequence in C-terminal and showed different tissue distribution in rabbit.
2. Identification of native alpha_1 adrenoceptor subtypes : Native alpha_1 adrenoceptors were examined in radioligand binding and functional experiments and identified in the following tissues ; alpha_<1A> and alpha_<1L> in human prostate, alpha_<1L> in human urethra, alpha_<1B> in human aorta, alpha_<1A> and alpha_<1L> in rat prostate and rabbit iris.
3. Functional analysis of alpha_1 adrenoceptors with cytosensor : Human alpha_<1a> alpha_<1b> and alpha_<1d> adrenoceptors were stably expressed in CHO cells and the extracellular acidification rate (EAR) was measured with cytosensor. EAR increased concentration-dependently in response to alpha agonists such as noradrenaline and clonidine. Detailed analyses of concentration-response urves revealed full agonist, partial agonist, spare receptor and propriety of Schild plot, showing that classical receptor theory is applicable to this system.
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