| Project/Area Number |
62480123
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| Research Category |
Grant-in-Aid for General Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
General pharmacology
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| Research Institution | Keio University |
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Principal Investigator |
KATO Ryuichi School of Medicine, Keio University, 医学部, 教授 (40112685)
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| Co-Investigator(Kenkyū-buntansha) |
SASAKAWA Nobuyuki School of Medicine, Keio University, 医学部, 助手 (20187107)
NAKAKI Toshio School of Medicine, Keio University, 医学部, 助手 (30164148)
YAMAMOTO Satoshi School of Medicine, Keio University, 医学部, 助教授 (50138129)
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| Project Period (FY) |
1987 – 1988
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| Project Status |
Completed (Fiscal Year 1988)
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| Budget Amount *help |
¥5,800,000 (Direct Cost: ¥5,800,000)
Fiscal Year 1988: ¥1,800,000 (Direct Cost: ¥1,800,000)
Fiscal Year 1987: ¥4,000,000 (Direct Cost: ¥4,000,000)
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| Keywords | chromaffin cells / Ca^<++> mobilization / inositol phosphate / nicotinic receptor / 牛副腎髄質培養クロマフィン細胞 / イノシトール三リン酸 / 細胞内遊離Ca^<2+> / サイクリックGMP / 培養日数 |
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| Research Abstract |
The mechanism of functional shift from muscarinic to nicotinic cholinergic receptors involved in cytosolic Ca^<++> mobilization and inositol triphosphate (IP_3) during the primary culture of adrenal chromaffin cells was studied. At 0.5 day in culture, muscarine, a specific agonist for muscarinic receptors, caused a greater effect on intracellular Ca^<2+> mobilization and the accumulation of Ins(1,3,4)P_3 than did the nicotinic-specific agonist nicotine. On the contrary, at 5 days, nicotine produced a greater effect on the accumulation of Ins(1,3,4)P_3 and intracellular calcium mobilization than did muscarine. Furthermore, at 0.5 day, the muscarinic antagonist atropine strongly inhibited the increase in InsP_3 accumulation that was induced by the nonspecific agonist carbachol, whereas at 5 days the inhibitory effect of atropine was greatly lowered. On the other hand, the nicotinic receptor antagonists hexamethonium and - tubocurarine showed a much higher inhibitory potency at 5 days compared with 0.5 day in culture. Binding experiments with a muscarinic ligand excluded the possibility that the reduction in muscarinic effects on InsP_3 and intracellular Ca^<2+> mobilization were due to disappearance of the muscarinic receptor itself. These data show that cholinergic receptors linked to the accumulation of InsP_3 and Ca^<2+> mobilization functionally shift from muscarinic to nicotinic during primary culture of adrenal chromaffin cells.
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