Project/Area Number |
04454139
|
Research Category |
Grant-in-Aid for General Scientific Research (B)
|
Allocation Type | Single-year Grants |
Research Field |
神経・筋肉生理学
|
Research Institution | Saga Medical School |
Principal Investigator |
KUBA Kenji Saga Medical School, Physiology, Professor, 医学部, 教授 (60080561)
|
Co-Investigator(Kenkyū-buntansha) |
NOHMI Mitsuo Saga Medical School, Center for M.S.R.E, Associate Professor, 医学部, 助教授 (80117209)
|
Project Period (FY) |
1992 – 1993
|
Project Status |
Completed (Fiscal Year 1993)
|
Budget Amount *help |
¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 1993: ¥2,700,000 (Direct Cost: ¥2,700,000)
|
Keywords | Intracellular Ca^<2+> / Ca^<2+> -induced Ca^<2+> release / Ca^<2+> influx / Bullfrog sympathetic ganglion cells / Rabbit otic ganglion cells / Cylic ADP-ribose / Mitochondria Cyclosporin-A / サイクロスポリンA / Ca^<2+>誘起性Ca^<2+>遊離 / cyclic ADP-ribose / Ca^<2+>感受性プローブ / 落射蛍光法 / 紫外レーザー共焦点顕微鏡法 / パッチクランプ法 |
Research Abstract |
The mechanism of intracellular Ca^<2+> release and its physiological functions were studied in cultured bullfrog sympathetic and rabbit otic ganglion cells, using fura-2 or indo-1 fluorescence redording techniques with a photomultiplier or confocal laser-scanning microscope and shole cell patch clamp techniques. Ryanodine-sensitive Ca^<2+> -induced Ca^<2+> release (CICR) in bullfrog sympathetic neurones were voltage-dependently activated throughout the cytoplasm by Ca^<2+> influx produced by a depolarizing voltage pulse (> 100 ms), but only in the submembrane regions by Ca^<2+> influx caused by action potentials (> 10 Hz, 100 pulses). Under the effects of intracellular cyclic ADP-ribose, tetanic action potentials activated propagating CICR. iIn cultured rabbit otic ganglion cells, when the extracellular Ca^<2+> was reduced to a level < 0.1 mM, a small Ca^<2+> entry produced by a high K^+ -induced depolarization caused a propagating Ca^<2+> release from mitochondria which was blocked by cyclosprin A. These two mechanisms may operate in ceurones in situ depending on the extracellular Ca^<2+> levels that would be altered by activities of neighboring neurones.
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