TY - JOUR
T1 - Reversed effect of caffeine on non-contractile and contractile Ca2+ mobilization operated by acetylcholine receptor in mouse diaphragm muscle
AU - Kimura, Ikuko
AU - Kondoh, Takashi
AU - Tsuneki, Hiroshi
AU - Kimura, Masayasu
PY - 1991/6/10
Y1 - 1991/6/10
N2 - Caffeine effects on contractile and acetylcholine receptor-related non-contractile Ca2+ mobilization were investigated in phrenic nerve-diaphragm muscles of mice with neostigmine. Caffeine enhanced at 0.25-5 mM, and decreased at 7-20 mM the total amount of contractile Ca2+-aequorin luminescence (Ca2+ transients), but only decreased at 2-10 mM non-contractile Ca2+ transients. Pretreatment with formamide (2 M for 30 min) abolished contractile Ca2+ transients, but did not affect non-contractile ones. These results suggest that non-contractile Ca2+ mobilization is not due to direct Ca2+ release from sarcoplasmic reticulum, but due to direct modulation by nicotinic acetylcholine receptor.
AB - Caffeine effects on contractile and acetylcholine receptor-related non-contractile Ca2+ mobilization were investigated in phrenic nerve-diaphragm muscles of mice with neostigmine. Caffeine enhanced at 0.25-5 mM, and decreased at 7-20 mM the total amount of contractile Ca2+-aequorin luminescence (Ca2+ transients), but only decreased at 2-10 mM non-contractile Ca2+ transients. Pretreatment with formamide (2 M for 30 min) abolished contractile Ca2+ transients, but did not affect non-contractile ones. These results suggest that non-contractile Ca2+ mobilization is not due to direct Ca2+ release from sarcoplasmic reticulum, but due to direct modulation by nicotinic acetylcholine receptor.
KW - Caffeine
KW - Contractile Ca transient
KW - Excitation-contraction coupling
KW - Formamide
KW - Nicotinic acetylcholine receptor
KW - Non-contractile Ca transient
KW - Skeletal muscle
UR - http://www.scopus.com/inward/record.url?scp=0025759255&partnerID=8YFLogxK
U2 - 10.1016/0304-3940(91)90886-X
DO - 10.1016/0304-3940(91)90886-X
M3 - 学術論文
C2 - 1881613
AN - SCOPUS:0025759255
SN - 0304-3940
VL - 127
SP - 28
EP - 30
JO - Neuroscience Letters
JF - Neuroscience Letters
IS - 1
ER -