INOSITOL TRISPHOSPHATE AND THAPSIGARGIN DISCRIMINATE ENDOPLASMIC-RETICULUM STORES OF CALCIUM IN RAT-BRAIN

被引:93
作者
VERMA, A
HIRSCH, DJ
HANLEY, MR
THASTRUP, O
CHRISTENSEN, SB
SNYDER, SH
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,75 N WOLFE ST,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT PHARMACOL & MOLEC SCI,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT PSYCHIAT,BALTIMORE,MD 21205
[4] UNIV CALIF DAVIS,SCH MED,DEPT BIOL CHEM,DAVIS,CA 95616
[5] UNIV COPENHAGEN,RIKSHOSP,DEPT CLIN CHEM,DK-2100 COPENHAGEN,DENMARK
[6] ROYAL DANISH SCH PHARM,DEPT ORGAN CHEM,DK-2100 COPENHAGEN,DENMARK
关键词
D O I
10.1016/0006-291X(90)90747-B
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ATP dependent Ca2+ accumulation into oxalate-loaded rat brain microsomes is potently inhibited by thapsigargin with an IC50 of 2 nM and maximal inhibition at 10 nM. Approximately 15% of the total A23187-releasable microsomal calcium store is insensitive to thapsigargin concentrations up to 100 μM. Inositol-1,4,5-trisphosphate (IP3) maximally inhibits 40% of the net Ca2+ accumulation by whole brain microsomes. Its effects are non-additive with thapsigargin suggesting that the IP3-sensitive Ca2+ pool is a subset of the thapsigargin sensitive Ca2+ pool. Marked regional differences occur in Ca2+ transport rates and sensitivity to both thapsigargin and IP3. © 1990.
引用
收藏
页码:811 / 816
页数:6
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