Abstract：
:The binding of nimodipine, a 1,4-dihydropyridine Ca2+ channel antagonist, and of Bay K 8644, a Ca2+ channel activator, was measured in several regions of rat brain and compared to the distribution of K+ depolarization-induced 45Ca2+ uptake into synaptosomes. The maximum binding densities (Bmax) of [3H]nimodipine and [3H]Bay K 8644 were not significantly different one from the other, but differed according to brain region with binding being highest in the olfactory bulb and hippocampus, intermediate in the caudate nucleus and cerebral cortex (various regions), and lowest in the cerebellum [563 to 107 fmol/mg protein (mean)]. The KD values, [3H]nimodipine = 1.8 X 10(-10) M (mean) and [3H]Bay K 8644 = 1.4 X 10(-9) M (mean), did not differ according to region. Depolarization-induced 45Ca2+ uptake in synaptosomes occurred as fast (1 sec) and slow (10 sec) components distinguished by their selective occurrence in choline-containing and pre-depolarized preparations respectively. Distribution of the fast component of uptake paralleled that of [3H]nimodipine binding, being least in the cerebellum and greatest in the hippocampus and cortex, but the magnitude of the slow phase of 45Ca2+ uptake did not vary in the three brain regions studied.
journal_name
Biochem Pharmacoljournal_title
Biochemical pharmacologyauthors
Skattebøl A,Triggle DJdoi
10.1016/0006-2952(87)90575-2subject
Has Abstractpub_date
1987-12-01 00:00:00pages
4163-6issue
23eissn
0006-2952issn
1873-2968pii
0006-2952(87)90575-2journal_volume
36pub_type
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