Abstract:
:The insoluble fraction of ox-brain, which had previously been shown to have a non-linear affinity for Na+ and K+, was prepared. Acetylcholine (1 x 10(-8) mol/l and 1 x 10(-7) mol/l) reduced the affinity of the fraction for Na+ and K+ to zero, while at 1 x 10(-6) mol/l, the affinity for the cations was almost as high as in the absence of the transmitter; the affinities for Na+ and K+ were particularly high, when the supernatant concentrations of these ions exceeded 80-100 mM. Addition of eserine (3 x 10(-5) mol/l) considerably modified the response of the fraction to acetylcholine (1 x 10(-5) mol/l). Atropine (1 x 10(-8) mol/l) in the absence or presence of acetylcholine (1 x 10(-5), or 1 x 10(-4) mol/l) reduced the affinity of the fraction for Na+ and K+ to zero. Epinephrine (3 x 10(-10) mol/l) lowered the affinity for Na+ and K+, while ergotamine itself (1 x 10(-5) mol/l) reduced it to zero. The addition of both epinephrine and ergotamine at the latter concentrations restored the affinity of the fractions for Na+ and K+ to what it had been in the absence of the transmitter or antagonist, previously reported. Norepinephrine (3 x 10(-10) mol/l), or ouabain (1 x 10(-7) mol/l) reduced the affinity of the fraction for Na+ and K+ to zero. Thus, the transmitters and antagonists altered the affinity of the insoluble fraction for Na+ and K+ non-linearity, dependent upon their concentrations, the concentrations of the cations, and the interaction of transmitter and antagonist.
journal_name
Neurochem Resjournal_title
Neurochemical researchauthors
Ahmed N,Hillman Hdoi
10.1007/BF00969636subject
Has Abstractpub_date
1989-02-01 00:00:00pages
179-84issue
2eissn
0364-3190issn
1573-6903journal_volume
14pub_type
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