Affiliation:
1. Department of Biochemistry, Institute of Psychiatry (British Postgraduate Medical Federation, University of London), London, S.E. 5
Abstract
1. Sample from the neocortex and piriform cortex of guinea pigs and rats were incubated in inulin-containing glucose–saline. Their intracellular (non-inulin) space contained 19–27μequiv. of Na+/g. of original tissue. These values were stable between 30 and 100min. after incubation commenced, but addition of 22NaCl to the neocortical samples showed them to be associated with a flux of 400μequiv. of Na+/g. of tissue/hr. 2. Addition of 0·5–10mm-l-glutamic acid or 0·1mm-N-methyl-dl-aspartic acid rapidly increased the tissue's Na+ content; N-acetyl-dl-aspartic acid was without action. 3. During the first 1–1·5min. after the addition of l-glutamic acid to neocortical samples their Na+ content increased at 600μequiv./g. of tissue/hr., and the rate of 22Na+ influx corresponded to 1230μequiv. of Na+/g./hr. These rates were calculated to be sufficiently rapid to account for loss of the tissue's normal membrane potential within 1–2sec. of the addition of the acid. 4. In addition, a rapid but more limited loss of K+ took place after the addition of l-glutamic acid or the methylaspartic acid; on continued incubation tissue K+ content increased, as also did the intracellular volume of the tissue, from its original 670μl./g. to 1100μl./g. 5. Interpretation of these and of associated changes is offered in terms that involve a cation pump and the permeability changes associated with the nerve impulse.
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