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Mobility and transport of magnesium in squid giant axons
Author(s) -
Baker P. F.,
Crawford A. C.
Publication year - 1972
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1972.sp010062
Subject(s) - axoplasm , chemistry , magnesium , axon , egta , biophysics , choline , calcium , analytical chemistry (journal) , inorganic chemistry , biochemistry , anatomy , chromatography , biology , organic chemistry
1. The Mg content of axons obtained from Loligo forbesi averaged 6·4 ± 0·8 m‐mole/kg axoplasm. 2. A small patch of radioactive 28 Mg injected into an axon broadened considerably. A similar patch of 45 Ca showed hardly any broadening. The self‐diffusion coefficient of Mg in axoplasm is about 2 × 10 −6 cm 2 /sec which is at least twenty times greater than that of Ca. 3. Under the influence of an applied electric field Mg migrated towards the cathode. Its mobility was about half of that of Mg in free solution. This suggests that the concentration of ionized Mg in squid axoplasm is between 2 and 3 m‐mole/kg axoplasm. The mobility of Mg was not changed by poisoning the axon fully. 4. Mg influx and Mg efflux were roughly the same and equal to about 1 p‐mole/cm 2 sec. Mg efflux was reduced by poisoning with cyanide and by replacement of external Na by choline. Removal of external K or Ca had little effect and removal of external Mg tended to increase the efflux. 5. The dependence of Mg efflux on Na seems not to be secondary to changes in Ca because it persists in the absence of external Ca and in axons pre‐injected with EGTA. The form of the dependence on Na ions approximates to a simple rectangular hyperbola. 6. Replacement of external Na by Li or choline increased Mg influx. Mg influx was unaffected by cyanide. 7. Mg efflux was reduced to an average of 15% by poisoning with cyanide or DNP. The efflux could be recovered by injection of ATP. Inhibition persisted in axons pre‐injected with EGTA, showing that it is not secondary to a rise in Ca i . 8. During nervous activity there is an extra entry of Mg. For axons immersed in sea water this extra Mg entry per impulse is roughly the same as the extra Ca entry per impulse.