Literature DB >> 5716849

Ionic environment of neurones and glial cells in the brain of an amphibian.

M W Cohen, H M Gerschenfeld, S W Kuffler.   

Abstract

1. Experiments were performed to determine the relative contribution of the blood plasma and of the cerebrospinal fluid (c.s.f.) to the ionic environment of neurones and glial cells within the brain of the amphibian Necturus maculosus.2. The concentrations in the blood plasma of untreated control animals were 99 +/- 2 mM for Na(+) and 2.0 +/- 0.1 mM for K(+). In the c.s.f. the corresponding values were 112 +/- 2 mM-Na(+) and 1.9 +/- 0.1 mM-K(+).3. By keeping animals in K(+)-rich water it was possible to raise chronically the concentrations of K(+) in the blood plasma up to almost 5 times the normal value, close to 9 mM, while the c.s.f. concentration of K(+) was only doubled, to about 4 mM. This behaviour of Necturus, tending to keep the K(+) in the c.s.f. low, resembles that of mammals.4. The membrane potential of glial cells in the optic nerve can be used as an accurate indicator for determining the K(+) concentration in the intercellular spaces. Such determinations were made in vivo, and it was shown that the glial cells adjust their membrane potential to the changes of K(+) concentrations in the c.s.f. and not to those of the blood plasma. In contrast, the membrane potential of skeletal muscle fibres changes according to the K(+) concentration in the blood plasma.5. It is concluded that the cells within the optic nerve are surrounded by an ionic environment which corresponds to that of the c.s.f. and not to that of the blood plasma. The intercellular spaces are open and ions diffuse freely into them from the c.s.f. A homeostatic mechanism operates, keeping the ion concentrations around neurones and glia within a narrow range and relatively independent of large changes in the blood plasma. This may provide relative stability for the signalling system. Similarities between the optic nerve and other parts of the central nervous system in respect to their relation to c.s.f. and blood are discussed. It seems likely that the mechanisms which control the electrolyte concentrations are similar in Necturus and in mammals.

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Year:  1968        PMID: 5716849      PMCID: PMC1351804          DOI: 10.1113/jphysiol.1968.sp008564

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  23 in total

1.  The influence of potassium and chloride ions on the membrane potential of single muscle fibres.

Authors:  A L HODGKIN; P HOROWICZ
Journal:  J Physiol       Date:  1959-10       Impact factor: 5.182

2.  Vital staining of the hematoencephalic barrier by silver nitrate and trypan blue, and cytological comparisons of the neurohypophysis, pineal body, area postrema, intercolumnar tubercle and supraoptic crest.

Authors:  G B WISLOCKI; E H LEDUC
Journal:  J Comp Neurol       Date:  1952-06       Impact factor: 3.215

3.  Neuroglial cells: physiological properties and a potassium mediated effect of neuronal activity on the glial membrane potential.

Authors:  S W Kuffler
Journal:  Proc R Soc Lond B Biol Sci       Date:  1967-06-06

4.  Studies on the permeability of the blood-retinal barrier. IV. Junctional complexes of the retinal vessels and their role in the permeability of the blood-retinal barrier.

Authors:  M Shakib; J G Cunha-Vaz
Journal:  Exp Eye Res       Date:  1966-07       Impact factor: 3.467

5.  Relation of potassium concentration in choroidplexus fluid to that in plasma.

Authors:  A Ames; K Higashi; F B Nesbett
Journal:  J Physiol       Date:  1965-12       Impact factor: 5.182

6.  The distribution within the brain of ferritin injected into cerebrospinal fluid compartments. II. Parenchymal distribution.

Authors:  M W Brightman
Journal:  Am J Anat       Date:  1965-09

7.  Distribution of 14C-labeled sucrose, inulin, and dextran in extracellular spaces and in cells of the leech central nervous system.

Authors:  J G Nicholls; D E Wolfe
Journal:  J Neurophysiol       Date:  1967-11       Impact factor: 2.714

8.  Physiological properties of glial cells in the central nervous system of amphibia.

Authors:  S W Kuffler; J G Nicholls; R K Orkand
Journal:  J Neurophysiol       Date:  1966-07       Impact factor: 2.714

9.  Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia.

Authors:  R K Orkand; J G Nicholls; S W Kuffler
Journal:  J Neurophysiol       Date:  1966-07       Impact factor: 2.714

10.  The ultrastructural basis of capillary permeability studied with peroxidase as a tracer.

Authors:  M J Karnovsky
Journal:  J Cell Biol       Date:  1967-10       Impact factor: 10.539

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  20 in total

1.  The natural history of neuroglia: an agenda for comparative studies.

Authors:  Theodore Holmes Bullock
Journal:  Neuron Glia Biol       Date:  2004-05

2.  Active transport of 131-I across the blood-brain barrier.

Authors:  H Davson; J R Hollingsworth
Journal:  J Physiol       Date:  1973-09       Impact factor: 5.182

3.  Protein size and cerebrospinal fluid composition.

Authors:  K Felgenhauer
Journal:  Klin Wochenschr       Date:  1974-12-15

4.  Transport of potassium at the blood-brain barrier.

Authors:  M W Bradbury; M B Segal; J Wilson
Journal:  J Physiol       Date:  1972-03       Impact factor: 5.182

5.  The effect of chronic osmotic disturbance on the concentrations of cations in cerebrospinal fluid.

Authors:  M W Bradbury; C R Kleeman
Journal:  J Physiol       Date:  1969-09       Impact factor: 5.182

6.  The thiosulphate (35S) space in the CNS of rats after ventriculo-cisternal perfusion.

Authors:  A Baethmann; U Steude; S Horsch; W Brendel
Journal:  Pflugers Arch       Date:  1970       Impact factor: 3.657

7.  The ontogenesis of haematoencephalic cation transport processes in the rhesus monkey.

Authors:  L Z Bito; R E Myers
Journal:  J Physiol       Date:  1970-05       Impact factor: 5.182

8.  Efflux mechanism contributing to the stability of the potassium concentration in cerebrospinal fluid.

Authors:  M W Bradbury; B Stulcová
Journal:  J Physiol       Date:  1970-06       Impact factor: 5.182

9.  The effects of certain anaesthetic and anti-convulsant drugs on the CSF potassium fluxes of the dog.

Authors:  J Halliday; A T Moir
Journal:  Br J Pharmacol       Date:  1974-09       Impact factor: 8.739

10.  Bicarbonate and chloride of rat brain during infusion-induced changes in bicarbonate concentration of blood.

Authors:  J Weyne; J L Pannier; G Demeester; I Leusen
Journal:  Pflugers Arch       Date:  1970       Impact factor: 3.657

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