In vitro and in vivo physiology of low nanomolar concentrations of Zn2+ in artificial cerebrospinal fluid
Artificial cerebrospinal fluid (ACSF), i.e., brain extracellular medium, which includes Ca 2+ and Mg 2+ , but not other divalent cations such as Zn 2+ , has been used for in vitro and in vivo experiments. The present study deals with the physiological significance of extracellular Zn 2+ in ACSF. Spo...
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Published in | Scientific reports Vol. 7; no. 1; p. 42897 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
17.02.2017
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Artificial cerebrospinal fluid (ACSF), i.e., brain extracellular medium, which includes Ca
2+
and Mg
2+
, but not other divalent cations such as Zn
2+
, has been used for
in vitro
and
in vivo
experiments. The present study deals with the physiological significance of extracellular Zn
2+
in ACSF. Spontaneous presynaptic activity is suppressed in the stratum lucidum of brain slices from young rats bathed in ACSF containing 10 nM ZnCl
2
, indicating that extracellular Zn
2+
modifies hippocampal presynaptic activity. To examine the
in vivo
action of 10 nM ZnCl
2
on long-term potentiation (LTP), the recording region was perfused using a recording electrode attached to a microdialysis probe. The magnitude of LTP was not modified in young rats by perfusion with ACSF containing 10 nM ZnCl
2
, compared to perfusion with ACSF without Zn
2+
, but attenuated by perfusion with ACSF containing 100 nM ZnCl
2
. Interestingly, the magnitude of LTP was not modified in aged rats even by perfusion with ACSF containing 100 nM ZnCl
2
, but enhanced by perfusion with ACSF containing 10 mM CaEDTA, an extracellular Zn
2+
chelator. The present study indicates that the basal levels of extracellular Zn
2+
, which are in the range of low nanomolar concentrations, are critical for synaptic activity and perhaps increased age-dependently. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/srep42897 |