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PMID: 3024751 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The gap junction channel. Its aqueous nature as indicated by deuterium oxide effects.

Biophysical journal ·Vol. 50 ·No. 5 ·1986-11-00 ·Pages 1003-7

Verselis V, Brink PR

Abstract

The effects of temperature and solvent substitution with deuterium oxide (D2O) on axoplasmic (ga) and gap junctional (gj) conductances were examined in the earthworm septate median giant axon (MGA). The temperature coefficients (Q10) for ga and gj were 1.4 and 1.5, respectively, between 5 and 15 degrees C. Substitution with D2O rapidly reduced both ga and gj by 20% and increased the Q10's to 1.5 and 1.8, respectively. The reduction in ga upon substitution with D2O and with cooling in either solvent reflects the changes that occur in solvent viscosity, which indicates that ion mobility in axoplasm, as in free solution, is primarily governed by viscous properties of the solvent. The similar initial reduction observed for gj suggests that solvent occupies the gap junction channel volume and influences transjunctional ion mobility. With time there was a further reduction in gj at 20 degrees C and a larger Q10 in D2O. The enhanced effects of D2O on gj cannot be accounted for by solvent viscosity alone and may be due to an increased hydration of the channels and/or the transport ions and by isotope effects of hydrogen-deuterium exchange on the channel protein that reduce gj.

MeSH Terms
Animals Deuterium Deuterium Oxide Electric Conductivity Intercellular Junctions/physiology Membrane Potentials Microelectrodes Oligochaeta Water
Chemicals
Water Deuterium Deuterium Oxide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Verselis V
Brink P R
References (12)
12 references, click to expand
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Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
0006-3495
Published
1986-11-00
Pages
1003-7
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC1329826
Subset
IM
Grants
NIGMS NIH HHS · GM 24905 · United States
NHLBI NIH HHS · HL 31299 · United States
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