spacer gif spacer gif spacer gif spacer gif Online submission spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by SCHOFIELD, P. K.
Right arrow Articles by TREHERNE, J. E.
Right arrow Search for Related Content
PubMed
Right arrow Articles by SCHOFIELD, P. K.
Right arrow Articles by TREHERNE, J. E.
Journal of Experimental Biology 109,307-318 (1984)
Published by Company of Biologists 1984


Potentials Associated With the Blood-Brain Barrier of an Insect: Recordings from Identified Neuroglia

P. K. SCHOFIELD 1, L. S. SWALES 2, and J. E. TREHERNE 2

1 A.F.R.C. Unit of Insect Neurophysiology and Pharmacology, Department of Zoology, The University, Downing St, Cambridge, CB2 3EJ, U.K.
2 A.F.R.C. Unit of Insect Neurophysiology and Pharmacology, Department of Zoology, The University Downing St, Cambridge, CB2 3EJ, U.K.

The blood-brain barrier of the insect nervous system is thought to be formed by the neuroglia. It is associated with a positive interstitial potential relative to the bathing medium (‘sheath’ potential), and with positive changes in potential that can be induced by raising the potassium level in the bathing medium. In central nervous connectives of the cockroach, Periplaneta americana, these potential differences (p.d.s) were measured just below the perineurium at the same magnitude as comparable p.d.s recorded deeper, indicating that they are produced by the perineurium. The interstitial p.d. apparently results from the presence of a paracellular resistance, and from the generation of less electromotive force (e.m.f.) by the basolateral membrane than by the apical (adglial). Recordings from cells identified by injection of peroxidase showed that the initial change in interstitial p.d. induced by high K was accompanied by: a depolarization of greater magnitude across the basolateral membrane, a small depolarization of the apical membrane, and no depolarization of sub-perineurial glial cells or axons. It therefore appears that the depolarization of the basolateral membrane by high K gives rise, by electrical coupling, to the shift in interstitial p.d. and the depolarization of the apical membrane. There was then a gradual depolarization of all membranes, consistent with a leak of K into the sub-perineurial interstitial system, and where the depolarization of the basolateral membrane would be produced by coupling to the apical. If the perineurium contains an intercellular resistance, then it must restrict diffusion of water-soluble substances.

Key words: Electrophysiology, glia, blood-brain barrier, insect, Periplaneta americana

Accepted on October 27, 1983







© The Company of Biologists Ltd 1984