Home LiteratureArticle Details
PMID: 2443623 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Use-dependent block of excitatory amino acid currents in cultured neurons by ketamine.

Journal of neurophysiology ·Vol. 58 ·No. 2 ·1987-08-00 ·Pages 251-66

MacDonald JF, Miljkovic Z, Pennefather P

Abstract

1. Mouse hippocampal neurons grown in dissociated cell culture were patch clamped using a whole cell voltage clamp (discontinuous switching clamp) technique. The currents generated by pressure applications of excitatory amino acids were studied over a wide range of holding potentials, and current-voltage curves were plotted. Excitatory amino acids that activated the N-methyl-D-aspartic acid (NMDA) receptor demonstrated some degree of desensitization with repeated applications, whereas the currents observed in response to kainic acid (KAI) did not. Desensitization could be minimized by keeping the frequency of application sufficiently low (i.e., less than 0.1 Hz). 2. The short-acting dissociative anaesthetic, ketamine (2-50 microM), selectively blocked L-aspartic acid (L-Asp), NMDA, and L-glutamic acid (L-Glu) currents while sparing those in response to KAI. Therefore, ketamine is a relatively selective blocker of the NMDA response versus that (those) activated by KAI. 3. The block by ketamine of excitatory amino acid currents is highly voltage dependent. Concentrations of ketamine that had little effect on outward current responses at depolarized potentials were quite effective at blocking inward current responses at hyperpolarized potentials. In contrast, DL-2-amino-5-phosphonovaleric acid (APV) was equally effective at blocking both inward and outward currents (voltage independent). The voltage dependence of ketamine (a positively charged molecule) could be accounted for if ketamine blocked the NMDA response by binding to a site that experienced 55% of the membrane field. 4. In the presence of ketamine, peak inward currents evoked by repeated applications of NMDA, L-Asp, or L-Glu progressively declined to a steady-state level of block (use-dependent block). This decrement occurred at frequencies much lower than those that were employed to demonstrate desensitization (in the absence of ketamine). Moving the membrane potential to depolarized values did not, in itself, relieve the ketamine block. However, if the appropriate excitatory amino acid (L-Asp, NMDA, L-Glu) was applied during the period of depolarization, a relief of the block could be demonstrated. No recovery from the blockade occurred with periods of rest (no amino acid application) as long as 5 min. Furthermore, no recovery was observed even when ketamine was washed out of the bathing solution until the appropriate agonist was applied. Thus recovery from blockade, like development of blockade, was use dependent.(ABSTRACT TRUNCATED AT 400 WORDS)

MeSH Terms
Amino Acids/physiology Animals Aspartic Acid/analogs & derivatives,pharmacology,physiology Cells, Cultured Electric Conductivity Glutamates/physiology Glutamic Acid Hippocampus/drug effects,physiology Ion Channels/drug effects,physiology Kainic Acid/pharmacology Ketamine/pharmacology Membrane Potentials/drug effects Mice N-Methylaspartate Spinal Cord/drug effects,physiology
Chemicals
Amino Acids Glutamates Ion Channels Aspartic Acid Glutamic Acid N-Methylaspartate Ketamine Kainic Acid
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
MacDonald J F
Playfair Neurosciences Unit, Toronto Western Hospital, Ontario, Canada.
Miljkovic Z
Pennefather P
Article Info
Journal
Journal of neurophysiology
Abbr.
J Neurophysiol
ISSN
0022-3077
Published
1987-08-00
Pages
251-66
Language
English
Region
United States
NLM ID
0375404
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com