Abstract

Using grease seal techniques on rat cerebral cortical slices and on frog hemisected spinal cords, bath applied N- methyl- d-aspartate (NMDA; 10–160 μM) and quinolinate (0.25–8 mM) induced dose-dependent depolarisations. These depolarising responses, but not those to quisqualate or kainate, were reduced by 2-amino-5-phosphono-valerate (2-AP5; 10–100 μM), magnesium (0.1–10 mM) and ketamine (10–100 μM). A novel dose-dependent hyperpolarising response to quinolinate (0.1–2 mM) but not to NMDA was observed only on frog motoneurones, and this was not reduced by classical amino acid receptor antagonists.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.