Differential actions of 3-(4-chlorophenyl) glutamic acid stereoisomers and l-trans-pyrrolidine-2,4-dicarboxylic acid upon l-homocysteic acid- and l-glutamic acid-induced responses from rat spinal motoneurones

doi:10.1016/0028-3908(95)00124-7

Paper

Differential actions of 3-(4-chlorophenyl) glutamic acid stereoisomers and l-trans-pyrrolidine-2,4-dicarboxylic acid upon l-homocysteic acid- and l-glutamic acid-induced responses from rat spinal motoneurones

Published Dec 1, 1995 · D. Chalmers, D. Jane, D. Sunter

Neuropharmacology

Q1 SJR score

4

Citations

0

Influential Citations

Full textSemantic Scholar

Abstract

Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.

In Vitro Study

Study Snapshot

Chlorpheg stereoisomers selectively potentiate responses evoked by l-homocysteic acid in neonatal rat motoneurones, supporting the existence of multiple excitatory amino acid uptake sites.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Differential actions of 3-(4-chlorophenyl) glutamic acid stereoisomers and l-trans-pyrrolidine-2,4-dicarboxylic acid upon l-homocysteic acid- and l-glutamic acid-induced responses from rat spinal motoneurones

References

Citations