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pmid: 9172154
Non-specific metabotropic glutamate receptor (mGluR) agonists have previously been shown to potentiate responses of spinal neurones to ionotropic glutamate receptor agonists. In this study we show that LY354740, which is a highly selective Group 2 mGluR agonist with nanomolar potency in vitro, also mimics the above effects following local ejection on spinal neurones in vivo, an action which is blocked by a Group 2 antagonist. Despite its polar nature, LY354740 is also active given either by the i.v. or the oral route (2.5-20 mg/kg) and thus will be a useful agent for investigating the role of Group 2 mGluRs both physiologically and clinically.
Neurons, Drug Evaluation, Preclinical, Administration, Oral, Stereoisomerism, Iontophoresis, Receptors, Metabotropic Glutamate, Rats, Bridged Bicyclo Compounds, Spinal Cord, Injections, Intravenous, Excitatory Amino Acid Agonists, Animals, Female, Rats, Wistar, Injections, Spinal
Neurons, Drug Evaluation, Preclinical, Administration, Oral, Stereoisomerism, Iontophoresis, Receptors, Metabotropic Glutamate, Rats, Bridged Bicyclo Compounds, Spinal Cord, Injections, Intravenous, Excitatory Amino Acid Agonists, Animals, Female, Rats, Wistar, Injections, Spinal
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 28 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |