BJA Advance Access published online on March 10, 2006
British Journal of Anaesthesia, doi:10.1093/bja/ael046
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1 Institute of Pharmacology and Toxicology, Tzu Chi University, Hualien, Taiwan, R.O.C.; Department of Health, Yuli Hospital, Executive Yuan, Hualien, Taiwan, R.O.C.
* To whom correspondence should be addressed. Background. Group I metabotropic glutamate receptors (mGluRs) have been reported to regulate N-methyl-D-aspartate (NMDA) receptor function in various brain regions. The selective mGluR5 antagonist 2-methyl-6-(phenylethynyl)-pyridine (MPEP) can potentiate NMDA antagonists such as PCP and MK-801-induced behavioural responses. In the present study, the role of group I mGluRs on ketamine- and propofol-induced general anaesthesia was examined. Methods. Mice were pretreated with various doses of the group I mGluR agonist (S)-3,5-dihydroxyphenylglycine (DHPG), selective mGluR5 agonist (RS)-2-chloro-5-hydroxyphenylglycine (CHPG), mGluR1 antagonist 7-(hydroxyimino)cyclopropa[b]chromen-1a-carboxylate ethyl ester (CPCCOEt) and mGluR5 antagonist MPEP followed by administration of ketamine (120 mg kg-1) or propofol (140 mg kg-1) to induce anaesthesia. The duration of loss of righting reflex was recorded. Results. DHPG and CHPG antagonized and MPEP potentiated ketamine-induced anaesthesia in a dose-dependent manner. CPCCOEt was in effective. However, propofol-induced anaesthesia was not affected after manipulating mGluR1 and mGluR5 receptors. Conclusions. mGluR5 receptors play an important role in modulation of anaesthesia induced by ketamine, but not propofol.
Accepted January 6, 2006
Laboratory Investigation
Ketamine, but not propofol, anaesthesia is regulated by metabotropic glutamate 5 receptors
J.-H. Sou 1,
M.-H. Chan 2,
and
H.-H. Chen 2 *
2 Institute of Pharmacology and Toxicology, Tzu Chi University, Hualien, Taiwan, R.O.C.
H.-H. Chen, E-mail: hwei{at}mail.tcu.edu.tw
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