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Korean J Anesthesiol > Volume 44(5); 2003 > Article
Korean Journal of Anesthesiology 2003;44(5):701-708.
DOI: https://doi.org/10.4097/kjae.2003.44.5.701   
Spinal Antinociceptive Mechanism of Isoflurane and Enflurane via the GABAA Receptor in Rats.
Dae Ki Choi, Young Kook Kim, Kyung Don Ham, Jai Hyun Hwang
Department of Anesthesiology, University of Ulsan College of Medicine, Seoul, Korea. jhhwang@amc.seoul.kr
Abstract
Background
Several studies have suggested that the spinal cord may be an important site of anesthetic action and have established that general anesthetics potentiate the effects of GABA at the GABAA receptor. It was, therefore, hypothesized that the suppression of nocifensive movements during anesthesia is due to an enhancement of GABAA receptor-mediated transmission. Therefore, the aim of this study was to determine behaviorally whether intrathecal GABA, glycine, or opioid receptor antagonists may change the anesthetic effect of isoflurane and enflurane.
Methods
The minimal alveolar concentration (MAC) of isoflurane and enflurane was determined in Sprague-Dawley rats, by the tail-clamp technique. First, MAC was determined and then concentration of each inhalation agent was increased by 0.2% from the sub-MAC level. Moving latencies were observed after the intrathecal administration of each receptor antagonist. Rectal temperature was measured and maintained at a steady level during the experiment.
Results
The spinal antinociceptive effects of isoflurane and enflurane were significantly reversed by the GABAA receptor antagonist bicuculline and picrotoxin (P < 0.05). The rectal temperature was well maintained within the range of 37-39 degrees C.
Conclusions
Our results suggest that the general anesthesia induced by isoflurane and enflurane, which are similar in terms of their action mechanism, is likely to be related to the spinal GABAA receptor system.
Key Words: Antagonism; enflurane; GABAA receptor; isoflurane; MAC; spinal cord


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