J Korean Pain Soc.
1999 Nov;12(2):177-182.
Effect of Adrenergic Receptors on the Nerve Conduction in Rat Sciatic Nerves
- Affiliations
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- 1Department of Anesthesiology, College of Medicine, University of Ulsan, Korea. ychoi@www.amc.seoul.kr
- 2Department of Physiology, Yonsei University College of Medicine, Korea.
- 3Department of Anesthesiology, College of Medicine, ChungBuk National University, Korea.
Abstract
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BACKGROUND: Clonidine, an a adrenergic agonist blocks nerve conduction. However, in our previous
experiment we found that adrenaline neither blocks nerve conduction by itself nor augment nerve
conduction blockade by lidocaine near clinical concentrations. Possible explanations are:
1) there may be antagonism between some of adrenergic receptors, 2) clonidine may block nerve
conduction via non-adrenergic mechanism. The purpose of this study is to obtain dose-response
curves of several different forms of adrenergic receptor agonist to see the relative potencies
of each adrenergic receptors to block nerve conduction.
METHODS
Recordings of compound action potentials of A-fiber components (A-CAPs) were obtained
from isolated sciatic nerves of adult male Sprague-Dawley rats. Nerve sheath of the sciatic
nerve was removed and desheathed nerve bundle was mounted on a recording chamber. Single pulse
stimuli (0.5 msec, supramaximal stimuli) were repeatedly applied (2Hz) to one end of the nerve
and recordings of A-CAPs were made on the other end of the nerve. Dose-response curves of
epinephrine, phenylephrine, isoproterenol, clonidine were obtained.
RESULTS
ED50 of each adrenergic agonist was: 4.51 x 10(-2)M for epinephrine; phenylephrine,
7,74 x 10(-2)M; isoproterenol, 9.61 x 10(-2)M; clonidine, 1.57 x 10(-3)M.
CONCLUSION
This study showed that only clonidine, a 2 adrenergic agonist, showed some nerve
blocking action while other adrenergic agonists showed similar poor degree of nerve blockade.
This data suggest that non-effectiveness of epinephrine in blocking nerve conduction is not from
the antagonism between adrenergic receptors.