Journal
PAIN
Volume 103, Issue 1-2, Pages 49-55Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1016/S0304-3959(02)00375-5
Keywords
tricyclic antidepressants; local anesthetics; sciatic nerve block; voltage-gated sodium channel; neuropathic pain
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Funding
- NIGMS NIH HHS [GM48090, GM35401] Funding Source: Medline
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dAmitriptyline, nortriptyline, imipramine, doxepin, desipramine, protriptyline, trimipramine, and maprotiline are tricyclic antidepressants (TCAs) used orally in treating major depressive disorders. Recent studies showed that amitriptyline is more potent in blocking the sciatic nerve functions in vivo by local injection than bupivacaine, a long-acting local anesthetic. We therefore tested whether various TCAs could likewise act as local anesthetics in vivo after single injection via the rat sciatic notch. The duration of complete sciatic nerve blockade by TCAs and the time to reach full recovery were measured with neurobehavioral assays and compared with results from bupivacaine. Amitriptyline, doxepin, and imipramine at 5 mM elicited a longer complete sciatic nerve blockade than did bupivacaine at 15.4 mM (0.5%), whereas trimipramine and desipramine at 5 mM produced a shorter blockade. In contrast, nortriptyline, protriptyline, and maprotiline failed to elicit complete sciatic nerve blockade. Thus, TCAs have very different efficacy as local anesthetics in vivo. The duration of rat sciatic nerve blockade in vivo by TCAs is not well correlated with the 50% inhibitory concentration (IC50) of TCAs in blocking human cardiac Nav 1.5 Na+ channels expressed in human embryonic kidney cells. With this in vitro expression system, TCAs appear more potent than bupivacaine as Na+ channel blockers in Nav 1.5 Na+ channels. We suggest that the ability of TCAs to pass through various membrane barriers within peripheral nerve trunks is crucial to their local anesthetic efficacy in vivo. TCAs with a tertiary amine appear more effective in penetrating these membrane barriers than TCAs with a secondary amine. (C) 2002 International Association for the Study of Pain. Published by Elsevier Science B.V. All rights reserved.
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