Article Text
Abstract
Background and Objectives The propyl group of ropivacaine (N-propyl-2′,6′-pipecoloxylidide hydrochloride) could be responsible for conferring some sensory selectivity to this drug. Thus, adding a propyl group to experimental local anesthetics (LAs) (e.g., the tricyclic antidepressants amitriptyline and doxepin) to increase sensory selectivity may be useful. We, therefore, synthesized N-propyl amitriptyline and N-propyl doxepin and investigated a potential predominance of sensory/nociceptive block over motor block (differential block) in a rat sciatic nerve block model. In addition, tetrodotoxin (TTX), a naturally occuring Na+ channel blocker, was coinjected to investigate whether it increased block duration.
Methods A 0.2-mL test dose of N-propyl amitriptyline and N-propyl doxepin, at a concentration of 1, 2.5, 5, and 10 mM, (alone or in combination with TTX at a concentration of 20 μM) was injected by the subfascial sciatic nerve approach. Motor function and sensory function (nociception) were evaluated by the force a rat's hind limb produced when pushing against a balance and the reaction to pinch, respectively.
Results N-propyl amitriptyline and N-propyl doxepin demonstrated prolonged block duration, with N-propyl amitriptyline displaying significant differential block at higher concentrations (5 and 10 mM). The combination of either of these drugs with TTX increased the potency as well as the efficacy. Neurotoxicity commenced at concentrations of 5 to 10 mM.
Conclusions Detailed histopathologic nerve toxicity evaluations are justified to determine whether N-propyl amitriptyline has potential as a more sensory-selective local anesthetic at lower concentrations or as a predominantly sensory-selective neurolytic agent at higher concentrations.
- Amitriptyline
- Doxepin
- Rats
- Ropivacaine
- Subfascial
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Footnotes
This study was supported by National Institutes of Health (research grants: no. GM48090 to GKW, no. GM64051 to PG, and no. NS18715 to RRM), Bethesda, MD.