Tonic blocking action of meperidine on Na+ and K+channels in amphibian peripheral nerves

• Published in: Anesthesiology (Philadelphia) Vol. 92; no. 1; pp. 147 - 155
• Main Authors: BRÄU, M. E, KOCH, E. D, VOGEL, W, HEMPELMANN, G
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott 2000
• Subjects: Analgesics, Opioid - pharmacology; Anesthetics, Local - pharmacology; Anesthetics. Neuromuscular blocking agents; Animals; Binding Sites - drug effects; Biological and medical sciences; Dose-Response Relationship, Drug; Lidocaine - pharmacology; Medical sciences; Membrane Potentials - drug effects; Meperidine - pharmacology; Neuropharmacology; Patch-Clamp Techniques; Peripheral Nerves - drug effects; Pharmacology. Drug treatments; Potassium Channels - drug effects; Sodium Channels - drug effects; Xenopus laevis; Peripheral nerve; Pethidine; Xenopus laevis; Amphibia; Blocking; Opiates; Salientia; Ionic channel; Narcotic analgesic; In vitro; Local anesthetic; Vertebrata; Sodium; Animal; Mechanism of action; Potassium
• ISSN: 0003-3022; 1528-1175
• DOI: 10.1097/00000542-200001000-00026

Among opioids, meperidine (pethidine) also shows local anesthetic activity when applied locally to peripheral nerve fibers and has been used for this effect in the clinical setting for regional anesthesia. This study investigated the blocking effects of meperidine on different ion channels in peripheral nerves. Experiments were conducted using the outside-out configuration of the patch-clamp method applied to enzymatically prepared peripheral nerve fibers of Xenopus laevis. Half-maximal inhibiting concentrations were determined for Na+ channels and different K+ channels by nonlinear least-squares fitting of concentration-inhibition curves, assuming a one-to-one reaction. Externally applied meperidine reversibly blocked all investigated channels in a concentration-dependent manner, i.e., voltage-activated Na+ channel (half-maximal inhibiting concentration, 164 microM), delayed rectifier K+ channels (half-maximal inhibiting concentration, 194 microM), the calcium-activated K+ channel (half-maximal inhibiting concentration, 161 microM), and the voltage-independent flicker K+ channel (half-maximal inhibiting concentration, 139 microM). Maximal block in high concentrations of meperidine reached 83% for delayed rectifier K+ channels and 100% for all other channels. Meperidine blocks the Na+ channel in the same concentration range as the local anesthetic agent lidocaine (half-maximal inhibiting concentration, 172 microM) but did not compete for the same binding site as evaluated by competition experiments. Low concentrations of meperidine (1 nM to 1 microM) showed no effects on Na+ channels. The blockade of Na+ and delayed rectifier K+ channels could not be antagonized by the addition of naloxone. It is concluded that meperidine has a nonselective inhibitory action on Na+ and K+ channels of amphibian peripheral nerve. For tonic Na+ channel block, neither an opioid receptor nor the the local anesthetic agent binding site is the target site for meperidine block.