Dexmedetomidine Prolongs Lidocaine Intravenous Regional Anesthesia in Rats by Blocking the Hyperpolarization-Activated Cation Current

Purpose: Intravenous regional anesthesia (IVRA) using lidocaine provides effective localized analgesia but its duration is limited.The mechanism by which dexmedetomidine enhances lidocaine IVRA is unclear but may involve modulation of hyperpolarizationactivated cyclic nucleotide-gated (HCN) channels.Materials and Methods: Lidocaine IVRA with varying dexmedetomidine concentrations was performed in the tails of Sprague-Dawley rats.Tail-flick and tail-clamping tests assessed IVRA analgesia and anesthesia efficacy and duration.Contributions of α 2 adrenergic receptors and HCN channels were evaluated by incorporating an α adrenergic receptor antagonist, the HCN channel inhibitor ZD7288, and the HCN channel agonist forskolin.Furthermore, whole-cell patch clamp electrophysiology quantified the effects of dexmedetomidine on HCN channels mediating hyperpolarization-activated cation current (I h ) in isolated dorsal root ganglion neurons.Results: Dexmedetomidine dose-dependently extended lidocaine IVRA duration and analgesia, unaffected by α 2 receptor blockade.The HCN channel inhibitor ZD7288 also prolonged lidocaine IVRA effects, while the HCN channel activator forskolin shortened effects.In dorsal root ganglion neurons, dexmedetomidine concentration-dependently inhibited I h amplitude and shifted the voltagedependence of HCN channel activation.Conclusion: Dexmedetomidine prolongs lidocaine IVRA duration by directly inhibiting HCN channel activity, independent of α 2 adrenergic receptor activation.This HCN channel inhibition represents a novel mechanism underlying the anesthetic and analgesic adjuvant effects of dexmedetomidine in IVRA.