TY - JOUR
T1 - Comparative Analysis of Intrathecal Lidocaine Combined With Guanfacine or Dexmedetomidine on Nociceptive and Motor Blockade in Rats
AU - Chou, An Kuo
AU - Chiu, Chong Chi
AU - Chen, Yu Wen
AU - Hung, Ching Hsia
AU - Wang, Jhi Joung
N1 - Publisher Copyright:
© 2025 Société Française de Pharmacologie et de Thérapeutique. Published by John Wiley & Sons Ltd.
PY - 2025/12
Y1 - 2025/12
N2 - The aim of this study was to examine the effects of intrathecal lidocaine combined with guanfacine or dexmedetomidine on nociceptive and motor blockade, in comparison to clonidine. Using a rat model of intrathecal injection, we evaluated the effects of lidocaine combined with guanfacine, dexmedetomidine, or clonidine on nociceptive and motor blockade. The dose-dependent effects of guanfacine on spinal nociceptive and motor blockade were compared to those of lidocaine, a well-known local anesthetic. Guanfacine (0.46 μmol/kg, 3 mM), dexmedetomidine (0.02 μmol/kg, 0.1 mM), or clonidine (1.52 μmol/kg, 10 mM) alone produced no spinal nociceptive or motor blockade. Co-administration of guanfacine (0.46 μmol/kg) or dexmedetomidine (0.02 μmol/kg) with lidocaine (3.14 or 8.38 μmol/kg) prolonged the duration of spinal blockade, an effect attenuated by yohimbine (0.76 μmol/kg), which alone produced no spinal nociceptive or motor blockade. In contrast, the addition of clonidine (1.52 μmol/kg) did not enhance the duration of lidocaine-induced spinal blockade. Guanfacine produced a dose-dependent spinal blockade of both nociceptive and motor functions. The potency ranking (ED50, 50% effective dose) of spinal blockade showed that guanfacine and lidocaine were equal. Guanfacine resulted in a markedly longer spinal block duration than lidocaine at equivalent anesthetic doses (ED25, ED50, and ED75). In summary, co-administration of subeffective doses of guanfacine or dexmedetomidine with lidocaine prolonged the duration of spinal blockade, likely involving α2-adrenergic receptors, whereas subeffective doses of clonidine did not. Guanfacine produced dose-dependent spinal blockade and was equipotent to lidocaine. At equianesthetic doses, guanfacine produced a longer duration of blockade than lidocaine.
AB - The aim of this study was to examine the effects of intrathecal lidocaine combined with guanfacine or dexmedetomidine on nociceptive and motor blockade, in comparison to clonidine. Using a rat model of intrathecal injection, we evaluated the effects of lidocaine combined with guanfacine, dexmedetomidine, or clonidine on nociceptive and motor blockade. The dose-dependent effects of guanfacine on spinal nociceptive and motor blockade were compared to those of lidocaine, a well-known local anesthetic. Guanfacine (0.46 μmol/kg, 3 mM), dexmedetomidine (0.02 μmol/kg, 0.1 mM), or clonidine (1.52 μmol/kg, 10 mM) alone produced no spinal nociceptive or motor blockade. Co-administration of guanfacine (0.46 μmol/kg) or dexmedetomidine (0.02 μmol/kg) with lidocaine (3.14 or 8.38 μmol/kg) prolonged the duration of spinal blockade, an effect attenuated by yohimbine (0.76 μmol/kg), which alone produced no spinal nociceptive or motor blockade. In contrast, the addition of clonidine (1.52 μmol/kg) did not enhance the duration of lidocaine-induced spinal blockade. Guanfacine produced a dose-dependent spinal blockade of both nociceptive and motor functions. The potency ranking (ED50, 50% effective dose) of spinal blockade showed that guanfacine and lidocaine were equal. Guanfacine resulted in a markedly longer spinal block duration than lidocaine at equivalent anesthetic doses (ED25, ED50, and ED75). In summary, co-administration of subeffective doses of guanfacine or dexmedetomidine with lidocaine prolonged the duration of spinal blockade, likely involving α2-adrenergic receptors, whereas subeffective doses of clonidine did not. Guanfacine produced dose-dependent spinal blockade and was equipotent to lidocaine. At equianesthetic doses, guanfacine produced a longer duration of blockade than lidocaine.
UR - https://www.scopus.com/pages/publications/105022522072
UR - https://www.scopus.com/pages/publications/105022522072#tab=citedBy
U2 - 10.1111/fcp.70057
DO - 10.1111/fcp.70057
M3 - Article
C2 - 41267192
AN - SCOPUS:105022522072
SN - 0767-3981
VL - 39
JO - Fundamental and Clinical Pharmacology
JF - Fundamental and Clinical Pharmacology
IS - 6
M1 - e70057
ER -