Systemic, but not intrathecal, ketamine produces preemptive analgesia in the rat formalin model

Acta Anaesthesiol Sin. 2001 Sep;39(3):123-7.

Abstract

Background: We investigated the antinociceptive effects of pre- or posttreatment of intrathecal or intravenous ketamine on formalin-induced pain behaviors.

Methods: Rats were divided into 4 groups of 7 rats each and 2 control groups (saline). Rats received ketamine 1 mg/kg intrathecally (i.t.) through a catheter either 15 min before or 5 min after formalin. In the other groups, they received ketamine 1 mg/kg intravenously (i.v.) through a catheter either 1 min before or 5 min after the formalin. Pain related behavior was quantified by counting the incidence of flinching of the injected paw for 60 min. Formalin induced a biphasic fliching (phase 1, 0-5 min; phase 2, 10-60 min after formalin injection) of injected paw. The inter-group (control, pre, and posttreatment groups) comparisons were performed separately for route of administration (i.t. or i.v.) and phase 1 and 2 using one-way ANOVA and Tukey test.

Results: Flinches of phase 1 were not different among the three i.t. groups. The total flinches of phase 2 were reduced by posttreatment with i.t. ketamine (P < 0.05); In contrast, i.v. ketamine was effective only when given as a pretreatment. Flinches of phase 1 and 2 were reduced by pretreatment with i.v. ketamine (P < 0.05).

Conclusions: Intrathecal ketamine was an analgesic even when administered as a posttreatment, whereas intravenous ketamine produced effective preemption only when given as a pretreatment.

MeSH terms

  • Analgesia*
  • Analgesics / administration & dosage*
  • Animals
  • Formaldehyde
  • Hyperalgesia / drug therapy
  • Injections, Intravenous
  • Injections, Spinal
  • Ketamine / administration & dosage*
  • Male
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Analgesics
  • Formaldehyde
  • Ketamine