Cue properties of oral and transdermal nicotine in the rat

Psychopharmacology (Berl). 1988;96(3):281-4. doi: 10.1007/BF00216050.

Abstract

In a standard two-lever drug discrimination paradigm, rats were trained to discriminate nicotine 0.5 mg/kg PO from saline. Injections occurred 15 min before the session. Subjects reached the training criterion in a mean of 38 sessions. Nicotine PO, SC, and IP generated similar dose-effect curves (ED50 = 0.073 mg/kg PO, 0.076 mg/kg SC, 0.090 mg/kg IP); the dose-effect curve for transdermal (TD) administration fell approximately 1 log unit to the right (ED50 = 1.34 mg/kg). The percentage of rats choosing the nicotine-appropriate lever peaked at 15 min and gradually decreased to 50% or less by 180 min for nicotine PO and TD, a time-decay function similar to that previously shown for SC administration. The nicotinic cholinergic agonist cytisine (0.5-8.0 mg/kg) PO and TD produced up to 56% nicotine-appropriate responding, while the muscarinic cholinergic agonist arecoline (1.0-4.0 mg/kg) PO and TD produced only saline-appropriate responding. The nicotine cue did not generalize to the cholinergic antagonist mecamylamine (0.125-0.5 mg/kg) PO or TD; mecamylamine 0.5 mg/kg PO but not TD completely blocked the PO and TD nicotine cues. These results show that an approximately equal cue occurs with PO, IP, and SC administration, and that the TD cue is considerably weaker. The significance of the procedure as an animal analog of human transdermal nicotine intake is discussed.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Cutaneous
  • Administration, Oral
  • Alkaloids / pharmacology
  • Animals
  • Azocines
  • Conditioning, Operant / drug effects
  • Cues*
  • Dose-Response Relationship, Drug
  • Female
  • Mecamylamine / pharmacology
  • Nicotine / administration & dosage
  • Nicotine / antagonists & inhibitors
  • Nicotine / pharmacology*
  • Ovariectomy
  • Quinolizines
  • Rats
  • Reinforcement Schedule
  • Time Factors

Substances

  • Alkaloids
  • Azocines
  • Quinolizines
  • cytisine
  • Mecamylamine
  • Nicotine