The emergence of insulin resistance following a chronic high-fat diet regimen coincides with an increase in the reinforcing effects of nicotine in a sex-dependent manner

Neuropharmacology. 2021 Dec 1:200:108787. doi: 10.1016/j.neuropharm.2021.108787. Epub 2021 Sep 24.

Abstract

The present study assessed the sex-dependent effects of insulin resistance on the reinforcing effects of nicotine. Female and male rats received a chronic high-fat diet (HFD) or regular diet (RD) for 8 weeks. A subset of rats then received vehicle or a dose of streptozotocin (STZ; 25 mg/kg) that induces insulin resistance. To assess insulin resistance, glucose levels were measured 15, 30, 60, 120, and 180 min after an insulin injection (0.75 U/kg). Nine days later, the rats were given extended access to intravenous self-administration (IVSA) of nicotine (0.015, 0.03, 0.06 mg/kg) in an operant box where they consumed their respective diet ad libitum and performed responses for water deliveries. Each nicotine dose was delivered for 4 days with 3 intermittent days of abstinence in their home cage. The day after the last IVSA session, physical signs were compared following administration of mecamylamine (3.0 mg/kg) to precipitate nicotine withdrawal. The results revealed that there were no changes in insulin resistance or nicotine intake in HFD alone rats regardless of sex. Insulin resistance was observed in HFD-fed rats that received STZ, and the magnitude of this effect was greater in males versus females. Our major finding was that nicotine intake was greater among HFD + STZ female rats as compared to males. Lastly, the physical signs of withdrawal were similar across all groups. Our results suggest that females diagnosed with disorders that disrupt insulin signaling, such as diabetes may be at risk of greater vulnerability to nicotine use due to enhanced reinforcing effects of this drug.

Keywords: Diabetes; Insulin resistance; Nicotine; Sex differences; Tobacco use.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Blood Glucose
  • Diabetes Mellitus, Experimental / pathology*
  • Diet, High-Fat*
  • Dose-Response Relationship, Drug
  • Female
  • Insulin Resistance / physiology*
  • Male
  • Mecamylamine / pharmacology
  • Nicotine / pharmacology*
  • Rats
  • Rats, Wistar
  • Reinforcement, Psychology
  • Sex Factors
  • Streptozocin / pharmacology

Substances

  • Blood Glucose
  • Streptozocin
  • Mecamylamine
  • Nicotine