# Effectiveness of pharmacotherapies for diabetes on nicotine, food, and water intake in insulin-resistant rats

**Authors:** Sebastian Ortegon, Priscilla Giner, Bryan Cruz, Luis M. Carcoba, Benjamin Clapp, Deborah J. Clegg, Laura E. O’Dell

PMC · DOI: 10.3389/adar.2023.11812 · Advances in Drug and Alcohol Research · 2024-01-04

## TL;DR

This study found that insulin, but not other diabetes medications, reduced nicotine intake in insulin-resistant rats fed a high-fat diet.

## Contribution

The study demonstrates that insulin, but not dapagliflozin or bromocriptine, can normalize nicotine intake in insulin-resistant rats.

## Key findings

- HFD-fed rats consumed more nicotine than RD controls, regardless of sex.
- Insulin, but not dapagliflozin or bromocriptine, normalized nicotine intake in HFD-fed rats.
- The HFD plus STZ regimen successfully induced insulin resistance in both female and male rats.

## Abstract

The intersectionality between diabetes medications and nicotine consumption was assessed in female and male rats. Briefly, the rats were fed a high-fat diet (HFD) or regular diet (RD) for 4 weeks. Then separate groups received vehicle or a low dose of streptozotocin (STZ; 25 mg/kg). Three days later, insulin resistance was assessed by measuring plasma glucose levels for 180 min following an injection of insulin (0.75 U/kg). The rats were then prepared with jugular catheters, and they were given 23 h access to nicotine intravenous self-administration (IVSA) in 4 days cycles with 3 days of forced abstinence in their home cages where they consumed their respective diet. During the IVSA sessions, operant responses for food and water and changes in body weight were recorded. Prior to administration of the pharmacotherapies, the rats were given access to two doses of nicotine (0.015 then 0.03 mg/kg for the remainder of the study). Then, daily injections of the pharmacotherapies were given at the onset of dark cycle (6 p.m.) in the following order: 1) dapagliflozin (3.0 then 10.0 mg/kg), 2) insulin (0.75 U/kg twice), and 3) bromocriptine (3.0 then 10.0 mg/kg). The results suggest that our HFD+STZ regiment induced insulin resistance in female and male rats. Also, the HFD-fed rats displayed higher nicotine intake than RD controls, regardless of sex. Administration of insulin, but not dapagliflozin or bromocriptine, normalized nicotine intake in HFD-fed rats to control levels. These results have clinical implications regarding the potential efficacy of insulin to control excessive nicotine intake in persons with diabetes.

## Linked entities

- **Chemicals:** streptozotocin (PubChem CID 29327), dapagliflozin (PubChem CID 9887712), insulin (PubChem CID 70678557), bromocriptine (PubChem CID 31101), nicotine (PubChem CID 942)
- **Diseases:** diabetes (MONDO:0005015)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** insulin (MESH:D007333), diabetes (MESH:D003920)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10880793/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC10880793/full.md

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Source: https://tomesphere.com/paper/PMC10880793