Evidence map›Paper›PMID 38389818›Full record

ArticleAdvances in drug and alcohol research2023

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

Sebastian Ortegon, Priscilla Giner, Bryan Cruz, Luis M Carcoba, Benjamin Clapp, Deborah J Clegg, Laura E O'Dell

Abstract read
In one paragraph

Article in Advances in drug and alcohol research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Sebastian OrtegonDepartment of Psychology, The University of Texas at El Paso, El Paso, TX, United States.
Priscilla GinerDepartment of Psychology, The University of Texas at El Paso, El Paso, TX, United States.
Bryan CruzDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, United States.
Luis M CarcobaDepartment of Psychology, The University of Texas at El Paso, El Paso, TX, United States.
Benjamin ClappTexas Tech University Health Science Center-El Paso, Paul Foster School of Medicine, El Paso, TX, United States.
Deborah J CleggTexas Tech University Health Science Center-El Paso, Paul Foster School of Medicine, El Paso, TX, United States.
Laura E O'DellDepartment of Psychology, The University of Texas at El Paso, El Paso, TX, United States.

Funding

Summer Mentoring And Research Training: Methods In Neuroscience of Drug-abuse (SMART-MIND)R25DA033613 · NIDA · UNIVERSITY OF TEXAS EL PASO · PI Karina C Canaba, LAURA ELENA ODELL · 2012 to 2026
$1.5M
Preventative Biomarkers and Potential Pharmacotherapies for Nicotine Use and DiabetesR16GM145551 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI ODELL, LAURA ELENA · 2022 to 2025
$614k
NIDA NIH HHS R25 DA033613NIGMS NIH HHS R16 GM145551
6 · The paper itself

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.

Indexed as

high fat dietinsulininsulin resistancesex differencestobacco

Identifiers

PMID38389818
PMCPMC10880793

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.