Evidence map›Paper›PMID 40620576›Full record

ArticleJournal of pain research2025

Intravenous Streptozotocin Induces Variants in Painful Diabetic Peripheral Neuropathy in Female Mice.

Michelle A Hagenimana, Audrey R Green, Jessica A Tierney, Melissa E Lenert, Michael D Burton

Abstract read
In one paragraph

Article in Journal of pain research, 2025. 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

5 · Who and what money

Authors and funding

5 authors.

Michelle A Hagenimana *Laboratory of Neuroimmunology and Behavior, Department of Neuroscience, Center for Advanced Pain Studies (CAPS), School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.ORCID 0009-0003-1574-0618
Audrey R Green *Laboratory of Neuroimmunology and Behavior, Department of Neuroscience, Center for Advanced Pain Studies (CAPS), School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.ORCID 0000-0001-5219-4554
Jessica A TierneyLaboratory of Neuroimmunology and Behavior, Department of Neuroscience, Center for Advanced Pain Studies (CAPS), School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.ORCID 0000-0003-2615-5847
Melissa E LenertLaboratory of Neuroimmunology and Behavior, Department of Neuroscience, Center for Advanced Pain Studies (CAPS), School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.ORCID 0000-0002-5504-4700
Michael D BurtonLaboratory of Neuroimmunology and Behavior, Department of Neuroscience, Center for Advanced Pain Studies (CAPS), School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.ORCID 0000-0002-0628-824X

Funding

The role of cell-specific TLR4 in Diabetic Peripheral NeuropathyR21DK130015 · NIDDK · UNIVERSITY OF TEXAS DALLAS · PI BURTON, MICHAEL D · 2022 to 2024
$577k
Identification of Sex Differences in Monocytes and Metabolism in the Maintenance of Chronic Muscle PainF99NS129173 · NINDS · UNIVERSITY OF TEXAS DALLAS · PI LENERT, MELISSA ELIZABETH · 2022 to 2023
$89k
NIDDK NIH HHS R21 DK130015NINDS NIH HHS F99 NS129173
6 · The paper itself

Abstract

Purpose: At least half of the 34 million diabetic patients in the US develop painful diabetic peripheral neuropathy (DPN). Recent evidence suggests that there are sex differences in the prevalence and mechanisms underlying pathological pain states. However, due to technical limitations in murine models, there is a dearth of the use of females in diabetic neuropathy research. There is a need to develop a reproducible model to induce painful DPN in both sexes. The predominately used model employs streptozotocin (STZ) administration via intraperitoneal injections. This strategy consistently induces diabetic pathology in males, but not females. We set out to enhance a current murine DPN model by identifying a method for inducing diabetic pathologies in male and female mice and tracking the development of painful neuropathy. Methods: Painful DPN was induced in both male and female mice through five daily intravenous injections of STZ. Metrics of diabetic pathology and pain behaviors were assessed across the development of painful DPN. To investigate neuronal sensitivity, calcium imaging assessing dorsal root ganglia neurons was performed. Results: We found that after intravenous administration of STZ, both male and female mice exhibited elevated blood glucose levels, impaired glucose tolerance, and increased mechanical and thermal hypersensitivity. Interestingly, we observed a subset of STZ-insensitive animals that displayed comparable elevated glucose levels to the STZ-sensitive animals. Calcium imaging was performed to investigate neuronal sensitivity and we found that both male and female mice with diabetic pathology had a lower latency to peak capsaicin-induced response compared to their control counterparts. Conclusion: Our findings demonstrate that intravenous administration of STZ can induce comparable diabetic neuropathy in male and female mice and opens the door for future preclinical studies on diabetic neuropathy.

Indexed as

diabetic peripheral neuropathyfemalesglucose tolerance testhyperglycemiamalessex differencesSTZ

Identifiers

PMID40620576
PMCPMC12229165

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Registered trials

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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.