Evidence map›Paper›PMID 27584552›Full record

ReviewCurrent protocols in mouse biology2016

Peripheral Neuropathy in Mouse Models of Diabetes.

Corinne G Jolivalt, Katie E Frizzi, Lucie Guernsey, Alex Marquez, Joseline Ochoa, Maria Rodriguez, Nigel A Calcutt

Open access · greenAbstract readReview
In one paragraph

Review in Current protocols in mouse biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 3 pooled it
5.8field-weighted citation impact, top 4% of its field
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

70 citing papers in PubMed, 3 syntheses or guidelines pooled it, 123 citations in OpenAlex.

  1. Pooled it
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  7. iRhom2 deletion protects against diabetic neuropathy by suppressing neuroinflammation.The Journal of pharmacology and experimental therapeutics · 2026
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10 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Corinne G JolivaltDepartment of Pathology, University of California San Diego, La Jolla, California.
Katie E FrizziDepartment of Pathology, University of California San Diego, La Jolla, California.
Lucie GuernseyDepartment of Pathology, University of California San Diego, La Jolla, California.
Alex MarquezDepartment of Pathology, University of California San Diego, La Jolla, California.
Joseline OchoaDepartment of Pathology, University of California San Diego, La Jolla, California.
Maria RodriguezDepartment of Pathology, University of California San Diego, La Jolla, California.
Nigel A CalcuttDepartment of Pathology, University of California San Diego, La Jolla, California.
University of California, San Diego · US

Funding

Cholinergic constraint and diabetic neuropathyR01NS081082 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CALCUTT, NIGEL A. · 2013 to 2017
$1.6M
Comorbidity of Alzheimer's disease and Diabetes: pathologic mechanism and therapyR01AG039736 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JOLIVALT, CORINNE · 2011 to 2015
$1.6M
Muscarinic receptor antagonists as a therapy for diabetic neuropathyR21DK102032 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CALCUTT, NIGEL A. · 2014 to 2016
$428k
NIA NIH HHS R01 AG039736NIDDK NIH HHS R21 DK102032NINDS NIH HHS R01 NS081082
6 · The paper itself

Abstract

Peripheral neuropathy is a frequent complication of chronic diabetes that most commonly presents as a distal degenerative polyneuropathy with sensory loss. Around 20% to 30% of such patients may also experience neuropathic pain. The underlying pathogenic mechanisms are uncertain, and therapeutic options are limited. Rodent models of diabetes have been used for more than 40 years to study neuropathy and evaluate potential therapies. For much of this period, streptozotocin-diabetic rats were the model of choice. The emergence of new technologies that allow relatively cheap and routine manipulations of the mouse genome has prompted increased use of mouse models of diabetes to study neuropathy. In this article, we describe the commonly used mouse models of type 1 and type 2 diabetes, and provide protocols to phenotype the structural, functional, and behavioral indices of peripheral neuropathy, with a particular emphasis on assays pertinent to the human condition. © 2016 by John Wiley & Sons, Inc.

Indexed as

AnimalsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Diabetic NeuropathiesDisease Models, AnimalMiceallodyniacorneal confocal microscopyhyperalgesiahypoalgesianerve conduction velocitynerve morphometryperipheral neuropathyskin biopsytype 1 diabetestype 2 diabetes

Identifiers

PMID27584552
PMCPMC5023323
OpenAlexW2508596879

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.