Evidence map›Paper›PMID 21945451›Full record

ArticlePhysiology & behavior2012

Depressive phenotypes evoked by experimental diabetes are reversed by insulin.

Nancy Ho, Darrick T Balu, Monica R F Hilario, Julie A Blendy, Irwin Lucki

Abstract read
In one paragraph

Article in Physiology & behavior, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.7field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 56 citations in OpenAlex.

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  9. Insulin modulates the strong reinforcing effects of nicotine and changes in insulin biomarkers in a rodent model of diabetes.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
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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

5 authors at 1 institution in 1 country.

Nancy HoSchool of Nursing, University of Pennsylvania, 418 Curie Boulevard, Philadelphia, PA 19104, USA.
Darrick T Balu
Monica R F Hilario
Julie A Blendy
Irwin Lucki
University of Pennsylvania · US

Funding

Regulation of Neurogenesis by Stress and AntidepressantsU01MH072832 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI LUCKI, IRWIN · 2005 to 2007
$1.7M
Regulation of Hippocampal Neurogenesis by AntidepressantsR01MH086599 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI LUCKI, IRWIN · 2010 to 2013
$1.6M
Role of Corticosterone on Hippocampal Cell Proliferation in Mice with DiabetesF31NR010853 · NINR · UNIVERSITY OF PENNSYLVANIA · PI HO, NANCY · 2008 to 2010
$102k
NIMH NIH HHS R01 MH086599NIMH NIH HHS R01 MH86599NIMH NIH HHS U01 MH072832NINR NIH HHS F31 NR010853
6 · The paper itself

Abstract

Clinical studies suggest a bidirectional relationship between diabetes and depression, where diabetes may increase risk for depressive symptoms and depression may increase risk for diabetes. Preclinical models examining the effects of diabetes on brain and behavior can provide insights to the pathophysiology underlying this relationship. The current study comprehensively examined, in C57BL/6 mice, the development of depressive phenotypes evoked by diabetes induced by streptozotocin (STZ) and determined if insulin treatment was able to reverse the diabetes-related changes on brain and affective behavior. Since anxiety is often comorbid with mood disturbances, behavioral tests for both anxiety and depression were administered. Possible physiological correlates of behavioral changes, including hippocampal cell proliferation, brain derived neurotrophic factor, and plasma corticosterone, were also measured. STZ-induced diabetes resulted in increased immobility in the tail suspension test, increased intracranial self-stimulation thresholds, decreased hippocampal cell proliferation, and increased corticosterone levels. Insulin treatment, on the other hand, reduced hyperglycemia, reversed the behavioral effects, and returned hippocampal cell proliferation and corticosterone to levels comparable to the control group. Anxiety-related behaviors were unaffected. This study showed that experimental diabetes in the mouse produced depressive phenotypes that were reversed by insulin therapy. Changes in reward-related behaviors and hippocampal cell proliferation may be useful markers to identify therapeutic interventions for comorbid diabetes and depression.

Indexed as

Analysis of VarianceAnimalsBlood GlucoseBrainBrain-Derived Neurotrophic FactorBromodeoxyuridineCell ProliferationCorticosteroneDepressionDiabetes Mellitus, ExperimentalDisease Models, AnimalElectric StimulationHindlimb SuspensionHippocampusHypoglycemic AgentsImmobility Response, TonicBlood GlucoseBrain-Derived Neurotrophic FactorBromodeoxyuridineCorticosteroneHypoglycemic AgentsInsulin

Identifiers

PMID21945451
PMCPMC3237925
OpenAlexW1989622995

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.