Evidence map›Paper›PMID 33004912›Full record

ArticleScientific reports2020

Deficits in hippocampal neurogenesis in obesity-dependent and -independent type-2 diabetes mellitus mouse models.

Jacqueline A Bonds, Aashutosh Shetti, Terilyn K L Stephen, Marcelo G Bonini, Richard D Minshall, Orly Lazarov

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
4.9field-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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
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  9. Journal of diabetes and metabolic disorders · 2025
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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

6 authors at 2 institutions in 1 country.

Jacqueline A BondsDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, 578 CME (M/C 512), 808 South Wood Street, Chicago, IL, 60612, USA.
Aashutosh ShettiDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, 578 CME (M/C 512), 808 South Wood Street, Chicago, IL, 60612, USA.
Terilyn K L StephenDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, 578 CME (M/C 512), 808 South Wood Street, Chicago, IL, 60612, USA.
Marcelo G BoniniDivision of Hematology/Oncology, Department of Medicine, Feinberg School of Medicine and The Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine of Northwestern University, Chicago, IL, 60612, USA.
Richard D MinshallDepartment of Anesthesiology, University of Illinois at Chicago, Chicago, IL, 60612, USA.ORCID https://orcid.org/0000-0003-3164-475X
Orly LazarovDepartment of Anatomy and Cell Biology, University of Illinois at Chicago, 578 CME (M/C 512), 808 South Wood Street, Chicago, IL, 60612, USA. olazarov@uic.edu.ORCID http://orcid.org/0000-0002-5887-948X
University of Illinois Chicago · USNorthwestern University · US

Funding

The role of PS1 in regulation of adult neurogenesis in the intact and Alzheimer?sR01AG033570 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Orly Lazarov · 2009 to 2026
$5.6M
Plasticity circuits in Alzheimer s diseaseRF1AG033570 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LAZAROV, ORLY · 2020 to 2021
$2.9M
Mechanisms underlying sporadic Alzheimer's diseaseR01AG060238 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LAZAROV, ORLY · 2018 to 2022
$2.4M
Training program in the biology and translational research on Alzheimer's diseaseand related dementiasT32AG057468 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Stephanie M Cologna, Orly Lazarov · 2017 to 2026
$2.3M
Acceleration of AD Phenotypes in Asymptomatic Mouse ModelsR01AG062251 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LAZAROV, ORLY · 2018 to 2022
$2.2M
Macrophage Redox State in Sterilizing and Injurious InflammationR01AI131267 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BONINI, MARCELO G. · 2017 to 2021
$2.1M
Environmental Arsenic in the Subtype Specification of Breast CancerR01ES028149 · NIEHS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BONINI, MARCELO G. · 2018 to 2022
$1.8M
Signaling pathways regulating hippocampal neurogenesis in the adult mouseR21AG061628 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LAZAROV, ORLY · 2019 to 2020
$440k
Environmental Arsenic Exposures and Breast Cancer Subtype SpecificationR56ES028149 · NIEHS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BONINI, MARCELO G. · 2017 to 2017
$185k
NIAID NIH HHS R01 AI131267NIA NIH HHS AG033570NIA NIH HHS AG033570-S1NIA NIH HHS AG033570-S2NIA NIH HHS AG057468NIA NIH HHS AG060238NIA NIH HHS AG061628NIA NIH HHS AG062251NIA NIH HHS R01 AG033570NIA NIH HHS R01 AG060238NIA NIH HHS R01 AG062251NIA NIH HHS R21 AG061628NIA NIH HHS RF1 AG033570NIA NIH HHS T32 AG057468NIA NIH HHS T32AG057468NIEHS NIH HHS R01 ES028149NIEHS NIH HHS R56 ES028149NIH HHS AI131267NIH HHS ES028149
6 · The paper itself

Abstract

Hippocampal neurogenesis plays an important role in learning and memory function throughout life. Declines in this process have been observed in both aging and Alzheimer's disease (AD). Type 2 Diabetes mellitus (T2DM) is a disorder characterized by insulin resistance and impaired glucose metabolism. T2DM often results in cognitive decline in adults, and significantly increases the risk of AD development. The pathways underlying T2DM-induced cognitive deficits are not known. Some studies suggest that alterations in hippocampal neurogenesis may contribute to cognitive deterioration, however, the fate of neurogenesis in these studies is highly controversial. To address this problem, we utilized two models of T2DM: (1) obesity-independent MKR transgenic mice expressing a mutated form of the human insulin-like growth factor 1 receptor (IGF-1R) in skeletal muscle, and (2) Obesity-dependent db/db mice harboring a mutation in the leptin receptor. Our results show that both models of T2DM display compromised hippocampal neurogenesis. We show that the number of new neurons in the hippocampus of these mice is reduced. Clone formation capacity of neural progenitor cells isolated from the db/db mice is deficient. Expression of insulin receptor and epidermal growth factor receptor was reduced in hippocampal neurospheres isolated from db/db mice. Results from this study warrant further investigation into the mechanisms underlying decreased neurogenesis in T2DM and its link to the cognitive decline observed in this disorder.

Indexed as

AnimalsCell ProliferationCognitive DysfunctionDiabetes Mellitus, Type 2HippocampusMiceMice, TransgenicNeural Stem CellsNeurogenesisNeuronsObesityReceptor, IGF Type 1Receptors, LeptinIgf1r protein, mouseReceptor, IGF Type 1Receptors, Leptin

Identifiers

PMID33004912
PMCPMC7530538
OpenAlexW3091591777

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.