Evidence map›Paper›PMID 33572986›Full record

ArticleInternational journal of molecular sciences2021

Delayed Administration of Angiotensin Receptor (AT2R) Agonist C21 Improves Survival and Preserves Sensorimotor Outcomes in Female Diabetic Rats Post-Stroke through Modulation of Microglial Activation.

LaDonya Jackson-Cowan, Wael Eldahshan, Selin Dumanli, Guangkuo Dong, Sarah Jamil, Yasir Abdul, Waleed Althomali, Babak Baban, Susan C Fagan, Adviye Ergul

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Microglia at the blood brain barrier in health and disease.Frontiers in cellular neuroscience · 2024
    Review
  4. The Angiotensin ATPharmacological reviews · 2022
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. 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

10 authors at 3 institutions in 1 country.

LaDonya Jackson-CowanDepartment of Medicine, Augusta University/University of Georgia Medical Partnership, Athens, GA 30602, USA.
Wael EldahshanProgram in Clinical and Experimental Therapeutics, University of Georgia College of Pharmacy, Augusta, GA 30912, USA.
Selin DumanliDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
Guangkuo DongDepartment Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.
Sarah JamilDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
Yasir AbdulDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
Waleed AlthomaliProgram in Clinical and Experimental Therapeutics, University of Georgia College of Pharmacy, Augusta, GA 30912, USA.
Babak BabanDepartment of Oral Biology, Dental College of Georgia, Augusta, GA 30912, USA.ORCID 0000-0002-3144-2288
Susan C FaganProgram in Clinical and Experimental Therapeutics, University of Georgia College of Pharmacy, Augusta, GA 30912, USA.
Adviye ErgulCharlie Norwood Veterans Affairs Medical Center, Augusta, GA 30912, USA.ORCID 0000-0003-0873-6015
Georgia College & State University · USMedical University of South Carolina · USAugusta University · US

Funding

Treating Depression and Enhancing Locomotor Recovery Post-strokeP20GM109040 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KAUTZ, STEVEN A. · 2014 to 2024
$23.5M
Vascular Injury and Recovery in Diabetic Ischemic StrokeRF1NS083559 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ERGUL, ADVIYE · 2020 to 2022
$2.4M
Progressive Post Stroke Cognitive Impairment:Mechanisms & InterventionR01NS104573 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ERGUL, ADVIYE, SHENOY, SOMANATH P RAMMOHAN · 2018 to 2022
$2.3M
Vascular Injury and Recovery in Diabetic Ischemic StrokeR01NS083559 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ERGUL, ADVIYE · 2014 to 2018
$1.9M
Cerebral Arteriole Structure/Function in Diabetic Ischemic Brain InjuryI01BX000347 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI ERGUL, ADVIYE · 2009 to 2025
–
BLR&D Research Career Scientist Award ApplicationIK6BX004471 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI ERGUL, ADVIYE · 2019 to 2025
–
BLRD VA I01 BX000347BLRD VA IK6 BX004471NIGMS NIH HHS P20 GM109040NIH HHS RFI NS083559NINDS NIH HHS R01 NS083559NINDS NIH HHS R01 NS104573NINDS NIH HHS RF1 NS083559TL1 TR002382TL1 UL1TR002378Veterans Affairs (VA) Merit Review BX000347
6 · The paper itself

Abstract

About 70% of stroke victims present with comorbid diseases such as diabetes and hypertension. The integration of comorbidities in pre-clinical experimental design is important in understanding the mechanisms involved in the development of stroke injury and recovery. We recently showed that administration of compound C21, an angiotensin II type 2 receptor agonist, at day 3 post-stroke improved sensorimotor outcomes by lowering neuroinflammation in diabetic male animals. In the current study, we hypothesized that a delayed administration of C21 would also lower chronic inflammation post-stroke in diabetic female animals. Young female diabetic rats were subjected to 1 h of middle cerebral artery occlusion (MCAO). Three days post-stroke, rats were administered C21 or vehicle in drinking water at a dose of 0.12 mg/kg/day for 4 weeks. The impact of C21 on microglial polarization was analyzed by flow cytometry in vivo and in vitro. Compound 21 treatment improved fine motor skills after MCAO through modulation of the microglia/macrophage inflammatory properties. In addition, C21 increased M2 polarization and reduced the M1:M2 ratio in vitro. In conclusion, delayed administration of C21 downregulates post-stroke inflammation in female diabetic animals. C21 may be a useful therapeutic option to lower neuro-inflammation and improve the post-stroke recovery in diabetes.

Indexed as

AnimalsAnti-Inflammatory AgentsCell LineCognitionDiabetes Mellitus, ExperimentalFemaleInfarction, Middle Cerebral ArteryMiceMicrogliaNeuroprotective AgentsRatsRats, WistarReceptor, Angiotensin, Type 2StrokeAnti-Inflammatory AgentsNeuroprotective AgentsReceptor, Angiotensin, Type 2AT2 receptordiabetesischemic strokemicroglial polarizationneuro-inflammation

Identifiers

PMID33572986
PMCPMC7866408
OpenAlexW3126683517

What OpenQuestion holds

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LicenceCC BY
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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.