Evidence map›Paper›PMID 33540122›Full record

ArticleVascular pharmacology2021

Interleukin-10 does not contribute to the anti-contractile nature of PVAT in health.

R K Kumar, L M Kaiser, C E Rockwell, S W Watts

Open access · greenAbstract read
In one paragraph

Article in Vascular pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

0 citing papers in PubMed, 6 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 1 institution in 1 country.

R K KumarDepartment of Pharmacology and Toxicology, Michigan State University, MI, USA. Electronic address: kalyanak@msu.edu.
L M KaiserDepartment of Pharmacology and Toxicology, Michigan State University, MI, USA.
C E RockwellDepartment of Pharmacology and Toxicology, Michigan State University, MI, USA.
S W WattsDepartment of Pharmacology and Toxicology, Michigan State University, MI, USA.
Michigan State University · US

Funding

SIGNALING MECHANISMS IN ARTERIES AND VEINS IN HYPERTENSIONP01HL070687 · NHLBI · MICHIGAN STATE UNIVERSITY · PI WATTS, STEPHANIE W · 2003 to 2019
$22.8M
The role of Nrf2 in immune cell polarization and allergyR01ES024966 · NIEHS · MICHIGAN STATE UNIVERSITY · PI ROCKWELL, CHERYL ELIZABETH · 2016 to 2020
$2.1M
NHLBI NIH HHS P01 HL070687NIEHS NIH HHS R01 ES024966
6 · The paper itself

Abstract

Perivascular adipose tissue (PVAT) is protective and reduces contraction of blood vessels in health. PVAT is composed of adipocytes, multiple types of immune cells and stromal cells. Interleukin (IL)-10, an anti-inflammatory cytokine usually produced by T cells, B cells and macrophages, was identified as one of the highly expressed (mRNA) cytokines in the mesenteric PVAT of healthy rats. One report suggested that exogenous IL-10 causes relaxation of mouse mesenteric arteries, also suggesting that IL-10 maybe a potential anti-contractile factor. Hence, we hypothesized that PVAT-derived IL-10 causes vasorelaxation and/or reduces vasoconstriction, thus contributing to the anti-contractile nature of PVAT in health. Mesenteric arteries from rats and mice expressed the receptor for IL-10 (in tunica intima and media) as determined by immunohistochemistry. Mesenteric resistance arteries for rats and superior mesenteric artery for mice were used for isometric contractility studies. Increasing concentrations [0.4-100 ng/mL] of recombinant rat/mouse (rr/mr) IL-10 or vehicle was directly added to half-maximally constricted (phenylephrine, PE) vessels (without PVAT, with endothelium). IL-10 did not cause a direct vasorelaxation. Further, the ability of rrIL-10 to cause a rightward or downward shift of a vasoconstriction-response curve was tested in the rat. The vessels were incubated with rrIL-10 [100 ng/mL or 10 ng/mL] or vehicle for 1.5 h in the tissue bath followed by a cumulative PE [10

Indexed as

VasoconstrictionVasodilationAdipose TissueAnimalsCells, CulturedFemaleInterleukin-10MaleMesenteric ArteriesMiceMice, Inbred C57BLMice, KnockoutParacrine CommunicationRatsRats, Sprague-DawleyReceptors, Interleukin-10IL10 protein, mouseInterleukin-10Receptors, Interleukin-10Anti-contractileIL-10Perivascular adipose tissueVascular toneVasorelaxation

Identifiers

PMID33540122
PMCPMC8174099
OpenAlexW3126162706

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.