Evidence map›Paper›PMID 32243770›Full record

ReviewAmerican journal of physiology. Heart and circulatory physiology2020

Crossing signals: bioactive lipids in the microvasculature.

Dawid S Chabowski, Katie E Cohen, Ossama Abu-Hatoum, David D Gutterman, Julie K Freed

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Heart and circulatory physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Structural basis of prostaglandin efflux by MRP4.Nature structural & molecular biology · 2024
    Article
  6. Role of ceramides in diabetic foot ulcers (Review).International journal of molecular medicine · 2023
    Review
  7. Article
  8. Article
  9. Review
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 2 institutions in 2 countries.

Dawid S ChabowskiDivision of Cardiology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Katie E CohenDivision of Cardiology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Ossama Abu-HatoumDepartment of Surgery, HaEmek Medical Center, Technion Medical School, Haifa, Israel.
David D GuttermanDivision of Cardiology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0003-2814-7867
Julie K FreedCardiovascular Center, Medical College of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0002-9367-2281
Medical College of Wisconsin · USEmek Medical Center · IL

Funding

Novel Regulatory Mechanisms in the Human MicrocirculationR01HL135901 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI GUTTERMAN, DAVID D. · 2017 to 2020
$1.7M
NOVEL ROLE OF SPHINGOLIPIDS IN MAINTAINING VASCULAR HOMEOSTASISK08HL141562 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI FREED, JULIE K · 2019 to 2023
$851k
NHLBI NIH HHS K08 HL141562NHLBI NIH HHS R01 HL135901
6 · The paper itself

Abstract

The primary function of the arterial microvasculature is to ensure that regional perfusion of blood flow is matched to the needs of the tissue bed. This critical physiological mechanism is tightly controlled and regulated by a variety of vasoactive compounds that are generated and released from the vascular endothelium. Although these substances are required for modulating vascular tone, they also influence the surrounding tissue and have an overall effect on vascular, as well as parenchymal, homeostasis. Bioactive lipids, fatty acid derivatives that exert their effects through signaling pathways, are included in the list of vasoactive compounds that modulate the microvasculature. Although lipids were identified as important vascular messengers over three decades ago, their specific role within the microvascular system is not well defined. Thorough understanding of these pathways and their regulation is not only essential to gain insight into their role in cardiovascular disease but is also important for preventing vascular dysfunction following cancer treatment, a rapidly growing problem in medical oncology. The purpose of this review is to discuss how biologically active lipids, specifically prostanoids, epoxyeicosatrienoic acids, sphingolipids, and lysophospholipids, contribute to vascular function and signaling within the endothelium. Methods for quantifying lipids will be briefly discussed, followed by an overview of the various lipid families. The cross talk in signaling between classes of lipids will be discussed in the context of vascular disease. Finally, the potential clinical implications of these lipid families will be highlighted.

Indexed as

AnimalsEnzyme AssaysFatty AcidsFluorometryHumansMass SpectrometryMicrovesselsPhospholipidsSignal TransductionSphingolipidsFatty AcidsPhospholipidsSphingolipidsepoxyeicosatrienoic acidslysophospholipidsmicrovasculatureprostanoidssphingolipids

Identifiers

PMID32243770
PMCPMC7541955
OpenAlexW3014561006

What Socratic holds

Textmetadata
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 Socratic graph.