Evidence map›Paper›PMID 28915321›Full record

ReviewComprehensive Physiology2017

Regulation and Functions of the Renin-Angiotensin System in White and Brown Adipose Tissue.

Mandana Pahlavani, Nishan S Kalupahana, Latha Ramalingam, Naima Moustaid-Moussa

Open access · greenAbstract readReview
In one paragraph

Review in Comprehensive Physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

61 citing papers in PubMed, 2 syntheses or guidelines pooled it, 111 citations in OpenAlex.

  1. Pooled it
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  19. The Association of M235T Genetic Polymorphism inJournal of personalized medicine · 2024
    Article
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1 more citing papers are in PubMed but not listed here.

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 2 institutions in 2 countries.

Mandana PahlavaniDepartment of Nutritional Sciences and Obesity Research Cluster, Texas Tech University, Lubbock, Texas, USA.
Nishan S KalupahanaDepartment of Nutritional Sciences and Obesity Research Cluster, Texas Tech University, Lubbock, Texas, USA.
Latha RamalingamDepartment of Nutritional Sciences and Obesity Research Cluster, Texas Tech University, Lubbock, Texas, USA.
Naima Moustaid-MoussaDepartment of Nutritional Sciences and Obesity Research Cluster, Texas Tech University, Lubbock, Texas, USA.
Texas Tech University · USUniversity of Peradeniya · LK

Funding

Anti-obesity effects of omega 3 fatty acids in brown adipose tissueR15AT008879 · NCCIH · TEXAS TECH UNIVERSITY · PI MOUSTAID-MOUSSA, NAIMA · 2016 to 2018
$799k
NCCIH NIH HHS R15 AT008879
6 · The paper itself

Abstract

The renin angiotensin system (RAS) is a major regulator of blood pressure, fluid, and electrolyte homeostasis. RAS precursor angiotensinogen (Agt) is cleaved into angiotensin I (Ang I) and II (Ang II) by renin and angiotensin converting enzyme (ACE), respectively. Major effects of Ang II, the main bioactive peptide of this system, is mediated by G protein coupled receptors, Angiotensin Type 1 (AGTR1, AT1R) and Type 2 (AGTR2, AT2R) receptors. Further, the discovery of additional RAS peptides such as Ang 1-7 generated by the action of another enzyme ACE2 identified novel functions of this complex system. In addition to the systemic RAS, several local RAS exist in organs such as the brain, kidney, pancreas, and adipose tissue. The expression and regulation of various components of RAS in adipose tissue prompted extensive research into the role of adipose RAS in metabolic diseases. Indeed, animal studies have shown that adipose-derived Agt contributes to circulating RAS, kidney, and blood pressure regulation. Further, mice overexpressing Agt have high blood pressure and increased adiposity characterized by inflammation, adipocyte hypertrophy, and insulin resistance, which can be reversed at least in part by RAS inhibition. These findings highlight the importance of this system in energy homeostasis, especially in the context of obesity. This overview article discusses the depot-specific functions of adipose RAS, genetic and pharmacological manipulations of RAS, and its applications to adipogenesis, thermogenesis, and overall energy homeostasis. © 2017 American Physiological Society. Compr Physiol 7:1137-1150, 2017.

Indexed as

Adipose Tissue, BrownAdipose Tissue, WhiteAnimalsBlood PressureEnergy MetabolismHomeostasisHumansRenin-Angiotensin System

Identifiers

PMID28915321
PMCPMC7561006
OpenAlexW2785958313

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.