Evidence map›Paper›PMID 32521775›Full record

ReviewBiomedicines2020

Free Fatty Acid Receptors 2 and 3 as Microbial Metabolite Sensors to Shape Host Health: Pharmacophysiological View.

Sidharth P Mishra, Prashantha Karunakar, Subhash Taraphder, Hariom Yadav

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 1 pooled it
4.3field-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

74 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

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14 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 3 institutions in 2 countries.

Sidharth P MishraDepartment of Internal Medicine, Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA.ORCID 0000-0001-7586-846X
Prashantha KarunakarDepartment of Biotechnology, PES University, Bangalore, Karnataka 560085, India.ORCID 0000-0002-5304-5363
Subhash TaraphderDepartment of Animal Genetics and Breeding, West Bengal University of Animal and Fishery Science, Kolkata, West-Bengal 700037, India.
Hariom YadavDepartment of Internal Medicine, Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA.ORCID 0000-0003-4504-1597
Wake Forest University · USPES University · INWest Bengal University of Animal and Fishery Sciences · IN

Funding

Congressionally Directed Medical Research Programs W81XWH-18-1-0118, W81XWH-19-1-0236National Institutes of Health R01AG01891, P30AG21332, UL1TR001420
6 · The paper itself

Abstract

The role of the gut microbiome in human health is becoming apparent. The major functional impact of the gut microbiome is transmitted through the microbial metabolites that are produced in the gut and interact with host cells either in the local gut environment or are absorbed into circulation to impact distant cells/organs. Short-chain fatty acids (SCFAs) are the major microbial metabolites that are produced in the gut through the fermentation of non-digestible fibers. SCFAs are known to function through various mechanisms, however, their signaling through free fatty acid receptors 2 and 3 (FFAR2/3; type of G-coupled protein receptors) is a new therapeutic approach. FFAR2/3 are widely expressed in diverse cell types in human and mice, and function as sensors of SCFAs to change several physiological and cellular functions. FFAR2/3 modulate neurological signaling, energy metabolism, intestinal cellular homeostasis, immune response, and hormone synthesis. FFAR2/3 function through Gi and/or Gq signaling, that is mediated through specific structural features of SCFAs-FFAR2/3 bindings and modulating specific signaling pathway. In this review, we discuss the wide-spread expression and structural homologies between human and mice FFAR2/3, and their role in different human health conditions. This information can unlock opportunities to weigh the potential of FFAR2/3 as a drug target to prevent human diseases.

Indexed as

FFAR2FFAR3gutimmunemicrobiotaSCFA

Identifiers

PMID32521775
PMCPMC7344995
OpenAlexW3033113803

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.