Evidence map›Paper›PMID 32973502›Full record

ArticleFrontiers in pharmacology2020

Resveratrol Modulates the Gut Microbiota and Inflammation to Protect Against Diabetic Nephropathy in Mice.

Ting-Ting Cai, Xiao-Long Ye, Ru-Run Li, Hui Chen, Ya-Yun Wang, Hui-Juan Yong, Ming-Lin Pan, Wei Lu, Ying Tang, Heng Miao and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed, 4 pooled it
12.0field-weighted citation impact, top 1% 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

112 citing papers in PubMed, 4 syntheses or guidelines pooled it, 192 citations in OpenAlex.

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52 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

15 authors at 3 institutions in 2 countries.

Ting-Ting CaiDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Xiao-Long YeDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ru-Run LiDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Hui ChenDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ya-Yun WangDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Hui-Juan YongDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ming-Lin PanDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Wei LuDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ying TangDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Heng MiaoDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Antoine M SnijdersBiological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, United States.
Jian-Hua MaoBiological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, United States.
Xing-Yin LiuDepartment of Pathogen Biology-Microbiology Division, Key Laboratory of Pathogen of Jiangsu Province, Nanjing Medical University, Nanjing, China.
Yi-Bing LuDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Da-Fa DingDepartment of Endocrinology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Second Affiliated Hospital of Nanjing Medical University · CNLawrence Berkeley National Laboratory · USNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral administration of resveratrol is able to ameliorate the progression of diabetic nephropathy (DN); however, its mechanisms of action remain unclear. Recent evidence suggested that the gut microbiota is involved in the metabolism therapeutics. In the current study, we sought to determine whether the anti-DN effects of resveratrol are mediated through modulation of the gut microbiota using the genetic db/db mouse model of DN. We demonstrate that resveratrol treatment of db/db mice relieves a series of clinical indicators of DN. We then show that resveratrol improves intestinal barrier function and ameliorates intestinal permeability and inflammation. The composition of the gut microbiome was significantly altered in db/db mice compared to control db/m mice. Dysbiosis in db/db mice characterized by low abundance levels of

Indexed as

diabetic nephropathygut–kidney axisgut microbiomeinflammationresveratrol

Identifiers

PMID32973502
PMCPMC7466761
OpenAlexW3079127461

What Socratic 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 Socratic graph.