Evidence map›Paper›PMID 36059948›Full record

ArticleFrontiers in pharmacology2022

Dapagliflozin protects against nonalcoholic steatohepatitis in db/db mice.

Panshuang Qiao, Yingli Jia, Ang Ma, Jinzhao He, Chen Shao, Xiaowei Li, Shuyuan Wang, Baoxue Yang, Hong Zhou

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–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

13 citing papers in PubMed.

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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

9 authors.

Panshuang QiaoDepartment of Pharmacology and Department of the Integration of Chinese and Western Medicine and Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.
Yingli JiaDepartment of Pharmacology and Department of the Integration of Chinese and Western Medicine and Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.
Ang MaDepartment of Pharmacology and Department of the Integration of Chinese and Western Medicine and Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.
Jinzhao HeDepartment of Pharmacology and Department of the Integration of Chinese and Western Medicine and Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.
Chen ShaoThe Department of Pathology, Beijing You An Hospital, Capital Medical University, Beijing, China.
Xiaowei LiDepartment of Pharmacology and Department of the Integration of Chinese and Western Medicine and Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.
Shuyuan WangDepartment of Pharmacology and Department of the Integration of Chinese and Western Medicine and Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.
Baoxue YangDepartment of Pharmacology and Department of the Integration of Chinese and Western Medicine and Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.
Hong ZhouDepartment of Pharmacology and Department of the Integration of Chinese and Western Medicine and Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD), which is the most common liver disease, is associated with type 2 diabetes mellitus and metabolic syndrome. Although there is no consensus on the treatment of NAFLD, growing evidence suggests that tight glycemic control would contribute to the improvement of NAFLD. However, some insulin sensitizers cannot improve NAFLD, especially nonalcoholic steatohepatitis (NASH). Whether insulin-independent hypoglycemic drug dapagliflozin, a sodium-glucose cotransporter-2 inhibitor, may improve NAFLD keeps unclear. Therefore, 12-week-old male C57BL/6 wild-type and db/db mice were treated with 1 mg/kg dapagliflozin or vehicle for 12 weeks. Dapagliflozin alleviated NASH, manifesting as decreased alanine aminotransferase and NAFLD activity score in db/db mice. Also, dapagliflozin reduced

Indexed as

de novo lipogenesisfibrosisinflammationnonalcoholic fatty liver diseasesodium-glucose cotransporter-2 inhibitor

Identifiers

PMID36059948
PMCPMC9437261

What OpenQuestion holds

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Registered trials

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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.