Evidence map›Paper›PMID 34285530›Full record

ArticleDiabetes, metabolic syndrome and obesity : targets and therapy2021

Qihu Preparation Ameliorates Diabetes by Activating the AMPK Signaling Pathway in db/db Mice.

Hongfang Zeng, Xiaoli Li, Duanfang Zhou, Ning Wang, Xiaoping Yu, Liangyuan Long, Hao Cheng, Shuyu Zhou, Zhengze Shen, Weiying Zhou

Open access · goldAbstract read
In one paragraph

Article in Diabetes, metabolic syndrome and obesity : targets and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
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

10 authors at 5 institutions in 1 country.

Hongfang Zeng *Department of Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing, People's Republic of China.
Xiaoli Li *Department of Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing, People's Republic of China.
Duanfang ZhouDepartment of Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing, People's Republic of China.
Ning WangWest China Biopharm Research Institute, West China Hospital, Chengdu, Sichuan Province, 610041, People's Republic of China.
Xiaoping YuDepartment of Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing, People's Republic of China.
Liangyuan LongDepartment of Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing, People's Republic of China.
Hao ChengChina Company 18th, College of Pharmacy, Army Medical University, Chongqing, 400038, People's Republic of China.
Shuyu ZhouChina Company 18th, College of Pharmacy, Army Medical University, Chongqing, 400038, People's Republic of China.
Zhengze ShenDepartment of Pharmacy, Yongchuan Hospital Affiliated to Chongqing Medical University, Chongqing, 400016, People's Republic of China.ORCID 0000-0002-2752-896X
Weiying ZhouDepartment of Pharmacology, College of Pharmacy, Chongqing Medical University, Chongqing, People's Republic of China.
Chongqing University · CNArmy Medical University · CNChongqing Medical and Pharmaceutical College · CNChongqing Medical University · CNSichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo examine the pharmacological effects of Qihu on type 2 diabetes mellitus using db/db mice. MATERIALS AND

methodsThirty-seven db/db mice were randomly divided into the following 5 groups: diabetes model control group (DM group; n = 7), administered with the adjuvant 0.3% carboxymethyl cellulose-Na; positive control group (Met group; n = 8), administered with metformin (0.13 g/kg bodyweight); Qihu-L group (n = 7), administered with a low dose of Qihu (0.75 g/kg bodyweight), Qihu-M group (n = 7), administered with a medium dose of Qihu (1.5 g/kg bodyweight); Qihu-H group (n = 8), administered with a high dose of Qihu (3.0 g/kg bodyweight). BKS mice (n = 8) were used as the negative control group. The db/db mice were administered with drugs through oral gavage for 28 days. The random blood glucose levels, glucose tolerance test, bodyweight, food intake, and blood lipid levels of the mice were measured during the experimental period. The liver and pancreas tissues were collected for pathological, quantitative real-time polymerase chain reaction, and Western blotting analyses.

resultsCompared with the DM group, the Qihu groups exhibited decreased bodyweight gain. The blood glucose levels in the Qihu-L, Qihu-M, and Qihu-H were 31.46%, 43.73%, and 51.83%, respectively, lower than those in the DM group. The triglyceride levels were significantly downregulated and the swelling and steatosis of the hepatocytes were significantly lower in the Qihu-M and Qihu-H groups than in the DM group. Qihu downregulated the expression of IL-1β, IL-6, and TXNIP and upregulated the AMP-activated protein kinase (AMPK) signaling pathway in the pancreas and liver tissues of db/db mice.

conclusionThe anti-diabetic effects of Qihu are mediated through the activation of the AMPK/Txnip signaling and the downregulation of the secretion of inflammatory factors in db/db mice.

Indexed as

anti-inflammatoryT2DMTCMTraditional Chinese medicineTXNIPtype 2 diabetes mellitus

Identifiers

PMID34285530
PMCPMC8286761
OpenAlexW3182184396

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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.