Evidence map›Paper›PMID 26064395›Full record

ArticleInternational journal of clinical and experimental medicine2015

Chinese medicine Jinlida (JLD) ameliorates high-fat-diet induced insulin resistance in rats by reducing lipid accumulation in skeletal muscle.

Sha-Sha Zang, An Song, Yi-Xuan Liu, Chao Wang, Guang-Yao Song, Xiao-Ling Li, Ya-Jun Zhu, Xian Yu, Ling Li, Chen-Xi Liu and 2 more

Abstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

12 authors.

Sha-Sha ZangDepartment of Geratology, The Affiliated Hospital of Hebei University, School of Medicine Baoding 071000, Hebei Province, China.
An SongDepartment of Clinical Medicine, Shandong University Jinan 250012, Shandong Province, China.
Yi-Xuan LiuDepartment of Internal Medicine, Hebei Medical University Shijiazhuang, 050017, Hebei Province, China.
Chao WangDepartment of Clinical Medical Research Center and Geriatric Key Laboratory, Hebei General Hospital Shijiazhuang 050051, Hebei Province, China.
Guang-Yao SongDepartment of Endocrinology, Hebei General Hospital Shijiazhuang 050051, Hebei Province, China.
Xiao-Ling LiDepartment of Endocrinology, Bethune International Peace Hospital Shijiazhuang, 050000, Hebei Province, China.
Ya-Jun ZhuDepartment of Endocrinology, Hebei General Hospital Shijiazhuang 050051, Hebei Province, China.
Xian YuDepartment of Endocrinology, Hebei General Hospital Shijiazhuang 050051, Hebei Province, China.
Ling LiDepartment of Internal Medicine, Hebei Medical University Shijiazhuang, 050017, Hebei Province, China.
Chen-Xi LiuDepartment of Internal Medicine, Hebei Medical University Shijiazhuang, 050017, Hebei Province, China.
Jun-Cong KangDepartment of Internal Medicine, Hebei Medical University Shijiazhuang, 050017, Hebei Province, China.
Lu-Ping RenDepartment of Endocrinology, Hebei General Hospital Shijiazhuang 050051, Hebei Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present paper reports the effects of Jinlida (JLD), a traditional Chinese medicine which has been given as a treatment for high-fat-diet (HFD)-induced insulin resistance. A randomized controlled experiment was conducted to provide evidence in support of the affects of JLD on insulin resistance induced by HFD. The affect of JLD on blood glucose, lipid, insulin, adiponectin, alanine aminotransferase (ALT), aspartate aminotransferase (AST) and total bilirubin (TBIL) in serum and lipid content in skeletal muscle was measured. Genes and proteins of the AMPK signaling pathway were analyzed by real time RT-PCR and Western blot. Adiponectin receptor 1 and 2 (ADIPOR1, ADIPOR2) and other genes involved in mitochondrial function and fat oxidation were analyzed by real time RT-PCR. Histological staining was also performed. JLD or pioglitazone administration ameliorated fasting plasma levels of glucose, insulin, triglyceride (TG), total cholesterol (TC), ALT, AST and non-esterified fatty acid (NEFA) (P < 0.05). Treatment with JLD or pioglitazone significantly reverted muscle lipid content (P < 0.05). JLD (1.5 g/kg) significantly increased plasma adiponectin concentration by 60.17% and increased AMPK and acetyl-CoA carboxylase (ACC) phosphorylation in skeletal muscle (P < 0.05). JLD administration increased levels of ADIPOR1 and ADIPOR2 by 1.48 and 1.29 respectively. Levels of genes involved in mitochondrial function and fat oxidation were increased. This study provides the molecular mechanism by which JLD ameliorates HFD-induced insulin resistance in rats.

Indexed as

AMP-activated protein kinaseinsulin resistanceJinlida (JLD)lipid accumulationmitochondriaskeletal muscle

Identifiers

PMID26064395
PMCPMC4443229

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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.