Evidence map›Paper›PMID 36262166›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2022

Fufang Fanshiliu Decoction Revealed the Antidiabetic Effect through Modulating Inflammatory Response and Gut Microbiota Composition.

Leyu Li, Guoxin Huang, Tingbo Chen, Hui Lin, Ruiyan Xu, Jinyan Cheng, Ying Hu, Weibo Dai, Gengting Dong

Abstract read
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Article in Evidence-based complementary and alternative medicine : eCAM, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

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0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Review
  2. Article
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  5. Article
  6. Frontiers in microbiology · 2024
    Article
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  9. Review
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.

Leyu LiPharmacology Laboratory, Zhongshan Hospital of Traditional Chinese Medicine, Zhongshan, Guangdong, China.
Guoxin HuangClinical Research Center, Shantou Central Hospital, Shantou, Guangdong, China.ORCID https://orcid.org/0000-0001-8128-7135
Tingbo ChenCollege of Health Industry, Zhongshan Torch Polytechnic, Zhongshan, Guangdong, China.
Hui LinPharmacology Laboratory, Zhongshan Hospital of Traditional Chinese Medicine, Zhongshan, Guangdong, China.
Ruiyan XuPharmacology Laboratory, Zhongshan Hospital of Traditional Chinese Medicine, Zhongshan, Guangdong, China.
Jinyan ChengPharmacology Laboratory, Zhongshan Hospital of Traditional Chinese Medicine, Zhongshan, Guangdong, China.
Ying HuPharmacology Laboratory, Zhongshan Hospital of Traditional Chinese Medicine, Zhongshan, Guangdong, China.
Weibo DaiPharmacology Laboratory, Zhongshan Hospital of Traditional Chinese Medicine, Zhongshan, Guangdong, China.ORCID https://orcid.org/0000-0002-0719-4026
Gengting DongPharmacology Laboratory, Zhongshan Hospital of Traditional Chinese Medicine, Zhongshan, Guangdong, China.ORCID https://orcid.org/0000-0001-7785-0351

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Diabetes mellitus brings serious threats and financial burdens to human beings worldwide. Fufang Fanshiliu decoction (FFSLD), a traditional Chinese medicine formula showing great antidiabetic effects, has been used in clinics for many years. Objective: This study aims to explore the underlying therapeutic mechanisms of FFSLD in Type II diabetes mellitus (T2DM). Methods: Sprague-Dawley rats induced by high-fat diet feeding combined with streptozotocin injection were used to establish the T2DM model. All rats were randomly divided into 6 groups: control, model, metformin, high dosage, middle dosage, and low dosage of FFSLD. After 4 weeks of treatment, serum, intestinal mucosa, and fecal samples were collected for further analysis. ELISA was used to detect the diabetic-related serum indicators and proinflammation cytokines. Gene or protein expressions of mitogen-activated protein kinase (MAPK), interleukin 1 beta (IL-1 Results: FFSLD effectively recovered the diabetic-related biochemical indexes by reducing fasting blood glucose (FBG), total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-C), insulin, and increasing high-density lipoprotein cholesterol (HDL-C). Furthermore, FFSLD significantly ameliorated the abnormal levels of proinflammation cytokines including IL-1 Conclusion: These results suggest that FFSLD alleviates diabetic symptoms in T2DM rats through regulating GM composition and inhibiting inflammatory response, which clarify the therapeutic mechanism of FFSLD on T2DM and provide a theoretical basis for its further clinical application.

Identifiers

PMID36262166
PMCPMC9576391

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