Evidence map›Paper›PMID 25815030›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2015

Therapeutic Effects of TianDiJingWan on the Aβ 25-35-Induced Alzheimer's Disease Model Rats.

Zhijie Li, Qing Tong, Huifang Xu, Li Hu, Rong Zhao, Fang Zhou, Wei Pan, Li Zhou

Open access · hybridAbstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Huang-Pu-Tong-Qiao Formula Ameliorates Tau Phosphorylation by Inhibiting the CaM-CaMKIV Pathway.Evidence-based complementary and alternative medicine : eCAM · 2020
    Article
  4. Article
  5. Article
  6. Review
  7. Protective effects ofNeural regeneration research · 2017
    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

8 authors at 2 institutions in 1 country.

Zhijie LiDepartment of Encephalopathy, Wuhan Hospital of Traditional Chinese Medicine, Wuhan 430030, China.
Qing TongDepartment of Pharmacy, Tongji Hospital Affiliated with Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Huifang XuDepartment of Encephalopathy, Wuhan Hospital of Traditional Chinese Medicine, Wuhan 430030, China.
Li HuDepartment of Encephalopathy, Wuhan Hospital of Traditional Chinese Medicine, Wuhan 430030, China.
Rong ZhaoDepartment of Encephalopathy, Wuhan Hospital of Traditional Chinese Medicine, Wuhan 430030, China.
Fang ZhouDepartment of Encephalopathy, Wuhan Hospital of Traditional Chinese Medicine, Wuhan 430030, China.
Wei PanDepartment of Encephalopathy, Wuhan Hospital of Traditional Chinese Medicine, Wuhan 430030, China.
Li ZhouDepartment of Encephalopathy, Wuhan Hospital of Traditional Chinese Medicine, Wuhan 430030, China.
Wuhan City Chinese Medicine Hospital · CNTongji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The main purpose of this study was to demonstrate the therapeutic effects and mechanism of TDJW, a modern Chinese medicine prescription developed based on the basic traditional Chinese medicine theory of "tonifying the kidney essence," on the Aβ 25-35-induced AD rats. The AD model was established by the intracerebroventricular administrations of Aβ 25-35 into the hippocampus CA1 tissue of SD male rats. 72 rats were randomly divided into six groups: sham operation, AD model, donepezil, high TDJW group, medium TDJW group, and low TDJW group. After oral administration of TDJW, the results of Morris water maze and step-down test showed that the learning and memory abilities of AD rats were significantly improved. And biochemical measurement demonstrated that Ach and Glu in hippocampus tissues of AD rats were increased as well. Moreover, the Aβ deposits and p-Tau aggregations in hippocampus CA1 tissues of AD rats were attenuated as observed in the micrographs of immunohistochemistry study, and the results of ELISA indicated that the expressions of TNF-α, IL-1β, and IL-6 in hippocampus tissues were significantly decreased. In conclusion, the present study demonstrated that TDJW could be used as a promising therapeutic agent for the clinical applications of AD treatment in patients.

Identifiers

PMID25815030
PMCPMC4357045
OpenAlexW2050051794

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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.