Evidence map›Paper›PMID 35846873›Full record

ArticleAnalytical cellular pathology (Amsterdam)2022

Metabolomics-Based Pharmacodynamic Analysis of Zhuang Yao Shuang Lu Tong Nao Granules in a Rat Model of Ischemic Cerebral Infarction.

Yang Zhai, Yangling Chen, Yihui Luo, Xiaoping Mei, Lin Wu, Xueni Mo, Min Zou, Mingzhao Zhou, Yangling Wu, Guangshan Zheng and 3 more

Abstract read
In one paragraph

Article in Analytical cellular pathology (Amsterdam), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Yang ZhaiGraduate School, Guangxi University of Chinese Medicine, China.
Yangling ChenGraduate School, Guangxi University of Chinese Medicine, China.
Yihui LuoGuangxi International Zhuang Medicine Hospital, China.
Xiaoping MeiGuangxi International Zhuang Medicine Hospital, China.
Lin WuDepartment of Neurology, Guangxi University of Chinese Medicine, China.
Xueni MoDepartment of Neurology, Guangxi University of Chinese Medicine, China.
Min ZouGuangxi International Zhuang Medicine Hospital, China.
Mingzhao ZhouGuangxi International Zhuang Medicine Hospital, China.
Yangling WuGuangxi International Zhuang Medicine Hospital, China.
Guangshan ZhengGuangxi International Zhuang Medicine Hospital, China.
Peng YangGuangxi International Zhuang Medicine Hospital, China.
Qingyu HeFaculty of Chinese Medicine Science, Guangxi University of Chinese Medicine, China.
Rui ChenFaculty of Chinese Medicine Science, Guangxi University of Chinese Medicine, China.ORCID https://orcid.org/0000-0003-4558-4479

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study used a metabolomic approach to reveal changes in the levels of metabolic biomarkers and related metabolic pathways before and after Zhuang Yao Shuang Lu Tong Nao granule (YHT) treatment in rats with cerebral ischemia. The neurological deficit scores were significantly higher in the MCAO_R group than in the NC group, indicating that the mice had significantly impaired motor functions. The YHT group had significantly lower scores than the MCAO_R group, suggesting that YHT significantly improved motor function in rats. TTC staining of the brain tissue revealed that YHT significantly reduced the area of cerebral infarction in the treated rats. The MCAO_R group was better separated from the NC rent, sham, and YHT groups via metabolomic PCA. Moreover, there were significant differences in the differential metabolites between the MACO_R and YHT groups. Eighteen common differential metabolites were detected between the MACO_R and NC groups, MACO_R and sham groups, and MACO_R and YHT groups, indicating that YHT significantly increased the levels of various metabolites in the serum of cerebral ischemic stroke (CIS) rats. Moreover, a total of 23 metabolic pathways were obtained. We identified 11 metabolic pathways with the most significant effects in the bubble plots. In conclusion, from a systems biology perspective, this metabolomics-based study showed that YHT could be used to treat ischemic stroke by modulating changes in endogenous metabolites.

Indexed as

Brain IschemiaIschemic StrokeAnimalsCerebral InfarctionDisease Models, AnimalMetabolomicsMiceRatsRats, Sprague-Dawley

Identifiers

PMID35846873
PMCPMC9277214

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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.