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ArticleMetabolic brain disease2024

ChangPu YuJin Tang improves Tourette disorder symptoms by modulating amino acid neurotransmitters in IDPN model rats.

Man-Qi Lu, Zheng-Gang Shi, Jing Shang, Lü Gao, Lei Gao, Wei-Jiao Gao

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Article in Metabolic brain disease, 2024. 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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5 · Who and what money

Authors and funding

6 authors.

Man-Qi LuClinical College of Chinese Medicine, Gansu University Of Chinese Medicine, Lanzhou, 730000, Gansu, P.R. China.ORCID 0000-0002-7119-5621
Zheng-Gang ShiClinical College of Chinese Medicine, Gansu University Of Chinese Medicine, Lanzhou, 730000, Gansu, P.R. China. shizhenggang007@163.com.ORCID 0009-0005-9740-1066
Jing ShangClinical College of Chinese Medicine, Gansu University Of Chinese Medicine, Lanzhou, 730000, Gansu, P.R. China.ORCID 0009-0008-7783-0033
Lü GaoShanxi University Of Chinese Medicine Third Clinical Medical College Pediatric Teaching and Research Department, Taiyuan, 140100, Shanxi, China.ORCID 0009-0005-5189-5507
Lei GaoClinical College of Chinese Medicine, Gansu University Of Chinese Medicine, Lanzhou, 730000, Gansu, P.R. China.ORCID 0009-0005-5240-3084
Wei-Jiao GaoClinical College of Chinese Medicine, Gansu University Of Chinese Medicine, Lanzhou, 730000, Gansu, P.R. China.ORCID 0009-0007-1276-4752

Funding

National Natural Science Foundation of China 81960886Natural Science Foundation of Gansu Province 20YF3FA041Shanxi Provincial Administration of Traditional Chinese Medicine Project 2022ZYYC257Shanxi Provincial Department of Education Science and Technology Innovation Project 2022L357
6 · The paper itself

Abstract

introductionChangpu Yujin Tang(CPYJT), a Chinese herbal compound, is an effective therapeutic strategy for pediatric patients with Tourette disorder (TD). Therefore, this work aims to investigate the therapeutic mechanisms of CPYJT.

methodsBehavioral and cellular ultrastructural evaluation of the therapeutic effects of CPYJT in TD model rats. Colorimetric methods, reverse transcription‑quantitative PCR, and Western Blot were used to measure the altered levels of GLU, GABA, and the levels of VGLUT1, GLUD1, GABRA3, and GAD65 in the cortex, striatum, and thalamus of the TD model rats after 7, 14, 21, and 28 days of CPYJT administration.

resultsCPYJT significantly reduced stereotypic behavior and motor behavior scores in TD model rats. CPYJT ameliorates myelin structural damage in TD model rat neuronal cells. CPYJT decreased GLU content, elevated GABA content, decreased GLUD1 and VGLUT1 levels, and elevated GAD65 and GABRA3 levels in TD model rats' cortex, striatum, and thalamus. CPYJT has different regulatory time points in the cortex, striatum, and thalamus for critical factors of amino acid-based neurotransmission.

conclusionCPYJT protects behavioral and structural damage of neuronal cells in multiple brain regions in TD model rats.

Indexed as

Disease Models, AnimalDrugs, Chinese HerbalNeurotransmitter AgentsTourette SyndromeAmino AcidsAnimalsBraingamma-Aminobutyric AcidMaleRatsRats, Sprague-DawleyAmino AcidsDrugs, Chinese Herbalgamma-Aminobutyric AcidNeurotransmitter AgentsChangpu Yujin TangGamma-aminobutyric acidGlutamateTourette disorder (TD)

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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.