Effect of borneol, moschus, storax, and acorus tatarinowii on expression levels of four amino acid neurotransmitters in the rat corpus striatum
The present study collected cerebrospinal fluid samples from the corpus striatum in rats treated with borneol, moschus, storax, and acorus tatarinowii using brain microdialysis technology. Levels of excitatory neurotransmitters aspartic acid and glutamate, as well as inhibitory neurotransmitters gly...
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Published in | Neural regeneration research Vol. 7; no. 6; pp. 440 - 444 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
India
Medknow Publications & Media Pvt. Ltd
25.02.2012
Pharmacy of Traditional Chinese Medicine, Drugs Supply Centre of PLA General Hospital, Beijing 100853, China Department of Pharmacy, Shijiazhuang Fourth Hospital, Shijiazhuang 050011, Hebei Province, China%Pharmacy of Traditional Chinese Medicine, Drugs Supply Centre of PLA General Hospital, Beijing 100853, China Medknow Publications & Media Pvt Ltd |
Subjects | |
Online Access | Get full text |
ISSN | 1673-5374 1876-7958 |
DOI | 10.3969/j.issn.1673-5374.2012.06.006 |
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Summary: | The present study collected cerebrospinal fluid samples from the corpus striatum in rats treated with borneol, moschus, storax, and acorus tatarinowii using brain microdialysis technology. Levels of excitatory neurotransmitters aspartic acid and glutamate, as well as inhibitory neurotransmitters glycine and ~-aminobutyric acid, were measured in samples using reversed-phase high-performance liquid chromatography, phosphate gradient elution, and fluorescence detection. Results showed that concentrations of all four amino acid neurotransmitters significantly increased in the corpus striatum following treatment with borneol or moschus, but effects due to borneol were more significant than moschus. Acorus tatarinowii treatment increased ~-aminobutyric acid expression, but decreased glutamate concentrations. Storax increased aspartic acid concentrations and decreased glycine expression. Results demonstrated that borneol and moschus exhibited significant effects on con amino acid neurotransmitter expression; storax exhibited excitatory effects and acorus tatarinowii resulted in inhibitory effects. |
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Bibliography: | The present study collected cerebrospinal fluid samples from the corpus striatum in rats treated with borneol, moschus, storax, and acorus tatarinowii using brain microdialysis technology. Levels of excitatory neurotransmitters aspartic acid and glutamate, as well as inhibitory neurotransmitters glycine and ~-aminobutyric acid, were measured in samples using reversed-phase high-performance liquid chromatography, phosphate gradient elution, and fluorescence detection. Results showed that concentrations of all four amino acid neurotransmitters significantly increased in the corpus striatum following treatment with borneol or moschus, but effects due to borneol were more significant than moschus. Acorus tatarinowii treatment increased ~-aminobutyric acid expression, but decreased glutamate concentrations. Storax increased aspartic acid concentrations and decreased glycine expression. Results demonstrated that borneol and moschus exhibited significant effects on con amino acid neurotransmitter expression; storax exhibited excitatory effects and acorus tatarinowii resulted in inhibitory effects. acorus tatarinowii; amino acid; borneol; microdialysis; high-performance liquid chromatography; moschus; neurotransmitter; resuscitation drugs; storax 11-5422/R ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Author contributions: Na Zhang and Ping Liu had full access to all data and participated in data integrity and data analysis. All authors were responsible for data collection, interpretation, and study design. Na Zhang, Pharmacist, Pharmacy of Traditional Chinese Medicine, Drugs Supply Centre of PLA General Hospital, Beijing 100853, China; Department of Pharmacy, Shijiazhuang Fourth Hospital, Shijiazhuang 050011, Hebei Province, China |
ISSN: | 1673-5374 1876-7958 |
DOI: | 10.3969/j.issn.1673-5374.2012.06.006 |