Dracocephalum moldavica aqueous extract induces sedation and general CNS inhibition in mice
The aqueous extract of Dracocephalum moldavica prolonged pentobarbital-induced sleeping time, induced sedation in the hole-board test, decreased spontaneous activity, and impaired motor coordination in mice. The LD50 was 470 mg/kg body weight, and the main compounds were acacetin, apigenin, and luteolin-7-O-β-D-(6″-O-malonyl)-glucoside derivatives.
Evidence Score
Study Evidence
Study 1. Neuropharmacological study of Dracocephalum moldavica L. (Lamiaceae) in mice: sedative effect and chemical analysis of an aqueous extract.
observationalMartínez-Vázquez M, Estrada-Reyes R, Martínez-Laurrabaquio A, López-Rubalcava C, Heinze G · Journal of ethnopharmacology (2012)
Result:
Mechanism Graph
Limitations
- ⚠Study conducted only in mice, not in humans
- ⚠No specific mechanism of action was identified (e.g., receptor binding assays)
- ⚠Anxiolytic and antidepressant effects were not observed, limiting therapeutic scope
Frequently Asked Questions
What is Dracocephalum moldavica used for traditionally?▼
It is used in Mexican traditional medicine as a tranquilizer and for relief of nervous conditions.
Did the extract show anxiolytic or antidepressant effects?▼
No, the extract did not show anxiolytic effects in the avoidance exploratory behavior test or hole-board test, and it was not effective in the forced swimming test for antidepressant-like effects.
What were the main chemical compounds identified in the extract?▼
The main compounds were acacetin, apigenin, and luteolin-7-O-β-D-(6″-O-malonyl)-glucoside derivatives, as determined by HPLC-ESI-MS.
What was the acute toxicity of the extract?▼
The LD50 was 470 mg/kg body weight, indicating moderate toxicity in mice.
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References
- 1.Martínez-Vázquez M, Estrada-Reyes R, Martínez-Laurrabaquio A, López-Rubalcava C, Heinze G. "Neuropharmacological study of Dracocephalum moldavica L. (Lamiaceae) in mice: sedative effect and chemical analysis of an aqueous extract.." Journal of ethnopharmacology, 2012. PMID: 22469767 DOI: 10.1016/j.jep.2012.03.028