2016, Number 1
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Salud Mental 2016; 39 (1)
Anxiolytic and sedative-like effects of flavonoids from Tilia americana var. mexicana: GABAergic and serotonergic participation
Aguirre-Hernández E, González-Trujano ME, Terrazas T, Herrera SJ, Guevara-Fefer P
Language: English
References: 32
Page: 37-46
PDF size: 405.13 Kb.
ABSTRACT
Introduction
The inflorescences of
Tilia americana var.
mexicana are used as an
infusion in Mexican traditional medicine due to their tranquilizing
effects; however, pharmacological and phytochemical studies of the
leaves are lacking.
Objective
In this research, the anxiolytic and sedative-like efficacy of the
Tilia
americana var.
mexicana leaves was compared to that obtained with
its inflorescences and flavonoids therein identified, as well as the possible
mechanism of action.
Methods
The sorted and dried inflorescences and leaves were macerated subsequently
in hexane, ethyl acetate and methanol. The methanol extracts
were qualitative- and quantitative-analyzed by HPLC, using commercial
flavonoids standards selected on the basis of their previously
reported presence in
Tilia species. The pharmacological activity was
evaluated in CD-1 mice in the tests: open-field, elevated plus-maze,
hole-board, and the sodium pentobarbital-induced sleep potentiation
test. In regard to the mechanism of action, participation of benzodiazepine
and 5-HT
1A serotonin receptors was tested with the respective
antagonists: flumazenil and WAY100635.
Results
The presence of quercetin, rutin and isoquercitrin was confirmed in
the extracts of the inflorescences and leaves. The anxiolytic-like effects
were the same between the two organs, which were inhibited in the
presence of flumazenil and WAY100635.
Discussion and conclusion
Our results provide evidence that the extracts of the leaves of
T. americana
var.
mexicana are as efficacious as the inflorescences to produce
anxiolytic and sedative-like effects, where flavonoids like quercetin,
rutin and isoquercitrin are partially responsible for these activities
by the involvement of GABA/BDZ and 5HT
1A serotonergic receptors.
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