2011
DOI: 10.1016/j.jep.2011.09.010
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The standardized extract of Loeselia mexicana possesses anxiolytic activity through the γ-amino butyric acid mechanism

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Cited by 22 publications
(10 citation statements)
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“…The open field test was conducted after the aforementioned behavioral tests, allowing us to exclude possible nonspecific locomotor effects of antagonists or FAT treatments. In the open field test, we found that none of the GABA A antagonists alone or the FAT-M at the doses tested produced any significant changes on motor activity, similar to previous reports [4, 11, 13, 35]. Additionally, the dose administered of bicuculline and picrotoxin did not produce behaviour linked to seizures (i.e., facial/ear twitching, myoclonic jerks, among others), which are detected with higher doses than those used in the present study.…”
Section: Discussionsupporting
confidence: 92%
“…The open field test was conducted after the aforementioned behavioral tests, allowing us to exclude possible nonspecific locomotor effects of antagonists or FAT treatments. In the open field test, we found that none of the GABA A antagonists alone or the FAT-M at the doses tested produced any significant changes on motor activity, similar to previous reports [4, 11, 13, 35]. Additionally, the dose administered of bicuculline and picrotoxin did not produce behaviour linked to seizures (i.e., facial/ear twitching, myoclonic jerks, among others), which are detected with higher doses than those used in the present study.…”
Section: Discussionsupporting
confidence: 92%
“…In this animal model, rats or mice that display anxiety-like behavior usually show a reduction of open-arm exploration, reflected by a decrease in the time spent in the open arms. Animals treated with clinically effective anxiolytic drugs (e.g., diazepam) [3436], some neurosteroids with anxiolytic-like potency (e.g., progesterone and allopregnanolone) [3739], and some extracts from medicinal plants with reputed anxiolytic properties exhibit an increase in the total time spent in the open arms [40, 41], which is considered an anxiolytic-like effect at the experimental level.…”
Section: Discussionmentioning
confidence: 99%
“…Scopoletin shows MAO inhibition activity in a dose-dependent fashion, with IC 50 values of 19.4 μg/mL [19]. In addition, daphnoretin a bicoumarin of scopoletin and umbelliferone exhibits significant anxiolytic activity in EPM model [21-23]. It has been also suggested that coumarin derivatives interact with the benzodiazepine binding site of the GABA-A receptor [24].…”
Section: Discussionmentioning
confidence: 99%