Aloysia deserticola (rica-rica) essential oil impairs inhibitory synaptic transmission in hippocampal CA1 pyramidal neurons
7 affiliations
- 1Centro de Neurobiología y Fisiopatología Integrativa (CENFI), Laboratorio de Neuroplasticidad, Instituto de Fisiología, Facultad de Ciencias, Universidad de Valparaíso
- 2Millennium Nucleus of Neuroepigenetics and Plasticity (EpiNeuro)
- 3Centro Interdisciplinario de Neurociencia de Valparaíso (CINV), Facultad de Ciencias, Universidad de Valparaíso
- 4Facultad de Farmacia, Escuela de Química y Farmacia, Laboratorio de Química de Metabolitos Bioactivos Universidad de Valparaíso
- 5Programa de Doctorado en Ciencias, Mención Neurociencia, Universidad de Valparaíso
- 6Facultad de Ciencias de la Vida, Universidad Viña del Mar
- 7Centro de Investigación, Desarrollo e Innovación de Productos Bioactivos (CInBIO), Universidad de Valparaíso
Abstract
Aloysia deserticola is an aromatic plant native to the Chilean Andean highlands that has traditionally been used in herbal preparations. Although a previous behavioral study reported the anxiolytic and antidepressant-like effects of rica-rica essential oil in an animal model, its neurophysiological actions at cellular and synaptic levels remain largely unexplored. In this study, we characterized A. deserticola essential oil (AD-EO) using gas chromatography–mass spectrometry (GC–MS) and examined its acute effects on GABAergic synaptic transmission via whole-cell patch-clamp recordings from CA1 pyramidal neurons in acute dorsal hippocampal slices obtained from C57BL/6 J mice. GC–MS analysis revealed an enriched thujone chemical profile, with peaks tentatively identified as α- and β-thujone accounting for 89.06% and 3.38% of the total chromatographic area, respectively. Application of AD-EO to the bath reduced evoked inhibitory postsynaptic current (eIPSC) amplitude in a concentration-dependent manner and shortened eIPSC decay kinetics. This is consistent with a postsynaptic contribution to the suppression of inhibitory signaling. At intermediate-to-high estimated thujone-equivalent concentrations, AD-EO increased the paired-pulse ratio. Coefficient-of-variation analysis supported the presence of an additional presynaptic component. Consistent with these findings, AD-EO reduced the frequency and amplitude of miniature inhibitory postsynaptic currents. Furthermore, the effects on eIPSC amplitude and the paired-pulse ratio were reversible following washout. Together, these results demonstrate that AD-EO suppresses inhibitory synapses in CA1 pyramidal neurons via effects consistent with pre- and postsynaptic locus . These results provide electrophysiological evidence that AD-EO modulates hippocampal inhibitory transmission and support further investigation of the mechanisms underlying the neurophysiological actions of this complex natural preparation.
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BibTeX
@article{ahumada2026aloysia,
title = {{Aloysia deserticola (rica-rica) essential oil impairs inhibitory synaptic transmission in hippocampal CA1 pyramidal neurons}},
author = {Juan Ahumada and Pablo Morel-Alonso and Nicole Vidal-Herrera and Koyam Morales-Weil and Waleska Vera and Marco Fuenzalida},
journal = {Frontiers in Pharmacology},
year = {2026},
month = oct,
doi = {10.3389/fphar.2026.1917739},
url = {https://www.frontiersin.org/articles/10.3389/fphar.2026.1917739/full},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Aloysia deserticola (rica-rica) essential oil impairs inhibitory synaptic transmission in hippocampal CA1 pyramidal neurons
AU - Juan Ahumada
AU - Pablo Morel-Alonso
AU - Nicole Vidal-Herrera
AU - Koyam Morales-Weil
AU - Waleska Vera
AU - Marco Fuenzalida
PY - 2026
DA - 2026/10/14
JO - Frontiers in Pharmacology
DO - 10.3389/fphar.2026.1917739
UR - https://www.frontiersin.org/articles/10.3389/fphar.2026.1917739/full
AB - Aloysia deserticola is an aromatic plant native to the Chilean Andean highlands that has traditionally been used in herbal preparations. Although a previous behavioral study reported the anxiolytic and antidepressant-like effects of rica-rica essential oil in an animal model, its neurophysiological actions at cellular and synaptic levels remain largely unexplored. In this study, we characterized A. deserticola essential oil (AD-EO) using gas chromatography–mass spectrometry (GC–MS) and examined its acute effects on GABAergic synaptic transmission via whole-cell patch-clamp recordings from CA1 pyramidal neurons in acute dorsal hippocampal slices obtained from C57BL/6 J mice. GC–MS analysis revealed an enriched thujone chemical profile, with peaks tentatively identified as α- and β-thujone accounting for 89.06% and 3.38% of the total chromatographic area, respectively. Application of AD-EO to the bath reduced evoked inhibitory postsynaptic current (eIPSC) amplitude in a concentration-dependent manner and shortened eIPSC decay kinetics. This is consistent with a postsynaptic contribution to the suppression of inhibitory signaling. At intermediate-to-high estimated thujone-equivalent concentrations, AD-EO increased the paired-pulse ratio. Coefficient-of-variation analysis supported the presence of an additional presynaptic component. Consistent with these findings, AD-EO reduced the frequency and amplitude of miniature inhibitory postsynaptic currents. Furthermore, the effects on eIPSC amplitude and the paired-pulse ratio were reversible following washout. Together, these results demonstrate that AD-EO suppresses inhibitory synapses in CA1 pyramidal neurons via effects consistent with pre- and postsynaptic locus . These results provide electrophysiological evidence that AD-EO modulates hippocampal inhibitory transmission and support further investigation of the mechanisms underlying the neurophysiological actions of this complex natural preparation.
SN - 1663-9812
ER -