Lavender improves sleep through olfactory perception and GABAergic neurons of the central amygdala

The use of lavender as sleep aid or hypnotic agent can be traced back as early as ancient Romans and Greeks. Yet, objective experimental data on whether and how lavender enhances sleep duration or/and sleep quality remain lacking. We aimed to characterize the sleep-wake regulating effects of lavender in the mouse and to demonstrate the brain targets and neural circuits involved. A self-made precise odor delivery system combined with chronic polysomnographic recordings was employed to assess the sleep-wake effects of inhalation with lavender essential oil (LEO, extracted from lavender) and its different constituents during the light and dark phases in free-moving C57BL/6J mice. Neuroviral labeling, in situ hybridization and pharmacogenetics were combined to identify the neural circuits and targets involved. Finally, an insomniac model of DL-4-Chlorophenylalanine (PCPA)-treated mice was established to examine the sleep-inducing potential of LEO. We found that inhalation of LEO with a concentration at 25.0% during the light (inactive) phase significantly shortened the latency to non-rapid eye movement (NREM) sleep, increased the total amount of NREM sleep at the expense of wakefulness (W), and enhanced cortical EEG slow wave activities, notably delta power spectra density. We further identified linalool, d-limonene, 1,8-cineole, linalyl acetate and terpinene-4-ol as the major effective sleep-promoting monomer components. Importantly, we found that LEO no longer produced any of the above sleep-promoting effect following either nasal injection of zinc sulfate which interrupts the olfactory pathway, or pharmacogenetics silencing of central amygdala GABAergic neurons. Finally, LEO reestablished NREM sleep with short latency in PCPA-treated insomniac mice , effects comparable with those induced by a potent sedative diazepam. We have characterized the quantitative and qualitative sleep-promoting effects of LEO and its effective components via the olfactory pathway and central amygdala GABA neuronal targets. The hypnotic property of LEO is reinforced by its ability to restore sleep in insomnia. Our study thus establishes a neurobiological basis for aromatherapy of sleep disorders using lavender.

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Publication Details

Journal
Journal of Ethnopharmacology
Published
2024-10-18
DOI
https://doi.org/10.1016/j.jep.2024.118942
Citations
10
Primary Topic
Sleep and Wakefulness Research
Type
article
Field-Weighted Citation Impact
3.43

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article

Lavender improves sleep through olfactory perception and GABAergic neurons of the central amygdala

Yu-Feng Shao, Jin-Xian Gao, Yu-Nong Chen, Jian‐Sheng Lin et al.
10 citations
Journal of Ethnopharmacology
Sleep and Wakefulness Research
3.43
article

Lavender improves sleep through olfactory perception and GABAergic neurons of the central amygdala

Yu-Feng Shao, Jin-Xian Gao, Yu-Nong Chen, Jian‐Sheng Lin, Jun-Fan Xie, Yiping Hou, Weiwei Chu, Karen Spruyt, Le Xin, Xing-Wen Yang, Guizhong Yan, Can Wang, Yanli Ren
article en
10 citations

Abstract

The use of lavender as sleep aid or hypnotic agent can be traced back as early as ancient Romans and Greeks. Yet, objective experimental data on whether and how lavender enhances sleep duration or/and sleep quality remain lacking. We aimed to characterize the sleep-wake regulating effects of lavender in the mouse and to demonstrate the brain targets and neural circuits involved. A self-made precise odor delivery system combined with chronic polysomnographic recordings was employed to assess the sleep-wake effects of inhalation with lavender essential oil (LEO, extracted from lavender) and its different constituents during the light and dark phases in free-moving C57BL/6J mice. Neuroviral labeling, in situ hybridization and pharmacogenetics were combined to identify the neural circuits and targets involved. Finally, an insomniac model of DL-4-Chlorophenylalanine (PCPA)-treated mice was established to examine the sleep-inducing potential of LEO. We found that inhalation of LEO with a concentration at 25.0% during the light (inactive) phase significantly shortened the latency to non-rapid eye movement (NREM) sleep, increased the total amount of NREM sleep at the expense of wakefulness (W), and enhanced cortical EEG slow wave activities, notably delta power spectra density. We further identified linalool, d-limonene, 1,8-cineole, linalyl acetate and terpinene-4-ol as the major effective sleep-promoting monomer components. Importantly, we found that LEO no longer produced any of the above sleep-promoting effect following either nasal injection of zinc sulfate which interrupts the olfactory pathway, or pharmacogenetics silencing of central amygdala GABAergic neurons. Finally, LEO reestablished NREM sleep with short latency in PCPA-treated insomniac mice , effects comparable with those induced by a potent sedative diazepam. We have characterized the quantitative and qualitative sleep-promoting effects of LEO and its effective components via the olfactory pathway and central amygdala GABA neuronal targets. The hypnotic property of LEO is reinforced by its ability to restore sleep in insomnia. Our study thus establishes a neurobiological basis for aromatherapy of sleep disorders using lavender.

Journal of EthnopharmacologyVol. 337
Université Claude Bernard Lyon 1 (FR), Weifang Medical University (CN), Centre National de la Recherche Scientifique (FR), Inserm (FR), Université Paris Cité (FR), Sorbonne Paris Cité (FR), Centre de Recherche en Neurosciences de Lyon (FR), Assistance Publique – Hôpitaux de Paris (FR), Xi'an Medical University (CN), Gansu Provincial Hospital (CN), Hôpital Robert-Debré (FR), Paris Cardiovascular Research Center (FR), Centre Hospitalier Le Vinatier (FR), Anshan Hospital (CN), NeuroDiderot (FR), Lanzhou University (CN)
Natural Science Foundation of Xinjiang Province, National Natural Science Foundation of China, State Administration of Foreign Experts Affairs, China Scholarship Council
Openalex Percentile: Top 7%
Sleep and Wakefulness Research
3.43
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