4.4 Article

Sedative effects of l-menthol, d-camphor, phenylethyl alcohol, and geraniol

Journal

JOURNAL OF NATURAL MEDICINES
Volume 75, Issue 2, Pages 319-325

Publisher

SPRINGER JAPAN KK
DOI: 10.1007/s11418-020-01470-1

Keywords

Sedative effect; l-menthol; d-camphor; Phenylethyl alcohol; Geraniol

Funding

  1. Santen Pharmaceutical Co., Ltd.

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This study found that fragrance components added to eye drops such as l-menthol, d-camphor, phenylethyl alcohol, and geraniol have sedative effects on mice. The optimal concentrations for each component were determined, with geraniol showing a biphasic sedative action. This research provides a new perspective on the pharmacological properties of eye drop additives.
Various essential oils from plants and fragrance components such as monoterpenes have been discovered to reduce spontaneous movements in mice; thus, it has been made clear that the odor itself has the sedative activity. In the present study, we examined the sedative activity of the odors of fragrance components added to eye drops; l-menthol, d-camphor, phenylethyl alcohol, and geraniol, which are often used as refreshers or preservatives. Each fragrance component was administered by the inhalation route to mice, and the sedative effects were evaluated using an open field test. The results showed that four components administered via inhalation to mice significantly decreased the amount of spontaneous motor activity in a dose-dependent manner, indicating that all four components have a sedative effect. The optimal concentrations at which l-menthol, d-camphor, phenylethyl alcohol, and geraniol showed the highest sedative activity were 4 x 10(-2) mg per cage, 4 x 10(-4) mg per cage, 4 x 10(-2) mg per cage, and both 4 x 10(-4) and 4 x 10(-2) mg per cage, respectively. The AUC graph of geraniol was represented as a W-shaped curve, suggesting that the sedative action of geraniol was biphasic. The present finding demonstrates a new perspective on a possible pharmacological property of eye drop additives used with no expected pharmacological functions.

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