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May 17, 2026Plants2 citationsOpen Access

Neuropharmacological Validation of Clinopodium pulchellum (Panizara): Unveiling the Anxiolytic and Antidepressant Mechanism via In Vivo Models and Molecular Docking

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JVJuan E. Valdiviezo-CamposRFRamiro Fiestas-JacintoKOKaryn A. Olascuaga-Castillo

Key Points

  • The study aims to evaluate the anxiolytic and antidepressant effects of Clinopodium pulchellum and characterize its phytochemical components.
  • Hydrodistillation to obtain essential oil, analyzed using GC–MS and GC–FID.
  • In vivo assays conducted with the aqueous extract at 200 mg·kg−1.
  • Molecular docking to assess binding affinities with serotonergic and ion channel targets.
  • The essential oil contained 15 volatile compounds, with β-caryophyllene (22.9%) and linalool (19.1%) as predominant.
  • In vivo, the extract significantly increased open-arm exploration and reduced immobility time by 37% compared to the stress group.
  • Molecular docking showed favorable binding affinities for β-caryophyllene and others, with suitable pharmacokinetic properties indicated.

Abstract

(1) Background: Clinopodium pulchellum (Kunth) Govaerts (Panizara) is an aromatic Andean medicinal plant traditionally used in Peru to manage nervous disorders, insomnia, and digestive complaints; however, its neuropharmacological properties remain poorly validated. This study aimed to evaluate the anxiolytic- and antidepressant-like effects of C. pulchellum and to characterize its phytochemical profile as supportive evidence. (2) Methods: The essential oil was obtained by hydrodistillation and analyzed using GC–MS and GC–FID. (3) Results: Fifteen volatile compounds were identified based on retention indices and mass spectral data, with β-caryophyllene (22.9%) and linalool (19.1%) as the most representative constituents, while other compounds were tentatively identified. The aqueous extract showed total phenolic and flavonoid contents of 34.15 mg GAE/g and 29.44 mg QE/g, respectively, and moderate antioxidant activity (DPPH = 2.36 mg TE/g; ABTS = 3.33 mg TE/g). In vivo assays revealed that EOCP at 200 mg·kg−1 significantly increased open-arm exploration in the elevated plus maze and reduced immobility time in the CUMS–forced swim test by 37% compared with the stress group, although the effect was lower than that of reference drugs. Molecular docking analysis indicated favorable binding affinities of β-caryophyllene, humulene, and aromandendrene with serotonergic and ion channel targets, while ADMET predictions suggested suitable pharmacokinetic properties. (4) Conclusions: These findings indicate that the observed neuropharmacological effects may be associated with the presence of bioactive terpenoids typical of Lamiaceae, supporting the traditional use of C. pulchellum. However, further studies are required to confirm the identity of uncommon constituents and to elucidate the mechanisms underlying its biological activity.

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Cite This Study

Valdiviezo-Campos et al. (2026) studied this question.

synapsesocial.com/papers/6a095c3f7880e6d24efe24e9https://doi.org/10.3390/plants15101511
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