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ArticleNaunyn-Schmiedeberg's archives of pharmacology2024

Role of TRPA1 in the pharmacological effect triggered by the topical application of trans-anethole in mice.

Larissa Gonzaga Santos, Janiana Raíza Jentsch Matias de Oliveira, Mayara Alves Amorim, Vitor Hélio de Souza Oliveira, Eunice André

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Article in Naunyn-Schmiedeberg's archives of pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Larissa Gonzaga SantosDepartment of Pharmacology, Federal University of Paraná, Curitiba, Paraná, 81531-980, Brazil.
Janiana Raíza Jentsch Matias de OliveiraDepartment of Pharmacology, Federal University of Paraná, Curitiba, Paraná, 81531-980, Brazil.
Mayara Alves AmorimDepartment of Pharmacology, Federal University of Paraná, Curitiba, Paraná, 81531-980, Brazil.
Vitor Hélio de Souza OliveiraDepartment of Pharmacology, Federal University of Paraná, Curitiba, Paraná, 81531-980, Brazil.
Eunice AndréDepartment of Pharmacology, Federal University of Paraná, Curitiba, Paraná, 81531-980, Brazil. eunice.andre@ufpr.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 307183/2021-1
6 · The paper itself

Abstract

purposeThis study investigated the pharmacological effects of topical trans-anethole, a natural compound found in anise, star anise, and fennel essential oils, and its relationship with the transient receptor potential of ankyrin 1 (TRPA1).

methodsThe effects of topical anethole were assessed by eye wiping, nociceptive behaviour, and ear oedema in mice. Histological evaluations were performed on the ears of the animals topically treated with anethole.

resultsAnethole caused less eye irritation than capsaicin (a TRPV1 agonist) and allyl isothiocyanate (a TRPA1 agonist). Anethole (250 and 500 nmol/20 µL/paw) promoted neurogenic nociception in the paw (20.89 ± 3.53 s and 47.56 ± 8.46 s, respectively) compared with the vehicle (0.88 ± 0.38 s). HC030031 (56.1 nmol/20 µL/paw), a TRPA1 antagonist, abolished this nociceptive response. Anethole (4, 10, and 20 µmol/20 µL/ear) induced ear oedema (30.25 ± 4.78 μm, 78.00 ± 3.74 μm, and 127.50 ± 27.19 μm, respectively) compared with the vehicle (5.00 ± 0.5 μm). HC030031 (56.1 nmol/20 µL/ear) inhibited the oedema induced by anethole (10 µmol/20 µL/ear). Ears pre-treated with anethole or allyl isothiocyanate on the first day and re-exposed to these compounds on the third day showed a reduction in oedema (68.16 ± 6.04% and 38.81 ± 8.98.9%, respectively). Cross-desensitisation between anethole and allyl isothiocyanate was observed. Histological analysis confirmed the beneficial effects of anethol.

conclusionAs repeated topical applications of anethole induce the desensitisation of TRPA1, we suggest its clinical application as a topical formulation for treating skin diseases or managing pain associated with this receptor. Anethole may also have advantages over capsaicin and allyl isothiocyanate because of its low pungency and pleasant aroma.

Indexed as

Allylbenzene DerivativesAnisolesTRPA1 Cation ChannelAdministration, TopicalAnimalsCapsaicinEdemaIsothiocyanatesMaleMiceAllylbenzene Derivativesallyl isothiocyanateanetholeAnisolesCapsaicinIsothiocyanatesTRPA1 Cation ChannelTrpa1 protein, mouseAntiedematogenicDesensitizationNociceptionTrans-anethole; transient receptor potential of ankyrin 1

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.