Anxiolytic and Antidepressant-like Effects of Monoterpene Tetrahydrolinalool and In silico Approach of new Potential Targets

Author:

Scotti Luciana1,Rayff da Silva Pablo2,Diniz NunesPazos Natalia2,Karla Silva do Nascimento Gonzaga Thallita2,Cabral de Andrade Jéssica2,Brito Monteiro Álefe2,Caroline Ribeiro Portela Anne2,Fernandes Oliveira Pires Hugo2,dos Santos Maia Mayara1,Vilar da Fonsêca Diogo3,T. Scotti Marcus1,Maria Barbosa Filho José4,Pergentino de Sousa Damião4,Francisco Bezerra Felipe Cícero2,Nóbrega de Almeida Reinaldo2

Affiliation:

1. Cheminformatics Laboratory, Institute of Drugs and Medicines Research, Federal University of Paraíba, 58051-900, Via Ipê Amarelo, S/N, João Pessoa, Paraíba, Brazil

2. Psychopharmacology Laboratory, Institute of Drugs and Medicines Research, Federal University of Paraíba, 58051-085, Via Ipê Amarelo, S/N, João Pessoa, Paraíba, Brazil

3. Collegiate of Medicine, Federal University of São Francisco Valley, 48607-190, Rua Aurora, S/N, Bahia, Brazil

4. Pharmaceutical Chemistry Laboratory, Department of Pharmaceutical Sciences, Federal University of Paraíba, 58051-900, Via Ipê Amarelo, S/N, João Pessoa, Brazil

Abstract

Introduction: Although drugs currently available for the treatment of anxiety and de-pression act through modulation of the neurotransmission systems involved in the neurobiology of the disorder, yet they often present side effects, which can impair patient adherence to treatment. Methods: This has driven the search for new molecules with anxiolytic and antidepressant potential. Aromatic plants are rich in essential oils, and their chemical constituents, such as monoterpenes, are being studied for these disorders. This study aims to evaluate the anxiolytic and antidepressant-like potential of the monoterpene tetrahydrolinalool in in vivo animal models and review pharmacologi-cal targets with validation through molecular docking. Male Swiss mice (Mus musculus) were treat-ed with THL (37.5-600 mg kg-1 p.o.) and submitted to the elevated plus maze, open field, rotarod, and forced swim tests. In the elevated plus-maze, THL at doses of 37.5 and 75 mg kg-1 induced a significant increase in the percentage of entries (72.7 and 64.3% respectively), and lengths of stay (80.3 and 76.8% respectively) in the open arms tests. Results: These doses did not compromise locomotor activity or motor coordination in the animals. In the open field, rotarod tests, and the forced swimming model, treatment with THL significantly reduced immobility times at doses of 150, 300, and 600 mg kg-1, and by respective percentages of 69.3, 60.9 and 68.7%. Conclusion: In molecular docking assay, which investigated potential targets, THL presented satis-factory energy values for: nNOs, SGC, IL-6, 5-HT1A, NMDAr, and D1. These demonstrate the po-tential of THL (a derivative of natural origin) in in vivo and in silico models, making it a drug can-didate.

Funder

Coordination for the Improvement of Higher Education Personnel (Capes) - Brazil

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,General Medicine

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