Planta Med 2011; 77(3): 236-241
DOI: 10.1055/s-0030-1250315
Biological and Pharmacological Activity
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Anxiolytic Effects of a Semipurified Constituent of Guaraná Seeds on Rats in the Elevated T-Maze Test

Camila Marroni Roncon1 , Camila Biesdorf de Almeida1 , Traudi Klein1 , João Carlos Palazzo de Mello1 , Elisabeth Aparecida Audi1
  • 1Department of Pharmacy and Pharmacology, State University of Maringá, Maringá, PR, Brazil
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Publikationsverlauf

received March 23, 2010 revised July 26, 2010

accepted August 5, 2010

Publikationsdatum:
15. September 2010 (online)

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Abstract

The objective of this study was to investigate the effects of chronic administration of a semi-purified extract (Purified Extract A – PEA; 4, 8, or 16 mg/kg) of Paullinia cupana (guaraná) seeds on rats submitted to the elevated T-maze (ETM) model of generalized anxiety and panic disorders. The selective serotonin (5-HT) reuptake inhibitor (SSRI) paroxetine (PAR; 3 mg/kg), was used as a positive control. To evaluate possible serotonergic and dopaminergic neurotransmission involvement in the action of PEA during the ETM test, ineffective doses of metergoline (MET; 5-HT2A/2C antagonist receptor) or sulpiride (SUL; dopaminergic receptor antagonist) were acutely administered together with the PEA. The locomotion of the rats was assessed in a circular arena following each drug treatment. Both PEA (8 and 16 mg/kg) and PAR (3 mg/kg) increased one-way escape latencies from the open arm of the ETM, indicating a panicolytic effect compared to the control group. MET, in higher doses (1, 2 or 3 mg/kg), produced a panicolytic effect in the ETM test, whereas SUL did not (10, 20 or 40 mg/kg). The panicolytic effect produced by PEA (8 mg/kg) was blocked by both MET (2 mg/kg) and SUL (20 mg/kg), whereas the panicolytic effect produced by PAR (3 mg/kg) was blocked only by MET (2 mg/kg). These results show that chronic treatment with PEA produces a panicolytic effect during the ETM test, and that the dopaminergic and the serotonergic neurotransmission systems are involved in this effect.

References

Prof. Dr. Elisabeth Aparecida Audi

Department of Pharmacy and Pharmacology
State University of Maringá

Av. Colombo, 5790

Zona 7, CEP

87020-900 Maringá, PR

Brazil

Telefon: + 55 44 30 11 48 44

Fax: + 55 44 32 61 49 99

eMail: eaaudi@uem.br