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Brazilian Archives of Biology and Technology

Print version ISSN 1516-8913On-line version ISSN 1678-4324

Braz. arch. biol. technol. vol.49 no.4 Curitiba July 2006

http://dx.doi.org/10.1590/S1516-89132006000500005 

HUMAN AND ANIMAL HEALTH

 

Sedative and anxiolytic effects of methanolic extract from the leaves of Passiflora actinia

 

 

Kely Cristina dos SantosI; Stella Maris Tessaro Figura KurtzI; Simony Davet MüllerII; Maique Weber BiavattiII; Rúbia Maria Monteiro Weffort de OliveiraIII; Cid Aimbiré de Moraes SantosI, *

ILaboratório de Farmacognosia; Departamento de Farmácia; Universidade Federal do Paraná; Rua Prefeito Lothario Meissner, 3400; Jd. Botânico; cid@ufpr.br; 80210-170 - Curitiba - PR -Brasil
IINúcleo de Investigações Químico-Farmacêutica; Universidade do Vale do Itajaí; C. P. 360; 88302-20; Itajaí - SC -Brasil
IIIDepartamento de Farmácia e Farmacologia; Universidade Estadual de Maringá; Av. Colombo, 5790; Jardim Universitário; Bloco K-80; 87020-900; Maringá -PR - Brasil

 

 


ABSTRACT

Leaves from several Passiflora species are largely employed in the Brazilian folk medicine as anxiolytic and sedative. In this work the anxiolytic, sedative-like properties and liquid chromatography analysis of methanolic extract of Passiflora actinia were evaluated. The methanol extract and all of its fractions presented significant sedative-like effect in elevated plus-maze and open field tests. Only the aqueous fraction of the methanol extract showed selective anxiolytic activity (30 mg/kg). Chromatographic analysis of the active fractions showed the presence of isovitexin and absence of the classical Passiflora b-carboline alkaloids or flavonoids such as vitexin, rutin, swertisin, hesperidin and orientin. The tincture obtained from P. actinia leaves presented 0.27 mg/ml of isovitexin and absence of vitexin.

Key words: Anxiolytic, sedative, isovitexin, Passiflora actinia, Passifloraceae


RESUMO

Folhas de diversas espécies de Passiflora são amplamente empregadas na medicina popular brasileira como ansiolítica e sedativa. Neste trabalho, as propriedades ansiolíticas e sedativas e análise por cromatografia líquida dos extratos metanólicos de Passiflora actinia foram avaliados. O extrato metanólico e todas as suas frações apresentaram efeitos sedativos significativos nos testes de labirinto em cruz elevada e campo aberto. Somente a fração aquosa do extrato metanólico mostrou seletiva atividade sedativa (30 mg/kg). Análise cromatográfica das frações ativas mostraram a presença de isovitexina e ausência dos alcalóides b-carbolínicos clássicos de Passiflora ou flavonóides como vitexina, rutina, swertisina, hesperidina e orientina. A tintura obtida de P. actinia (folhas) apresentou 0,27 mg/ml de isovitexina e ausência de vitexina.


 

 

INTRODUCTION

In folk medicine, some wildspread Passiflora's species have been used for their sedative and anxiolytic effects. The principal bioactive compounds described in this genus are C-glycosil flavonoids (vitexin, isovitexin, orientin, isoorientin and apigenin) and b-carbolinic alkaloids (harman, harmin, harmalin, harmol and harmalol) (Blumenthal et al., 2000). Some reports have pointed out the harman alkaloids (Alonso, 1998) as the bioactive constituents of Passiflora incarnata Linneu, one of the species of Passiflora that have been extensively studied chemically and biologically (Dhawan et al., 2001; Soulimani et al., 1997). Others indicate the flavonoid chrysin (Wolfman et al., 1994; Zanoli et al., 2000) or even maltol (Aoyagi et al., 1974) as the putative substances responsible for the tranquilizer activities.

Passiflora actinia Hooker (vernacular name: maracujá-do-mato) is a liana widely distributed through Southern Brazil. Unlikely P. incarnata, so far there has been no report in literature about this species. It grows very well on the Brazilian soil (Cervi, 1981), which makes it a potential alternative for P. incarnata. The aim of the present study was to evaluate the possible anxiolytic and sedative properties of P. actinia methanol extract and its fractions in mice. Chromatographic analyses were performed in order to investigate the presence of some compounds previously described in the genus with hypothetical activity on these two parameters at the central nervous system (CNS).

 

MATERIALS AND METHODS

Plant material

Leaves of P. actinia Hooker were collected in Canguiri's Farm, Pinhais, Paraná, Brazil (November 2001) and the plant was identified by Dr. Armando Cervi. A voucher specimen was deposited at the Department of Botany Herbarium (UPCB nº 30.831), Universidade Federal do Paraná, PR, Brazil.

Preparation of extracts and fractions

The dried and powdered P. actinia leaves (750 g) were exhaustively and successively extracted in a Soxhlet apparatus with petroleum ether, CHCl3 and MeOH. Subsequently, the MeOH extract (100 g) was suspended in distilled water (1000 ml), shaken in water-iced bath for 8 h and refrigerated for 12 h. An aliquot (800 ml) of the filtered extract was alkalinized by NaHCO3 (pH 9.5) and partitioned sequentially with n-hexane and CHCl3 to yield 6.78 g and 3.77 g, respectively after drying the solvents under vacuum. The remaining H2O extract (aqueous fraction, 70.3 g) was subjected to column chromatography (aluminum oxide 90 Merck, activity I-II seg. Brokmann) eluted with a gradient of CHCl3-MeOH-H2O. The resulting joined fractions 3-6 (A, 1.8 g), 7-13 (B, 2.7 g) and 14-16 (C, 2.3 g) were subjected to liquid chromatography (LC) analysis and to biological tests as well as the crude MeOH extract and its fractions. The dosage form (tincture) was prepared with 45% ethanol in water, according to the Brazilian Pharmacopoeia 2nd Edition and Newall et al (1996).

Chromatographic analysis

HPLC analyses were performed using a Shimadzu LC-10AD (Tokyo, Japan) pump, a Luna RPC18 (5 µm), (250 x 4.6 mm i.d., 5 µm) column from Phenomenex (Torrance, CA, USA), a Shidmadzu SPD-M10A photodiode array detector and a Shimadzu CTO-10A column oven fit to 30ºC. A Rheodyne manual injector model 7725i was used for sample injection (Rohnert Park, CA, USA). All reagents used were HPLC grade. The C-glycosil flavonoids and the harmane alkaloids analyses consisted of linear gradient system with a flow-rate of 1 and 0.8 ml/min respectively, at 30 ºC.

Gradient elution for flavonoids analysis was: 1-20 min 10% solvent B (MeOH) and (10%) C (MeCN) in A (H2O-HOAc, 100:0.5, pH 2.88), 20-30 min 15% B and C in A, 30-35 min 20% B and C in A. The C-flavonoids (orientin, swertisin, vitexin, isovitexin) and also rutin and hesperidin were monitored at 340 nm. Gradient elution for alkaloids analysis was: 0-5 min 12% solvent B (MeOH) and 32% solvent C (MeCN) in A (phosphate buffer, pH 8.0), 5-18 min 20% B and 40% C in A, 18-30 min 12% B and 32% C in A. The harmane alkaloids harman, harmin, harmalol, harmol and harmaline (Fluka) were monitored at 350 nm. For the qualitative flavonoid analysis an isocratic elution mode (MeCN-H2O-HOAc 18:82:0,5) with a 1 ml/min flow rate was also employed. Extracts and standards were diluted in MeOH/H2O (1:1) (1:10 and 2:100 v/v respectively), filtered over regenerated cellulose membrane of 0.45 µm pore diameter (Schleicher and, Schuell, Dassel, Germany) and injected (20 µl).Isovitexin was determined in the plant material by external standard method (Snyder et al., 1997) at a concentration of 20 µg/ml diluted in triplicate to 4.0; 8.0; 12.0; 16.0 and 20.0 µg/ml. The software Shimadzu Class-VP 5.03 was used to fit the regression curve and for calculating the corresponding correlation coefficient. All samples were analysed in triplicate

Animals

Male albino-Swiss mice (30-45 g), housed in groups (n=5) with free access to food and water in a temperature controlled room (23±1ºC) with a 12 h light dark cycle, were used. The animals were allowed to acclimate to the testing room for at least 1 h prior the behavioral testing, which occurred between 9 to 12 am. The experiments were carried out according to the National Institute of Health Guide for Care and Use of Laboratory Animals, and all efforts were made to minimize animal suffering.

Treatments

Methanol extract (100, 300 and 600 mg/kg), as well as n-hexane, CHCl3 and aqueous crude fractions (30, 100 and 300 mg/kg), and chromatographic fractions A to C (10, 30 and 100 mg/kg) of P. actinia were administered intraperitoneally (i.p.) 30 min before the behavioural tests at a volume of 10 ml/kg. The extracts and fractions were solubilized in saline (NaCl, 0.9%) while n-hexane and CHCl3 crude fractions were solubilized in saline containing 2% DMSO. Diazepam (Dienpax, Sanofi-Wintrop Lab., Brazil, 1.0 mg/kg), used as a reference drug (positive control), was dissolved in FBB (propyleneglycol 60%, benzyl alcohol 2% in water) immediately before i.p. administration.

Behavioural tests

Elevated plus maze: The method initially suggested by Handley and Mithani (1984) was employed with minor modifications (Lister, 1987). The mice were individually placed in the center of the elevated plus maze and were allowed 5 min for free exploration. All sessions were videotaped. Afterwards, the number of open and enclosed arm entries, and time spent on open arms were manually registered. The percentage of open arm entries (100 x open/total entries) and the percentage of time spent in the open arms (100 x open/open + enclosed) were calculated for each animal.

Open field: Immediately after the elevated plus maze test, the animals were placed into the center of the open field in order to measure the locomotor activity (Royce, 1977). The animals could explore the space during 5 min. Sessions were videotaped and subsequently, hand operated counters and stopwatches were used to score the number of crossings (number of square floor units entered) and rearing (number of times the animal stood on hind legs).

Statistical analysis: The data were analyzed by t Student test or one-way analysis of variance (ANOVA) followed by the Tukey's test for multiple comparisons.

 

RESULTS

Chromatographic analysis

The chromatographic analysis of the active crude methanol extract and of the generated fractions showed absence of the classical b-carboline tested alkaloids (harman, harmin, harmalol, harmol and harmaline). The methanol extract and the aqueous fraction presented similar profile when analyzed under the flavonoid conditions. Only isovitexin was found in quantifiable amounts while traces of vitexin were detected in the fractions B and C. The flavonoids swertisin, rutin, orientin and hesperidin were not found in all fractions and extract tested. The methanolic extract, aqueous crude fraction, fractions B and C clearly presented other unidentified flavonoids than isovitexin according to their UV profile in the PDA detector. Quantitative HPLC analysis of P. actinia tincture showed 0.27 mg/ml of isovitexin, absence of vitexin and the presence of some other unidentified flavonoids. CHCl3 and n-hexane fractions, as well as fraction A did not show a flavonoid profile in the PDA detector.

Behavioral tests

As seen in Fig. 1, the reference drug, diazepam (1 mg/kg), increased the percentage of entries (t=3.7, df=16, p=0.0022) and of the time (t=3.6, df=16, p=0.0026) spent in the open arms of the elevated plus maze, without changing the number of enclosed arm entries.

 

 

Acute treatment with crude methanol extract of P. actinia at 300 and 600 mg/kg, significantly decreased the percentage of entries (F3,40 = 7.0, p<0.05) and the percentage of time spend in the open arms (F3,40 = 9.8, p<0.05, Fig. 2) of the elevated plus maze. In addition, the same doses significantly decreased the number of enclosed arm entries (F3,40 = 5.2, p<0.05).

 

 

The administration of the aqueous crude fraction of P. actinia 30 mg/kg (Fig. 3) produced a significant increase in the percentage of entries (F3,46 = 6.7, p<0.05) and in the percentage of time spent in the open arms of the elevated plus maze (F3,46 = 10.46, p<0.05) without any change in the number of enclosed entries. Higher doses of this fraction (100 and 300 mg/kg), significantly decreased the number enclosed arm entries (F3,46 = 20.5, p<0.001). The n-hexane and CHCl3 fractions failed to modify the parameters analyzed in the elevated plus maze test (data not shown). Fraction C showed a significant effect on the enclosed entries at doses of 30 and 100 mg/kg (F3.39 = 7.1, p<0.05).

 

 

As shown in Fig. 4, fraction A (10, 30 and 100 mg/kg; F3.41 = 30.5) and fraction B (10, 30 and 100 mg/kg, F3.41 = 12.1) also significantly (p<0.05) decreased the number of enclosed entries. However, only the fraction C produced a significant decrease in the percentage of open arm entries (F3.41=5.24, p<0.05) in the elevated plus maze. All together these results show a general decrease in the animal locomotion's activity.

 

 

The effects of P. actinia methanol extract and fractions on the open field test are shown in Table 1. The administration of methanol extract of P. actinia produced a significant decrease in the number of rearing (300 and 600 mg/kg, F3,40 = 6.2, p<0.05) and crossings (600 mg/kg, F3.40 = 4.5, p<0.05). Both doses of 100 and 300 mg/kg aqueous crude fraction of P. actinia decreased the number of rearing (F3,46 = 21.4, p<0.05) while only dose of 300 mg/kg significantly altered the number of crossings (F3,46 = 15.14, p<0.001). A significant decreased effect on locomotor activity of the animals was observed with fractions A and B at dose of 100 mg/kg either for the number of rearing (A, F3,41 = 34.20, p<0.001; B, F3,41 = 6.2, p<0.001 ) or number of crossings (A, F3,41 = 15.65, p<0.001; B, F3,41 = 3.6, p<0.05) (Table 1). Fraction C (30 and 100 mg/kg) also produced a significant decrease in the number of rearing (F3,39 = 7.7, p<0.05) and crossings (100 mg/kg, F3,39 = 2.9, p<0.05).

 

DISCUSION

The elevated plus maze test has been recognized as a valuable model able to predict anxiolytic or anxiogenic effects of drugs in rodents (Lister, 1987; Pellow and File, 1986). While anxiolytic compounds typically increase the percentage of open arms entries as well as the time spend in open arms, anxiogenics have the opposite effects. In addition, the number of the enclosed entries has been used as a parameter reflecting general motor activity. Confirming previous results (Bhattacharya, Mitra, 1991), the i.p. administration of diazepam (1 mg/kg) resulted in anxiolytic-like effect, characterized by an increase in the percentage of exploration in the open arms of the plus maze (Fig. 1). The methanol extract (300 and 600 mg/kg), otherwise, decreased the entries and time spent in the open arms (Fig. 2). Although this is usually interpreted as an anxiogenic effect, the extract administration also decreased the number of enclosed arms entries as well as the number of crossings and rearings in the open field test (Table 1), suggesting a sedative-like effect more than an anxiogenic effect. Furthermore, a decreased general activity was also observed after the administration of A, B and C fractions in lower doses as compared to the methanol extract, suggesting a major concentration of the putative active principle.

Interestingly, only the aqueous fraction at 30 mg/kg presented a selective anxiolytic effect evidenced by an increase of the percentage of open entries and time spent in the open arms without changing the number of enclosed entries (Fig. 3). Different results were described by Soulimani et al. (1997) using P. incarnata extracts. The authors observed that the aqueous extracts (400 and 800 mg/ kg) induced sedative effects while the hydroalcoholic extract (400 mg/kg) produced anxiolytic effect. Furthermore, the observed different effects were attributed to the solvents used to prepare the extracts. In the present work, the aqueous extract of P. actinia produced anxiolytic and sedative effect depending on the doses administered (Fig. 3).

In fact, sedative activity has been related to strong doses, while anxiolytic activity has been related to weak doses of plant extracts or reference drugs such as clorazepate (Rolland et al., 1991).

Although several reports have shown psychotropic effects for different species of Passiflora, there is no consensus about which substances are responsible for these effects. Increasing number of evidence point out the flavonoids as the responsible for the pharmacological effects. Vitexin, isovitexin, orientin, isoorientin (De-Paris et al., 2002) or chrysin (Wolfman et al., 1994; Zanoli, et al., 2000; Medina et al., 1990), have been involved in promoting the CNS effects. Recently, De Paris et al. (2002) have shown a correlation between the content of flavonoids found in aqueous extracts from Passiflora species and their psychotropic actions. In addition, Rocha et al. (2002) have suggested that orientin and isoorientin could be responsible for the observed anxiolytic-like effect of a butanolic fraction from Cecropia glazioui. However, controversial works report that pure vitexin and isovitexin showed no activity in CNS tests (Speroni and Minghetti, 1988) while orientin presented very mild anxiolytic effects (Okuyiama et al., 1996).

In this work isovitexin was present in most of the active extracts (methanol, aqueous, B and C fractions). Interestingly, in the fraction A, one of those that showed the highest sedative activity at 100 mg/kg (Fig. 2), none of the classical bioactive flavonoids analysed were identified by LC. Also, the UV profile in the PDA detector did not indicate the presence of other unknown flavonoid, due to the absence of characteristic absorption spectra of this class of compounds. The classical alkaloid standards (harman, harmin, harmaline, harmol and harmalol) could not be detected in the methanol extract or fractions.

The results showed that methanol extract and fractions obtained from P. actinia leaves demonstrated sedative and anxiolytic activities. Possibly, the anxiolytic and sedative activities observed in this work were not only dependent on the flavonoid or alkaloid content and other compounds belonging to different phytochemical classes were involved in the biological response observed in this work. Further studies would be necessary to evaluate the contribution of other substances for the activity showed as it still remains to be determined which components were responsible for these effects.

 

ACKNOWLEDGEMENTS

The authors thank Prof. Dr. A. Cervi (Universidade Federal do Paraná) for identification the plant material.

 

REFERENCES

Alonso, J. R. (1998), Tratado de fitomedicina: bases clínicas y farmacológicas. Buenos Aires: ISIS. pp.786-792.        [ Links ]

Aoyagi, N.; Kimura R. and Murata T. (1974), Studies on Passiflora incarnata dry extract. I. Isolation of maltol and pharmacological action of maltol and ethyl maltol. Chem. Pharm. Bull., 22, 1008-1013.        [ Links ]

Bhattacharya, S. K. and Mitra, S. K.(1991), Anxiolytic activity of Panax ginseng roots: an experimental study. J. Ethnopharmacol., 34, 87-92.        [ Links ]

Blumenthal, M.; Goldberg, A. and Brinckmann, J. (2000), Herbal Medicine: Expanded Comission E Monographs. Integrative Medicine, Newton Communications. pp.293-296.        [ Links ]

Cervi, A. C. (1981), Revisão do gênero Passiflora L. (Passifloraceae) do Estado do Paraná, Brasil. PhD. Thesis, Faculdad de Biologia, Universidad de Barcelona. Barcelona.        [ Links ]

De-Paris, F.; Petry, R. D.; Reginatto, F. H.; Gosmann, G.; Quevedo, J.; Salgueiro, J. B.; Kapczinski, F;; González-Ortega, G. and Schenkel, E. P. (2002), Pharmacochemical Study of Aqueous Extracts of Passiflora alata Dryander and Passiflora edulis Sims. Acta Farm. Bonaerense, 21, 5-8.        [ Links ]

Dhawan, K.; Kumar, S. and Sharma, A. (2001), Anti-anxiety studies on extracts of Passiflora incarnata Linneaus. J. Ethnopharmacol., 78, 165-170.        [ Links ]

Handley, S. L. and Mithani, S. (1984), Effects of alpha-adrenoceptors agonists and antagonists in a maze-exploration of fear-motivated behaviour. Naunyn. Schmiedebergs Arch. Pharmacol., 324, 1-5.        [ Links ]

Lister, R. G. (1987), The use of a plus-maze to measure anxiety in the mouse. Psychopharmacol., 92, 180-185.        [ Links ]

Medina, J. H.; Paladini, A. C.; Wolfman, C.; Levi de Stein, M.; Calvo. D.; Diaz, L. E. and Pena, C. (1990), Chrysin (5,7-di-OH-flavone), a naturally-occurring ligand for benzodiazepine receptors, with anticonvulsant properties. Biochemical Pharmacol. 40, 2227-2230.        [ Links ]

Newall, C. A.; Anderson, L. A. and Phillipson, J. D. (1996), Herbal medicines. A guide for health-care professionals. The Pharmaceutical Press, London, 206-207.        [ Links ]

Okuyama, E.; Okamoto, Y.; Yamazaki, M. and Satake, M. (1996), Pharmacologically active components of a Peruvian medicinal plant, huanarpo (Jatropha cilliata). Chem Pharmac Bull, 44, 333-336.        [ Links ]

Pellow, S. and File, S. E. (1986), Anxiolytic and anxiogenic drug effects on exploratory activity in an elevated plus-maze: a novel test of anxiety in the rat. Pharmacol. Biochem. Behav., 24, 525-529.        [ Links ]

Rocha, F. F.; Lapa, A. J. and Lima, T. C. (2001), Evaluation of the anxiolytic-like effects of Cecropia glazioui Sneth in mice. Pharmacol. Biochem. Behav., 71, 183-190.        [ Links ]

Rolland, A.; Fleurentin, J.; Lanhers, M. C.; Younos, C.; Misslin, R.; Mortier, F. and Pelt, J. M. (1991), Behavioural effects of the American traditional plant Eschscholzia californica: sedative and anxiolytic properties. Planta Med., 57, 212-216.        [ Links ]

Royce, J. R. (1977), On the construct vality of open-field measures, Psychological Bull., 84, 1098-1106.        [ Links ]

Snyder, L. R.; Kirkland, J. J. and Glajch, J. L. (1997), Practical LC Methods Development. 2. ed. New York: John Wiley and Sons. 655 pp.        [ Links ]

Soulimani, R.; Younos, C.; Jarmouni, S.; Bousta, D.; Misslin, R. and Mortier, F. (1997), Behavioural effects of Passiflora incarnata L. and its indole alkaloid and flavonoid derivatives and maltol in the mouse. J. Ethnopharmacol., 57, 11-20.        [ Links ]

Speroni, E. and Minghetti, A. (1988), Neuropharmacological activity of extracts from Passiflora incarnata. Planta Med., 54, 488-491.        [ Links ]

Wolfman, C.; Viola, H.; Paladini. A.; Dajas, F. and Medina, J. F. (1994), Possible anxiolytic effects of chrysin, a central benzodiazepine receptor ligand isolated from Passiflora coerulea. Pharmacol. Biochem. Behav., 47, 1-4.        [ Links ]

Zanoli, P. R.; Avallone, R. and Baraldi, M. (2000), Behavioral characterisation of the flavonoids apigenin and chrysin. Fitoterapia, 71, S117-S123.        [ Links ]

 

 

Received: November 03, 2004;
Revised: August 22, 2005;
Accepted: March 28, 2006.

 

 

* Author for correspondence

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