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Phenols, flavonoids and antioxidant activity of aqueous and methanolic extracts of propolis (Apis mellifera L.) from Algarve, South Portugal

Abstract

Propolis is a resinous substance collected by honeybees to seal honeycomb, which has been used in folk medicine due to its antimicrobial and antioxidant properties. In the present study, water and methanol were used to extract phenols and flavonoids from propolis collected in thirteen different areas in the Algarve region during the winter and spring. The ABTS•+, DPPH•, and O2•- scavenging capacity, and metal chelating activity were also evaluated in the propolis samples. Methanol was more effective than water in extracting total phenols (2.93-8.76 mg/mL) (0.93-2.81 mg/mL). Flavones and flavonols were also better extracted with methanol (1.28-2.76 mg/mL) than with water (0.031-0.019 mg/mL). The free radical scavenging activity, ABTS (IC50=0.006-0.036 mg/mL), DPPH (IC50=0.007-0.069 mg/mL) and superoxide (IC50=0.001-0.053 mg/mL), of the samples was also higher in methanolic extracts. The capacity for chelating metal ions was higher in aqueous extracts (41.11-82.35%) than in the methanolic ones (4.33-29.68%). Propolis from three locations of Algarve region were richer in phenols and had better capacity for scavenging free ABTS and DPPH radicals than the remaining samples. These places are part of a specific zone of Algarve known as Barrocal.

Algarve; propolis; antioxidant activity


RESEARCH PAPER

Phenols, flavonoids and antioxidant activity of aqueous and methanolic extracts of propolis (Apis mellifera L.) from Algarve, South Portugal

Maria Graça MiguelI, * * Corresponding author ; Susana NunesII; Susana Anahi DandlenII; Ana Maria CavacoII; Maria Dulce AntunesI

ICentro de Biotecnologia Vegetal, Faculdade de Ciências e Tecnologia, Universidade do Algarve - UAlg, Faro, Portugal, e-mail: mgmiguel@ualg.pt

IIFaculdade de Ciências e Tecnologia, Universidade do Algarve - UAlg, Faro, Portugal

ABSTRACT

Propolis is a resinous substance collected by honeybees to seal honeycomb, which has been used in folk medicine due to its antimicrobial and antioxidant properties. In the present study, water and methanol were used to extract phenols and flavonoids from propolis collected in thirteen different areas in the Algarve region during the winter and spring. The ABTS+, DPPH, and O2- scavenging capacity, and metal chelating activity were also evaluated in the propolis samples. Methanol was more effective than water in extracting total phenols (2.93-8.76 mg/mL) (0.93-2.81 mg/mL). Flavones and flavonols were also better extracted with methanol (1.28-2.76 mg/mL) than with water (0.031-0.019 mg/mL). The free radical scavenging activity, ABTS (IC50=0.006-0.036 mg/mL), DPPH (IC50=0.007-0.069 mg/mL) and superoxide (IC50=0.001-0.053 mg/mL), of the samples was also higher in methanolic extracts. The capacity for chelating metal ions was higher in aqueous extracts (41.11-82.35%) than in the methanolic ones (4.33-29.68%). Propolis from three locations of Algarve region were richer in phenols and had better capacity for scavenging free ABTS and DPPH radicals than the remaining samples. These places are part of a specific zone of Algarve known as Barrocal.

Keywords: Algarve; propolis; antioxidant activity.

1 Introduction

Propolis is a resinous substance collected by honeybees from leaf buds and exudates from various plant sources, which is employed to seal and repair honeycomb. Propolis has several functions in beehives: seal holes in the hives, exclude draught, protect against external invaders, and mummify their carcasses. In addition to these functions, propolis is also important for bees in the prevention of growth and decomposition of micro-organisms (Pietta et al., 2002; Santos et al., 2002; Salomão et al., 2004).

Usually, propolis is not used as raw material but rather as an extract, and several solvents have been used to obtain these extracts. Ethanol 70 %, methanol, or water have been referred as good solvents to extract polyphenolic compounds from propolis (Gómez-Caravaca et al., 2006; Martos et al., 1997; Cao et al., 2004; Nakajima et al., 2007).

Propolis generally contains several types of compounds, such as polyphenols (flavonoids and phenolic acids and their esters), terpenoids, steroids, and aminoacids (Kumazawa et al., 2004). Polyphenols that can be found in the resinous part of raw propolis have been proved to inhibit specific enzymes, stimulate some hormones and neurotransmitters, scavenge free radicals, and prevent multiplication of micro-organisms (Cao et al., 2004; Sforcin, 2007). However, such properties can change depending on the composition and polyphenols content that in turn depend on several factors including season, vegetation of the area, geographical origin, and the state of propolis (fresh or aged) (Cao et al., 2004).

In Brazil, there is legislation to regulate the quality of ethanol extract of propolis (Tagliacollo & Orsi, 2011); however, in Portugal, only very recently has there been studies concerning the chemical and biological properties of propolis from Portugal (Falcão et al., 2010; Miguel et al., 2010; Cardoso et al., 2011; Valente et al., 2011; Silva et al., 2012).

In the present study, two solvents, water and methanol, were used to extract phenols, including flavonoids, from propolis collected in various areas of Algarve, south Portugal, during two different seasons (winter and spring). Gum rockrose, rosemary, lavender, strawberry tree, and carob tree predominated in the areas where the samples of propolis were collected.

2 Materials and methods

2.1 Propolis

Several samples of propolis were collected in various areas of Algarve during two collection times (winter and spring 2008/2009) for analysis of phenol content and antioxidant activity (Table 1).

2.2 Analysis

Aqueous and methanolic extracts

Propolis (1.0 g) was divided into small pieces and extracted with 10 mL of water at 80 °C for 3 h, as reported elsewhere (Midorikawa et al., 2001). This extract was used for analysis of the aqueous extract. The residue was further extracted with methanol (100 mL) under reflux for 3 h, filtered, and evaporated under reduced pressure without reaching dryness; the final volume was adjusted with methanol. This extract was used for analysis of the methanolic extract.

Total phenolic content

Total phenolic content was determined according to the Folin-Ciocalteau colorimetric method (Singleton; Rossi, 1965). Pinocembrin was used as standard for the calibration curve. The sample (0.5 mL) and 2 mL of sodium carbonate (75 g/L) were added to 2.5 mL of 10% (w/v) Folin-Ciocalteau reagent. After 30 min of reaction at room temperature, absorbance was measured at 765 nm.

Flavone and flavonol content

The content of these groups of compounds was quantified as described by Ahn et al. (2007). Briefly, 0.5 mL of 2% AlCl3-ethanol solution was added to 0.5 mL of sample or standard. After 1 h at room temperature, absorbance was measured at 420 nm. Quercetin was used as a standard for the construction of the calibration curve.

Flavanone and dihydroflavonol content

The total quantification of flavanone and dihydroflavonol compounds was performed as reported by Popova et al. (2004). Briefly, an aliquot (1 mL) of the sample or standard and 2 mL DNP (2,4-dinitrophenylhydrazine) solution (1 g DNP in 2 mL 96% sulphuric acid, diluted to 100 mL with methanol) were heated at 50 °C for 50 min. After cooling at room temperature, the mixture was diluted to 10 mL with 10% KOH in methanol (w/v). A sample (1 mL of the resulting solution) was added to 10 mL methanol and diluted to 50 mL with methanol. Absorbance was measured at 486 nm.

ABTS+ free radical-scavenging activity

The determination of ABTS+ radical scavenging activity was carried out as reported by Dorman & Hiltunen (2004). Briefly, the ABTS+ radical was generated by the reaction of an (7 mM) ABTS aqueous solution with K2S2O8 (2.45 mM) in the dark for 16 h adjusting the absorbance at 734 nm to 0.700 at room temperature. The samples (10 µL) were added to 1490 µL ABTS+, absorbance at 734 nm was read immediately (A0) and after 6 min (A1). Several concentrations were measured, and the percentage inhibition [(A0-A1/A0) x 100] was plotted against the phenol content and IC50 was determined (concentration of total phenol able to scavenger 50% of ABTS+ free radical).

DPPH free radical-scavenging activity

Fifty microlitres of various concentrations of propolis samples were added to 2 mL of 60 µM methanolic solution of DPPH. Absorbance measurements were read at 517 nm after 20 min of incubation time at room temperature (A1). Absorbance of a blank sample containing the same amount of methanol and DPPH solution acted as the negative control (A0). The percentage inhibition [(A0-A1/A0) × 100] was plotted against the phenol content and IC50 was determined.

Scavenging ability of superoxide anion radical

Scavenging ability of superoxide anion radical was evaluated as previously reported by Nagai et al. (2003). The procedure was initiated by mixing 1.2 mL of 0.05 M sodium carbonate buffer (pH 10.5), 0.1 mL of 3 mM xanthine, 0.1 mL of 3 mM ethylenediaminetetraacetic acid disodium salt (EDTA), 0.1 mL of 0.75 mM nitroblue tetrazolium (NBT), and 0.1 mL of propolis sample. After holding at 25 °C for 10 min, the reaction was started by adding 6 mU xanthine oxidase (XOD) and was carried out at 25 °C for 20 min. Next, the reaction was stopped by adding 0.1 mL of 6 mM CuCl2. The absorbance of the reaction mixture was measured at 560 nm. The amount of the formazan that was reduced from NBT by superoxide was measured, and the inhibition rate was determined. IC50 was calculated by plotting in a graphic the inhibition ratio against the content of total phenols.

Chelating metal ions

The degree of chelating ferrous ions by propolis was evaluated according to the method described by Wang et al. (2004). The samples were incubated with 0.05 mL of FeCl2.4H2O (2 mM). The reaction was initiated by adding 5 mM ferrozine (0.2 mL) and after 10 min, absorbance was read at 562 nm. An untreated sample served as the control. The percentage of chelating ability was determined according to the formula: (A0-A1)/A0 × 100, where A0 is the absorbance of the untreated sample and A1 the absorbance of the propolis sample.

2.3 Statistical analysis

The significant differences between the antioxidant activities, phenols, and flavonoids of the different samples of propolis were determined by two-way ANOVA and Duncan's Multiple-Range Test using the SPSS 16.0 software (SPSS Inc.). Correlations between phenol, flavonoids and antioxidant activity were determined by Pearson correlation coefficient. In each zone and for each season of the year six samples that served as replications were taken.

3 Results and discussion

The levels of phenols in the aqueous extracts of propolis from various areas of Algarve are shown in Table 2. During the winter, the highest amounts were found in the samples from Ame (2.61 mg/mL) and Arr (2.81 mg/mL), in contrast to those of Mad (0.93 mg/mL). In the same season, methanolic extracts from Ame (8.10 mg/mL) and Arr (8.76 mg/mL) also had higher amounts of phenols than that of the remaining methanolic extracts (Table 3). However, it is important to stress that the phenol content found in methanolic extracts were about 3-4 times higher than that found in the aqueous extracts. Park et al. (1998) also found that water was not a good solvent to extract phenols from propolis. Some authors (Park & Ikegaki, 1998) reported lower absorption in water extracts of propolis than in ethanolic extracts, in spite of similar absorption spectra at wavelengths in the range 200-500 nm. During spring, relative higher amounts of phenols in the aqueous extracts were found in samples from Ame (2.65 mg/mL), Arr (2.27 mg/mL), Pes (2.34 mg/mL), and Cal (2.36 mg/mL) (Table 2). In the same season, phenol amounts in the methanolic extracts of Ame (7.02 mg/mL), Arr (6.40 mg/mL), and Pes (7.62 mg/mL) were 6 mg/mL higher than those found during the winter (Table 3). The samples of VCV also had relatively higher amounts of total phenols (6.24 mg/mL).

The effects of the geographic origin on the chemical composition of propolis and its biological activities have already been reported (Bankova et al., 2000; Kumazawa et al., 2004; Bankova, 2005). In Portugal, extracts of propolis collected in Trás-os-Montes (Northest) and Beira Interior also had different phenol concentrations (Moreira et al., 2008). In the same region (Algarve), it was found in the present study that different places showed different phenol contents.

Flavanones and dihydroflavonols were 20-30 times higher compared to flavonols and flavones in the aqueous extracts (Table 2). In contrast, the values of these two groups of flavonoids were of the same order of magnitude in the methanolic extracts (Table 3). Owing to their phenolic nature, flavonoids are quite polar but are poorly water soluble, which can explain the higher concentrations of these two groups of flavonoids in methanolic extracts than in the aqueous extracts (Table 2 and 3). However, it is noteworthy that water was less effective in extracting flavones and flavonols than flavanones and dihydroflavonols. Comparing the concentrations of flavones and flavonols in both extraction solvents (Table 2 and 3), the methanolic extracts had about 10 times more flavones and flavonols than the aqueous extracts, while for flavanones and dihydroflavonols, the values were twice as high.

The most commonly studied propolis types include those from Europe, North America, non-tropic regions of Asia, Russia, Brazil, Cuba, Venezuela, the Pacific region (Okinawa, Taiwan), and the Canary Islands (Bankova, 2005). Flavones, flavanones and cinnamic acids and their esters are the major constituents of the European propolis (Bankova, 2005). Cinnamic acids and their esters may constitute the remaining phenols present in the propolis samples of the present study, which were not quantified.

Aqueous extracts of propolis collected from Arr in the winter were the richest in flavones and flavonols and flavanones and dihydroflavonols (0.029 and 0.85 mg/ml, respectively), while in the spring, Cal was the place where higher amounts of those flavonoids were found (0.031 and 0.92 mg/mL, respectively) (Table 2). With regards to the methanolic extracts in the winter samples, those with the highest amounts of flavones and flavonols were found in the extracts from Ame (2.17 mg/mL), Arr (2.76 mg/mL), and Pes (2.45 mg/mL), whereas those from Arr (2.54 mg/mL) had significant higher levels of flavanones and dihydroflavonols than those of other areas (Table 3). In the spring, the samples from Pes had generally higher concentrations of flavones and flavonols, and flavanones and dihydroflavonols (2.49 mg/mL and 2.88 mg/mL, respectively) than those from the other places. The sole exception was the sample from Ame, which had the same concentration of flavanones and dihydroflavonols as the sample from Pes.

As for the concentrations of total phenols and flavonoids, it seems that an increase in phenols leads to an increase in flavonoids. In fact, a significant correlation between total phenols and flavones and flavonols was obtained either in aqueous or methanolic extracts (r=0.791 and r=0.917, respectively) at the P<0.01 level in a two-tailed Pearson correlation. Significant correlations between total phenols and flavanones and dihydroflavonols were also obtained (r=0.917 and r=0.478, respectively) (Table 4).

According to the results obtained in the present study, total phenols, flavanones, and dihydroflavonols showed significant differences between collection seasons in the methanolic extracts. They were significantly higher (P<0.05) for phenols in the winter than in the spring, while the opposite occurred for flavanones and dihydroflavonols. In the aqueous extracts such significant differences were only observed in flavones and flavonols, which were higher in the spring.

Tables 5 and 6 show the antioxidant activity of propolis samples, extracted with water and methanol, respectively, collected in different areas of Algarve, during the winter and spring.

In the majority of the aqueous samples, it was not possible to determine the concentration of phenols able to scavenge 50% of the free radicals; therefore the values were given as percentage of free radical scavenging ability of the samples when the same volume of extract was used (Table 4).

The aqueous extracts of propolis collected in Ame, Arr, and Pes, either in the winter or spring, had the best ability to scavenge ABTS and DPPH free radicals and the superoxide anion radical. In the spring, the VCV samples had similar capacity to scavenge superoxide anion radicals (Table 5). The best activity found in the propolis extracts from Ame, Arr, and Pes may be related to their higher content of phenols, including flavonoids (Table 2) (Kähkönen et al., 1999). The antioxidant ability of propolis from different origins has been reported: propolis from Argentine (Isla et al., 2001, 2005; Lima et al., 2009); Brazil (Nagai et al., 2003; da Silva et al., 2006; Cabral et al., 2009); China (Ahn et al., 2007); Colombia (Palomino et al., 2009); Greece and Cyprus (Kalogeropoulos et al., 2009); Iran (Mohammadzadeh et al., 2007); Japan (Kumazawa et al., 2007); Korea (Ahn et al., 2004); Taiwan (Chen et al., 2008), and Turkey (Geckil et al., 2005). Recently, the antioxidant activity has also been reported for propolis from Northern and Southern Portugal (Moreira et al., 2008; Miguel et al., 2010).

Relating the biological activity of propolis extracts with the concentration of individual phenol components may be difficult according to some authors; hence, it is preferable to compare family of compounds with their biological activity (Bankova, 2005). Nevertheless, there are some authors that have been able to relate antioxidant activity to specific compounds, such as kaempferol and phenethyl caffeate (Kumazawa et al., 2004) or prenylated flavonoids (Kumazawa et al., 2007). In the present study, it was only possible to confirm the direct relationship between antioxidant activity and phenol content. In fact, a significant correlation between total phenols and scavenging free DPPH radicals (r=0.831), free ABTS radicals (r=0.870), and superoxide anion radicals (r=0.628) was obtained at the P<0.01 level in a two-tailed Pearson correlation (Table 4). The same significant correlation was also observed when comparing flavones and flavonols with DPPH, ABTS, and superoxide scavenging ability (r=0.711, r=0.579 and r=0.424, respectively). With regards to the flavanones and dihydroflavonols, this correlation was only verified with ABTS (Table 3).

When the extraction was performed with methanol, higher quantity of phenols were extracted, as reported above, corresponding to higher antioxidant activity that allow determining IC50 values, which was not possible when water was used as the extraction solvent. In methanol extracts, the samples from Ame, Arr, and Pes were the best in terms of scavenging free ABTS and DPPH radicals, either in the winter or spring (Table 6). In the spring, VCV revealed to be also a good scavenger of free radicals. As for the superoxide anion radicals, the extracts from VCV were the best for quenching this free radical in both collection seasons, along with samples from Pes and Sar, but only in the spring. The correlation between phenols and ABTS or DPPH does exist although it is an inverse correlation because the activity in this case is measured as the concentration of phenols able to scavenge free radicals; therefore, the lower concentration of phenols corresponds to the best activity. The correlations found between phenols and ABTS or DPPH were r= - 0.683 and r= - 0.583, respectively. For superoxide and phenols no significant correlation was found, neither for superoxide and flavanones and dihydroflavonols (Table 4). Flavones and flavonols correlated well with all free radicals assayed (Table 4).

The capacity of the methanolic extracts assayed in the present study to scavenge free radicals revealed that samples from Ame, Arr, and Pes were better than those reported by some authors for other propolis samples from different origins (China, Korea, Argentine, Brazil, China, Hungary, Thailand, Ukraine, Uzbekistan, Australia, Bulgaria, New Zealand, South Africa, and United States) (Kumazawa et al., 2004; Ahn et al., 2004; 2007). In our case, 7-12 µg/mL of phenol content in methanolic extracts was able to quench 50% of free ABTS and DPPH radicals, values significantly lower than those described by those authors that reported values ranging from 20 to 500 µg/mL.

Superoxide scavenging capacity of water extracts of Brazilian propolis has already been reported by some authors (Nagai et al., 2003). These authors found that 1 mg/mL propolis scavenged 87% of superoxide anion radicals. This value is relatively high when compared to the values found in the present study, mainly those resulting from methanolic extraction. In this case, the samples from VCV, Pes, and Sar with phenol content ranging from 10-16 µg/mL were able to quench 50% of superoxide anion radical.

Phenols, flavanones and flavonols, and flavanones and dihydroflavonols correlated well with DPPH and ABTS, in both collection seasons; on the other hand, this was not so evident with superoxide anion radical, mainly when comparing the capacity for quenching these radicals with flavanones and dihydroflavonols content.

The chelating activity of the aqueous extracts of propolis was unexpectedly better than that of the methanolic assays (Tables 5 and 6); in perfect contrast to those found for free radical scavenging and also in contrast to that reported by some other authors (Geckil et al., 2005). Studying Turkish propolis, these authors found that ethanolic extracts were better chelating agents than the aqueous extracts. Some authors (van Acker et al., 1996), investigating the chelating activity of some individual flavonoids, found that naringin, pelargonidin, phloridzin, and hesperitin had no chelating activity, contrary to apigenin, diosmin, phloretin, fisetin, cyanidanol, taxifolin, and naringenin, which presented good chelating properties. Therefore, different phenolic components present in aqueous and methanolic extracts, as for example, flavonoids, may have contributed to these results.

In the winter and spring, the aqueous extracts from Sob and Ame presented the best chelating activities (82.35 and 71.34%, respectively), whereas the methanolic extracts from Mad (29.68 and 13.99% in winter and spring, respectively) showed the best activity independent on the collection season (Tables 5 and 6).

According to the results obtained in the present study, the capacity of methanolic extracts to scavenge free ABTS and DPPH radicals showed significant differences between the collection seasons; and it was significantly higher (P<0.05) in the spring than in the winter.

In the aqueous extracts, the significant differences between the collection seasons were observed in ABTS, DPPH, and superoxide scavenging activities and also in the amounts of flavanones and dihydroflavonols. Nevertheless such variation was greatly dependent on the collection place. The other compounds studied did not show significant differences.

4 Conclusion

This study allowed concluding that phenols, flavones, flavonols, flavanones, and dihydroflavonols from propolis of Algarve were better extracted with methanol than with water. The capacity of water to extract flavones and flavonols was substantially lower than that of methanol (about ten times lower).

From the 13 places where the propolis samples were collected, only three (Ame, Arr, and Pes) proved the richest in phenols with consequent better capacity to scavenge free DPPH and ABTS radicals (Ame, Arr, Pes, and in some cases VCV). Ame, Arr, and Pes are part of zone in Algarve called Barrocal, from where the flora was not determined in the present study.

The chelating activity of the propolis samples was better in the aqueous extracts than in the methanolic extracts. In this case, the samples from Sob, Ame, and Mad proved the most effective in chelating metal ions.

In the methanolic extracts, significant differences between the winter and spring were observed in the content of total phenols, and flavanones and dihydroflavonols, in the scavenging of free ABTS and DPPH radicals and in chelating metal ions. As for the aqueous extracts, these differences were found in the content of flavanones and dihydroflavonols and in the scavenging of free ABTS, DPPH, and superoxide radicals.

Acknowledgments

The authors are grateful to Mr. Helder Guia for the propolis supply, to "Cruz Alta, Lda." for granting the scholarship, and for the financial support provided by CDCTPV (Portugal). This study was also funded by CEOT and the Programa Nacional de Re-equipamento Científico (PNRC) - FCT (Fundação para a Ciência e a Tecnologia) (REEQ/601/EEI/2005) and the POCI 2010 - FEDER. Ana M. Cavaco is an assistant researcher of CEOT funded by FCT under Programa Ciência 2008 (Contratação de Doutorados para o Sistema Científico e Tecnológico Nacional).

Received 04 Nov., 2012

Accepted 03 May, 2013 (005923)

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    Corresponding author
  • Publication Dates

    • Publication in this collection
      25 Apr 2014
    • Date of issue
      Mar 2014

    History

    • Accepted
      03 May 2013
    • Received
      04 Nov 2012
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