Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2012 / Article

Research Article | Open Access

Volume 2012 |Article ID 464238 | https://doi.org/10.1155/2012/464238

Noorlidah Abdullah, Siti Marjiana Ismail, Norhaniza Aminudin, Adawiyah Suriza Shuib, Beng Fye Lau, "Evaluation of Selected Culinary-Medicinal Mushrooms for Antioxidant and ACE Inhibitory Activities", Evidence-Based Complementary and Alternative Medicine, vol. 2012, Article ID 464238, 12 pages, 2012. https://doi.org/10.1155/2012/464238

Evaluation of Selected Culinary-Medicinal Mushrooms for Antioxidant and ACE Inhibitory Activities

Academic Editor: Y. Ohta
Received14 Jan 2011
Revised31 Mar 2011
Accepted12 Apr 2011
Published18 Jun 2011

Abstract

Considering the importance of diet in prevention of oxidative stress-related diseases including hypertension, this study was undertaken to evaluate the in vitro antioxidant and ACE inhibitory activities of selected culinary-medicinal mushrooms extracted by boiling in water for 30 min. Antioxidant capacity was measured using the following assays: DPPH free radical scavenging activity, -carotene bleaching, inhibition of lipid peroxidation, reducing power ability, and cupric ion reducing antioxidant capacity (CUPRAC). Antioxidant potential of each mushroom species was calculated based on the average percentages relative to quercetin and summarized as Antioxidant Index (AI). Ganoderma lucidum (30.1%), Schizophyllum commune (27.6%), and Hericium erinaceus (17.7%) showed relatively high AI. Total phenolics in these mushrooms varied between 6.19 to 63.51 mg GAE/g extract. In the ACE inhibitory assay, G. lucidum was shown to be the most potent species (IC50 = 50 g/mL). Based on our findings, culinary-medicinal mushrooms can be considered as potential source of dietary antioxidant and ACE inhibitory agents.

1. Introduction

Reactive oxygen species (ROS) have been implicated in food deterioration as well as pathogenesis of various human diseases and aging-related disorders [1]. Epidemiological studies have revealed the close association between intake of food rich in antioxidants such as vegetables, fruits, and cereals with prevention of the aforementioned pathologies [2]. Intake of exogenous antioxidants is crucial to maintain an adequate level of antioxidants in order to balance the ROS especially when human in vivo antioxidant defence and repair systems are considered to be insufficient to totally prevent the damage. Oxidative stress has been linked to hypertension—imbalance in superoxide and nitric oxide production will lead to reduced vasodilation [3]. If hypertension persists for a long period, it could be one of the risk factors for strokes, heart diseases, and eventually leading to chronic renal failure.

Synthetic antioxidants that are widely used in the food industry such as butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), and tert-butylated hydroxyquinine (TBHQ) have been reported to be carcinogenic; thus, their use has been restricted [4]. Treatments by administration of antihypertensive drugs, for example, inhibitors of the angiotensin I-converting enzyme (ACE) aim to reduce blood pressure and lower the risk of hypertension complications. However, the use of synthetic ACE inhibitors such as captopril and enalapril caused serious side effects including dry cough, skin rashes, and allergic reactions [5]. This situation has prompted the search for potential antioxidant and ACE inhibitors from natural sources.

Combination of both biological activities in one multifunctional preparation, especially in food, was suggested to be useful for controlling the risk of cardiovascular diseases [6]. In fact, Münzel and Keaney [3] proposed that ACE inhibitors possess novel antioxidant strategy by improving vasoconstriction, increasing bioactivity of nitric oxide, and inhibiting vascular superoxide production at its source. Therefore, consumption of antioxidant-rich foods which possess ACE inhibitory activity can be considered as an alternative therapy for treatment of hypertension especially for prehypertensive patients whose blood pressure is marginally or mildly high but not high enough to warrant the prescription of blood-pressure-lowering medications as suggested by Chen et al. [7].

Mushrooms are considered as functional food with physiological beneficial constituents [1] and consumption of several mushrooms such as Agaricus bisporus, Lentinula edodes, and Pleurotus spp. has become popular over the years. The broad medicinal values of mushrooms have a promising future as a branch of alternative medicine [8] and hence, scientific research directed to validation of claimed medicinal properties is vital. Mushroom decoctions in folk medicine often involve the use of hot water to extract soluble components from the fruiting body. Accordingly, crushed or small pieces of the fruiting body are boiled and the resulting decoction is consumed. Besides that, mushrooms are usually not eaten raw but subjected to various food processing procedures so that they will be more readily assimulated by digestion [9]. Hence, it can be said that preparation of hot water extracts similate cooking conditions—the typical way of how edible mushrooms are consumed.

Information obtained from analysis using hot water extracts was considered a better indicator of biological activities especially upon consumption [10, 11]. Since most reports on biological properties of mushrooms utilised various organic solvents for preparation of extracts, it is rather difficult to make comparisons between different laboratories taking into account variation in the procedures. Evaluation of several mushroom species using the same set of procedures is vital for accurate and fair comparison of biological activities studied. Hence, the objective of this study is to analyse the in vitro antioxidant and ACE inhibitory activities of hot water extracts of selected culinary-medicinal mushrooms.

2. Materials and Methods

2.1. Mushroom Collection

Fourteen species of culinary-medicinal mushrooms used in this study (Table 1) were obtained from mushroom farms and supermarkets in Selangor, Malaysia. The samples were identified and authenticated by experts in the Mushroom Research Centre, University of Malaya; voucher specimens were deposited in the University of Malaya herbarium (KLU).


Mushroom speciesTotal phenolic content
Scientific nameCommon name(s)(mg GAE/g extract)

Agrocybe sp.Black poplar mushroom; yangimatusutake (Japanese)
Auricularia auricular-judaeJelly mushroom; Judas’s ear fungus; kikurage “tree-jelly fish” (Japanese); mù ěr “wood ear” (Chinese)
Flammulina velutipesGolden needle mushroom; enokitake (Japanese); ū (Chinese)
Ganoderma lucidumReishi (Japanese); l ngzh (Chinese)
Hericium erinaceusLion’s mane mushroom; yamabushitake “mountain-hidden mushroom” (Japanese); hóutóugū “monkey head mushroom” (Chinese)
Lentinula edodesForest mushroom, shiitake “shii mushrooms” (Japanese); xiānggū “fragrant mushroom” (Chinese)
Pleurotus cystidiosusAbalone oyster; summer oyster mushroom
Pleurotus eryngiiKing oyster; king trumpet mushroom; French horn mushroom; eringi (Japanese); xìngbàogū “almond abalone mushroom” (Chinese)
Pleurotus flabellatusPink oyster mushroom
Pleurotus floridaWhite oyster mushroom
Pleurotus sajor-cajuGrey oyster mushroom
Schizophyllum communeBracket fungus; spilt-gill fungus; liezhejun (Chinese)
Termitomyces heimii“Termite nest fungus”
Volvariella volvaceaePaddy straw mushroom; fukurotake (Japanese); cǎogū (Chinese)

Positive controls

Quercetin
Butylated hydroxyanisole (BHA)
Ascorbic acid*

Values were expressed as mean ± standard deviation of three replicate determinations.
Mean values in a column with different lowercase letters (a–k) indicate significant difference at .
*The value is an estimation of total reducing capacity of ascorbic acid instead of its phenolic content.
2.2. Preparation of Mushroom Hot Water Extracts

All mushroom fruiting bodies were cleaned, cut into smaller pieces, and boiled in distilled water at the ratio of 1 : 10 (w/v) at 100°C for 30 min. Boiled mushrooms were cooled to room temperature, removed by using Whatman No. 1 filter paper and hot water extracts obtained were freeze-dried (Labconco). The extracts were kept in desiccator at room temperature for further analysis.

2.3. Estimation of Total Phenolic Content

Total phenolic content of the mushroom extracts was estimated using Folin-Ciocalteu reagent according to the method of Slinkard and Singleton [12] with some modifications. Initially, 250 μL of each mushroom extract was mixed with 250 μL of 10% Folin-Ciocalteu reagent, followed with the addition of 500 μL of saturated sodium carbonate (10% aqueous solution) after 2 min of incubation at room temperature. The mixture was kept in the dark for 1 h before absorbance was taken at 750 nm. A calibration curve using gallic acid (2–10 μg/mL) was prepared. Total phenolic content of the mushroom extracts was expressed as gallic acid equivalents (GAEs), which reflect the phenolic content as the amount of gallic acid (mg) in 1 g of extract.

2.4. Antioxidant Capacity Assays

In all assays, quercetin, butylated hydroxyanisole (BHA), and ascorbic acid were used as positive control.

2.5. Scavenging Effect on 1,1-Diphenyl-2-Picrylhydrazyl (DPPH) Radicals

The DPPH free radical scavenging activity of the extracts was measured according to the method of Brand-Williams et al. [13]. Stock solution of each mushroom extract (50 mg/mL) was diluted to a concentration in the range of 0.1 to 50 mg/mL. For the test, 3.9 mL of 0.06 mM DPPH radical (Sigma) was added to 0.1 mL of mushroom extract. Reaction mixture was vortexed and absorbance was measured at 515 nm using a spectrophotometer with methanol as the blank. The decrease in absorbance was monitored at 0 min, 1 min, 2 min, and every 15 min until the reaction has reached a plateau. The time taken to reach the steady state was determined by one-way analysis of variance (ANOVA). The DPPH free radical scavenging activity, expressed as percentage of radical scavenging activity, was calculated as follows: where A0 is the absorbance of 0.06 mM methanolic DPPH only whereas As is the absorbance of the reaction mixture.

2.6. -Carotene Bleaching Activity

-carotene bleaching activity of the mushroom extracts was evaluated using β-carotene-linoleic acid model system previously described [14] with some modifications. Briefly, 2 mg of -carotene in 10 mL chloroform was mixed with 40 μL of linoleic acid and 400 μL of Tween 80 emulsifier. Chloroform was allowed to evaporate under vacuum, prior to addition of 100 mL of distilled water with vigorous shaking. Then, 4.8 mL of the mixture was transferred into tubes containing different concentrations of extract. Upon addition of the emulsion into each tube, the zero time absorbance was measured at 470 nm using a spectrophotometer. The emulsion system was incubated for 2 h at 50°C.

2.7. Inhibition of Lipid Peroxidation of Buffered Egg Yolk

The ability of mushroom extracts to inhibit lipid peroxidation was determined according to the method of Daker et al. [15]. The reaction mixture contained 1 mL of fowl egg yolk emulsified with 0.1 M phosphate buffer (pH 7.4) to obtain a final concentration of 25 g/L and 100 μL of 1000 μM Fe2+. The stock solution of each mushroom extract (360 mg/mL) was prepared and then diluted to final extract concentrations of 0.1–30 mg/mL. The mixture was incubated at 37°C for 1 h before being treated with 0.5 mL of freshly prepared 15% trichloroacetic acid (TCA) and 1.0 mL of 1% thiobarbituric acid (TBA). The reaction tubes were further incubated in boiling water bath for 10 min. Once cooled to room temperature, the tubes were centrifuged at for 10 min to remove precipitated protein. Finally, 100 μL of supernatant was subjected to an absorbance reading at 532 nm to measure the formation of thiobarbituric acid reactive substances (TBARS). Buffered egg with Fe2+ only was used as control in this assay. The percentage inhibition was calculated from the following equation: where A0 is the absorbance of the control whereas As is the absorbance of the sample.

2.8. Reducing Power Ability

Reducing power of the mushroom extracts was determined according to the method of Öztürk et al. [16]. Diluted mushroom extracts were mixed with 2.5 mL of 0.2 M phosphate buffer (pH 6.6) and 2.5 mL of 1% potassium ferricyanide. Reaction mixtures were incubated at 50°C for 20 min. After the addition of 2.5 mL of 10% TCA, the mixture were centrifuged for 10 min at 1 000 rpm. Then, 2.5 mL of the supernatant were mixed with 2.5 mL of distilled water and 0.5 mL of 0.1% ferric chloride. Absorbance was measured at 700 nm against a blank.

2.9. Cupric-Ion-Reducing Antioxidant Capacity (CUPRAC)

CUPRAC assay was performed according to the method by Öztürk et al. [16] with some modifications. The test mixture contained 1 mL of 10 mM of copper (II), 7.5 mM neocuproine, and 1 M ammonium acetate buffer (pH 7.0). Briefly, 1 mL of diluted mushroom extracts in the concentration range of 0.1–20 mg/mL were added to the reaction tubes to achieve final volume of 4 mL. The tubes were incubated for 30 min at room temperature before absorbance at 450 nm was recorded against a blank.

2.10. Antioxidant Index (AI)

The Antioxidant Index as proposed by Puttaraju et al. [17] was used to grade the selected culinary-medicinal mushrooms on the basis of their antioxidant potential. Mushroom extracts were graded in a numerical scale based on quercetin which is considered to be equivalent to 100 (Table 5). AI represents the average relative percentages compared to quercetin obtained using five different methodologies for evaluation of antioxidant capacity described above.

2.11. ACE Inhibitory Assay

The ACE inhibitory activity assay was performed according to the method by Nakamura et al. [18] with some modifications. Briefly, 200 L of 5 mM hippuryl-L-histidine-L-leucine (HHL) (Sigma) solution was mixed with 50 L of each mushroom extract and the mixture was preincubated at 37°C for 3 min. The reaction was initiated by the addition of 20 L of 0.1 U/mL ACE (Sigma) solution and the mixture was again incubated at 37°C for 30 min. The reaction was terminated with the addition of 250 L of 1 N HCl. Then, 1.5 mL of ethyl acetate was added to extract the hippuric acid liberated by the reaction. The solution was centrifuged for 10 min; the ethyl acetate layer was then aspirated and evaporated under vacuum condition. The dried hippuric acid was redissolved in 1 mL of distilled water and measured spectrophotometrically at 228 nm. The ACE inhibitory activity of the mushroom extracts was determined by the following equation: where A is the absorbance of ACE and mushroom extracts, B is the absorbance of ACE and HHL and C is the absorbance of HHL only.

2.12. Statistical Analysis

All analysis was performed in triplicates and data was recorded as means ± standard deviation. Analysis was carried out using one-way analysis of variance (ANOVA) in Statgraphics Plus for Windows 3.0. The test stated any significant differences between the means at 95% () level were considered as statistically significant. Correlation and regression analysis were carried out using the Microsoft EXCEL.

3. Results and Discussion

3.1. Estimation of Total Phenolic Content

Considering the physiological importance of phenolic compounds and their contribution towards total antioxidant capacity, Folin-Ciocalteu method was used to estimate the total phenolic content of mushroom extracts. It must be noted that this reagent does not react exclusively with phenolics, but other reducing agents, for example, ascorbic acid as well [19, 20]. Hence, results of this test therefore reflect the total reducing capacity of the mushroom extracts and positive controls tested. Despite its tendency to overestimate the level of phenolics, this method is still widely employed prior to quantitative measurement of phenolics using high-performance liquid chromatography (HPLC) [21]. As shown in Table 1, total phenolic content of mushroom extracts tested varied from 6.19 to 63.51 mg GAE/g extract with G. lucidum having the highest phenolic content (63.51 ± 1.11 mg GAE/g extract).

Phenolic acids were reported to be the main phenolic compounds in mushrooms [21]. According to Puttaraju et al. [17], gallic acid, tannic acid, protocatechuic acid, and gentisic acids were some of the major phenolics detected in water extracts of several indigenous edible mushrooms from India. Besides, several authors have reported the correlation between the polarity of extraction solvent and phenolic content of resulting extracts [17, 22]. For instance, the phenolic content of H. erinaceus hot water extract in this study was determined to be  mg GAE/g extract, which was higher than that of methanolic extracts of fresh (0.26 mg GAE/g extract), oven-dried (2.37 mg GAE/g extract), and freeze-dried fruiting bodies (0.78 mg GAE/g extract) of the same species [23].

3.2. Antioxidant Capacity of Mushrooms

There is no single, universal method capable of providing an accurate, comprehensive picture of antioxidant profile because several mechanisms underlying antioxidant activity have been proposed including termination of free radical mediated chain reaction, hydrogen donation, chelation of catalytic ions, and elimination of peroxides [24]. Thus, a single assay is not sufficient to measure the total antioxidant capacity of the mushrooms. Moon and Shibamoto [25] recommended that a combination of electron scavenging and lipid peroxidation assays be used. The use of simplified model systems that closely resemble the main features of a given food system was suggested by Kulišić et al. [26]. Multiple assays based on different antioxidant mechanisms are crucial in providing a more reliable approach to assess the antioxidant capacity of the mushrooms. In the present study, a total of five methods—DPPH free radical scavenging activity, -carotene bleaching, inhibition of lipid peroxidation, reducing power ability, and CUPRAC— were used.

3.3. Scavenging Effect on DPPH Free Radicals

One of the most common methods for determination of antioxidant capacity is the DPPH free radical scavenging activity assay which relies on the reduction of methanolic DPPH solution in the presence of a hydrogen donating compound (antioxidant). The resulting decolourisation upon absorption of hydrogen from the antioxidant is stoichiometric with respect to the degree of reduction and the remaining DPPH, measured after a certain time, corresponds inversely to the radical scavenging activity of the antioxidant [27].

As shown in Table 2, the scavenging activity of mushroom extracts towards DPPH free radicals was expressed in terms of IC50. Since a lower IC50 value indicates stronger ability of the extracts to act as DPPH radical scavengers, then it is obvious that the positive controls were excellent DPPH radical scavengers with quercetin exhibited >100-fold higher scavenging activity (IC50 = 0.03 mg/mL) compared to the mushroom extracts (IC50 = 5.28–39.05 mg/mL). Investigated mushrooms showed DPPH free radical scavenging activity, acting possibly as primary antioxidants as suggested by Tsai et al. [11]. G. lucidum exhibited significant radical scavenging activity with IC50 of  5.28 mg/mL, followed by Agrocybe sp. and P. eryngii having IC50 of 9.56 and 15.42 mg/mL respectively. Apparently, F. velutipes displayed the weakest scavenging activity with an IC50 of 39.05 mg/mL.


DPPH free radical scavenging activity -carotene bleaching assayLipid peroxidation
Mushroom speciesIC50 (mg/mL)IC50 (mg/mL)Percentage of inhibition at 10 mg/mL

Agrocybe sp.
Auricularia auricular-judae
Flammulina velutipes
Ganoderma lucidum
Hericium erinaceus
Lentinula edodes
Pleurotus cystidiosus
Pleurotus eryngii
Pleurotus flabellatus
Pleurotus florida
Pleurotus sajor-caju
Schizophyllum commune
Termitomyces heimii
Volvariella volvaceae

Positive controls  

Quercetin
Butylated hydroxyanisole (BHA)
Ascorbic acid

Values were expressed as mean ± standard deviation of three replicate determinations.
Mean values in a column with different lowercase letters (a–h) indicate significant difference at .

The ability of hot water extract of other mushrooms to quench free radicals has been reported earlier. Hot water extracts of mature and baby Ling chih (Ganoderma tsugae Murrill) showed excellent antioxidant activities with low IC50 of 0.30 and 0.40 mg/mL, respectively [10]. In their study, Chirinang and Intarapichet [28] noticed that the radical scavenging activity of water extract of Pleurotus ostreatus (IC50 = 11.56 mg/mL) was better than that of P. sajor-caju (IC50 = 13.38 mg/mL) probably due to higher content of phenolic compounds and dietary fibres. Agaricus blazei, Agrocybe cylindracea, and Boletus edulis displayed moderate DPPH scavenging activities with IC50 of 13.75, 26.98, and 15.78 mg/mL, respectively [11]. It has been reported that the IC50 of hot water extract of Hypsizygus marmoreus was 4.19 mg/mL [29] whereas the white mutant strain of the same species was less effective with an IC50 of 18.85 mg/mL [30].

3.4. -Carotene Bleaching Activity

For evaluation of antioxidant capacity of compounds in emulsions, the -carotene bleaching assay is recommended. Food systems usually comprise of multiple phases where lipid and water coexist with some emulsifiers [31] so it may be feasible to include this assay in our study. Briefly, oxidation of linoleic acid in the emulsion generated radicals which in turn caused the loss of the yellow colour of -carotene. The presence of antioxidants will minimize the extent of -carotene bleaching by neutralizing the radicals [32].

The antioxidant capacities of the mushroom extracts as determined by the β-carotene bleaching method were also as expressed as IC50 values as shown in Table 2. Low IC50 values were noted for quercetin and BHA but a relatively higher IC50 value for ascorbic acid suggests it is a weak antioxidant based on the results of this assay despite the fact it is a well-known, polar antioxidant. Our results are in agreement to the previous reports which pointed out that ascorbic acid did not show its antioxidant activity under similar assay [31]. Such phenomenon was termed as “polar paradox” whereby polar antioxidants remaining in the aqueous phase of the emulsion are more diluted in lipid phase and thus, they are less effective [32].

Comparison of -carotene bleaching activity of mushrooms with the positive controls revealed that S. commune ( mg/mL) showed comparable activity with quercetin (IC50 = 1.86 mg/mL) and even more potent than BHA ( mg/mL). Apart from that, three mushroom species, namely, G. lucidum, H. erinaceus, and L. edodes ( mg/mL) were more effective than ascorbic acid ( mg/mL). The antioxidant activity of F. velutipes was the weakest, as evidenced by an IC50 that is approximately 20-fold higher than that of S. commune and quercetin.

Apparently, some wild mushrooms demonstrated better inhibition activity in similar assay. Several Portuguese wild mushrooms were reported to show good antioxidant activities as evidenced by IC50 in the range of 0.71 to 7.48 mg/mL except for Hydnum repandum which had a higher IC50 of 28.72 mg/mL [33]. In the concentration of 4–20 mg/mL, water extract of Lentinula edodes (52.7–75.9%) showed better antioxidant activities than that of V. volvaceae (31.8–65.2%) [22].

3.5. Inhibition of Lipid Peroxidation of Buffered Egg Yolk

Lipid peroxidation induced by free radical species results in break down of membrane integrity, affecting its fluidity and permeability [1]. The initial step, that is, peroxidation of polyunsaturated fatty acid components in low-density lipoproteins of membrane produces several byproducts which can damage biomolecules. Transition ions may either generate hydroxyl radicals to initiate the lipid peroxidation process or propagate the chain process via decomposition of lipid hyperoxides [25].

In our study, the lipid peroxidation induced by Fe2+ was estimated by the presence of TBARS. The ability of the mushroom extracts to inhibit peroxidation of phospholipids in egg yolk is included in Table 2. At the concentration of 10 mg/mL, inhibition of lipid peroxidation by the mushroom extracts was moderate (30.54–57.18%) whereas quercetin, BHA, and ascorbic acid showed higher inhibition percentage (77.92–81.93%). G. lucidum exhibited highest inhibition of lipid peroxidation of 57.18%, followed by P. florida and A. auricular-judae with inhibition percentage of 56.58% and 56.41%, respectively. Both V. volvacea and P. flabellatus have comparable percentage of lipid peroxidation inhibition of 50.09% and 50.00%, respectively.

The ability of mushroom extracts to inhibit lipid peroxidation on rat brain homogenate has been reported by Cheung and Cheung [34] who indicated that the dichloromethane subfraction of V. volvacea ( mg/mL) and L. edodes ( mg/mL) were active in inhibiting lipid peroxidation. Phellinus linteus was reported to inhibit FeCl2-induced lipid peroxidation in rat brain homogenate with an IC50 of 0.485 mg/mL [35].

3.6. Reducing Power Ability

The ability of mushroom extracts to donate electrons could be evaluated using the reducing power assay. In the presence of antioxidants, the Fe3+-ferricyanide complex is reduced to the ferrous form, Fe2+ and the latter can be monitored by measuring the formation of Perl’s Prussian blue at 700 nm; higher absorbance indicates greater reducing power [16].

The ability of the mushrooms extracts and controls to reduce Fe3+ to Fe2+ at different concentrations are shown in Table 3. At the concentration of 0.50 mg/ml, the positive controls that is quercetin, BHA, and ascorbic acid exhibited high-reducing capacity of 2.506, 2.405, and 2.380, respectively, which were distinctively higher than that of any mushroom extracts (0.011–0.060). Mushroom extracts showed variable reducing capacity and overall, the reducing capacity of mushroom extracts increased with increasing concentration. Amongst the mushrooms, G. lucidum showed marked increase in reducing power ability of 0.063 to 0.453 in the tested concentration of 0.01 to 1.00 mg/mL. At 1.00 mg/mL, the reducing power of G. lucidum was 0.453 and this was in accordance to work by Mau et al. [10] who reported that the reducing power of mature and baby Ling chih (G. tsugae Murrill) was 0.48 and 0.44, respectively. Agrocybe sp. and P. florida demonstrated comparative increase in reducing power ability of 0.054–0.193 and 0.053–0.110, respectively. Our results for Agrocybe sp. were actually comparable to Tsai et al. [36] who reported that reducing power of hot water extracts of Agrocybe cylindracea was 0.22 at 1.00 mg/mL.


Mushroom speciesAbsorbance values (at 700 nm) of mushroom extracts of different concentrations (mg/mL)
0.050.100.501.00

Agrocybe sp.
Auricularia auricular-judae
Flammulina velutipes
Ganoderma lucidum
Hericium erinaceus
Lentinula edodes
Pleurotus cystidiosus
Pleurotus eryngii
Pleurotus flabellatus
Pleurotus florida
Pleurotus sajor-caju
Schizophyllum commune
Termitomyces heimii
Volvariella volvaceae

Positive controls*  

Quercetin
Butylated hydroxyanisole (BHA)
Ascorbic acid

Values were expressed as mean ± standard deviation of three replicate determinations.
Mean values in a column with different lower case letters (a–g) indicate significant difference at .
*Absorbance values for positive controls were measured at the concentration of 0.50 mg/mL.

The oyster mushrooms (Pleurotus spp.) exhibited relatively low reducing power of 0.040–0.081 and 0.043–0.165 at the concentration of 0.50 and 1.00 mg/mL, respectively. Lee et al. [37] in their study reported that Pleurotus citrinopileatus showed better reducing power ability than all Pleurotus spp. tested in this study. Similarly, Kim et al. [38] found that Pleurotus cornucopiae has better reducing capacity than Pleurotus ostreatus and Pleurotus salmoneostramineus. The reducing power ability of mushrooms can be attributed to the presence of reductones which reacts with peroxides and certain precursors to halt peroxides formation as well as hydrogen-donating ability of these extracts leading to termination of radical chain reactions.

3.7. CUPRAC Assay

The CUPRAC assay utilised copper(II)-neocuproine (CU(II)-Nc) reagent as the chromogenic oxidizing agent. It is based on the measurement of absorbance at 450 nm by the formation of stable complex between neocuproine and copper (I) [16]. CUPRAC of the mushroom extracts was assessed and compared to that of the positive controls. As shown in Table 4, CUPRAC of the mushroom extracts was dependent on the concentration of extract. As expected, the positive controls showed more pronounced CUPRAC than the mushroom extracts. At the concentration of 0.50 mg/mL, CUPRAC of quercetin, BHA and ascorbic acid were 2.110, 1.958, and 1.791, respectively. At similar concentrations, G. lucidum exhibited significantly higher CUPRAC of 1.058 than other mushroom species. To the best of our knowledge, this is the first report on evaluation of antioxidant activity of hot water extracts of mushroom fruiting bodies by the CUPRAC method. Recently, Omar et al. [39] showed the CUPRAC of Lentinus squarrosulus mycelial extract (0.50 mg/mL) was 0.20 ± 0.03 which was lower than CUPRAC of hot water extract of some of the mushrooms studied (Table 4).


Mushroom speciesAbsorbance values (at 450 nm) of mushroom extracts of different concentrations (mg/mL)
0.100.501.005.0010.00

Agrocybe sp.
Auricularia auricular-judae
Flammulina velutipes
Ganoderma lucidum
Hericium erinaceus
Lentinula edodes
Pleurotus cystidiosus
Pleurotus eryngii
Pleurotus flabellatus
Pleurotus florida
Pleurotus sajor-caju
Schizophyllum commune