Phenolic composition and functional properties of wild mint (Mentha longifolia var. calliantha (Stapf) Briq.)

ABSTRACT

Mints (Mentha species) are widely used as food, medicine, spice, and flavoring agents. At the present work, phenolics profile of infusion and ethanol extract of Mentha longifolia was determined using an RP–HPLC–DAD system. Total bioactive contents, radical scavenging, reducing power, metal chelating, and enzyme inhibitory activities relevant to Alzheimer’s disease, diabetes mellitus, and skin disorders were evaluated. Sixteen phenolic compounds (ten phenolic acids and six flavonoids) were identified in the extracts in which sinapic acid (7132 µg/g extract) and rosmarinic acid (6260 µg/g extract) were the most abundant compounds. Strong antioxidant effects were observed in 1,1-diphenyl-2-picrylhydrazyl radical, 2,2ʹ-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), cupric ion reducing activity, ferric reducing antioxidant power, phosphomolybdenum, and metal chelating assays. Results indicated selective acetylcholinesterase inhibitory activity and high α-amylase and α-glucosidase inhibitory potential. Findings showed that M. longifolia has promising health benefits due to its high concentration of useful phenolic compounds and has great potential for possible applications in the preparation of functional ingredients.

KEYWORDS:

• Alzheimer’s disease
• Diabetes mellitus
• Functional foods
• Herbal tea
• Mint
• Nutraceuticals

Introduction

The genus Mentha L. (Mentheae, Nepetoideae) belonging to the Lamiaceae family is consisted of mostly perennial aromatic herbs with invasive creeping rhizomes frequently living in wet habitations.^[1,2] According to the plant list database (http://www.theplantlist.org), this genus contains around 56 accepted taxa including 42 species distributed worldwide especially in temperate and subtemperate regions. Mentha represents in Iran by seven species including Mentha longifolia.^[3] These plants, because of their multiple utilities, are very popular for humankind since antiquity. Mentha species are of big economic value today and largely consumed in pharmaceutical, beverage, confectionary, culinary, perfume, food, cosmetic, and tobacco industries.^[4–6]

Mints have been using traditionally for centuries as flavoring, condiment, herbal tea, fresh vegetable, infusion, decoction, and distillate.^[7,8] They are also used as breath freshener, carminative, choleretic, anti-infective, anti-inflammatory, antiemetic, diaphoretic, antispasmodic, analgesic, stimulant, emmenagogue, anticatarrhal, diuretic, antiallergic, stomach tonic, and insecticidal agents.^[9,10] Accordingly, fresh, dried, and processed mints are empirically used in herbal medicine for treatment of several health problems and discomforts like gastric acidities, aerophagia, nausea, flatulence, vomiting, ulcerative colitis, stomach aches, dyspepsia, diarrhea, jaundice, liver complaints, anorexia, cramps, bronchitis, throat infections, and viral hepatitis.^[11,12]

The genus Mentha is globally a phenomenal source of essential oil production. Beside the widely growing populations, Mentha piperita, Mentha spicata, and Mentha arvensis are vastly cultivated worldwide, mainly for their essential oil yield.^[13,14] Mentha species are also rich in phenolic compounds, especially in phenolic acids and flavonoids.^[15,16] Generally, biologic activities of mint species mostly originate from their phenolics and essential oil components.^[17,18]

M. longifolia known as hors or wild mint is a sharply scented widespread species, breeding multi-flowered spike-shaped inflorescences. M. longifolia is a well-known overconsumed medicinal plant.^[3] It is used to provide household spices, infusion, additive, food, decoction, and distillate.^[19] Its pungent scent could repel mosquito and also keep the rodents away from the stored grains. Several bioactivities such as antibacterial, antifungal, antioxidant, anticandidal, pesticidal, insecticidal, antimutagenic, anticancer, calcium channel blocking, cyclooxygenase, and HIV 1 inhibitory properties have been reported for this species. Also, some remedial effects namely sedative, spasmolytic, diaphoretic, antipruritic, carminative, antiseptic, choleretic, central nervous system stimulant, antihistamine, diuretic, and hepatoprotective traits of M. longifolia have been verified.^[20–25] Chemically variable M. longifolia, based on the morphologically discriminating characteristics, is subdivided into nine varieties in Iran, including var. calliantha (Stapf) Briq. The later taxon of wild mint is nominated in the Flora of Iran as an endemic plant, but it occurs in eastern Anatolia too.

To the best of our knowledge, there is not any information about the phytoconstituents and biological activities of M. longifolia var. calliantha (Stapf) Briq. Accordingly, at the present work, the phenolics profile of infusion and ethanolic extract of this plant are examined to find its bioactive metabolites. In addition, to explore its health benefits, several biological activities of M. longifolia such as radical scavenging, reducing power, metal chelating, and its enzyme inhibitory properties relevant to diabetes mellitus (DM), skin disorders, and Alzheimer’s disease (AD) are investigated.

Materials and methods

Plant material

The aerial plant parts including flowers, leaves, and juvenile stems were collected during flowering stage in early spring 2015 from Urmia, West Azerbaijan province of Iran, and authenticated by Mr. Shahram Bahadori (taxonomist) as M. longifolia var. calliantha (Stapf) Briq. In addition, a voucher specimen was deposited in Herbarium of Urmia Pharmacy School (HUPS-177), Urmia, Iran.

Preparation of extracts

The ethanol extract of the aerial parts of M. longifolia was obtained using maceration method. An amount of 50 g crushed dried material was extracted using 500 mL of EtOH. The extraction was performed by shaking at room temperature during 72 h. Finally, the extract was passed through a paper filter and the filtrated solution was concentrated by a rotary evaporator at 40°C. For preparation of the infusion, 50 g of the plant material was suspended in 500 mL of hot distilled water. The mixture was shaken for 10 min and the extract was centrifuged and filtered using paper filter. The obtained solution was lyophilized and stored in −18°C until analysis.

Profiling of phenolic compounds by RP–HPLC–DAD

Phenolic metabolites were analyzed using RP–HPLC–DAD (Shimadzu Scientific Instruments, Kyoto, Japan). Separation procedure was carried out at 30°C on Eclipse XDB C-18 reversed-phase column (250 mm × 4.6 mm length, 5 µm particle size, Agilent, Santa Clara, CA, USA). The eluates were detected at 278 nm. The phenolic compounds of the ethanolic and water extracts were determined using a previously modified method.^[26] Twenty-three standard phenolic compounds were used for the analysis including gallic acid, protocatechuic acid, catechin, p-hydroxybenzoic acid, chlorogenic acid, caffeic acid, epicatechin, syringic acid, vanillin, p-coumaric acid, ferulic acid, sinapic acid, benzoic acid, o-coumaric acid, rutin, hesperidin, rosmarinic acid, eriodictyol, cinnamic acid, quercetin, luteolin, kaempferol, and apigenin. Retention times, UV spectra, and comparison with commercial standard compounds were used for the characterization and quantitative analysis of phenolic compounds. The results were expressed as µg/g of dry extracts using external calibration curves.

Total phenolic content and total flavonoid content

The total phenolic content (TPC) of the extracts was determined using Folin–Ciocalteu method with slight modification ^[27] and expressed as gallic acid equivalents (GAEs/g sample). Briefly, 20 μL of sample solution in methanol (2 mg/mL) was mixed with 100 μL of Folin–Ciocalteu reagent (1:10). After 6 min, 80 μL sodium carbonate 7.5% is added into the reaction mixture. The absorbance is measured at 740 nm after 2 h of incubation in the dark at 25°C. The TPC of the extracts is expressed as mg of gallic acid equivalents per g of samples (mg GAE/g) through the calibration curve with gallic acid. Total flavonoid content is determined using AlCl₃ method with some modifications^[28] and the results are expressed as rutin equivalents (REs/g sample). In brief, 20 μL of mint samples or a standard solution of rutin (1–200 μg/mL) is diluted using 60 μL of MeOH and 10 μL of AlCl₃ (5%). Afterward, 10 μL of 0.5 M potassium acetate is added and the total volume is made up to 200 μL by distilled water. The solution is well and the absorbance read at 415 nm after 30 min. All assays were carried out in triplicate, and mean values of flavonoid content were expressed as mg of rutin equivalents per g of extracts calculated according to the standard calibration curve.

Total antioxidant activity

The total antioxidant activity of the plant samples was evaluated by phosphomolybdenum method with slight modification.^[29] The results are expressed as trolox equivalents as standard antioxidant compound (mmol TEs/g extract). In this direction, sample solution (0.3 mL) was combined with 3 mL of reagent solution including 0.6 M sulfuric acid, 28 mM sodium phosphate, and 4 mM ammonium molybdate. The sample absorbance was read at 695 nm after 90 min incubation at 95°C. Total antioxidant capacity is expressed as equivalents of trolox as determined by the equation of the standard trolox curve.

Radical scavenging activity

The radical scavenging activities of the extracts against 1,1-diphenyl-2-picrylhydrazyl radical (DPPH) and also on 2,2ʹ-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) radical cation (ABTS) were estimated.^[30–32] Results were expressed as mean ± SD of trolox equivalents from three independent experiments (mg TEs/g extract). Twenty microliters of samples or standard antioxidant butylated hydroxy toluene (BHT), which is dissolved in methanol in several concentrations, are mixed with 180 μL of 0.1 mM DPPH solution. Discoloration of mixtures is measured at 517 nm after 30 min. In ABTS assay, ABTS⁺ radical cation is produced directly by reaction of 7 mM ABTS solution with 2.45 mM potassium persulfate in 12–16 h in dark at the room temperature. Prior to beginning the assay, ABTS solution was diluted with methanol to an absorbance of 0.700 ± 0.02 at 734 nm. Sample solution (1 mL) was added to ABTS solution (2 mL) and mixed. The sample absorbance was read at 734 nm after 30 min incubation at room temperature. The ABTS radical cation scavenging activity was expressed as equivalents of trolox, according to the equation obtained from the standard trolox curve.

Reducing power activity

The cupric ion reducing activity (CUPRAC) and the ferric reducing antioxidant power (FRAP) assays were determined according to the previously published methods with some modifications.^[33,34] The results of both CUPRAC and FRAP assays were expressed as equivalents of trolox (mg TEs/g sample). For CUPRAC test, sample solution (0.5 mL) was added to reaction mixture containing CuCl₂ (1 mL, 10 mM), neocuproine (1 mL, 7.5 mM), and NH₄Ac buffer (1 mL, 1 M, pH 7.0). Similarly, a blank was prepared by adding sample solution (0.5 mL) to reaction mixture (3 mL) without CuCl₂. Afterward, the sample and blank absorbances were read at 450 nm after 30 min incubation at room temperature. The absorbance of the blank was subtracted from that of the sample. CUPRAC activity was expressed as equivalents of trolox according to the equation obtained from the standard trolox graph. In FRAP assay, sample solution (0.1 mL) was added to premixed FRAP reagent (2 mL) containing acetate buffer (0.3 M, pH 3.6), 2,4,6-tris(2-pyridyl)-s-triazine (10 mM) in 40 mM HCl and ferric chloride (20 mM) in a ratio of 10:1:1 (v/v/v). Then, the sample absorbance was read at 593 nm after a 30-min incubation at room temperature. FRAP activity was expressed as equivalents of trolox according to the equation obtained from the standard trolox graph.

Metal chelating activity

The metal chelating activity of plant samples was estimated using ferrous ions chelating method according to a previously described procedure.^[34] The metal chelating activity values were expressed as equivalents of EDTA (mg EDTAE/g). Briefly, sample solution (2 mL) was added to FeCl₂ solution (0.05 mL, 2 mM). The reaction was initiated by the addition of 5 mM ferrozine (0.2 mL). Similarly, a blank was prepared by adding sample solution (2 mL) to FeCl₂ solution (0.05 mL, 2 mM) and water (0.2 mL) without ferrozine. Then, the sample and blank absorbances were read at 562 nm after 10 min incubation at room temperature. The absorbance of the blank was subtracted from that of the sample. The metal chelating activity was expressed as equivalents of EDTA according to the equation obtained from the standard EDTA graph.

Enzyme inhibitory activity

Enzyme inhibitory properties of M. longifolia were investigated using ELISA plate reader against α-glucosidase (from Saccharomyces cerevisiae, EC 3.2.1.20, Sigma) and α-amylase (ex-porcine pancreas, EC 3.2.1.1, Sigma) as acarbose equivalents (mmol ACEs/g extract), acetylcholinesterase (AChE) (electric ell AChE, Type-VI-S, EC 3.1.1.7, Sigma) and butyrylcholinesterase (BChE) (horse serum BChE, EC 3.1.1.8, Sigma) as galantamine equivalents (mg GALAEs/g extract), and tyrosinase (from mushroom, EC 1.14.18.1, Sigma) as kojic acid equivalents (mg KAEs/g extract) using previously published methods.^[35]

Statistical analysis

All experiments were carried out in triplicate. The results are expressed as mean value ± standard deviation (SD). Data analysis was performed using SPSS v.16.0. Differences between means were determined by one-way analysis of variance (ANOVA) followed by Duncan’s post hoc test for multiple comparisons with control. A value of p < 0.05 was considered as indicative of statistical significance.

Results and discussion

Phenolics profiling

Phenolic compounds are one the most abundant natural products in foods. They occupy the major portion of phytochemicals in plants. In the last decades, these compounds have received a great attention from the scientific community against public health problems due to their antioxidant potential and their role in management of several disorders such as diabetes, cancer, neurodegeneration, and cardiovascular diseases.

At the present work, a comparative RP–HPLC–DAD analysis was performed between ethanolic extract and infusion of M. longifolia as a common medicinal herb. In this direction, 23 standard phenolic compounds were used in analysis which revealed the presence of 16 compounds (10 phenolic acids and 6 flavonoids) in the tested samples. Comparative study shows that both of ethanolic extract and infusion of M. longifolia share the presence of all phenolic compounds but with different amounts. Table 1 lists the concentration of phenolic compounds, belonging to the different classes of polyphenols, measured by RP–HPLC–DAD system in both infusion and ethanolic extract of M. longifolia. The structures of the identified phenolics are shown in Fig. 1. Sinapic acid and rosmarinic acid are the most abundant phenolic component in both of the samples, followed by hesperidin and o-coumaric acid. Previous studies on Mentha species indicated the presence of several phenolic compounds in the genus like caffeic acid, rosmarinic acid, and diosmin in M. spicata, M. pulegium, and M. rotundifolia.^[36] Elansary and coworkers investigated phenolics compound of four Mentha species and reported rosmarinic acid and caffeic acid as the major metabolites.^[37] Phenolics profiling of M. australis, an Australian native mint, revealed the presence of neoponcirin, rosmarinic acid, narirutin, chlorogenic acid, biochanin, caffeic acid, apigenin, hesperetin, and naringenin.^[38] Phenolic compounds of M. spicata were analyzed by UHPLC-ESI–MSⁿ. The analysis suggested that this species is rich in rosmarinic acid and its derivatives, salvianolic acids, hydroxybenzoic acids, caffeoylquinic acids, hydroxycinnamic acids, flavanones, and flavones.^[39] According to our literature review and also the results of this work, Mentha species are rich in phenolic compounds and especially phenolic acids. Moreover, it seems that rosmarinic acid is the most abundant phenolic compound in the genus.

Table 1. Quantitative analysis for determination of phenolic components in the infusion and ethanol extract of M. longifolia.

		Samples		Analytical characteristics
No.	Phenolic compounds	Infusion	Ethanol extract	Linear range (ppm)	r^2	LOD (ppm)	LOQ (ppm)
1	Gallic acid	72 ± 4	2 ± 0.2	0.20–25.0	0.9993	0.075	0.227
2	Protocatechuic acid	6 ± 0.2	7 ± 0.2	0.20–25.0	0.9991	0.086	0.260
3	(+)-Catechin	nd	nd	0.90–113	0.9988	0.172	0.522
4	p-Hydroxybenzoic acid	nd	nd	0.20–25.0	0.9994	0.007	0.020
5	Chlorogenic acid	64 ± 1	27 ± 1	0.35–45.0	0.9988	0.080	0.241
6	Caffeic acid	119 ± 3	86 ± 2	0.16–21.0	0.9993	0.054	0.162
7	(−)-Epicatechin	nd	nd	0.50–66.0	0.9990	0.170	0.514
8	Syringic acid	33 ± 2	9 ± 0.1	0.05–12.0	0.9995	0.030	0.090
9	Vanillin	31 ± 1	6 ± 0.1	0.08–10.0	0.9995	0.020	0.060
10	p-Coumaric acid	15 ± 0.8	5 ± 0.1	0.04–6.0	0.9996	0.066	0.199
11	Ferulic acid	nd	nd	0.12–17.0	0.9993	0.004	0.011
12	Sinapic acid	7132 ± 32	4604 ± 27	0.12–17.0	0.9993	0.017	0.053
13	Benzoic acid	nd	nd	0.85–55.0	0.9998	0.111	0.335
14	o-Coumaric acid	328 ± 1.8	134 ± 0.7	0.24–32.0	0.9988	0.023	0.069
15	Rutin	96 ± 7	45 ± 1	0.40–56.0	0.9989	1.113	3.373
16	Hesperidin	481 ± 28	248 ± 2	0.43–55.0	0.9992	1.080	3.280
17	Rosmarinic acid	6260 ± 60	2225 ± 46	0.02–7.0	0.9998	0.148	0.447
18	Eriodictyol	14 ± 0.3	25 ± 0.3	0.33–21.0	0.9998	0.140	0.410
19	trans-Cinnamic acid	79 ± 2	15 ± 0.5	0.02–7.0	0.9998	0.148	0.447
20	Quercetin	nd	nd	0.40–55.0	0.9999	0.013	0.040
21	Luteolin	162 ± 4	84 ± 0.4	0.13–17.0	0.9999	0.020	0.060
22	Kaempferol	nd	nd	0.05–15.0	0.9996	0.021	0.062
23	Apigenin	124 ± 4	94 ± 4	0.17–11.0	0.9997	0.034	0.104

Figure 1. Phenolic compounds identified and quantified in infusion and ethanol extract of Mentha longifolia.

Total phenolic and flavonoid contents

Phenolic and flavonoid compounds exert vital bioactivities in the prevention and/or treatment of several public health problems such as diabetes, atherosclerosis, Parkinson’s disease, cancer, and AD. Total phenolic and flavonoid contents of the infusion and ethanol extract of M. longifolia are presented in Table 2. The infusion is contained higher TPC (92.38 mg GAEs/g extract) than ethanol extract (67.05 mg GAEs/g). Similarly, it has higher total flavonoid content (46.18 mg REs/g extract) than ethanol extract (23.68 mg REs/g). This is in accordance with HPLC analysis in which the concentrations of phenolics in infusion generally are more than those in ethanol extract (Table 2). High concentration of phenolic and flavonoid compounds in M. longifolia indicates that it has strong potential health benefits. This is in agreement with previous work which showed the presence of high phenolic and flavonoid content in M. longifolia and other Mentha species.^[37]

Table 2. Total bioactive compounds and total antioxidant activity of M. longifolia.

	Total bioactive compounds		Total antioxidant activity
Samples	Total phenolic (mg GAEs/g extract)^a	Total flavonoid (mg REs/g extract)^b	Phosphomolybdenum (mmol TEs/g extract)^c
Infusion	92.38 ± 0.43^d	46.18 ± 0.20	0.75 ± 0.02
Ethanol extract	67.05 ± 0.85	23.68 ± 0.20	0.64 ± 0.01

^aGAEs: Gallic acid equivalents.

^bREs: Rutin equivalents.

^cTEs: Trolox equivalents.

^dValues expressed are means ± SD of three parallel measurements.

Antioxidant activity

Accumulation of free radicals results in oxidative stress in the human body and, as a consequence, leads to several diseases such as cancer, diabetes, cardiovascular, and neurodegenerative disorders.^[40,41] Moreover, synthetic and commercial antioxidant compounds such as Butylated hydroxyanisole (BHA) and BHT have some side effects like liver damage and gastrointestinal disorders. The antioxidant capacity of plant extracts or essential oils should be measured using several different methods. Each of these assays is based on different mechanisms. In fact, utilizing just one method could not explore the antioxidant ability of natural extracts because of their complex composition. Accordingly, antioxidant activity of natural products should be investigated using several different assays to get accurate and comparable data. In this direction, single electron transfer, hydrogen atom transfer, and metal chelating are the major mechanisms in which the antioxidants could deactivate the oxidative process.

To this end, at the present study, the antioxidant effects of infusion and ethanol extract of M. longifolia were evaluated using six different methods including radical scavenging (DPPH and ABTS), metal ion reducing (FRAP and CUPRAC), total antioxidant (phosphomolybdenum), and metal chelating assays. Generally, both the plant samples showed strong radical scavenging activities (Table 3). Also, they indicated remarkable metal ion reducing power (Table 4). Fe²⁺ ions could create the hydroxyl radicals and then initiate lipid peroxidation which leads to serious health damages. Promising total antioxidant activity (Table 2) and moderate metal chelating activities (Table 4) were also observed for tested samples. In comparison, in all of the antioxidant assays, infusion sample exhibited higher antioxidant activity than ethanol extract. This observation could be easily interpreted according to their total phenolics and total flavonoids contents, and also individual phenolics concentration. As noted above, the concentration of phenolic acids and flavonoids (well-known antioxidant compounds) in infusion is higher than ethanol extract. Phenolic compounds could reduce oxidative damages in body through scavenging free radicals, chelating, and reducing metal ions which are responsible to formation of reactive oxygen species (ROS). Previous studies on several mints showed that infusion and methanolic extracts have strong antioxidant activities in DPPH assay with IC₅₀ values ranging from 9.3 to 14.8 µg/mL.^[37] In view of phytochemicals of Mentha species, flavonoids and phenolic acids are the main classes of natural compounds found in the extracts and infusions of Mentha plants.^[8,17] So, these secondary metabolites could be responsible for observed antioxidant potential of M. longifolia. These findings are in agreement with previous works on the genus Mentha.^[42–44] According to relatively high amounts of phenolic compounds in M. longifolia and their antioxidant potential which were confirmed using several in vitro assays, this species could be considered for possible applications in food industries.

Table 3. Radical scavenging activity of infusion and ethanol extract of M. longifolia.

	Radical scavenging activity
Samples	DPPH radical (mg TEs/g extract)^a	ABTS radical cation (mg TEs/g extract)^a
Infusion	195.96 ± 0.94^b	269.25 ± 9.04
Ethanol extract	162.08 ± 3.90	242.06 ± 1.53

^aTEs: Trolox equivalents.

^bValues expressed are means ± SD of three parallel measurements.

Table 4. Reducing power and metal chelating activity of the infusion and ethanol extract of M. longifolia.

	Reducing power activity		Metal chelating activity
Samples	CUPRAC (mg TEs/g sample)^a	FRAP (mg TEs/g sample)^a	Chelating effect (mg EDTAEs/g sample)^b
Infusion	454.99 ± 4.48^c	346.20 ± 0.17	7.31 ± 0.44
Ethanol extract	371.30 ± 5.21	239.87 ± 3.95	9.29 ± 0.24

^aTEs: Trolox equivalents.

^bEDTAEs: EDTA equivalents.

^cValues expressed are means ± SD of three parallel measurements.

Therapeutic target enzymes inhibitory activity

There are several disorders, in which inhibition of key enzymes activity is considered as an effective strategy in treatment of public health problems. In this regard, screening of natural products for their enzyme inhibitory activities is an important method to discovery of new drugs. The prevalence of AD and DM is rising and it is estimated to increase significantly in the following decades. In this direction, at the present study, inhibitory activity of infusion and ethanol extract of M. longifolia (a common functional tea) against key enzymes involved in AD, DM, and skin disorders were investigated.

Cholinesterases inhibition

AChE and BChE inhibitors are effective drugs for management of AD which is a neurodegenerative disorder.^[45,46] As the world population ages, it is necessary more and more to find treatments for AD.^[47] Both plant samples showed moderate AChE inhibitory potential (1.32 and 1.25 mg GALAEs/g sample for infusion and ethanol extract, respectively) but they were inactive against BChE in tested concentration (Table 5). Results indicated that active compounds in these samples could be selective inhibitors of AChE. This is in agreement with a previous work in which several extracts from Mentha species showed selective AChE inhibitory activity and Linarin (acacetin-7-O-β-d-rutinoside) was identified as the active compound from the flower extract of M. arvensis.^[48] There are some evidences in the literature showing the potential of dietary phenolics for treatment of AD.^[49] So, phenolic metabolites (especially phenolic acids) of M. longifolia may be responsible for observed AChE inhibitory activity.

Table 5. Enzyme inhibitory activities of the infusion and ethanol extract of M. longifolia.

	Anti-Alzheimer’s disease effect		Antidiabetic effect		Skin care effect
Samples	AChE inhibition (mg GALAEs/g sample)^a	BChE inhibition (mg GALAEs/g sample)^a	α-Amylase inhibition (mmol ACEs/g sample)^b	α-Glucosidase inhibition (mmol ACEs/g sample)^b	Tyrosinase inhibition (mg KAEs/g sample)^c
Infusion	1.32 ± 0.02^d	na^e	0.43 ± 0.04	5.90 ± 0.10	na
Ethanol extract	1.25 ± 0.01	na	0.59 ± 0.03	5.68 ± 0.18	na

^aGALAEs: Galantamine equivalents.

^bACEs: Acarbose equivalents.

^cKAEs: Kojic acid equivalents.

^dValues expressed are means ± SD of three parallel measurements.

^eNot active.

α-Amylase and α-glucosidase inhibition

α-Amylase and α-glucosidase inhibitors may be considered as glucose level reducing drugs for the treatment of DM. These enzymes catalyze carbohydrates to their monomers and increase the glucose level of blood. There are several drugs for treatment of type 2 diabetes in the market such as metformin, acarbose, and miglitol. These drugs have some negative effects on human health. So, discovery of new and natural effective antidiabetic drugs with more activity and less side effects is warranted. In this work, M. longifolia was investigated for its antidiabetic potential for the first time. Infusion and ethanol extract of the plant exhibited moderate α-amylase inhibitory activity and strong α-glucosidase inhibitory potential (Table 5). In view of active compounds, phenolic acids and flavonoids are well known for antidiabetic potential due to their enzyme inhibitory effects.^[26,50,51]

Tyrosinase inhibition

The infusion and ethanol extract of M. longifolia were evaluated for their tyrosinase inhibitory activity in vitro (Table 5). None of the tested samples showed enzyme inhibitory potential in test concentrations.

Conclusion

Wild mint (M. longifolia) is a useful functional food. At the present study, M. longifolia var. calliantha (Stapf) Briq. was investigated for its phytochemicals and functional properties for the first time. To this end, infusion and ethanol extract of this herb were evaluated for their enzyme inhibitory and antioxidant activities comprehensively. Antioxidant, antidiabetic, and neuroprotective effects of wild mint were confirmed using in vitro assays. HPLC analysis showed the presence of phenolic compounds with health benefits in the herb as responsible bioactive components. Findings indicated that M. longifolia has great nutritional value and thus, it could be considered as a source of natural agents for designing new functional ingredients. However, further pharmacological and phytochemical investigations are essential to establish solid grounds for future utilization of this herb in food and nutraceutical industries.

Declaration of interest

The authors declare that there are no conflicts of interest.

Additional information

Funding

This work was supported by Urmia University of Medical Sciences [Project Number 2032].