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Molecules 2014, 19(1), 767-782; doi:10.3390/molecules19010767
Published: 9 January 2014
Abstract: The present study aimed to evaluate acetylcholinesterase (AChE) inhibitory and antioxidant activities of Lamiaceae medicinal plants growing wild in Croatia. Using Ellman’s colorimetric assay all tested ethanolic extracts and their hydroxycinnamic acid constituents demonstrated in vitro AChE inhibitory properties in a dose dependent manner. The extracts of Mentha x piperita, M. longifolia, Salvia officinalis, Satureja montana, Teucrium arduini, T. chamaedrys, T. montanum, T. polium and Thymus vulgaris at 1 mg/mL showed strong inhibitory activity against AChE. The antioxidant potential of the investigated Lamiaceae species was assessed by DPPH• scavenging activity and total antioxidant capacity assays, in comparison with hydroxycinnamic acids and trolox. The extracts differed greatly in their total hydroxycinnamic derivatives content, determined spectrophotometrically. Rosmarinic acid was found to be the predominant constituent in most of the investigated medicinal plants (by RP-HPLC) and had a substantial influence on their AChE inhibitory and antioxidant properties, with the exception of Teucrium species. These findings indicate that Lamiaceae species are a rich source of various natural AChE inhibitors and antioxidants that could be useful in the prevention and treatment of Alzheimer’s and other related diseases.
Alzheimer’s disease (AD), the most common cause of dementia, is a progressive age-related neurodegenerative disorder which is becoming a serious public health issue and a massive economic burden. AD patients lose their memory, their cognitive abilities and even their personalities may change dramatically. These changes are due to the progressive dysfunction and death of nerve cells responsible for the storage and processing of information . AD arises as a result of malfunction of different biochemical pathways. Multiple pathogenic factors, including aggregated amyloid-β-peptide and tau protein, excessive transition metals, oxidative stress and reduced acetylcholine (ACh) levels have been implicated in AD pathology . Acetylcholinesterase (AChE), the predominant cholinesterase in the brain, hydrolyzes ACh to choline and acetate, thereby terminating the effect of this neurotransmitter at cholinergic synapses. Therefore, AChE is the target of cholinesterase inhibitors used for addressing the cholinergic deficit in AD patients. Despite decades of research and advances in our understanding of its aetiology and pathogenesis, current pharmacotherapeutic options for AD are still very limited and represent an area of need that is currently unmet. The leading AD therapeutics involve AChE inhibitors, resulting in increased acetylcholine concentrations in the synaptic cleft and enhanced cholinergic transmission [3,4]. Compounds showing an AChE inhibitory effect are also used for the treatment of senile dementia, myastenia gravis, Parkinson’s disease and ataxia . Taking into account that the inhibition of AChE has been one of the most used strategies for treating AD and that existing drugs are effective only against mild to moderate type of disease while presenting considerable side effects, the search for new sources of effective and selective antiacetylcholinesterase agents with fewer side effects is imperative. The free radical and oxidative stress theories of aging suggest that oxidative damage is a major player in the degeneration of cells. In this respect, recent findings clearly indicate that oxidative damage is one of the earliest events in the pathogenesis of AD, so targeting oxidative stress could be considered beneficial in both its prevention and treatment .
Owing to their richness in secondary metabolites that exhibit a remarkable diversity of both chemical structures and biological activities, medicinal plants are being recognized as promising sources of lead compounds for new drugs targeting neurodegenerative diseases [7,8,9]. Croatia is one of Europe’s most biodiversity-rich countries due to its unique geographical position. As an integral part of the Mediterranean area, its flora is represented by a high number of species and subspecies, in total 5,516 taxa belonging to 184 families, among which Lamiaceae could be considered one of the richest in medicinal plants . Lamiaceae species have been reported to possess a wide range of biological activity, and a wide diversity of phytochemicals. Essential oils, hydroxycinnamic acids and flavonoids were found as the major bioactive constituents of the most common Lamiaceae species, such as thyme, rosemary, peppermint, sage, lemon balm and oregano . The essential oil composition of Thymus vulgaris can vary greatly and various chemotypes have been recorded, particularly regarding thymol and carvacrol. Other constituents of thyme include rosmarinic acid and flavonoids (luteolin, eriodictyol, apigenin and some methylated flavones) [12,13]. Rosemary leaves contain an essential oil whose composition may vary according to the plant chemotype (eucalyptol, camphor-borneol and α-pinene-verbenone types are distinguished). Rosmarinic acid and flavonoids as well as diterpenes, which are structural derivatives of carnosic acid, belong to the phenolic fraction [14,15]. Menthol and menthone are the major components of peppermint essential oil. The phenolic constituents of peppermint include rosmarinic acid and several flavonoids, primarily eriocitrin, luteolin and hesperidin . The essential oil of Salvia officinalis is characterized by a high amount of α- and β-thujone. The non-volatile fraction of sage is mainly composed of various diterpenes, phenolic acids and flavonoids [17,18]. Lemon balm yields only a small quantity of essential oil, with citral and citronellal as the principal components. It also contains hydroxycinnamic acids (rosmarinic, p-coumaric and caffeic acids) and flavonoids, e.g., luteolin, quercetin, apigenin and kaempferol . The composition of Origanum vulgare essential oil from different geographical origins is most commonly characterised by carvacrol and thymol as the major components, though the proportions vary widely. The phenolic compounds including flavonoids and phenolic acids are another kind of abundant constituent in oregano . Investigation of the species belonging to the genus Teucrium revealed the presence of diterpenes, triterpenes, phytosterols, iridoids, flavonoids and essential oils [21,22]. It was found that Lavandula species contain essential oil, triterpenes, coumarins, hydroxycinnamic acids and flavonoids . Most of the chemical studies on Micromeria and Calamintha species were carried out for investigation of their volatile constituents and flavonoids [24,25,26].
A large number of species belonging to the genus Calamintha, Lavandula, Mentha, Melissa, Origanum, Rosmarinus, Salvia, Teucrium and Thymus has traditionally been used in Croatia and neighbouring countries to treat respiratory diseases, gastrointestinal problems and various nervous system disorders [27,28,29]. Some of them have been investigated for their antioxidant and neuroprotective effects using various in vitro and in vivo methods. These activities have mostly been attributed to the presence of polyphenols, particularly rosmarinic acid [30,31,32,33]. Along with other more common hydroxycinnamates, such as caffeic, ferulic, p-coumaric and chlorogenic acid, rosmarinic acid is widely distributed in the plant kingdom, occurring particularly in species of the Lamiaceae and Boraginaceae families. Recent biological and pharmacological studies have shown that this phytochemical possesses many beneficial effects, including antiviral, antibacterial, antioxidant, antiinflammatory, antiangiogenic, antidepressive, anticancer and antihepatotoxic activities [11,34,35].
Aiming to discover new and promising sources of potential anti-AD drugs, the present study was undertaken to evaluate the antiacetylcholinesterase and antioxidant properties of selected Croatian medicinal plants belonging to the Lamiaceae family. Additionally, their hydroxycinnamic acid profiles were investigated.
2. Results and Discussion
2.1. Acetylcholinesterase (AChE) Inhibitory Activity
Over the past two decades, cholinesterase inhibition has become the most widely employed clinical approach to treating the symptoms of AD. Various plants and phytochemical substances have demonstrated AChE inhibitory activity and thus could be beneficial in the treatment of neurodegenerative disorders such as AD . In this study, the ethanolic extracts of 26 medicinal plants of the Lamiaceae family growing in Croatia were comparatively tested for their inhibitory activity against AChE at concentrations of 0.25, 0.50 and 1 mg/mL by in vitro Ellman’s method. To the best of our knowledge, there are no literature data for most of the tested plants concerning the AChE inhibitory properties of their polar extracts, with the exception of Rosmarinus officinalis [30,36,37,38,39], Lavandula angustifolia [37,38,40], Salvia officinalis , Mentha x piperita [36,41], M. longifolia , M. pulegium [39,41], Melissa officinalis [37,40,42], Teucrium polium [36,42], Satureja montana  and Micromeria juliana . Since Lamiaceae species were found to be rich in phenolic acids as active constituents that significantly contribute to their neuroprotective properties , the anti-AChE activities of rosmarinic, caffeic, chlorogenic and ferrulic acid were also examined in this study. The plant alkaloid galanthamine was used as the reference AChE inhibitor.
All tested ethanolic extracts possessed the ability to inhibit AChE in a dose dependent manner (Figure 1). However, significant differences in AChE inhibitory properties were established between the tested plants, and values of 0%–35.8%, 0%–62.5% and 20.8%–97.0% were obtained for tested concentrations of 0.25, 0.50 and 1 mg/mL, respectively. The most potent plant extracts, with AChE inhibition rates above 75% at 1 mg/mL, were those of Mentha x piperita, M. longifolia, Salvia officinalis, Satureja montana, Teucrium arduini, T. chamaedrys, T. montanum, T. polium and Thymus vulgaris. Ethanolic extracts (1 mg/mL) of Calamintha grandiflora, C. officinalis, Lavandula angustifolia, L. x intermedia, Melissa officinalis, Micromeria graeca, M. thymifolia, Rosmarinus officinalis and Satureja subspicata demonstrated moderate inhibitory activity (50.5%–68.1%). On the other hand, Acinos arvensis, Calamintha sylvatica, Clinopodium vulgare, Marrubium incanum, Mentha pulegium, Micromeria croatica, M. juliana and Origanum vulgare did not achieve 50% inhibition of enzyme activity.
The tested hydroxycinnamic acids at 0.25 and 0.50 mg/mL inhibited 30.0%–48.9% and 73.6%–86.6% of AChE activity, respectively, which was generally a stronger effect than the tested extracts exerted, though at the highest concentration examined, their AChE inhibition (88.1%–96.7%) was comparable to the activity of the extracts found as the most potent. Galanthamine, used as the reference AChE inhibitor, demonstrated a similar effect at a 1,000 times lower concentration (IC50 = 0.122 ± 0.004 μg/mL). These results also confirmed previous findings of several medicinal plants reported to show AChE inhibitory activity, such as Rosmarinus officinalis [37,39], Salvia officinalis , Lavandula angustifolia [37,40] and Teucrium polium .
2.2. Antioxidant Activity
Since age is a primary risk factor for the majority of AD cases, oxidative stress is inevitably involved in the pathogenesis of AD. Oxidative stress is an imbalance between reactive oxygen species (ROS) production and the intracellular capacity for removing ROS, subsequently leading to excessive damage of DNA, lipids, carbohydrates and proteins in the cell. Neural cells, which suffer functional (ataxia) or sensory loss (dementia) in neurodegenerative diseases, are considered to be more susceptible to oxidative damage as compared to other body tissues. The brain is highly sensitive to oxidative stress as it is rich in peroxidizable fatty acids, has a high oxygen demand and a relative paucity of cellular- and tissue-specific antioxidant mechanisms [6,7]. Antioxidants can delay, inhibit or prevent the oxidation of oxidizable materials by scavenging free radicals and diminishing oxidative stress. The plant kingdom offers a wide range of compounds exhibiting antioxidant activities, especially plant polyphenols that have been investigated with the intent of finding compounds that can protect against a number of diseases related to oxidative stress and free radical-induced damage [45,46].
The free-radical scavenging activities of the ethanolic extracts of selected Lamiaceae species were evaluated by the commonly used DPPH assay, in comparison with pure hydroxycinnamic acids and trolox as a reference antioxidant. DPPH• is a stable free radical compound with a characteristic absorption at a wavelength of 517 nm. Antioxidants upon interaction with DPPH• either transfer an electron or hydrogen atom to DPPH•, thus neutralizing its free radical character. The colour of the reaction mixture changes from purple to yellow resulting in an absorbance decrease. The degree of discolouration indicates the scavenging potential of the antioxidants [47,48]. As shown in Table 1, all the tested samples demonstrated DPPH• scavenging activity in a concentration dependant manner, with a wide range of IC50 values from 3.08 µg/mL to 43.97 µg/mL. The ethanolic extract of Satureja subspicata exhibited the most effective radical scavenging ability, followed by Origanum vulgare (4.19 µg/mL) and Salvia officinalis (4.81 µg/mL). Some other tested plants, such as Rosmarinus officinalis, Teucrium polium, T. chamaedrys, Micromeria thymifolia, Melissa officinalis, Teucrium montanum, Mentha longifolia, M. x piperita, Micromeria graeca and Satureja montana, also showed potent antioxidant activity (IC50 = 5.06–9.95 µg/mL). Caffeic, rosmarinic, and chlorogenic acids with IC50 values of 0.36, 1.01 and 1.69 μg/mL, respectively, demonstrated the strongest antioxidative properties, even significantly stronger than trolox (IC50 = 1.99 µg/mL), while ferulic acid was a weaker free radical scavenger (IC50 = 3.56 µg/mL).
The total antioxidant capacities of Lamiaceae ethanolic extracts in comparison with hydroxycinnamic acids were evaluated using the phosphomolybdenum method. This assay is based on the reduction of Mo(VI) to Mo(V) by the antioxidant compounds and the subsequent formation of a green phosphate/Mo(V) complex at acidic pH with a maximal absorption at 695 nm . The obtained results, expressed as trolox equivalents (TE), are presented in Table 1. All investigated samples were active in a concentration dependent manner. Among investigated plants, Melissa officinalis, Salvia officinalis, Mentha longifolia, Origanum vulgare, Teucrium montanum, Mentha x piperita, Teucrium chamaedrys and Satureja montana possessed the highest total antioxidant capacities ranging between 717.41 mg TE/g and 855.78 mg TE/g. Hydroxycinnamic acids were much more active than tested extracts with values of 1240.65–1940.38 mg TE/g. Their potency decreased in the following order: caffeic acid > ferulic acid > rosmarinic acid > chlorogenic acid. Our results are in agreement with previous research on hydroxicinnamic acids [49,50,51] and suggest their great possible influence on antioxidant effects of the tested Lamiaceae extracts.
|Table 1. Antioxidant activities of the ethanolic extracts of selected Lamiaceae species and their phenolic acid constituents.|
|Plant part used||Extract yield a||DPPH radical scavenging activity||Total |
|Acinos arvensis (Lam.) Dandy||L0111||Aerial part||15.47||17.50 ± 0.42||254.97 ± 2.68|
|Calamintha grandiflora (L.) Moench||L0141||Aerial part||5.80||10.75 ± 0.22||609.03 ± 0.38|
|Calamintha officinalis Moench||L0142||Aerial part||9.02||16.45 ± 0.32||650.65 ± 3.44|
|Calamintha sylvatica Bromf.||L0143||Aerial part||11.62||18.61 ± 0.50||449.84 ± 3.82|
|Clinopodium vulgare L.||L0151||Aerial part||7.98||17.39 ± 0.13||473.62 ± 1.53|
|Lavandula angustifolia Mill.||L1101||Flower||11.05||31.62 ± 0.84||577.95 ± 13.76|
|Lavandula x intermedia Emeric ex Loisel.||L1102||Flower||16.86||43.97 ± 0.47||439.03 ± 15.29|
|Marrubium incanum Desr.||L1141||Aerial part||4.31||11.82 ± 0.33||502.54 ± 1.15|
|Melissa officinalis L.||L1151||Leaf||5.79||7.74 ± 0.01||855.78 ± 6.12|
|Mentha longifolia (L.) Huds.||L1173||Aerial part||7.34||8.43 ± 0.28||830.38 ± 6.12|
|Mentha pulegium L.||L1176||Aerial part||7.52||24.27 ± 0.21||518.49 ± 22.17|
|Mentha x piperita L.||L1175||Leaf||5.62||8.88 ± 0.13||790.38 ± 19.11|
|Micromeria croatica (Pers.) Schott||L1181||Aerial part||7.24||29.48 ± 0.51||530.11 ± 26.37|
|Micromeria graeca (L.) Benth. ex Reich.||L1184||Aerial part||7.42||8.79 ± 0.01||580.11 ± 3.06|
|Micromeria juliana (L.) Benth. ex Rchb.||L1185||Aerial part||4.69||17.52 ± 0.33||403.62 ± 21.79|
|Micromeria thymifolia (Scop.) Fritsch||L1189||Aerial part||6.67||6.53 ± 0.13||478.49 ± 7.64|
|Origanum vulgare L.||L1202||Aerial part||13.47||4.19 ± 0.04||803.89 ± 0.76|
|Rosmarinus officinalis L.||L1241||Leaf||19.32||5.06 ± 0.01||602.00 ± 3.44|
|Salvia officinalis L.||L1259||Leaf||12.40||4.81 ± 0.30||838.22 ± 12.61|
|Satureja montana L.||L1263||Aerial part||7.39||9.95 ± 0.06||717.41 ± 1.53|
|Satureja subspicata Bartl. ex Vis.||L1264||Aerial part||17.60||3.08 ± 0.04||406.59 ± 19.11|
|Teucrium arduini L.||L1301||Aerial part||12.48||18.06 ± 0.68||530.11 ± 30.96|
|Teucrium chamaedrys L.||L1304||Aerial part||11.34||5.97 ± 0.11||792.81 ± 11.85|
|Teucrium montanum L.||L1308||Aerial part||14.44||7.78 ± 0.13||771.19 ± 8.03|
|Teucrium polium L.||L1309||Aerial part||15.67||5.90 ± 0.12||589.30 ± 14.52|
|Thymus vulgaris L.||L1318||Aerial part||7.25||12.27 ± 0.07||679.83 ± 12.96|
|Phenolic acid constituent|
|Rosmarinic acid||1.01 ± 0.07||1894.84 ± 10.51|
|Chlorogenic acid||1.69 ± 0.02||1240.65 ± 59.24|
|Caffeic acid||0.36 ± 0.03||1940.38 ± 5.35|
|Ferulic acid||3.56 ± 0.36||1923.62 ± 0.20|
|Trolox (referent antioxidant)||1.99 ± 0.03||-|
a Extract yield expressed as percentage weight of air-dried plant material.
2.3. Content and Composition of Hydroxycinnamic Acids
The contents of total hydroxycinnamic derivatives in the ethanolic extracts of selected Lamiaceae species were determined spectrophotometrically and expressed as mg rosmarinic acid per g of dry plant extract (Table 2). The presented results revealed that the extracts differed greatly in hydroxycinnamic acids content, ranging from 10.75 mg/g to 173.10 mg/g. Satureja subspicata contained the highest amount of these polyphenolic compounds, whereas their lowest level was found in Teucrium arduini. In addition to Satureja subspicata, the extracts of Mentha x piperita, Origanum vulgare, Satureja montana, Salvia officinalis, Micromeria graeca, Mentha longifolia, Micromeria thymifolia, Melissa officinalis, Calamintha grandiflora and Thymus vulgaris were also characterized by a high hydroxycinnamic acids content (72.98–157.45 mg/g).
|Table 2. Content and composition of hydroxycinnamic derivatives of Lamiaceae ethanolic extracts.|
|Medicinal plant||Plant part used||Total hydroxycinnamic derivatives a||Rosmarinic acid b||Chlorogenic acid b||Caffeic acid b||Ferulic acid b|
|Acinos arvensis||Aerial part||36.58 ± 0.42||2.21||26.06||3.53||nd|
|Calamintha grandiflora||Aerial part||75.42 ± 0.74||24.08||2.01||0.37||nd|
|Calamintha officinalis||Aerial part||30.17 ± 0.44||3.82||6.88||0.57||nd|
|Calamintha sylvatica||Aerial part||31.65 ± 0.19||0.70||11.18||0.74||nd|
|Clinopodium vulgare||Aerial part||27.12 ± 0.71||12.27||2.25||0.56||nd|
|Lavandula angustifolia||Flower||42.64 ± 0.19||3.31||3.22||nd||1.31|
|Lavandula x intermedia||Flower||26.00 ± 0.38||3.04||1.00||0.33||0.11|
|Marrubium incanum||Aerial part||57.78 ± 1.25||5.01||1.14||0.47||nd|
|Melissa officinalis||Leaf||77.70 ± 0. 94||39.48||1.16||1.05||nd|
|Mentha longifolia||Aerial part||80.06 ± 1.76||22.33||1.50||1.18||nd|
|Mentha pulegium||Aerial part||34.83 ± 0.38||12.72||1.64||0.72||nd|
|Mentha x piperita||Leaf||157.45 ± 2.71||61.05||1.78||2.15||0.50|
|Micromeria croatica||Aerial part||30.13 ± 0.33||9.95||1.26||0.70||nd|
|Micromeria graeca||Aerial part||81.76 ± 0.76||18.41||1.26||0.79||0.27|
|Micromeria juliana||Aerial part||41.50 ± 0.25||21.62||1.29||0.91||0.28|
|Micromeria thymifolia||Aerial part||79.86 ± 1.51||26.50||13.22||2.98||0.93|
|Origanum vulgare||Aerial part||129.16 ± 0.76||37.73||nd||1.12||nd|
|Rosmarinus officinalis||Leaf||55.57 ± 0.47||18.94||1.18||0.63||nd|
|Salvia officinalis||Leaf||86.86 ± 0.59||18.72||1.13||0.80||0.77|
|Satureja montana||Aerial part||95.29 ± 0.66||31.11||1.19||0.65||nd|
|Satureja subspicata||Aerial part||173.10 ± 1.68||46.11||1.62||1.78||nd|
|Teucrium arduini||Aerial part||10.75 ± 0.72||nd||1.75||nd||0.97|
|Teucrium chamaedrys||Aerial part||18.58 ± 0.97||1.03||4.06||nd||1.37|
|Teucrium montanum||Aerial part||15.11 ± 1.67||nd||2.25||2.36||1.70|
|Teucrium polium||Aerial part||13.91 ± 0.42||nd||2.19||2.36||1.38|
|Thymus vulgaris||Aerial part||72.98 ± 0.18||32.80||1.18||2.07||0.49|
a Content determined spectrophotometrically and expressed as mg rosmarinic acid/g of extract; b Content determined by HPLC and expressed as mg/g of extract; nd – not detected.
Furthermore, RP-HPLC analyses of rosmarinic, chlorogenic, caffeic and ferulic acids, as the most common free hydroxycinnamic acids present in Lamiaceae species [11,52,53], were carried out and the obtained results are presented in Table 2. The main components of most of the tested extracts were rosmarinic (0.70–61.05 mg/g) and chlorogenic acids (1.00–26.06 mg/g), while caffeic (0.33–3.53 mg/g) and ferulic acids (0.11–1.70 mg/g) were generally less abundant. Figure 2 shows the respective HPLC profiles of ten ethanolic extracts containing more than 20 mg/g of rosmarinic acid found to be the predominant constituent of most of the investigated Lamiaceae species. These results highlight Mentha x piperita, Satureja subspicata and Melissa officinalis as rich sources of rosmarinic acid, while Acinos arvenis had a high content of chlorogenic acid (26.06 mg/g).
The obtained results showed a very strong positive correlation between rosmarinic acid and total hydroxycinnamic acids content (r = 0.905, p < 0.001), indicating the great contribution of rosmarinic acid to the content of total hydroxycinnamic acids in Lamiaceae species. Comparing the total hydroxycinnamic acids content with the chlorogenic, caffeic and ferulic acid contents, no significant correlations were observed (r values range from −0.313 to 0.234 with p = 0.119–0.353). The influence of rosmarinic acid content on AChE inhibitory and antioxidant properties of the tested Lamiaceae species was also evaluated. No significant correlation was found between rosmarinic acid content and AChE inhibitory activity at 1 mg/mL (r = 0.150, p = 0.465). However, a moderate positive correlation was observed (r = 0.533, p = 0.011) between rosmarinic acid content and anti-AChE activity (1 mg/mL) for the investigated plants, excluding Teucrium species. The correlation between rosmarinic acid content and DPPH activity for all plant extracts was moderate (r = −0.441, p = 0.024), and even strong for plant extracts excluding Teucrium species (r = −0.614, p = 0.002). There was no statistically significant correlation between rosmarinic acid content and total antioxidant capacity (r = 0.344, p = 0.086), while a moderate correlation was observed in comparing the investigated Lamiaceae species excluding Teucrium species (r = 0.507, p = 0.016). These results are consistent with previously published data [30,31,32,54], and therefore, rosmarinic acid is highly likely to contribute substantially to AChE inhibitory and antioxidant activities of most studied Lamiaceae species. However, the notable activity of tested Teucrium species containing low amounts of hydroxycinnamic acids could be attributed to their terpenic components which are well-known to possess anti-AChE properties . On the other hand, their significant antioxidant properties likely depend on flavonoids and other present phenolic compounds . The findings suggest that Lamiaceae extracts that contain both terpenes and polyphenols could affect different targets, including AChE activity and oxidative stress.
3.1. Plant Material and Extraction Procedure
A total of 26 wild-growing Lamiaceae species used in this study (Table 1) were collected before (leaves) and during the flowering period (aerial parts and flowers), between May and September 2011, in Croatia. The plant material was identified at the Department of Pharmacognosy, Faculty of Pharmacy and Biochemistry, University of Zagreb, Croatia, where the voucher specimens have been deposited. Air-dried and pulverized plant material (5.00 g) was extracted with ethanol (50 mL) for 30 min using an ultrasonic bath. The extract was then filtered through Whatman No. 1 paper and concentrated to dryness under a vacuum on a rotary evaporator at 50 °C. The extraction yields are given in Table 1.
Acetylcholinesterase (AChE) from electric eel (Type-VI-S, EC 184.108.40.206), acetylthiocholine iodide (ATChI), ammonium molybdate, chlorogenic acid (≥95%), 2,2-diphenyl-1-picryl-hydrazyl (DPPH•), 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB), galanthamine hydrobromide, sodium molybdate, sodium nitrite, rosmarinic acid (96%) and Trizma base were obtained from Sigma-Aldrich (St. Louis, MO, USA). Sodium hydroxide and sodium phosphate were purchased from Kemika (Zagreb, Croatia). Caffeic acid (≥95%), ferulic acid (≥98%) and trolox (≥98%) were obtained from Fluka (Buchs, Switzerland). All other chemicals and reagents used were of analytical grade.
3.3. Acetylcholinesterase (AChE) Inhibition Assay
The AChE inhibitory activities of the Lamiaceae extracts and their phenolic acid constituents were determined using modified Ellman’s colorimetric method described by Conforti et al. . In brief, 1900 μL of 50 mM Tris-HCl buffer (pH 8.0), 40 μL of 0.02 U/mL AChE and 20 μL of tested solution (0.25–1 mg/mL) were mixed and pre-incubated for 30 min at 4 °C. The reaction was then initiated with the addition of 20 μL of 10 mM DTNB and 20 μL of 12 mM ATChI. AChE activity was determined spectrophotometrically through measuring the change in ultraviolet absorbance of an assay solution at 412 nm over a period of 10 min at 25 °C. Galanthamine (0.03–1 μg/mL) was used as positive control. Percentage enzyme inhibition was calculated by comparing the enzymatic activity with, and without inhibitor. The experiment was run in triplicate.
3.4. DPPH Free Radical Scavenging Assay
The free radical scavenging activities of the investigated Lamiaceae extracts and their phenolic acid constituents were evaluated using the stable DPPH radicals according to the previously reported method . Briefly, 0.1 mM solution of DPPH in ethanol was prepared and 1 mL of this solution was added to 3 mL of the ethanolic sample solution. The samples were assayed in a range of 0.2–100 μg/mL. After incubation for 30 min in the dark at room temperature, the absorbance was measured spectrophotometrically at 517 nm. Trolox was used as the reference antioxidant compound. The assay was carried out in triplicate. The capability to scavenge the DPPH radicals was calculated using the following equation: (%) = (1 − A1/A0) × 100, where A0 is the absorbance of the control reaction and A1 is the absorbance in the presence of sample, corrected for the absorbance of sample itself. The concentrations of samples that provide 50% inhibition (IC50) were obtained by interpolation from linear regression analysis.
3.5. Total Antioxidant Capacity Assay
The total antioxidant capacities of the studied Lamiaceae plant extracts and their phenolic acid constituents were evaluated by the phosphomolybdenum method previously described by Vladimir-Knežević et al. . An aliquot of sample solution in ethanol (0.3 mL, 50 and 100 μg/mL) was combined in a vial with reagent solution (2.7 mL) containing 0.6 M sulfuric acid, 28 mM sodium phosphate and 4 mM ammonium molybdate. The reaction mixture was incubated at 95 °C for 90 min. After cooling to room temperature, the absorbance was measured spectrophotometrically at 695 nm. The assay was run in triplicate. The antioxidant capacity of the sample was expressed as trolox equivalents (TE), utilizing a calibration curve of trolox.
3.6. Determination of Total Hydroxycinnamic Derivatives
For the determination of total hydroxycinnamic acids content, the following procedure described in European Pharmacopoeia was performed . Briefly, the plant extract (0.200 g) was mixed with 50% ethanol (80 mL) and boiled in a water bath under a reflux condenser for 30 min. The cooled extract was filtered into a 100 mL volumetric flask, the filter rinsed, and diluted to 100.0 mL with 50% ethanol. The obtained solution served as stock solution. Test solution was prepared by mixing stock solution (1.0 mL) with 0.5 M hydrochloric acid (2 mL), 2 mL of a solution prepared by dissolving 10 g of sodium nitrite and 10 g of sodium molybdate in 100 mL of water, dilute sodium hydroxide (2 mL, 8.5%) and diluted to 10.0 mL with water. The absorbance of the test solution was immediately measured spectrophotometrically at 505 nm, using a compensation solution prepared by diluting 1.0 mL of the stock solution. Each sample was tested in triplicate and the content of total hydroxycinnamic derivatives was expressed as mg of rosmarinic acid per g of dry plant extract.
3.7. HPLC Analysis
The hydroxycinnamic acids composition of the selected Lamiaceae species was studied using a slightly modified method of Fecka and Turek . HPLC analysis was conducted on an Agilent 1100 Series instrument (Agilent Technologies, Santa Clara, CA, USA) equipped with an Agilent auto sampler, a quaternary pump, a column thermostat, and a photodiode array detector. The separation was achieved using a LichroCART®250-4 column (250 mm × 4.0 mm i.d.) packed with LiChrospher® 100 RP-18e (5 μm). The mobile phase consisted of acidified acetonitrile (5% formic acid in acetonitrile, solvent A) and acidified water (5% formic acid in water, solvent B). The gradient employed was as follows: 0 min, 15% A; 25 min, 35% A; 27 min, 70% A; 32 min, 70% A; 33 min, 100% A; 38 min, 100% A. The flow rate was 0.9 mL/min. The injection volume for the sample was 20 μL. All chromatographic experiments were performed at 20 °C. Polyphenolic profiles of plant extracts were recorded at a wavelength of 330 nm. Chromatographic data were acquired and processed using HP ChemStation software. Phenolic acids were identified based on their chromatographic retention times and UV spectra, and quantified by comparing integrated peak areas to calibration curves prepared with corresponding analytical standards. The results were expressed in mg per g of the dry extract. All HPLC analyses were run in duplicate.
3.8. Statistical Analysis
The data analysis was performed using Microsoft Excel 2007 software and MedCalc for Windows (version 220.127.116.11.). The results were tested for normal distribution by Kolmogorov-Smirnov test. Correlations were assessed using Pearson’s correlation coefficient (r) and p < 0.05 was considered statistically significant.
This paper presents the results of a comparative study of AChE inhibitory and antioxidant activities of a large number of Lamiaceae medicinal plants, providing the first-ever data for most of them. Of the 26 tested ethanolic extracts, eight did not achieve 50% inhibition of AChE at a concentration of 1 mg/mL, whereas nine extracts showed strong inhibitory activity, achieving values over 75%. These findings suggest the great influence of the rosmarinic acid content and total hydroxycinnamic derivatives on the AChE inhibitory properties of tested plants, with the exception of Teucrium species, whose exceptional effects on AChE could be associated with other constituents such as terpenes. All the tested extracts also demonstrated moderate to strong antioxidant activities, primarily due to their high levels of polyphenols. The obtained results showed that Lamiaceae species containing multifunctional phenolic and terpenic components that can affect different targets, such as AChE activity and oxidative stress, may have great relevance in the prevention and therapy of AD and other neurodegenerative disorders.
This work was supported by the Ministry of Science, Education and Sports of Republic of Croatia (Project No. 006-0061117-1238) and bilateral Croatian-Austrian project (NatProd AD), and also partially supported by the scholarship awarded to Jelena Vladić by CEEPUS III Network.
SVK made significant contribution to conception and design of the study, collection and identification of the plants, interpretation of data and writing of the manuscript. BB participated in the design of the study, collection and extraction of plant materials, phytochemical analysis, enzyme assay, data analysis and manuscript writing. MK contributed to collection and extraction of plant materials, enzyme assay, data analysis and manuscript preparation. JV was involved in the antioxidant and phytochemical assays. ADLN carried out part of the phytochemical analysis. AHB participated in the study design and coordination and revised the manuscript critically. All authors read and approved the final manuscript.
Conflicts of Interest
The authors declare no conflict of interest.
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