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Keywords Kúcové slová: 1. INTRODUCTION Salvia officinalis L. (sage) is a common aromatic plant of the Lamiaceae family, widely cultivated for its medicinal and culinary purposes. Sage shows various biological activities and medicinal properties: antioxidant, antibacterial, antifungal, anti-inflammatory, antispasmodic, astringent and antihidrotic (Bouaziz et al., 2009; Martins et al., 2015; Lu & Foo, 2001; Baricevic et al., 2001; Khan et al., 2011; British Herbal Compendium, 2006). The predominant medicinally valuable compounds are monoterpenes in essential oil (- and -thujones, 1,8-cineol, camphor), diterpenes (carnosic * E-mail: firstname.lastname@example.org © Acta Facultatis Pharmaceuticae Universitatis Comenianae acid, carnosol), triterpenes (ursolic and oleanolic acids) and phenolics phenolic acids (especially caffeic acid and their depside forms, e.g. rosmarinic acid) and flavonoids (luteoline and apigenine derivatives). The main antioxidative effect of Salvia officinalis was reported to relate to the presence of carnosic acid, carnosol, and hydroxycinnamic derivatives, especially rosmarinic acid (Cuvelier et al., 1996). Hydroxycinnamic derivatives are sometimes described as ,,Lamiaceae or Labiatae tannins" since they may be adsorbed by hide powder to some extent in methods for the determination of tannins in herbal drugs. However, they are not genuine tannins (British Herbal Compendium, 2006). Pharmacopoeial assays usually require the quantification of essential oil in herbal drugs originating from Lamiaceae plant species (more precisely from the Nepetoideae subfamily species). Sometimes the total hydroxycinnamic derivatives or specifically rosmarinic acid quantification is required (as in Rosmarini folium, Melissae folium). For Salviae officinalis folium, the European Pharmacopoeia (8th Edition) includes the essential oil assay (Ph. Eur. 8, 2014). The content and composition of sage essential oil has been studied extensively in previous years. Changes in its content due to external and internal influences, e.g. locality, climatic conditions, plant phenophase, as well as content differences in respective plant parts are reported in previous studies (Grella & Picci, 1988; Tekeová, 1993; Tekeová & Havassy, 1993; Rasmussen et al., 1971; Tekeová & Felklová, 1993; Tekeová et al., 1994). Contemporary research also focuses on sage phenolic compounds that show antioxidant activity. Factors influencing their accumulation in respective plant organs and links to e.g. plant phenophase have not yet been studied well so far. This inspired the present study that quantifies total hydroxycinnamic derivatives and rosmarinic acid in sage leaf and stem samples from different harvest times. Individual opposite leaf pairs have been studied as well. specimens were deposited at the Herbarium, Department of Pharmacognosy and Botany, Faculty of Pharmacy, Comenius University in Bratislava. 2.2. Biological evaluation and secondary metabolites determination Phenolic compounds were quantified both in dry leaves (average sample), and in individual leaf pairs samples, as well as in stems. Biological evaluation was carried out on 10 sample shoots. Chemical analyses were carried out on average samples gained from 100 shoots. Measurements were performed in triplicate. 2.2.1. Total hydroxycinnamic derivatives (THD) (Arnow's spectrophotometric assay) THD content was quantified using a spectrophotometric method that employs Arnow's reagent according to the European Pharmacopoeia (Ph. Eur. 8, 2014). Two extraction solvents, ethanol (50 % V/V) and methanol, were used, respectively. Measuring conditions: 505 nm; spectrophotometer Genesys 6 (Thermo Electron Corporation, UK). THD percentage was calculated with reference to the dried drug and expressed as rosmarinic acid content. 2.2.2. Rosmarinic acid (RA) (HPLC assay) Rosmarinic acid content was quantified using a previously published HPLC method (Tóth et al., 2003). The plant materials were extracted with methanol in Soxhlet's apparatus (3 hours). Measuring conditions: HPLC set: ECOM (Czech Republic, gradient elution: methanol and orthophosphoric acid (pH 2.5), column: LiChrospher 100 (RP-18(e), 5 m, 125×4 mm), liquid-liquid pre-separation, UVD: 320 nm. RA percentage was calculated using the external standard method (rosmarinic acid, Aldrich, USA) based on peak area, with reference to the dried drug. 2. MATERIAL AND METHODS 2.1. Plant material Salvia officinalis L. cv. `Krajová' plants were grown in climate conditions of Southwest Slovakia, in the Medicinal Plants Garden, Faculty of Pharmacy, Comenius University in Bratislava. A 3-years-old culture was planted on a light sand-loam soil in a sunny location. Non-flowering tops were harvested at 3 different times of year: at the end of May and in mid-June in the vegetative development phase, and in July in the flowering phase, respectively. Subsequently, a second harvest was carried out in September (of plants first harvested in June). Harvests were generally carried out in the afternoon of sunny days. Plant shoots were dried at room temperature. Dry shoots were separated into: individual opposite leaf pairs, side branches, and stems. These fractions were stored separately in paper sachets at room temperature. Voucher 3. RESULTS AND DISCUSSION Sage (Salvia officinalis L.) is native to the Mediterranean area, but can be successfully cultivated in Central European climatic conditions, including Slovak Republic. Our previous cultivation experience with the domestic cultivar `Krajová' shows that several harvests in the course of one year are possible (Tekeová, 1993). Both sage leaf and whole herb constitute herbal drugs of pharmacopoeial quality. The Pharmacopoea Bohemoslovaca listed a herb monograph Herba salviae (PhBs IV, 1987). The currently valid monograph of the European Pharmacopoeia describes the leaf Salviae officinalis folium (Ph. Eur. 8, 2014). The recommended time for leaf harvest lies in the phenophase before flowering, or at the beginning of flowering at latest (May/July), as leaf essential Figure 1. Salvia officinalis L. cv. `Krajová' May harvest plant organ weight percentage in herb compared to RA content [%]. RA content rosmarinic acid content ([%] in dry aerial plant organs), VT vegetative top, 1p 1st opposite leaf pair (2p to 4p subsequent leaf pairs), S 3 side branches (length 0.5 to 3 cm), St stem. Values are presented as average value. Figure 2. Salvia officinalis L. cv. `Krajová' June harvest plant organ weight percentage in herb compared to RA content [%]. RA content rosmarinic acid content ([%] in dry aerial plant organs), VT vegetative top, 1p 1st opposite leaf pair (2p to 6p subsequent leaf pairs), S side branches of different length (S 3 0.5 to 3 cm, S 6 3.5 to 6 cm), St stem. Values are presented as average value. oil content decreases during the flowering phase (June/ August) (Heeger, 1956). Another important reason to carry out an earlier harvest in our climatic conditions is the risk of plant culture frost damage in winter, after the first harvest has been carried out at the flowering phase, and the subsequent second harvest was shifted to later autumn (Heeger, 1956). This work deals with the total hydroxycinnamic derivatives (THD) and rosmarinic acid (RA) content quantification in aerial parts of the domestic cultivar Salvia officinalis L. `Krajová' in the course of one vegetation year. Whole nonflowering tops were harvested. The first harvest was carried out at three different times of the year: at the end of May and in mid-June in the vegetative development phase, and in July in the flowering phase, respectively. Subsequently, a second harvest was carried out in September (of plants first harvested in June). Shoots from the May and June harvests grew 4, and 6 opposite leaf pairs in average, respectively. Longest leaves were 7 8 cm long (without petiole). Only non-flowering tops were cut of flowering plants in July. These shoots showed 11 opposite leaf pairs in average; the longest leaf was 8.6 cm long (Table 1). Leaves placed on the middle part of the stem represented the largest weight portion of the whole leaf samples. Stems counted for 17.5 28 % of whole herb weight (Fig. 1 4). A spectrophotometric pharmacopoeial method (Ph. Eur. 8, 2014) was employed for the quantification of total hydroxycinnamic derivatives (THD), as published in the Rosmarini folium monograph assay. The Salviae officinalis folium monograph requires the assay for essential oil instead of the THD assay. The extraction solvent for the pharmacopoeial THD assay is ethanol (50 % V/V), whereas methanol has often been employed for the rosmarinic acid (RA) extraction (Gracza & Ruff, 1984; Baskan et al., 2007). Water-ethanolic leaf extracts (50 % V/V) of whole shoots samples (Salviae officinalis folium) showed small variations only in THD content in the course of one year: from 3.06 % to 3.52 %, with maxima in May and September samples. Stems of all first harvests contained 1.33 1.54 % THD only. Table 1. Salvia officinalis L. cv. `Krajová' leaf length, and THD quantification [%] in leaf pairs linked to harvest time and extraction solvent Vegetative phase May Leaf length [cm] VT 1p 2p 3p 4p 5p 6p 7p 8p 9p 10p 11p S3 S6 S 10 3.58 0.33 3.43 0.30 3.30 0.21 2.96 0.18 3.80 0.24 3.93 0.29 3.4 0.5 5.9 1.1 7.2 1.2 6.9 1.5 THD [%] 50% EtOH 6.21 0.60 2.44 0.17 2.57 0.31 3.05 0.34 1.45 0.15 Leaf length MeOH [cm] 4.81 0.39 2.65 0.27 1.96 0.13 2.24 0.20 1.30 0.14 3.9 0.9 6.5 1.1 7.7 0.6 7.9 1.0 7.8 0.8 7.3 1.3 June THD [%] 50% EtOH 5.14 0.44 3.38 0.29 2.76 0.19 2.27 0.31 2.95 0.24 3.35 0.16 3.03 0.12 Leaf length MeOH [cm] 5.70 0.37 3.51 0.29 2.02 0.21 1.70 0.07 2.38 0.13 2.31 0.26 1.98 0.10 3.4 0.7 4.4 0.4 5.8 0.5 6.5 0.6 6.8 0.9 7.1 0.9 7.5 0.8 8.2 0.9 8.6 0.9 8.2 0.2 8.4 0.1 Flowering phase July THD [%] 50% EtOH 6.09 1.63 4.50 0.20 3.06 0.19 2.34 0.45 2.27 0.13 2.32 0.33 2.22 0.31 2.49 0.35 2.62 0.10 2.73 0.88 3.15 0.83 2.59 0.15 3.29 0.30 3.50 0.27 2.93 0.19 Leaf length MeOH [cm] 6.03 0.36 3.79 0.13 2.14 0.16 1.38 0.26 1.19 0.27 1.21 0.09 0.89 0.06 1.00 0.02 1.47 0.12 1.60 0.14 1.53 0.15 1.19 0.10 3.00 0.29 2.07 0.17 1.85 0.10 3.91 0.28 3.22 0.15 3.88 0.19 3.37 0.23 3.1 0.6 4.9 0.4 5.8 0.5 5.9 0.7 5.5 0.7 5.2 0.7 4.4 0.5 Second harvest September THD [%] 50% EtOH 4.70 0.45 3.49 0.38 2.71 0.24 2.94 0.28 2.98 0.27 3.08 0.23 3.51 0.35 3.75 0.31 MeOH 4.96 0.26 3.38 0.19 2.6 0.15 2.56 0.13 1.99 0.13 2.41 0.14 2.75 0.12 2.37 0.11 THD total hydroxycinnamic derivatives content expressed as rosmarinic acid ([%] in dry leaves), VT vegatative top, 1p 1st opposite leaf pair (2p to 11p subsequent leaf pairs), S side branches of different length (S 3 0.5 to 3 cm, S 6 3.5 to 6 cm, S 10 6.5 to 10 cm), 50% EtOH ethanol (50 % V/V) extract, MeOH methanol extract. Values are presented as average value (bold) ± standard deviation. Figure 3. Salvia officinalis L. cv. `Krajová' July harvest plant organ weight percentage in herb compared to RA content [%]. RA content rosmarinic acid content ([%] in dry aerial plant organs), VT vegetative top, 1p 1st opposite leaf pair (2p to 11p subsequent leaf pairs), S side branches of different length (S 3 0.5 to 3 cm, S 6 3.5 to 6 cm, S 10 6.5 to 10 cm), St stem. Values are presented as average value. Figure 4. Salvia officinalis L. cv. `Krajová' September (second) harvest plant organ weight percentage in herb compared to RA content [%]. RA content rosmarinic acid content ([%] in dry aerial plant organs), VT vegetative top, 1p 1st opposite leaf pair (2p to 7p subsequent leaf pairs), S side branches of different length (S 3 0.5 to 3 cm, S 6 3.5 to 6 cm), St stem. Values are presented as average value. Stems of the second harvest increased their THD content to percentages comparable to leaf samples, on the contrary. This applies mostly to the fleshy top part of the stems. Methanolic extracts showed THD contents lower by about ¼ compared to the water-ethanolic leaf extracts (Table 2). Common sage THD percentages have been reported to be in the range of 3.5 % (Lamaison et al., 1990). Our domestic cultivar `Krajová' shows slightly lower percentages that but still obey the pharmacopoeial criteria of other Lamiaceae herbal drugs monographs, e.g. Rosmarini folium: min. 3 % (Ph. Eur. 8, 2014). Rosmarinic acid (RA) quantification was carried out using a previously published method (Tóth et al., 2003). Leaves and stems RA percentages showed very similar trends compared to the THD content, with maxima in youngest-grown shoots (May and September): leaves 0.76 1.65 %, and stems 0.19 0.83 % of RA, respectively. The RA leaf content showed a marked decrease during the flowering phenophase (July). Other authors have reported higher September RA percentages as well (Areias et al., 2000). Reference values for sage leaf RA content range from 0.2 % to 1.4 % (Janicsák et al., 1999; Wang et al., 2004). European Pharmacopoeia's Lamiaceae herbal drugs monographs HPLC assays, e.g. Melissae folium, require RA contents not lower than 1.0 % (Ph. Eur. 8, 2014). Stems show generally low RA content, except for fleshy top parts, which in some cases showed RA contents even exceeding leaf RA percentages (Table 2). Table 2. Salvia officinalis L. cv. `Krajová' THD and RA quantification [%] in leaf and stem samples linked to harvest time and extraction solvent Vegetative phase May 3.52 0.25 2.77 0.31 1.65 0.12 1.46 0.13 1.10 0.10 0.60 0.04 2.17 0.31 2.48 0.23 1.70 0.14 June 3.26 0.33 2.57 0.21 1.31 0.04 1.33 0.10 0.51 0.26 0.20 0.03 1.84 0.11 1.66 0.13 0.89 0.09 Flowering phase July 3.06 0.31 1.36 0.11 0.76 0.08 1.54 0.11 0.62 0.25 0.19 0.03 1.78 0.16 2.05 0.17 0.69 0.05 Second harvest September 3.33 0.29 2.41 0.17 1.57 0.12 3.04 0.23 2.39 0.15 0.83 0.14 3.36 0.19 2.83 0.21 1.84 0.22 Extract 50% EtOH THD Leaf RA MeOH MeOH 50% EtOH THD Whole RA Stem 50% EtOH THD Top part RA MeOH MeOH MeOH MeOH THD total hydroxycinnamic derivatives content expressed as rosmarinic acid ([%] in dry leaves), RA rosmarinic acid content ([%] in dry leaves), 50% EtOH ethanol (50 % V/V) extract, MeOH methanol extract. Values are presented as average value (bold) ± standard deviation. Differences in THD and RA contents observed in sage whole shoot leaf samples (Salviae officinalis folium) are notably influenced by the content of these active compounds in the respective leaf pairs. Highest contents of the quantified phenolics are present in top-most shoot parts, and decrease basipetally (Table 2, Fig. 1 4). This illustrates the influence that the cut shoot's number of leaf pairs shows on the overall quality of the herbal drug Salviae officinalis folium. These results complement well findings of some of our previous works with the domestic cultivar Salvia officinalis L `Krajová' (Tekeová & Felklová, 1993), and confirm that leaves of sage shoots top parts should be the primary harvest source of high-quality herbal drug both from the point of high essential oil and phenolics (THD and RA) contents. First harvest can be carried out as early as in May. Such plant cultures allow even for three harvests in the course of one year (Tekeová, 1993), and such herbal drug (mainly plant material originating from subsequent harvests) shows both sufficient essential oil and phenolics (THD and RA) contents (the Ph. Eur. 8 criterion for the essential oil assay in Salviae officinalis folium is minimum 12 mL/kg, i.e. 1.2 % V/m). Leaves of autumn harvests comprise the expectation of higher thujone contents (Tekeová & Havassy, 1993). 4. CONCLUSION Leaves of sage (Salvia officinalis L. cv. `Krajová') shoots top parts are the best source of high-quality herbal drug both from the point of high essential oil (Tekeová, 1993), and phenolics (THD and RA) contents. The leaf content of the studied phenolics decreases during the flowering phenophase (this is in agreement with previous observations of lower essential oil contents in the flowering phenophase). Both leaves and stems originating in the plant material gained in a subsequent second harvest show higher phenolics (THD and RA) contents. Acknowledgements This study was partially supported by a grant project of the VEGA agency, No. VEGA 2/0044/15.
Acta Facultatis Pharmaceuticae Universitatis Comenianae – de Gruyter
Published: Jun 1, 2015
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