Antiplatelet activity of methanol extracts of Rhizoplaca melanophthalma and Umbilicaria krascheninnikovii, two saxicolous lichens from the Maule Region, Chile

Introduction

Lichens are symbiotic organisms usually composed of a fungal partner (mycobiont) and one or more photosynthetic partners (photobiont), which is most often either a green alga or a cyano bacterium or both [1,2]. Although the dual nature of most lichens is now widely recognized, it is less commonly known that some lichens are symbioses involving three (tripartite lichens) or more partners [3].

In general, lichens exist as discrete thalli and are implicitly treated as individuals in many studies, even though they may be a symbiotic entity involving species from three kingdoms. Some li chen metabolites are widely used for medicinal and industrial purposes [4-6]. Currently there is increased interest in finding natural secondary metabolites of lichens that are useful in the treatment of cardiovascular diseases due to the prolonged use of other synthetic compounds, such as salicylic acid (aspirin), that are regularly used to control these diseases but often with side effects [7]. The identification of such compounds has become urgent because projections have shown that cardiovascular diseases could become the leading causes of death by 2020 [8-10].

Therefore, the aims of the present study were to:

a) obtain crude extracts of two Rhizoplaca melanophthalma and Umbilicaria krascheninnikovii lichen species using solvents of different polarity

b) assess the antiaggregant activity of crude methanol extracts against ADP and TRAP-6, determine the inhibitory minimal concentration; and

c) identify compounds responsible for antiplatelet activity.

Materials and Methods

Collection and identification of lichen samples

Two saxicolous lichen species — Rhizoplaca melanophthalma (Ram.) Leuck. & Poelt (Lecanoraceae) and Umbilicaria krascheninnikovii (Savicz) Zahlbr (Umbilicariaceae) — were collected in January 2017 from the Maule Region of Chile. The lichens were obtained from rocky systems surrounding Lake Maule (30°04’ S; 70°30’ W), located 50 km west of Talca at an altitude of 2300 m above sea level. The lichen material was identified by Jae-Seoun Hur of Souchon University, South Korea, and Iris Pereira of University of Talca, Chile. The specimens were deposited in the herbarium of the University of Talca (UTAL).

Preparation of Extract

Lichen material was cleaned, dried, weighed and put in labelled Erlenmeyer flasks. Metabolites were then extracted from samples using four solvents in decreasing order of polarity: hexane, dichloromethane, ethyl acetate and methanol. Extractions were performed by adding 300 mL of solvent to material of U. krascheninnikovii and 250 mL to material of R. melanophthalma (ratio of 1:2 weight/solvent) followed by sonication for 1 h (Transsonic T460) [11]. The product of each sonication was filtered using a Watson N° 1 filter. This procedure was repeated for 30 min for each solvent. The filtrates were then subjected to rotary evaporation at 35 ± 5ºC under reduced pressure to remove the solvent and obtain a concentrate of each extract. The concentrate was then suspended in chloroform and dispensed into small vials of known weight to reduce the loss of material. After complete evaporation of chloroform, each vial was weighed. Only methanol extracts were used to assess antiaggregant activity due to the high availability of this extract.

Preparation of Lichen Extract Standards

Methanol extracts of both lichen species were suspended to give a final reaction volume of 520 μL. A final crude methanol extract concentration of 1.0 mg/mL was used with DMSO (dimethyl sulfoxide) as a solvent to a final concentration of 0.5% with distilled water added to complete 1 mL. The standard solutions were kept at 4 °C until time of use.

Preparation of Platelet-Rich Plasma

Platelets were obtained from healthy volunteers with no history of hematological diseases and who had not consumed aspirin during the previous week nor consumed any alcohol, which could affect platelets or the coagulation cascade. All volunteers provided informed consent prior to the collection of platelets. The protocols were approved by the Ethics Committee of the University of Talca (N° 2017005). Venous blood from the cubical fossa was collected into tubes and mixed with 3.2% sodium citrate at a 9:1 ratio (BD Vacutainer ® Franklin Lakes, NJ USA) [12]. Samples were stabilized for 5 min, after which they were centrifuged at 1000 rpm for 10 min to obtain platelet-rich plasma (PRP). The PRP was then analysed using a hematological counter (ADVIA 60 Haematology System, Bayer) and adjusted to 200,000 platelets/μL with platelet-poor plasma (PPP).

Preparation of Platelet-Poor Plasma

Platelet-poor plasma was obtained by centrifuging an aliquot of PRP at 3500 rpm for 10 min. Very platelet-poor plasma was obtained by centrifuging an aliquot of PPP at 12000 rpm for 5 min and used as a control in the platelet aggregation study.

Agonists

Platelet aggregation was initiated by the addition of 8μM of ADP (Sigma Chemical Co., St. Louis, USA) and 30 μM of TRAP-6 (H8365, Bachem Bioscience Inc., California, USA). Samples were then frozen until immediately prior to assays.

Measurement of aggregation based on blood absorbance and platelet aggregation turbidimetry

Platelet aggregation was measured by aggregometry as described by Born (1970), with minor modifications. Specifically, optical density was measured at 630 nm [13] using a spectrophotometer (Cecil, CE1021) coupled to a motor that generated constant agitation, and the addition of refractory bricks to maintain the temperature at 37°C.

Platelet aggregation of PRP was analysed based on variation in the optic density of plasma using the method described by Born (1970). Aggregation was induced with ADP and TRAP-6, in separate assays. Specifically, 480 μL of PRP, adjusted to 200,000 platelets/ μL, was placed in a reaction container and homogenized with a magnetic stirrer, after which it was mixed with 20 μL of extract and incubated for 5 min.

Minimum Inhibitory Concentration

Approximate minimum inhibitory concentration was determined using methanol extracts of R. melanophthalma because previous results showed them to have the highest inhibitory effect. Nine pre-established concentrations of methanol extract were added to samples to generate an aggregation inhibition curve, from which the concentration that inhibited 50% of the aggregation was determined.

Obtaining Fractions

The methanol extracts of both species were fractionated by preparative TLC to assess and identify the fractions with major activity.

Preparation of Plates for Thin-Layer Chromatography

Plates containing 20 × 20 cm silica gel at a thickness of 0.25 mm were used as the solid phase, while a 9:1 mixture of ethyl acetate and methanol was used as the mobile phase because this mixture of solvents showed greater separation of the bands in TLC in this study. The TLC plates were visualized using UV light.

Electrospray ionization mass spectrometry (ESI-MS)

High resolution ESI(-)-MS analysis was performed with a hybrid double-quadrupole (Qq) and orthogonal time-of-flight (Tof) mass spectrometer (Qtof Micro, Waters) operating at 5,200 resolution with a mass accuracy of 10 ppm. The nebulizer temperature was 100 °C, and the ESI and mass spectrometer were operated in the negative ion mode. The cone and extractor potential were set to 30 and 0 V, respectively. The scan range was 50-1000 m/z. Tandem mass spectrometric [ESI(-)-MS/MS] experiments were performed using the product ion scan mode via Q1 mass selection of the desirable product ion, q2 collision-induced dissociation (CID) with Argon, and orthogonal TOF mass analysis of the CID ionic fragments. The collision energy ranged from 15 to 25 eV, depending on the dissociation labiality of the precursor ion. ESI-MS experiments employing total methanol extracts obtained from R. melanophthalma achieved the spectra depicted in Figure 1 for fractions B and C.

Statistical Analyses

The % total aggregation (measured at 5 min), % of maximum aggregation, incline and area under curve were measured and expressed as the average for each assay ± the standard deviation. The averages for each parameter were compared using SPSS 15.0 (Statistical Product and Service Solutions) with p < 0.05 considered significant.

Results and Discussion

Extraction with different solvents of lesser to greater concentration gave a total of five crude extracts for each species with a total yield of 8.458% for R. melanophthalma and 5.889% for U. krascheninnikovii. Crude methanol extracts were the highest (Table 1).

Due to difficulty with the dissolution of other compounds with solvents without damaging platelet function, only the antiplatelet effects of crude methanol extracts were measured. Methanol extracts were investigated at a final concentration of 1 mg/mL. The agonists used were ADP (8 μM) and TRAP-6 (30 μM), and DMSO 0.5% was used as the negative control. (Figure 2) shows the inhibitory effects of extracts of R. melanophthalma and U. krascheninnikovii on platelet aggregation in vitro induced by ADP (8 μM) in PRP

Table 1: Weight of extract obtained with solvents of different polarity and percentage of total yield of each species.

Table 2: Antiaggregant effect of crude methanol extracts of two lichen species from the Maule region activated by TRAP-6 (30 μM).

Figure 1: Mass spectra of fractions of crude methanol extract (A) Fraction 1 of R. melanophthalma, (B) Fraction 2 of R. melanophthalma, (C) Fraction 3 of R. melanophthalma.

Figure 2: Inhibitory effect of the platelet aggregation in vitro induced by ADP (8 μM) in PRP (negative control, NC, methanol extract of R.melanophthalma 1 mg/mL (R) and U. krascheninnikovii 1 mg/mL (U).

Preparative TLC plates yielded five fractions for U. krascheninnikovii and three for R. melanophthalma, which were dissolved with DMSO/H₂O at a ratio of 13:87 with a final concentration of 0.5 mg/ mL (Table 4).

Secondary metabolites were identified by ESI-MS [14]. The analyses of the spectra according to MS/MS fragmentations and high-resolution MS showed the presence barbaric and usnic acids as secondary metabolites in fractions B and C of the crude extract of R. melanopthtalma. These acids were thusly considered as potentially responsible for the observed antiplatelet activity (Figure 1). Despite having obtained five crude extracts for all solvents, only methanol extract was investigated due to its high availability and high capacity to extract hydrophilic compounds, which facilitates its solubility at the time of use. The fractions of the extract were then dissolved in 0.5 % DMSO, since it is known to provide good results for methanol extracts [15]. Fractions from R. melanophthalma exhibited greater inhibitory effects than those from U. krascheninnikovii at a concentration of 1 mg/mL, even though this concentration did not correspond to the minimal inhibitory concentration (IC50) (Figure 2).

The fractions obtained from the methanol extracts of both species had lower inhibitory effects when used with the agonist ADP (8μm) (Figures 4 & 5). The specific metabolites responsible for the observed antiplatelet activity could not be determined from the mass spectra of peaks shown by mass spectroscopy. Nevertheless, the secondary metabolites identified in this study are known to have different biological activities: barbaric acid (358.9 m/z) is known for its herbicidal effect [16,17] and antiplatelet activity [18] atranorin (373.9 m/z) is known for its antinociceptive and anti-inflammatory effects [19-21] and usnic acid (342.9 m/z) is known for its antibacterial activity [22-25], phytotoxic activity against algae [26] and antiplatelet activity [18,27,28].

Figure 3: Curve of inhibition of the platelet aggregation in vitro induced by ADP (8 μM) in PRP by crude methanol extracts of R. melanophthalma.

Figure 4: Inhibitory effect of the platelet aggregation in vitro induced by ADP (8 μM) in PRP of the fractions of crude methanol extracts of R. melanophthalma. R 0.5%: Crude methanol extract of R. melanophthalma, FR1: Fraction 1, FR2: Fraction 2, FR3: Fraction 3, NC: Negative Control (DMSO 0.5%).

Figure 5: Inhibitory effect of the platelet aggregation in vitro induced by ADP (8 μM) of the fractions of crude methanol extracts of U. krascheninnikovii in PRP. U 0.5: crude methanol extract of U. krascheninnikovii, FU1: Fraction 1, FU2: Fraction 2, FU3: Fraction 3, FU4: Fraction 4, FU5: Fraction 5, NC: negative Control (DMSO 0.5%).

Table 3: Antiaggregant effect of crude methanol extracts of two lichen species from the Maule region activated by ADP (8 μM).

Table 4: Antiaggregant effect of methanol extracts of two lichen species from the Maule region activated by ADP (8 μM).

Table 5: Approximate inhibitory minimum concentration (IC50) of R. melanophthalma induced by ADP (8 μM).

Despite the difficulty in determining which secondary metabolites had antiplatelet activity, it can be assumed that usnic acid is the compound responsible since this metabolite was found in fractions B and C of R. melanophthalma (Figure 1) and antiplatelet activity has been previously reported for other lichen species that contain this metabolite [18,27,28].

Although no assays were performed in vivo, the in vitro assays performed here showed promising results for antiplatelet activity. The methanol extract of R. melanophthalma showed inhibitory effects on ADP-induced platelet aggregation, with IC50 < 1.0 mg/mL (Table 5 & Figure 3). This IC50 value is considerably lower than the that obtained with methanol extracts of Usnea longissima, where the IC50 was 3.6 mg/mL [18]. It is important to point out that the in vitro assays of the present study were conducted under experimental conditions similar to those used by Lee and Kim (2005). Apart from the compounds detected in fractions B and C, there is a third, yet unidentified, compound whose peak is 327.9 m/z (Figure 1).

Recent studies have shown that acetone extracts of R. melanophthalma have anticancer activity against lung cancer cell lines. This activity has been attributed to the presence of a metabolite corresponding to usnic acid [29,30] which does not rule out this compound as being responsible for antiplatelet activity.

Conclusions

Of the three most abundant metabolites found in the different fractions of R. melanophthalma, usnic acid and barbaric acid have been previously reported to have antiplatelet activity. Furthermore, these two compounds have been shown to have high antioxidant activity, as detected in other lichen species [18,31].

The IC₅₀ value of the antiplatelet activity of Rhizoplaca melanophthalma is at a lower concentration than those described for the other lichen species studied so far.

Acknowledgments

The authors acknowledge support from Project PIEI: Química y Bio-orgánica en Recursos Naturales and to Instituto de Ciencias Biológicas, University of Talca, Talca, Chile.

Declaration of Interest

The authors declare no conflicts of interest.

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