; Lucia Ungvarská Maľučká
; Aneta Salayová
; Jarmila Harvanová
; Peter Očenáš
Authors place of work:
University of Veterinary Medicine and Pharmacy, Košice, Slovak Republic
Published in the journal:
Čes. slov. Farm., 2015; 64, 202-205
44<sup>th</sup> Conference drug synthesis and analysis
Cordyceps sinensis is the fungi parasiting larvae, pupae and imagoes of insect as well as fruiting bodies of truffles of the genus Elaphomyces1). The fungi is known in both traditional Chinese medicine and in modern medicinal methods. It is used as a dietary supplement (CORDYCEPS MRL.®, ACAI DETOX®). The fact of Cordyceps sinensis consequence is supported by many scientific studies, which have shown its positive effects, for example in anti-tumor therapy2), in the treatment of HIV/AIDS, asthma, liver diseases and it also has a positive effect on female fertility etc.3). Chemical compounds are responsible for these properties, which is currently characterized by the parasite. It was found that the fungi are rich in natural substances such as cordycepin, cordycepic acid, respectively, D-mannitol4–6), polysaccharides7, 8), nucleotides9), proteins and amino acids10, 11).
This paper is focused on the basic research of studied biologically active compounds (nucleosides, amino acids) identification. To date nucleosides are believed to be the active compounds in Cordyceps12). Several methods including thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC) and nuclear magnetic resonance spectroscopy (NMR) have been used for the identification of the compounds under study.
The mushrooms for extraction were obtained dried and grinded from the Technical University of Zvolen, Faculty of Forestry, in co-operation with team of Ing. Martin Paulík, PhD.
For the identification of biologically active compounds occurrring in Cordyceps sinensis we used methanolic extracts of eight fungi samples (1–8). For the separation of the content compounds thin layer chromatography was used (silica gel plates by Kiesselgel 60 F254 from Merck) in chloroform. Detection of chromatographs was provided by UV light at 254 nm and by freshly prepared 2% ninhydrine in methanol. For HPLC detection on a UHPLC Ultimate 3000 (ThermoScientific) a DAD detector was used. The measurements were performed at the temperature of 25 °C on the column Polaris 5 C18-A 250 ⋅ 4,6 mm (Varian), the injection volumes were 20 μl, flow rate was 1 ml/min. The mobile phase consisted of 2% acetonitrile hypergrade for chromatography (Merck) in water for chromatography (Merck). Standards were purchased: cytidine and uridine (Sigma-Aldrich), guanosine and adenosine (Acros Organics), thymidine (ABCR) and inosine (Calbiochem). NMR spectra were measured on a Varian VNMRS 600 MHz in D2O (Merck).
Samples of Cordyceps sinensis for analysis were prepared by extraction in methanol. 10 g of crude mushroom was mixed in boiling methanol for 8 h and then filtered. The solvent was evaporated and the extract was dried under vacuum. Extraction yields: 7.1% (1), 2.2% (2), 8.0% (3), 4.8% (4), 8.3% (5), 7.6% (6), 15.1% (7), 9.1% (8).
Samples were filtered through a 0.22 μm syringe filters before HPLC analysis. Concentrations of samples prepared as water solution were 10 mg/ml.
From the extract of sample 7 we obtained a fraction crystallized from methanol, which we used for NMR experiments (1H NMR, 13C NMR, DEPT, gCOSY, gNOESY, gHSQC and gHMBC) in amount of 20 mg dissolved in 0.6 ml of D2O.
Results and discussion
In all samples the presence of the nucleosides adenosine, cytidine, uridine, inosine, guanosine and thymidine was studied (Fig. 1).
Figure 2 shows typical chromatograms of nucleoside standards and an example of a C. sinensis extract (6). The results showed that the components were obviously variant depending on different cultivation conditions of Cordyceps sinensis.
In all samples all nucleosides under study were not determined. The qualitative analysis showed that all nucleosides studied are represented only in samples 2, 3, 4, 5. In other samples cytidine (sample 8), inosine (samples 1, 6 and 7), and guanosine (sample 1) did not occur. These results demonstrate that qualitative parameters of the compounds under study are affected by cultivation conditions of fungi.
With regard to the identification of chemical structures contained in Cordyceps sinensis, NMR analysis, which is an invaluable source of new information on the molecular structure, is only little employed.
A NMR study of the extract fraction achieved by crystallisation from methanol (sample 7) was provided. The TLC and HPLC analyses performed the presence of five compounds in an approximately equal amount. As we could not identify the compounds, we used NMR analysis. On the basis of 1D (1H NMR, 13C NMR, DEPT) and 2D (gCOSY, gNOESY, gHSQC and gHMBC) NMR experiments, we defined the structure of five amino acids. The chemical shifts (δδ, ppm) are described in Table 1. The chemical shifts correlated with the database13).
HPLC-UV/VIS and NMR analyses were performed for qualitative determination of nucleosides in Cordyceps sinensis fungi. Six nucleosides were determined by HPLC and five unknown compounds were identified by NMR as amino acids.
The authors would like to acknowledge the contribution of Assoc. Prof. RNDr. Ján Imrich, CSc., and RNDr. Mária Vilková, PhD., from the Laboratory of NMR, Faculty of Science, UPJŠ, Košice, to the measurements of NMR spectra.
Conflicts of interest: none
RNDr. Zdenka Bedlovičová, PhD.
University of Veterinary Medicine and Pharmacy
Komenského 73, 04181 Košice, Slovak Republic
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