#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

The immunomodulatory activity of the extracts and complexes of biologically active compounds of Galium verum L. herb


Authors: Igor L. Shinkovenko;  Natalia V. Kashpur;  Tatiana V. Ilyina;  Alla M. Kovalyova;  Olga V. Goryacha;  Oleh M. Koshovyi;  Erica L. Toryanyk;  Olena V. Kryvoruchko
Published in: Čes. slov. Farm., 2018; 67, 25-29
Category: Original Article

Overview

The present article discusses the results of an immunomodulatory activity of Galii veri herba, Galium verum herb (Galium verum L., Rubiaceae) fluid water extract and the effect of the polysaccharide and phenolic complexes of the letter on the immunomodulatory activity. The same extract was fractionated into a polysaccharide complex (PSC) and a polyphenolic complex (PPC). In the obtained substances, the contents of hydroxycinnamic derivates, flavonoids and polyphenols were determined spectrophotometrically; polysaccharides were quantified gravimetrically; the immunomodulatory activity of the substances was determined in the reaction of lymphocyte blast transformation. It has been established that the fluid extract of Galium verum herb contains 6.3% polysaccharides, 4.2% hydroxycinnamic derivates expressed as chlorogenic acid, 0.4% flavonoids expressed as rutin, 3.7% polyphenols expressed as gallic acid. PPC contains 4.48% hydroxycinnamic derivates expressed as chlorogenic acid, 0.43% flavonoids expressed as rutin, and 3.95% polyphenols expressed as gallic acid. The lowest immunomodulatory activity was found for PPC. A significantly higher activity was determined for PSC. The highest immunomodulatory activity was established for the fluid extract at a dilution of 1/20, its activity being by 59.4% higher compared with the lymphocyte spontaneous transformation and by 18.5% higher than that of the reference substance PHA. The obtained results enable an assumption of a synergistic effect of PPC and PSC of Galium verum herb fluid extract on the potency of its immunomodulatory activity.

Key words:

Galium verum L. • immunomodulatory activity • lymphocyte blast transformation • fluid water extract • polysaccharide complex • polyphenols complex

Introduction

The secondary immunodeficiency disorders present a severe challenge for the modern society. The use of immunosuppressive drugs, chemotherapy, malnutrition, chronic diseases and metabolic disorders are among root causes of secondary immunodeficiencies1). Since all these conditions lead to serious biochemical disturbances affecting different organ systems, correction of these changes requires a complex and long-term treatment. Considering the above-mentioned, a search for immunomodulators of plant origin is among the topical issues facing pharmacy2–4). Herbal medicinal products uniquely combine a low toxicity, an affinity to the human body and a wide range of biological activities (antioxidant, anti-inflammatory, immunostimulating, antiviral, antimicrobial, etc.) causing a multifaceted beneficial effect on the impaired body functions, which is of great importance in the treatment of the secondary immunodeficiencies5–9). On the pharmaceutical market of Ukraine, the line of immunomodulators of plant origin is rather limited. Therefore, it is currently important for medicine and pharmacy to seek for and develop effective domestic herbal medicinal products with an immunomodulatory effect. In Ukrainian folk medicine Galii veri herba, Galium verum herb (Galium verum L., Rubiaceae) is used as antibacterial, haemostatic, choleretic and immunostimulant agent10). The herb of Galium verum contains iridoids, flavonoids, coumarins etc. The aim of the present article is to discuss the effect of the fluid water extract of Galium verum herb, polysaccharide complex (PSC) and polyphenolic complex (PPC) on the functional activity of lymphocytes in the reaction of lymphocyte blast transformation (RLBT).

Experimental part

Plant materials

Galium verum herb was harvested at full flowering stage in the Kharkiv region (Ukraine) in the summer of 2016. Herbarium samples (No. 20062016-25062016) are deposited at the Department of Pharmacognosy (National University of Pharmacy, Ukraine).

Preparation of extracts

A three-fold water extraction (30 min each) was carried out at a general ratio of the plant material : solvent of 1 : 10 on heating. Three extracts were combined, concentrated on a vacuum rotary evaporator to a ratio of plant material – finished product of 1 : 1.

At the same time, under the same conditions, an extract was obtained from which polysaccharides were precipitated with three volumes of 96% ethanol, separated by centrifugation (10 min, 3000 rpm), re-washed with 96% ethanol and centrifuged under the same conditions. The resulting polysaccharide complex was dried to an air-dry state (PSC). The filtrate remaining after polysaccharides precipitation was concentrated to a ratio of plant material – finished product of 1 : 1 (PPC – polyphenolic complex).

Preliminary phytochemical screening of Galium verum herb fluid water extract, PSC and PPC

The preliminary phytochemical screening was performed to identify the main groups of biologically active compounds (BAC) of Galium verum L. herb fluid water extract, PSC and PPC, namely sugars, flavonoids, polyphenols by a reaction with Fehling’s solution, by a cyanidin reaction, and a reaction with lead acetate and ferric chloride.

Quantification of main groups of BACs

Polysaccharides were quantified gravimetrically after complete drying at room temperature taking into account the loss on drying11, 12). PSC’s monosaccharides after acidic hydrolysis were quantified by the spectrometric method using the reaction with picric acid (as glucose, λ = 463 nm) according to the procedures developed by Minin et al.13). In Galium verum L. herb fluid water extract and PPC, the content of hydroxycinnamic derivates was determined by direct spectrophotometry (as chlorogenic acid, λ = 325 nm) according to Yezerska et al.14), Spagnol et al.15); flavonoids were quantified by the method of differential spectrophotometry with aluminium chloride (as rutin, λ = 410 nm)16); polyphenols were quantified by direct spectrophotometry (as gallic acid, λ = 270 nm) according to Kovalyova et al.17), Koshovyi et al.18). All assays were performed in triplicate.

Study of immunomodulatory activity

The study of the immunomodulatory activity of PSC was carried out at the dose which corresponds to polysaccharide content in the fluid water extract, i.e. 0.63 g of PSC were dissolved in 10 mL of purified water. To study the immunomodulatory activity of Galium verum L. herb fluid water extract and PPC, 10 mL of each substance were used. Before the RLBT, the fluid water extract, PPC and solution of polysaccharides were prepared in ratios of 1/200, 1/20, 1/10. 100 μL of substances were added to 100 μL of primary cultures of immunocompetent cells.

The immunomodulatory activity of the substances was studied in vitro in a reaction of lymphocyte blast transformation (RLBT)19, 20).

As the sample for substance testing, the mononuclear cells (lymphocytes) removed from venous heparinized blood (donated blood, Kharkiv Regional Blood Banking Centre, UA) by ficoll-verographine gradient density centrifugation (density 1.077 g/mL) (Research and Production Enterprise “PanEco”, RU) by the standard technique21), were used (Protocol of the Сommittee on Biomedical Ethics of SO “Mechnikov Institute of Microbiology and Immunology” No. 2 of May 16, 2017).

The cells obtained were cultured in medium 199 with an addition of 10% bovine foetal serum (Thermo Fisher Scientific, BR), 2 mM L-glutamine (Altera Holding, RU), 100 μg/mL gentamicin (LEK (CZ). A suspension of 1 million cells per 1mL of the culture medium with the addition of substances was incubated for 15–18 hours in a thermostat at 37 °C, in a 5% CO2 atmosphere with saturated water vapour.

The intensity of the proliferative reaction was evaluated by the indexes of DNA synthesis activation recorded by the treatment of samples with antiBrdU Antibody (3H579) monoclonal antibodies (Santa Cruz Biotechnology, USA) at the concentration of 100 mg/mL. After the final sample preparation, numerical data on the total number of cells and the percentage of blast forms in the samples were established for a flow cytometric analysis with fluorescence detection.

It is known that vegetable lectin phytohemagglutinin (PHA) (Research and Production Enterprise “PanEco”, RU) is a mitogen for all T-lymphocytes22). Therefore, in order to determine the quality of the cell cultivating environment, as well as to study the potential proliferative activity of the major populations of T-lymphocytes (donated blood, Kharkiv Regional Blood Banking Centre, UA), the mitogenic stimulation of lymphocytes by PHA at a concentration of 2.5 μg/mL was performed as the control. RLBT without the addition of the substances under study (spontaneous blast transformation) was also evaluated.

Equipment

A spectrophotometer EvolutionTM 60S UV-Visible (Thermo Fisher Scientific, USA), electronic analytical scales AN 100 “Axis” (AXIS, PL), an electrical temperature chamber ТС80М-3 (Medlabortekhnika, UA), a centrifuge OPN – 3 (Phizpribor, RU), a microscope ZEISS Primo Star (ZEISS, DE), a pipette Thermo Scientific, Lait series 1–200 μl (Thermo Fisher Scientific, USA), a pipette Thermo Scientific, Lait series 1–50 μl (Thermo Fisher Scientific, USA), a pipette Thermo Scientific, Lait series 1–1000 μl (Thermo Fisher Scientific, USA), a pipette Thermo Scientific, Lait series 1–20 μl (Thermo Fisher Scientific, USA), a CO2 incubator (Binder, DE), a bioanalyzer Agilent 2100 (Agilent, DE).

Chemicals

The purified water used for the extraction complied with the requirements of the State Pharmacopoeia of Ukraine23); chemicals used for phytochemical screening and quantification of the main groups of BACs: ethanol (ACS reagent, Fisher Scientific, USA), hydrochloric acid, p.a. (Sobstar, Zaporizhia, UA), acetic acid, puriss. (PJSC AZOT, UA), lead (II) acetate, p.a. (Unikhim Ltd., RU), aluminum chloride, p.a., granulated zinc, p.a. (PC Uralskiy zavod khimicheskih reaktivov, RU), ferric (III) chloride, puriss. (Sigma-Aldrich, USA), Fehling’s solutions (Biochem Chemopharma, FR), picric acid, p.a. (Sigma-Aldrich, USA), gallic acid, chlorogenic acid and rutin were of analytical grade (Merck, DE).

Statistical analysis

All statistical analyses were performed using Microsoft Office Excel 200724). Differences between groups were statistically analysed using one-way analysis of variance (ANOVA). The results were expressed as mean ± standard deviation (SD). P values less than 0.05 were considered statistically significant.

Result and discussion

Phytochemical screening of Galium verum herb fluid water extract, PSC and PPC

The fluid water extract, polysaccharide complex and polyphenolic complex of Galium verum herb were obtained for the first time and their phytochemical profiles were characterized for the first time too.

The phytochemical screening of G. verum herb fluid water extract revealed the presence of reducing sugars, flavonoids, polyphenols. The results obtained correspond with previous studies aimed at the research of phytochemical constituencies of Galium species25–27).

Quantification of main groups of BACs

When quantifying the main groups of BACs, it was established that the fluid water extract contained 6.3% polysaccharides, 4.2% hydroxycinnamic derivates expressed as chlorogenic acid, 0.4% flavonoids expressed as rutin, 3.7% polyphenols expressed as gallic acid. PPC contains 4.48% hydroxycinnamic derivates expressed as chlorogenic acid, 0.43% flavonoids expressed as rutin, 3.95% polyphenols expressed as gallic acid. In PSC the content of monosaccharides was 26.70%; taking into account the loss on drying (7.2%), the total ash was 23.61%.

Since the fluid extract was obtained at the ratio of the plant material – finished product 1 : 1, we could compare the content of BACs in the fluid extract with the content of BACs in the plant material.

There are no available articles discussing the phytochemical profile of water extracts of Galium species, but in comparison with the data provided by Vlase L, Mocan A, Hanganu D, et al.25) and taking into account the differences in the extracts used, the content of hydroxycinnamic derivates and polyphenols in the fluid extract and PPC is higher, and the content of flavonoids is significantly lower.

Reaction of lymphocyte blast transformation in vitro

The immunomodulatory activity of Galium verum herb fluid water extract and the effect of the polysaccharide and phenolic compounds of the latter on the immunomodulatory activity were studied for the first time.

It has been established that all the substances under study greatly stimulate the transformational activity of peripheral blood mononuclear cells. The activity under the influence of substances increases from 26.6% (PPC at dilution of 1/200) to 59.4% (fluid extract at dilution of 1/20) compared with spontaneous lymphocyte blast transformation. Table 1 shows the effect of substances of Galium verum L. herb on the indices of lymphocyte blast transformation.

1. The effect of substances of Galium verum L. on the indices of lymphocyte blast transformation (X ± m), n = 5
The effect of substances of Galium verum L. on the indices of lymphocyte blast transformation (X ± m), n = 5
PPC – polyphenolic complex, PSC – polysaccharide complex, PHA – phytohemagglutinin, RLBT – the reaction of lymphocyte blast transformation
*Р < 0.05 in comparison with the indices of control

The highest activity was found for Galium verum water fluid extract at a dilution of 1/20, its activity being by 59.4% higher than that of the lymphocyte spontaneous transformation and by 18.5% higher than that of the reference substance PHA. Somewhat lower indexes were found for the extract at a dilution of 1/200, its activity being by 54.4% higher than that of the lymphocyte spontaneous transformation and by 13.5% higher than that of PHA; the lowest activity was exhibited at a dilution of 1/10, its activity being by 53.1% higher than that of the lymphocyte spontaneous transformation and by 11.1% higher than that of PHA.

The water solution of PSC showed a significant activity at a dilution of 1/10 (its activity was by 51.1% higher than that of the lymphocyte spontaneous transformation and by 10.2% higher than that of PHA), at a dilution of 1/20 its activity being by 53.4% higher than that of the lymphocyte spontaneous transformation and by 12.5% higher than that of PHA, at a dilution of 1/200 its activity being by 40.7% higher than that of the lymphocyte spontaneous transformation and almost comparable with PHA activity.

The lowest activity was found for PPC: at a dilution of 1/10 its activity was by 36.7% higher than that of the lymphocyte spontaneous transformation and by 4.2% lower than that of PHA; at a dilution of 1/20 its activity was by 37.3% higher than that of the lymphocyte spontaneous transformation and by 3.6% lower than that of PHA; at a dilution of 1/200 its activity was by 26.6% higher than that of the lymphocyte spontaneous transformation and by 14.3% lower than that of PHA.

In our previous study, we reported the immunomodulatory effects of two Asperula species (Rubiaceae family) which are native herbs used for the treatment of inflammatory diseases in Ukrainian traditional medicine28).

According to research articles available in the public domain, only for one species of the genus – Galium mite – the immunomodulatory activity was studied 29). It was concluded that the methanol extract of the aerial part of G. mite mildly increases the proliferation of human lymphocytes at the concentrations of less than 10 µg/ml and inhibits their proliferation at higher doses in a dose-dependent manner. As the results of our study have shown, all the substances of Galium verum L. herb and especially fluid water extract are characterized by a stimulating effect on the transformational activity of human lymphocytes. We can assume that different effects of G. verum L. herb water extract and methanol extract of aerial part of G. mite on human lymphocyte proliferation can be explained by differences in the phytochemical profiles of species and extracts under study.

PHA increased the level of RLBT by 40.9% compared with the lymphocyte spontaneous transformation.

On average, the most potent stimulation of immunocompetent cell functional activity was observed in 100 μL of the substances under study at a dilution of 1/20.

The obtained results suggested a synergistic effect of the polysaccharide complex and the phenolic complex of Galium verum herb fluid water extract on the potency of immunomodulating activity.

The obtained data provided the basis for an in-depth study of the mechanisms of immunomodulatory activity of the substances of Galium verum herb in order to develop on their basis medicinal products for immune correction of the conditions occurring in violation of the cooperative function of immunocompetent cells and the correction of weakening of nonspecific resistance factors.

Conclusion

Fluid water extracts of Galium verum herb were obtained for the first time; their chemical composition and immunomodulatory activity were studied. Galium verum herb fluid extract and polysaccharide complex greatly stimulate the transformational activity of blood immunocompetent cells. The obtained results confirmed the prospect of further study of substances of Galium verum in order to search for new drugs and principles of immunodeficiency correction.

Acknowledgments

This study was supported by the Laboratory of Immunorehabilitology of the Mechnikov Institute of Microbiology and Immunology of National Academy of Sciences of Ukraine.

Conflicts of interest: The authors have declared no financial relationships with any organizations that might have an interest in the submitted work; no any other relationships or activities that could appear to have influenced the submitted work.

I. L. Shinkovenko • T. V. Ilyina • A. M. Kovalyova • Assistant Lecturer Olga V. Goryacha, Ph.D. (∗) • O. M. Koshovyi • E. L. Toryanyk • O. V. Kryvoruchko

National University of Pharmacy, Kharkiv, Ukraine

Valentunivska 4, 61168 Kharkiv, Ukraine

e-mail: helgagnosy@gmail.com

N. V. Kashpur

SO Mechnikov Institute of Microbiology and Immunology, Kharkiv, Ukraine


Sources

1.    Chinen J., Shearer W. Secondary Immunodeficiencies, including HIV infection. Journal of Allergy and Clinical Immunology 2010; 125(2), 195–203.

  2.   Xiubao C., Yuanxiao Z., Changxin S., Stewart A.K. Mechanism of immunomodulatory drugs’ action in the treatment of multiple myeloma. Acta Biochim. Biophys. Sin. (Shanghai) 2014; 46(3), 240–253.

  3.   Alamgir M., Uddin S. J. Recent advances on the ethnomedicinal plants as immunomodulatory agents. Ethnomedicine: A Source of Complementary Therapeutics 2010; 4, 227–244.

  4.   Uorakkottil I., Deepshikha P. K., Vidhu A., Punnooth P. N. A Review on Hepatoprotective and Immunomodulatory Herbal Plants. Pharmacogn Rev. 2016; 10(19), 66–70.

  5.   Pushpa R., Nishant R., Kumar N., Gautam P. Antiviral potential of medicinal plants: an overview. Int. Res. J. Pharm. 2013; 4(6), 8–16.

  6.   Silva N. C. C., Fernandes Jr A. Biological properties of medicinal plants: a review of their antimicrobial activity. J. Venom. Anim. Toxins incl. Trop. Dis. 2010; 16(3), 402–413.

  7.   Ambriz-Pérez D. L., Leyva-López N., Gutierrez-Grijalva E. P., Heredia J. B. Phenolic compounds: Natural alternative in inflammation treatment. A review. Cogent Food & Agriculture. 2016; 2(1): 1131412.

  8.   Mohamed S. I. A., Jantan I., Haque M.A. Naturally occurring immunomodulators with antitumor activity: An insight on their mechanisms of action. Int. Immunopharmacol. 2017; 50, 291–304.

  9.   Kure Ch., Timmer J., Stough C. The immunomodulatory effects of plant extracts and plant secondary metabolites on chronic neuroinflammation and cognitive aging: a mechanistic and Empirical Review. Front Pharmacol. 2017; 8, 117.

10.   Abubakirov N. K., Belenovskaya L. M., Grushvitskaya I. V., et al. Plant resources of the USSR: Flowering plants, their chemical composition and use; Families Caprifoliaceae-Plantaginaceae, Leningrad: Nauka 1990, 326 p. (in Russian)

11.   The State Pharmacopoeia of Ukraine / State enterprise “Scientific and Expert Pharmacopoeial Centre”, First edition, Kharkiv: RІREG, 2001; 556 p. (in Ukrainian).

12.   The State Pharmacopoeia of Ukraine / State enterprise “Scientific and Expert Pharmacopoeial Centre”, First edition, first supplement, Kharkiv: RІREG, 2004; 494 p. (in Ukrainian).

13.   Minin S. A., Kauhova E. I. Chemistry & Technologies of phytopreparations. Moscow: Heotar – Honey, 2004, 516 p. (in Russian).

14.   Yezerska O., Kalynyuk T., Vronska L. Quantitative determination of hydroxycinnamic acids in Chicory root. Chemistry and Chemical Technology 2013; 7(3), 247–250.

15.   Spagnol C. M. , Oliveira Th. S., Lucia Borges V. I., Corrêa M. A., Salgado H. R. N. Validation of caffeic acid in emulsion by UV-Spectrophotometric method. Physical Chemistry 2015; 5(1), 16–22.

16.   The State Pharmacopoeia of Ukraine / State enterprise “Scientific and Expert Pharmacopoeial Centre”, First edition, second supplement, Kharkiv: RІREG, 2008; 617 p. (in Ukrainian).

17.   Kovalyova A. A., Georgievskiy G. V., Kovalyov V. M., Komisarenko A. M. et al. Development of new piflamin medicine standardization methods. Farmakom 2002; 2, 92 –97 (in Ukrainian).

18.   Koshovyi O. M., Zagayko A. L., Kolychev I. A., Akhmedov E. Yu., et al. Phytochemical study of the dry extract from bilberry leaves. Azerbaijan Pharmaceutical and Pharmacotherapy Journal 2016; 1, 18–23 (in Russian).

19.   Korneeva M. N., Novokhatskii A. S., Grebenyuk V. N., Kerimov S. G. Use of the lymphocyte blast transformation reaction to assess the state of cellular immunity. Bulletin of Experimental Biology and Medicine 1989; 107(4), 533–535.

20.   Bashirova D. K., Kochnev O. S., Davletkil’deev F. A., Lagutina M. V. Immunologic activity of human lymph cells in the lymphocyte blast transformation reaction. Biull. Eksp. Biol. Med. 1980; 89(1), 33–35.

21.   Bulanova E. G., Budagyan V. M., Yarilin A. A., Mazurenko N. N. Expression of protooncogenes during lymphocyte activation by growth factors. http://protein.bio.msu.ru/biokhimiya/contents/v62/full/62091191.html

22.   Movafagh A., Heydary Н., Mortazavi-Tabatabaei S. A., Azargashb E. The significance application of indigenous phytohemagglutinin (PHA) mitogen on metaphase and cell culture procedure. Iran. J. Pharm. Res. 2011; 10 (4), 895–903.

23.   The State Pharmacopoeia of Ukraine / State enterprise “Scientific and Expert Pharmacopoeial Centre”, First edition, fourth supplement, Kharkiv: RІREG, 2011; 538 p. (in Ukrainian).

24.   Zulfiqar A., Bhaskar S. B. Basic statistical tools in research and data analysis. Indian J Anaesth. 2016; 60(9), 662–669.

25.   Zhao C., Shao J., Cao D., Zhang Y., Li X. Chemical constituents of Galium verum. Zhongguo Zhong Yao Za Zhi 2009; 34(21), 2761–2764.

26.   Vlase L., Mocan A., Hanganu D., Benedec D., Gheldiu A., Crișan G. Comparative study of polyphenolic content, antioxidant and antimicrobial activity of four Galium species (Rubiaceae). Digest Journal of Nanomaterials and Biostructures 2014; 9(3), 1085–1094.

27.   Ghiţă G., Necula R., Trifan A., Gille E., Zamfirache M. M., Stănescu U. Investigations regarding the phytochemical study of some samples of Galium verum L. and Galium album Mill. Analele Ştiinţifice ale Universităţii „Al. I. Cuza” Iaşi s. II a. Biologie vegetală. 2012; 58(1), 45–50.

28.   Kashpur N. V., Yurchenko N. S., Ilyina T. V., Kovalyova A. M., Goryacha О. V., Smilyanska M. V., Peremot S. D. The immunomodulatory effect of Asperula odorata L. and Asperula humifusa M. Bieb. Besser dry extracts. Clinical Pharmacy 2015; 19(1), 56–58.

29.   Amirghofran Z., Javidnia K., Bahmani M., Azadmehr A., Esmaeilbeig M. The effect of the methanol extract of Galium mite on the cellular immunity and antibody synthesis. Journal of Immunoassay and Immunochemistry 2011; 32, 157–169.

Labels
Pharmacy Clinical pharmacology
Topics Journals
Login
Forgotten password

Enter the email address that you registered with. We will send you instructions on how to set a new password.

Login

Don‘t have an account?  Create new account

#ADS_BOTTOM_SCRIPTS#