Possibilities of use of plant derived nonstarch polysaccharides in clinical practice


Inhibition of Pglycoprotein transporter protein (ABCB1protein, Pgp) is a promising method to increase the effectiveness of pharmacotherapy in different pathologies: neoplastic diseases, epilepsy, cerebral circulation disorders. Pgp is a large transmembrane protein that provides efflux of a wide range of endo and xenobiotics from cells, and plays a significant role in pharmacokinetics of many medical drugs. Nowadays not a single synthetic inhibitor of the transporter is used in clinical practice due to nonselectivity of action, toxicity and high cost. Medicinal herbal remedies possess different pharmacological and therapeutic effects, rarely cause side effects and are economically accessible. This review presents the results of experiments in which affiliation of the oligo and polysaccharides to substrates and inhibitors of Pgp was analyzed, and which precondition further studies of other plant derived polysaccharides. Possibilities of using plant derived nonstarch polysaccharides in complex therapy of tumors are described, since along with potential inhibition of the transporter, they possess an antitumor effect and can also assist in correction of side effects of cytostatics. The prospects of using plant derived nonstarch polysaccharides for improvement of the effectiveness of neuroprotective therapy are presented, because they not only can increase the penetration of neuroprotective drugs across the bloodbrain barrier through Pgp inhibition, but also possess their own neuroprotective activity, as well as a number of pharmacological effects that can give a positive result in the complex treatment of brain pathologies. Thus investigations of plant nonstarch polysaccharides, their isolation and development of medical drugs on their basis is a promising direction of modern medicine.

Full Text

An important problem of modern medicine is resistance of diseases to pharmacotherapy. One of causes of ineffectiveness of medical drugs is considered to be enhanced activity of glycoprotein-P transporter protein (ABCB1-protein, Pgp), which removes medical substances that are its substrates, out of target cells, or reduces their concentration in blood and tissues [1].

Pgp is a large transmembrane protein with a wide substrate specificity that provides efflux of numerous endo- and xenobiotics including medical drugs, out of cell [1]. It was first found in tumor tissue where its intense functioning causes reduction in the permeability of cell membranes to antitumor drugs leading to the phenomenon of multidrug resistance [2]. In further studies Pgp was found in many organs and tissues of humans and animals (gastrointestinal tract, liver, kidneys, tissues barriers), thus it is believed to play a key role in pharmacokinetics of medial drugs.

Being localized in enterocytes, the transporter decreases absorption of substrates in the intestine; in histohematic barriers (hematoencephalic, hematoovarian, hemato-testicular and hematoplacental) it prevents entry of substrates to the sequestered organs; besides, it mediates release of substrates from hepatocytes and renal epithelium into the lumen of bile ducts and of renal tubules [1, 3]. Of special attention is the function of the transporter in hematoencephalic barrier, since increase in its activity in the barrier may reduce the effectiveness of antiepileptic and neuroprotective therapy [1, 3]. Taking the above into account, inhibition of Pgp transporter protein is a prospective way to increase effectiveness of pharmacotherapy of some pathologies.

At present three generations of Pgp inhibitors has been developed. Their brief char-

acteristics are given in Table 1.

Table 1.Characteristics of Pgp Inhibitors [4-6]







Verapamil, yohimbine, quinidine, cyclosporin, reserpine, tamoxifen, toremifene, triflyoroperazine

Non-selective, low affinity to Pgp

They are substrates of Pgp, of other transporters and enzymatic systems of metabolism; possess pharmacological activity; to achieve transporter inhibition high doses are required


Dexniguldipine, dexverapamil, dofequidar fumarate [MS-209], valspodar [PSC 833]

Possess higher specificity as compared to the first generation inhibitors

They are substrates of Pgp and of other transporters and enzymatic systems


Вiricodar [VX-710], сyclopro-pyldibenzosuberanezosuquidar [LY335979], elacridar [GF120918/GG918], laniquidar [R101933], mitotane [NSC-38721], tariquidar [XR9576], ONT-093, HM30181

High specificity; selective and effective inhibition of Pgp



 The optimal synthetic transporter inhibitors are those of the third generation, possessing low toxicity and selectivity of action. However, their application may lead to enhancement of side effects of the prescribed medical drugs. Thus, use of tariquidar is associated with increase in the concentration of cytostatic and antiepileptic drugs not only in the target cells, but also in blood plasma with the result of development of unwanted drug-related reactions [7]. It is worth noting that Pgp inhibitors of the third generation are costly. Thus, at the moment synthetic inhibitors of transporter protein are not used in clinical practice.

An important direction in the development of modern pharmacology is search and investigation of new medical drugs of plant origin [8]. Plant derived medical drugs possess certain advantages: they are capable of various pharmacological effects, possess a wide range of therapeutic actions, seldom induce side effects including allergic reactions, and are affordable [9].

Polysaccharides of plant origin possess these advantages, they are actively used in medicine in the form of galenical preparations containing a complex of active substances. Thus, roots of sweatweed (Аlthaea officinalis L.) are used as an expectorating drug in the form of a syrup; thallus of luminaria (Lami-naria japonica Aresch) are used as a laxative; mucus of flax seeds (Linum usitatissimum L.) is used as a softening and coating agent, etc. [10].

Recently, research works have been conducted concerning pharmacological activity of non-starch polysaccharides (non-hydro-lysable with amylase) of higher plants and algae, and development of medical drugs on their basis containing individual substances.

Application of non-starch plant polysaccharides as Pgp inhibitors is possible due to their chemical structure, since molecules of polysaccharides often contain functional groups characteristic of blockers of the transporter protein. [11]. Such chemical structure is inherent to the so called inlay polysaccharides and water-soluble pectins (structural heteropolysaccharides) which contain amino sugars, polypeptide chains and uronic acids that can form ester groups. Besides, structure of polysaccharides permits to introduce additional functional groups into their molecules by chemical synthesis. It should be noted that polysaccharides contain high-electronegative atoms of oxygen which make electron pairs for formation of intramolecular hydrogen bonds and bonds with Pgp molecule.

In some works affiliation of poly- and oligosaccharides to substrates of the transporter is shown. One of mechanisms of changing the functional activity of Pgp consists in the interaction of a substance with parts of its molecule (substrate-binding and other sites) with probable alteration of its spatial structure, therefore substrates of the transporter are considered its potential inhibitors [12].

It was found that processing of culture of cells overexpressing Pgp with modified cyclodextrin (heptakis (2,6-di-O-methyl)-beta-cyclodextrin) increases permeability of membranes to the transporter substrates in both directions, that is, it decreases activity of the transporter, probably due to derangement of microenvironment in the membrane [13].

In in vitro experiment on the culture of tumor cells it was found that heparin which is a negatively charged high-sulfated polysaccharide, increases penetration of chemopre-parations – Pgp substrates – into cells through suppression of the functional activity of the transporter. This phenomenon may be associated with the ability of heparin to interact with the extracellular proteins (growth factors, matrix components) and to modulate their activity by its charge [14]. In a study on the culture of human breast tumor cells MDA-MB231, intracellular penetration of the transporter substrate – calcein-AM – was analyzed, and it was shown that unfractionated heparin inhibits functioning of Pgp [15].

It is found that some resin glycosides (glycolipids, or lipo-oligosaccharides) obtained from seeds of Ipomoea alba increase susceptibility of the culture of chemoresistant cells of human breast carcinoma to vinblastine [16].

It was identified in in vitro experiment that oligomers of hyaluronic acid promote penetration of doxorubicin into tumor cells of peripheral nerve sheaths and also increase cytotoxicity of the drug in vivo [17].

It was shown that incubation of the culture of Pgp-expressing tumor cells within 4 hours with solid lipid nanoparticles (stearic acid and surfactant: lecithin and poloxamer) with paclitaxel subject to modification by ultrasound with use of 2-hydroxypropyl-β-cyclodextrin system resulted in accumulation of the chemical drug inside the cell to a higher extent than in incubation with classic transporter inhibitor – verapamil [18].

Dextran-based nanoparticles were found to be promising for delivery of doxorubicin to multidrug-resistant tumor cells [19].

The results of the mentioned experiments suggest further study of use of other available plant polysaccharides as Pgp inhibitors.

Of special attention is a propable use of non-starch plant polysaccharides for complex treatment of tumors, since besides potential inhibiton of transporter and increase in pene-tration of chemical drugs into tumor cells, some polysaccharides can produce antitumor effect of their own. Thus, it was found that plant polysaccharides reduce growth and metastasizing of blastomas due to induction of apoptosis in tissues [20]. It was also shown that butyric acid synthesized in the intestine in fermentation of polysaccharides, promotes differentiation and apoptosis of cells of colon carcinoma and suppresses their proliferation, possessing antineoplastic effect [21].

In experiments on mice with Lewis car-cinoma increase in the activity of chemotherapy was found in combined use of cyclo-phosphan and polysaccharide complex of sweet calamus rhizome and its fractions. The most expressed antitumor and antimetastatic activity was characteristic of the acidic fraction of the complex [22].

It was shown that the mechanism of antitumor effect of pectin polysaccharides containing D-galacturonic acid is based on their ability to interact with specific receptors on  the membrane of macrophages which results in formation of cytokines and tumor necrosis factor [20]. Polysaccharides containing gala-cturonan enhance expression of MHC complex on the surface of tumor cells thus activating immune cells that participate in antitumor protection [23].

It was found that introduction of polysaccharides of sweet calamus rhizome in case of cyclophosphan-induced immune depression, stimulates specific T-type immune response increasing the activity of cells of lymph nodes toward tumor cells [24].

Plant derived polysaccharides may correct side effects of cytostatics. It was shown in experiments on mice with Lewis carcinoma that water-soluble polysaccharides of foalfoot (Tussilago farfara L.) and sweet calamus rhizome reduce hepatotoxicity of paclitaxel [25]. Plant polysaccharides can effectively reduce gastrotoxicity of antitumor drugs: antiulcer effect was found in fucoidans, chitosan, colloid bismuth-pectin complex, low-esterified pectins [26-28]. Pectin polysaccharides may also be considered as prebiotics for correction of intestinal dysbiosis associated with intake of cytostatics [29].

Of interest is a possibility of using plant derived polysaccharides to improve the effectiveness of neuroprotective therapy, since they can not only increase penetration of neuroprotectors across the hematoencephalic barrier by potential inhibition of Pgp, but possess neuroprotective activity of their own, as well as some pharmacological effects, that may add to the positive result of complex treatment of pathologies of the brain.

Nitric oxide (NO) in high concentration is known to cause damage and death of neurons [30]. Sulfated polysaccharides produce a neuroprotective effect through inhibition of NO-synthase [31]. Fucoidan isolated from Laminaria japonica alga in the concentration 125 µg/ml decreases release of nitric oxide in microglial cells by inhibition of phosphorylation of mitogen-activated protein kinase and of intracellular signal-regulated kinase [32]. In the dose 62.5 µg/ml the polysaccharide decreases expression of CD11b receptors on the surface of granulocytes, natural killers and macrophages. Fucoidan produces a protective effect for proliferation of astrocytes through regulation of inducible NO synthase [33].

Inhibitory effect of fucoidan isolated from kelp Fucus vesiculosis on synthesis of nitric oxide was shown in cultures of BV2 glial cells and C6 glioma cells induced by proinflammatory cytokines (tumor necrosis factor α, γ-interferon and interleukin 1β) [34].

Oxidative stress is an important pathogenetic factor of many neurologic diseases. In in vitro and in vivo experiments the antioxidant effect of fucoidan isolated from kelp Laminaria japonica was demonstrated [35]. This effect of polysaccharide results from block of production of oxygen radicals and from increase in the levels of glutathione peroxidase, superoxide dismutase and malon-dialdehyde [35]. Antioxidant activity is also found in polysaccharides of some higher plants – mountain ash, St. John’s wort, and carregeenans [36].

Hypolipidemic, anticoagulation and antiischemic effects of non-starch polysaccharides may assist in complex therapy of acute disorder in brain circulation.

Hypolipidemic effect of polysaccharides (chitosan, fucoidans and others) consist in prevention of absorption of cholesterol in the intestine, increase in relative concentration of hydrophobic bile acids which more powerfully than hydrophilic ones inhibit activity of cholesterol-7α-hydroxylase, and in suppression of synthesis of cholesterol in the liver under influence of short-chain fatty acids (propionic, acetic and butyric acid) produced in fermentation of polysaccharides [37]. Besides, chitosan can form ionic complexes with fats including cholesterol, and inhibit their absorption and recirculation from the intestine into the liver [37].

Anticoagulation effect is found in pectins. They change the characteristic of fibrin meshwork so that it becomes more permeable, loses strength and readily lyses [38]. 

Fucoidans can activate formation of vessels and produce an antiischemic effect. Binding with fibroblast growth factors, they protect them against proteolysis and promote angiogenesis [39]. Besides, high-molecular fucoidans induce liberation of glucosamino-glycan-bound stromal factor-1 which mobilizes progenitors of stem cells of the bone marrow participating in angiogenesis [40].

Thus, it seems reasonable to evaluate affiliation of non-starch polysaccharides of some plants (alecost, foalfoot, calamus root, kelp) possessing gastroprotective, hepatopro-tective, antioxidant, membranoprotective [26-41], and also antitumor and neuroprotective [34] effects, to glycoprotein-P inhibitors. Isolation, modification and development of medical drugs on the basis of plant derived polysaccharides is a promising direction of modern pharmacology. A study of specific activity of non-starch plant derived polysaccharides including their ability to inhibit glycoprotein-P transporter protein, permits to clarify peculiarities of their pharmacokinetics and pharmacodynamics and to optimize pharmacotherapy of some diseases.


About the authors

Ivan V. Chernykh

Ryazan State Medical University

Email: p34-66@yandex.ru
ORCID iD: 0000-0002-5618-7607
SPIN-code: 5238-6165

PhD in Biological sciences, Assistant of the Department of General Chemistry and Pharmachemistry

Russian Federation, 9, Vysokovoltnaja str., Ryazan, 390026

Ekarina E. Kirichenko

Ryazan State Medical University

Email: p34-66@yandex.ru
ORCID iD: 0000-0002-5950-7952
SPIN-code: 1895-6145

PhD in Biological sciences, Assistant of the Department of General Chemistry and Pharmachemistry

Russian Federation, 9, Vysokovoltnaja str., Ryazan, 390026

Aleksey V. Shchulkin

Ryazan State Medical University

Email: p34-66@yandex.ru
ORCID iD: 0000-0003-1688-0017
SPIN-code: 2754-1702

MD, PhD, Assistant Professor of Pharmacology Department with Course of Pharmacy of Continuing Professional Education Faculty

Russian Federation, 9, Vysokovoltnaja str., Ryazan, 390026

Natalia M. Popova

Ryazan State Medical University

Author for correspondence.
Email: p34-66@yandex.ru
ORCID iD: 0000-0002-5166-8372
SPIN-code: 7553-9852

MD, PhD, Senior Teacher of Pharmacology Department with Course of Pharmacy of Continuing Professional Education Faculty

Russian Federation, 9, Vysokovoltnaja str., Ryazan, 390026

Anna A. Kotlyarova

Ryazan State Medical University

Email: p34-66@yandex.ru
ORCID iD: 0000-0002-0676-7558
SPIN-code: 9353-0139

Assistant of Pharmacology Department with Course of Pharmacy of Continuing Professional Education Faculty

Russian Federation, 9, Vysokovoltnaja str., Ryazan, 390026


  1. Kukes VG, Grachev SV, Sychev DA, et al. Metabolizm lekarstvennykh sredstv. Nauchnye osnovy personalizovannoy meditsiny: rukovodstvo dlya vrachey. Moscow: GEOTARMedia; 2008. (In Russ).
  2. Liu ZH, Ma YL, He YP, et al. Tamoxifen reverses the multidrugresistance of an established human cholangiocarcinoma cell line in combined chemotherapeutics. Molecular Biology Reports. 2010;14:16977. doi: 10.1007/s110330100291z
  3. Yakusheva EN, Chernykh IV, Shchulkin AV, et al. Pglycoprotein expression in brain during ischemiareperfusion. I.P. Pavlov Russian Medical Biological Herald. 2015;23(4):4450. (In Russ).
  4. Lomovskaya O, Bostian KA. Practical applications and feasibility of efflux pump inhibitors in the clinic – a vision for applied use. Biochemical Pharmacology. 2006;71(7):9108. doi: 10.1016/j.bcp.2005.12.008
  5. Darby RA, Callaghan R, Mcmahon RM. Pglycoprotein inhibition; the past, the present and the future. Current Drug Metabolism. 2011;12(8): 72231. doi: 10.2174/138920011798357006
  6. Pusztai L, Wagner P, Ibrahim N, et al. Phase II study of tariquidar, a selective Pglycoprotein inhibitor, in patients with chemotherapyresistant, advanced breast carcinoma. Cancer. 2005;104(4):68291. doi: 10.1002/cncr.21227
  7. Srivalli KMR, Lakshmi PK. Overview of Pglycoprotein inhibitors: a rational outlook. Brazilian Journal of Pharmaceutical Sciences. 2012;48(3): 35367. doi: 10.1590/S198482502012000300002
  8. Shchulkin AV, Popova NM, Chernykh IV. The original and generic drugs: current state of the problem. Science of Young (Eruditio Juvenium). 2016;2:305. (In Russ).
  9. Engalycheva EE, Yakusheva EN, Sychev IA, et al. Study of hepatoprotective activity of flowers tansy polysaccharide complex I.P. Pavlov Russian Medical Biological Herald. 2015;23(2):505. (In Russ).
  10. Zubov AA. Ispol'zovaniye preparatov iz morskikh vodorosley dlya profilaktiki i lecheniya patologicheskikh sostoyaniy. Ekologiya cheloveka. 1998;3:2731. (In Russ).
  11. Poongavanam V, Haider N, Ecker GF. Fingerprintbased in silico models for the prediction of Pglycoprotein substrates and inhibitors. Bioorganic&Medicinal Chemistry. 2012;20(18): 538895. doi: 10.1016/j.bmc.2012.03.045
  12. Carrigos M, Mir LM, Orlowski S. Competitive and NonCompetitive Inhibition of the MultidrugResistanceAssociated Pglycoprotein ATPase. European Journal of Biochemistry. 1997;244(2): 66473. doi: 10.1124/mol.62.6.1288
  13. Fenivesi F, Fenivesi E, Szente L, et al. Pglycoprotein inhibition by membrane cholesterol modulation. European Journal of Pharmaceutical Science. 2008;34(45):23642. doi:10.1016/ j.ejps.2008.04.005
  14. Cheng JW, Zhang LJ, Hou YQ, et al. Association between MDR1 C3435T polymorphism and refractory epilepsy in the Chinese population: A systematic review and metaanalysis. Epilepsy Behavior. 2014;36:1739. doi:10.1016/ j.yebeh.2014.05.007
  15. Angelini A, Febbo CD, Ciofani G, et al. Inhibition of Pglycoproteinmediated multidrug resistance by unfractionated heparin: a new potential chemosensitizer for cancer therapy. Cancer Biology & Therapy. 2005;4(3):31317. doi: 10.4161/cbt.4.3.1503
  16. CruzMorales S, CastanedaGomez J, RosasRamirez D, et al. Resin Glycosides from Ipomoea alba Seeds as Potential Chemosensitizers in Breast Carcinoma Cells. Journal of Natural Products. 2016;79(12):3093104. doi: 10.1021/acs.jnatprod.6b00782
  17. Slomiany MG, Grass GD, Robertson AD, et al. Hyaluronan, CD44, and Emmprin Regulate Lactate Efflux and Membrane Localization of Monocarboxylate Transporters in Human Breast Carcinoma Cells. Cell, Tumor, and Stem Cell Biology. 2009;69(4):1293301. doi: 10.1158/00085472
  18. Baek JS, Cho CW. 2‐Hydroxypropyl ‐β‐cyclodextrin‐modified SLN of paclitaxel for overcoming P‐glycoprotein function in multidrug‐resistant breast cancer cells. Journal of Pharmacy and Pharmacology. 2013;65(1):728. doi: 10.1111/j.20427158. 2012.01578.x
  19. Kobayashi E, Iyer AK, Hornicek FJ, et al. Lipidfunctionalized Dextran Nanosystems to Overcome Multidrug Resistance in Cancer: A Pilot Study. Clinical Orthopaedics and Related Research. 2013;471(3):91525. doi:10.1007/ s1199901226102
  20. Niu YC, Liu JC, Zhao XM, et al. A low molecular weight polysaccharide isolated from Agaricus Blazei suppresses tumor growth and angiogenesis in vivo. Oncology Reports. 2009; 21(1):14552. doi: 10.3892/or_00000201
  21. Hague A, Elder DJE, Hicks DJ, et al. Apoptosis in colorectal tumorcells. Induction by the shortchain fattyacids butyrate, propionate and acetate and by the bilesalt deoxycholate. International Journal of Cancer. 1995;60:4006. doi: 10.1002/ijc.2910600322
  22. Safonova EA, Guriev AM, Razina TG, et al. Increase of chemotherapy efficiency by means of fractions isolated from polysaccharides complex Acorus Calamus L. Rossiyskiy bioterapevticheskiy zhurnal. 2012;11(4):558. (In Russ).
  23. Iguchi C, Nio Y, Takeda T, et al. Plant polysaccharide PSK: cytostatic effects on growth and invasion; modulating effect on the expression of HLA and adhesion molecules on human gastric and colonic tumor cell surface. Anticancer research. 2001;21:100713.
  24. Lopatina KA, Guryev AM, Razina TG, et al. Influence of polysaccharides from acorus calamus rizomes on functional activity of murine limphnode cells after experimental tumor chemotherapy. Sibirskiy onkologicheskiy zhurnal. 2006;3:5963. (In Russ).
  25. Safonova EA, Razina TG, Zueva EP, et al. Prospects for the use of plant polysaccharides in complex treatment of malignant tumors. Experimental and Clinical Pharmacology. 2012; 75(9):427. (In Russ).
  26. Yamamoto Y, Suzuki T, Hirano M, et al. Effect of fucoidan and fucoidan containing tea on gastric ulcer and nonulcer dyspepsia. The Japanese Journal of Pharmacology. 2000;28:6370.
  27. Ito M, Ban A, Ishihara M. Antiulcer effects of chitin and chitosan, healty foods in rats. The Japanese Journal of Pharmacology. 2000;82: 21825. doi: 10.1254/jjp.82.218
  28. Katayama H, Nishimura T, Ochi S, et al. Sustained release liquid preparation using sodium alginate for eradication of Нelicobacter pylori. Biological and Pharmaceutical Bulletin. 1999; 22:5560. doi: 10.1254/jjp.82.218
  29. Gibson GR, Roberfroid MB. Dietary modulation of the human colonic microbiota: introducing the concept of prebiotics. Nutrition Journal. 1995;125(6):14012. doi: 10.1093/jn/ 125.6.1401
  30. Block ML, Zecca L, Hong JS. Microgliamediated neurotoxicity: uncovering the molecular mechanisms. Nature Reviews Neuroscience. 2007;8(1):5769. doi: 10.1038/nrn2038
  31. Besednova NN, Somova LM, Gulyaev SA, et al. Neuroprotective effects of sulfated polysaccharides from seaweed. Vestnik rossiyskoy akademii meditsinskikh nauk. 2013;68(5):529. (In Russ).
  32. Cui YQ, Zhang LJ, Zhang T, et al. Inhibitory effect of fucoidan on nitrit oxide production in lipopolysaccharideactivated primary microglia. Clinical And Experimental Pharmacology And Physiology. 2010;37:4228. doi:10.1111/ j.14401681.2009.05314.x
  33. Lee HR, Do H, Lee SR, et al. Effects of fucoidan on neuronal сell proliferation assotiation with NO production through the iNOS pathway. Journal of Food Science and Nutrition. 2007;12:748. doi: 10.3746/jfn.2007.12.2.074
  34. Do H, Pyo S, Sohn EH. Suppression of iNOS expression by fucoidan is mediated by regulation of p38 MAPK, JAK/STAT, AP1 and IFR1, and dependents on upregulation of scavenger receptor B1 expression in TNFα and IFNγstimulated C6 glioma cells. Journal of Nutritional Biochemistry. 2010;21(8):6719. doi: 10.1016/j.jnutbio.2009.03.013
  35. Luo D, Zhang Q, Wang H., et al. Fucoidan protects against dopaminergic neuron death in vivo and in vitro. European Journal of Pharmacology. 2009;617(13):3340. doi: 10.1016/j. ejphar.2009.06.015
  36. Zlobin AA, Martinson YA, Ovechkina IA, et al. Sostav i svoystva pektinovykh polisakharidov zveroboya prodyryavlennogo Hypericum perforatum L. Khimiya rastitel'nogo syr'ya. 2011;1:338. (In Russ).
  37. Kryzhanovsky SP, Bogdanovich LN, Besednova NN, et al. Hypolipidemic AND antiinflammatory effects of polysaccharides marine brown kelps in patients with dyslipidemia. Fundamental research. 2014;10:93100. (In Russ).
  38. Huang R, Du Y, Yang J, et al. Influence of functional groups on the in vitro anticoagulant activity of chitosan sulfate. Carbohydrate Research. 2003;338:4839. doi: 10.1055/s00311299848
  39. Matou S, Helley D, Chabut D, et al. Effect of fucoidan on fibroblast growth factor2induced angiogenesis in vitro. Thrombosis Research. 2002; 106:21321. doi: 10.1016/S00493848 (02)001366
  40. Millet J, Jouault CS, Mauray S, et al. Antithrombotic and anticoagulant activities of a low molecular weight fucoidan. Journal of Thrombosis and Haemostasis. 1999;81:3915.
  41. Yakusheva EN, Engalycheva EE, Sychev IA, Shchulkin AV. Pharmacological evaluation polysaccharide complex flowers tansy. Fundamental research. 2015;2(4):4554. (In Russ).

Copyright (c) 2018 Chernykh I.V., Kirichenko E.E., Shchulkin A.V., Popova N.M., Kotlyarova A.A.

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