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Central European Journal of Immunology
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vol. 35

Experimental immunology
The in vitro effect of Uncaria tomentosa water and ethanol extract on the metabolic activity of blood granulocytes in mice

Julita Nowakowska
Ewa Sommer
Andrzej Czubaj
Mieczysław Kuraś
Ewa Skopińska-Różewska

Centr Eur J Immunol 2010; 35 (2): 69-72
Online publish date: 2010/05/10
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In recent years natural preparations of the plant origination have been both more popular and effective. Among them plants originated from rainforests of Middle and South America raise huge interest. It is believed that over 80% of plant species inhabited in mountain areas of Amazon possess medical properties. One of them is Uncaria tomentosa (una de gato, cat’s claw, vilcacora) of the Rubiaceae family [1]. For hundreds years it has been used by Indians in treating various diseases including cancers [1-3]. Wide medical activity of this plant results from many biologically active compounds such as oxindole alkaloids, including pentacyclic (POA, e.g. pteropodine, isopteropodine, speciophylline, uncarine F, mitraphilline, isomitraphilline) and tetracyclic ones (TOA, rhynchophylline, isor­hynchophylline) [4]. As shown by Keplinger et al., alkaloid content differs in various parts of plant and changes according to seasons of a year [2]. Besides alkaloids many other phytochemicals were identified, including glycosides of quinic acid, triterpenes (ursolic and oleaonlic acids), sterols (stigmasterol and kampesterol), polyphenols, phenolic and catechin tannins and uncaric acids [5-7]. On the basis of different results an extract from U. tomentosa was classified as a preparation of antyproliferative or cytostatic [8-10], anti-inflammatory [11, 12], anti-mutagenic [13], antioxidative [14, 15], contraceptive [16], anti-bacterial [17] and anti-viral [2] properties. In addition, preparations of U. tomentosa showed immunostimulating activity by increasing rats’ leucocytosis in vivo and by stimulating proliferation of isolated lymphocytes. It also induced higher leukocytosis in healthy people [18, 19]. It has been shown that Uncaria extract would effectively stimulate lymphocyte-dependent immunity [20]. Additional research on toxicity carried out on experimental animals showed that U. tomentosa extracts are not toxic [21]. Therefore U. tomentosa was legitimated as medicinal plant on the 1st International Conference concerning U. tomentosa in Geneva in 1994 year. Due to its wide chemical content and its amazing properties U. tomentosa has been more and more popular all over the world including Poland. The preparations of U. tomentosa have been more widely applied in prevention and treating many diseases e.g. cancers. In this case they are used as a supplement of synthetic medicaments, particularly between radiotherapy and chemotherapy sessions. It was observed that activity of these preparations might work directly, inhibiting cancer cell divisions or indirectly by improving immunology system.
In the present paper we evaluate the in vivo influence of U. tomentosa bark water and ethanol extract on the metabolic activity of blood granulocytes in mice.

Materials and methods
Preparation of extracts
The bark of the U. tomentosa used for obtaining preparations originated from Peru and was supplied by A-Z Medica Spółka z o.o. Gdańsk, Poland. The voucher material has been deposited at the Laboratory of Phytochemistry, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznań.
One gram of the bark was extracted in 10 ml of distilled water or 96% ethanol for 8 h at 37°C. Then, the extracts were centrifuged (MLW K70D) for 15 min at 4000 rpm. Supernatants were evaporated on Speed-Vac and next exsiccated with P2O5. All these extracts were analyzed by HPLC. Content of total alkaloids in different cat’s claw preparations expressed in mg/100 g: water extract 430 mg and ethanol extract 3480 mg [22]. Both dry extracts were dissolved in 10% ethyl alcohol before administration to the animals.
The study was performed on 8-10-weeks old female inbred Balb/c mice, 20–22 γ of body mass, delivered from the Polish Academy of Sciences breeding colony. For all experiments animals were handled according to the Polish law on the protection of animals and NIH (National Institutes of Health) standards. All experiments were accepted by the local Ethical Committee (nr 347/2004).
In vivo experiment
Uncaria extracts were administered to Balb/c mice per os in 7 daily doses of 200 g (each group consisted of 10 mice). These dose corresponded to 100 mg given to 70 kg person (applying the coefficient equal 7 for adjusting differences between mouse and human in relation of the surface to body mass). Mice received drugs by Eppendorff pipette, in 40 l of 10% ethyl alcohol, for 7 days. Control mice (16 animals) were fed 40 l of 10% ethyl alcohol. On the day 8th mice were bled in anaesthesia from retro-orbital plexus and sacrificed with Morbital.
Chemiluminescence test
Chemiluminescence test (CL) was measured using the method of Easmon and Cole with some modifications [9, 10] at room temperature, in scintillation counter (RackBeta 1218, KB, Sweden). Briefly: samples of 0.05 ml heparinised blood were diluted 1 : 4 with PBS (Biomed Lublin, Poland) supplemented with 0.1% BSA (Sigma-Aldrich, USA) and 0.1% glucose (Polfa, Poland). Next, 0.05 ml of this diluted blood was mixed with 0.2 ml of luminol (Sigma-Aldrich, USA) solution (10-5 M) in PBS and placed in a scintillation counter in the “out of coincidence” mode for background chemiluminescence measurement. Then, the cells were activated by addition of 0.02 ml solution of opsonised Zymosan (10 mg/ml) and chemiluminescence activity was measured for the next 15 min. Estimating the number of leukocytes and blood smears examination were performed by routine methods and the results were shown as the maximum value of chemiluminescence (cpm) obtained for 103 granulocytes.
Statistical analysis
Paired, normally distributed data were analyzed using the t-Student test.

The results from the effect of U. tomentosa bark two extract feeding on chemiluminescence activity of mouse blood grnulocytes in vitro are presented on the Fig. 1 (granulocyte activity test) and Table 1 (statistical significance of number of blood leukocytes and chemiluminescent activity). As can be seen from the table, water extract highly stimulated granulocyte chemiluminescence but ethanol extract slightly decreased the O2-production and number of leukocytes.

Our experiments with chemiluminescence test showed in vivo immunostimulatory effect of U. tomentosa water extracts on mice granulocytes activity. Granulocytes provide the first line of defence against microbal pathogens and kill several of them. The essential part of killing process is the generation of reactive oxygen species during the oxidative burst. This process leads to the emission of light proportional to free radical quantity-chemiluminescence (CL) [23].
The results obtained show that the water extract highly stimulated granulocyte chemiluminescence whereas ethanol extract gave slightly inhibitory effect. Similar stimulatory properties were observed during research on the influence of extracts of Rhodiola rosea and Rhodiola quadrifida on mice splenocytes chemokinetic activity [24]. Uncaria water extract proved to be a strong immunostimulator of non-specific cellular defence, depending on the first line cells, granulocytes. Earlier experiments performed by us concerned evaluation of the effect of U. tomentosa water extract on the course of Pseudomonas aeruginosa infection in mice. Our results demonstrated that extract does not directly work on bacteria however it inhibits bacterial infection as an immunomodulating substance [17].
Content of total alkaloids measured by HPLC in both extracts showed that ethanol extract has tenfold more alkaloids then water extract. It was shown that high concentrated extract of these substances did not activate granulocytes. Moreover it has slightly decreased the total number of leukocytes. Besides the above-mentioned alkaloids, over fifty different compounds have been identified, including tannins, pentacyclic triterpenes with a variety of ursolic acid derivatives, quinovic acid glycosides, sterols and procyanidins many of which with strong immunostimulating properties [5].
It might been suggested that daily dose of 100 mg per day of Uncaria water extract in human would effectively stimulate granulocyte-dependent immunity. Use of dietary supplements containing U. tomentosa bark ethanol extract in the same daily doses might be dangerous because of the potential suppression of the first line defence against microbal pathogens infection.

The authors would like to thank Norbert Czubaj for his help in translating this text to English.

1. Reinhard KH (1997): Uncaria tomentosa (Willd) DC. – Cat`s claw, Una de Gato oder Katzenkralle. Zeitschr Phytother 18: 112-121.
2. Keplinger K, Laus G, Wurm M et al. (1999): Uncaria tomentosa (Willd) DC. – etnomedicinal use and new pharmacological, toxicological and botanical results. J Etnopharmacol 64: 23-34.
3. Reinhard K H (1999): Uncaria tomentosa (Willd) DC.: Cat`s claw, Una de Gato,or Saventaro. J Altern Complement Med 5: 143-151.
4. Keplinger K, Wagner H, Kreutzkamp B (1989): Oxindole alkaloids having properties stimulating the immunologic system. Washington, D.C.: United States Patent # 4844901.
5. Heitzman M, Neto C C, Winiarz E et al. (2005): Ethnobotany, phyochemistry and pharmacology of Uncaria (Rubiaceae). Phytochemistry 66: 5-29.
6. Aquino R, De Simone F, Vinceri F F et al. (1990). New polyhydroxylated triterpenes from Uncaria tomentosa. J Nat Products 53: 559-564.
7. Aquino R, De Feo V, De Simone F (1991): Plant metabolites. New compounds and antiinflamatory activity of Uncaria tomentosa. J Nat Products 54: 453-459.
8. Sheng Y, Pero R W, Amiri A et al. (1998): Induction of apoptosis and inhibition of proliferation in human tumor cells treated with extracts of Uncaria tomentosa. Anticancer Res 18: 3363-3368.
9. Riva L, Coradini D, Di Drozo G et al. (2001): The antiproliferative effects of Uncaria tomentosa extracts on growth of breast cancer cell line. Anticancer Res 21: 2457-2462.
10. Riva L, Coradini D, Di Drozo G et al. (2001): The antiproliferative effects of Uncaria tomentosa extracts on growth of breast cancer cell line. Anticancer Res 21: 2457-2462.
11. Sandoval M, Charbonnet RM, Okuchama N et al. (2000): Cat’s claw inhibits TNF- production and scavenges free radicals: role in cytoprotection. Free Radical Biol. & Med. 29: 71-78.
12. Aquino R, De Feo V, De Simone F et al. (1991): Plant metabolites. New compounds and antiinflamatory activity of Uncaria tomentosa. J Nat. Products 54: 453-459.
13. Rizzi R, Bianchi A, Feo V et al. (1993): Mutagenic and antymutagenic activites of Uncaria tomentosa and its extracts. J Etnopharmacol 38: 63-77.
14. Gonçalves C, Dinis T, Batista MT (2005): Antioxidant properties of proanthocyanidins of Uncaria tomentosa bark decoction: a mechanism for anti-inflammatory activity. Phytochemistry 66: 89-98.
15. Pilarski R, Zieliński H, Ciesiołka D (2006): Antioxidant activity of ethanolic and aqueous extracts of Uncaria tomentosa (Willd.) DC. J Ethnopharmacol 104: 18-23.
16. Salazar EL, Jayme V (1998): Depletioin of specific binding sites for estrogen receptor by Uncaria tomentosa. Proceedings West Pharm Soc 41: 123-124.
17. Nowakowska J, Bany J, Zdanowska D (2009): The effect of the bark water extract Uncaria tomentosa on the Pseudomonas aeruginosa infection in mice. Centr Eur J Immunol 34: 162-165.
18. Sheng Y, Bryngelsson C, Pero RW (2000): Enhanced DNA repair, immune function and reduced toxicity of C-MED.-100TM, a nowelaqueous extract from Uncaria tomentosa. J Ethnopharmacol 69: 115-126.
19. Wurm M, Kacani L, Laus G et al. (1998): Pentacyclic oxindole alcaloids from Uncaria tomentosa induce human endothelial cells to release a lymphocyte-proliferation-regulating factor. Planta Med 64: 701-704.
20. Nowakowska J, Sommer E, Czubaj A et al. (2009): The effect of Uncaria tomentosa bark water extract on chemokinetic activity of spleen lymphocytes in mice. Centr Eur J Immunol 34: 235-238.
21. Santa Maria S, Lopez A, Diaz MM et al. (1997): Evaluation of toxicity of Uncaria tomentosa by bioassays in vitro. J Ethnopharmacol 57: 183-187.
22. Pilarski R, Poczekaj-Kostrzewska M, Ciesiołka D et al. (2007): Antiproliferative activity of various Uncaria tomentosa preparations on HL-60 promielocytic leucemia cells. Pharmacol Rep 59: 565-572.
23. Allen RC, Stjenholm RL, Steel RH (1972): Evidence for the generation of an electronic excitation state in human polymorphonuclear leucocytes and its participation in bacterial acrivity. Biochem Biophys Res Commun 47: 679-684.
24. Skopińska-Różewska E, Bychawska E, Białas-Chromiec B et al. (2009): The in vivo effect of Rhiodiola rosea and Rhodiola quadrifida hydro-alcoholic extracts on chemokinetic activity of spleen lymphocytes in mice. Centr Eur J Immunol 34: 43-45.
Copyright: © 2010 Polish Society of Experimental and Clinical Immunology This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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