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cat’s claw

What is cat’s claw

Cat’s claw is a woody creeper vine that grows wild in the Amazon rainforest and other tropical areas of Central and South America 1. Its thorns resemble a cat’s claws. Cat’s claw is naturally distributed in South America, mainly in Peru and Brazil as well as in Central America, and it is traditionally used as a medicinal plant. The two most common Cat’s claw species are Uncaria tomentosa and Uncaria guianensis that belong to Rubiaceae family. Most commercial preparations of Cat’s claw contain Uncaria tomentosa. Using cat’s claw for health dates back to the Inca civilization. Cat’s claw historical uses have included for contraception, inflammation, cancer, and viral infections, and to stimulate the immune system. Today, cat’s claw is used as a dietary supplement for a variety of health conditions including viral infections (such as herpes and HIV), Alzheimer’s disease, cancer, arthritis, rheumatism, asthma, diverticulitis, peptic ulcers, colitis, gastritis, hemorrhoids, parasites, cirrhosis, diabetes, hypertension, stroke and leaky bowel syndrome. The bark and root of cat’s claw are used to make liquid extracts, capsules, tablets, and tea. However, there have been very few high quality clinical trials (studies done in people) of cat’s claw. And there’s no conclusive scientific evidence based on studies in people that supports using cat’s claw for any health purpose. Recently as study using Cat’s claw (Uncaria tomentosa) as adjuvant treatment was carried out with 40 patients who had undergone complete breast cancer resection, which was histologically diagnosed as Invasive Ductal Carcinoma—Stage II 2. Adjuvant treatment is an additional cancer treatment given after the primary cancer treatment to lower the risk that the cancer will come back. Adjuvant therapy may include chemotherapy, radiation therapy, hormone therapy, targeted therapy, or biological therapy. The Cat’s claw (Uncaria tomentosa) dose used was 300 mg dry extract per day. The rsearch found that Cat’s claw is effective in the recovery from neutropenia induced by chemotherapy in women diagnosed with Invasive Ductal Carcinoma—Stage II. Cat’s claw (Uncaria tomentosa) enables the stimulation of the immune system, increasing resistance to diseases when the body is immunosuppressed due to stress, malnutrition, or due to the effect of some medication 2.

Few side effects such as gastrointestinal complaints (nausea, diarrhea, stomach discomfort), kidney effects, nervous system disorders, and an increased risk of bleeding with anticoagulant therapy have been reported for cat’s claw when taken in small amounts. Women who are pregnant or trying to become pregnant should avoid using cat’s claw because of its past use for preventing and aborting pregnancy.

Around 50 compounds have been isolated from Cat’s claw, from which approximately 35 chemical markers can be considered exclusive to this species, including triterpenes 3, alkaloids 4 and polyphenols 5. The special interest on Cat’s claw plant is due to the fact that numerous scientific studies report a wide variety of biological activities 6, such as immunomodulatory properties 5, as well as their antioxidant, anti-inflammatory and cardiovascular effects and protective properties against cancer, among others 7.

Although originally attributed to alkaloids, recent studies suggest that the health effects derived from Cat’s claw could be attributed to a synergistic interaction among different chemical compounds present in this plant 8. Of particular interest are polyphenols, for which there is strong evidence of having multiple molecular targets, modulating pro-inflammatory gene expression, interacting with phospholipid membranes 9 and modulating pathways related to chronic inflammation and energy metabolism 10.

When considering subclasses of polyphenols, Cat’s claw barks show variable contents, with procyanidin dimers as the most abundant group in Los Chiles (7971.4 µg/g of extract) aqueous extract, followed by Sarapiqui (6085.3–6464.1 µg/g of extract) in ethanolic and aqueous extracts, respectively. In contrast, extracts from Cat’s claw leaves showed a more uniform subclass distribution, for instance, all extracts are particularly rich in propelargonidin dimers (7904.3–14,390.8 µg/g of extract), followed by procyanidin dimers (3593.1–9988.8 µg/g of extract) and flavalignans-cinchonains (1074.6–7058.0 µg/g of extract).

In summary, this study 11 shows that independently of the Cat’s claw plant origin, leaves extracts exhibit high contents of phenolic compounds and more importantly high contents of proanthocyanidins derivatives, mainly propelargonidin dimers and procyanidin dimers. These compounds are linked to diverse bioactivities, for instance due to their antioxidant capacity, as shown in reports for commercial dietary products from grape 12 and cocoa 13, which suggest these Cat’s claw (Uncaria tomentosa) extracts’ potential for further studies.

Table 1. Phenolic composition of aqueous extracts from Cat’s claw (Uncaria tomentosa) bark and leaves

Leaves ExtractsBark Extracts
CompoundASLCPASRASLCPASR
Concentration (µg/g Extract)
Hydroxybenzoic acids
Benzoic acid71.2 ± 6.950.3 ± 0.8225.8 ± 7.6120.0 ± 9.8343.0 ± 23.260.3 ± 5.81181.6 ± 89.013.0 ± 0.5
Salicylic acid27.7 ± 2.322.9 ± 0.424.7 ± 1.129.0 ± 1.920.1 ± 1.856.4 ± 0.9105 ± 6.9197.6 ± 1.4
4-hydroxybenzoic acid35.2 ± 1.1143.6 ± 3.2200.0 ± 4.741.1 ± 1.1113.7 ± 7.722.7 ± 1.1164.7 ± 6.637.6 ± 1.9
Protocatechuic acid60.5 ± 1.4323.0 ± 5.5495.5 ± 13.2120.5 ± 6.9983.8 ± 61.6292.2 ± 9.6696.5 ± 52.3808.0 ± 18.7
Gallic acid47.4 ± 1.2188.5 ± 5.719.5 ± 1.410.7 ± 0.942.6 ± 3.325.3 ± 1.327.9 ± 2.928.3 ± 0.4
Vainillinic acid5.8 ± 0.19.5 ± 0.910.7 ± 0.34.8 ± 0.194.8 ± 6.684.8 ± 8.3136.7 ± 7.545.2 ± 2.3
Syringic acid3.4 ± 0.06.9 ± 0.16.8 ± 0.14.4 ± 0.220.5 ± 1.026.8 ± 1.521.9 ± 0.512.7 ± 0.1
∑ Hydroxybenzoic acids251.3744.8983.0330.31618.5568.52334.31142.5
Hydroxycinnamic acids
p-cumaric acid11.2 ± 1.142.9 ± 3.218.1 ± 4.737.5 ± 1.15.5 ± 7.75.2 ± 1.18.6 ± 6.62.2 ± 1.9
Caffeic acid13.9 ± 0.791.4 ± 1.438.4 ± 0.915.3 ± 0.512.7 ± 0.615.9 ± 1.414.4 ± 1.37.3 ± 0.6
Ferulic acid22.2 ± 0.746.1 ± 3.359.4 ± 2.031.2 ± 1.622.7 ± 1.112.2 ± 0.611.0 ± 0.514.3 ± 1.0
Isoferulic acid15.4 ± 0.27.8 ± 0.712.0 ± 0.310.9 ± 1.0ndndndnd
∑ Hydroxycinnamic acids62.7188.3128.094.940.933.234.123.8
Flavan-3-ols: monomers
(+)-Catechin1170.3 ± 30.5947.2 ± 39.71181.0 ± 11.71592.5 ± 32.2112.4 ± 2.8691.5 ± 24.8185.3 ± 18.4555.8 ± 26.2
(−)-Epicatechin3346.5 ± 46.61901.7 ± 39.62179.4 ± 68.82954.5 ± 73.0835.1 ± 27.83302.9 ± 194.21032.9 ± 19.33827.0 ± 76.6
∑ Monomers4516.82848.83360.44547.0947.43994.41218.34382.8
Flavan-3-ols: procyanidin dimers
Procyanidin B11233.6 ± 39.01536.6 ± 16.0829.4 ± 16.3887.1 ± 19.668.2 ± 1.8587.2 ± 25.5105.4 ± 10.8327.4 ± 10.1
Procyanidin B22415.6 ± 35.61651.0 ± 26.91085.5 ± 24.91291.9 ± 29.81085.3 ± 20.84011.4 ± 297.61061.2 ± 78.33777.0 ± 68.0
Procyanidin B31119.1 ± 32.02417.8 ± 34.3893.1 ± 36.31383.2 ± 32.753.2 ± 1.7350.3 ± 17.570.2 ± 2.3158.8 ± 9.5
Procyanidin B43642.9 ± 96.53888.7 ± 79.01886.0 ± 57.92979.5 ± 68.7479.8 ± 5.52720.8 ± 159.0681.5 ± 48.61715.3 ± 5.2
Procyanidin B5317.1 ± 4.0159.5 ± 7.4137.6 ± 8.2191.0 ± 7.372.6 ± 2.7301.8 ± 18.950.4 ± 3.6448.3 ± 12.2
Procyanidin B7158.8 ± 12.2164.2 ± 10.147.3 ± 2.7118.4 ± 2.1ndndndnd
Procyanidin B (5.47 min)154.8 ± 11.0171.0 ± 12.963.2 ± 1.1116.5 ± 6.7ndndndnd
Procyanidin B (9.27 min)68.1 ± 2.4nd20.2 ± 1.479.0 ± 6.4ndndnd37.3 ± 1.2
∑ Procyanidin dimers9110.09988.84962.27046.61759.07971.41968.76464.1
Flavan-3-ols: propelargonidin dimers
Propelargonidin dimer (4.43 min)4978.9 ± 161.54125.9 ± 84.34689.4 ± 185.54477.4 ± 235.322.3 ± 1.6126.2 ± 6.646.8 ± 2.7115.3 ± 2.1
Propelargonidin dimer (5.01 min)3369.6 ± 102.62661.0 ± 39.53179.5 ± 23.32981.4 ± 52.4118.3 ± 4.1346.7 ± 15.794.2 ± 9.0257.0 ± 4.7
Propelargonidin dimer (5.65 min)5209.1 ± 59.92602.3 ± 23.32935.9 ± 60.42748.8 ± 69.6238.5 ± 5.81135.2 ± 71.3213.2 ± 19.71153.2 ± 13.6
Propelargonidin dimer (9.27 min)833.2 ± 5.1352.8 ± 2.8298.9 ± 24.8339.6 ± 3.117.6 ± 1.056.8 ± 2.79.2 ± 0.983.2 ± 4.5
∑ Propelargonidin dimers14,390.89742.111,103.710,547.3396.61664.9363.31608.7
Flavan-3-ols: procyanidin trimers
Trimer T2nd104.6 ± 11.3ndndnd235.1 ± 25.2ndnd
Procyanidin C1303.7 ± 9.0190.7 ± 6.364.3 ± 0.6106.3 ± 3.9480.8 ± 45.42006.3 ± 169.3323.2 ± 2.12148.3 ± 70.4
Trimer B (5.78 min)176.6 ± 13.9395.7 ± 15.4101.3 ± 6.7145.1 ± 8.586.6 ± 3.8473.6 ± 16.954.5 ± 3.8585.0 ± 13.9
∑ Procyanidin trimers480.3691.0165.6251.4567.42715.1377.72733.4
Flavalignans
Cinchonain (7.37 min)937.8 ± 21.5325.4 ± 18.0258.3 ± 11.3354.8 ± 25.8183.4 ± 6.9391.8 ± 8.6107.2 ± 4.2213.1 ± 10.4
Cinchonain (9.05 min)786.9 ± 9.8420.4 ± 5.3249.6 ± 20.9522.8 ± 19.818.9 ± 1.149.5 ± 2.822.5 ± 1.215.3 ± 0.3
Cinchonain (9.30 min)977.6 ± 20.8565.4 ± 17.4335.5 ± 16.7570.8 ± 20.224.7 ± 0.655.7 ± 2.624.0 ± 1.221.4 ± 1.1
Cinchonain (12.27 min)809.3 ± 11.3301.3 ± 7.4231.2 ± 11.9337.9 ± 19.1189.3 ± 2.6325.7 ± 11.9115.6 ± 9.3207.9 ± 7.3
∑ Flavalignans3511.61612.41074.61786.3416.3822.7269.4457.7

Abbreviations: AS =Asomat; LC = Los Chiles; PA = Palacios; SR = Sarapiquí; nd = not detected.

[Source 11]

Table 2. Phenolic composition of ethanolic extracts from Cat’s claw (Uncaria tomentosa) bark and leaves

Leaves ExtractsBark Extracts
CompoundASLCPASRASLCPASR
Concentration (µg/g Extract)
Hydroxybenzoic acids
Benzoic acid46.3 ± 0.288.9 ± 9.8165.9 ± 8.864.8 ± 4.31053.4 ± 41.95102.6 ± 69.51567.6 ± 22.020.1 ± 1.4
Salicylic acid12.0 ± 1.110.0 ± 0.512.4 ± 0.612.0 ± 0.627.6 ± 0.5175.4 ± 2.3100.8 ± 7.1110.0 ± 3.3
4-hydroxybenzoic acid19.9 ± 0.723.2 ± 1.3124.3 ± 4.426.2 ± 1.4203.0 ± 6.2117.2 ± 4.6176.2 ± 15.342.2 ± 2.2
Protocatechuic acid25.7 ± 1.861.4 ± 1.0118.4 ± 3.348.5 ± 2.8932.9 ± 21.5283.8 ± 4.3742.1 ± 61.7326.5 ± 9.2
Gallic acid5.8 ± 0.310.5 ± 0.111.5 ± 0.62.8 ± 0.128.1 ± 1.732.5 ± 1.115.8 ± 1.115.4 ± 0.2
Vainillinic acid3.5 ± 0.05.8 ± 0.212.6 ± 0.64.4 ± 0.1150.3 ± 6.6412.1 ± 16.7147.7 ± 10.547.0 ± 1.8
Syringic acidnd3.4 ± 0.35.3 ± 0.2nd40.9 ± 2.182.7 ± 3.022.4 ± 1.312.5 ± 0.1
∑ Hydroxybenzoic acids113.2203.2450.4158.62436.16206.32772.6573.8
Hydroxycinnamic acids
p-cumaric acid4.6 ± 0.78.1 ± 1.322.5 ± 4.422.1 ± 1.49.9 ± 6.27.6 ± 4.64.8 ± 15.32.6 ± 2.2
Caffeic acid5.3 ± 0.57.5 ± 0.37.4 ± 0.45.4 ± 0.39.0 ± 0.67.5 ± 0.710.8 ± 1.04.5 ± 0.2
Ferulic acid10.2 ± 1.017.9 ± 0.930.1 ± 1.916.7 ± 1.531.5 ± 1.132.4 ± 3.211.8 ± 0.921.7 ± 0.8
Isoferulic acid14.4 ± 0.1nd7.7 ± 0.2nd21.0 ± 1.538.9 ± 4.0ndnd
∑ Hydroxycinnamic acids34.533.667.744.371.386.427.428.8
Flavan-3-ols: monomers
(+)-Catechin615.1 ± 6.7674.2 ± 16.0412.0 ± 14.11173.2 ± 33.466.4 ± 5.567.7 ± 4.7100.7 ± 8.4181.1 ± 11.3
(−)-Epicatechin2163.7 ± 62.31554.3 ± 52.91097.2 ± 31.82159.0 ± 45.3712.6 ± 44.0978.3 ± 38.91444.3 ± 142.23148.6 ± 64.9
∑ Monomers2778.82228.51509.23332.2779.01046.01545.03329.6
Flavan-3-ols: procyanidin dimers
Procyanidin B1621.5 ± 13.41114.6 ± 40.6313.6 ± 8.4769.6 ± 27.923.2 ± 0.921.8 ± 1.599.0 ± 8.2170.5 ± 5.8
Procyanidin B21363.7 ± 35.71399.3 ± 24.3539.1 ± 18.2992.1 ± 36.8527.4 ± 19.8378.5 ± 20.21592.3 ± 55.92792.9 ± 83.7
Procyanidin B3830.0 ± 26.62353.2 ± 16.1687.6 ± 11.41708.5 ± 93.719.2 ± 1.014.2 ± 0.269.3 ± 1.668.3 ± 3.4
Procyanidin B42476.6 ± 41.93931.9 ± 108.91711.8 ± 13.63172.6 ± 73.6370.9 ± 15.7319.1 ± 17.01866.0 ± 86.12015.7 ± 10.4
Procyanidin B5291.0 ± 6.4268.7 ± 8.3122.6 ± 9.9217.2 ± 3.472.9 ± 2.853.9 ± 0.1292.0 ± 5.6744.6 ± 13.6
Procyanidin B7161.4 ± 9.3267.6 ± 6.185.5 ± 4.8170.5 ± 14.5ndndnd112.2 ± 5.5
Procyanidin B (5.47 min)137.8 ± 9.6263.3 ± 7.596.0 ± 10.6184.3 ± 13.2ndnd65.1 ± 4.3123.1 ± 9.4
Procyanidin B (9.27 min)53.4 ± 2.2nd36.8 ± 2.876.0 ± 9.4ndndnd58.0 ± 3.3
∑ Procyanidin dimers5935.49598.53593.17290.81013.6787.43983.86085.3
Flavan-3-ols: propelargonidin dimers
Propelargonidin dimer (4.43 min)3239.3 ± 63.13067.8 ± 72.33644.5 ± 59.84660.6 ± 105.09.9 ± 1.022.0 ± 0.816.4 ± 2.468.7 ± 5.7
Propelargonidin dimer (5.01 min)2503.6 ± 26.92179.3 ± 22.12926.1 ± 37.83343.7 ± 57.185.7 ± 6.058.0 ± 5.1153.6 ± 6.4231.7 ± 18.0
Propelargonidin dimer (5.65 min)3253.4 ± 12.52177.2 ± 33.12178.4 ± 82.62480.8 ± 38.0112.8 ± 4.377.6 ± 2.4308.0 ± 13.8895.5 ± 24.3
Propelargonidin dimer (9.27 min)795.7 ± 30.3480.0 ± 15.5471.1 ± 20.5576.8 ± 21.012.2 ± 1.212.4 ± 0.842.3 ± 1.3143.8 ± 5.7
∑ Propelargonidin dimers9792.07904.39220.211,061.9220.6169.9520.21339.7
Flavan-3-ols: procyanidin trimers
Trimer T2ndndndndndndndnd
Procyanidin C1243.4 ± 25.4260.6 ± 13.269.7 ± 0.4181.2 ± 9.137.8 ± 0.4nd744.6 ± 10.81636.2 ± 76.2
Trimer B (5.78 min)ndndndndndndndnd
∑ Procyanidin trimers243.4260.669.7181.237.80.0744.61636.2
Flavalignans
Cinchonain (7.37 min)1723.6 ± 23.51011.9 ± 17.8567.2 ± 14.4773.0 ± 33.1236.0 ± 15.1170.7 ± 9.8745.7 ± 20.4447.7 ± 2.5
Cinchonain (9.05 min)2010.3 ± 17.01816.3 ± 48.4744.3 ± 23.41544.1 ± 77.119.7 ± 1.220.7 ± 2.663.8 ± 5.128.4 ± 1.4
Cinchonain (9.30 min)1795.3 ± 31.11901.5 ± 32.5773.9 ± 23.11358.0 ± 65.722.7 ± 2.025.8 ± 0.956.0 ± 2.534.6 ± 1.9
Cinchonain (12.27 min)1528.8 ± 20.7900.5 ± 14.5486.7 ± 16.2727.2 ± 23.3285.3 ± 10.1217.3 ± 12.9710.2 ± 25.7471.9 ± 17.3
∑ Flavalignans7058.05630.12572.04402.1563.7434.41575.7982.6

Abbreviations: AS =Asomat; LC = Los Chiles; PA = Palacios; SR = Sarapiquí; nd = not detected.

[Source 11]

Figure 2. Cat’s claw bioactive compounds chemical structure

Cat's claw bioactive compounds chemical structure

Regarding polyphenols, Cat’s claw studies are scarce and mainly focused on a particular subclass, for instance on hydroxycinnamic acids 14, flavonols 15, flavan-3-ols 16 and cinchonains 17. Recently, a detailed characterization of Cat’s claw leaves, bark, stem and wood has been reported indicating a high flavan-3-ol content, particularly in procyanidin dimers and trimers, propelargonidin dimers and cinchonain-type flavalignans 18 in leaves and bark. Also, assessment of biological activities of Cat’s claw proanthocyanidins showed evidence on the relationship between proanthocyanidin contents and antioxidant capacity, antimicrobial effect against Staphylococcus aureus, Enterococcus faecalis and Pseudomonas aeruginosa respiratory pathogens 19, and in vitro cytotoxicity, with high selectivity for AGS gastric and SW620 colon adenocarcinoma cell lines, mainly attributed to the content of propelargonidin dimers 20.

These promising results about the bioactivity of Cat’s claw proanthocyanidin extracts and their potential health effects were subject of an industrial patent 21 and prompted the need to further explore the viability of elaborating polyphenolic extracts form Cat’s claw using food-grade solvents (i.e., aqueous or ethanolic extracts) with potential use as dietary supplements.

Previous studies carried out with Cat’s claw aqueous and ethanolic extracts indicated antioxidant activity in vitro 22 and other biological activities such as important effects on mono- nuclear blood cells 23 with 95% ethanol extracts; however, detailed characterization of the extracts was not performed.

The efficacy and safety of this plant in improving osteoarthritis of the knee have been tested on 45 patients who have been divided into 2 groups (placebo and active); the active group has demonstrated some degrees of remission after 4 weeks by inhibiting TNF-α and diminishing PGE2 production 24. In a 24-week double-blind placebo-controlled trial which has been performed for evaluating the effect of high purified extract of Cat’s claw in rheumatoid arthritis patients, Cat’s claw extract has been administered along with Sulfasalazine or Hydroxy chloroquine; modest benefit of Cat’s claw herb in alleviating pain, swelling, and tenderness of joint has been shown in the treatment group in comparison with the placebo group 25. There is a report of Cat’s claw causing remarkable remission in enteritis in rats which has been observed 26. Edible extract of Cat’s claw has had protective action against respiratory inflammation in mice 27. Pivotal mechanism of Cat’s claw is inhibition of iNOS and NF-κB expression that in turn have downregulated TNF-α, IL-1α, 1β, 10 and 17 successively. Also, little inactivation effect on COX-1 and COX-2 has been expressed through an in vivo study 28. Cat’s claw plant’s bark has demonstrated anti-inflammatory action exactly the same as dexamethasone in an animal model, while it has attenuated about 40% of IL-4 while dexamethasone has not 29.

Figure 1. Cat’s claw

cat's claw

Cat’s claw benefits

Apart from numerous laboratory test tube and animals studies to test hypotheses, currently there is no clinical study data to support Cat’s claw use for any condition. Suggested anti-inflammatory, anticancer, and immune system stimulant properties are largely based on in vitro and limited animal studies.

Cat’s claw dosage

Clinical trials are generally lacking to support appropriate dosages. One gram of root bark given 2 to 3 times daily is a typical dose, while 20 to 30 mg of a root bark extract has been recommended.

Cat’s claw side effects

Currently no clinical study data to comment of cat’s claw side effects and long term safety. There are reports of side effects such as gastrointestinal complaints (nausea, diarrhea, stomach discomfort), kidney effects, nervous system disorders, and an increased risk of bleeding with anticoagulant therapy are possible for cat’s claw when taken in small amounts. Women who are pregnant or trying to become pregnant should avoid using cat’s claw because of its past use for preventing and aborting pregnancy. Information regarding safety and efficacy during pregnancy and lactation is lacking.

Cat’s claw products should be avoided before and after surgery, as well as by those using immunosuppressant therapy and in children due to lack of safety data.

Case reports are generally lacking; however, there is a reported interaction with HIV protease inhibitors.

References
  1. Anti-inflammatory activity of two different extracts of Uncaria tomentosa (Rubiaceae). Aguilar JL, Rojas P, Marcelo A, Plaza A, Bauer R, Reininger E, Klaas CA, Merfort I. J Ethnopharmacol. 2002 Jul; 81(2):271-6. https://www.ncbi.nlm.nih.gov/pubmed/12065162/
  2. Santos Araújo M do C, Farias IL, Gutierres J, et al. Uncaria tomentosa—Adjuvant Treatment for Breast Cancer: Clinical Trial. Evidence-based Complementary and Alternative Medicine : eCAM. 2012;2012:676984. doi:10.1155/2012/676984. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395261/
  3. Rizzi R., Re F., Bianchi A., De Feo V., De Simone F., Bianchi L., Stivala L.A. Mutagenic and antimutagenic activities of Uncaria tomentosa and its extracts. J. Ethnopharmacol. 1993;38:63–77. doi: 10.1016/0378-8741(93)90080-O
  4. Sandoval M., Okuhama N.N., Zhang X.J., Condezo L.A., Lao J., Angeles F.M., Musah R.A., Bobrowski P., Miller J.S. Anti-inflammatory and antioxidant activities of cat’s claw (Uncaria tomentosa and Uncaria guianensis) are independent of their alkaloid content. Phytomedicine. 2002;9:325–337. doi: 10.1078/0944-7113-00117
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  6. Heitzman M.E., Neto C.C., Winiarz E., Vaisberg A.J., Hammond G.B. Ethnobotany, Phytochemistry and Pharmacology of Uncaria (Rubiaceae) Phytochemistry. 2005;66:5–29. doi: 10.1002/chin.200517286 https://www.ncbi.nlm.nih.gov/pubmed/15649507
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  8. Falkiewicz B., Lukasiak J. Vilcacora [Uncaria tomentosa (Willd.) DC and Uncaria guianensis (Aublet) Gmell.]—A review of published scientific literature. Case Rep. Clin. Pract. Rev. 2001;2:305–316
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  12. Quality assessment of commercial dietary antioxidant products from Vitis vinifera L. grape seeds. Monagas M, Hernández-Ledesma B, Garrido I, Martín-Alvarez PJ, Gómez-Cordovés C, Bartolomé B. Nutr Cancer. 2005; 53(2):244-54.
  13. Cádiz-Gurrea M.L., Lozano-Sanchez J., Contreras-Gámez M., Legeai-Mallet L., Fernández-Arroyo S., Segura-Carretero A. Isolation, comprehensive characterization and antioxidant activities of Theobroma cacao extract. J. Funct. Foods. 2014;10:485–498. doi: 10.1016/j.jff.2014.07.016
  14. Pavei C., Kaiser S., Borre G.L., Ortega G.G. Validation of a LC Method for Polyphenols Assay in Cat’s Claw (Uncaria tomentosa) J. Liquid Chromatogr. Relat. Technol. 2010;33:1551–1561. doi: 10.1080/10826076.2010.503753
  15. Desmarchelier C., Mongelli E., Coussio J., Ciccia G. Evaluation of the in vitro antioxidant activity in extracts of Uncaria tomentosa (willd.) DC. Phytother. Res. 1997;11:254–256. doi: 10.1002/(SICI)1099-1573(199705)11:3<254::AID-PTR76>3.0.CO;2-5
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