JOURNAL OF THE CZECH PHARMACEUTICAL SOCIETY AND THE SLOVAK PHARMACEUTICAL SOCIETY

Čes. slov. farm. 2014, 63(2):55-70 | DOI: 10.36290/csf.2014.012

Selected natural phenolic compounds - potential treatment for peripheral neuropathy?

Karel ©mejkal
University of Veterinary and Pharmaceutical Sciences Brno, Faculty of Pharmacy, Department of Natural Drugs, Brno, Czech Republic

Neuropathic pain is a syndrome comprising pain caused by a lesion or dysfunction of the nervous system, or resulting from lesions or diseases of the somatosensory system. Neuropathic pain is often connected with adverse effects of chemotherapy administered because of cancer, infiltration of the nervous tissue with cancer cells, neurodegeneration and diabetes mellitus. Disbalance in the production of various cytokines plays an important role in the pathogenesis of many of the diseases connected with neuropathies. These cytokines comprise in particular interleukins IL-1β, IL-15, and IL-6, tumour necrosis factors, and prostaglandins. The biochemistry of the production of cytokines is directed by nuclear factors, which affect the expression of the mRNA for the respective cytokines or enzymes metabolizing the cytokines. The main nuclear factor which regulates the expression of cytokines is NF-κB. Because of insufficient effectiveness or adverse effects of the pharmacological treatment of peripheral neuropathy, many patients seek supportive or adjuvant therapy. Natural compounds which modulate the production of inflammatory cytokines may reduce the symptoms of neuropathies. Many natural phenolic compounds belong to substances affecting the activity of NF-κB and consequently the activity of cytokines which are regulated by this substance. The aim of this mini-review is to present information about three natural phenols which are potentially usable for the treatment of neuropathies: curcumin, resveratrol and mangiferin, and bring attention to the practical usability thereof. Curcumin and mangiferin are active constituents of plants; they have been used for centuries in traditional medicine. Biological effects of resveratrol have been known for a relatively short time; since the discovery of the so-called French paradox, attention has been focused on resveratrol. This summary includes particularly the information related to the influence on the activity of NF-κB, expression of anti-inflammatory cytokines, and antiradical activity, because imbalance between the creation and degradation of free radicals plays an important role in the activation of NF-κB and in inflammatory processes. It also briefly summarizes basic information concerning bioavailability, metabolism and practical application of the aforementioned substances.

Keywords: phenols; curcumin; mangiferin; NF-κB; peripheral neuropathy; resveratrol

Received: February 25, 2014; Accepted: March 6, 2014; Published: February 1, 2014  Show citation

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©mejkal K. Selected natural phenolic compounds - potential treatment for peripheral neuropathy? Čes. slov. farm. 2014;63(2):55-70. doi: 10.36290/csf.2014.012.
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References

  1. Höke A. Animal Models of Peripheral Neuropathies. Neurotherapeutics 2012; 9, 262-269. Go to original source... Go to PubMed...
  2. Iyer S, Tanenberg R. J. Pharmacologic management of diabetic peripheral neuropathic pain. Expert Opin. Pharmacother. 2013; 14, 1765-1775. Go to original source... Go to PubMed...
  3. Finkel T. Oxygen radicals and signaling. Curr. Opin. Cell Biol 1998; 10, 248-253. Go to original source... Go to PubMed...
  4. Garrido-Suárez B. B., Garrido G., Delgado R., Bosch F., Del C. Rabí M. A Mangifera indica L. Extract Could Be Used to Treat Neuropathic Pain and Implication of Mangiferin. Molecules 2010; 15, 9035-9045. Go to original source... Go to PubMed...
  5. Carozzi V. A. Ceresa C. The Role of Glutamate in Diabetic and in Chemotherapy Induced Peripheral Neuropathies and its Regulation by Glutamate Carboxypeptidase II. Curr. Med. Chem. 2012; 19, 1261-1268. Go to original source... Go to PubMed...
  6. Nickel F. T., Seifert F., Lanz S., Maihöfner C. Mechanisms of neuropathic pain. Eur. Neuropsychopharmacol. 2012; 22, 81-91. Go to original source... Go to PubMed...
  7. Finnerup N. B., Sindrup S. H., Jensen T. S. The evidence for pharmacological treatment of neuropathic pain. Pain 2010; 150, 573-581. Go to original source... Go to PubMed...
  8. Head K. A. Peripheral Neuropathy: Pathogenic Mechanisms and Alternative Therapies. Altern. Med. Rev. 2006; 11, 294-329.
  9. He S. M., Chan E., Zhou S. F. ADME properties of herbal medicines in humans: evidence, challenges and strategies. Curr. Pharm. Des. 2011; 17, 357-407. Go to original source... Go to PubMed...
  10. Jayaprakasha G. K., Jagan Mohan Rao L., Sakariah K. K. Chemistry and biological activities of C. longa. Trends Food Sci. & Technol. 2005; 16, 533-548. Go to original source...
  11. Shishodia S., Sethi G., Aggarwal B. B. Curcumin: Getting Back to the Roots. Ann. N.Y. Acad. Sci. 2005; 1056, 206-217. Go to original source... Go to PubMed...
  12. Lee W. H., Loo C. Y., Bebawy M., Luk F., Mason R. S., Rohanizadeh, R. Curcumin and its Derivatives: Their Application in Neuropharmacology and Neuroscience in the 21st Century. Curr. Neuropharmacol. 2013; 11, 338-378. Go to original source... Go to PubMed...
  13. Maheshwari R. K., Singh A. K., Gaddipati J., Srimal R. C. Multiple biological activities of curcumin: A short review. Life Sci. 2006; 78, 2081-2087. Go to original source... Go to PubMed...
  14. Esatbeyoglu T., Huebbe P., Insa E. M. A., Chin D., Wagner A. E., Rimbach G. Curcumin - From Molecule to Biological Function. Angew. Chem. Int. Ed. 2012; 51, 5308-5332. Go to original source... Go to PubMed...
  15. Singh U., Barik, A., Singh, B. G., Priyadarsini, K. I. Reactions of reactive oxygen species (ROS) with curcumin analogues: Structure-activity relationship. Free Rad. Res. 2011; 45, 317-325. Go to original source... Go to PubMed...
  16. Feng, J.-Y., Liu Z.-Q. Phenolic and Enolic Hydroxyl Groups in Curcumin: Which Plays the Major Role in Scavenging Radicals? J. Agric. Food Chem. 2009; 57, 11041-11046. Go to original source... Go to PubMed...
  17. Ak T., Gulcin I. Antioxidant and radical scavenging properties of curcumin. Chem. Biol. Interact. 2008; 174, 27-37. Go to original source... Go to PubMed...
  18. Calabrese V., Bates T. E., Mancuso C., Cornelius C., Ventimiglia B., Cambria M. T., Di Renzo L., De Lorenzo A., Dinkova-Kostova A. T. Curcumin and the cellular stress response in free radical-related diseases. Mol. Nutr. & Food Res. 2008; 52, 1062-1073. Go to original source... Go to PubMed...
  19. Zhang H.-Y., Yang D.-P., Tang G.-Y. Multipotent antioxidants: from screening to design. Drug Discov. Today 2006; 11, 749-754. Go to original source... Go to PubMed...
  20. Mattson M. P. Dietary factors, hormesis and health. Ageing Res. Rev. 2008; 7, 43-48. Go to original source... Go to PubMed...
  21. Ray P. D., Huang B.-W., Tsuji Y. Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling. Cell. Signal 2012; 24, 981-990. Go to original source... Go to PubMed...
  22. Appiah-Opong R., Commandeur J. N. M., Istyastono E., Bogaards J. J., Vermeulen N. P. Inhibition of human glutathione S-transferases by curcumin and analogues. Xenobiotica 2009; 39, 302-311. Go to original source... Go to PubMed...
  23. Sharma R. A., McLelland H. R., Hill K. A., Ireson C. R., Euden S. A., Manson M. M., Pirmohamed M., Marnett L. J., Gescher A. J., Steward W. P. Pharmacodynamic and pharmacokinetic study of oral Curcuma extract in patients with colorectal cancer. Clin. Cancer Res. 2001; 7, 1894-1900.
  24. Balogun E., Hoque M., Gong P., Killeen E., Green C. J., Foresti R., Alam J., Motterlini R. Curcumin activates the haem oxygenase-1 gene via regulation of Nrf2 and the antioxidant-responsive element. Biochem. J. 2003; 371, 887-905. Go to original source... Go to PubMed...
  25. Schrader C., Schiborr C., Frank J., Rimbach G. Curcumin induces paraoxonase 1 in cultured hepatocytes in vitro but not in mouse liver in vivo. Br. J. Nutr. 2010; 105, 167-170. Go to original source... Go to PubMed...
  26. Naik S. R., Thakare V. N., Path S. R. Protective effect of curcumin on experimentally induced inflammation, hepatotoxicity and cardiotoxicity in rats: Evidence of its antioxidant property. Exp. Toxicol. Pathol. 2011; 63, 419-431. Go to original source... Go to PubMed...
  27. Jena S., Chainy G. B. N., Dandapat J. Expression of antioxidant genes in renal cortex of PTU-induced hypothyroid rats: effect of vitamin E and curcumin. Mo. Biol. Rep. 2012; 39, 1193-1203. Go to original source... Go to PubMed...
  28. Dickinson D. A., Moellering D. R., Iles K. E., Patel R. P., Levonen A.-L., Wigley A., Darley-Usmar V. M., Forman H. J. Cytoprotection against Oxidative Stress and the Regulation of Glutathione Synthesis. Biol. Chem. 2005; 384, 527-537. Go to original source... Go to PubMed...
  29. Wu J., Li Q., Wang X., Yu S., Li L., Wu X., Chen Y., Zhao J., Zhao Y. Neuroprotection by Curcumin in Ischemic Brain Injury Involves the Akt/Nrf2 Pathway. PLoS One 2013; 8, e59843. Go to original source... Go to PubMed...
  30. He L. F., Chen H. J., Qian L. H., Chen G. Y., Buzby J. S. Curcumin protects pre-oligodendrocytes from activated microglia in vitro and in vivo. Brain Res. 2010; 1339, 60-69. Go to original source... Go to PubMed...
  31. Zhu Y. G., Chen X. C., Chen Z. Z., Zeng Y. Q., Shi G. B., Su Y. H., Peng X. Curcumin protects mitochondria from oxidative damage and attenuates apoptosis in cortical neurons. Acta Pharmacol. Sin. 2004; 25, 1606-1612.
  32. Darvesh A. S., Carroll R. T., Bishayee A., Novotny N., Geldenhuys W. J., Van der Schyf C. J. Curcumin and neurodegenerative diseases: a perspective. Exp. Opin. Inv. Drug. 2012; 21, 1123-1140. Go to original source... Go to PubMed...
  33. Balasubramanyam M., Koteswari A. A., Kumar R. S., Monickaraj S. F., Maheswari J. U., Mohan V. Curcumin-induced inhibition of cellular reactive oxygen species generation: Novel therapeutic implications. J. Biosci. 2003; 28, 715-721. Go to original source... Go to PubMed...
  34. Bremner P., Heinrich M. Natural products as targeted modulators of the nuclear factor-kappa B pathway. J. Pharm. Pharmacol. 2002; 54, 453-472. Go to original source... Go to PubMed...
  35. Sharma S., Kulkarni S. K., Agrewala J. N., and Chopra K. Curcumin attenuates thermal hyperalgesia in a diabetic mouse model of neuropathic pain. Eur. J. Pharmacol. 2006; 536, 256-261. Go to original source... Go to PubMed...
  36. Zhao X., Xu Y, Zhao Q., Chen C. R., Liu A. M., Huang Z. L. Curcumin exerts antinociceptive effects in a mouse model of neuropathic pain: descending monoamine system and opioid receptors are differentially involved. Neuropharmacol. 2012; 62, 843-854. Go to original source... Go to PubMed...
  37. Anand P., Kunnumakkara A. B., Newman R. A., Aggarwal B. B. Bioavailability of Curcumin: Problems and Promises. Mol. Pharm. 2007; 4, 807-818. Go to original source... Go to PubMed...
  38. Wahlstrom B., Blennow G. A. study on the fate of curcumin in the rat. Acta Pharmacol. Toxicol. (Copenhagen) 1978; 43, 86-92. Go to original source... Go to PubMed...
  39. Lao C. D., Ruffin M. T., Normolle D., Heath D. D., Murray S. I., Bailey J. M., Boggs M. E., Crowell J., Rock C. L., Brenner D. E. Dose escalation of a curcuminoid formulation. BMC Complement. Altern. Med. 2006; 6, 10. doi: 10.1186/1472-6882-6-10. Go to original source... Go to PubMed...
  40. Cheng A. L., Hsu C. H., Lin J. K., Hsu M. M., Ho Y. F., Shen T. S., Ko J. Y., Lin J. T., Lin B. R., Ming-Shiang W., Yu H. S., Jee S. H., Chen G. S., Chen T. M., Chen C. A., Lai M. K., Pu Y. S., Pan M. H., Wang Y. J., Tsai C. C., Hsieh C. Y. Phase I clinical trial of curcumin, a chemopreventive agent, in patients with high-risk or pre-malignant lesions. Anticancer Res. 2001; 21, 2895-900.
  41. Shoba G., Joy D., Joseph T., Majeed M., Rajendran R., Srinivas P. S. Influence of piperine on the pharmacokinetics of curcumin in animals and human volunteers. Planta Med. 1998; 64, 353-356. Go to original source... Go to PubMed...
  42. Garcea G., Jones D. J., Singh R., Dennison A. R., Farmer P. B., Sharma R. A., Steward W. P., Gescher A. J., Berry D. P. Detection of curcumin and its metabolites in hepatic tissue and portal blood of patients following oral administration. Br. J. Cancer 2004; 90, 1011-1015. Go to original source... Go to PubMed...
  43. Metzler M., Pfeiffer E., Schulz S. I., Dempe J. S. Curcumin uptake and metabolism. Biofactors 2013; 39, 14-20. Go to original source... Go to PubMed...
  44. Wang K., Qiu F. Curcuminoid Metabolism and its Contribution to the Pharmacological Effects. Curr. Drug Metab. 2013; 14, 791-806. Go to original source... Go to PubMed...
  45. Pari L., Tewas D., Eckel J. Role of curcumin in health and disease. Arch. Physiol. Biochem. 2008; 114, 127-149. Go to original source... Go to PubMed...
  46. Goel A., Kunnumakkara A. B., Aggarwal B. B. Curcumin as ''Curecumin'': From kitchen to clinic. Biochem. Pharmacol. 2008; 75, 787-809. Go to original source... Go to PubMed...
  47. Deodhar S. D., Sethi R., Srimal R. C. Preliminary study on antirheumatic activity of curcumin (diferuloyl methane). Indian J. Med. Res. 1980; 71, 632-634.
  48. Satoskar R. R., Shah S. J., Shenoy S. G. Evaluation of antiinflammatory property of curcumin (diferuloyl methane) in patients with postoperative inflammation. Int. J. Clin. Pharmacol. Ther. Toxicol. 1986; 24, 651-654.
  49. Lal B., Kapoor A. K., Asthana O. P., Agrawal P. K., Prasad R., Kumar P., Srimal R.C. Efficacy of curcumin in the management of chronic anterior uveitis. Phytother. Res. 1999; 13, 318-322. Go to original source...
  50. Lal B., Kapoor A. K., Agrawal P. K., Asthana O. P., Srimal R. C. Role of curcumin in idiopathic inflammatory orbital pseudotumours. Phytother. Res. 2000; 14, 443-447. Go to original source...
  51. Sharma R. A., Euden S. A., Platton S. L., Cooke D. N., Shafayat A., Hewitt H. R., Marczylo T. H., Morgan B., Hemingway D., Plummer S. M., Pirmohamed M., Gescher A. J., Steward W. P. Phase I clinical trial of oral curcumin: biomarkers of systemic activity and compliance. Clin. Cancer Res. 2004; 10, 6847-6854. Go to original source... Go to PubMed...
  52. Bundy R., Walker A. F., Middleton R. W., Booth J. Turmeric extract may improve irritable bowel syndrome symptomology in otherwise healthy adults: a pilot study. J. Altern. Complement. Med. 2004; 10, 1015-1018. Go to original source... Go to PubMed...
  53. Durgaprasad S., Pai C. G., Vasanthkumar ??, Alvres J. F., Namitha S. A pilot study of the antioxidant effect of curcumin in tropical pancreatitis. Indian J. Med. Res. 2005; 122, 315-318.
  54. Holt P. R., Katz S., Kirshoff R. Curcumin therapy in inflammatory bowel disease: a pilot study. Dig. Dis. Sci. 2005; 50, 2191-2193. Go to original source... Go to PubMed...
  55. Hanai H., Iida T., Takeuchi K., Watanabe F., Maruyama Y., Andoh A., Tsujikawa T., Fujiyama Y., Mitsuyama K., Sata M., Yamada M., Iwaoka Y., Kanke K., Hiraishi H., Hirayama K., Arai H., Yoshii S., Uchijima M., Nagata T., Koide Y. Curcumin maintenance therapy for ulcerative colitis: randomized, multicenter, double-blind, placebo-controlled trial. Clin. Gastroenterol. Hepatol. 2006; 4, 1502-1506. Go to original source... Go to PubMed...
  56. Neves A. R., Lúcio M., Lima J. L. C., Reis S. Resveratrol in Medicinal Chemistry: A Critical Review of its Pharmacokinetics, Drug-Delivery, and Membrane Interactions. Curr. Med. Chem. 2012; 19, 1663-1681. Go to original source... Go to PubMed...
  57. Pervaiz S. Resveratrol: from grapevines to mammalian biology. Faseb J. 2003; 17, 1975-1985. Go to original source... Go to PubMed...
  58. Ector B. J., Magee J. B., Hegwood C. P., Coign M. J. Resveratrol concentration in muscadine berries, juice, pomace, purees, seeds, and wines. Am. J. Enol. Viticult. 1996; 47, 57-62. Go to original source...
  59. Bavaresco L., Mattivi F., De Rosso M., Flamini R. Effects of Elicitors, Viticultural Factors, and Enological Practices on Resveratrol and Stilbenes in Grapevine and Wine. Mini-Rev. Med. Chem. 2012; 12, 1366-1381. Go to original source... Go to PubMed...
  60. Hasan M. M., Cha M., Bajpai V. K., Baek K.-H. Production of a major stilbene phytoalexin, resveratrol in peanut (Arachis hypogaea) and peanut products: a mini review. Rev. Environ. Sci. Biotechnol. 2013; 12, 209-221. Go to original source...
  61. Peng W, Qin R, Li X, Zhou H. Botany, phytochemistry, pharmacology, and potential application of Polygonum cuspidatum Sieb.et Zucc.: A review. J. Ethnopharmacol. 2013; 148, 729-745. Go to original source... Go to PubMed...
  62. Harikumar K. B., Aggarwal B. B. Resveratrol - A multitargeted agent for age-associated chronic diseases. Cell Cycle 2008; 7, 1020-1035. Go to original source... Go to PubMed...
  63. Yoo Y. J., Saliba A. J., Prenzler P. D. Should Red Wine Be Considered a Functional Food? Compr. Rev. Food Sci. F. 2010; 9, 530-551. Go to original source... Go to PubMed...
  64. Catalgol B., Batirel S., Taga Y., Ozer N. K. Resveratrol: French paradox revisited. Front. Pharmacol. 2012; 3, 141. doi: 10.3389/fphar.2012.00141. Go to original source... Go to PubMed...
  65. Singh N., Agrawal M., Doré S. Neuroprotective Properties and Mechanisms of Resveratrol in in Vitro and in Vivo Experimental Cerebral Stroke Models. ACS Chem. Neurosci. 2013; 4, 1151-1162. Go to original source... Go to PubMed...
  66. Zhang F., Liu J., Shi J.-S. Anti-inflammatory activities of resveratrol in the brain: Role of resveratrol in microglial activation. Eur. J. Pharmacol. 2010; 636, 1-7. Go to original source... Go to PubMed...
  67. Bandyopadhyay U., Das D., Banerjee R. K. Reactive oxygen species: Oxidative damage and pathogenesis. Curr. Sci. 1999; 77, 658-666.
  68. King R. E., Bomser J. A., Min D. B. Bioactivity of Resveratrol. Compr. Rev. Food Sci. F. 2006; 5, 65-70. Go to original source...
  69. Zhang F., Shi J. S., Zhou H., Wilson B., Hong J. S., Gao H. M. Resveratrol Protects Dopamine Neurons Against Lipopolysaccharide-Induced Neurotoxicity through Its Anti-Inflammatory Actions. Mol. Pharmacol. 2010; 78, 466-477. Go to original source... Go to PubMed...
  70. Stünkel W., Campbell R. M. Sirtuin 1 (SIRT1): The Misunderstood HDAC. J. Biomol. Screen. 2011; 16, 1153-1169. Go to original source... Go to PubMed...
  71. Donmez G. The neurobiology of sirtuins and their role in neurodegeneration. Trends Pharmacol. Sci. 2012; 33, 494-501. Go to original source... Go to PubMed...
  72. Piotrowska H., Kucinska M., Murias M. Biological activity of piceatannol: Leaving the shadow of resveratrol. Mutat. Res. - Rev. Mutat. Res. 2011; 750, 60-82. Go to original source... Go to PubMed...
  73. Storniolo C. E., Moreno J. J. Resveratrol metabolites have an antiproliferative effect on intestinal epithelial cancer cells. Food Chem. 2012; 134, 1385-1391. Go to original source... Go to PubMed...
  74. Cottart C. H., Nivet-Antoine V., Laguillier-Morizot C., Beaudeux J. L. Resveratrol bioavailability and toxicity in humans. Mol. Nutr. Food Res. 2010; 54, 7-16. Go to original source... Go to PubMed...
  75. Smoliga J. M., Baur J. A., Hausenblas H. A. Resveratrol and health - A comprehensive review of human clinical trials. Mol. Nutr. Food Res. 2011; 55, 1129-1141. Go to original source... Go to PubMed...
  76. Kennedy D. O., Wightman E. L., Reay J, L., Lietz G., Okello E. J., Wilde A., Haskell C. F. Effects of resveratrol on cerebral blood flow variables and cognitive performance in humans: a double-blind, placebo-controlled, crossover investigation. Am. J. Clin. Nutr. 2010; 91, 1590-1597. Go to original source... Go to PubMed...
  77. Ghanim H., Sia C. L., Korzeniewski K., Lohano T., Abuaysheh S., Marumganti A., Chaudhuri A., Dandona P. A Resveratrol and Polyphenol Preparation Suppresses Oxidative and Inflammatory Stress Response to a High-Fat, High-Carbohydrate Meal. J. Clin. Endocrinol. Metab. 2011; 96, 1409-1414. Go to original source... Go to PubMed...
  78. Ghanim H., Sia C. L., Abuaysheh S., Korzeniewski K., Korzeniewski K., Patnaik P., Marumganti A., Chaudhuri A., Dandona P. An antiinflammatory and reactive oxygen species suppressive effects of an extract of Polygonum cuspidatum containing resveratrol. J. Clin. Endocrinol. Metab. 2010; 95, E1-E8. Go to original source... Go to PubMed...
  79. Almeida L., Vaz-da-Silva M., Falcao A., Soares E., Soares E., Costa R., Loureiro A. I., Fernandes-Lopes C., Rocha J. F., Nunes T., Wright L., Soares-da-Silva P. Pharmacokinetic and safety profile of transresveratrol in a rising multiple-dose study in healthy volunteers. Mol. Nutr. Food Res. 2009; 53, S7-S15. Go to original source... Go to PubMed...
  80. Boocock D. J., Faust G. E. S., Patel K. R., Schinas A. M., Brown V. A., Ducharme M. P., Booth T. D., Crowell J. A., Perloff M., Gescher A. J., Steward W. P., Brenner D. E. Phase I dose escalation pharmacokinetic study in healthy volunteers of resveratrol, a potential cancer chemoprotective agent. Cancer Epidemiol. Biomarkers. Prev. 2007; 16, 1246-1252. Go to original source... Go to PubMed...
  81. Matkowski A, Ku¶ P, Góralska E, WoĽniak D. Mangiferin - a bioactive xanthonoid, not only from mango and not just antioxidant. Mini Rev. Med. Chem. 2013; 13, 439-455. Go to original source...
  82. Qin J. P., Deng J. G., Feng X., Wang Q., Wang S. B. Quantitative RP-LC Analysis of Mangiferin and Homomangiferin in Mangifera indica L. Leaves and in Mangifera persiciforma CY Wu et TL Ming Leaves. Chromatographia 2008; 68, 955-960. Go to original source...
  83. Mirza R. H., Chi N., Chi Y. Therapeutic Potential of the Natural Product Mangiferin in Metabolic Syndrome. J. Nutrit. Ther. 2013; 2, 74-79. Go to original source...
  84. Denisova O. A., Glyzin V. I., Patudin A. V., Gavrilenko B. D. Determination of the Content of the Xanthone Glycoside Mangiferin in Iris, Gentiana and Hedysarum Plants. Khim-Farm. Z. 1980; 14, 76-77.
  85. Islam M. N., Yoo H. H., Lee J., Nam J. W., Seo E. K., Jin C., Kim D. H. Simultaneous Determination of Bioactive Xanthone Glycosides and Norlignans from Ethanolic Extract of Anemarrhena asphodeloides by Liquid Chromatography. J. AOAC Int. 2008; 91, 1271-1277. Go to original source...
  86. Vyas A., Syeda K., Ahmad A., Padhye S., Sarkar F. H. Perspectives on Medicinal Properties of Mangiferin. Mini Rev. Med. Chem 2012; 12, 412-425. Go to original source... Go to PubMed...
  87. Masibo M., He Q. Major Mango Polyphenols and Their Potential Significance to Human Health. Compr. Rev. Food Sci. F. 2008; 7, 309-319. Go to original source... Go to PubMed...
  88. Campos-Esparza M. R., Sanchez-Gomez M. V., Matute C. Molecular mechanisms of neuroprotection by two natural antioxidant polyphenols. Cell Calcium 2009; 49, 358-368. Go to original source... Go to PubMed...
  89. Bhatia H. S., Candelario-Jalil E., Pinheiro de Oliveira A., Olajide O. A., Martínez-Sánchez G., Fiebich B. L. Mangiferin inhibits cyclooxygenase-2 expression and prostaglandin E2 production in activated rat microglial cells. Arch. Biochem. Biophys. 2008; 477, 253-258. Go to original source... Go to PubMed...
  90. Lopes S. C., da Silva A. V., Arruda B. R., Morais T. C., Rios J. B., Trevisan M. T., Rao V. S., Santos F. A. Peripheral antinociceptive action of mangiferin in mouse models of experimental pain: Role of endogenous opioids, KATP-channels and adenosine. Pharmacol. Biochem. Behav. 2013; 110, 19-26. Go to original source... Go to PubMed...
  91. Izquierdo T., Espinosa de Los Monteros-Zuñiga A., Cervantes-Durán C., Lozada M. C., Godínez-Chaparro B. Mechanisms underlying the antinociceptive effect of mangiferin in the formalin test. Eur. J. Pharmacol. 2013; 718, 393-400. Go to original source... Go to PubMed...
  92. Yoshikawa M., Nishida N., Shimoda H., Takada M., Kawahara Y., Matsuda H. Polyphenol constituents from salacia species: quantitative analysis of mangiferin with glucosidase and aldose reductase inhibitory activities. Yakugaku Zasshi 2001; 121, 371-378. Go to original source... Go to PubMed...
  93. Delarue J., Magnan C. Free fatty acids and insulin resistance. Curr. Opin. Clin. Nutr. Metab. Care 2007; 10, 142-148. Go to original source... Go to PubMed...
  94. Hu H. G., Wang M. J., Zhao Q. J., Liao H. L., Cai L. Z., Song Y., Zhang J., Yu S. C., Chen W. S., Liu C. M., Wu Q. Y. Synthesis of mangiferin derivatives as protein tyrosine phosphatase 1B inhibitors. Chem. Nat. Comp. 2007; 43, 663-666. Go to original source...
  95. Hou S., Wang F., Li Y., Li Y., Wang M., Sun D., Sun C. Pharmacokinetic study of mangiferin in human plasma after oral administration. Food Chem. 2012; 132, 289-294. Go to original source... Go to PubMed...
  96. Hattori M., Shu Y.-Z., Tomimori T., Kobashi K., Namba T. A bacterial cleavage of the C-glucosyl bond of mangiferin and bergenin. Phytochemistry 1989; 28, 1289-1290. Go to original source...
  97. Wang H., Ye G., Ma C.-H., Tang Y.-H., Fan M.-S., Li Z.-X., Huang C. G. Identification and determination of four metabolites of mangiferin in rat urine. J. Pharm. Biomed. Anal. 2007; 45, 793-798. Go to original source... Go to PubMed...
  98. Pardo-Andreu G. L., Philip S. J., Riano A., Sanchez C., Viada C., Nunez-Selles A. J., Delgado R. Mangifera indica L. (Vimang) protection against serum oxidative stress in elderly humans. Arch. Med. Res. 2006; 37, 158-164. Go to original source... Go to PubMed...
  99. Nunez-Selles A., Paez-Betancourt E., Amaro-Gonzalez D., Acosta-Esquijarosa J., Aguero-Aguero J., Capote-Hernandez R. Oficina Cubana De La Propiedad Industrial Patent 2002, Cuba patent No. 1814.
  100. Menkovic N., Juranic Z., Stanojkovic T., Raonic-Stevanovic T., Savikin K., Zdunic G., Borojevic N. Radioprotective Activity of Gentiana lutea Extract and Mangiferin. Phytother. Res. 2010; 24, 1693-1696. Go to original source... Go to PubMed...
  101. Cruz-Correa M., Shoskes D. A., Sanchez P., Zhao R., Hylind L. M., Wexner S. D., Giardiello F. M. Combination treatment with curcumin and quercetin of adenomas in familial adenomatous polyposis. Clin. Gastroenterol. Hepatol. 2006; 4, 1035-1038. Go to original source... Go to PubMed...
  102. Verma S. P., Salamone E., Goldin B. Curcumin and genistein, plant natural products, show synergistic inhibitory effects on the growth of human breast cancer MCF-7 cells induced by estrogenic pesticides. Biochem. Biophys. Res. Commun. 1997; 233, 692-696. Go to original source... Go to PubMed...
  103. Fang J. Y., Hung C. F., Chiu H. C., Wang J. J., Chan T. F. Efficacy and irritancy of enhancers on the in-vitro and in-vivo percutaneous absorption of curcumin. J. Pharm. Pharmacol. 2003; 55, 593-601. Go to original source... Go to PubMed...
  104. Sun M., Su X., Ding B., He X., Liu X., Yu A., Lou H., Zhai G. Advances in nanotechnology-based delivery systems for curcumin. Nanomedicine 2012; 7, 1085-1100. Go to original source... Go to PubMed...
  105. Bansal S. S., Goel M., Aqil F., Vadhanam M. V., Gupta R. C. Advanced Drug Delivery Systems of Curcumin for Cancer Chemoprevention. Cancer Prev. Res. 2011; 4, 1158-1171. Go to original source... Go to PubMed...
  106. Amri A., Chaumeil J. C., Sfar S., Charrueau C. Administration of resveratrol: What formulation solutions to bioavailability limitations? J. Control. Release 2012; 158, 182-193. Go to original source... Go to PubMed...
  107. Bhattacharya S., Sanyal A. K., Ghosal S. Monoamine Oxidase-Inhibiting Activity of Mangiferin Isolated from Canscora-Decussata. Naturwissenschaften 1972; 59, 651-651. Go to original source... Go to PubMed...
  108. Niu Y., Lu W., Gao L., Lin H., Liu X., Li L. Reducing effect of mangiferin on serum uric acid levels in mice. Pharm. Biol. 2012; 50, 1177-1182. Go to original source... Go to PubMed...
  109. Aftab N., Vieira A. Antioxidant Activities of Curcumin and combinations of this curcuminoid with other phytochemicals. Phytother. Res. 2010; 24, 500-502. Go to original source... Go to PubMed...
  110. Du Q., Hu B., An H.-M., Shen K.-P., DengS., Wei M.-M. Synergistic anticancer effects of curcumin and resveratrol in Hepa1-6 hepatocellular carcinoma cells. Oncol. Rep. 2013; 29, 1851-1858. Go to original source... Go to PubMed...
  111. Majumdar A. P., Banerjee S., Nautiyal J., Patel B. B., Patel V., Du J., Yu Y., Elliott A. A., Levi E., Sarkar F. H. Curcumin synergizes with resveratrol to inhibit colon cancer. Nutr. Cancer 2009; 61, 544-553. Go to original source... Go to PubMed...
  112. Masuelli L., Marzocchella L., Focaccetti C., Tresoldi I., Palumbo C., Izzi V., Benvenuto M., Fantini M., Lista F., Tarantino U., Modesti A., Galvano F., Bei B. Resveratrol and diallyl disulfide enhance curcumin-induced sarcoma cell apoptosis. Front. Biosci. 2012; 17, 498-508. Go to original source... Go to PubMed...
  113. Csaki C., Mobasheri A., Shakibaei M. Synergistic chondroprotective effects of curcumin and resveratrol in human articular chondrocytes: inhibition of IL-1β-induced NF-κB-mediated inflammation and apoptosis. Arthritis Res. Ther. 2009; 11, R165. doi: 10.1186/ar2850 Go to original source... Go to PubMed...




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