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Abstract

Saccharum officinarum is a tropical perennial grass of the GRAMINEAE family. It is 3–4 m tall, approx 5 cm in diameter, with unbranched stems, which have many nodes and short conspicuous internodes filled with solid, juicy pulp. Each stem produces its own root system. Two types of roots develop: the first type, from the primordia of the cutting after planting, are thin and branched, and the second type, from the primordia of the tillers, which are thick, fleshy, and less branched. With age, all roots become brown, shrivel, and die. Leaves are up to 1.5 m long, falling from the lower stems when they wither. Each leaf consists of linear-lanceolate blade, up to 10 cm wide in the base, narrowing into sheath clasping the stem, sharp serrate on the margin and siliceous. The midrib is prominent and broad, white and concave on the upper surface, and green below.

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References

  1. Gamez, R., R. Mas, M. Noa, et al. Effects of chronic administration of D-003, a mixture of sugar cane wax high molecular acids, in beagle dogs. Drugs Exp Clin Res 2004; 30(2): 75–88.

    PubMed  CAS  Google Scholar 

  2. Amer, S., K.J. Na, M. El-Abasy, M. Motobu, Y. Koyama, K. Koge, and Y. Hirota. Immunostimulating effects of sugar cane extract on X-ray radiation induced immunosuppression in the chicken. Int Immunopharmacol 2004; 4(1): 71–77.

    Article  PubMed  CAS  Google Scholar 

  3. Mendoza, S., M. Noa, R. Mas, and N. Mendoza. Effect of D-003, a mixture of high molecular weight primary acids from sugar cane wax, on paracetamol-induced liver damage in rats. Int J Tissue React 2003; 25(3): 91–98.

    PubMed  CAS  Google Scholar 

  4. Takara, K., D. Matsui, K. Wada, T. Ichiba, I. Chinen, and Y. Nakasone. New phenolic compounds from Kokuto, non-centrifuged cane sugar. Biosci Biotechnol Biochem 2003; 67(2): 376–379.

    Article  PubMed  CAS  Google Scholar 

  5. Ledon, N., A. Casaco, V. Rodriguez, et al. Anti-inflammatory and analgesic effects of a mixture of fatty acids isolated and purified from sugar cane wax oil. Planta Med 2003; 69(4): 367–369.

    Article  PubMed  CAS  Google Scholar 

  6. Arruzazabala, M.L., D. Carbajal D, R. Mas R, S. Valdes, and V. Molina V. Pharmacological interaction between Policosanol and nitroprusside in rats. J Med Food 2001; 4(2): 67–70.

    Article  PubMed  CAS  Google Scholar 

  7. Noa, M., S. Mendoza, R. Mas, and N. Mendoza. Effect of D-003, a mixture of high molecular weight primary acids from sugar cane wax, on CL4C-in-duced liver acute injury in rats. Drugs Exp Clin Res 2002; 28(5): 177–183.

    PubMed  CAS  Google Scholar 

  8. Gamez, R., R. Mas, M. Noa, et al. Six-month toxicity study of oral administration of D-003 in Sprague Dawley rats. Drugs R D 2002; 3(6): 375–386.

    Article  PubMed  CAS  Google Scholar 

  9. Menendez, R., A.M. Amor, I. Rodeiro, et al. Policosanol modulates HMG-CoA reductase activity in cultured fibroblasts. Arch Med Res 200; 32(1): 8–12.

    Google Scholar 

  10. Gamez, R., R. Mas, M. Noa, et al. Acute and oral subchronic toxicity of D-003 in rats. Toxicol Lett 2000; 118(1–2): 31–41.

    Article  PubMed  CAS  Google Scholar 

  11. Menendez, R., V. Fraga, A.M. Amor, R.M. Gonzalez, and R. Mas. Oral administration of policosanol inhibits in vitro copper ion-induced rat lipo-protein peroxidation. Physiol Behav 1999; 67(1): 1–7.

    Article  PubMed  CAS  Google Scholar 

  12. Molina Cuevas, V., M.L. Arruzazabala, D. Carbajal Quintana, R. Mas Ferreiro, and S. Valdes Garcia. Effect of policosanol on arterial blood pressure in rats. Study of the pharmacological interaction with nifedipine and propranolol. Arch Med Res 1998; 29(1): 21–24.

    PubMed  CAS  Google Scholar 

  13. Fraga, V., R. Menendez, A.M. Amor, R.M. Gonzalez, S. Jimenez, and R. Mas. Effect of policosanol on in vitro and in vivo rat liver microsomal lipid peroxidation. Arch Med Res 1997; 28(3): 355–360.

    PubMed  CAS  Google Scholar 

  14. Mesa, A. R., R. Mas, M. Noa, et al. Toxicity of policosanol in beagle dogs: one-year study. Toxicol Lett 1994; 73(2): 81–90.

    Article  PubMed  CAS  Google Scholar 

  15. Carbajal, D., M. L. Arruzazabala, R. Mas, V. Molina, and S. Valdes. Effect of policosanol on experimental thrombosis models. Prostaglandins Leukot Es-sent Fatty Acids 1994; 50(5): 249–251.

    Article  CAS  Google Scholar 

  16. Arruzazabala, M. L., D. Carbajal, R. Mas, V. Molina, S. Valdes, and A. Laguna. Cholesterol-lowering effects of policosanol in rabbits. Biol Res 1994; 27(3–4): 205–208.

    PubMed  CAS  Google Scholar 

  17. Hikino, H., M. Takahashi, C. Konno, A. Ishimori, T. Kawamura, and T. Namiki. Effect of glycans of Saccharum officinarum on carbohydrate and lipid metabolism of rats. J Ethnopharmacol 1985; 14(2–3): 261–268.

    Article  PubMed  CAS  Google Scholar 

  18. Chinen, I., K. Oouchi, H. Tamaki, and N. Fukuda. Purification and properties of thermostable beta-xylosidase from immature stalks of Saccharum officinarum L. (sugar cane). J Biochem (Tokyo) 1982; 92(6): 1873–1881.

    CAS  Google Scholar 

  19. Chinen, I., T. Nakamura, and N. Fukuda. Purification and properties of alpha-galactosidase from immature stalks of Saccharum officinarum (sugar cane). J Biochem (Tokyo) 1981; 90(5): 1453–1461.

    CAS  Google Scholar 

  20. Mas, R., G. Castano, J. Fernandez, et al. Long-term effects of policosanol on obese patients with Type II hypercholesterolemia. Asia Pacific J Clin Nutr 2004; 13(Suppl): S102.

    Google Scholar 

  21. Mas, R., G. Castano, J. Fernandez, et al. Long-term effects of policosanol on older patients with Type 2 diabetes. Asia Pacific J Clin Nutr 2004; 13(Suppl):S101.

    Google Scholar 

  22. Murphy, K. J., D. A. Saint, and P. R. Howe. Lack of effect of sugar cane and sunflower seed policosanols on plasma cholesterol in rabbits. Asia Pacific J Clin Nutr 2004;13(Suppl): S69.

    Google Scholar 

  23. El-Abasy, M., M. Motobu, K. Nakamura, K. Koge, T. Onodera, O. Vainio, P. Toivanen, and Y. Hirota. Preventive and therapeutic effects of sugar cane extract on cyclophosphamide-induced immunosuppression in chickens. Int Immunopharmacol 2004; 4(8): 983–990.

    Article  PubMed  CAS  Google Scholar 

  24. Noa, M., R. Mas, S. Mendoza, R. Gamez, and N. Mendoza. Effects of D-003, a mixture of high molecular weight aliphatic acids from sugar cane wax, on bones from ovariectomized rats. Drugs Exp Clin Res 2004; 30(1): 35–41.

    PubMed  CAS  Google Scholar 

  25. Menendez, R., R. Mas, J. Perez, R.M. Gonzalez, and S. Jimenez. Oral administration of D-003, a mixture of very long chain fatty acids prevents casein-induced endogenous hypercholesterolemia in rabbits. Can J Physiol Pharmacol 2004; 82(1): 22–29.

    Article  PubMed  CAS  Google Scholar 

  26. Holt, S., V.D. Jong, E. Faramus, T. Lang, and J. Brand Miller. A bioflavonoid in sugar cane can reduce the postprandial glycaemic response to a high-GI starchy food. Asia Pacific J Clin Nutr 2003; 12(Suppl): S66.

    Google Scholar 

  27. Mendoza, S., R. Gamez, R. Mas, and E. Goicochea. Effects of D-003, a mixture of long-chain aliphatic primary acids, fluvastatin and the combined therapy of D-003 plus fluvastatin on the lipid profile of normocholesterolemic rabbits. Int J Tissue React 2003; 25(3): 81–89.

    PubMed  CAS  Google Scholar 

  28. Barba, T. F., C.A. Barba, D. Sole, and C.K. Naspitz. Non-specific broncho-provocation with metacholine in children before and during sugar cane burning in Catanduva-SP. J Pediatr (Rio J) 1998; 74(3): 228–232.

    Google Scholar 

  29. Varady, K. A., Y. Wang, and P. J. Jones. Role of policosanols in the prevention and treatment of cardiovascular disease. Nutr Rev 2003; 61(11): 376–383.

    Article  PubMed  Google Scholar 

  30. Carbajal, D., M. L. Arruzazabala, M. Noa, et al. Protective effect of D-003 on experimental spinal cord ischemia in rabbits. Prostaglandins Leuko Es-sent Fatty Acids 2004; 70(1): 1–6.

    Article  CAS  Google Scholar 

  31. Carbajal, D., M. Noa, V. Molina, et al. Effect of D-003 on isoproterenol-induced myocardial necrosis in rats. J Med Food 2003; 6(1): 13–18.

    Article  PubMed  CAS  Google Scholar 

  32. Wang, Y.W., P.J. Jones, I. Pischel, and C. Fairow. Effects of policosanols and phytosterols on lipid levels and cholesterol biosynthesis in hamsters. Lipids 2003; 38(2): 165–170.

    Article  PubMed  CAS  Google Scholar 

  33. Tamaki, H., S. L. Man, Y. Ohta, N. Katsuyama, and I. Chinen. Inhibition of osteoporosis in rats fed with sugar cane wax. Biosci Biotechnol Biochem 2003; 67(2): 423–425.

    Article  PubMed  CAS  Google Scholar 

  34. Gamez, R., J. E. Gonzalez, I. Rodeiro, et al. In vivo genotoxic evaluation of D-003, a mixture of very long chain aliphatic acids. J Med Food 2001; 4(2): 85–91.

    Article  PubMed  CAS  Google Scholar 

  35. Gamez, R., C. L. Aleman, R. Mas, et al. A 6-month study on the toxicity of high doses of Policosanol orally administered to Sprague-Dawley rats. J Med Food 2001; 4(2): 57–65.

    Article  PubMed  CAS  Google Scholar 

  36. El-Abasy, M., M. Motobu, T. Sameshima, K. Koge, T. Onodera, and Y. Hirota. Adjuvant effects of sugar cane extracts (SCE) in chickens. J Vet Med Sci 2003; 65(1): 117–119.

    Article  PubMed  Google Scholar 

  37. Castano, G., R. Mas, L. Fernandez, et al. Comparison of the efficacy and tolerability of policosanol with atorvastatin in elderly patients with type II hypercholesterolaemia. Drugs Aging 2003; 20(2): 153–163.

    Article  PubMed  CAS  Google Scholar 

  38. El-Abasy, M., M. Motobu, K. Shimura, et al. Immunostimulating and growth-promoting effects of sugar cane extract (SCE) in chickens. J Vet Med Sci 2002; 64(11): 1061–1063.

    Article  PubMed  Google Scholar 

  39. Rodriguez, M. D., R. Gamez, J. E. Gonzalez, H. Garcia, C. P. Acosta, and E. Goicochea. Lack of developmental toxicity of D-003: a mixture of long-chain fatty acids in rats. Food Chem Toxicol 2003; 41(1): 89–93.

    Article  PubMed  CAS  Google Scholar 

  40. Molina, V., M. L. Arruzazabala M. L, D. Carbajal, and R. Mas. D-003, a potential antithrombotic compound isolated from sugar cane wax with effects on arachidonic acid metabolites. Prostaglandins Leuko Essent Fatty Acids 2002; 67(1): 19–24.

    Article  CAS  Google Scholar 

  41. McCarty, M.F. Policosanol safely down-regulates HMG-CoA reductase-potential as a component of the Esselstyn regimen. Med Hypotheses 2002; 59(3): 268–279.

    Article  PubMed  CAS  Google Scholar 

  42. Gamez, R., I. Rodeiro, I. Fernandez, and P.C. Acosta. Preliminary evaluation of the cytotoxic and genotoxic potential of D-003: mixture of very long chain fatty acids. Teratog Carcinog Mutagen 2002; 22(3): 175–181.

    Article  PubMed  CAS  Google Scholar 

  43. Menendez, R., R. Mas, A. M. Amor, et al. Inhibition of rat lipoprotein lipid peroxidation by the oral administration of D-003, a mixture of very long-chain saturated fatty acids. Can J Physiol Pharmacol 2002; 80(1): 13–21.

    Article  PubMed  CAS  Google Scholar 

  44. Takara, K., D. Matsui, K. Wada, T. Ichiba, and Y. Nakasone. New antioxidative phenolic glycosides isolated from Kokuto non-centrifuged cane sugar. Biosci Biotechnol Biochem 2002; 66(1): 29–35.

    Article  PubMed  CAS  Google Scholar 

  45. Castano, G., R. Mas, L. Fernandez, J. Illnait, R. Gamez, and E. Alvarez. Effects of policosanol 20 versus 40 mg/ day in the treatment of patients with type II hypercholesterolemia: a 6-month double-blind study. Int J Clin Pharmacol Res 2001; 21(1): 43–57.

    PubMed  CAS  Google Scholar 

  46. Mirkin, A., R. Mas, M. Martinto, et al. Efficacy and tolerability of policosanol in hypercholesterolemic postmenopausal women. Int J Clin Pharmacol Res 2001; 21(1): 31–41.

    PubMed  CAS  Google Scholar 

  47. Menendez, R., R. Mas, A. M. Amor, I. Rodeiros, R. M. Gonzalez, and J. L. Alfonso. Inhibition of cholesterol biosynthesis in cultured fibroblasts by D-003, a mixture of very long chain saturated fatty acids. Pharmacol Res 2001; 44(4): 299–304.

    Article  PubMed  CAS  Google Scholar 

  48. Costa, M. J., L. H. Moraes, F. M. Bion, M. A. Rivera, L. S. Moura, and M. L. Conceicao. Efficacy evaluation of the molasses supplementation in normal and depleted rats diet. Arch Latinoam Nutr 2000; 50(4): 341–345.

    PubMed  CAS  Google Scholar 

  49. Noa, M., R. Mas, and R. Mesa. A comparative study of policosanol vs lovastatin on intimal thickening in rabbit cuffed carotid artery. Pharmacol Res 2001; 43(1): 31–37.

    Article  PubMed  CAS  Google Scholar 

  50. Molina, V., M. L. Arruzazabala, D. Carbajal, R. Mas, and S. Valdes. Antiplatelet and antithrombotic effect of D-003. Pharmacol Res 2000; 42(2): 137–143.

    Article  PubMed  CAS  Google Scholar 

  51. Arruzazabala, M. L., M. Noa, R. Menendez, R. Mas, D. Carbajal, S. Valdes, and V. Molina. Protective effect of policosanol on atherosclerotic lesions in rabbits with exogenous hypercholesterolemia. Braz J Med Biol Res 2000; 33(7): 835–840.

    Article  PubMed  CAS  Google Scholar 

  52. Molina, V., M. L. Arruzazabala, D. Carbajal, et al. Effect of policosanol on cerebral ischemia in Mongolian gerbils. Braz J Med Biol Res 1999; 32(10): 1269–1276.

    Article  PubMed  CAS  Google Scholar 

  53. Re, L., S. Barocci, C. Capitani, et al. Effects of some natural extracts on the acetylcholine release at the mouse neuromuscular junction. Pharmacol Res 1999; 39(3): 239–245.

    Article  PubMed  CAS  Google Scholar 

  54. Noa, M., R. Mas, and R. Mesa. Effect of policosanol on intimal thickening in rabbit cuffed carotid artery. Int J Car-diol 1998; 67(2): 125–132.

    Article  CAS  Google Scholar 

  55. Ferriolli, E., R. O. Dantas, R. B. Oliveira, and F. J. Braga. The influence of ageing on oesophageal motility after ingestion of liquids with different viscosities. Eur J Gastroenterol Hepatol 1996; 8(8): 793–798.

    PubMed  CAS  Google Scholar 

  56. Noa, M., M. C. de la Rosa, and R. Mas. Effect of policosanol on foam-cell formation in carrageenan-induced granulomas in rats. J Pharm Pharmacol 1996; 48(3): 306–309.

    PubMed  CAS  Google Scholar 

  57. Aleman, C. L., M. N. Puig, E. C. Elias, et al. Carcinogenicity of policosanol in mice: an 18-month study. Food Chem Toxicol 1995; 33(7): 573–578.

    Article  PubMed  CAS  Google Scholar 

  58. Noa, M., R. Mas, M. C. de la Rosa, and J. Magraner. Effect of policosanol on lipofundin-induced atherosclerotic lesions in rats. J Pharm Pharmacol 1995; 47(4): 289–291.

    PubMed  CAS  Google Scholar 

  59. Agata, H., N. Kondo, A. Yomo, et al. Sensitization to sugar cane pollen in Okinawan allergic children. Asian Pacific J Allergy Immunol 1994; 12(2): 151–154.

    CAS  Google Scholar 

  60. Menendez, R., S. I. Fernandez, A. Del Rio, et al. Policosanol inhibits cholesterol biosynthesis and enhances low density lipoprotein processing in cultured human fibroblasts. Biol Res 1994; 27(3–4): 199–203.

    PubMed  CAS  Google Scholar 

  61. Arruzazabala, M. L., V. Molina, D. Carbajal, S. Valdes, and R. Mas. Effect of policosanol on cerebral ischemia in Mongolian gerbils: role of prostacyclin and thromboxane A2. Prostaglandins Leuko Essent Fatty Acids 1993; 49(3): 695–697.

    Article  CAS  Google Scholar 

  62. Arruzazabala, M. L., D. Carbajal, R. Mas, M. Garcia, and V. Fraga. Effects of Policosanol on platelet aggregation in rats. Thromb Res 1993; 69(3): 321–327.

    Article  PubMed  CAS  Google Scholar 

  63. Frencken, J. E., P. Rugarabamu, and J. Mulder. The effect of sugar cane chewing on the development of dental caries. J Dent Res 1989; 68(6): 1102–1104.

    PubMed  CAS  Google Scholar 

  64. Oji, E. O. Locally available plant materials for use as ophthalmic surgical swabs. Ann R Coll Surg Engl 1986; 68(6): 307–309.

    PubMed  CAS  Google Scholar 

  65. Shanmugasundaram, E. R., and K. R. Shanmugasundaram. An Indian herbal formula (SKV) for controlling voluntary ethanol intake in rats with chronic alcoholism. J Ethnopharmacol 1986; 17(2): 171–182.

    Article  PubMed  CAS  Google Scholar 

  66. Sho, H., I. Chinen, and N. Fukuda. Effects of Okinawan sugar cane wax and fatty alcohol on serum and liver lipids in the rat. J Nutr Sci Vitaminol (Tokyo) 1984; 30(6): 553–559.

    CAS  Google Scholar 

  67. Li, X. Y., R. Nolte, and W. Vogt. Natural antibodies against a polysaccharide (Bo) from sugar cane mediate its complement-activating effect. Immunobiology 1983; 164(2): 110–117.

    PubMed  CAS  Google Scholar 

  68. Li, X., and W. Vogt. Activation of the classical complement pathway by a polysaccharide from sugar cane. Immunopharmacology 1982; 5(1): 31–38.

    Article  PubMed  CAS  Google Scholar 

  69. Sho, H., I. Chinen, K. Uchihara, and N. Fukuda. Effects of Okinawan sugar cane rind on serum and liver cholesterol and triglyceride levels in the rat. J Nutr Sci Vitaminol (Tokyo) 1981; 27(5): 463–470.

    CAS  Google Scholar 

  70. Grant, E.C. Food allergies and migraine. Lancet 1979; 1(8123): 966–969.

    Article  PubMed  CAS  Google Scholar 

  71. Varavithya, W., P. Posayanond, K. Tontisirin, L. Chernjitra, and C. Kashemsant. Oral hydration in infantile diarrhoea. Southeast Asian J Trop Med Public Health 1978; 9(3): 414–419.

    PubMed  CAS  Google Scholar 

  72. West, G. B. Glucans and dextrans in rats and man. Int Arch Allergy Appl Immunol 1978; 56(4): 380–382.

    PubMed  CAS  Google Scholar 

  73. Baird, I. M., R. L. Walters, P. S. Davies, M. J. Hill, B. S. Drasar, and D. A. Southgate. The effects of two dietary fiber supplements on gastrointestinal transit, stool weight and frequency, and bacterial flora, and fecal bile acids in normal subjects. Metabolism 1977; 26(2): 117–128.

    Article  PubMed  CAS  Google Scholar 

  74. Fahey, G. C., J. E. Williams, and G.A. McLaren. Influence of molasses lignin-hemicellulose fractions in rat nutrition. J Nutr 1976; 106(10): 1447–1451.

    PubMed  CAS  Google Scholar 

  75. Dumaswala, U. J., R. U. Dumaswala, and A. Venkataraman. The relative effect of dietary fats and carbohydrates on lipid metabolism in the albino rat. 1: Ital J Biochem 1976; 25(4): 289–303.

    PubMed  CAS  Google Scholar 

  76. Walters, R. L., I. M. Baird, P. S. Davies, et al. Effects of two types of dietary fibre on faecal steroid and lipid excretion. Br Med J 1975; 2(5970): 536–538.

    PubMed  CAS  Google Scholar 

  77. Suwal, P. N. Medicinal plants of Nepal. Ministry of Forests, Department of Medicinal Plants, Thapathali, Kathmandu, Nepal 1970.

    Google Scholar 

  78. Couvee. Compilation of herbs, plants, crops supposed to be effective in various complaints and illness. J Sci Res 1952; 1S: 1.

    Google Scholar 

  79. Ahmad, Y.S. A note on the plants of medicinal value found in Pakistan. Government of Pakistan Press, Karachi, 1957.

    Google Scholar 

  80. Lin, Y. C., J. T. Huang and H. C. Hsiu. Studies on the hypoglycemic activity of the medicinal herbs. Formosan Med Assoc 1964; 63(8): 400–404.

    CAS  Google Scholar 

  81. Pongpan, A., W. Avirutnant, and P. Chumsri. Some Thai plants as substrates for microbial protein production. Mahidol Univ J Pharm Sci 1983; 10(1): 15–18.

    Google Scholar 

  82. Kimura, Y., H. Okua, N. Shoji, T. Taemto, and S. Arichi. Effects of non-sugar fraction in black sugar on lipid and carbohydrate metabolism. Part II. New compounds inhibiting elevation of plasma insulin. Planta Med 1984; 1984(5): 469–473.

    Article  Google Scholar 

  83. Yadava, V. S., and K. Misra. Vanilloyl-1-O-beta-D-glucoside acetate from the roots of Saccharum officinarum. Indian J Chem Ser B 1989; 28(1): 875–877.

    Google Scholar 

  84. Morita, I., S. Morishita, T. Tatsumi, and S. Kako. Invert sugar having high inversion. Patent-Japan Kokai-74 134,852 1974.

    Google Scholar 

  85. Doepke, W., and U. Hess. Obtaining phytosterol mixtures from oil fraction sof sugar cane waxes. Patent-Ger (East) 1974; 104,513.

    Google Scholar 

  86. Ferber, L., and F. G. Carpenter. Plant pigments as colorants in cane sugar. US Agr Res Serv South Reg ARS 1975; 51: 23.

    Google Scholar 

  87. Da Gloria, N. A., and A. A. Rodella. Inorganic quantitative analysis of sugar cane juice, vinasse, and molasses. I. Calcium, magnesium, potassium, sulfur and phosphorus determination in single extract. An Esc Super Agr Luiz Dr Queiroz Univ Sao Paulo 1972; 29: 5.

    Google Scholar 

  88. Dubey, R. C., and K. Misra. Flavonoids of sugar cane. J Indian Chem Soc 1974; 51: 653.

    CAS  Google Scholar 

  89. Misra, K. and R. C. Dubey. Anthocyanin of sugarcane. Curr Sci 1974; 43: 544A.

    Google Scholar 

  90. Kapadia, G. J., E. B. Chung, B. Ghosh, et al. Carcinogenicity of some folk medicinal herbs in rats. J Nat Cancer Inst 1978; 60: 683–686.

    PubMed  CAS  Google Scholar 

  91. Kuhnie, J. A., P. H. Moore, W. F. Haddon, and M. M. Fitch. Identification of gibberellins from sugar cane plants. J Plant Growth Regul 1983; 2(1): 59–71.

    Article  Google Scholar 

  92. Patron, N. H., P. Smith, and T. J. Mabry. Identification of flavonoid compounds in HPLC separation of sugar cane colorants. Int Sugar J 1985; 87(1043): 213–215.

    CAS  Google Scholar 

  93. Goswami, P. C., H. D. Singh, and J. N. Baruah. Isolation of phytosterols from sugarcane press mud and microbial conversion of the phytosterols to 17-ketosteroids. Curr Sci 1984; 53917): 917–919.

    CAS  Google Scholar 

  94. Taahashi, M., C. Konno, and H. Hikino. Isolation and hypoglycemic activity of saccharin A, B, C, D, E, and F, glycans of Saccharum officinarum stalks. Planta Med 1985; 1985(3): 258–260.

    Article  Google Scholar 

  95. Kato, A., J. I. Azuma, and T. Koshijima. Isolation and identification of a new feruloylated tetrasaccharide from bagasse lignin-carbohydrate complex containing phenolic acid. Agr Biol Chem 1987; 51(6): 1691–1693.

    CAS  Google Scholar 

  96. Smith, R. M., and M. Martin-Smith. Triterpen methyl ethers in leaf waxes of Saccharum and related genera. Phytochemistry 1978; 17(8): 1307–1312.

    Article  CAS  Google Scholar 

  97. Seetharam, K. A., and J.S. Pasricha. Condiments and contact dermatitis of the finger-tips. Indian J Dermatol Venerol Leprol 1987; 53(6): 325–328.

    Google Scholar 

  98. De A Ribeiro, R., F. Barros, M. Margarida, et al. Acute diuretic effects in conscious rats produced by some medicinal plants used in the state of Sao Paulo, Brasil. J Ethnopharmacol 1988; 24(1): 19–29.

    Article  Google Scholar 

  99. Takagi, S. Isolation of polysaccharides as pharmaceuticals from sugarcane and its molasses. Patent-Japan Kokai Tokkyo Koho-61 83,130 1986; 13 pp.

    Google Scholar 

  100. Holdsworth, D., and T. Rali. A survey of medicinal plants of the southern Highlands, Papua New Guinea. Int J Crude Drug Res 1989; 27(1): 1–8.

    Google Scholar 

  101. Vicente, C., J. L. Mateos, M. M. Pedrosa, and M.E. Legaz. High-performance liquid chromatographic determination of sugars and polyols in extracts of lichens and sugarcane juice. J Chromatogr 1991; 553(1/2): 271–283.

    Article  CAS  Google Scholar 

  102. Misra, C. S., and K. Misra. Dimethyl apigenin 4′-O-beta-D-glucopyranoside from Saccharum officinarum leaves. Curr Sci 1978; 47: 152.

    CAS  Google Scholar 

  103. Irvine, J. E. Variation of non-sucrose solids in sugarcane. I. Potassium. Sugar J 1978; 41(5): 28–30.

    CAS  Google Scholar 

  104. Misra, K., and C. S. Misra. Flavonoids of Saccharum officinarum flowers. Indian J Chem Ser B 1979; 18: 88.

    Google Scholar 

  105. Jin, Y. N., H. Z. Liang, C. Y. Cao, Z. W. Wang, R. S. Shu, and X. Y. Li. Immunological activity of bagasse polysaccharides. Chung-Kuo Yao Li Hsueh Pao 1981; 2: 269–275.

    PubMed  CAS  Google Scholar 

  106. Bhattacharjee, J. W., R. P. Saxena, and S.H. Zaidi. Experimental studies on the toxicity of bagasse. Environ Res 1980; 23: 68–76.

    Article  PubMed  CAS  Google Scholar 

  107. Kato, A., J. Azuma, and T. Koshijima. A new feruloylated trisaccharide from bagasse. Chem Lett 1983; 1983(1): 137–140.

    Article  Google Scholar 

  108. Mabry, T. J., Y. L. Liu, J. Pearce, et al. New flavonoids from sugarcane (Saccharum). J Nat Prod 1984; 47(1): 127–130.

    Article  CAS  Google Scholar 

  109. Achamaas, G., and R. Thawornset. Phytochemical and anticancer screening of Schefflera leucantha and Saccharum officinarum. Undergraduate Special Project Report 1980; 69 pp.

    Google Scholar 

  110. Hirschhorn, H. H. Botanical remedies of the former Dutch East Indies (Indonesia). I. Eumycetes, Pteridpohyta, Gymnospermae, Angiospermae (Monocotyledons only). J Ethnopharmacol 1983; 7(2): 123–156.

    Article  PubMed  CAS  Google Scholar 

  111. Martinez, M. A. Medicinal plants used in a Totonac community of the Sierra Norte del Puebla: Tuzamapan de Galeana, Puebla, Mexico. J Ethnopharmacol 1984; 11(2): 203–221.

    Article  Google Scholar 

  112. Aswal, B. S., D. S. Bahakuni, A. K. Goel, K. Kar, B. N. Mehrotra, and K.C. Mukherjee. Screening of Indian plants for biological activity: part X. Indian J Exp Biol 1984; 22(6): 312–332.

    PubMed  CAS  Google Scholar 

  113. De A Ribeiro, R., M. M. R. Fiuza de Melo, F. de Baroz, C. Gomes, and G. Troln. Acute antihypertensive effect in conscious rats produced by some medicinal plants used in the state of Sao Paulo. J Ethnopharmacol 1986; 15(3): 261–269.

    Article  Google Scholar 

  114. Hedberg, I., O. Hedberg, P. J. Madati, K. E. Mshigeni, E. N. Mshiu, and G. Samuelsson. Inventory of plants used in traditional medicine in Tanzania. Part III. Plants of the families Papillion-aceae-Vitaceae. J Ethnopharmacol 1983; 9(2/3): 237–260.

    Article  PubMed  CAS  Google Scholar 

  115. Li, X., B. Damerau, and W. Vogt. Influence of a bagasse glucan (B-O) on leukocyte aggregation and accumulation. Chung-Kuo Yao Li Hsueh Pao 1985; 6(2): 137–140.

    PubMed  CAS  Google Scholar 

  116. Hikino, H., M. Takahashi, C. Konno, A. Ishimori, T. Kawamura, and T. Namiki. Effect of glycans of Saccharum officinarum on carbohydrate and lipid metabolism of rats. J Ethnopharmacol 1985; 14(2/3): 261–268.

    Article  PubMed  CAS  Google Scholar 

  117. Anis, M., and M. Iqbal. Antipyretic utility of some Indian plants in traditional medicine. Fitoterapia 1986; 57(1): 52–55.

    Google Scholar 

  118. Caceres, A., L. M. Giron, and A. M. Martinez. Diuretic activity of plants used for the treatment of urinary ailments in Guatemala. J Ethnopharmacol 1987; 19(3): 233–245.

    Article  PubMed  CAS  Google Scholar 

  119. Caceres, A., L. M. Giron, S. R. Alvarado, and M.F. Torres. Screening of antimicrobial activity of plants popularly used in Guatemala for the treatment of dermatomucosal diseases. J Ethnopharmacol 1987; 20(3): 223–237.

    Article  PubMed  CAS  Google Scholar 

  120. Costa, M., L. C. di Stasi, M. Kirizawa, S. L. J. Mendacolli, C. Gomez, and G. Trolin. Screening in mice of some medicinal plants used for analgesic purposes in the state of Sao Paulo. J Ethnopharmacol 1989; 27(1/2): 25–33.

    Article  PubMed  CAS  Google Scholar 

  121. Darias, V., L. Bravo, R. Rabanal, C. Sanchez Mateo, R. M. Gonzalez Luis, and A. M. Hernandez Perez. New contribution to the ethnopharmacological study of the Canary Islands. J Ethnopharmacol 1989; 25(1): 77–92.

    Article  PubMed  CAS  Google Scholar 

  122. Vedavathy, S., K. N. Rao, M. Rajaiah, and N. Nagaraju. Folklore information from Ryalaseema region, Andhra Pradesh for family planning and birth control. Int J Pharmacog 1991; 29(2): 113–116.

    Google Scholar 

  123. Aleman, C. L., R. Mas, C. Hernandez, I. Rodeiro, E. Cerejido, M. Noa, A. Capote, R. Menedez, A. Amor, V. Fraga, V. Sotolongo, and S. Jimenez. A 12-month study of policosanol oral toxicity in Sprague Dawley rats. Toxicol Lett 1994; 70(1): 77–87.

    Article  PubMed  CAS  Google Scholar 

  124. Seabrook, W. B. adventures in Arabia among the Bedouins, Druses, Whirling Dervishes & Yezidee devil worshipers. Blue Ribbon Book, New York 1927; 99–105

    Google Scholar 

  125. Holdsworth, D. K. Traditional medicinal plants of Rarotonga, Cook Islands. Part II. Int J Pharmacog 1991; 29(1): 71–79.

    Article  Google Scholar 

  126. Lin, C. C. Crude drugs used for the treatment of diabetes mellitus in Taiwan. Amer J Chin Med 1992; 20(3/4): 269–279.

    Article  CAS  Google Scholar 

  127. Kimura, Y., H. Okuda, and S. Arichi. Effects of non-sugar fraction in black sugar on lipid and carbohydrate metabolism: part I. Planta Med 1984; 1984(4): 465–468

    Article  Google Scholar 

  128. McGhie, T. Analysis of sugarcane flavonoids by capillary zone electrophoresis. J Chromatogr 1993; 534(1): 107–112.

    Article  Google Scholar 

  129. Hope, B. E., D. G. Massey, and G. Massey-Fournier. Hawaiian Materia Medica for asthma. Hawaiian Med J 1993; 52(6): 160–166.

    CAS  Google Scholar 

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(2005). Saccharum officinarum. In: Medicinal Plants of the World, Volume 3. Humana Press. https://doi.org/10.1007/978-1-59259-887-8_13

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