Diabetes mellitus is a chronic metabolic disease which is a serious global problem. Many antidiabetic therapies focus on improving insulin sensitivity, increasing insulin production, and/or decreasing the level of blood glucose. Hesperetin is a flavanoid commonly found in many herbal medicines and food. Hesperetin seem to demonstrate adequate properties. Animal studies were carried out for 45days and at the end of 45th day blood samples were collected and various biochemical parameters were measured using autoanalyser. They can inhibit enzymes involved in glucose metabolism, prevent the development of insulin resistance and normalize plasma glucose and insulin levels. This synthetic drug apart from producing a hypoglycemic effect has also been found to manifest hypolipidemic and anti-obesity activity. Hesperetin is also promising agents in the prevention of diabetic complications. They have strong antioxidant activity and inhibit the formation of advanced glycation end products, implicated in the pathogenesis of diabetic nephropathy, embryopathy, and neuropathy or impaired wound healing. Until now very few clinical studies have been concerned with the application of Hesperetin in treating diabetes. Our experimental findings with respect to the mechanism of action of synthetic compound in Streptozotocin induced diabetic rats suggest that it enhances insulin secretion by the islets of langerhans and enhances glucose utilization. However, due to their great therapeutic potential, these compounds deserve special attention.
Published in | Journal of Cancer Treatment and Research (Volume 5, Issue 1) |
DOI | 10.11648/j.jctr.20170501.11 |
Page(s) | 1-6 |
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Copyright © The Author(s), 2017. Published by Science Publishing Group |
Hesperetin, Insulin, Hypoglycemic Effect, Hypolipidemic Activity
[1] | American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes care. 2011; 34 (1) 62-68. |
[2] | Kim JJ, Ramesh T, Kim JS. Protective effects of chrysanthemum Flower extract against streptozotocin-induced oxidative damage in diabetes mice. Journal of medicinal plant research. 2012; 6 (4): 22-630. |
[3] | Huizinga MM, Rothman RL. Addressing diabetes pandemic. A comprehensive approach Indian J. Med. Res. 2006; 124: 481-484. |
[4] | Eze ED, Mohammed A, Musa KY, Tanko Y, Isa AS. Effect of ethanolic leaf extract of mucunapruriens (fabaceae) on lipid profile in alloxan-induced diabetes wister rats. British J pharm Toxicol. 2012; 3 (3): 102-109. |
[5] | WHO use of glycated Haemoglobin (HbAlc) in the diagnosis of diabetes mellitus. Abbreviated report of a WHO consultation. 2011; 1-25. |
[6] | Ahmed MF. Kazim SM, Ghori SS, Mehjabeen SS, Ahmed SE, Ali SM. Ibrahim M. Antidiabetes activity of vincabosea extracts in alloxan- induced diabetes rats. International journal of endocrinology. Article ID 841090, 2010: 1-6. |
[7] | Laakso M. Heart in diabetes: A microvascular disease Diabetes care. 2011; 34 (2): 145-149. |
[8] | Cao H, Hininger-Favier I, Kelly M. A, Benaraba R, Dawson H. D, Coves S, Roussel A. M, and Anderson R. A, J. Agric. Food C., 55, 6372-6378 (2007). |
[9] | Horcajada, M. N., Habauzit, V., Trzeciakiewicz, A., Morand, C., Gil-Izquierdo, A., Mardon, J., Lebecque, P., Davicco, M. J., Chee, W. S. S., Coxam, V., Offord, E., J. Appl. Physiol. 2008, 104, 648. |
[10] | Szkudelski. The Mechanism of Alloxan and Streptozotocin Action in B Cells of the Rat Pancreas. Physiol. Res. 2001; 50: 536-546. |
[11] | Ramachandran V, Saravanan R. Efficacy of asiatic acid, a pentacyclic triterpene on attenuating the key enzymes activities of carbohydrate metabolism in streptozotocin-induced diabetic rats. Phytomedicine 2013; 20: 230-236. |
[12] | Rajamani U, Joseph D, Roux S, Essop MF. The hexosamine biosynthetic pathway can mediate myocardial apoptosis in a rat model of diet-induced insulin resistance. Acta Physiol 2011; 202: 151-157. |
[13] | Gomathi D, Ravikumar G, Kalaiselvi M, Devaki K, Uma C, Protective effect of the whole plant extract of Evolvulus alsinoides on glycoprotein alterations in streptozotocin induced diabetic rats. J Acu Dis 2013; 2: 148-150. |
[14] | Pari L, Rajeswari N. Protective role of coumarin on plasma and tissue glycoprotein components in streptozotocin-nicotinamide induced hyperglycemic rats. Int J Biol Med Res 2010; 1: 61-65. |
[15] | Ciftci G, Cenesiz S, Yarim GF, Nisbet O, Nisbet C, Cenesiz M, Guvene D. Effect of fluoride exposure on serum glycoprotein pattern and sialic acid level in rabbits. Biol Trace Elem Res 2010; 133: 51-59. |
[16] | Romero AC, Ibuki FK, Nogueira FN. Sialic acid reduction in the saliva of streptozotocin induced diabetic rats. Arch Oral Biol 2012; 57: 1189-1193. |
[17] | Pari L, Srinivasan S. Preventive effect of diosmin, a bioflavonoid, on glycoprotein changes in streptozotocin-nicotinamide-induced type 2 diabetic rats. In J Pharm Sci Res 2010; 10: 89-95. |
[18] | Coppack, S. W., Jenson, M. D., Miles, J. M. 1994. Invivo regulation of lipolysis in human. J. Lipid Res., 35: 177-193. |
[19] | Ohno, T., Horio, F., Tanaka, S., Terada, M., Namikawa, T. and Kitoh, J. 2000. Fatty liver and hyperlipidemia in IDDM of streptozotocin treated shrews. Life Sci., 66: 125-131. |
APA Style
J. Revathy, S. Sheik Abdullah. (2017). The Role of Hesperetin in the Management of Diabetes Mellitus and Its Complications. Journal of Cancer Treatment and Research, 5(1), 1-6. https://doi.org/10.11648/j.jctr.20170501.11
ACS Style
J. Revathy; S. Sheik Abdullah. The Role of Hesperetin in the Management of Diabetes Mellitus and Its Complications. J. Cancer Treat. Res. 2017, 5(1), 1-6. doi: 10.11648/j.jctr.20170501.11
AMA Style
J. Revathy, S. Sheik Abdullah. The Role of Hesperetin in the Management of Diabetes Mellitus and Its Complications. J Cancer Treat Res. 2017;5(1):1-6. doi: 10.11648/j.jctr.20170501.11
@article{10.11648/j.jctr.20170501.11, author = {J. Revathy and S. Sheik Abdullah}, title = {The Role of Hesperetin in the Management of Diabetes Mellitus and Its Complications}, journal = {Journal of Cancer Treatment and Research}, volume = {5}, number = {1}, pages = {1-6}, doi = {10.11648/j.jctr.20170501.11}, url = {https://doi.org/10.11648/j.jctr.20170501.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jctr.20170501.11}, abstract = {Diabetes mellitus is a chronic metabolic disease which is a serious global problem. Many antidiabetic therapies focus on improving insulin sensitivity, increasing insulin production, and/or decreasing the level of blood glucose. Hesperetin is a flavanoid commonly found in many herbal medicines and food. Hesperetin seem to demonstrate adequate properties. Animal studies were carried out for 45days and at the end of 45th day blood samples were collected and various biochemical parameters were measured using autoanalyser. They can inhibit enzymes involved in glucose metabolism, prevent the development of insulin resistance and normalize plasma glucose and insulin levels. This synthetic drug apart from producing a hypoglycemic effect has also been found to manifest hypolipidemic and anti-obesity activity. Hesperetin is also promising agents in the prevention of diabetic complications. They have strong antioxidant activity and inhibit the formation of advanced glycation end products, implicated in the pathogenesis of diabetic nephropathy, embryopathy, and neuropathy or impaired wound healing. Until now very few clinical studies have been concerned with the application of Hesperetin in treating diabetes. Our experimental findings with respect to the mechanism of action of synthetic compound in Streptozotocin induced diabetic rats suggest that it enhances insulin secretion by the islets of langerhans and enhances glucose utilization. However, due to their great therapeutic potential, these compounds deserve special attention.}, year = {2017} }
TY - JOUR T1 - The Role of Hesperetin in the Management of Diabetes Mellitus and Its Complications AU - J. Revathy AU - S. Sheik Abdullah Y1 - 2017/03/17 PY - 2017 N1 - https://doi.org/10.11648/j.jctr.20170501.11 DO - 10.11648/j.jctr.20170501.11 T2 - Journal of Cancer Treatment and Research JF - Journal of Cancer Treatment and Research JO - Journal of Cancer Treatment and Research SP - 1 EP - 6 PB - Science Publishing Group SN - 2376-7790 UR - https://doi.org/10.11648/j.jctr.20170501.11 AB - Diabetes mellitus is a chronic metabolic disease which is a serious global problem. Many antidiabetic therapies focus on improving insulin sensitivity, increasing insulin production, and/or decreasing the level of blood glucose. Hesperetin is a flavanoid commonly found in many herbal medicines and food. Hesperetin seem to demonstrate adequate properties. Animal studies were carried out for 45days and at the end of 45th day blood samples were collected and various biochemical parameters were measured using autoanalyser. They can inhibit enzymes involved in glucose metabolism, prevent the development of insulin resistance and normalize plasma glucose and insulin levels. This synthetic drug apart from producing a hypoglycemic effect has also been found to manifest hypolipidemic and anti-obesity activity. Hesperetin is also promising agents in the prevention of diabetic complications. They have strong antioxidant activity and inhibit the formation of advanced glycation end products, implicated in the pathogenesis of diabetic nephropathy, embryopathy, and neuropathy or impaired wound healing. Until now very few clinical studies have been concerned with the application of Hesperetin in treating diabetes. Our experimental findings with respect to the mechanism of action of synthetic compound in Streptozotocin induced diabetic rats suggest that it enhances insulin secretion by the islets of langerhans and enhances glucose utilization. However, due to their great therapeutic potential, these compounds deserve special attention. VL - 5 IS - 1 ER -