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dc.contributor.authorIsnaeni, Farida Nur
dc.contributor.authorArsanti, Lily
dc.contributor.authorPratiwi, Woro Rukmi
dc.date.accessioned2013-04-30T04:51:21Z
dc.date.available2013-04-30T04:51:21Z
dc.date.issued2011-06
dc.identifier.citationAdam, J.M.F., 2000. Klasifikasi dan Kriteria Diagnosis Diabetes Melitus yang Baru. Cermin Dunia Kedokteran (127) : 37-40 Alvarez, J.F., Barbera, A., Nadal, B., Barcelo-Batllori, S., Piquer, S., Claret, M., Guinovart, J.J., and Gomis, R., 2004. Stable and Functional regeneration of pancreatic Beta-Cell Population in nSTZ-rats treated with Tungstate. Diabetologia 47 : 470-477 Anonim. Asuhan Keperawatan Diabetes Mellitus, http://www.rusari.com. Diakses tanggal 3 Juli 2008. Anonim. Chitase Specificity, http://www.sigmaaldrich.com. Diakses : tanggal 3 Juli 2008. Anonim, Chitosanase Specificity, http://www.sigmaaldrich.com. Diakses : tanggal 3 Juli 2008. Anonim. Islets of Langerhans. http://www.histol.chuvashia.com/atlas-en/digestive03en.htm. Diakses: tanggal 3 Juli 2008. Anonim, Qingdao Reach International Inc. http://www.tradekey.com. Diakses : tanggal 19 Juli 2008. Baynes, J.W. and Thorpe, S.R., 1999. Role of oxidative Stress in Diabetic Complication. Diabetes 48 Departemen Kesehatan RI, 2005. Pharmaceutical Care untuk Penyakit Diabetes Mellitus, Jakarta, Bina Kefarmasian dan Alat Kesehatan Departemen Kesehatan RI Hayashi, K. and Ito, M., 2002. Antidiabetic Action of Low Molecular Weight Chitosan in Genetically Obese Diabetic KK-A Mice. Biol. Pharm, Bull, 25(2) : 188— 192 y Hendromartono, 2009. Current Update in the Management of Type 2 Diabetes, Surabaya. Divisi Endokrinologi dan Metabolisme RS Dr. Soetomo Hennen, W.J., 1996. Chitosan, Woodland Publishing Inc. Johansen, J.S., Harris, A.K., Rychly, D.J., and Ergul, A., 2005. Oxidative Stress and The Use of Antioxidant in Diabetes , Lingking Basic Science to Clinical practice. Biomed Central Junqueira, L.C., Carneiro, J., and Kelley, R.O., 1995. Histologi Dasar Edisi 8. Jakarta , Penerbit Buku Kedokteran EGC. Lee, H.W., Park, Y.S., Choi, J.W., Yi, S.Y., and Shin, W.S., 2003. Antidiabetic Effects of Chitosan Oligosaccharides in Neonatal Streptozotocin-Induced Noninsulin-Dependent Diabetes Mellitus in Rats. Biol. Pharm. Bull. 26(8) 1100—1103 Li, Q., Dunn, E.T., Grandmaison, E.W., and Goosen, M.F.A., 1992. Application and Properties of Chitosan dalam , Application of Chitin and Chitosan, Pennsylvania. Technomic Publishing Compani Inc. Li Xue, W., She Li, X., Zhang., Hui Liu, Y., Lun Wang, Z., and Juan Zhang, R., 2007. Effect of Trigonella Foenum-Graecum (Fenugreek) Extract on Blood Glucose, Blood Lipid and Hemorheological Properties in Streptozotocin-Induced Diabetic Rats. Asia pac J Clin Nutr 16 : 422-426 Liu, B., Liu, W.S., Han, B.Q., and Sun, Y.Y., 2007. Antidiabetic Effects of Chitooligosaccharides on Pancreatic Islet Cells in Streptozotocin-Induced Diabetic Rats. World Journal of Gastroenterology 13(5): 725-731 Utami, P., 2004, Terapi Jus untuk Diabetes Mellitu. Jakarta , Agro Media Pustaka Vincent, A.M., Russell, J.W., Low, P., and Feldman, E.L., 2004. Oxidative Stress in the Pathogenesis of Diabetic Neuropathy. Endocrine Review 25(4): 612-628 Walujani, A., 2003. Mengawasi Suplemen Melindungi Konsumen. http://kompas- cetak.com. Diakses : tanggal 3 Juli 2008. WHO, 1999. Definition, Diagnosis and Classification of Diabetes Mellitus and its Complications. Departement of Noncommunicable Disease Surveillance Geneva Yao, H.T., Huang, S.Y., and Chiang, M.T., 2008. A Comparative Study on Hypoglycemic and Hypocholesterolemic Effects of High and Low molecular Weight Chitosan in Streptozotocin-Induced Diabetic Rats. Food and Chemical Toxicology 46 , 1525–1534 Yassin, M.M. and Mwafy, S.N., 2007. Protective Potential of Glimepiride and Nerium oleander Extract on Lipid Profile, Body Growth Rate, and Renal Function in Streptozotocin-Induced Diabetic Rats. Turk J Biol 31 : 95-102 Yuan, W.P., Liu, B., liu, C.H., Wang, X.J., Zhang, M.S., and Meng, X.M., Xia, X.K., 2009. Antioxidant Activity of Chito-Oligosaccharides on Pancreatic Islet Cells in Streptozotocin-Induced Diabetes in Rats. World J Gastroenteral, 15(11) : 1339-1345en_US
dc.identifier.issn1979-7621
dc.identifier.urihttp://hdl.handle.net/11617/2942
dc.description.abstractDiabetes Mellitus (DM) is a disease that will increase in the future, and most of them occur in developing countries. In addition, DM also causes many complications. Therefore, the alternative medication is needed to help treatment. One of the substances suspected having hypoglycemic effects is chitosan. Researcher find that chitosan oligosaccarides (hydrolysis of chitosan) have a dietary fiber and hypoglycemic effect on the Wistar rat. However, the hypoglycemic effect of chitosan itself is not yet known. This research was conducted to determine the hypoglycemic effect of chitosan. The aim of this research was to explore the effect of chitosan on blood glucose level and histology of pancreas in diabetic Sprague dawley rat induced by alloxan. Fourteen Sprague dawley male rats, aging 2 months, weighing 141-201 grams were divided randomly into 2 treatment groups. Group I (P1) were given alloxan 80 mg / kg BW i.v until diabetic and then chitosan 500mg/kg BW; group II (P2) were given alloxan and then metformin 9mg/dose. Both groups were provided with standard diet and drinking water ad libitum. In day 0, 7, 14, 21, and 28 blood glucose level was measured. The rats were sacrified after 28 days treatment then the pancreatic organ taken for the histologic examination. The slide had been made using paraffin method and smeared by Kromium Hematoxilin Floxin. Slides were analyzed by measuring the islet’s diameter and the number of pancreatic â cell. Result of this research showed that chitosan decreased blood glucose level every week in DM rats (p <0.05). There was not any significant difference of blood glucose level between the two groups on the measurement on day 0 and 7 (p> 0.05) and there was significant differences of blood glucose level between the two groups on the measurement on day 14, 21, and 28 (p<0,05). Diameter size and the number of â cells in both groups did not have significant differences (p> 0.05). This research conclude that oral administration of chitosan 500mg/kg BW had similar hypoglycemic effect, even better compared with the metformin 9mg/dose.en_US
dc.publisherlppmumsen_US
dc.subjectChitosanen_US
dc.subjectMetforminen_US
dc.subjectAlloxanen_US
dc.subjectDiabetes Mellitusen_US
dc.subjectSprague Dawleyen_US
dc.titlePENGARUH PEMBERIAN CHITOSAN TERHADAP KADAR GLUKOSA DARAH DAN HISTOLOGI PANKREAS TIKUS Sprague dawley YANG DIINDUKSI ALOKSANen_US
dc.typeArticleen_US


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