Suweg Flour (Amorphophallus Campanulatus) Potential Reducing TNF-α Levels in Model Diabetic Rats

Ika Setyawati

Abstract


Diabetes mellitus (DM) is a chronic disease and it is called as a silent killer because this disease is unrecognized by the diabetics. However, when it is already known the complication is occurred. It is recognized by the increase of blood glucose level (hyperglycemia) as the main character of Diabetes Mellitus (DM). This condition causes the increase of the Reactive Oxygen Species (ROS) in a chronic condition.  Then, insulin resistance is caused by the oxidative stress in fat, muscle and liver tissue. Moreover, insulin resistance produces several oxidative stress mediators including  (TNF- α). This research aims to determine the effect of suweg flour (Amorphophallus campanulatus) on TNF-α level in rats diabetic model. The method used in the research was an experimental laboratory of pre-post control group test conducted in 28 days. The subjects of this research were 25 Rattus Novergicus wistar strains, (P1) positif control (P2), standart (P3) and two treatment groups (P4 and P5). The data were gained by measuring the level of TNF-α before and after receiving the suweg flour enzyme-linked immunosorbent assay (ELISA). The data were analyzed by paired sample t-test. This research showed a significant correlation between suweg flour and TNF-α levels (p = 0.000). A significant correlation was discovered in all treatment groups (P4 and P5). The results of this research can be concluded that the administration of suweg flour (Amorphophallus campanulatus) can decrease of TNF-α levels in rats diabetic model.


Keywords


Amorphophallus campanulatus; TNF-; Diabetes mellitus

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References


International Diabetes Federation. IDF Diabetes Atlas Eight Edition 2017, 8.

Saeedi, pouya, et al. 2019.Global and region diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9th edition. Belgium. Elsevier B.V.

Roglic, G., World Health Organization (Eds.), 2016.Global report on diabetes. World Health Organization, Geneva, Switzerland.

Papatheodorou, K., Papanas, N., Banach, M., Papazoglou, D., Edmonds, M., 2016. Complications of Diabetes 2016. J. Diabetes Res. 2016, 1–3. https://doi.org/10.1155/2016/6989453

Setiati, S., Alwi, I., W.Sudoyo, A., Simadibrata, M., Setyohadi, B., Syam, A.F., 2017. Ilmu Penyakit Dalam, VI. ed, 2. Interna Publishing, Jakarta.

Ingaramo PI, Ronco MT, Frances DE, Monti JA, Pisani GB, Ceballos MP, Galleano M, Carrillo MC, Carnovale CE. Tumor necrosis factor alpha pathways develops liver apoptosis in type 1 diabetes mellitus. Mol Immunol. 2011. 48:1397–1407.

Diaz-Flores M, Angeles-Mejia S, Baiza-Gutman LA, Medina-Navarro R, Hernandez-Saavedra D, Ortega-Camarillo C, Roman-Ramos R, Cruz M, Alarcon-Aguilar FJ. Effect of an aqueous extract of Cucurbita ficifolia Bouche on the glutathione redox cycle in mice with STZ-induced diabetes. J Ethnopharmacol. 2012.144:101–108.

Elmarakby AA, Sullivan JC. Relationship between oxidative stress and inflammatory cytokines in diabetic nephropathy. Cardiovasc Ther. 2012. 30:49–59.

Faria, A., Persaud, S.J., Cardiac oxidative stress in diabetes: Mechanisms and therapeutic potential. Pharmacol. Ther. 2017.172, 50–62. https://doi.org/10.1016/j.pharmthera. 2016.11.013

Tangvarasittichai, S., Oxidative stress, insulin resistance, dyslipidemia and type 2 diabetes mellitus. World J. Diabetes 2015.6, 456. https://doi.org/10.4239/wjd.v6.i3.456

Swaroop, J.J., rajarajeswari, D., and naidu, J.N. Association of TNF-α with Insulin Resistance in type 2 Diabetes Mellitus. Indian J Med Res. 2012. Jan; 135(1): 127-130. (Journal)

Moller DE. Potential role of TNF alpha in the pathogenesis of insulin resistance and type 2 diabetes. Ternd Endocrinol Metab. 2000;11:212-7. (Journal)

Aguirre V, Uchida T, Yenush L., Davis R, White MF. The c-Jun NH2-terminal kinase promotes insulin resistance during association with insulin receptor substrate-1 and phosphorylation of Ser (307) J Biol Chem. 2000;275:9047-54. (Journal)

Noctor, G., Lelarge-Trouverie, C., Mhamdi, A., The metabolomics of oxidative stress. Phytochemistry. 2015. 112, 33–53. https://doi.org/10.1016/j.phytochem.2014.09.002

Handayani, T., 2019. Analysis of Nutrient and Anti-Nutrient Compositions of “Suweg” (Amorphophallus paeoniifolius) Cultivated in Java 8.

Hasan, V., Astuti, S., 2011. Glicemyc Index of Oyek And Tiwul From Arrowroot 16, 17.

Jain, S.K., Rains, J.L., Croad, J.L. Effect of Chromium Niacinate and Chromium Picolinate Supplementation on Lipid Peroxidation, TNF-α, IL-6, CRP, Glycated Hemoglobin, Triglycerides and Cholesterol Levels in blood of Streptozotocin-treated Diabetic Rats. Free Radic Biol Med. 2007 October 15; 43(8): 1124–1131. doi:10.1016/j.freeradbiomed.2007.05.019.

Ansil, P.N., Nitha, A., Prabha, S.P., Wills, P.J., Jazaira, V., Latha, M.S., Protective effect of Amorphophallus campanulatus (Roxb.) Blume.tuber against thioacetamide induced oxidative stress in rats. Asian Pac. J. Trop. Med. 2011. 4, 870–877. https://doi.org/10.1016/S1995-7645(11)60211-3

Pisoschi, A.M., Pop, A., The role of antioxidants in the chemistry of oxidative stress: A review. Eur. J. Med. Chem. 2015. 97, 55–74. https://doi.org/10.1016/j.ejmech.2015.04.040

Ahmad, M., Akhtar, M.S., Malik, T., Gilani, A.H., 2000. Hypoglycaemic action of the flavonoid fraction of Cuminum nigrum seeds. Phytother Res 4.

Loizzo, M.R., Lecce, G.D., Boselli, E., Menichini, F., Frega, N.G., Inhibitory Activity Of Phenolic Compounds From Extra Virgin Olive Oils On The Enzymes Involved In Diabetes, Obesity And Hypertension: Bioactivity Of Olive Oil Polyphenolic Extracts. J. Food Biochem. 2011. 35, 381–399. https://doi.org/10.1111/j.1745-4514.2010.00390.x

Hoa, N.K., Norberg, A., Sillard, R., Van Phan, D., Thuan, N.D., Dzung, D.T.N., Jornvall, H., Ostenson, C.-G., The possible mechanisms by which phanoside stimulates insulin secretion from rat islets. J. Endocrinol. 2007.192, 389–394. https://doi.org/10.1677/joe.1.06948

Newsholme, P., Cruzat, V.F., Keane, K.N., Carlessi, R., de Bittencourt, P.I.H., Molecular mechanisms of ROS production and oxidative stress in diabetes. Biochem. J. 2016.473, 4527–4550. https://doi.org/10.1042/BCJ20160503C

Kunwar, A., Priyadarsini, K.I., Free radicals, oxidative stress and importance of antioxidants in human health. J Med Allied Sci 2011.1, 8.

M. S. H. Akash, K. Rehman, and A. Liaqat, “: role in development of insulin resistance and pathogenesis of type 2 diabetes mellitus,” Journal of Cellular Biochemistry, 2018. vol. 119, no. 1, pp. 105–110




DOI: https://doi.org/10.18196/mm.200246

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