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The effects of vanadyl sulfate on glutathione, lipid peroxidation and nonenzymatic glycosylation levels in various tissues in experimental diabetes

Yıl 2021, Cilt: 51 Sayı: 1, 73 - 78, 30.04.2021

Öz

Background and Aims: Diabetes mellitus is characterized by hyperglycemia which over time leads to serious damage of several body systems. Vanadium ions and their complexes have been demonstrated to have various insulin-mimetic and antidiabetic effects. The object of the present work was to investigate the effect of vanadyl sulfate (VS) on serum total lipid and protein parameters, glutathione, lipid peroxidation and nonenzymatic glycosylation levels in cardiac, lens, lung and skeletal muscle tissues of STZ diabetic rats. Methods: Randomly selected 6.0 - 6.5 month old Swiss Albino rats were separated into two diabetic and two control groups. A single intraperitoneal injection of 65 mg/kg streptozotocin (STZ) in 0.01 M citrate buffer (pH 4.5) was used to induce diabetes. 100 mg/kg VS was administered daily to one of the controls and one of the diabetic groups. On the 60th day of the experiment, serum total lipid and total protein levels were determined. Results: Tissue samples were taken and used for determination of glutathione (GSH), lipid peroxidation (LPO) and nonenzymatic glycosylation (GSH) and protein levels. Conclusion: According to the results, treatment with VS reversed the effects of diabetes by exerting antioxidant properties and preventing damage caused by diabetes on various tissues along with some serum parameters.

Kaynakça

  • • Akgun-Dar, K., Bolkent, S,. Yanardag, R., & Tunali, S. (2007). Vanadyl sulfate protects against streptozotocin-induced morphological and biochemical changes in rat aorta. Cell Biochemistry & Function, 25, 603-609.
  • • Anderson, R. E., Rapp, L. M., & Wiegand, R. D. (1984). Lipid peroxidation and retinal degeneration. Current Eye Research, 3, 223-227.
  • • Bao, F. J., Deng, M. L., Zheng, X. B., Li, N. A., Zhao, Y. P. Cao, S. Yua, A., Wang, Q. M., Huang, J. H., & Elsheikh, A. (2017). Effects of diabetes mellitus on biomechanical properties of the rabbit cornea. Experimental Eye Research, 161, 82-88.
  • • Beutler, E. (1975). Glutathione in red blood cell metabolism; In A manual of biochemical methods, 2nd ed. Grune and Stratton, New York, pp. 112–114.
  • • Bohlin, C., Praestgaard, E., Baumann, M. J., Borch, K., Praestgaard, J., Monrad, R. N., & Westh, P. (2013). A comparative study of hydrolysis and transglycosylation activities of fungal α-glucosidases. Applied Microbiology and Biotechnology, 97, 159-169.
  • • Bolkent, S., Bolkent, S., Yanardag, R., & Tunali, S. (2005). Protective effect of vanadyl sulfate on the pancreas of streptozotocininduced diabetic rats. Diabetes Research and Clinical Practice, 70, 103–109.
  • • Cai, L., Li, W., Wang, G., Guo, L., Jiang, Y., & Kang, Y. J. (2002). Hyperglycemia- induced apoptosis in mouse myocardium: mitochondrial cytochrome C-mediated caspase-3 activation pathway. Diabetes, 51, 1938-1948.
  • • Cayir, A., Ugan, R. A., Albayrak, A. D., Kose, E., Akpinar, Y., Cayir, H. T., Atmaca, Bayraktutan Z., & Kara M. (2015). The lung endothelin system: a potent therapeutic target with bosentan for the amelioration of lung alterations in a rat model of diabetes mellitus. Journal of Endocrinological Investigation, 38, 987–998.
  • • Chen, Y., Tanga, S., Chend, Y., Zhang, R., Zhoua, M., Wanga, C., Fenga, N., & Wu, Q. (2019). Structure-activity relationship of procyanidins on advanced glycation end products formation and corresponding mechanisms. Food Chemistry, 279, 679-687.
  • • Dennis, R. J., Maldonado, D., Rojas, M. X., Aschner, P., Rondón, M., Charry, L., & Casas, A. (2010). Inadequate glucose control in type 2 diabetes is associated with impaired lung function and systemic inflammation: a cross-sectional study. BioMed Central, 10, 38.
  • • Djelić, N., Radaković, M., Borozan, S., Dimirijević-Srećković, V., Pajović, N., Vejnović, B., Borozan, N., Bankoglu, E. E., Stopper, H., & Stanimirović, Z. (2019). Oxidative stress and DNA damage in peripheral blood mononuclear cells from normal, obese, prediabetic and diabetic persons exposed to adrenaline in vitro. Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 843, 81-89.
  • • Ding, W., Hasegawa, T., Hosaka, H., Peng, D., Takahashi, K., & Seko, Y. (2001). Effect of long-term treatment with vanadate in drinking water on KK mice with genetic non-insulin-dependent diabetes mellitus. Biological Trace Element Research, 80, 159-174.
  • • Domingo, J. L., & Gómez, M. (2016). Vanadium compounds for the treatment of human diabetes mellitus: A scientific curiosity? A review of thirty years of research. Food and Chemical Toxicology, 95, 137-141.
  • • El Hadi, H., Vettor R., & Rossato, M. (2019). Cardiomyocyte mitochondrial dysfunction in diabetes and its contribution in cardiac arrhythmogenesis. Mitochondrion, 46, 6-14.
  • • Frings, C. S., Fendley, T. W., Dunn, R. T. & Queen C. A. (1972). Improved determination of total serum lipids by the sulfo-phosphovanillin reaction. Clinical Chemistry, 18, 673-674.
  • • Griesmacher, A., Kindhauser, M., Andert, S. E., Schreiner, W., Toma, C., Knoebl, P., Pietschmann, P., Prager, R., Schnack, C., Schemthaner, G., & Mueller, M. M. (1995). Enhanced serum levels of thiobarbituric- acid-reactive substances in diabetes mellitus. The American Journal of Medicine, 98, 469-475.
  • • Gupta, D., Raju, J., Prakash, J., & Baquer, N. Z. (1999). Change in the lipid profile, lipogenic and related enzymes in the livers of experimental diabetic rats: effect of insulin and vanadate. Diabetes Research and Clinical Practice, 46, 1-7.
  • • Hajarnavis A. M., & Bulakh P. M. (2019). Anticataract effects of S. cumini and A. marmelos on goat lenses in an experimental diabetic cataract model, Journal of Ayurveda and Integrative Medicine, https://doi.org/10.1016/j.jaim.2019.08.001.
  • • Heyliger, C. E., Tahiliani, A. G., & McNeill, J. H. (1985). Effect of vanadate on elevated blood glucose and depressed cardiac performance of diabetic rats. Science, 227, 1474-1477. • Irving E., & Stoker A. W. (2017). Vanadium compounds as PTP inhibitors. Molecules, 22, 2269.
  • • Jound, A., Lambert, E., Stauffacher, W., & Renold, A. E. (1969). Diabetogenic action of streptozotocin. Relationship of dose to metabolic response. Journal of Clinical Investigation, 48, 2129–2139.
  • • Kim, A. D., Zhang, R., Kang, K. A., You, H. J., & Hyun, J. W. (2011). Increased glutathione synthesis following Nrf2 activation by vanadyl sulfate in human chang liver cells. International Journal of Molecular Sciences, 12, 8878-8894.
  • • Kim, C. H., Kim, H. K., Kim, E. H., Bae, S. J., Jung, Y. J., Choi, J., & Park, J. Y. (2015). Association of restrictive ventilatory dysfunction with the development of prediabetes and type 2 diabetes in Koreans. Acta Diabetologica, 52, 357-363.
  • • Lavelli, V., Sri Harsha, P. S. C., Ferranti, P., Scarafoni, A., & Iametti, S. (2016). Grape skin phenolics as inhibitors of mammalian α-glucosidase and α-amylase effect of food matrix and processing on efficacy. Food & Function, 7, 1655-1663.
  • • Ledwozyw, A., Michalak, J., Stepien, A., & Kadziolka, A. (1986). The relationship between plasma triglycerides, cholesterol, total lipids and lipid peroxidation products during human atheroschlerosis. Clinica Chimica Acta, 155, 275-283.
  • • Lee, W. S., & Kim, J. (2017). Diabetic cardiomyopathy: where we are and where we are going. The Korean Journal of Internal Medicine, 32, 404-421.
Yıl 2021, Cilt: 51 Sayı: 1, 73 - 78, 30.04.2021

Öz

Kaynakça

  • • Akgun-Dar, K., Bolkent, S,. Yanardag, R., & Tunali, S. (2007). Vanadyl sulfate protects against streptozotocin-induced morphological and biochemical changes in rat aorta. Cell Biochemistry & Function, 25, 603-609.
  • • Anderson, R. E., Rapp, L. M., & Wiegand, R. D. (1984). Lipid peroxidation and retinal degeneration. Current Eye Research, 3, 223-227.
  • • Bao, F. J., Deng, M. L., Zheng, X. B., Li, N. A., Zhao, Y. P. Cao, S. Yua, A., Wang, Q. M., Huang, J. H., & Elsheikh, A. (2017). Effects of diabetes mellitus on biomechanical properties of the rabbit cornea. Experimental Eye Research, 161, 82-88.
  • • Beutler, E. (1975). Glutathione in red blood cell metabolism; In A manual of biochemical methods, 2nd ed. Grune and Stratton, New York, pp. 112–114.
  • • Bohlin, C., Praestgaard, E., Baumann, M. J., Borch, K., Praestgaard, J., Monrad, R. N., & Westh, P. (2013). A comparative study of hydrolysis and transglycosylation activities of fungal α-glucosidases. Applied Microbiology and Biotechnology, 97, 159-169.
  • • Bolkent, S., Bolkent, S., Yanardag, R., & Tunali, S. (2005). Protective effect of vanadyl sulfate on the pancreas of streptozotocininduced diabetic rats. Diabetes Research and Clinical Practice, 70, 103–109.
  • • Cai, L., Li, W., Wang, G., Guo, L., Jiang, Y., & Kang, Y. J. (2002). Hyperglycemia- induced apoptosis in mouse myocardium: mitochondrial cytochrome C-mediated caspase-3 activation pathway. Diabetes, 51, 1938-1948.
  • • Cayir, A., Ugan, R. A., Albayrak, A. D., Kose, E., Akpinar, Y., Cayir, H. T., Atmaca, Bayraktutan Z., & Kara M. (2015). The lung endothelin system: a potent therapeutic target with bosentan for the amelioration of lung alterations in a rat model of diabetes mellitus. Journal of Endocrinological Investigation, 38, 987–998.
  • • Chen, Y., Tanga, S., Chend, Y., Zhang, R., Zhoua, M., Wanga, C., Fenga, N., & Wu, Q. (2019). Structure-activity relationship of procyanidins on advanced glycation end products formation and corresponding mechanisms. Food Chemistry, 279, 679-687.
  • • Dennis, R. J., Maldonado, D., Rojas, M. X., Aschner, P., Rondón, M., Charry, L., & Casas, A. (2010). Inadequate glucose control in type 2 diabetes is associated with impaired lung function and systemic inflammation: a cross-sectional study. BioMed Central, 10, 38.
  • • Djelić, N., Radaković, M., Borozan, S., Dimirijević-Srećković, V., Pajović, N., Vejnović, B., Borozan, N., Bankoglu, E. E., Stopper, H., & Stanimirović, Z. (2019). Oxidative stress and DNA damage in peripheral blood mononuclear cells from normal, obese, prediabetic and diabetic persons exposed to adrenaline in vitro. Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 843, 81-89.
  • • Ding, W., Hasegawa, T., Hosaka, H., Peng, D., Takahashi, K., & Seko, Y. (2001). Effect of long-term treatment with vanadate in drinking water on KK mice with genetic non-insulin-dependent diabetes mellitus. Biological Trace Element Research, 80, 159-174.
  • • Domingo, J. L., & Gómez, M. (2016). Vanadium compounds for the treatment of human diabetes mellitus: A scientific curiosity? A review of thirty years of research. Food and Chemical Toxicology, 95, 137-141.
  • • El Hadi, H., Vettor R., & Rossato, M. (2019). Cardiomyocyte mitochondrial dysfunction in diabetes and its contribution in cardiac arrhythmogenesis. Mitochondrion, 46, 6-14.
  • • Frings, C. S., Fendley, T. W., Dunn, R. T. & Queen C. A. (1972). Improved determination of total serum lipids by the sulfo-phosphovanillin reaction. Clinical Chemistry, 18, 673-674.
  • • Griesmacher, A., Kindhauser, M., Andert, S. E., Schreiner, W., Toma, C., Knoebl, P., Pietschmann, P., Prager, R., Schnack, C., Schemthaner, G., & Mueller, M. M. (1995). Enhanced serum levels of thiobarbituric- acid-reactive substances in diabetes mellitus. The American Journal of Medicine, 98, 469-475.
  • • Gupta, D., Raju, J., Prakash, J., & Baquer, N. Z. (1999). Change in the lipid profile, lipogenic and related enzymes in the livers of experimental diabetic rats: effect of insulin and vanadate. Diabetes Research and Clinical Practice, 46, 1-7.
  • • Hajarnavis A. M., & Bulakh P. M. (2019). Anticataract effects of S. cumini and A. marmelos on goat lenses in an experimental diabetic cataract model, Journal of Ayurveda and Integrative Medicine, https://doi.org/10.1016/j.jaim.2019.08.001.
  • • Heyliger, C. E., Tahiliani, A. G., & McNeill, J. H. (1985). Effect of vanadate on elevated blood glucose and depressed cardiac performance of diabetic rats. Science, 227, 1474-1477. • Irving E., & Stoker A. W. (2017). Vanadium compounds as PTP inhibitors. Molecules, 22, 2269.
  • • Jound, A., Lambert, E., Stauffacher, W., & Renold, A. E. (1969). Diabetogenic action of streptozotocin. Relationship of dose to metabolic response. Journal of Clinical Investigation, 48, 2129–2139.
  • • Kim, A. D., Zhang, R., Kang, K. A., You, H. J., & Hyun, J. W. (2011). Increased glutathione synthesis following Nrf2 activation by vanadyl sulfate in human chang liver cells. International Journal of Molecular Sciences, 12, 8878-8894.
  • • Kim, C. H., Kim, H. K., Kim, E. H., Bae, S. J., Jung, Y. J., Choi, J., & Park, J. Y. (2015). Association of restrictive ventilatory dysfunction with the development of prediabetes and type 2 diabetes in Koreans. Acta Diabetologica, 52, 357-363.
  • • Lavelli, V., Sri Harsha, P. S. C., Ferranti, P., Scarafoni, A., & Iametti, S. (2016). Grape skin phenolics as inhibitors of mammalian α-glucosidase and α-amylase effect of food matrix and processing on efficacy. Food & Function, 7, 1655-1663.
  • • Ledwozyw, A., Michalak, J., Stepien, A., & Kadziolka, A. (1986). The relationship between plasma triglycerides, cholesterol, total lipids and lipid peroxidation products during human atheroschlerosis. Clinica Chimica Acta, 155, 275-283.
  • • Lee, W. S., & Kim, J. (2017). Diabetic cardiomyopathy: where we are and where we are going. The Korean Journal of Internal Medicine, 32, 404-421.
Toplam 25 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Eczacılık ve İlaç Bilimleri, Sağlık Kurumları Yönetimi
Bölüm Original Article
Yazarlar

Sevim Tunalı Bu kişi benim 0000-0003-3363-1290

Refiye Yanardağ Bu kişi benim 0000-0003-4185-4363

Yayımlanma Tarihi 30 Nisan 2021
Gönderilme Tarihi 10 Nisan 2020
Yayımlandığı Sayı Yıl 2021 Cilt: 51 Sayı: 1

Kaynak Göster

APA Tunalı, S., & Yanardağ, R. (2021). The effects of vanadyl sulfate on glutathione, lipid peroxidation and nonenzymatic glycosylation levels in various tissues in experimental diabetes. İstanbul Journal of Pharmacy, 51(1), 73-78.
AMA Tunalı S, Yanardağ R. The effects of vanadyl sulfate on glutathione, lipid peroxidation and nonenzymatic glycosylation levels in various tissues in experimental diabetes. iujp. Nisan 2021;51(1):73-78.
Chicago Tunalı, Sevim, ve Refiye Yanardağ. “The Effects of Vanadyl Sulfate on Glutathione, Lipid Peroxidation and Nonenzymatic Glycosylation Levels in Various Tissues in Experimental Diabetes”. İstanbul Journal of Pharmacy 51, sy. 1 (Nisan 2021): 73-78.
EndNote Tunalı S, Yanardağ R (01 Nisan 2021) The effects of vanadyl sulfate on glutathione, lipid peroxidation and nonenzymatic glycosylation levels in various tissues in experimental diabetes. İstanbul Journal of Pharmacy 51 1 73–78.
IEEE S. Tunalı ve R. Yanardağ, “The effects of vanadyl sulfate on glutathione, lipid peroxidation and nonenzymatic glycosylation levels in various tissues in experimental diabetes”, iujp, c. 51, sy. 1, ss. 73–78, 2021.
ISNAD Tunalı, Sevim - Yanardağ, Refiye. “The Effects of Vanadyl Sulfate on Glutathione, Lipid Peroxidation and Nonenzymatic Glycosylation Levels in Various Tissues in Experimental Diabetes”. İstanbul Journal of Pharmacy 51/1 (Nisan 2021), 73-78.
JAMA Tunalı S, Yanardağ R. The effects of vanadyl sulfate on glutathione, lipid peroxidation and nonenzymatic glycosylation levels in various tissues in experimental diabetes. iujp. 2021;51:73–78.
MLA Tunalı, Sevim ve Refiye Yanardağ. “The Effects of Vanadyl Sulfate on Glutathione, Lipid Peroxidation and Nonenzymatic Glycosylation Levels in Various Tissues in Experimental Diabetes”. İstanbul Journal of Pharmacy, c. 51, sy. 1, 2021, ss. 73-78.
Vancouver Tunalı S, Yanardağ R. The effects of vanadyl sulfate on glutathione, lipid peroxidation and nonenzymatic glycosylation levels in various tissues in experimental diabetes. iujp. 2021;51(1):73-8.