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Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi

Year 2018, Volume: 22 Issue: Special, 277 - 284, 05.10.2018

Abstract

Bu çalışmanın temel amacı Tip 2 diyabetle indüklenen testis hasarında oksidatif stresin baskılanmasında sulu çam çıra ekstresinin olası etkilerini araştırmaktır.  Çalışmada 49 adet 2,5 aylık erkek sıçanlar tercih edildi. Sıçanlar; kontrol, diyabet ve farklı dozlardan oluşan diyabet+çam çırası olmak üzere gruplara ayrıldı (D+Ç100, D+Ç200, D+Ç400).  Kontrol grubu dışındaki sıçanlara 45 mg/kg streptozotozin (STZ) intraperitonal olarak verilerek Tip-2 diyabet oluşturuldu.  Diyabet oluşumundan sonra sıçanların içme sularına farklı dozlarda (100 g/L, 200 g/L, 400 g/L) çam çıra ekstresi eklenerek suya serbest olarak erişimleri sağlandı.  Deneysel uygulamalar 10 hafta sürdü.  Kontrol grubu ile karşılaştırıldığında, diyabet grubunda MDA seviyesinin kayda değer düzeyde arttığı (p<0.001), total protein düzeyinin ise önemli düzeyde azaldığı (p<0.05) belirlendi.  Diyabet grubu ile karşılaştırıldığında çıra suyu verilen gruplarda MDA düzeyinin önemli düzeyde azaldığı (p<0.001), protein seviyesinin ise önemli düzeyde yükseldiği (D+Ç100) (p<0.05) belirlendi. İncelenen diğer parametrelerde (α-tokoferol, palmitik, oleik, linoleik asit ve doza bağlı diğer parametreler) ise istatistiksel açıdan anlamlı değişiklikler tespit edildi (p<0.05, p<0.01, p<0.001). Sonuç olarak, sulu çam çıra ekstresinin oksidatif stres seviyesini azaltarak testiküler hasarı azaltmada potansiyel olarak yararlı olduğu gözlenmiştir.

References

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  • [2] Yigitturk, G., Acara, A. C., Erbas, O., Oltulu, F., Yavasoglu, N. U., Uysal, A., Yavasoglu, A. 2017. The antioxidant role of agomelatine and gallic acid on oxidative stress in STZ induced type I diabetic rat testes. Biomed Pharmacother, 87, 240-246.
  • [3] Adedara, I. A., Awogbindin, I. O., Anamelechi, J. P., Farombi, E. O. 2015. Garcinia kola seed ameliorates renal, hepatic, and testicular oxidative damage in streptozotocin-induced diabetic rats. Pharm Biol, 53(5), 695-704.
  • [4] Li, M., Liu, Z., Zhuan, L., Wang, T., Guo, S., Wang, S., Liu, J., Ye, Z. 2013. Effects of apocynin on oxidative stress and expression of apoptosis-related genes in testes of diabetic rats. Mol Med Rep, 7(1), 47-52.
  • [5] Rohdewald, P. 2002. A review of the French maritime pine bark extract (pycnogenol), a herbal medication with a diverse clinical pharmacology. Int J Clin Pharmacol Ther, 40, 158–168.
  • [6] Lee, I. C., Ko, J. W., Park, S. H., Shin, N. R., Shin, I.S., Kim, Y. B., Kim, J. C. 2017. Ameliorative effects of pine bark extract on cisplatin-induced acute kidney injury in rats. Ren Fail, 39(1), 363-371.
  • [7] Guo, Q., Zhao, B., Packer, L. 1999. Electron spin resonance study of free radicals formed from a procyanidin-rich pine (Pinus maritima) bark extract, pycnogenol. Free Radic Biol Med, 27, 1308–1312.
  • [8] Maritim, A., Dene, B. E., Sanders, R. A., Watkins, J.B. 2003. Effects of pycnogenol treatment on oxidative stress in streptozotocin-induced diabetic rats. J Biochem Mol Toxicol, 17, 193–198.
  • [9] McGrath, K. C., Li, X. H., McRobb, L. S., Heather, A. K. 2015. Inhibitory Effect of a French Maritime Pine Bark Extract-Based Nutritional Supplement on TNF-α-Induced Inflammation and Oxidative Stress in Human Coronary Artery Endothelial Cells. Evid Based Complement Alternat Med, 2015, 260530.
  • [10] Eryilmaz, A., Eliyatkin, N., Demirci, B., Basal, Y., Kurt Omurlu, I., Gunel, C., Aktas, S., Toka, A., Basak S. 2016. Protective effect of Pycnogenol on cisplatin-induced ototoxicity in rats. Pharm Biol, 54(11), 2777-2781.
  • [11] Erdal, N., Gürgül, S., Kavak, S., Yildiz, A., Emre, M. 2011. Deterioration of bone quality by streptozotocin (STZ)-induced type 2 diabetes mellitus in rats. Biol Trace Elem Res, 140(3), 342-53.
  • [12] Dewanjee, S., Das, A. K., Sahu, R., Gangopadhyay, M. 2009. Antidiabetic activity of Diospyros peregrina fruit: effect on hyperglycemia, hyperlipidemia and augmented oxidative stress in experimental type 2 diabetes. Food Chem Toxicol, 47(10), 2679-85.
  • [13] Demir, E., Yılmaz, Ö. 2014. Streptozotosin ile Tip-1 diyabet oluşturulan sıçanlarda acı badem yağının serum ve eritrositlerdeki bazı biyokimyasal parametrelere etkisi. Marmara Pharmaceutical Journal, 18, 13-21.
  • [14] Ohkawa, H., Ohishi, N., Yagi, K. 1979. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem, 95(2), 351-8.
  • [15] Lowry, O. H., Rosebrough, N. J., Farr, A. L., Randall, R. J., 1951. Protein measurement with the folin phenol reagent. Journal of Biological Chemistry,193, 265-275.
  • [16] Hara, A., Radin, N. S., 1978. Lipid extraction of tissues with a low-toxicity solvent. Anal Biochem, 90(1), 420-6.
  • [17] Christie, W. W. 1992. Gas chromatography and lipids. The Oil Press, Glasgow, 302s.
  • [18] Tvrzická, E., Vecka, M., Staňková, B., Žák, A., 2002. Analysis of fatty acids in plasma lipoproteins by gas chromatography–flame ionization detection: Quantitative aspects. Analytica Chimica Acta, 465, 337-350.
  • [19] Sánchez-Machado, D. I., López-Hernández, J., Paseiro-Losada, P. 2002. High-performance liquid chromatographic determination of alpha-tocopherol in macroalgae. J Chromatogr A, 976(1-2), 277-84.
  • [20] López-Cervantes, J., Sánchez-Machado, D. I., Ríos-Vázquez, N. J. 2006. High-performance liquid chromatography method for the simultaneous quantification of retinol, alpha-tocopherol, and cholesterol in shrimp waste hydrolysate. J Chromatogr A, 1105(1-2), 135-9.
  • [21] Yi, J., Cheng, C., Li, X., Zhao, H., Qu, H., Wang, Z., Wang, L. 2017. Protective mechanisms of purified polyphenols from pinecones of Pinus koraiensis on spleen tissues in tumor-bearing S180 mice in vivo. Food Funct, 8(1), 151-166.
  • [22] Aruoma, O. I. 1998. Free radicals, oxidative stress, andantioxidants in human health and disease. Journal of the American oil chemists' society, 72(2), 199-212.
  • [23] Bajaj, S., Khan, A. 2012. Antioxidants and diabetes. Indian J Endocrinol Metab, 16(Suppl 2), S267–S271.
  • [24] Rahimi-Madiseh, M., Malekpour-Tehrani, A., Bahmani, M., Rafieian-Kopaei, M. 2016. The research and development on the antioxidants in prevention of diabetic complications. Asian Pac J Trop Med, 9(9),825-31.
  • [25] Packer, L., Rimbach, G., Virgili, F. 1999. Antioxidant activity and biologic properties of a procyanidin-rich extract from pine (Pinus maritima) bark, pycnogenol. Free Radic Biol Med, 27(5-6), 704-24.
  • [26] Iravani, S., Zolfaghari, B. 2014. Phytochemical analysis of Pinus eldarica bark. Res Pharm Sci, 9(4), 243-50.
  • [27] Babaee, F., Safaeian, L., Zolfaghari, B., Haghjoo Javanmard, S. 2016. Cytoprotective Effect of Hydroalcoholic Extract of Pinus eldarica Bark against H2O2-Induced Oxidative Stress in Human Endothelial Cells. Iran Biomed J, 20(3), 161-7.
  • [28] Nain, P., Saini, V., Sharma, S., Nain, J. 2012. Antidiabetic and antioxidant potential of Emblica officinalis Gaertn. leaves extract in streptozotocin-induced type-2 diabetes mellitus (T2DM) rats. J Ethnopharmacol, 142(1), 65-71.
  • [29] Florence, N. T., Benoit, M. Z., Jonas, K., Alexandra, T., Désiré, D. D., Pierre, K., Théophile, D. 2014. Antidiabetic and antioxidant effects of Annona muricata (Annonaceae), aqueous extract on streptozotocin-induced diabetic rats. J Ethnopharmacol, 151(2), 784-90.
  • [30] Saliu, J. A., Oboh, G., Omojokun, O. S., Rocha, J. B., Schetinger, M. R., Guterries, J., Stefanello, N., Carvalho, F., Schmatz, R., Morsch, V. M., Boligon, A. 2016. Effect of dietary supplementation of Padauk (Pterocarpus soyauxii) leaf on high fat diet/streptozotocin induced diabetes in rats' brain and platelets. Biomed Pharmacother, 84, 1194-1201.
  • [31] Bal, R., Türk, G., Tuzcu, M., Yilmaz, O., Ozercan, I., Kuloglu, T., Gür, S., Nedzvetsky, V. S., Tykhomyrov, A. A., Andrievsky, G. V., Baydas, G., Naziroglu, M. 2011. Protective effects of nanostructures of hydrated C(60) fullerene on reproductive function in streptozotocin-diabetic male rats. Toxicology, 282(3), 69-81.
  • [32] Shrilatha, B., Muralidhara. 2007. Early oxidative stress in testis and epididymal sperm in streptozotocin-induced diabetic mice: its progression and genotoxic consequences. Reprod Toxicol, 23(4), 578-87.
  • [33] Won, S. B., Jung, G. Y., Kim, J., Chung, Y. S., Hong, E. K., Kwon, Y. H. 2013. Protective effect of Pinus koraiensis needle water extract against oxidative stress in HepG2 cells and obese mice. J Med Food, 16(7), 569-76.
  • [34] Devaraj, S., Vega-López, S., Kaul, N., Schönlau, F., Rohdewald, P., Jialal, I. 2002. Supplementation with a pine bark extract rich in polyphenols increases plasma antioxidant capacity and alters the plasma lipoprotein profile. Lipids, 37(10), 931-4.
  • [35] Parveen, K., Khan, M. R., Mujeeb, M., Siddiqui W. A. 2010. Protective effects of Pycnogenol on hyperglycemia-induced oxidative damage in the liver of type 2 diabetic rats. Chem Biol Interact, 186(2), 219-27.
  • [36] Rizvi, S., Raza, S. T., Ahmed, F., Ahmad, A., Abbas, S., Mahdi, F. 2014. The role of vitamin E in human health and some diseases. Sultan Qaboos Univ Med J, 14(2), 157-65.
  • [37] Gavazza, M., Catalá, A. 2001. The effect of alpha-tocopherol on the lipid peroxidation of mitochondria and microsomes obtained from rat liver and testis. Mol Cell Biochem, 225(1-), 121-8.
  • [38] De, A., Singh, M. F., Singh, V., Ram, V., Bisht, S. 2016. Treatment effect of l-Norvaline on the sexual performance of male rats with streptozotocin induced diabetes. Eur J Pharmacol, 771, 247-54.
  • [39] Hamden, K., Jaouadi, B., Carreau, S., Aouidet, A., El-Fazaa, S., Gharbi, N., Elfeki, A. 2010. Potential protective effect on key steroidogenesis and metabolic enzymes and sperm abnormalities by fenugreek steroids in testis and epididymis of surviving diabetic rats. Arch Physiol Biochem, 116(3), 146-55.
  • [40] Arikawe, A. P., Oyerinde, A., Olatunji-Bello, I. I., Obika, L. F. 2012. Streptozotocin diabetes and insulin resistance impairment of spermatogenesis in adult rat testis: central vs. local mechanism. Niger J Physiol Sci, 27(2), 171-9.
  • [41] Huang, Y. S., Horrobin, D. F., Manku, M. S., Mitchell, J., Ryan, M. A. 1984. Tissue phospholipid fatty acid composition in the diabetic rat. Lipids, 19(5), 367-70.
  • [42] Ntambi, J. M. 1995. The regulation of stearoyl-CoA desaturase (SCD). Prog. Lipid Res, 34, 139–150.
  • [43] Miyazaki, M., Gomez, F. E., Ntambi, J. M. 2002. Lack of stearoyl-CoA desaturase-1 function induces a palmitoyl-CoA Delta6 desaturase and represses the stearoyl-CoA desaturase-3 gene in the preputial glands of the mouse. J. Lipid Res, 43, 2146–2154.
  • [44] Nakamura, M. T., Nara T. Y. 2004. Structure, function, and dietary regulation of delta6, delta5, and delta9 desaturases. Annu Rev Nutr, 24, 345-76.
  • [45] Wilder, P. J., Coniglio J. G. 1984. The effects of streptozotocin diabetes and of dietary protein content on the composition and metabolism of testicular lipids. Proc Soc Exp Biol Med, 177(3), 399-405.
  • [46] Hurtado de Catalfo, G. E., De Gómez Dumm, I. N. 1998. Lipid dismetabolism in Leydig and Sertoli cells isolated from streptozotocin-diabetic rats. Int J Biochem Cell Biol, 30(9), 1001-10.
  • [47] Hu, Q., Ishii, E., Nakagawa, Y. 1994. Differential changes in relative levels of arachidonic acid in major phospholipids from rat tissues during the progression of diabetes. J Biochem, 115(3), 405-408.
  • [48] Romanelli, F., Valenca, M., Conte, D., Isidori, A., Negro-Vilar, A. 1995. Arachidonic acid and its metabolites effects on testosterone production by rat Leydig cells. J Endocrinol Invest, 18(3), 186-93.
  • [49] Chan, A. C. 1993. Partners in defense, vitamin E and vitamin C. Can J Physiol Pharmacol, 71(9), 725-31.
  • [50] Burczynski, J. M., Southard, S. J., Hayes, J. R., Longhurst, P. A., Colby, H. D. 2001. Changes in mitochondrial and microsomal lipid peroxidation and fatty acid profiles in adrenal glands, testes, and livers from alpha-tocopherol-deficient rats. Free Radic Biol Med, 30(9), 1029-35.
Year 2018, Volume: 22 Issue: Special, 277 - 284, 05.10.2018

Abstract

References

  • [1] Koroglu, P., Senturk, G. E., Yucel, D., Ozakpinar, O. B., Uras, F., Arbak, S. 2015. The effect of exogenous oxytocin on streptozotocin (STZ)-induced diabetic adult rat testes, Peptides, 63, 47-54.
  • [2] Yigitturk, G., Acara, A. C., Erbas, O., Oltulu, F., Yavasoglu, N. U., Uysal, A., Yavasoglu, A. 2017. The antioxidant role of agomelatine and gallic acid on oxidative stress in STZ induced type I diabetic rat testes. Biomed Pharmacother, 87, 240-246.
  • [3] Adedara, I. A., Awogbindin, I. O., Anamelechi, J. P., Farombi, E. O. 2015. Garcinia kola seed ameliorates renal, hepatic, and testicular oxidative damage in streptozotocin-induced diabetic rats. Pharm Biol, 53(5), 695-704.
  • [4] Li, M., Liu, Z., Zhuan, L., Wang, T., Guo, S., Wang, S., Liu, J., Ye, Z. 2013. Effects of apocynin on oxidative stress and expression of apoptosis-related genes in testes of diabetic rats. Mol Med Rep, 7(1), 47-52.
  • [5] Rohdewald, P. 2002. A review of the French maritime pine bark extract (pycnogenol), a herbal medication with a diverse clinical pharmacology. Int J Clin Pharmacol Ther, 40, 158–168.
  • [6] Lee, I. C., Ko, J. W., Park, S. H., Shin, N. R., Shin, I.S., Kim, Y. B., Kim, J. C. 2017. Ameliorative effects of pine bark extract on cisplatin-induced acute kidney injury in rats. Ren Fail, 39(1), 363-371.
  • [7] Guo, Q., Zhao, B., Packer, L. 1999. Electron spin resonance study of free radicals formed from a procyanidin-rich pine (Pinus maritima) bark extract, pycnogenol. Free Radic Biol Med, 27, 1308–1312.
  • [8] Maritim, A., Dene, B. E., Sanders, R. A., Watkins, J.B. 2003. Effects of pycnogenol treatment on oxidative stress in streptozotocin-induced diabetic rats. J Biochem Mol Toxicol, 17, 193–198.
  • [9] McGrath, K. C., Li, X. H., McRobb, L. S., Heather, A. K. 2015. Inhibitory Effect of a French Maritime Pine Bark Extract-Based Nutritional Supplement on TNF-α-Induced Inflammation and Oxidative Stress in Human Coronary Artery Endothelial Cells. Evid Based Complement Alternat Med, 2015, 260530.
  • [10] Eryilmaz, A., Eliyatkin, N., Demirci, B., Basal, Y., Kurt Omurlu, I., Gunel, C., Aktas, S., Toka, A., Basak S. 2016. Protective effect of Pycnogenol on cisplatin-induced ototoxicity in rats. Pharm Biol, 54(11), 2777-2781.
  • [11] Erdal, N., Gürgül, S., Kavak, S., Yildiz, A., Emre, M. 2011. Deterioration of bone quality by streptozotocin (STZ)-induced type 2 diabetes mellitus in rats. Biol Trace Elem Res, 140(3), 342-53.
  • [12] Dewanjee, S., Das, A. K., Sahu, R., Gangopadhyay, M. 2009. Antidiabetic activity of Diospyros peregrina fruit: effect on hyperglycemia, hyperlipidemia and augmented oxidative stress in experimental type 2 diabetes. Food Chem Toxicol, 47(10), 2679-85.
  • [13] Demir, E., Yılmaz, Ö. 2014. Streptozotosin ile Tip-1 diyabet oluşturulan sıçanlarda acı badem yağının serum ve eritrositlerdeki bazı biyokimyasal parametrelere etkisi. Marmara Pharmaceutical Journal, 18, 13-21.
  • [14] Ohkawa, H., Ohishi, N., Yagi, K. 1979. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem, 95(2), 351-8.
  • [15] Lowry, O. H., Rosebrough, N. J., Farr, A. L., Randall, R. J., 1951. Protein measurement with the folin phenol reagent. Journal of Biological Chemistry,193, 265-275.
  • [16] Hara, A., Radin, N. S., 1978. Lipid extraction of tissues with a low-toxicity solvent. Anal Biochem, 90(1), 420-6.
  • [17] Christie, W. W. 1992. Gas chromatography and lipids. The Oil Press, Glasgow, 302s.
  • [18] Tvrzická, E., Vecka, M., Staňková, B., Žák, A., 2002. Analysis of fatty acids in plasma lipoproteins by gas chromatography–flame ionization detection: Quantitative aspects. Analytica Chimica Acta, 465, 337-350.
  • [19] Sánchez-Machado, D. I., López-Hernández, J., Paseiro-Losada, P. 2002. High-performance liquid chromatographic determination of alpha-tocopherol in macroalgae. J Chromatogr A, 976(1-2), 277-84.
  • [20] López-Cervantes, J., Sánchez-Machado, D. I., Ríos-Vázquez, N. J. 2006. High-performance liquid chromatography method for the simultaneous quantification of retinol, alpha-tocopherol, and cholesterol in shrimp waste hydrolysate. J Chromatogr A, 1105(1-2), 135-9.
  • [21] Yi, J., Cheng, C., Li, X., Zhao, H., Qu, H., Wang, Z., Wang, L. 2017. Protective mechanisms of purified polyphenols from pinecones of Pinus koraiensis on spleen tissues in tumor-bearing S180 mice in vivo. Food Funct, 8(1), 151-166.
  • [22] Aruoma, O. I. 1998. Free radicals, oxidative stress, andantioxidants in human health and disease. Journal of the American oil chemists' society, 72(2), 199-212.
  • [23] Bajaj, S., Khan, A. 2012. Antioxidants and diabetes. Indian J Endocrinol Metab, 16(Suppl 2), S267–S271.
  • [24] Rahimi-Madiseh, M., Malekpour-Tehrani, A., Bahmani, M., Rafieian-Kopaei, M. 2016. The research and development on the antioxidants in prevention of diabetic complications. Asian Pac J Trop Med, 9(9),825-31.
  • [25] Packer, L., Rimbach, G., Virgili, F. 1999. Antioxidant activity and biologic properties of a procyanidin-rich extract from pine (Pinus maritima) bark, pycnogenol. Free Radic Biol Med, 27(5-6), 704-24.
  • [26] Iravani, S., Zolfaghari, B. 2014. Phytochemical analysis of Pinus eldarica bark. Res Pharm Sci, 9(4), 243-50.
  • [27] Babaee, F., Safaeian, L., Zolfaghari, B., Haghjoo Javanmard, S. 2016. Cytoprotective Effect of Hydroalcoholic Extract of Pinus eldarica Bark against H2O2-Induced Oxidative Stress in Human Endothelial Cells. Iran Biomed J, 20(3), 161-7.
  • [28] Nain, P., Saini, V., Sharma, S., Nain, J. 2012. Antidiabetic and antioxidant potential of Emblica officinalis Gaertn. leaves extract in streptozotocin-induced type-2 diabetes mellitus (T2DM) rats. J Ethnopharmacol, 142(1), 65-71.
  • [29] Florence, N. T., Benoit, M. Z., Jonas, K., Alexandra, T., Désiré, D. D., Pierre, K., Théophile, D. 2014. Antidiabetic and antioxidant effects of Annona muricata (Annonaceae), aqueous extract on streptozotocin-induced diabetic rats. J Ethnopharmacol, 151(2), 784-90.
  • [30] Saliu, J. A., Oboh, G., Omojokun, O. S., Rocha, J. B., Schetinger, M. R., Guterries, J., Stefanello, N., Carvalho, F., Schmatz, R., Morsch, V. M., Boligon, A. 2016. Effect of dietary supplementation of Padauk (Pterocarpus soyauxii) leaf on high fat diet/streptozotocin induced diabetes in rats' brain and platelets. Biomed Pharmacother, 84, 1194-1201.
  • [31] Bal, R., Türk, G., Tuzcu, M., Yilmaz, O., Ozercan, I., Kuloglu, T., Gür, S., Nedzvetsky, V. S., Tykhomyrov, A. A., Andrievsky, G. V., Baydas, G., Naziroglu, M. 2011. Protective effects of nanostructures of hydrated C(60) fullerene on reproductive function in streptozotocin-diabetic male rats. Toxicology, 282(3), 69-81.
  • [32] Shrilatha, B., Muralidhara. 2007. Early oxidative stress in testis and epididymal sperm in streptozotocin-induced diabetic mice: its progression and genotoxic consequences. Reprod Toxicol, 23(4), 578-87.
  • [33] Won, S. B., Jung, G. Y., Kim, J., Chung, Y. S., Hong, E. K., Kwon, Y. H. 2013. Protective effect of Pinus koraiensis needle water extract against oxidative stress in HepG2 cells and obese mice. J Med Food, 16(7), 569-76.
  • [34] Devaraj, S., Vega-López, S., Kaul, N., Schönlau, F., Rohdewald, P., Jialal, I. 2002. Supplementation with a pine bark extract rich in polyphenols increases plasma antioxidant capacity and alters the plasma lipoprotein profile. Lipids, 37(10), 931-4.
  • [35] Parveen, K., Khan, M. R., Mujeeb, M., Siddiqui W. A. 2010. Protective effects of Pycnogenol on hyperglycemia-induced oxidative damage in the liver of type 2 diabetic rats. Chem Biol Interact, 186(2), 219-27.
  • [36] Rizvi, S., Raza, S. T., Ahmed, F., Ahmad, A., Abbas, S., Mahdi, F. 2014. The role of vitamin E in human health and some diseases. Sultan Qaboos Univ Med J, 14(2), 157-65.
  • [37] Gavazza, M., Catalá, A. 2001. The effect of alpha-tocopherol on the lipid peroxidation of mitochondria and microsomes obtained from rat liver and testis. Mol Cell Biochem, 225(1-), 121-8.
  • [38] De, A., Singh, M. F., Singh, V., Ram, V., Bisht, S. 2016. Treatment effect of l-Norvaline on the sexual performance of male rats with streptozotocin induced diabetes. Eur J Pharmacol, 771, 247-54.
  • [39] Hamden, K., Jaouadi, B., Carreau, S., Aouidet, A., El-Fazaa, S., Gharbi, N., Elfeki, A. 2010. Potential protective effect on key steroidogenesis and metabolic enzymes and sperm abnormalities by fenugreek steroids in testis and epididymis of surviving diabetic rats. Arch Physiol Biochem, 116(3), 146-55.
  • [40] Arikawe, A. P., Oyerinde, A., Olatunji-Bello, I. I., Obika, L. F. 2012. Streptozotocin diabetes and insulin resistance impairment of spermatogenesis in adult rat testis: central vs. local mechanism. Niger J Physiol Sci, 27(2), 171-9.
  • [41] Huang, Y. S., Horrobin, D. F., Manku, M. S., Mitchell, J., Ryan, M. A. 1984. Tissue phospholipid fatty acid composition in the diabetic rat. Lipids, 19(5), 367-70.
  • [42] Ntambi, J. M. 1995. The regulation of stearoyl-CoA desaturase (SCD). Prog. Lipid Res, 34, 139–150.
  • [43] Miyazaki, M., Gomez, F. E., Ntambi, J. M. 2002. Lack of stearoyl-CoA desaturase-1 function induces a palmitoyl-CoA Delta6 desaturase and represses the stearoyl-CoA desaturase-3 gene in the preputial glands of the mouse. J. Lipid Res, 43, 2146–2154.
  • [44] Nakamura, M. T., Nara T. Y. 2004. Structure, function, and dietary regulation of delta6, delta5, and delta9 desaturases. Annu Rev Nutr, 24, 345-76.
  • [45] Wilder, P. J., Coniglio J. G. 1984. The effects of streptozotocin diabetes and of dietary protein content on the composition and metabolism of testicular lipids. Proc Soc Exp Biol Med, 177(3), 399-405.
  • [46] Hurtado de Catalfo, G. E., De Gómez Dumm, I. N. 1998. Lipid dismetabolism in Leydig and Sertoli cells isolated from streptozotocin-diabetic rats. Int J Biochem Cell Biol, 30(9), 1001-10.
  • [47] Hu, Q., Ishii, E., Nakagawa, Y. 1994. Differential changes in relative levels of arachidonic acid in major phospholipids from rat tissues during the progression of diabetes. J Biochem, 115(3), 405-408.
  • [48] Romanelli, F., Valenca, M., Conte, D., Isidori, A., Negro-Vilar, A. 1995. Arachidonic acid and its metabolites effects on testosterone production by rat Leydig cells. J Endocrinol Invest, 18(3), 186-93.
  • [49] Chan, A. C. 1993. Partners in defense, vitamin E and vitamin C. Can J Physiol Pharmacol, 71(9), 725-31.
  • [50] Burczynski, J. M., Southard, S. J., Hayes, J. R., Longhurst, P. A., Colby, H. D. 2001. Changes in mitochondrial and microsomal lipid peroxidation and fatty acid profiles in adrenal glands, testes, and livers from alpha-tocopherol-deficient rats. Free Radic Biol Med, 30(9), 1029-35.
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Ersin Demir

Ökkeş Yılmaz

Halise Sarıgül This is me

Publication Date October 5, 2018
Published in Issue Year 2018 Volume: 22 Issue: Special

Cite

APA Demir, E., Yılmaz, Ö., & Sarıgül, H. (2018). Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 22, 277-284.
AMA Demir E, Yılmaz Ö, Sarıgül H. Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi. J. Nat. Appl. Sci. October 2018;22:277-284.
Chicago Demir, Ersin, Ökkeş Yılmaz, and Halise Sarıgül. “Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi”. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi 22, October (October 2018): 277-84.
EndNote Demir E, Yılmaz Ö, Sarıgül H (October 1, 2018) Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi 22 277–284.
IEEE E. Demir, Ö. Yılmaz, and H. Sarıgül, “Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi”, J. Nat. Appl. Sci., vol. 22, pp. 277–284, 2018.
ISNAD Demir, Ersin et al. “Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi”. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi 22 (October 2018), 277-284.
JAMA Demir E, Yılmaz Ö, Sarıgül H. Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi. J. Nat. Appl. Sci. 2018;22:277–284.
MLA Demir, Ersin et al. “Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi”. Süleyman Demirel Üniversitesi Fen Bilimleri Enstitüsü Dergisi, vol. 22, 2018, pp. 277-84.
Vancouver Demir E, Yılmaz Ö, Sarıgül H. Sulu Çam Çıra Ekstresinin Diyabet Oluşturulan Sıçanların Testis Dokusu Üzerindeki Etkisi. J. Nat. Appl. Sci. 2018;22:277-84.

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