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Yıl 2020, Cilt: 4 Sayı: 3, 136 - 144, 30.12.2020
https://doi.org/10.30704/http-www-jivs-net.811491

Öz

Kaynakça

  • Abou-Seif, M. A. & Youssef, A. (2004). Evaluation of some biochemical changes in diabetic patients. Clinica Chimica Acta, 346, 161–170.
  • 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. Pharmaceutical Biology, 1, 695–704.
  • Afifi, M., Almaghrabi, O. A. & Kadasa, N. M. (2015). Ameliorative effect of zinc oxide nanoparticles on antioxidants and sperm characteristics in streptozotocin- induced diabetic rat testes. Biomedical Research International, 2, 1–6.
  • Agarwal, A., Makker, K. & Sharma, R. (2008). Clinical relevance of oxidative stress in male factor infertility: An update. American Journal of Reproduction and Immunology, 59, 2–11.
  • Agbaje, I. M., Rogers, D. A., McVicar, C. M., McClure, N., Atkinson, A. B., Mallidis, C. & Lewis, S. E. M. (2007). Insulin dependant diabetes mellitus: implications for male reproductive function. Human Reproduction, 22, 1871–7.
  • Akbarzadeh, A., Norouzian, D., Mehrabi, M. R. Jamshidi, Sh., Farhangi, A., Allah Verdi, A., Mofidian, S. M. A. & Lame Rad, B. (2007). Induction of diabetes by streptozotocin in rats. Indian Journal of Clinical Biochemestry, 22 (2), 60-64.
  • Akkati, S., Sam, K. G. & Tungha, G. (2011). Emergence of promising therapies in diabetes mellitus. Journal of Clinical Pharmacology, 51, 796–804.
  • Amaral, S., & Ramalho-Santos, J. (2014). Free radical biology and reproductive health in diabetes. In ‘Systems Biology of Free Radicals and Anti-Oxidants’. (Ed. I. Laher.) pp. 1–24. (Springer–Verlag: Berlin.)
  • American Diabetes Association. 2. Classification and diagnosis of diabetes: Standards of Medical Care in Diabetes (2019). Diabetes Care 2019; 42(Suppl. 1): S13–S28.
  • Amidu, N., Owiredu, W. K., Alidu, H., Sarpong, C., Gyasisarpong, C. K. & Quaye, L. (2013). Association between metabolic syndrome and sexual dysfunction among men with clinically diagnosed diabetes. Diabetology and Metabolic Syndrome, 5, 242–250.
  • Baccetti, B., Marca, L. A. & Piomboni, P. (2002). Insulin-dependent diabetes in men is associated with hypothalamo-pituitary derangement and with impairment in semen quality. Human Reproduction, 17, 2673-2677.
  • Bindu, B. & Podikunju, B. (2015). Performance evaluation of onion (Allium Cepa L. Var. Cepa) varieties for their suitability in kollam district. International Journal of Research in Agricultural Science, l (1), 18–20.
  • Butler, A. E., Janson, J., Bonner‑Weir, S., Ritzel, R., Rizza, R. A. & Butler, P. C. (2003). Beta‑cell deficit and increased beta‑cell apoptosis in humans with type 2 diabetes. Diabetes, 52, 102–110.
  • Cavallini, G. (2006). Male idiopathic oligoasthenoteratozoospermia. Asian Journal of Andrology. 8, 143–157.
  • Chae, M. R., Kang, S. J., Lee, K. P., Choi, B. R., Kim, H. K., Park, J. K., Kim, C. Y. & Lee, S.W. (2017). Onion (Allium cepa L.) peel extract (OPE) regulates human sperm motility via protein kinase C-mediated activation of the human voltage-gated proton channel. Andrology, 5(5), 979–989.
  • Cooke, D. W. & Plotnick, L. (2008). Type 1 diabetes mellitus in pediatrics. Pediatric Review, 29, 374–384.
  • Coskun, O., Kanter, M., Korkmaz, A. & Oter, S. (2005). Quercetin; a flavonoid antioxidant, prevents and protects streptozotocin-induced oxidative stress and beta-cell damage in rat pancreas. Pharmacology Research, 51, 117-123.
  • de Ancos, B., Colina-Coca, C., Gonzalex-Pena, D. & Sanchez-Moreno, C. (2015). Bioactive compounds from vegetable and fruit by-products. In Biotechnology of Bioactive Compounds. Sources and Applications. Section I, V. K. Gupta and M. G. Tuohy, Eds., pp. 3–36,Wiley Blackwell, 2015.
  • Dias, A. S., Porawski, M., Alonso, M., Marroni, N., Collado, P. S. & Gonzalez-Gallego, J. (2005). Quercetin decreases oxidative stress, NF-kappaB activation, and iNOS overexpression in liver of streptozotocin-induced diabetic rats. Journal of Nutrition, 135, 2299-2304.
  • Edeoga, H. O., Okwu, D. E. & Mbaebie, B. O. (2005). Phytochemical constituents of some Nigerian medicinal plants. African Journal of Biotechnology, 4 (7), 685-688.
  • Eizirik, D. L., Colli, M. L. & Ortis, F. (2009). The role of inflammation in insulitis and beta‑cell loss in type 1 diabetes. Nature Reviews Endocrinology, 5, 219–26.
  • Flesch, F. M. & Gadella, B. M. (2000). Dynamics of the mammalian sperm plasma membrane in the process of fertilization. Biochimica et Biophysica Acta, 1469, 197–235.
  • Folli, F., D. Corradi, P. Fanti, A. Davalli, A. Paez, A. Giaccari, C. Perego & G. Muscogiuri. (2011). The Role of Oxidative Stress in the Pathogenesis of Type 2 Diabetes Mellitus Micro- and Macrovascular Complications: Avenues for a Mechanistic-Based Therapeutic Approach. Current Diabetes Review, 7 (5), 313-324.
  • Freitas, J. P., Filipe, P. M. & Rodrigo, F. G. (1997). Lipid peroxidation intype 2 normolipidemic diabetic patients. Diabetes Research and Clinical Practice, 36, 71–75.
  • Ghanbari, E., Nejati, V., Najafi, G., Khazaei, M. & Babaei, M. (2015). Study on the effect of royal jelly on reproductive parameters in streptozotocin-induced diabetic rats. Internal Journal of Fertility and Sterility, 1, 113–120.
  • Griffiths, G., Trueman, L., Crowther, T., Thomas, B. & Smith, B. (2002). Onions—a global benefit to health. Phytotherapy Research, 16(7), 603–615.
  • Harrison, R. A. & Gadella, B. M. (2005). Bicarbonate‑induced membrane processing in sperm capacitation. Theriogenology, 63, 342–51.
  • Jequier, A. M. (2010). Semen analysis: a new manual and its application to the understanding of semen and its pathology. Asian Journal of Andrology, 12(1), 11–13.
  • Ji, Y. J., Yeni, L., Min, S. M., Ji, Y. K. & Oran, K. (2011). Effect of quercetin derivatives on diabetic animals. Nutrition & Metabolism, 8, 18-25.
  • Kahn, S. E., Hull, R. L. & Utzschneider, K. M. (2006). Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature. 444, 840–846.
  • Kameswara, R. B., Kesavulu, M. M., Guiri, R. & Apparao, C. H. (1999). Hepatic key enzyme in experimental diabetes. Journal of Ethnopharmacology, 91 (1) , 109-113.
  • Kanter, M., Aktas, C. & Erboga, M. (2013). Curcumin attenuates testicular damage, apoptotic germcell death, and oxidative stress in streptozotocin ‐induced diabetic rats. Molecular Nutrition and Food Research, 57, 1578-1585.
  • Khaki, A., Fathiazad, F., Nouri, M., Maleki, N. A., Khamnei, H. J. & Ahmadi, P. (2010). Beneficial effectsof quercetin on sperm parameters in streptozotocin‐induced diabetic male rats. Phytotherapy Research, 24, 1285-1291.
  • Kilarkaje, N., Al‑Hussaini, H. & Al‑Bader, M. M. (2014). Diabetes‑induced DNA damage and apoptosis are associated with poly (ADP ribose) polymerase 1 inhibition in the rat testis. European Journal of Pharmacology, 737, 29–40.
  • Kim, S. T. & Moley, K. H. (2008). Paternal effect on embryo quality in diabetic mice is related to poor sperm quality and associated with decreased glucose transporter expression. Reproduction. 136, 313–322.
  • Kobori, M., Masumoto, S., Akimoto, Y. & Takahashi, Y. (2009). Dietary quercetin alleviates diabetic symptoms and reduces streptozotocin-induced disturbance of hepatic gene expression in mice. Molecular Nutrition and Food Research, 53, 859-868.
  • 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. Fertility and Sterility, 2, 47–54.
  • Lee, B. K. & Jung, Y. S. (2016). Allium cepa extract and quercetin protect neuronal cells from oxida¬tive stress via PKC-ε inactivation/ERK1/2 ac¬tivation. Oxidative Medicine and Cellular Longevity, 2016, 2495624.
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Ameliorative effects of Allium cepa Linn. scaly leaves extract on reproductive dysfunctions in streptozotocin-induced diabetic Wistar rats

Yıl 2020, Cilt: 4 Sayı: 3, 136 - 144, 30.12.2020
https://doi.org/10.30704/http-www-jivs-net.811491

Öz

Diabetes mellitus, an endocrine and metabolic disorder characterized by hyperglycemia and low blood insulin or target organs insensitivity to insulin affects life quality due to its complications. Infertility is a complication in diabetes. Various agents have been used for research on diabetes-induced infertility globally, but there are little documented treatments for diabetes associated infertility. Allium cepa scaly leaves extract (ACSLE) possess anti-oxidant and anti-diabetic activities. This study investigated the effects of ACSLE on reproductive dysfunctions in male diabetic rats. Twenty eight male rats were assigned to 4 groups (n=7): CT (control); DNT (streptozotocin, 60 mg/kg once, intraperitoneal), DT1 and DT2 (streptozotocin, 60 mg/kg once, intraperitoneal, ACSLE 125 and 250 mg/kg rat/day respectively). Organ samples were obtained after 2 weeks and testicular weights recorded. Fasting blood glucose was determined using a digital glucometer. Sperm count, motility, viability and morphology were assessed microscopically. Testes were histologically evaluated. Glucose levels were reduced in DT1 and DT2 compared with DNT. Testes weights increased in DT1and DT2 compared with DNT. Sperm concentration increased in DT1 and DT2 compared with DNT motility increased in DT1 and DT2 compared with DNT; viability increased significantly in DT1 and DT2 compared with DNT. Abnormal sperm morphology decreased in DT1 and DT2 compared with DNT. Testes showed degenerated cells in DNT and no lesions in DT1 and DT2. Reduced blood glucose, improved testicular functions and morphology showed that ACSLE ameliorated reproductive dysfunctions associated with streptozotocin-induced diabetes in male Wistar rats.

Kaynakça

  • Abou-Seif, M. A. & Youssef, A. (2004). Evaluation of some biochemical changes in diabetic patients. Clinica Chimica Acta, 346, 161–170.
  • 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. Pharmaceutical Biology, 1, 695–704.
  • Afifi, M., Almaghrabi, O. A. & Kadasa, N. M. (2015). Ameliorative effect of zinc oxide nanoparticles on antioxidants and sperm characteristics in streptozotocin- induced diabetic rat testes. Biomedical Research International, 2, 1–6.
  • Agarwal, A., Makker, K. & Sharma, R. (2008). Clinical relevance of oxidative stress in male factor infertility: An update. American Journal of Reproduction and Immunology, 59, 2–11.
  • Agbaje, I. M., Rogers, D. A., McVicar, C. M., McClure, N., Atkinson, A. B., Mallidis, C. & Lewis, S. E. M. (2007). Insulin dependant diabetes mellitus: implications for male reproductive function. Human Reproduction, 22, 1871–7.
  • Akbarzadeh, A., Norouzian, D., Mehrabi, M. R. Jamshidi, Sh., Farhangi, A., Allah Verdi, A., Mofidian, S. M. A. & Lame Rad, B. (2007). Induction of diabetes by streptozotocin in rats. Indian Journal of Clinical Biochemestry, 22 (2), 60-64.
  • Akkati, S., Sam, K. G. & Tungha, G. (2011). Emergence of promising therapies in diabetes mellitus. Journal of Clinical Pharmacology, 51, 796–804.
  • Amaral, S., & Ramalho-Santos, J. (2014). Free radical biology and reproductive health in diabetes. In ‘Systems Biology of Free Radicals and Anti-Oxidants’. (Ed. I. Laher.) pp. 1–24. (Springer–Verlag: Berlin.)
  • American Diabetes Association. 2. Classification and diagnosis of diabetes: Standards of Medical Care in Diabetes (2019). Diabetes Care 2019; 42(Suppl. 1): S13–S28.
  • Amidu, N., Owiredu, W. K., Alidu, H., Sarpong, C., Gyasisarpong, C. K. & Quaye, L. (2013). Association between metabolic syndrome and sexual dysfunction among men with clinically diagnosed diabetes. Diabetology and Metabolic Syndrome, 5, 242–250.
  • Baccetti, B., Marca, L. A. & Piomboni, P. (2002). Insulin-dependent diabetes in men is associated with hypothalamo-pituitary derangement and with impairment in semen quality. Human Reproduction, 17, 2673-2677.
  • Bindu, B. & Podikunju, B. (2015). Performance evaluation of onion (Allium Cepa L. Var. Cepa) varieties for their suitability in kollam district. International Journal of Research in Agricultural Science, l (1), 18–20.
  • Butler, A. E., Janson, J., Bonner‑Weir, S., Ritzel, R., Rizza, R. A. & Butler, P. C. (2003). Beta‑cell deficit and increased beta‑cell apoptosis in humans with type 2 diabetes. Diabetes, 52, 102–110.
  • Cavallini, G. (2006). Male idiopathic oligoasthenoteratozoospermia. Asian Journal of Andrology. 8, 143–157.
  • Chae, M. R., Kang, S. J., Lee, K. P., Choi, B. R., Kim, H. K., Park, J. K., Kim, C. Y. & Lee, S.W. (2017). Onion (Allium cepa L.) peel extract (OPE) regulates human sperm motility via protein kinase C-mediated activation of the human voltage-gated proton channel. Andrology, 5(5), 979–989.
  • Cooke, D. W. & Plotnick, L. (2008). Type 1 diabetes mellitus in pediatrics. Pediatric Review, 29, 374–384.
  • Coskun, O., Kanter, M., Korkmaz, A. & Oter, S. (2005). Quercetin; a flavonoid antioxidant, prevents and protects streptozotocin-induced oxidative stress and beta-cell damage in rat pancreas. Pharmacology Research, 51, 117-123.
  • de Ancos, B., Colina-Coca, C., Gonzalex-Pena, D. & Sanchez-Moreno, C. (2015). Bioactive compounds from vegetable and fruit by-products. In Biotechnology of Bioactive Compounds. Sources and Applications. Section I, V. K. Gupta and M. G. Tuohy, Eds., pp. 3–36,Wiley Blackwell, 2015.
  • Dias, A. S., Porawski, M., Alonso, M., Marroni, N., Collado, P. S. & Gonzalez-Gallego, J. (2005). Quercetin decreases oxidative stress, NF-kappaB activation, and iNOS overexpression in liver of streptozotocin-induced diabetic rats. Journal of Nutrition, 135, 2299-2304.
  • Edeoga, H. O., Okwu, D. E. & Mbaebie, B. O. (2005). Phytochemical constituents of some Nigerian medicinal plants. African Journal of Biotechnology, 4 (7), 685-688.
  • Eizirik, D. L., Colli, M. L. & Ortis, F. (2009). The role of inflammation in insulitis and beta‑cell loss in type 1 diabetes. Nature Reviews Endocrinology, 5, 219–26.
  • Flesch, F. M. & Gadella, B. M. (2000). Dynamics of the mammalian sperm plasma membrane in the process of fertilization. Biochimica et Biophysica Acta, 1469, 197–235.
  • Folli, F., D. Corradi, P. Fanti, A. Davalli, A. Paez, A. Giaccari, C. Perego & G. Muscogiuri. (2011). The Role of Oxidative Stress in the Pathogenesis of Type 2 Diabetes Mellitus Micro- and Macrovascular Complications: Avenues for a Mechanistic-Based Therapeutic Approach. Current Diabetes Review, 7 (5), 313-324.
  • Freitas, J. P., Filipe, P. M. & Rodrigo, F. G. (1997). Lipid peroxidation intype 2 normolipidemic diabetic patients. Diabetes Research and Clinical Practice, 36, 71–75.
  • Ghanbari, E., Nejati, V., Najafi, G., Khazaei, M. & Babaei, M. (2015). Study on the effect of royal jelly on reproductive parameters in streptozotocin-induced diabetic rats. Internal Journal of Fertility and Sterility, 1, 113–120.
  • Griffiths, G., Trueman, L., Crowther, T., Thomas, B. & Smith, B. (2002). Onions—a global benefit to health. Phytotherapy Research, 16(7), 603–615.
  • Harrison, R. A. & Gadella, B. M. (2005). Bicarbonate‑induced membrane processing in sperm capacitation. Theriogenology, 63, 342–51.
  • Jequier, A. M. (2010). Semen analysis: a new manual and its application to the understanding of semen and its pathology. Asian Journal of Andrology, 12(1), 11–13.
  • Ji, Y. J., Yeni, L., Min, S. M., Ji, Y. K. & Oran, K. (2011). Effect of quercetin derivatives on diabetic animals. Nutrition & Metabolism, 8, 18-25.
  • Kahn, S. E., Hull, R. L. & Utzschneider, K. M. (2006). Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature. 444, 840–846.
  • Kameswara, R. B., Kesavulu, M. M., Guiri, R. & Apparao, C. H. (1999). Hepatic key enzyme in experimental diabetes. Journal of Ethnopharmacology, 91 (1) , 109-113.
  • Kanter, M., Aktas, C. & Erboga, M. (2013). Curcumin attenuates testicular damage, apoptotic germcell death, and oxidative stress in streptozotocin ‐induced diabetic rats. Molecular Nutrition and Food Research, 57, 1578-1585.
  • Khaki, A., Fathiazad, F., Nouri, M., Maleki, N. A., Khamnei, H. J. & Ahmadi, P. (2010). Beneficial effectsof quercetin on sperm parameters in streptozotocin‐induced diabetic male rats. Phytotherapy Research, 24, 1285-1291.
  • Kilarkaje, N., Al‑Hussaini, H. & Al‑Bader, M. M. (2014). Diabetes‑induced DNA damage and apoptosis are associated with poly (ADP ribose) polymerase 1 inhibition in the rat testis. European Journal of Pharmacology, 737, 29–40.
  • Kim, S. T. & Moley, K. H. (2008). Paternal effect on embryo quality in diabetic mice is related to poor sperm quality and associated with decreased glucose transporter expression. Reproduction. 136, 313–322.
  • Kobori, M., Masumoto, S., Akimoto, Y. & Takahashi, Y. (2009). Dietary quercetin alleviates diabetic symptoms and reduces streptozotocin-induced disturbance of hepatic gene expression in mice. Molecular Nutrition and Food Research, 53, 859-868.
  • 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. Fertility and Sterility, 2, 47–54.
  • Lee, B. K. & Jung, Y. S. (2016). Allium cepa extract and quercetin protect neuronal cells from oxida¬tive stress via PKC-ε inactivation/ERK1/2 ac¬tivation. Oxidative Medicine and Cellular Longevity, 2016, 2495624.
  • Machavarapu, M., Sindiri, M. K. & Vangalapati, M. (2017). Optimization of Physico-chemical Parameters for the Extraction of Flavonoids and Phenolic Components from the Skin of Allium cepa. Optimization. Journal of Physiology, 2(7), 110-121.
  • Mahesh, T. & Menon, V. P. (2004). Quercetin allievates oxidative stress in streptozotocin-induced diabetic rats. Phytotherapy Research, 18, 123-127.
  • Maiti, R., Jana, D., Das, U. K. & Ghosh, D. (2004). Antidiabetic effect of aqueous extract of seed of tamarindus indica in streptozotocin induced diabetic rats. Journal of Ethnopharmacology, 92, 85-91.
  • Marefati, N., Eftekhar, N., Kaveh, M., Boskabadi, J., Beheshti, F., Boskabady, M. H. (2018). The Effect of Allium cepa Extract on Lung Oxidant, Boskabadi,Antioxidant, and Immunological Biomarkers in Ovalbumin-Sensitized Rats. Medical Principles and Practice, 27, 122–128.
  • Marti, E., Mara, L., Marti, J. I., Muiño-Blanco, T. & Cebrián-Pérez, J. A. (2007). Seasonal variations in antioxidant enzyme activity in ram seminal plasma. Theriogenology. 67, 1446–1454.
  • Maxwell, S. R. J. & Lip, G. Y. H. (1997). Free radicals and antioxidants in cardiovascular disease. British Journal of Clinical Pharmacology, 44,307-317.
  • Melendez-Ramirez, L. Y., Richards, R. J. & Cefalu, W. T. (2010). Complications of type 1 diabetes. Journal of Endocrinology. 39, 351- 400.
  • Muthukumaran, J., Ramachandran, V., Ranga, R. A., Baojun, X., Stephen, S. M. C. (2018). Guava Leaf Extract Diminishes Hyperglycemia and Oxidative Stress, prevents𝛽-Cell Death, Inhibits Inflammation, and Regulates NF-kB Signaling Pathway in STZ Induced Diabetic Rats. Biomedical Research International, 5, 1-14.
  • Navarro-Casado, L., Juncos-Tobarra, M. A., Cha´fer-Rudilla, M., de Onzono, L. I., Bla´zquez-Cabrera, J. A. & Miralles-Garcı´a, J. M. (2010). Effect of experimental diabetes and STZ on male fertility capacity. Study in rats. Andrology, 31, 584–592.
  • Nile, A., Gansukh, E., Park, G. S., Kim, D. H. & Hariram Nile, S. (2020). Novel insights on the multi-functional properties of flavonol glucosides from red onion (Allium cepa L) solid waste- In vitro and in silico approach. Food Chemistry. 127650, https://doi.org/10.1016/j. foodchem.2020.127650
  • O.E.C.D. (Organization for Economic Co-operation and Development). (2008): OECD guidelines 407 for the testing of chemicals: Repeated Dose 28- day oral toxicity studies in rodents. https://ntp.niehs.nih.gov/iccvam/suppdocs/feddocs/oecd/oecdtg407-2008.pdf
  • Oliveira, P. F., Alves, M. G., Rato, L., Laurentino, S., Silva, J., Sa´, R., Barros, A., Sousa, M., Carvalho, R. A., Cavaco, J. E. & Socorro, S. (2012). Effect of insulin deprivation on metabolism and metabolismassociated gene transcript levels of in vitro cultured human Sertoli cells. Biochimica et Biophysica Acta, 1820, 84–89.
  • Oonk, R. B., Grootegoed, J. A. & van der Molen, H. J. (1985). Comparison of the effects of insulin and follitropin on glucose metabolism by Sertoli cells from immature rats. Molecular and Cellular Endocrinology, 42, 39-48.
  • Oonk, R. B. & Grootegoed, J. A. (1987). Identification of insulin receptors on rat Sertoli cells. Molecular and Cellular Endocrinology, 49, 51–62.
  • Palsamy, P., Sivakumar, S. & Subramanian, S. (2010). Resveratrol attenuates hyperglycemia-mediated oxidative stress, proinflammatory cytokines and protects hepatocytes ultrastructure in streptozotocin-nicotinamide-induced experimental diabetic rats. Chemico-Biologic Interaction, 186 (2), 200-210.
  • Park, J., Kim J. & Kim, M. K. (2007). Onion flesh and onion peel enhance antioxidant status in aged rats. Tokyo Journal of Nutrition Science and Vitaminology, 53, 21-29.
  • P´erez-Gregorio, R. M., Garc´ıa-Falc´on, M. S., Simal-G´andara, J., Rodrigues, A. S. & Almeida, D. P. F. (2010). Identification and quantification of flavonoids in traditional cultivars of red and white onions at harvest. Journal of Food Composition and Analysis, 23(6), 592–598.
  • Philippe, J., Raccah, D. (2009). Treating type 2 diabetes: how safe are current therapeutic agents? International Journal of Clinical Practice, 63, 321–332.
  • Prakash, D., Singh, B. N. & Upadhyay, G. (2007). Antioxidant and free radical scavenging activities of phenols fromonion (Allium cepa). Food Chemistry, 102(4), 1389–1393.
  • Ramachandran, A. (2014). Know the signs and symptoms of diabetes. Indian Journal of Medical Research, 140(5), 579-5816.
  • Rashid, K. & Sil P. C. (2015). Curcumin ameliorates testicular damage in diabetic rats by suppressing cellular stress-mediated mitochondria and endoplasmic reticulum-dependent apoptotic death. Biochimica Biophysica Acta, 3, 70–82.
  • Riserus, U., Willett, W. C. & Hu, F. B. (2009). Dietary fats and prevention of type 2 diabetes. Progress in Lipid Research, 48, 44–51.
  • Roldan, E., Sanchez-Moreno, C., de Anco, B. & Cano, M. P. (2008). Characterisation of onion (Alliumcepa L.) by-products as food ingredients with antioxidant and antibrowning properties. Food Chemistry, 108(3) , 907–916.
  • Rupeshkumar, M., Kavitha, K. & Haldar, P. K. (2014). The role of herbal plants in the diabetes mellitus therapy: an overview. International Journal of Applied Pharmacology, 6, 1–3.
  • Saeedi, P., Petersohn, I., Malanda, B., Karuranga, S., Unwin, N., Colagiuri, S., Guariguata, L., Motala, A. A., Ogurtsova, K., Shaw J. E., Bright, D. & Williams, R. (2019). Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9th edition. Diabetes Research and Clinical Practice, 157 (2019) 107843.
  • Santas, J., Almajano, M. P. & Carb´o, R. (2010). Antimicrobial and antioxidant activity of crude onion (Allium cepa, L.) extracts. International Journal of Food Science and Technology, 45(2) , 403–409.
  • Saumya, S. & Basha, P. M. (2016). Fluoride exposure aggravates the testicular damage and sperm quality in diabetic mice: protective role of Ginseng and Banaba. Biological Trace Element Research, 2, 1–14.
  • Scarano, W. R., Messias, A. G., Oliva, S. U., Klinefelter, G. R. & Kempinas, W. G. (2006). Sexual behaviour, sperm quantity and quality after short-term streptozotocin-induced hyperglycaemia in rats. International Journal of Andrology, 29, 482-488.
  • Schoeller, E. L., Albanna, G., Frolova, A. I. & Moley, K. H. (2012). Insulin rescues impaired spermatogenesis via the hypothalamicpituitary-gonadal axis in Akita diabetic mice and restores male fertility. Diabetes, 61, 1869–1878.
  • Sexton, W. J. & Jarow J. P. (1997). Effect of diabetes mellitus upon male reproductive function. Urology Research, 49, 508-513.
  • Shaath, N.A. & Flores, F. B. (1998). Egyptian onion oil, developments in Food Science. Journal of Nutrition, 40, 443-453.
  • Slimestad, R., Fossen, T. & V˚agen, I. M. (2007). Reviews. Onions: a source of unique dietary flavonoids. Journal of Agriculture and Food Chemistry, 55 (25), 10067–10080.
  • Smith, C., K. A. Lombard, E. B. Peffley, W. Liu. (2003). Genetic analysis of quercetin in onion (Allium cepa L.) 'Lady Raider'. Texas Journal of Agriculture and Natural Resources, 16, 24-28.
  • Tamtaji, O. R., Hossan, H., Sagyed, A. T., Mohamed, B., Seyed, M. T., Moshen, T. & Reza, A. (2017). Protective effects of red onion ethanolic extract on learning and memory impairments in animal of diabetes. Journal of Medicine, 6(3) , 249-257.
  • Tavares, R. S., Portela Joana, M. D., Sousa, M. I., MotaPaula, C., Ramalho-Santos, J. & Amaral, S. (2017). High glucose levels affect spermatogenesis: an in vitro approach. Reproduction Fertility and Development, 29(7), 1369 – 1378.
  • Tremellen, K. (2008). Oxidative stress and male infertility—a clinical perspective. Human Reproduction Update, 14 (3), 243–258.
  • Tsounapi, P., Honda, M., Dimitriadis, F., Kawamoto, B., Hikita, K., Muraoka, K., Saito, M., Sofikitis, N. & Takenaka, A. (2016). Impact of antioxidants on seminal vesicles function and fertilizing potential in diabetic rats. Asian Journal of Andrology, 2, 1–10.
  • Yanagimachi, R. (1994). Mammalian fertilization. Physiology of Reproduction, 1, 189–317.
Toplam 76 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Veteriner Cerrahi
Bölüm Araştırma Makaleleri
Yazarlar

Olushola Adeleye 0000-0002-2767-5564

Emmanuel Okoh Bu kişi benim

Adenike Adeleye Bu kişi benim

Fakilahyel Musa Mshelbwala Bu kişi benim

Abiodun Adetomiwa Bu kişi benim

James Apantaku Bu kişi benim

Ngozichukwu Aboajah Bu kişi benim

Ladoke Durotoye Bu kişi benim

Johnny Olufemi Olukunle Bu kişi benim

Yayımlanma Tarihi 30 Aralık 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 4 Sayı: 3

Kaynak Göster

APA Adeleye, O., Okoh, E., Adeleye, A., Mshelbwala, F. M., vd. (2020). Ameliorative effects of Allium cepa Linn. scaly leaves extract on reproductive dysfunctions in streptozotocin-induced diabetic Wistar rats. Journal of Istanbul Veterinary Sciences, 4(3), 136-144. https://doi.org/10.30704/http-www-jivs-net.811491

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