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The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System

Yıl 2026, Cilt: 13 Sayı: 1 , 134 - 149 , 30.03.2026
https://doi.org/10.34087/cbusbed.1623944
https://izlik.org/JA39XY72ZY

Öz

Aim; To assess the potential of gallic acid in stress-induced testicular damage and its impact on oxidative stress markers
Method; Twenty-eight male Sprague-Dawley rats were divided into four groups: Control (C), Gallic Acid (GA), Chronic Stress (CS), and Chronic Stress + Gallic Acid (CS+GA). The CS group experienced 6-hour immobilization stress for 15 days, while the GA group received 20 mg/kg oral gallic acid daily for 15 days. The CS+GA group received gallic acid before exposure to chronic immobility stress.
Histological, immunohistochemical and biochemical analyses were conducted, and data were analyzed using the SPSS program.
Results; Normal testicular morphology was observed in the Control and Gallic Acid groups. The Chronic Stress group exhibited impaired seminiferous tubules and increased oxidative stress markers. However, damage decreased in the Chronic Stress + Gallic Acid group, showing restored blood-testis barrier integrity.
Conclusion; Gallic acid demonstrated potential in reducing stress-induced testicular damage, suggesting its potential as a supportive agent in male infertility of unknown etiology.

Kaynakça

  • Acevedo-Rodriguez, A., Kauffman, A. S., Cherrington, B. D., Borges, C. S., Roepke, T. A., & Laconi, M. (2018). Emerging insights into hypothalamic-pituitary-gonadal axis regulation and interaction with stress signalling. J Neuroendocrinol, 30(10), e12590. https://doi.org/10.1111/jne.12590
  • Acikel-Elmas, M., Algilani, S. A., Sahin, B., Bingol Ozakpinar, O., Gecim, M., Koroglu, K., & Arbak, S. (2023). Apocynin Ameliorates Monosodium Glutamate Induced Testis Damage by Impaired Blood-Testis Barrier and Oxidative Stress Parameters. Life (Basel), 13(3). https://doi.org/10.3390/life13030822
  • Agarwal, A., Nallella, K. P., Allamaneni, S. S., & Said, T. M. (2004). Role of antioxidants in treatment of male infertility: an overview of the literature. Reprod Biomed Online, 8(6), 616-627. https://doi.org/10.1016/s1472-6483(10)61641-0
  • Aitken, R. J., Smith, T. B., Jobling, M. S., Baker, M. A., & De Iuliis, G. N. (2014). Oxidative stress and male reproductive health. Asian J Androl, 16(1), 31-38. https://doi.org/10.4103/1008-682x.122203
  • Al-Damegh, M. (2014). Stress-Induced Changes in Testosterone Secretion in Male Rats: Role of Oxidative Stress and Modulation by Antioxidants. Open Journal of Animal Sciences, 04, 70-78. https://doi.org/10.4236/ojas.2014.42010
  • Arai, M., Nakano, S., Okuno, F., Hirano, Y., Sujita, K., Kobayashi, T., Ishii, H., & Tsuchiya, M. (1989). Endotoxin-induced hypercoagulability: a possible aggravating factor of alcoholic liver disease. Hepatology, 9(6), 846-851. https://doi.org/10.1002/hep.1840090609
  • Behairy, A., El-Sharkawy, N. I., Saber, T. M., Soliman, M. M., Metwally, M. M. M., Abd El-Rahman, G. I., Abd-Elhakim, Y. M., & El Deib, M. M. (2020). The Modulatory Role of Vitamin C in Boldenone Undecylenate Induced Testicular Oxidative Damage and Androgen Receptor Dysregulation in Adult Male Rats. Antioxidants (Basel), 9(11). https://doi.org/10.3390/antiox9111053
  • Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem, 72, 248-254. https://doi.org/10.1006/abio.1976.9999 Cardoso, J. P., Cocuzza, M., & Elterman, D. (2019). Optimizing male fertility: oxidative stress and the use of antioxidants. World J Urol, 37(6), 1029-1034. https://doi.org/10.1007/s00345-019-02656-3
  • Cetinel, S., Ercan, F., Cikler, E., Contuk, G., & Sener, G. (2005). Protective effect of melatonin on water avoidance stress induced degeneration of the bladder. J Urol, 173(1), 267-270. https://doi.org/10.1097/01.ju.0000145891.35810.56
  • Chhillar, R., & Dhingra, D. (2013). Antidepressant-like activity of gallic acid in mice subjected to unpredictable chronic mild stress. Fundam Clin Pharmacol, 27(4), 409-418. https://doi.org/10.1111/j.1472-8206.2012.01040.x Chrousos, G. P. (2009). Stress and disorders of the stress system. Nat Rev Endocrinol, 5(7), 374-381. https://doi.org/10.1038/nrendo.2009.106
  • Chudzik, R., Jarosz, K., Gołębiowska, M., & Gołębiowska, B. (2017). Stress disease of the 21st century?. https://doi.org/10.5281/zenodo.839685.
  • Cikler, E., Ercan, F., Cetinel, S., Contuk, G., & Sener, G. (2005). The protective effects of melatonin against water avoidance stress-induced mast cell degranulation in dermis. Acta Histochem, 106(6), 467-475. https://doi.org/10.1016/j.acthis.2004.10.001
  • Esposito, P., Chandler, N., Kandere, K., Basu, S., Jacobson, S., Connolly, R., Tutor, D., & Theoharides, T. C. (2002). Corticotropin-releasing hormone and brain mast cells regulate blood-brain-barrier permeability induced by acute stress. J Pharmacol Exp Ther, 303(3), 1061-1066. https://doi.org/10.1124/jpet.102.038497
  • Fuchs, E., & Flïugge, G. (2006). Experimental animal models for the simulation of depression and anxiety. Dialogues Clin Neurosci, 8(3), 323-333. https://doi.org/10.31887/DCNS.2006.8.3/efuchs Hamada, A., Esteves, S. C., Nizza, M., & Agarwal, A. (2012). Unexplained male infertility: diagnosis and management. Int Braz J Urol, 38(5), 576-594. https://doi.org/10.1590/s1677-55382012000500002
  • Hervé, J. C., Derangeon, M., Sarrouilhe, D., & Bourmeyster, N. (2014). Influence of the scaffolding protein Zonula Occludens (ZOs) on membrane channels. Biochim Biophys Acta, 1838(2), 595-604. https://doi.org/10.1016/j.bbamem.2013.07.006
  • Johnsen, S. G. (1970). Testicular biopsy score count--a method for registration of spermatogenesis in human testes: normal values and results in 335 hypogonadal males. Hormones, 1(1), 2-25. https://doi.org/10.1159/000178170
  • Joo, J. S., Park, K., Ahn, K. Y., & Park, Y. I. (2006). The effect of long-term immobilization stress on spermatogenesis and testosterone production. Korean Journal of Urology, 47, 1197-1203.
  • Kırmızıkan, S., Karip, B. Z., Beyaztaş, H., Güler, E. M., Pasin, Ö., & Çikler, E. (2025). Ultrastructural testicular damage by water avoidance stress: therapeutic effects of nobiletin. Biotech Histochem, 100(4), 168-178. https://doi.org/10.1080/10520295.2025.2486454
  • Konturek, P. C., Brzozowski, T., & Konturek, S. J. (2011). Stress and the gut: pathophysiology, clinical consequences, diagnostic approach and treatment options. J Physiol Pharmacol, 62(6), 591-599.
  • Lobo, V., Patil, A., Phatak, A., & Chandra, N. (2010). Free radicals, antioxidants and functional foods: Impact on human health. Pharmacogn Rev, 4(8), 118-126. https://doi.org/10.4103/0973-7847.70902
  • M. B. AYCAN Et Al. , O. S. v. A., " Erciyes Üniversitesi Sağlık Bilimleri Dergisi , vol.9, no.1, pp.49-53, 2000 Marin, M. T., Cruz, F. C., & Planeta, C. S. (2007). Chronic restraint or variable stresses differently affect the behavior, corticosterone secretion and body weight in rats. Physiol Behav, 90(1), 29-35. https://doi.org/10.1016/j.physbeh.2006.08.021
  • Moreno, J. M., Rodríguez Gómez, I., Wangensteen, R., Osuna, A., Bueno, P., & Vargas, F. (2005). Cardiac and renal antioxidant enzymes and effects of tempol in hyperthyroid rats. Am J Physiol Endocrinol Metab, 289(5), E776-783. https://doi.org/10.1152/ajpendo.00611.2004
  • Musch, M. W., Walsh-Reitz, M. M., & Chang, E. B. (2006). Roles of ZO-1, occludin, and actin in oxidant-induced barrier disruption. Am J Physiol Gastrointest Liver Physiol, 290(2), G222-231. https://doi.org/10.1152/ajpgi.00301.2005
  • Mustafa, S., Wei, Q., Ennab, W., Lv, Z., Nazar, K., Siyal, F. A., Rodeni, S., Kavita, N. M. X., & Shi, F. (2019). Resveratrol Ameliorates Testicular Histopathology of Mice Exposed to Restraint Stress. Animals (Basel), 9(10). https://doi.org/10.3390/ani9100743
  • Olukole, S. G., Ola-Davies, E. O., Lanipekun, D. O., & Oke, B. O. (2020). Chronic exposure of adult male Wistar rats to bisphenol A causes testicular oxidative stress: Role of gallic acid. Endocr Regul, 54(1), 14-21. https://doi.org/10.2478/enr-2020-0003
  • Oyola, M. G., & Handa, R. J. (2017). Hypothalamic-pituitary-adrenal and hypothalamic-pituitary-gonadal axes: sex differences in regulation of stress responsivity. Stress, 20(5), 476-494. https://doi.org/10.1080/10253890.2017.1369523
  • Poritz, L. S., Garver, K. I., Green, C., Fitzpatrick, L., Ruggiero, F., & Koltun, W. A. (2007). Loss of the tight junction protein ZO-1 in dextran sulfate sodium induced colitis. J Surg Res, 140(1), 12-19. https://doi.org/10.1016/j.jss.2006.07.050
  • Rajan, V. K., & Muraleedharan, K. (2017). A computational investigation on the structure, global parameters and antioxidant capacity of a polyphenol, Gallic acid. Food Chem, 220, 93-99. https://doi.org/10.1016/j.foodchem.2016.09.178
  • Ramkumar, K. M., Vijayakumar, R. S., Vanitha, P., Suganya, N., Manjula, C., Rajaguru, P., Sivasubramanian, S., & Gunasekaran, P. (2014). Protective effect of gallic acid on alloxan-induced oxidative stress and osmotic fragility in rats. Hum Exp Toxicol, 33(6), 638-649. https://doi.org/10.1177/0960327113504792
  • Ribeiro, C. T., De Souza, D. B., Costa, W. S., Sampaio, F. J. B., & Pereira-Sampaio, M. A. (2018). Immediate and late effects of chronic stress in the testes of prepubertal and adult rats. Asian J Androl, 20(4), 385-390. https://doi.org/10.4103/aja.aja_68_17
  • Smith, C. (2012). Using Rodent Models to Simulate Stress of Physiologically Relevant Severity: When, Why and How. In X. Qian (Ed.), Glucocorticoids - New Recognition of Our Familiar Friend. IntechOpen. https://doi.org/10.5772/52045
  • Sogut, I., Oglakci, A., Kartkaya, K., Ol, K. K., Sogut, M. S., Kanbak, G., & Inal, M. E. (2015). Effect of boric acid on oxidative stress in rats with fetal alcohol syndrome. Exp Ther Med, 9(3), 1023-1027. https://doi.org/10.3892/etm.2014.2164
  • Theoharides, T. C., & Cochrane, D. E. (2004). Critical role of mast cells in inflammatory diseases and the effect of acute stress. J Neuroimmunol, 146(1-2), 1-12. https://doi.org/10.1016/j.jneuroim.2003.10.041
  • Zhou, J., Xi, Y., Zhang, J., Tang, J., Zhou, X., Chen, J., Nie, C., Zhu, Z., & Ma, B. (2020). Protective effect of Dioscorea zingiberensis ethanol extract on the disruption of blood-testes barrier in high-fat diet/streptozotocin-induced diabetic mice by upregulating ZO-1 and Nrf2. Andrologia, 52(3), e13508. https://doi.org/10.1111/and.13508

Gallik Asitin Hareketsizlik Stresinin Erkek Üreme Sisteminde Oluşturduğu Hasar Üzerine Antioksidan Etkisi

Yıl 2026, Cilt: 13 Sayı: 1 , 134 - 149 , 30.03.2026
https://doi.org/10.34087/cbusbed.1623944
https://izlik.org/JA39XY72ZY

Öz

Öz
Giriş ve Amaç: Bu çalışmada, gallik asidin stres kaynaklı testis hasarına karşı olası koruyucu etkisi ile oksidatif stres belirteçleri üzerindeki rolü araştırılmıştır.
Gereç ve Yöntemler: Toplam 28 adet erkek Sprague-Dawley sıçan dört gruba ayrıldı: Kontrol (C), Gallik Asit (GA), Kronik Stres (CS) ve Kronik Stres + Gallik Asit (CS+GA). CS grubuna, 15 gün boyunca her gün 6 saat süren hareketsizlik stresi uygulandı. GA grubuna 15 gün boyunca günde 20 mg/kg gallik asit oral yolla verildi. CS+GA grubuna gallik asit, stres protokolünden hemen önce verildi. Histolojik, immünohistokimyasal ve biyokimyasal analizler yapıldı ve elde edilen veriler SPSS programı kullanılarak analiz edildi.
Bulgular: Kontrol ve GA gruplarında normal testis morfolojisi gözlemlendi. CS grubunda, seminifer tübüllerde bozulma ve oksidatif stres belirteçlerinde artış saptandı. CS+GA grubunda ise bu hasarın azaldığı ve kan-testis bariyerinin bütünlüğünün kısmen korunduğu tespit edildi.
Sonuç: Gallik asit, stres kaynaklı testis hasarını azaltmada koruyucu etki göstermiştir. Bu etkisiyle, nedeni açıklanamayan erkek infertilitesine yönelik destekleyici bir ajan olarak potansiyel taşıyabilir.

Kaynakça

  • Acevedo-Rodriguez, A., Kauffman, A. S., Cherrington, B. D., Borges, C. S., Roepke, T. A., & Laconi, M. (2018). Emerging insights into hypothalamic-pituitary-gonadal axis regulation and interaction with stress signalling. J Neuroendocrinol, 30(10), e12590. https://doi.org/10.1111/jne.12590
  • Acikel-Elmas, M., Algilani, S. A., Sahin, B., Bingol Ozakpinar, O., Gecim, M., Koroglu, K., & Arbak, S. (2023). Apocynin Ameliorates Monosodium Glutamate Induced Testis Damage by Impaired Blood-Testis Barrier and Oxidative Stress Parameters. Life (Basel), 13(3). https://doi.org/10.3390/life13030822
  • Agarwal, A., Nallella, K. P., Allamaneni, S. S., & Said, T. M. (2004). Role of antioxidants in treatment of male infertility: an overview of the literature. Reprod Biomed Online, 8(6), 616-627. https://doi.org/10.1016/s1472-6483(10)61641-0
  • Aitken, R. J., Smith, T. B., Jobling, M. S., Baker, M. A., & De Iuliis, G. N. (2014). Oxidative stress and male reproductive health. Asian J Androl, 16(1), 31-38. https://doi.org/10.4103/1008-682x.122203
  • Al-Damegh, M. (2014). Stress-Induced Changes in Testosterone Secretion in Male Rats: Role of Oxidative Stress and Modulation by Antioxidants. Open Journal of Animal Sciences, 04, 70-78. https://doi.org/10.4236/ojas.2014.42010
  • Arai, M., Nakano, S., Okuno, F., Hirano, Y., Sujita, K., Kobayashi, T., Ishii, H., & Tsuchiya, M. (1989). Endotoxin-induced hypercoagulability: a possible aggravating factor of alcoholic liver disease. Hepatology, 9(6), 846-851. https://doi.org/10.1002/hep.1840090609
  • Behairy, A., El-Sharkawy, N. I., Saber, T. M., Soliman, M. M., Metwally, M. M. M., Abd El-Rahman, G. I., Abd-Elhakim, Y. M., & El Deib, M. M. (2020). The Modulatory Role of Vitamin C in Boldenone Undecylenate Induced Testicular Oxidative Damage and Androgen Receptor Dysregulation in Adult Male Rats. Antioxidants (Basel), 9(11). https://doi.org/10.3390/antiox9111053
  • Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem, 72, 248-254. https://doi.org/10.1006/abio.1976.9999 Cardoso, J. P., Cocuzza, M., & Elterman, D. (2019). Optimizing male fertility: oxidative stress and the use of antioxidants. World J Urol, 37(6), 1029-1034. https://doi.org/10.1007/s00345-019-02656-3
  • Cetinel, S., Ercan, F., Cikler, E., Contuk, G., & Sener, G. (2005). Protective effect of melatonin on water avoidance stress induced degeneration of the bladder. J Urol, 173(1), 267-270. https://doi.org/10.1097/01.ju.0000145891.35810.56
  • Chhillar, R., & Dhingra, D. (2013). Antidepressant-like activity of gallic acid in mice subjected to unpredictable chronic mild stress. Fundam Clin Pharmacol, 27(4), 409-418. https://doi.org/10.1111/j.1472-8206.2012.01040.x Chrousos, G. P. (2009). Stress and disorders of the stress system. Nat Rev Endocrinol, 5(7), 374-381. https://doi.org/10.1038/nrendo.2009.106
  • Chudzik, R., Jarosz, K., Gołębiowska, M., & Gołębiowska, B. (2017). Stress disease of the 21st century?. https://doi.org/10.5281/zenodo.839685.
  • Cikler, E., Ercan, F., Cetinel, S., Contuk, G., & Sener, G. (2005). The protective effects of melatonin against water avoidance stress-induced mast cell degranulation in dermis. Acta Histochem, 106(6), 467-475. https://doi.org/10.1016/j.acthis.2004.10.001
  • Esposito, P., Chandler, N., Kandere, K., Basu, S., Jacobson, S., Connolly, R., Tutor, D., & Theoharides, T. C. (2002). Corticotropin-releasing hormone and brain mast cells regulate blood-brain-barrier permeability induced by acute stress. J Pharmacol Exp Ther, 303(3), 1061-1066. https://doi.org/10.1124/jpet.102.038497
  • Fuchs, E., & Flïugge, G. (2006). Experimental animal models for the simulation of depression and anxiety. Dialogues Clin Neurosci, 8(3), 323-333. https://doi.org/10.31887/DCNS.2006.8.3/efuchs Hamada, A., Esteves, S. C., Nizza, M., & Agarwal, A. (2012). Unexplained male infertility: diagnosis and management. Int Braz J Urol, 38(5), 576-594. https://doi.org/10.1590/s1677-55382012000500002
  • Hervé, J. C., Derangeon, M., Sarrouilhe, D., & Bourmeyster, N. (2014). Influence of the scaffolding protein Zonula Occludens (ZOs) on membrane channels. Biochim Biophys Acta, 1838(2), 595-604. https://doi.org/10.1016/j.bbamem.2013.07.006
  • Johnsen, S. G. (1970). Testicular biopsy score count--a method for registration of spermatogenesis in human testes: normal values and results in 335 hypogonadal males. Hormones, 1(1), 2-25. https://doi.org/10.1159/000178170
  • Joo, J. S., Park, K., Ahn, K. Y., & Park, Y. I. (2006). The effect of long-term immobilization stress on spermatogenesis and testosterone production. Korean Journal of Urology, 47, 1197-1203.
  • Kırmızıkan, S., Karip, B. Z., Beyaztaş, H., Güler, E. M., Pasin, Ö., & Çikler, E. (2025). Ultrastructural testicular damage by water avoidance stress: therapeutic effects of nobiletin. Biotech Histochem, 100(4), 168-178. https://doi.org/10.1080/10520295.2025.2486454
  • Konturek, P. C., Brzozowski, T., & Konturek, S. J. (2011). Stress and the gut: pathophysiology, clinical consequences, diagnostic approach and treatment options. J Physiol Pharmacol, 62(6), 591-599.
  • Lobo, V., Patil, A., Phatak, A., & Chandra, N. (2010). Free radicals, antioxidants and functional foods: Impact on human health. Pharmacogn Rev, 4(8), 118-126. https://doi.org/10.4103/0973-7847.70902
  • M. B. AYCAN Et Al. , O. S. v. A., " Erciyes Üniversitesi Sağlık Bilimleri Dergisi , vol.9, no.1, pp.49-53, 2000 Marin, M. T., Cruz, F. C., & Planeta, C. S. (2007). Chronic restraint or variable stresses differently affect the behavior, corticosterone secretion and body weight in rats. Physiol Behav, 90(1), 29-35. https://doi.org/10.1016/j.physbeh.2006.08.021
  • Moreno, J. M., Rodríguez Gómez, I., Wangensteen, R., Osuna, A., Bueno, P., & Vargas, F. (2005). Cardiac and renal antioxidant enzymes and effects of tempol in hyperthyroid rats. Am J Physiol Endocrinol Metab, 289(5), E776-783. https://doi.org/10.1152/ajpendo.00611.2004
  • Musch, M. W., Walsh-Reitz, M. M., & Chang, E. B. (2006). Roles of ZO-1, occludin, and actin in oxidant-induced barrier disruption. Am J Physiol Gastrointest Liver Physiol, 290(2), G222-231. https://doi.org/10.1152/ajpgi.00301.2005
  • Mustafa, S., Wei, Q., Ennab, W., Lv, Z., Nazar, K., Siyal, F. A., Rodeni, S., Kavita, N. M. X., & Shi, F. (2019). Resveratrol Ameliorates Testicular Histopathology of Mice Exposed to Restraint Stress. Animals (Basel), 9(10). https://doi.org/10.3390/ani9100743
  • Olukole, S. G., Ola-Davies, E. O., Lanipekun, D. O., & Oke, B. O. (2020). Chronic exposure of adult male Wistar rats to bisphenol A causes testicular oxidative stress: Role of gallic acid. Endocr Regul, 54(1), 14-21. https://doi.org/10.2478/enr-2020-0003
  • Oyola, M. G., & Handa, R. J. (2017). Hypothalamic-pituitary-adrenal and hypothalamic-pituitary-gonadal axes: sex differences in regulation of stress responsivity. Stress, 20(5), 476-494. https://doi.org/10.1080/10253890.2017.1369523
  • Poritz, L. S., Garver, K. I., Green, C., Fitzpatrick, L., Ruggiero, F., & Koltun, W. A. (2007). Loss of the tight junction protein ZO-1 in dextran sulfate sodium induced colitis. J Surg Res, 140(1), 12-19. https://doi.org/10.1016/j.jss.2006.07.050
  • Rajan, V. K., & Muraleedharan, K. (2017). A computational investigation on the structure, global parameters and antioxidant capacity of a polyphenol, Gallic acid. Food Chem, 220, 93-99. https://doi.org/10.1016/j.foodchem.2016.09.178
  • Ramkumar, K. M., Vijayakumar, R. S., Vanitha, P., Suganya, N., Manjula, C., Rajaguru, P., Sivasubramanian, S., & Gunasekaran, P. (2014). Protective effect of gallic acid on alloxan-induced oxidative stress and osmotic fragility in rats. Hum Exp Toxicol, 33(6), 638-649. https://doi.org/10.1177/0960327113504792
  • Ribeiro, C. T., De Souza, D. B., Costa, W. S., Sampaio, F. J. B., & Pereira-Sampaio, M. A. (2018). Immediate and late effects of chronic stress in the testes of prepubertal and adult rats. Asian J Androl, 20(4), 385-390. https://doi.org/10.4103/aja.aja_68_17
  • Smith, C. (2012). Using Rodent Models to Simulate Stress of Physiologically Relevant Severity: When, Why and How. In X. Qian (Ed.), Glucocorticoids - New Recognition of Our Familiar Friend. IntechOpen. https://doi.org/10.5772/52045
  • Sogut, I., Oglakci, A., Kartkaya, K., Ol, K. K., Sogut, M. S., Kanbak, G., & Inal, M. E. (2015). Effect of boric acid on oxidative stress in rats with fetal alcohol syndrome. Exp Ther Med, 9(3), 1023-1027. https://doi.org/10.3892/etm.2014.2164
  • Theoharides, T. C., & Cochrane, D. E. (2004). Critical role of mast cells in inflammatory diseases and the effect of acute stress. J Neuroimmunol, 146(1-2), 1-12. https://doi.org/10.1016/j.jneuroim.2003.10.041
  • Zhou, J., Xi, Y., Zhang, J., Tang, J., Zhou, X., Chen, J., Nie, C., Zhu, Z., & Ma, B. (2020). Protective effect of Dioscorea zingiberensis ethanol extract on the disruption of blood-testes barrier in high-fat diet/streptozotocin-induced diabetic mice by upregulating ZO-1 and Nrf2. Andrologia, 52(3), e13508. https://doi.org/10.1111/and.13508
Toplam 34 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Biyokimya ve Hücre Biyolojisi (Diğer)
Bölüm Araştırma Makalesi
Yazarlar

İlayda Özge Polat 0000-0002-5904-9998

Kübra Bozali 0000-0003-2416-0773

Zeynep İnce 0000-0002-9278-8557

Seda Kırmızıkan 0000-0002-5652-778X

Eray Metin Güler 0000-0003-4351-1719

Esra Çikler 0000-0002-5756-5892

Gönderilme Tarihi 3 Şubat 2025
Kabul Tarihi 2 Haziran 2025
Yayımlanma Tarihi 30 Mart 2026
DOI https://doi.org/10.34087/cbusbed.1623944
IZ https://izlik.org/JA39XY72ZY
Yayımlandığı Sayı Yıl 2026 Cilt: 13 Sayı: 1

Kaynak Göster

APA Polat, İ. Ö., Bozali, K., İnce, Z., Kırmızıkan, S., Güler, E. M., & Çikler, E. (2026). The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System. Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi, 13(1), 134-149. https://doi.org/10.34087/cbusbed.1623944
AMA 1.Polat İÖ, Bozali K, İnce Z, Kırmızıkan S, Güler EM, Çikler E. The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System. CBU-SBED. 2026;13(1):134-149. doi:10.34087/cbusbed.1623944
Chicago Polat, İlayda Özge, Kübra Bozali, Zeynep İnce, Seda Kırmızıkan, Eray Metin Güler, ve Esra Çikler. 2026. “The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System”. Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi 13 (1): 134-49. https://doi.org/10.34087/cbusbed.1623944.
EndNote Polat İÖ, Bozali K, İnce Z, Kırmızıkan S, Güler EM, Çikler E (01 Mart 2026) The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System. Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi 13 1 134–149.
IEEE [1]İ. Ö. Polat, K. Bozali, Z. İnce, S. Kırmızıkan, E. M. Güler, ve E. Çikler, “The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System”, CBU-SBED, c. 13, sy 1, ss. 134–149, Mar. 2026, doi: 10.34087/cbusbed.1623944.
ISNAD Polat, İlayda Özge - Bozali, Kübra - İnce, Zeynep - Kırmızıkan, Seda - Güler, Eray Metin - Çikler, Esra. “The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System”. Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi 13/1 (01 Mart 2026): 134-149. https://doi.org/10.34087/cbusbed.1623944.
JAMA 1.Polat İÖ, Bozali K, İnce Z, Kırmızıkan S, Güler EM, Çikler E. The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System. CBU-SBED. 2026;13:134–149.
MLA Polat, İlayda Özge, vd. “The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System”. Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi, c. 13, sy 1, Mart 2026, ss. 134-49, doi:10.34087/cbusbed.1623944.
Vancouver 1.İlayda Özge Polat, Kübra Bozali, Zeynep İnce, Seda Kırmızıkan, Eray Metin Güler, Esra Çikler. The Antioxidant Effect Of Gallic Acid On The Damage Caused By Immobilization Stress To The Male Reproductive System. CBU-SBED. 01 Mart 2026;13(1):134-49. doi:10.34087/cbusbed.1623944