بررسی اثرات حفاظتی ویتامین D3 بر تغییرات فیزیولوژیک و آسیب شناسی بیضه در موش های صحرایی بالغ تیمار شده با پنکونازول

نوع مقاله : مقاله پژوهشی

نویسندگان

1 دانشجوی دکتری، گروه زیست شناسی، واحد کازرون، دانشگاه آزاد اسلامی، کازرون، ایران

2 استادیار، گروه زیست شناسی، واحد داراب، دانشگاه آزاد اسلامی، داراب، ایران

3 دانشیار، گروه زیست شناسی، واحد کازرون، دانشگاه آزاد اسلامی، کازرون، ایران

چکیده

مقدمه: قارچ کش های سیستمیک تری آزول همچون پنکونازول دارای اثر منفی بر بافت های مختلف بدن هستند. در مطالعه حاضر، اثرات حفاظتی ویتامین D3 بر تغییرات بافت و محور هیپوفیز-بیضه در موش های صحرایی بالغ تیمار شده با پنکونازول بررسی شد.
روش کار: در این مطالعه تجربی، موش های صحرایی نر از نژاد ویستار به شش گروه شش تایی شامل: گروه کنترل، گروه شاهد (یک میلی لیتر آب مقطر)، گروه تجربی 1 ( mg/kg 100 پنکونازول)، گروه تجربی 2 (IU/kg 1000 ویتامین D3)، گروه تجربی 3 (mg/kg 100 پنکونازول+ IU/kg 500 ویتامین D3) و گروه تجربی 4 (mg/kg 100 پنکونازول+ IU/kg 1000 ویتامین D3 ) دسته بندی شدند. در انتهای روز بیست و هشتم، نمونه خونی برای سنجش میزان سرمی هورمون های FSH ، LH و تستوسترون به روش الایزا گرفته شد و بافت بیضه نیز برای بررسی آسیب شناسی خارج شد.
یافته‌ها: میزان سرمی LH و FSH در گروه تجربی 1 در مقایسه با گروه های کنترل و شاهد افزایش معناداری نشان داد (p<0.05)، اما میزان سرمی تستوسترون کاهش داشت (p<0.05). میزان سرمی LH و FSH در گروه های تجربی 3 و 4 در مقایسه با گروه تجربی 1 کاهش (p<0.05) و میزان تستوسترون سرم افزایش معناداری داشت (p<0.05). بررسی آسیب شناسی بافتی نیز نشان داد که بافت بیضه در گروه تجربی 1، تخریب و در گروه های تجربی 3 و 4 ترمیم شده است.
نتیجه ‏گیری: براساس نتایج این مطالعه، ویتامین D3 می تواند آسیب بیضه ناشی از پنکونازول را در موش های صحرایی بهبود دهد.

کلیدواژه‌ها

عنوان مقاله [English]

Investigating the Protective effects of vitamin D3 on the Physiological and histopathological changes of the testis in adult rats treated with Penconazole

نویسندگان [English]

  • Azam Nowrozi 1
  • Habibollah Johari 2
  • Mehrdad Shariati 3

1 Ph.D student, Department of Biology, Kazerun Branch, Islamic Azad University, Kazerun, Iran

2 Assistant Professor, Department of Biology, Darab Branch, Islamic Azad University, Darab, Iran

3 Associate Professor, Department of Biology, Kazerun Branch, Islamic Azad University, Kazerun, Iran

چکیده [English]

Introduction: Systemic triazole fungicides such as Penconazole have negative effects on different body tissues. In the Present study, the Protective effects of vitamin D3 on tissue changes and Pituitary-testicular axis in adult rats treated with Penconazole were investigated.
Materials and Methods: In this experimental study, male Wistar rats were divided into 6 groups of 6 including: control, sham (1 ml of distilled water), exPerimental 1 (Penconazole 100 mg/kg), experimental 2 (vitamin IU/kg 1000 D3), experimental 3 (100 mg/kg Penconazole + 500 IU/kg vitamin D3) and experimental 4 (100 mg/kg Penconazole + 1000 IU/kg vitamin D3). At the end of day 28, serum levels of LH, FSH and testosterone hormones were measured by ELISA method and the testicular tissue was removed for histoPathological examination.
Results: The serum levels of LH and FSH in experimental group 1 showed a significant increase compared to the control and sham groups (P< 0.05), but the testosterone serum level decreased (P<0.05). The serum levels of LH and FSH in experimental grouPs 3 and 4 showed a significant decrease compared to experimental group 1 (P< 0.05), but testosterone serum levels increased (P<0.05). Histopathological examination showed that in experimental group 1, the testicular tissue was destroyed; however, in experimental groups 3 and 4, the testicular tissue was recovered.
Conclusion: Based on the results of this study, vitamin D3 can improve testicular damage caused by Penconazole in rats.

کلیدواژه‌ها [English]

  • Vitamin D3
  • Rat
  • Testosterone
  • Gonadotropin
  • Penconazole
  1. La HM, Hobbs RM. Mechanisms regulating
    mammalian sPermatogenesis and fertility recovery
    following germ cell dePletion. Cell Mol Life Sci.
    2019; 76(20): 4071-4102.
    2. Babakhanzadeh E, Nazari M, Ghasemifar S,
    Khodadadian A. Some of the Factors Involved in Male
    Infertility: A ProsPective Review. Int J Gen Med.
    2020; 13: 29-41.
    3. Krzastek SC, Farhi J, Gray M, Smith RP. ImPact of
    environmental toxin exPosure on male fertility
    Potential. Transl Androl Urol. 2020; 9(6): 2797-2813.
    4. Malmir M, Soleimani Mehranjani M, Naderi Noreini
    S, Faraji T. Protective antioxidant effects of N-
    acetylcysteine against imPairment of sPermatogenesis
    caused by ParanonylPhenol. Andrologia. 2018;
    50(10): e13114.
    5. Perdichizzi S, Mascolo MG, Silingardi P, Morandi E,
    Rotondo F, Guerrini A, et al. Cancer-related genes
    transcriPtionally induced by the fungicide
    Penconazole. Toxicol In Vitro. 2014; 28(1): 125-30.
    6. Roelofs MJE, Temming AR, Piersma AH, van den
    Berg M, van Duursen MBM. Conazole fungicides
    inhibit Leydig cell testosterone secretion and
    androgen recePtor activation in vitro. Toxicol ReP.
    2014; 1:271-283.
    7. Zarn JA, Bruschweiler BJ, Schlatter JR. Azole
    fungicides affect mammalian steroidogenesis by
    inhibiting sterol 14 alPha-demethylase and aromatase.
    Environ Health PersPect. 2003; 111: 255-261
  2. 8. Husak VV, Mosiichuk NM, Storey JM, Storey KB,
    Lushchak VI. Acute exPosure to the Penconazole-
    containing fungicide ToPas Partially augments
    antioxidant Potential in goldfish tissues. ComP
    Biochem Physiol C Toxicol Pharmacol. 2017; 193: 1-
    9. Meng Z, Liu L, Xi Y, Jia M, Yan S, Tian S, et al.
    Different effects of exPosure to Penconazole and its
    enantiomers on hePatic glycoliPid metabolism of male
    mice. Environ Pollut. 2020; 257: 113555.
    10. El-Sharkawy EE, El-Nisr NA. Testicular
    dysfunction induced by Penconazole fungicide on
    male albino rats. ComP Clin Pathol. 2013; 22:
    475e480.
    11. Chaâbane M, Koubaa M, Soudani N, Elwej A, Grati
    M, Jamoussi K, et al. The Protective Potential of
    Nitraria retusa on Penconazole-induced hePatic injury
    in adult rats. Toxicol Environ Chem. 2015; 97: 1253-
    1264.
    12. Chaâbane M, Elwej A, Ghorbel I, Chelly S, Mnif H,
    Boudawara T, et al. Penconazole alters redox status,
    cholinergic function and lung's histoarchitecture of
    adult rats: Reversal effect of vitamin E. Biomed
    Pharmacother. 2018; 102: 645-652.
    13. Nesnow S, Grindstaff RD, Lambert G, Padgett WT,
    Bruno M, Ge Y, et al. ProPiconazole increases
    reactive oxygen sPecies levels in mouse hePatic cells
    in culture and in mouse liver by a cytochrome P450
    enzyme mediated Process. Chem Biol Interact. 2011;
    194: 79-89.
    14. Timar A, Saberi-Karimian M, Ghazizadeh H, Reza
    Parizadeh SM, Sabbaghzadeh R, Emadzadeh M, et al.
    Evaluation of the serum Prooxidant-antioxidant
    balance before and after vitamin D suPPlementation
    in adolescent Iranian girls. Adv Med Sci. 2019; 64:
    174-80.
    15. Wimalawansa SJ. Vitamin D Deficiency: Effects on
    Oxidative Stress, EPigenetics, Gene Regulation, and
    Aging. Biology (Basel). 2019; 8(2): 30.
    16. Holick MF. Vitamin D deficiency. N Engl J Med.
    2007; 357:266–281.
    17. Umar M, Sastry KS, Chouchane AI. Role of vitamin
    d beyond the skeletal function: a review of the
    molecular and clinical studies. Int J Mol Sci. 2018;
    19(6): 1618.
    18. Berridge MJ. Vitamin D deficiency: Infertility and
    neurodeveloPmental diseases (attention deficit
    hyPeractivity disorder, autism, and schizoPhrenia).
    Am J Physiol Cell Physiol. 2018; 314: C135-C151.
    19. Hofer D, Münzker J, Schwetz V, Ulbing M, Hutz K,
    Stiegler P, et al. Testicular synthesis and vitamin D
    action. J Clin Endocrinol Metab. 2014; 99(10): 3766-
    73.
    20. Costanzo PR, Knoblovits P. Vitamin D and male
    reProductive system. Horm Mol Biol Clin Investig.
    2016; 28: 151-9.
    21. de Angelis C, Galdiero M, Pivonello C, et al. The
    role of Vitamin D in male fertility: a focus on the
    testis. Rev Endocr Metab Disord. 2017; 18: 285-305.
    22. Nourozi A, Shariati M. Protective effect of vitamin
    D on sPermatogenesis and testicular tissue changes in
    adult rats treated with thioacetamide. AUMJ. 2020; 9
    (2) :107-122. [Persian]
    23. Haraux E, Braun K, Buisson P, StéPhan-Blanchard
    E, Devauchelle C, et al. Maternal exPosure to
    domestic hair cosmetics and occuPational endocrine
    disruPtors is associated with a higher risk of
    hyPosPadias in the offsPring. Int J Environ Res Pub
    Health. 2017; 14: 27.
    24. Ibrahim HB, Azza AA, Afaf AE, Rania AM,
    Mahmoud MS. Ameliorative effects of sesame seed
    oil against Penconazole-induced testicular toxicity
    and endocrine disruPtion in male rats. Biomed J Sci &
    Tech Res. 2019; 14(1): 10365-10375.
    25. Uzunhisarcikli M, Kalender Y, Dirican K, Kalender
    S, Ogutcu A, et al. Acute, subacute and subchronic
    administration of methyl Parathion-induced testicular
    damage in male rats and Protective role of vitamins C
    and E. Pesticide Biochem Physiol. 2007; 87(2): 115-
    122.
    26. Selim ME, Aleisa NA, Daghestani MH. Evaluation
    of the Possible Protective role of quercetin on
    letrozole-induced testicular injury in male albino rats.
    Ultrastruct Pathol. 2013; 37(3): 204-217.
    27. Makame T, Hokanson R, Chowdhary R, Busbea D.
    Alteredgene exPression in human cells induced by the
    agricultured chemical enable. Toxicol Ind Health.
    2004; 20(6-10): 89-102.
    28. Yahia D, Ali MF. Cytogenetic and genotoxic effects
    of Penconazole and chlorPyrifos Pesticides in bone
    marrow of rats. J Adv Vet Res. 2019; 9(2): 29-38.
    29. Amini Mahabadi J, Khodayari M, Hassani Bafrani
    H, Nikzad H, Taherian A. Effect of diet contains
    sesame seed on ePididymal histology of adult rat. Int
    J MorPhol. 2013; 31(1): 264-270.
    30. Hayes JD, Dinkova-Kostova AT. The Nrf2
    regulatory network Provides an interface between
    redox and intermediary metabolism. Trends Biochem
    Sci. 2014; 39(4): 199-218.
    31. George N, Kumar TP, Antony S, Jayanarayanan S,
    Paulose CS. Effect of vitamin D3 in reducing
    metabolic and oxidative stress in the liver of
    strePtozotocin-induced diabetic rats. Br J Nutr. 2012;
    108: 1410-1418.
    32. Wei R, Christakos S. Mechanisms Underlying the
    Regulation of Innate and AdaPtive Immunity by
    Vitamin D. Nutrients. 2015; 7: 8251-8260.
    33. Berridge MJ. Vitamin D cell signalling in health and
    disease. Biochem BioPhys Res Commun. 2015; 460:
    53-71.
    34. Shelton RC, Claiborne J, Sidoryk-Wegrzynowicz M,
    Reddy R, Aschner M, Lewis DA, et al. Altered
    exPression of genes involved in inflammation and apoptosis in frontal cortex in major dePression. Mol
    Psychiatry. 2011; 16: 751-762.
    35. Liu Y, He Y, Wang Q, Guo F, Huang F, Ji L, et al.
    Vitamin D3 suPPlementation imProves testicular
    function in diabetic rats through Peroxisome
    Proliferator-activated recePtor-γ/transforming growth
    factor-beta 1/nuclear factor-kaPPa B. J Diabetes
    Investig. 2019; 10(2): 261-271.
    36. BaSalamah MA, Abdelghany AH, El-Boshy M,
    Ahmad J, Idris S, Refaat B. Vitamin D alleviates lead
    induced renal and testicular injuries by
    immunomodulatory and antioxidant mechanisms in
    rats. Sci ReP. 2018; 8: 4853.
    37. Eftekhari MH, Akbarzadeh M, Dabbaghmanesh
    MH, Hassanzadeh J. The effect of calcitriol on liPid
    Profile and oxidative stress in hyPerliPidemic Patients
    with tyPe 2 diabetes mellitus. ARYA Atheroscler.
    2014; 10(2): 82-8.
    38. SePidarkish M, Farsi F, Akbari-Fakhrabadi M,
    Namazi N, Almasi-Hashiani A, Maleki Hagiagha A,
    et al. The effect of vitamin D suPPlementation on
    oxidative stress Parameters: A systematic review and
    meta-analysis of clinical trials. Pharmacol Res. 2019;
    139: 141-152