DOI QR코드

DOI QR Code

The effect of streptozotocin induced diabetes on sperm function: a closer look at AGEs, RAGEs, MAPKs and activation of the apoptotic pathway

  • Omolaoye, Temidayo S. (Division of Medical Physiology, Faculty of Medicine and Health Sciences, Stellenbosch University) ;
  • Du Plessis, Stefan S. (Division of Medical Physiology, Faculty of Medicine and Health Sciences, Stellenbosch University)
  • Received : 2019.09.02
  • Accepted : 2020.01.29
  • Published : 2021.01.15

Abstract

This study was designed to (1) investigate the possible mechanisms through which diabetes-induced advanced glycation end products (AGEs) and receptor for AGEs (RAGE) activation can affect male reproductive function; and (2) corroborate the interaction of previously established independent pathways. Male albino Wistar rats (14-weeks old) weighing 250-300 g received either a single intraperitoneal injection of streptozotocin (30 mg/kg or 60 mg/kg), represented as STZ30 or STZ60 respectively, or citrate buffer (control). Diabetes mellitus (DM) was confirmed if plasma glucose levels were ≥14 mmol/L after 1 week. Animals were sacrificed after 8 weeks of treatment by an overdose of sodium pentobarbital (160 mg/kg body weight). The testes and epididymides were harvested. The testes were used for biochemical and Western blot analysis, while sperm was retrieved from the epididymis and analysed with computer-aided sperm analysis. The blood glucose levels of STZ60 animals were above the cut-off point and hence these animals were regarded as diabetic. Diabetic animals presented with a non-significant increase in AGE and RAGE expression. Diabetic animals showed a significant increase in the expression of cleaved caspase 3 compared to control (p<0.001), and these animals also presented with an increase in the expression of JNK (p<0.05), PARP (p=0.059) and p38 MAPK (p=0.1). Diabetic animals also displayed decreased catalase activity accompanied by a non-significant increase in malondialdehyde levels. Additionally, there was a significant decrease in the percentage of progressively motile spermatozoa (p<0.05) in diabetic animals. This study has shed some light on the interplay between DM, AGE, RAGE and mitogen-activated protein kinase signalling in the testes of diabetic rats, which can result in altered sperm function and contribute to male infertility. However, more studies are needed to better understand this complicated process.

Keywords

Acknowledgement

The authors would like to thank Dr. Michelle Smit-van Schalkwyk and Dr. Shantal Windvogel for the generous donation of tissue samples and Harry Crossley Foundation for the research grant provided.

References

  1. World Heallth Organization (2010) Diabetes fact sheet. NMH Fact Sheet February 2010
  2. World Health Organization (2014) Global report on diabetes, vol 58, pp 1-88. https://www.who.int/about/licensing/copyright_form/index.html. Accessed 19 Aug 2019
  3. Jacky B, Laura B, John AC, Nygren KG (2007) International estimates of infertility prevalence and treatment-seeking: potential need and demand for infertility medical care. Hum Reprod 22:1506-1512 https://doi.org/10.1093/humrep/dem046
  4. Zegers-Hochschild F, Adamson GD, de Mouzon J, Ishihara O, Mansour R, Nygren K, Sullivan E, Vanderpoel S (2009) International Committee for Monitoring Assisted Reproductive Technology (ICMART) and the World Health Organization (WHO) revised glossary of ART terminology, 2009. Hum Reprod 24:2683-2687 https://doi.org/10.1093/humrep/dep343
  5. Ceriello A (2000) Oxidative stress and glycemic regulation. Metabolism 49:27-29 https://doi.org/10.1016/S0026-0495(00)80082-7
  6. Delfino M, Imbrogno N, Elia J, Capogreco F, Mazzilli F (2007) Prevalence of diabetes mellitus in male partners of infertile couples. Minerva Urol Nefrol 59:131-135
  7. Rehman K, Beshay E (2001) Diabetes and male sexual function. J Sex Reprod Med 1:29-33
  8. Alves MG, Martins AD, Rato L, Moreira PI, Socorro S, Oliveira PF (2013) Molecular mechanisms beyond glucose transport in diabetes-related male infertility. Biochim Biophys Acta Mol Basis Dis 1832:626-635. https://doi.org/10.1016/j.bbadis.2013.01.011
  9. Ballester J, Rigau T, Rodriguez-Gil JE, Munoz MC, Dominguez J, Guinovart JJ (2004) Insulin-dependent diabetes affects testicular function by FSH- and LH-linked mechanisms. J Androl 25:706-719 https://doi.org/10.1002/j.1939-4640.2004.tb02845.x
  10. Maresch CC, Stute DC, Ludlow H, Hammes HP, de Kretser DM, Hedger MP, Linn T (2017) Hyperglycemia is associated with reduced testicular function and activin dysregulation in the Ins2Akita+/- mouse model of type 1 diabetes. Mol Cell Endocrinol 446:91-101. https://doi.org/10.1016/j.mce.2017.02.020
  11. Omolaoye TS, Skosana BT, du Plessis SS (2018) Diabetes mellitus-induction: effect of different streptozotocin doses on male reproductive parameters. Acta Histochem 120:103-109 https://doi.org/10.1016/j.acthis.2017.12.005
  12. Jelodar G, Khaksar Z, Pourahmadi M (2010) Endocrine profile and testicular histomorphometry in neonatal rats of diabetic mothers. Vet Arh 80:421-430
  13. Baccetti B, La Marca A, Piomboni P, Capitani S, Bruni E, Petraglia F, De Leo V (2002) Insulin-dependent diabetes in men is associated with hypothalamo-pituitary derangement and with impairment in semen quality. Hum Reprod 17:2673-2677 https://doi.org/10.1093/humrep/17.10.2673
  14. Jiang X, Zhang C, Xin Y, Huang Z, Tan Y, Huang Y, Wang Y, Feng W, Li X, Li W, Qu Y, Cai L (2013) Protective effect of FGF21 on type 1 diabetes-induced testicular apoptotic cell death probably via both mitochondrial- and endoplasmic reticulum stress-dependent pathways in the mouse model. Toxicol Lett 219:65-76. https://doi.org/10.1016/j.toxlet.2013.02.022
  15. Roessner C, Paasch U, Kratzsch J, Glander HJ, Grunewald S (2012) Sperm apoptosis signalling in diabetic men. Reprod Biomed 25:292-299 https://doi.org/10.1016/j.rbmo.2012.06.004
  16. Du Plessis SS, Agarwal A, Halabi J, Tvrda E (2015) Contemporary evidence on the physiological role of reactive oxygen species in human sperm function. J Assist Reprod Genet 32:509-520 https://doi.org/10.1007/s10815-014-0425-7
  17. Mangoli E, Talebi AR, Anvari M, Pourentezari M (2013) Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice. Iran J Reprod Med 11:53-60
  18. Chen J, Song M, Yu S, Gao P, Yu Y, Wang H, Huang L (2010) Advanced glycation endproducts alter functions and promote apoptosis in endothelial progenitor cells through receptor for advanced glycation endproducts mediate overpression of cell oxidant stress. Mol Cell Biochem 335:137-146 https://doi.org/10.1007/s11010-009-0250-y
  19. Ramasamy R, Vannucci SJ, Yan SS, Herold K, Yan SF, Schmidt AM (2005) Advanced glycation end products and RAGE: a common thread in ageing, diabetes, neurodegeneration, and inflammation. Glycobiology 15:16-28
  20. Li DX, Deng TZ, Lv J, Ke J (2014) Advanced glycation end products (AGEs) and their receptor (RAGE) induce apoptosis of periodontal ligament fibroblasts. Braz J Med Biol Res 47:1036-1043 https://doi.org/10.1590/1414-431X20143996
  21. Hoefen RJ, Berk BC (2002) The role of MAP kinases in endothelial activation. Vascul Pharmacol 38:271-273 https://doi.org/10.1016/S1537-1891(02)00251-3
  22. Mallidis C, Agbaje IM, Rogers DA, Glenn JV, Pringle R, Atkinson AB, Steger K, Stitt AW, McClure N (2009) Advanced glycation end products accumulate in the reproductive tract of men with diabetes. Int J Androl 32:295-305 https://doi.org/10.1111/j.1365-2605.2007.00849.x
  23. Committee for the Update of the Guide for the Care and Use of Laboratory Animals, National Research Council (2010) Guide for the care and use of laboratory animals, 8th edn. National Research Council, Washington
  24. Oyeyipo IP, Maartens PJ, du Plessis SS (2015) Diet-induced obesity alters kinematics of rat spermatozoa. Asian Pac J Reprod 4:235-239. https://doi.org/10.1016/j.apjr.2015.06.008
  25. Bradford MM, Bradford MM (1976) A rapid and sensitive microgram quantities of protein utilizing the priciple of protein dye biding. Anal Biochem 72:248-254 https://doi.org/10.1006/abio.1976.9999
  26. Marais E, Genade S, Huisamen B, Strijdom JG, Moolman JA, Lochner A (2001) Activation of p38 MAPK induced by a multi-cycle ischaemic preconditioning protocol is associated with attenuated p38 MAPK activity during sustained ischaemia and reperfusion. J Mol Cell Cardiol 33:769-778 https://doi.org/10.1006/jmcc.2001.1347
  27. Sexton WJ, Jarow JP (1997) Effect of diabetes mellitus upon male reproductive function. Urology 49:508-513 https://doi.org/10.1016/S0090-4295(96)00573-0
  28. Fedele D (2005) Therapy insight: sexual and bladder dysfunction associated with diabetes mellitus. Nat Clin Pract Urol 2:282 https://doi.org/10.1038/ncpuro0211
  29. Navarro-Casado L, Juncos-Tobarra MA, Chafer-Rudilla M, Iniguez De Onzono L, Blazquez-Cabrera JA, Miralles-Garcia JM (2010) Effect of experimental diabetes and STZ on male fertility capacity. Study in rats. J Androl 31:584-592 https://doi.org/10.2164/jandrol.108.007260
  30. Singh S, Malini T, Rengarajan S, Balasubramanian K (2009) Impact of experimental diabetes and insulin replacement on epididymal secretory products and sperm maturation in albino rats. J Cell Biochem 108:1094-1101 https://doi.org/10.1002/jcb.22337
  31. Vikram A, Tripathi DN, Ramarao P, Jena GB (2008) Intervention of D-glucose ameliorates the toxicity of streptozotocin in accessory sex organs of rat. Toxicol Appl Pharmacol 226:84-93 https://doi.org/10.1016/j.taap.2007.09.006
  32. Bhattacharya SM, Ghosh M, Nandi N (2014) Diabetes mellitus and abnormalities in semen analysis. J Obstet Gynaecol Res 40:167-171 https://doi.org/10.1111/jog.12149
  33. Adaramoye OA, Lawal SO (2014) Effect of kolaviron, a biflavonoid complex from Garcinia kola seeds, on the antioxidant, hormonal and spermatogenic indices of diabetic male rats. Andrologia 46:878-886 https://doi.org/10.1111/and.12160
  34. Giacco F, Brownlee M (2010) Oxidative stress and diabetic complications. Circ Res 107:1058-1070 https://doi.org/10.1161/CIRCRESAHA.110.223545
  35. Ricci G, Catizone A, Esposito R, Pisanti FA, Vietri MT, Galdieri M (2009) Diabetic rat testes: morphological and functional alterations. Andrologia 41:361-368 https://doi.org/10.1111/j.1439-0272.2009.00937.x
  36. Khaki A, Fathiazad F, Nouri M, Khaki AA, Maleki NA, Khamnei HJ, Ahmadi P (2010) Beneficial effects of quercetin on sperm parameters in streptozotocin-induced diabetic male rats. Phyther Res 24:1285-1291 https://doi.org/10.1002/ptr.3100
  37. Martin-Gallan P, Carrascosa A, Gussinye M, Dominguez C (2003) Biomarkers of diabetes-associated oxidative stress and antioxidant status in young diabetic patients with or without subclinical complications. Free Radic Biol Med 34:1563-1574 https://doi.org/10.1016/S0891-5849(03)00185-0
  38. Mullarkey CJ, Edelstein D, Brownlee M (1990) Free radical generation by early glycation products: a mechanism for accelerated atherogenesis in diabetes. Biochem Biophys Res Commun 173:932-939 https://doi.org/10.1016/S0006-291X(05)80875-7
  39. Mayorga-Torres BJM, Camargo M, Cadavid P, du Plessis SS, Cardona-Maya WD (2017) Are oxidative stress markers associated with unexplained male infertility? Andrologia 49:e12659 https://doi.org/10.1111/and.12659
  40. Buttke TM, Sandstrom PA (1994) Oxidative stress as a mediator of apoptosis. Immunol Today 15:7-10 https://doi.org/10.1016/0167-5699(94)90018-3
  41. Du Plessis SS, McAllister DA, Luu A, Savia J, Agarwal A, Lampiao F (2010) Effects of H2O2 exposure on human sperm motility parameters, reactive oxygen species levels and nitric oxide levels. Andrologia 42:206-210 https://doi.org/10.1111/j.1439-0272.2009.00980.x
  42. Mahfouz RZ, du Plessis SS, Aziz N, Sharma R, Sabanegh E, Agarwal A (2010) Sperm viability, apoptosis, and intracellular reactive oxygen species levels in human spermatozoa before and after induction of oxidative stress. Fertil Steril 93:814-821. https://doi.org/10.1016/j.fertnstert.2008.10.068
  43. Nicholl ID, Bucala R (1998) Advanced glycation endproducts and cigarette smoking. Cell Mol Biol (Noisy-le-grand) 44:1025-1033
  44. Valencia JV, Weldon SC, Quinn D, Kiers GH, DeGroot J, TeKoppele JM, Hughes TE (2004) Advanced glycation end product ligands for the receptor for advanced glycation end products: biochemical characterization and formation kinetics. Anal Biochem 324:68-78 https://doi.org/10.1016/j.ab.2003.09.013
  45. Chen S, Yin L, Xu Z, An FM, Liu AR, Wang Y, Yao WB, Gao XD (2016) Inhibiting receptor for advanced glycation end product (AGE) and oxidative stress involved in the protective effect mediated by glucagon-like peptide-1 receptor on AGE induced neuronal apoptosis. Neurosci Lett 612:193-198. https://doi.org/10.1016/j.neulet.2015.12.007
  46. Mallidis C, Agbaje I, Rogers D, Glenn J, McCullough S, Atkinson AB, Steger K, Stitt A, McClure N (2007) Distribution of the receptor for advanced glycation end products in the human male reproductive tract: prevalence in men with diabetes mellitus. Hum Reprod 22:2169-2177 https://doi.org/10.1093/humrep/dem156
  47. Yang J, Zhu T, Liu X, Zhang L, Yang Y, Zhang J, Guo M (2015) Heat shock protein 70 protects rat peritoneal mesothelial cells from advanced glycation end-products-induced epithelial-to-mesenchymal transition through mitogen-activated protein kinases/extracellular signal-regulated kinases and transforming growth fact. Mol Med Rep 11:4473-4481 https://doi.org/10.3892/mmr.2015.3271
  48. Wu Q, Li S, Li X, Sui Y, Yang Y, Dong L, Xie B, Sun Z (2015) Inhibition of advanced glycation endproduct formation by lotus seedpod oligomeric procyanidins through RAGE-MAPK signaling and NF-κB activation in high-fat-diet rats. J Agric Food Chem 63:6989-6998 https://doi.org/10.1021/acs.jafc.5b01082
  49. Taguchi A, Blood DC, Del-Toro G, Canet A, Lee DC, Qu W, Tanjl N, Lu Y, Lalla E, Fu C, Hofmann MA, Kislinger T, Ingram M, Lu A, Tanaka H, Hori O, Ogawa S, Stern DM, Schmidt AM (2000) Blockade of RAGE-amphoterin signalling suppresses tumour growth and metastases. Nature 405:354-360 https://doi.org/10.1038/35012626
  50. Ichijo H, Nishida E, Irie K, Dijke PT, Saitoh M, Moriguchi T, Takagi M, Matsumoto K, Miyazono K, Gotoh Y (1997) Induction of apoptosis by ASK1, a mammalian MAPKKK that activates SAPK/JNK and p38 signaling pathways. Science 275:90-94 https://doi.org/10.1126/science.275.5296.90
  51. Adhikary L, Chow F, Nikolic-Paterson DJ, Stambe C, Dowling J, Atkins RC, Tesch GH (2004) Abnormal p38 mitogen-activated protein kinase signalling in human and experimental diabetic nephropathy. Diabetologia 47:1210-1222 https://doi.org/10.1007/s00125-004-1437-0
  52. Farley N, Pedraza-Alva G, Serrano-Gomez D, Nagaleekar V, Aronshtam A, Krahl T, Thornton T, Rincon M (2006) p38 Mitogen-activated protein kinase mediates the Fas-induced mitochondrial death pathway in CD8+ T cells. Mol Cell Biol 26:2118-2129 https://doi.org/10.1128/MCB.26.6.2118-2129.2006
  53. Taylor CA, Zheng Q, Liu Z, Thompson JE (2013) Role of p38 and JNK MAPK signaling pathways and tumor suppressor p53 on induction of apoptosis in response to Ad-eIF5A1 in A549 lung cancer cells. Mol Cancer 12:1-11 https://doi.org/10.1186/1476-4598-12-1
  54. Park SJ, Kim IS (2005) The role of p38 MAPK activation in auranofin-induced apoptosis of human promyelocytic leukaemia HL-60 cells. Br J Pharmacol 146:506-513 https://doi.org/10.1038/sj.bjp.0706360
  55. Nys K, Van Laethem A, Michiels C, Rubio N, Piette JG, Garmyn M, Agostinis P (2010) A p38MAPK/HIF-1 pathway initiated by UVB irradiation is required to induce noxa and apoptosis of human keratinocytes. J Invest Dermatol 130:2269-2276. https://doi.org/10.1038/jid.2010.93
  56. Metzler-Guillemain C, Grillo J-M, Mitchell MJ, Karsenty G, Saias-Magnan J, Streichemberger E, Perrin J, Malzac P (2012) Case report of apoptosis in testis of four AZFc-deleted patients: increased DNA fragmentation during meiosis, but decreased apoptotic markers in post-meiotic germ cells. Hum Reprod 27:1939-1945 https://doi.org/10.1093/humrep/des128
  57. Manente L, Pecoraro S, Picillo E, Gargiulo U, Gargiulo P, De Luca A, Politano L (2015) Molecular evidence of apoptotic pathway activation in semen samples with high DNA fragmentation. Vivo (Brooklyn) 29:289-294