Search results

Filters

  • Journals
  • Authors
  • Keywords
  • Date
  • Type

Search results

Number of results: 2
items per page: 25 50 75
Sort by:
Download PDF Download RIS Download Bibtex

Abstract

The aim of this study was to determine the time-dependent effectiveness of photo-stimulation against bovine sperm cells using a multi-wavelength LED (Light Emitting Diode). Spermatological parameters were evaluated for viability, acrosome structure and motility. In addition, the effect of photo-stimulation on frozen-thawed sperm cells subjected to in vitro capacitation was evaluated in terms of changes in mitochondrial membrane potential. The study consisted of two separate experiments and a total of 32 sperm samples obtained from separate bulls were used. All sperm samples were obtained from Holstein bulls using an artificial vagina. Semen was diluted to a final concentration of 92 x 106 spermatozoa per ml in 0.25 ml straws. The sperm cells were frozen using the conventional method. Straws were kept in a 37°C water bath for 20 seconds and diluted 1:4 in phosphate buffered saline (PBS) to eliminate the potentially deleterious effect of glycerol, the main permeable cryoprotectant in the freezing medium for bull sperm. This dilution also helped in the evaluation of sperm quality parameters. In the first experiment, whereas the 15-10-15 showed no differences with the control, other treatments such as 10-10-10, 5-5-5, and 3-1-3 exhibited significantly higher percentages of viable spermatozoa at 24h. The results obtained for acrosome integrity were pretty much similar to those observed in the sperm viability assessment. In effect, while the treatment consisting of 15-10-15 had no positive effects, shorter treatments exerted a much more positive effect. The percentages of acrosome-intact spermatozoa in 2-1-2 and 1-1-1 were significantly higher than those obtained in the control. The significant differences in mitochondrial membrane potential were observed at 0, 2, 4 and 24h post-photo-stimulation in all treatments, except 15-10-15. The highest increase in the percentage of spermatozoa exhibiting high mitochondrial membrane potential was found in 10-10-10, 5-5-5 and 3-1-3 treatments. With regard to total and progressive motility, whereas 10-10-10 was the best regime, 5-5-5 and 3-1-3 treatments also had a positive effect. However, 15-10-15 appeared to have a stimulating effect upon progressive motility at 2h and 4h but later declined and showed no significant differences with regard to the control at 24h. In the second experiment, not immediately after thawing but after having been kept at room temperature for up to 24h, it was observed that there was no statistical difference in terms of viability, acrosome integrity and total/progressive motility between photostimulation and the control group. This indicates that photo- stimulation is less able to exert a beneficial effect when post-thawed sperm are not immediately stimulated. As a result it was determined that photo-stimulation at a pattern of 10-10-10, 5-5-5, 3-1-3 and, to a lesser extent 2-1-2, increases the resilience of frozen-thawed bull sperm when applied upon thawing.
Go to article

Bibliography


Abdel-Salam Z, Dessouki SH, Abdel-Salam SA, Ibrahim MA, Harith MA (2011) Green laser irradiation effects on buffalo semen. Theri-ogenology 75: 988-994.
Aitken RJ (1997) Molecular mechanisms regulating human sperm function. Mol Hum Reprod 3: 169-173.
Aitken RJ, West K M (1990) Analysis of the relationship between reactive oxygen species production and leucocyte infiltration in fractions of human semen separated on Percoll gradients. Int J Androl 13: 433-451.
Antognazza MR, Abdel Aziz I, Lodola F (2019) Use of Exo- genous and Endogenous Photomediators as Efficient ROS Modulation Tools: Results and Perspectives for Therapeutic Purposes. Oxid Med Cell Longev 2019: 2867516.
Avci P, Gupta A, Sadasivam M, Vecchio D, Pam Z, Pam N, Hamblin MR (2013) Low-level laser (light) therapy (LLLT) in skin: stimulating, healing, restoring. Semin Cutan Med Surg 32: 41-52.
Brand˜ao AC, Arruda RP, Andrade AF, Zaffalon FG, Tarrag´o OF, Visintin JA, Assumpção ME (2008) Effect of diode laser on motility, plasma and acrosomal membrane integrity, and mitochondrial membrane potential of cryopreserved stallion spermatozoa. Anim Reprod Sci 107: 309-310.
Breitbart H, Levinshal T, Cohen N, Friedmann H, Lubart R (1996) Changes in calcium transport in mammalian sperm mitochondria and plasma membrane irradiated at 633 nm (He-Ne laser). J Photochem Photobiol B 34: 117-121.
Bucak MN, Sariozkan S, Tuncer PB, Sakin F, Atessahin A, Kulaksiz R, Cevik M (2010) The effect of antioxidants on post-thawed Angora goat (Capra hircus ancryrensis) sperm parameters, lipid peroxidation and antioxidant activities. Small Rumin Res 89: 24-30.
Cohen N, Lubart R, Rubinstein S, Breitbart H (1998) Light irradiation of Mouse spermatozoa: Stimulation of in vitro fertilization and calcium signals. Photochem Photobiol 68: 407-413.
Corral-Baqués MI, Rivera MM, Rigau T, Rodríguez-Gil JE, Rigau J (2009) The effect of low-level laser irradiation on dog spermatozoa motility is dependent on laser output power. Lasers Med Sci 24: 703-713.
Cui L, Li XY, He DY, Chen L, Gong SL (2013) Study on microtexture of laser welded 5A90 aluminium-lithium alloys using electron backscattered diffraction. Sci Technol Weld 18: 204–209.
Dall Agnol MA, Nicolau RA, de Lima CJ, Munin E (2009) Comparative analysis of coherent light action (laser) versus non-coherent light (light-emitting diode) for tissue repair in diabetic rats. Lasers Med Sci 24: 909-916.
Darszon A, Treviño CL, Wood C, Galindo B, Rodríguez- -Miranda E, Acevedo JJ, Hernández-González EO, Beltrán C, Martínez-López P, Nishigaki T (2007) Ion channels in sperm motility and capacitation. Soc Reprod Fertil Suppl 65: 229-244.
de Almeida TG, Alves MB, Batissaco L, Torres MA, de Andrade AF, Mingoti RD, de Arruda RP, Celeghini EC (2019) Does low-level laser therapy on degenerated ovine testes improve post-thawed sperm characteristics? Lasers Med Sci 34: 1001-1009.
de Rezende MU, Varone BB, Martuscelli DF, Ocampos GP, Freire GM, Pinto NC, de Sousa MV (2022) Pilot study of the effect of therapeutic photobiomodulation on postoperative pain in knee arthroplasty. Braz J Anesthesiol 72: 159-161
Desan PH, Weinstein AJ, Michalak EE, Tam EM, Meesters Y, Ruiter M J, Horn E, Telner J, Iskandar H, Boivin DB, Lam RW (2007) A controlled trial of the Litebook light- -emitting diode (LED) light therapy device for treatment of Seasonal Affective Disorder (SAD). Bmc Psychiatry 7(1): 1-8.
Fekrazad E, Keyhan H, Fekrazad R, Tajik A (2014) Effect of Diode Lasers on Human Sperm Motility. Acad Res Int 5: 21-25.
Fernandes GH, de Carvalho PD, Serra AJ, Crespilho AM, Peron JP, Rossato C, Leal-Junior EC, Albertini R (2015) The effect of low-level laser irradiation on sperm motility, and integrity of the plasma membrane and acrosome in cryopreserved bovine sperm. PLoS One 10: e0121487.
Frangez HB, Frangez I, Verdenik I, Jansa V, Klun IV (2015) Photobiomodulation with light-emitting diodes improves sperm motility in men with asthenozoospermia. Lasers Med Sci 30: 235-240.
Garner DL, Johnson LA (1995) Viability assessment of mammalian sperm using SYBR-14 and propidium iodide. Biol Reprod 53: 276-284.
Huang YY, Nagata K, Tedford CE, McCarthy T, Hamblin MR (2013) Low-level laser therapy (LLLT) reduces oxidative stress in primary cortical neurons in vitro. J Biophotonics 6: 829-838.
Iaffaldano N, Meluzzi A, Manchisi A, Passarella S (2005) Improvement of stored turkey semen quality as a result of He-Ne laser irradiation. Anim Reprod Sci 85: 317-325.
Iaffaldano N, Paventi G, Pizzuto R, Di Iorio M, Bailey JL, Manchisi A, Passarella S (2016) Helium-neon Laser Irradiation of Cryopreserved Ram Sperm Enhances Cytochrome C Oxidase Activity and ATP Levels Improving Semen Quality. Theriogenology 86: 778-784.
Iaffaldano N, Rosato MP, Paventi G, Pizzuto R, Gambacorta M, Manchisi A, Passarella S (2010) The irradiation of rabbit sperm cells with He-Ne laser prevents their in vitro liquid storage dependent damage. Anim Reprod Sci 119: 123-129.
Kim CH, Ahn DC (2012) Coaxial monitoring of keyhole during Yb:YAG laser welding. Opt Laser Technol 44: 1874-1880.
Lubart R, Wollman Y, Friedmann H, Rochkind S, Laulicht I (1992) Effects of visible and near infrared lasers on cell cultures. J Photochem Photobiol B 12: 305-310.
Maia MS, Bicudo SD, Sicherle CC, Rodello L, Gallego IC (2010) Lipid peroxidation and generation of hydrogen peroxide in frozen-thawed ram semen cryopreserved in extenders with antioxidants. Anim Reprod Sci 122: 118-123.
Muiño R, Tamargo C, Hidalgo CO, Peña AI (2008) Identification of sperm subpopulations with defined motility characteristics in ejaculates from Holstein bulls: effects of cryopreservation and between-bull variation. Anim Reprod Sci 109: 27-39.
Nagy S, Jansen J, Topper EK, Gadella BM (2003) A triple- -stain flow cytometric method to assess plasma- and acrosome-membrane integri-ty of cryopreserved bovine sperm immediately after thawing in presence of egg-yolk particles. Biol Reprod 68: 1828-1835.
Ocaña-Quero JM, Gomez-Villamandos R, Moreno-Millan M, Santisteban-Valenzuela JM (1997) Biological effects of helium-neon (He-Ne) laser irradiation on acrosome reaction in bull sperm cells. J Photochem Photobiol B 40: 294-298.
Omur A, Balcı S (2020) Evaluatıon of the effects of photostimulation on freze-thawed bull sperm cells in terms of motility: preliminary as-sessment. CRYO2020 The 57th Annual Meeting Of The Society For Cryobiology. July 21-23. 97: 289-290
Omur AD, Coyan K (2016) Protective effects of the antioxidants curcumin, ellagic acid and methionine on motility, mitochondrial transmem-brane potential, plasma membrane and acrosome integrity in freeze-thawed Merino ram sperm. Vet Med 61: 10-16.
Pezo F, Zambrano F, Uribe P, Ramírez-Reveco A, Romero F, Sanchéz R (2018) LED-based red light photostimulation improves short-term response of cooled boar semen exposed to thermal stress at 37°C. Andrologia 51: e13237.
Prieto-Martínez N, Morató R, Muiño R, Hidalgo CO, Rodríguez-Gil JE, Bonet S, Yeste M (2017) Aquaglyceroporins 3 and 7 in bull spermatozoa: identification, localisation and their relationship with sperm cryotolerance. Reprod Fertil Dev 29: 1249-1259.
Rashid K, Sil PC (2015) Curcumin ameliorates testicular damage in diabetic rats by suppressing cellular stress mediated mitochondria and endoplasmic reticulum dependent apoptotic death. Biochim Biophys Acta 1852: 70-82.
Rodríguez-Gil JE (2019) Photostimulation and thermotaxis of sperm: Overview and practical implications in porcine reproduction. Theriogenology 137: 8-14.
Saltmarche AE (2008) Low level laser therapy for healing acute and chronic wounds-the extendicare experience. Int Wound J 5: 351-360.
Soares LE, Guirado MM, Berlingieri G, Ramires MC, Lyra LA, Teixeira IS, Oliveira, PC, Tateno RY, Palma LF, Campos L (2021) Intranasal photobiomodulation therapy for COVID-19-related olfactory dysfunction: a Brazilian multicenter case series. Photodiagnosis Photodyn Ther 36: 102574.
Wenbin Y, Wenzhong L, Mengzhao L, Baotian Z, Laizeng AI, Tongya L (1996) Effects of laser radiation on Saanen buck’s sperm energy metabolism. In: Proceedings of the sixth ınternational conference on goats. Beijing, China.
Wright C, Milne S, Leeson H (2014) Sperm DNA damage caused by oxidative stress: modifiable clinical, lifestyle and nutritional factors in male infertility. Rep Biomed Online 28: 684-703.
Yeste M, Codony F, Estrada E, Lleonart M, Baslasch S, Peña A, Bonet S, Rodríguez-Gil JE (2016) Specific LED-based red light photo-stimulation procedures improve overall sperm function and reproductive performance of boar ejaculates. Sci Rep 6: 22569.
You DY, Gao XD, Katayama S (2014) Review of laser welding monitoring. Sci Technol Weld Join 19: 181-201.
Go to article

Authors and Affiliations

A.D. Ömür
1 2 3

  1. Department of Reproduction and Artificial Insemination, Faculty of Veterinary Medicine, Atatürk University, 25240, Yakutiye/ Erzurum, Turkey
  2. Department of Biochemistry, Faculty of Veterinary Medicine, Atatürk University, 25240, Yakutiye/Erzurum, Turkey
  3. Department of Molecular Biology and Genetics, Faculty of Science, Atatürk University, 25240, Yakutiye/Erzurum, Turkey
Download PDF Download RIS Download Bibtex

Abstract

Twenty eight male Sprague Dawley rats (aged 3 months) were used in the study. The animals were given feed and water as ad libitum. Sprague dawley rats were randomly divided into 4 groups as 7 rats in each group. Except for the control one, aflatoxin B1 (7.5 μg / 200 g), resvera- trol (60 mg / kg) was administered to rats of 3 other groups. At the end of the 16th day, blood, semen and tissue specimens were taken by decapitation under ether anesthesia. When we evaluate the spermatological parameters, it is understood that resveratrol has a statistically significant difference in terms of sperm motility and viability (membrane integrity) compared to the control group and aflatoxin B1 administration groups, indicating a protective effect on spermatological parameters. In terms of pathological parameters - histopathological examination - in the control and resveratrol groups, seminiferous tubules were observed to be in normal structure. In the group treated with aflatoxin, the regular structure of the spermatogenic cells deteriorated and the seminiferous tubules became necrotic and degenerative. In the group treated with Afb1 + res, the decreasing of necrotic and degenerative changes were determined compared with in the group treated with aflatoxin. As immunohistochemical examination, cleaved caspase 3 expression was found to be very low in the control and resveratrol groups. Cleaved caspase 3 expression was severely exacerbated in seminiferous tubules in aflatoxin group but cleaved caspase 3 expression level decreased in Afb1 + res. In the biochemical direction, resveratrol has been shown to inhibit the adverse effects of aflatoxin on antioxidant levels and to show a protective effect. For this purpose, the use of resveratrol with antioxidant activity was investi- gated in preventing or ameliorating damage to aflatoxin B1. It has been concluded that resveratrol effectively prevent the aflatoxin-induced testicular damage and lipid peroxidation. It has also been shown that resveratrol has protective effects on sperm motility and viability.

Go to article

Authors and Affiliations

A.D. Omur
B. Yildirim
Y.S. Saglam
S. Comakli
M. Ozkaraca

This page uses 'cookies'. Learn more