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Мужское бесплодие. Применение цинка и антиоксидантов в терапии нарушений фертильности и воспалительных заболеваний мужских гениталий (клиническая лекция)
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Borisov V.V. Male infertility. The use of antioxidants and zinc in the treatment of fertility disorders and inflammatory diseases of male genitalia (clinical lecture). Consilium Medicum. 2015; 17 (7): 16–23. DOI: 10.26442/2075-1753_2015.7.16-23
Материалы доступны только для специалистов сферы здравоохранения. Авторизуйтесь или зарегистрируйтесь.
Ключевые слова: мужское бесплодие, фертильность, сперматогенез, инфекции, передаваемые половым путем, микроэлементы, оксидативный стресс, активные формы кислорода, антиоксиданты.
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Key words: male infertility, fertility, spermatogenesis, infections, sexually transmitted diseases, trace elements, oxidative stress, reactive oxygen species, antioxidants.
2. ВОЗ – Всемирная организация здравоохранения. Официальный сайт. http://www.who.int/ru/ / VOZ – Vsemirnaia organizatsiia zdravookhraneniia. Ofitsial'nyi sait. http://www.who.int/ru/ [in Russian]
3. Борисов В.В. Антиоксидативная терапия мужских сексуальных и репродуктивных расстройств. Consilium Medicum. 2014; 16 (7): 41. / Borisov V.V. Antioksidativnaia terapiia muzhskikh seksual'nykh i reproduktivnykh rasstroistv. Consilium Medicum. 2014; 16 (7): 41. [in Russian]
4. UroWeb.ru. Урологический информационный портал, 2015. / UroWeb.ru. Urologicheskii informatsionnyi portal, 2015. [in Russian]
5. Шадеркина В.А., Болотова Е.В. Проблема здоровья мальчиков в современной России. UroWeb.ru. Урологический информационный портал. 2015. / Shaderkina V.A., Bolotova E.V. Problema zdorov'ia mal'chikov v sovremennoi Rossii. UroWeb.ru. Urologicheskii informatsionnyi portal. 2015. [in Russian]
6. Lotti F, Corona G, Vitale P et al. Current smoking is associated with lower seminal vesicles and ejaculate volume, despite higher testosterone levels, in male subjects of infertile couples. Hum Reprod 2015; 30: 590–602.
7. Br Med J Open, 2015.
8. Тюзиков И.А., Калинченко С.Ю., Ворслов Л.О., Тишова Ю.А. Бесплодие: определение, эпидемиология, причины, классификация, критерии прогноза. Эксперим. и клин. урология. 2014; 2. / Tiuzikov I.A., Kalinchenko S.Iu., Vorslov L.O., Tishova Iu.A. Besplodie: opredelenie, epidemiologiia, prichiny, klassifikatsiia, kriterii prognoza. Eksperim. i klin. urologiia. 2014; 2. [in Russian]
9. Panda B, Dash C, Padhy RN, Routray P. Effect of age and abstinence on semen quality: A retrospective study in a teaching hospital Priyadarsini Sunanda. Asian Pacific J Reprod 2014.
10. Виноградов И.В., Страшнова А.Л., Афанасьева Л.М. и др. Применение различных методов оценки сперматозоидов в клинической практике. Материалы XI Конгресса «Мужское здоровье». М., 2010; с. 195–7. / Vinogradov I.V., Strashnova A.L., Afanas'eva L.M. i dr. Primenenie razlichnykh metodov otsenki spermatozoidov v klinicheskoi praktike. Materialy XI Kongressa «Muzhskoe zdorov'e». M., 2010; s. 195–7. [in Russian]
11. Божедомов В.А. Мужское бесплодие. М., 2009. / Bozhedomov V.A. Muzhskoe besplodie. M., 2009. [in Russian]
12. Zini A, Al-Hathal N. Antioxidant therapy in male infertility: fact or fiction? Asian J Androl 2011; 13: 374
13. Zini A, San Gabriel M, Baazeem A. Antioxidants and sperm DNA damage: a clinical perspective. J Assist Reprod Genet 2009; 26: 427–32.
14. Aitken RJ, de Iuliis GN, Finnie JM et al. Analysis of the relationships between oxidative stress, DNA damage and sperm vitality in a patient population: development of diagnostic criteria. Hum Reprod 2010; 25: 2415–26.
15. Fraga CG, Motchnik PA, Shigenaga MK et al. Ascorbic acid protects against endogenous oxidative DNA damage in human sperm. Proc Natl Acad Sci USA 1991; 88: 11003–6.
16. Iwasaki A, Gagnon C. Formation of reactive oxygen species in spermatozoa of infertile patients. Fertil Steril 1992; 57: 409–16.
17. Zini A, Sigman M. Are tests of sperm DNA damage clinically useful? Pros and cons. J Androl 2009; 30: 219–29.
18. Agarwal A, Nallella KP, Allamaneni SS, Said TM. Role of antioxidants in treatment of male infertility: an overview of the literature. Reprod Biomed Online 2004; 8: 616–27.
19. Aitken RJ, Paterson M, Fisher H et al. Redox regulation of tyrosine phosphorylation in human spermatozoa and its role in the control of human sperm function. J Cell Sci 1995; 108 (Pt. 5): 2017–25.
20. Griveau JF, Le Lannou D. Reactive oxygen species and human spermatozoa: physiology and pathology. Int J Androl 1997; 20: 61–9.
21. De Lamirande E, Jiang H, Zini A et al. Reactive oxygen species and sperm physiology. Rev Reprod 1997; 2: 48–54.
22. Aitken RJ, Clarkson JS. Cellular basis of defective sperm function and its association with the genesis of reactive oxygen species by human spermatozoa. J Reprod Fertil 1987; 81: 459–69.
23. De Lamirande E, Gagnon C. Reactive oxygen species and human spermatozoa. I. Effects on the motility of intact spermatozoa and on sperm axonemes. J Androl 1992; 13: 368–78.
24. Zini A, Garrels K, Phang D. Antioxidant activity in the semen of fertile and infertile men. Urology 2000; 55: 922–6.
25. Alvarez JG, Touchstone JC, Blasco L, Storey BT. Spontaneous lipid peroxidation and production of hydrogen peroxide and superoxide in human spermatozoa. Superoxide dismutase as major enzyme protectant against oxygen toxicity. J Androl 1987; 8: 338–48.
26. Twigg J, Fulton N, Gomez E et al. Analysis of the impact of intracellular reactive oxygen species generation on the structural and functional integrity of human spermatozoa: lipid peroxidation, DNA fragmentation and effectiveness of antioxidants. Hum Reprod 1998; 13: 1429–36.
27. Chabory E, Damon C, Lenoir A et al. Epididymis seleno-independent glutathione peroxidase 5 maintains sperm DNA integrity in mice. J Clin Invest 2009; 119: 2074–85.
28. Weir CP, Robaire B. Spermatozoa have decreased antioxidant enzymatic capacity and increased reactive oxygen species production during aging in the Brown Norway rat. J Androl 2007; 28: 229–40.
29. Zini A, de Lamirande E, Gagnon C. Low levels of nitric oxide promote human sperm capacitation in vitro. J Androl 1995; 16: 424–31.
30. Smith R, Vantman D, Ponce J, Escobar J, Lissi E. Total antioxidant capacity of human seminal plasma. Hum Reprod 1996; 11: 1655–60.
31. Zini A, De Lamirande E, Gagnon C. Reactive oxygen species in semen of infertile patients: levels of superoxide dismutase- and catalase-like activities in seminal plasma and spermatozoa. Int J Androl 1993; 16: 183–8.
32. Kobayashi T, Miyazaki T, Natori M, Nozawa S. Protective role of superoxide dismutase in human sperm motility: superoxide dismutase activity and lipid peroxide in human seminal plasma and spermatozoa. Hum Reprod 1991; 6: 987–91.
33. Zini A, Schlegel PN. Catalase mRNA expression in the male rat reproductive tract. J Androl 1996; 17: 473–80.
34. Thiele JJ, Friesleben HJ, Fuchs J, Ochsendorf FR. Ascorbic acid and urate in human seminal plasma: determination and interrelationships with chemiluminescence in washed semen. Hum Reprod 1995; 10: 110–5.
35. Kalthur G, Adiga SK, Upadhya D et al. Effect of cryopreservation on sperm DNA integrity in patients with teratospermia. Fertil Steril 2008; 89: 1723–7.
36. Tauber PF, Zaneveld LJ, Propping D, Schumacher GF. Components of human split ejaculates. I. Spermatozoa, fructose, immunoglobulins, albumin, lactoferrin, transferrin and other plasma proteins. J Reprod Fertil 1975; 43: 249–67.
37. Smith R, Vantman D, Ponce J et al. Total antioxidant capacity of human seminal plasma. Hum Reprod 1996; 11: 1655–60.
38. Lewis SE, Sterling ES, Young IS, Thompson W. Comparison of individual antioxidants of sperm and seminal plasma in fertile and infertile men. Fertil Steril 1997; 67: 142–7.
39. Sanocka D, Miesel R, Jedrzejczak P, Kurpisz MK. Oxidative stress and male infertility. J Androl 1996; 17: 449–54.
40. Lewis SE, Boyle PM, McKinney KA, Young IS, Thompson W. Total antioxidant capacity of seminal plasma is different in fertile and infertile men. Fertil Steril 1995; 64: 868–70.
41. Appasamy M, Muttukrishna S, Pizzey AR et al. Relationship between male reproductive hormones, sperm DNA damage and markers of oxidative stress in infertility. Reprod Biomed Online 2007; 14: 159–65.
42. Verit FF, Verit A, Kocyigit A et al. No increase in sperm DNA damage and seminal oxidative stress in patients with idiopathic infertility. Arch Gynecol Obstet 2006; 274: 339–44.
43. Hampl JS, Taylor CA, Johnston CS. Vitamin C deficiency and depletion in the United States: the Third National Health and Nutrition Examination Survey, 1988 to 1994. Am J Public Health 2004; 94: 870–5.
44. Мухина Ю.Г., Ключников С.О., Нетребенко О.К., Щеплягина Л.А. Клиническое значение нарушений метаболизма цинка. 2011. / Mukhina Iu.G., Kliuchnikov S.O., Netrebenko O.K., Shchepliagina L.A. Klinicheskoe znachenie narushenii metabolizma tsinka. 2011. [in Russian]
45. Ефремов Е.А., Охоботов Д.А., Мельник Я.И. Применение препарата Селцинк Плюс в комбинированной терапии хронического простатита и доброкачественной гиперплазии предстательной железы. Эксперим. и клин. урология, 2014. / Efremov E.A., Okhobotov D.A., Mel'nik Ia.I. Primenenie preparata Seltsink Plius v kombinirovannoi terapii khronicheskogo prostatita i dobrokachestvennoi giperplazii predstatel'noi zhelezy. Eksperim. i klin. urologiia, 2014. [in Russian]
46. Козаренко В.Г. Дефицит цинка у детей с задержкой роста и полового развития. Автореф. дис. … канд. мед. наук. СПб., 2008. / Kozarenko V.G. Defitsit tsinka u detei s zaderzhkoi rosta i polovogo razvitiia. Avtoref. dis. … kand. med. nauk. SPb., 2008. [in Russian]
47. Авцын А.П., Жаворонков А.А., Риш М.А. и др. Микроэлементозы человека: этиология, классификация, органопатология. М., 1991. / Avtsyn A.P., Zhavoronkov A.A., Rish M.A. i dr. Mikroelementozy cheloveka: etiologiia, klassifikatsiia, organopatologiia. M., 1991. [in Russian]
48. Алексеенко В.А., Алещукин Л.В. и др. Цинк и кадмий в окружающей среде. М., 1992. / Alekseenko V.A., Aleshchukin L.V. i dr. Tsink i kadmii v okruzhaiushchei srede. M., 1992. [in Russian]
49. Скальный А.В. Эколого-физиологическое обоснование эффективности использования макро- и микроэлементов при нарушениях гомеостаза у обследуемых из различных климатогеографических регионов. Дис. … д-ра мед. наук. М., 2000. / Skal'nyi A.V. Ekologo-fiziologicheskoe obosnovanie effektivnosti ispol'zovaniia makro- i mikroelementov pri narusheniiakh gomeostaza u obsleduemykh iz razlichnykh klimatogeograficheskikh regionov. Dis. … d-ra med. nauk. M., 2000. [in Russian]
50. Golubkina N.A., Alfthan G.V. The human selenium status in 27 regions of Russia. J Trace Elem Med Biol 1999; 13: 15–20.
51. Коровина Н.А. Профилактика рахита у детей: применение кальция. Лечащий врач. 2004; 1: 56–8. / Korovina N.A. Profilaktika rakhita u detei: primenenie kal'tsiia. Lechashchii vrach. 2004; 1: 56–8. [in Russian]
52. Ruel MT, Rivera JA, Santizo M-C et al. Impact of Zinc Supplementation on Morbidity From Diarrhea and Respiratory Infections Among Rural Guatemalan Children. Pediatrics 1997; 99: 808–13. [in Russian]
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1. Federal'naia sluzhba gosudarstvennoi statistiki. Ofitsial'nyi sait. http://www.gks.ru/ [in Russian]
2. VOZ – Vsemirnaia organizatsiia zdravookhraneniia. Ofitsial'nyi sait. http://www.who.int/ru/
[in Russian]
3. Borisov V.V. Antioksidativnaia terapiia muzhskikh seksual'nykh i reproduktivnykh rasstroistv. Consilium Medicum. 2014; 16 (7): 41. [in Russian]
4. UroWeb.ru. Урологический информационный портал, 2015. / UroWeb.ru. Urologicheskii informatsionnyi portal, 2015. [in Russian]
5. Shaderkina V.A., Bolotova E.V. Problema zdorov'ia mal'chikov v sovremennoi Rossii. UroWeb.ru. Urologicheskii informatsionnyi portal. 2015. [in Russian]
6. Lotti F, Corona G, Vitale P et al. Current smoking is associated with lower seminal vesicles and ejaculate volume, despite higher testosterone levels, in male subjects of infertile couples. Hum Reprod 2015; 30: 590–602.
7. Br Med J Open, 2015.
8. Tiuzikov I.A., Kalinchenko S.Iu., Vorslov L.O., Tishova Iu.A. Besplodie: opredelenie, epidemiologiia, prichiny, klassifikatsiia, kriterii prognoza. Eksperim. i klin. urologiia. 2014; 2. [in Russian]
9. Panda B, Dash C, Padhy RN, Routray P. Effect of age and abstinence on semen quality: A retrospective study in a teaching hospital Priyadarsini Sunanda. Asian Pacific J Reprod 2014.
10. Vinogradov I.V., Strashnova A.L., Afanas'eva L.M. i dr. Primenenie razlichnykh metodov otsenki spermatozoidov v klinicheskoi praktike. Materialy XI Kongressa «Muzhskoe zdorov'e». M., 2010; s. 195–7. [in Russian]
11. Божедомов В.А. Мужское бесплодие. М., 2009. / Bozhedomov V.A. Muzhskoe besplodie. M., 2009. [in Russian]
12. Zini A, Al-Hathal N. Antioxidant therapy in male infertility: fact or fiction? Asian J Androl 2011; 13: 374
13. Zini A, San Gabriel M, Baazeem A. Antioxidants and sperm DNA damage: a clinical perspective. J Assist Reprod Genet 2009; 26: 427–32.
14. Aitken RJ, de Iuliis GN, Finnie JM et al. Analysis of the relationships between oxidative stress, DNA damage and sperm vitality in a patient population: development of diagnostic criteria. Hum Reprod 2010; 25: 2415–26.
15. Fraga CG, Motchnik PA, Shigenaga MK et al. Ascorbic acid protects against endogenous oxidative DNA damage in human sperm. Proc Natl Acad Sci USA 1991; 88: 11003–6.
16. Iwasaki A, Gagnon C. Formation of reactive oxygen species in spermatozoa of infertile patients. Fertil Steril 1992; 57: 409–16.
17. Zini A, Sigman M. Are tests of sperm DNA damage clinically useful? Pros and cons. J Androl 2009; 30: 219–29.
18. Agarwal A, Nallella KP, Allamaneni SS, Said TM. Role of antioxidants in treatment of male infertility: an overview of the literature. Reprod Biomed Online 2004; 8: 616–27.
19. Aitken RJ, Paterson M, Fisher H et al. Redox regulation of tyrosine phosphorylation in human spermatozoa and its role in the control of human sperm function. J Cell Sci 1995; 108 (Pt. 5): 2017–25.
20. Griveau JF, Le Lannou D. Reactive oxygen species and human spermatozoa: physiology and pathology. Int J Androl 1997; 20: 61–9.
21. De Lamirande E, Jiang H, Zini A et al. Reactive oxygen species and sperm physiology. Rev Reprod 1997; 2: 48–54.
22. Aitken RJ, Clarkson JS. Cellular basis of defective sperm function and its association with the genesis of reactive oxygen species by human spermatozoa. J Reprod Fertil 1987; 81: 459–69.
23. De Lamirande E, Gagnon C. Reactive oxygen species and human spermatozoa. I. Effects on the motility of intact spermatozoa and on sperm axonemes. J Androl 1992; 13: 368–78.
24. Zini A, Garrels K, Phang D. Antioxidant activity in the semen of fertile and infertile men. Urology 2000; 55: 922–6.
25. Alvarez JG, Touchstone JC, Blasco L, Storey BT. Spontaneous lipid peroxidation and production of hydrogen peroxide and superoxide in human spermatozoa. Superoxide dismutase as major enzyme protectant against oxygen toxicity. J Androl 1987; 8: 338–48.
26. Twigg J, Fulton N, Gomez E et al. Analysis of the impact of intracellular reactive oxygen species generation on the structural and functional integrity of human spermatozoa: lipid peroxidation, DNA fragmentation and effectiveness of antioxidants. Hum Reprod 1998; 13: 1429–36.
27. Chabory E, Damon C, Lenoir A et al. Epididymis seleno-independent glutathione peroxidase 5 maintains sperm DNA integrity in mice. J Clin Invest 2009; 119: 2074–85.
28. Weir CP, Robaire B. Spermatozoa have decreased antioxidant enzymatic capacity and increased reactive oxygen species production during aging in the Brown Norway rat. J Androl 2007; 28: 229–40.
29. Zini A, de Lamirande E, Gagnon C. Low levels of nitric oxide promote human sperm capacitation in vitro. J Androl 1995; 16: 424–31.
30. Smith R, Vantman D, Ponce J, Escobar J, Lissi E. Total antioxidant capacity of human seminal plasma. Hum Reprod 1996; 11: 1655–60.
31. Zini A, De Lamirande E, Gagnon C. Reactive oxygen species in semen of infertile patients: levels of superoxide dismutase- and catalase-like activities in seminal plasma and spermatozoa. Int J Androl 1993; 16: 183–8.
32. Kobayashi T, Miyazaki T, Natori M, Nozawa S. Protective role of superoxide dismutase in human sperm motility: superoxide dismutase activity and lipid peroxide in human seminal plasma and spermatozoa. Hum Reprod 1991; 6: 987–91.
33. Zini A, Schlegel PN. Catalase mRNA expression in the male rat reproductive tract. J Androl 1996; 17: 473–80.
34. Thiele JJ, Friesleben HJ, Fuchs J, Ochsendorf FR. Ascorbic acid and urate in human seminal plasma: determination and interrelationships with chemiluminescence in washed semen. Hum Reprod 1995; 10: 110–5.
35. Kalthur G, Adiga SK, Upadhya D et al. Effect of cryopreservation on sperm DNA integrity in patients with teratospermia. Fertil Steril 2008; 89: 1723–7.
36. Tauber PF, Zaneveld LJ, Propping D, Schumacher GF. Components of human split ejaculates. I. Spermatozoa, fructose, immunoglobulins, albumin, lactoferrin, transferrin and other plasma proteins. J Reprod Fertil 1975; 43: 249–67.
37. Smith R, Vantman D, Ponce J et al. Total antioxidant capacity of human seminal plasma. Hum Reprod 1996; 11: 1655–60.
38. Lewis SE, Sterling ES, Young IS, Thompson W. Comparison of individual antioxidants of sperm and seminal plasma in fertile and infertile men. Fertil Steril 1997; 67: 142–7.
39. Sanocka D, Miesel R, Jedrzejczak P, Kurpisz MK. Oxidative stress and male infertility. J Androl 1996; 17: 449–54.
40. Lewis SE, Boyle PM, McKinney KA, Young IS, Thompson W. Total antioxidant capacity of seminal plasma is different in fertile and infertile men. Fertil Steril 1995; 64: 868–70.
41. Appasamy M, Muttukrishna S, Pizzey AR et al. Relationship between male reproductive hormones, sperm DNA damage and markers of oxidative stress in infertility. Reprod Biomed Online 2007; 14: 159–65.
42. Verit FF, Verit A, Kocyigit A et al. No increase in sperm DNA damage and seminal oxidative stress in patients with idiopathic infertility. Arch Gynecol Obstet 2006; 274: 339–44.
43. Hampl JS, Taylor CA, Johnston CS. Vitamin C deficiency and depletion in the United States: the Third National Health and Nutrition Examination Survey, 1988 to 1994. Am J Public Health 2004; 94: 870–5.
44. Mukhina Iu.G., Kliuchnikov S.O., Netrebenko O.K., Shchepliagina L.A. Klinicheskoe znachenie narushenii metabolizma tsinka. 2011. [in Russian]
45. Efremov E.A., Okhobotov D.A., Mel'nik Ia.I. Primenenie preparata Seltsink Plius v kombinirovannoi terapii khronicheskogo prostatita i dobrokachestvennoi giperplazii predstatel'noi zhelezy. Eksperim. i klin. urologiia, 2014. [in Russian]
46. Kozarenko V.G. Defitsit tsinka u detei s zaderzhkoi rosta i polovogo razvitiia. Avtoref. dis. … kand. med. nauk. SPb., 2008. [in Russian]
47. Avtsyn A.P., Zhavoronkov A.A., Rish M.A. i dr. Mikroelementozy cheloveka: etiologiia, klassifikatsiia, organopatologiia. M., 1991. [in Russian]
48. Alekseenko V.A., Aleshchukin L.V. i dr. Tsink i kadmii v okruzhaiushchei srede. M., 1992. [in Russian]
49. Skal'nyi A.V. Ekologo-fiziologicheskoe obosnovanie effektivnosti ispol'zovaniia makro- i mikroelementov pri narusheniiakh gomeostaza u obsleduemykh iz razlichnykh klimatogeograficheskikh regionov. Dis. … d-ra med. nauk. M., 2000. [in Russian]
50. Golubkina N.A., Alfthan G.V. The human selenium status in 27 regions of Russia. J Trace Elem Med Biol 1999; 13: 15–20.
51. Korovina N.A. Profilaktika rakhita u detei: primenenie kal'tsiia. Lechashchii vrach. 2004; 1: 56–8. [in Russian]
52. Ruel MT, Rivera JA, Santizo M-C et al. Impact of Zinc Supplementation on Morbidity From Diarrhea and Respiratory Infections Among Rural Guatemalan Children. Pediatrics 1997; 99: 808–13. [in Russian]
ГБОУ ВПО Первый Московский государственный медицинский университет им. И.М.Сеченова Минздрава России. 119991, Россия, Москва, ул. Трубецкая, д. 8, стр. 2
vvb56@yandex.ru
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I.M.Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation. 119991, Russian Federation, Moscow, ul. Trubetskaia, d. 8, str. 2
vvb56@yandex.ru