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Bir Çoklu Organ Toksini: Akrilamit

Yıl 2018, Cilt: 40 Sayı: 1, 94 - 100, 31.01.2018
https://doi.org/10.20515/otd.323209

Öz

Akrilamit, kullanımı
yaygın bir kimyasaldır. Çeşitli sanayi dallarından laboratuvara, yiyeceklerden
sigara dumanına kadar birçok yerde mevcuttur. 20. yüzyıl ortalarından beri
nörotoksik bir ajan olduğu bilinen akrilamitin 2002 yılında yiyeceklerde de
oluştuğu saptanmıştır. Akrilamit yüksek ısıya maruz kalan yiyeceklerde früktoz
ve glikoz gibi şekerlerin asparajin aminoasiti ile reaksiyonu sonucunda
oluşmaktadır. Yiyeceklerin içeriği, asparajin oranı, yiyeceklerin maruz kaldığı
işlem, sıcaklık ve diğer etmenler oluşacak akrilamit miktarını etkilemektedir.
Bu anlaşılınca akrilamitin nörotoksik etkileri dışında diğer etkileri de
araştırma konusu olmuştur. Yapılan çalışmalar sonucunda akrilamitin testis,
yumurtalık, karaciğer, akciğer, böbrek ve bağırsak gibi organlara etkisi olduğu
gösterilmiştir. Aynı zamanda Uluslararası Kanser Araştırmaları Ajansı
tarafından insanda kanser yapma olasılığı olan maddeler arasında sayılmaktadır.
Akrilamitin kanserojen özelliği deney hayvanlarında kanıtlansa da insanlarda
henüz kesin kanıtlar mevcut değildir. Günlük yaşamda akrilamit karşılaşma
kaçınılmaz bir durumdur. Yiyeceklerde uygulanan işlemlerin çoğunda akrilamit
oluşmaktadır. Böylece akrilamit içeren gıdalarla daha fazla karşı karşıya
kalanlar, özellikle de çocuklar için bir risk oluşabilir. Bu derlemede, zararlı
olduğu önceden gösterilen, ancak zarar potansiyeli henüz tam olarak
anlaşılamamış bir madde olan akrilamitin bedendeki etkileri tartışılarak
korunma önlemleri hakkında önerilerde bulunulmuştur.

Kaynakça

  • 1. Smith E. A., Oehme F. W. (1991). Acrylamide and polyacrylamide: a review of production, use, environmental fate and neurotoxicity. Rev Environ Health, 9(4), 215-28.
  • 2. Friedman M. (2003). Chemistry, Biochemistry, and Safety of Acrylamide. A Review. J Agr Food Chem, 51(16), 4504-26.
  • 3. Tareke E., Rydberg P., Karlsson P., Eriksson S., Törnqvist M. (2002). Analysis of Acrylamide, a Carcinogen Formed in Heated Foodstuffs. J Agric Food Chem, 50(17), 4998-5006.
  • 4. Mottram D. S., Wedzicha B. L., Dodson A. T. (2002). Acrylamide is formed in the Maillard reaction. Nature, 419(6906), 448-9.
  • 5. Claus A., Carle R., Schieber A. (2008). Acrylamide in cereal products: A review. J Cereal Sci, 47(2), 118-33.
  • 6. Capuano E., Fogliano V. (2011). Acrylamide and 5-hydroxymethylfurfural (HMF): A review on metabolism, toxicity, occurrence in food and mitigation strategies. LWT-Food sci technol, 44(4), 793-810.
  • 7. Mojska H., Gielecinska I., Cendrowski A. (2016). Acrylamide content in cigarette mainstream smoke and estimation of exposure to acrylamide from tobacco smoke in Poland. Ann Agric Environ Med, 23(3), 456-61.
  • 8. Dearfield K. L., Abernathy C. O., Ottley M. S., Brantner J. H., Hayes P. F. (1988). Acrylamide: its metabolism, developmental and reproductive effects, genotoxicity, and carcinogenicity. Mutat Res-Rev Genet 195(1), 45-77.
  • 9. Kuperman A. S. (1958). Effects of acrylamide on the central nervous system of the cat. Journal of Pharmacology and Experimental Therapeutics, 123(3), 180-92.
  • 10. Duda-Chodak A., Wajda L., Tarko T., Sroka P., Satora P. (2016). A review of the interactions between acrylamide, microorganisms and food components. Food Funct, 7(3), 1282-95.
  • 11. LoPachin R. M. (2004). The changing view of acrylamide neurotoxicity. Neurotoxicology, 25(4), 617-30.
  • 12. He F. S., Zhang S. L., Wang H. L., Li G., Zhang Z. M., Li F. L., et al. (1989). Neurological and electroneuromyographic assessment of the adverse effects of acrylamide on occupationally exposed workers. Scand J Work Environ Health, 15(2), 125-9.
  • 13. Hagmar L., xf, rnqvist M., Nordander C., Ros, xe, et al. (2001). Health effects of occupational exposure to acrylamide using hemoglobin adducts as biomarkers of internal dose. Scand J Work Environ Health 27(4), 219-26.
  • 14. Fullerton P. M., Barnes J. M. (1966). Peripheral Neuropathy in Rats Produced by Acrylamide. Br J Ind Med, 23(3), 210-21.
  • 15. Vanitha S., Thiagarajan V. R., Muthuraman A., Krishnan S., Aruna A., Tharabai R. (2015). Pharmacological evaluation of methanolic leaf extract of Swietenia mahagoni on acrylamide-induced neuropathic pain in rats. Toxicol Ind Health, 31(12), 1185-94.
  • 16. Rice J. M. (2005). The carcinogenicity of acrylamide. Mutat Res 580(1-2), 3-20.
  • 17. IARC. (1994). International Agency for Reseach on Cancer. Monographs on the evalution of the carcinogenic risk to humans., 60389-426.
  • 18. Sakamoto J., Hashimoto K. (1986). Reproductive toxicity of acrylamide and related compounds in mice — effects on fertility and sperm morphology. Arch Toxicol, 59(4), 201-5.
  • 19. Wang H., Huang P., Lie T., Li J., Hutz R. J., Li K., et al. (2010). Reproductive toxicity of acrylamide-treated male rats. Reprod Toxicol, 29(2), 225-30.
  • 20. Sega G. A., Generoso E. E., Brimer P. A., Malling H. V. (1990). Acrylamide exposure induces a delayed unscheduled dna synthesis in germ cells of male mice that is correlated with the temporal pattern of adduct formation in testis DNA. Environ Mol Mutagen, 16(3), 137-42.
  • 21. Yang H. J., Lee S. H., Jin Y., Choi J. H., Han D. U., Chae C., et al. (2005b). Toxicological effects of acrylamide on rat testicular gene expression profile. Reprod Toxicol, 19(4), 527-34.
  • 22. Tyl R. W., Marr M. C., Myers C. B., Ross W. P., Friedman M. A. (2000). Relationship between acrylamide reproductive and neurotoxicity in male rats. Reprod Toxicol, 14(2), 147-57.
  • 23. Gassner P., Adler I.-D. (1996). Induction of hypoploidy and cell cycle delay by acrylamide in somatic and germinal cells of male mice. Mutat Res-Gen Tox, 367(4), 195-202.
  • 24. Mahmood S. A. F., Amin K., Rahman H. S., Othman H. H. (2016). The Pathophysiological Effects of Acrylamide in Albino Wister Rats. IJMRHS, 5(7), 42-8.
  • 25. Duan X., Wang Q. C., Chen K. L., Zhu C. C., Liu J., Sun S. C. (2015). Acrylamide toxic effects on mouse oocyte quality and fertility in vivo. Sci Rep 5.
  • 26. Wei Q. W., Li J., Li X. M., Zhang L., Shi F. X. (2014). Reproductive toxicity in acrylamide-treated female mice. Reproductive Toxicology, 46121-8.
  • 27. Perreault S. D., Jeffay S. C. (1997). Glutathione depletion in hamster oocytes and ovary by acute exposure to acrylamide. Biol Reprod 56604.
  • 28. El- Bohi K. M., Moustafa G. G., El sharkawi N. I., Sabik L. M. E. (2011). Genotoxic effects of acrylamide in adult male albino rats liver J Am Sci, 7(1).
  • 29. Rawi S. M., Marie M.-A. S., Fahmy S. R., El-Abied S. A. (2012). Hazardous effects of acrylamide on immature male and female rats. Afr J Pharm Pharmacol, 6(18), 1367-86.
  • 30. Rajeh N. A., Al-Dhaheri N. M. (2017). Antioxidant effect of vitamin E and 5-aminosalicylic acid on acrylamide induced kidney injury in rats. Saudi Med J 38(2), 132-7.
  • 31. Totani N., Yawata M., Ojiri Y., Fujioka Y. (2007). Effects of trace acrylamide intake in Wistar rats. J Oleo Sci, 56(9), 501-6.
  • 32. Ghorbel I., Elwej A., Fendri N., Mnif H., Jamoussi K., Boudawara T., et al. (2017). Olive oil abrogates acrylamide induced nephrotoxicity by modulating biochemical and histological changes in rats. Ren Fail 39(1), 236-45.
  • 33. Ghorbel I., Chaabane M., Boudawara O., Kamoun N. G., Boudawara T., Zeghal N. (2016). Dietary unsaponifiable fraction of extra virgin olive oil supplementation attenuates lung injury and DNA damage of rats co-exposed to aluminum and acrylamide. Environ Sci Pollut Res, 23(19), 19397-408.
  • 34. Kacar S., Vejselova D., Kutlu H. M., Sahinturk V. (2017). Acrylamide-derived cytotoxic, anti-proliferative, and apoptotic effects on A549 cells. Hum Exp Toxicol, 960327117712386.
  • 35. Swamy M., Subbaiah K., Aumau B., Kamala K., Rao K., Raju K. (2013). Toxic effect of acrylamide on body weight, the study of antioxidants and histoarchitecture of heart in the developing chick embryo. Indian J Appl Res, 327-30.
  • 36. Ghorbel I., Khemakhem M., Boudawara O., Marrekchi R., Jamoussi K., Ben Amar R., et al. (2015). Effects of dietary extra virgin olive oil and its fractions on antioxidant status and DNA damage in the heart of rats co-exposed to aluminum and acrylamide. Food Funct, 6(9), 3098-108.
  • 37. Altinoz E., Turkoz Y., Vardi N. (2015). The protective effect of N-acetylcysteine against acrylamide toxicity in liver and small and large intestine tissues. Bratisl Lek Listy, 116(4), 252-8.
  • 38. Erdemli M. E., Dogan Z., Cigremis Y., Akgoz M., Altintoz E., Gecer M., et al. (2015). Amelioration of subchronic acrylamide toxicity in large intestine of rats by organic dried apricot intake. Turk J Biol 39(6), 872-8.
  • 39. Tomaszewska E., Dobrowolski P., Puzio I., Prost L., Kurlak P., Sawczuk P., et al. (2014). Acrylamide-induced prenatal programming of intestine structure in guinea pig. J Physiol Pharmacol, 65(1), 107-15.
  • 40. Sabo J. I., Djolai M., Zivojinov M., Fejsa A. L., Mocko-Kacanski M., Amidzic J. (2016). Effects of acute exposure to orally administrated acrylamide on histological structure of stomach tissue in Wistar rats. Virchows Archiv, 469S158-S.
  • 41. El-Mehi A. E., El-Sherif N. M. (2015). Influence of acrylamide on the gastric mucosa of adult albino rats and the possible protective role of rosemary. Tissue and Cell, 47(3), 273-83.
  • 42. Fang J., Liang C. L., Jia X. D., Li N. (2014). Immunotoxicity of acrylamide in female BALB/c mice. Biomed Environ Sci, 27(6), 401-9.

A Multiple Organ Toxicant: Acrylamide

Yıl 2018, Cilt: 40 Sayı: 1, 94 - 100, 31.01.2018
https://doi.org/10.20515/otd.323209

Öz

 Acrylamide is a chemical substance, the
utilization area of which is widespread. It is available in many places from
various industries to laboratories, from daily food to cigarette smoke. Acrylamide,
known as a neurotoxic agent since the middle of the 20th century, was found to
form in foods in 2002. Acrylamide forms as a result of the reaction between
asparagine and the reducing sugars such as fructose and glucose in the
high-temperature processed foods. The food ingredients, asparagine amount, food
processing method, temperature and other factors affect the amount of
acrylamide to form in foods. After the discovery of acrylamide formation in
foods, other effects of acrylamide became the subject of research. As a result
of these studies, the effect of acrylamide on the testis, ovaries, liver lung,
kidney, bowel organs has been revealed. Acrylamide is also categorized in the
substances that are probably carcinogenic to human by the International Agency
for Research on Cancer. Although acrylamide was proven to be carcinogenic for
experimental animals, there is no more definitive evidence for humans.
Acrylamide exposure is inevitable in daily life. Acrylamide forms as a result
of the majority of food processes. This may pose a risk for who exposes more to
acrylamide-containing foods, especially for children. In this review, the
bodily effects of acrylamide were discussed and suggestions for its protection
modalities were provided, which was previously shown to be harmful but its
exact potential toxicity has not yet been fully understood.

Kaynakça

  • 1. Smith E. A., Oehme F. W. (1991). Acrylamide and polyacrylamide: a review of production, use, environmental fate and neurotoxicity. Rev Environ Health, 9(4), 215-28.
  • 2. Friedman M. (2003). Chemistry, Biochemistry, and Safety of Acrylamide. A Review. J Agr Food Chem, 51(16), 4504-26.
  • 3. Tareke E., Rydberg P., Karlsson P., Eriksson S., Törnqvist M. (2002). Analysis of Acrylamide, a Carcinogen Formed in Heated Foodstuffs. J Agric Food Chem, 50(17), 4998-5006.
  • 4. Mottram D. S., Wedzicha B. L., Dodson A. T. (2002). Acrylamide is formed in the Maillard reaction. Nature, 419(6906), 448-9.
  • 5. Claus A., Carle R., Schieber A. (2008). Acrylamide in cereal products: A review. J Cereal Sci, 47(2), 118-33.
  • 6. Capuano E., Fogliano V. (2011). Acrylamide and 5-hydroxymethylfurfural (HMF): A review on metabolism, toxicity, occurrence in food and mitigation strategies. LWT-Food sci technol, 44(4), 793-810.
  • 7. Mojska H., Gielecinska I., Cendrowski A. (2016). Acrylamide content in cigarette mainstream smoke and estimation of exposure to acrylamide from tobacco smoke in Poland. Ann Agric Environ Med, 23(3), 456-61.
  • 8. Dearfield K. L., Abernathy C. O., Ottley M. S., Brantner J. H., Hayes P. F. (1988). Acrylamide: its metabolism, developmental and reproductive effects, genotoxicity, and carcinogenicity. Mutat Res-Rev Genet 195(1), 45-77.
  • 9. Kuperman A. S. (1958). Effects of acrylamide on the central nervous system of the cat. Journal of Pharmacology and Experimental Therapeutics, 123(3), 180-92.
  • 10. Duda-Chodak A., Wajda L., Tarko T., Sroka P., Satora P. (2016). A review of the interactions between acrylamide, microorganisms and food components. Food Funct, 7(3), 1282-95.
  • 11. LoPachin R. M. (2004). The changing view of acrylamide neurotoxicity. Neurotoxicology, 25(4), 617-30.
  • 12. He F. S., Zhang S. L., Wang H. L., Li G., Zhang Z. M., Li F. L., et al. (1989). Neurological and electroneuromyographic assessment of the adverse effects of acrylamide on occupationally exposed workers. Scand J Work Environ Health, 15(2), 125-9.
  • 13. Hagmar L., xf, rnqvist M., Nordander C., Ros, xe, et al. (2001). Health effects of occupational exposure to acrylamide using hemoglobin adducts as biomarkers of internal dose. Scand J Work Environ Health 27(4), 219-26.
  • 14. Fullerton P. M., Barnes J. M. (1966). Peripheral Neuropathy in Rats Produced by Acrylamide. Br J Ind Med, 23(3), 210-21.
  • 15. Vanitha S., Thiagarajan V. R., Muthuraman A., Krishnan S., Aruna A., Tharabai R. (2015). Pharmacological evaluation of methanolic leaf extract of Swietenia mahagoni on acrylamide-induced neuropathic pain in rats. Toxicol Ind Health, 31(12), 1185-94.
  • 16. Rice J. M. (2005). The carcinogenicity of acrylamide. Mutat Res 580(1-2), 3-20.
  • 17. IARC. (1994). International Agency for Reseach on Cancer. Monographs on the evalution of the carcinogenic risk to humans., 60389-426.
  • 18. Sakamoto J., Hashimoto K. (1986). Reproductive toxicity of acrylamide and related compounds in mice — effects on fertility and sperm morphology. Arch Toxicol, 59(4), 201-5.
  • 19. Wang H., Huang P., Lie T., Li J., Hutz R. J., Li K., et al. (2010). Reproductive toxicity of acrylamide-treated male rats. Reprod Toxicol, 29(2), 225-30.
  • 20. Sega G. A., Generoso E. E., Brimer P. A., Malling H. V. (1990). Acrylamide exposure induces a delayed unscheduled dna synthesis in germ cells of male mice that is correlated with the temporal pattern of adduct formation in testis DNA. Environ Mol Mutagen, 16(3), 137-42.
  • 21. Yang H. J., Lee S. H., Jin Y., Choi J. H., Han D. U., Chae C., et al. (2005b). Toxicological effects of acrylamide on rat testicular gene expression profile. Reprod Toxicol, 19(4), 527-34.
  • 22. Tyl R. W., Marr M. C., Myers C. B., Ross W. P., Friedman M. A. (2000). Relationship between acrylamide reproductive and neurotoxicity in male rats. Reprod Toxicol, 14(2), 147-57.
  • 23. Gassner P., Adler I.-D. (1996). Induction of hypoploidy and cell cycle delay by acrylamide in somatic and germinal cells of male mice. Mutat Res-Gen Tox, 367(4), 195-202.
  • 24. Mahmood S. A. F., Amin K., Rahman H. S., Othman H. H. (2016). The Pathophysiological Effects of Acrylamide in Albino Wister Rats. IJMRHS, 5(7), 42-8.
  • 25. Duan X., Wang Q. C., Chen K. L., Zhu C. C., Liu J., Sun S. C. (2015). Acrylamide toxic effects on mouse oocyte quality and fertility in vivo. Sci Rep 5.
  • 26. Wei Q. W., Li J., Li X. M., Zhang L., Shi F. X. (2014). Reproductive toxicity in acrylamide-treated female mice. Reproductive Toxicology, 46121-8.
  • 27. Perreault S. D., Jeffay S. C. (1997). Glutathione depletion in hamster oocytes and ovary by acute exposure to acrylamide. Biol Reprod 56604.
  • 28. El- Bohi K. M., Moustafa G. G., El sharkawi N. I., Sabik L. M. E. (2011). Genotoxic effects of acrylamide in adult male albino rats liver J Am Sci, 7(1).
  • 29. Rawi S. M., Marie M.-A. S., Fahmy S. R., El-Abied S. A. (2012). Hazardous effects of acrylamide on immature male and female rats. Afr J Pharm Pharmacol, 6(18), 1367-86.
  • 30. Rajeh N. A., Al-Dhaheri N. M. (2017). Antioxidant effect of vitamin E and 5-aminosalicylic acid on acrylamide induced kidney injury in rats. Saudi Med J 38(2), 132-7.
  • 31. Totani N., Yawata M., Ojiri Y., Fujioka Y. (2007). Effects of trace acrylamide intake in Wistar rats. J Oleo Sci, 56(9), 501-6.
  • 32. Ghorbel I., Elwej A., Fendri N., Mnif H., Jamoussi K., Boudawara T., et al. (2017). Olive oil abrogates acrylamide induced nephrotoxicity by modulating biochemical and histological changes in rats. Ren Fail 39(1), 236-45.
  • 33. Ghorbel I., Chaabane M., Boudawara O., Kamoun N. G., Boudawara T., Zeghal N. (2016). Dietary unsaponifiable fraction of extra virgin olive oil supplementation attenuates lung injury and DNA damage of rats co-exposed to aluminum and acrylamide. Environ Sci Pollut Res, 23(19), 19397-408.
  • 34. Kacar S., Vejselova D., Kutlu H. M., Sahinturk V. (2017). Acrylamide-derived cytotoxic, anti-proliferative, and apoptotic effects on A549 cells. Hum Exp Toxicol, 960327117712386.
  • 35. Swamy M., Subbaiah K., Aumau B., Kamala K., Rao K., Raju K. (2013). Toxic effect of acrylamide on body weight, the study of antioxidants and histoarchitecture of heart in the developing chick embryo. Indian J Appl Res, 327-30.
  • 36. Ghorbel I., Khemakhem M., Boudawara O., Marrekchi R., Jamoussi K., Ben Amar R., et al. (2015). Effects of dietary extra virgin olive oil and its fractions on antioxidant status and DNA damage in the heart of rats co-exposed to aluminum and acrylamide. Food Funct, 6(9), 3098-108.
  • 37. Altinoz E., Turkoz Y., Vardi N. (2015). The protective effect of N-acetylcysteine against acrylamide toxicity in liver and small and large intestine tissues. Bratisl Lek Listy, 116(4), 252-8.
  • 38. Erdemli M. E., Dogan Z., Cigremis Y., Akgoz M., Altintoz E., Gecer M., et al. (2015). Amelioration of subchronic acrylamide toxicity in large intestine of rats by organic dried apricot intake. Turk J Biol 39(6), 872-8.
  • 39. Tomaszewska E., Dobrowolski P., Puzio I., Prost L., Kurlak P., Sawczuk P., et al. (2014). Acrylamide-induced prenatal programming of intestine structure in guinea pig. J Physiol Pharmacol, 65(1), 107-15.
  • 40. Sabo J. I., Djolai M., Zivojinov M., Fejsa A. L., Mocko-Kacanski M., Amidzic J. (2016). Effects of acute exposure to orally administrated acrylamide on histological structure of stomach tissue in Wistar rats. Virchows Archiv, 469S158-S.
  • 41. El-Mehi A. E., El-Sherif N. M. (2015). Influence of acrylamide on the gastric mucosa of adult albino rats and the possible protective role of rosemary. Tissue and Cell, 47(3), 273-83.
  • 42. Fang J., Liang C. L., Jia X. D., Li N. (2014). Immunotoxicity of acrylamide in female BALB/c mice. Biomed Environ Sci, 27(6), 401-9.
Toplam 42 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Sağlık Kurumları Yönetimi
Bölüm DERLEMELER / REVIEWS
Yazarlar

Sedat Kaçar

Varol Şahintürk

Yayımlanma Tarihi 31 Ocak 2018
Yayımlandığı Sayı Yıl 2018 Cilt: 40 Sayı: 1

Kaynak Göster

Vancouver Kaçar S, Şahintürk V. Bir Çoklu Organ Toksini: Akrilamit. Osmangazi Tıp Dergisi. 2018;40(1):94-100.


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