Dergiler / Turkish Journal of Medical Sciences / 2020 / Cilt: 50 - Sayı: 2

The in vitro cytotoxic, genotoxic, and oxidative damage potentials of the oral artificial sweetener aspartame on cultured human blood cells

Sayfa
448–454
Yayın Tarihi
2020-03-01
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Conclusion: Overall, the obtained results showed that APM had genotoxicity potential and a concentration-dependent cytotoxic activity in human blood cells.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Background/aim: Aspartame APM, L-aspartyl-L-phenylalanine methylester is a low-calorie, nonsaccharide artificial sweetener widely used in foods and beverages.
📊
Temel Bulgular & Veri:Materials and methods: We aimed to evaluate the in vitro cytotoxic effects by using 3- 4,5-dimetylthiazol-2-yl -2,5-diphenyltetrazolium bromide MTT and lactate dehydrogenase release tests, genotoxic damage potential by using chromosome aberration CA assay, and antioxidant/oxidant activity by using total antioxidant capacity TAC and total oxidative stress TOS analysis in primary human whole blood cell cultures.
💡
Sonuç & Katkı:Conclusion: Overall, the obtained results showed that APM had genotoxicity potential and a concentration-dependent cytotoxic activity in human blood cells.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Aspartame · cytotoxicity · genotoxicity

Abstract

Background/aim: Aspartame APM, L-aspartyl-L-phenylalanine methylester is a low-calorie, nonsaccharide artificial sweetener widely used in foods and beverages. When metabolized by the body, APM is broken down into aspartic acid, phenylalanine amino acids, and a third substance, methanol. Since the amino acid phenylalanine serves as a neurotransmitter building block affecting the brain, and methanol is converted into toxic formaldehyde, APM has deleterious effects on the body and brain. Thus, its safety and, toxicity have been the subjects of concern ever since it was first discovered. Although many studies have been performed on it, due to the presence of conflicting data in the literature, there are still numerous question marks concerning APM. Therefore, the safety of aspartame was tested using in vitro methods. Materials and methods: We aimed to evaluate the in vitro cytotoxic effects by using 3- 4,5-dimetylthiazol-2-yl -2,5-diphenyltetrazolium bromide MTT and lactate dehydrogenase release tests, genotoxic damage potential by using chromosome aberration CA assay, and antioxidant/oxidant activity by using total antioxidant capacity TAC and total oxidative stress TOS analysis in primary human whole blood cell cultures. Results: The results of the MTT test showed that APM led to significant decreases in cell viability in a clear concentration-dependent manner. Moreover, an increase in CA frequency was found in the cells treated with APM. However, APM treatments did not cause any significant changes in TAC and TOS levels in whole blood cultures. Conclusion: Overall, the obtained results showed that APM had genotoxicity potential and a concentration-dependent cytotoxic activity in human blood cells.

🔖

Bu Makaleye Atıf Yap

ÇADIRCI, K., TOZLU, Ö. Ö., TÜRKEZ, H., MARDİNOĞLU, A. (2020). The in vitro cytotoxic, genotoxic, and oxidative damage potentials of the oral artificial sweetener aspartame on cultured human blood cells. Turkish Journal of Medical Sciences, Cilt: 50 - Sayı: 2, 448–454. https://ajindex.com/articles/113417

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (11)

  1. Ibrahim O. High intensity sweeteners chemicals structure, properties and applications. Natural Science and Discovery 2015
  2. 1(4): 88-94. doi: 10.20863/nsd.97334 2. Yang Q. Gain weight by “going diet?” Artificial sweeteners and the neurobiology of sugar cravings: Neuroscience 2010. Yale Journal of Biology and Medicine 2010
  3. 83(2): 101-108. 3. Gunby P. FDA approves aspartame as soft-drink sweetener. Journal of the American Medical Association 1983
  4. 250(7): 872-873. doi: 10.1001/jama.1983.03340070004002 4. Belpoggi F, Soffritti M, Padovani M, Degli Esposti D, Lauriola M et al. Results of long-term carcinogenicity bioassay on Sprague-Dawley rats exposed to aspartame administered in feed. Annals of the New York Academy of Sciences 2006
  5. doi: 10.1196/ annals.1371.080 5. Magnuson BA, Burdock GA, Doull J, Kroes RM, Marsh GM et al. Aspartame: a safety evaluation based on current use levels, regulations, and toxicological and epidemiological studies. Critical Reviews in Toxicology 2007
  6. 37(8): 629-727. doi: 10. 1080/10408440701516184 6. Finamor I, Pérez S, Bressan AC, Brenner CE, Rius-Pérez S et al. Chronic aspartame intake causes changes in the transsulphuration pathway, glutathione depletion and liver damage in mice. Redox Biology 2017
  7. doi: 10.1016/ j.redox. 2017. 01. 019. 7. Li X, Staszewski L, Xu H, Durick K, Zoller M et al. Human receptors for sweet and umami taste. Proceedings of the National Academy of Sciences of the United States of America. 2002
  8. 99(7): 4692-4696. doi: 10.1073/pnas.072090199 8. Sharma A, Amarnath S, Thulasimani M, Ramaswamy S. Artificial sweeteners as a sugar substitute: Are they really safe? Indian Journal of Pharmacology 2016
  9. 48(3): 237-240. doi: 10.4103/0253-7613.182888 9. Ashok I, Wankhar D, Sheeladevi R, Wankhar W. Longterm effect of aspartame on the liver antioxidant status and histopathology in Wistar albino rats. Biomedicine & Preventive Nutrition 2013
  10. 4(2): 229-305. doi: 10.1016/ j.bionut.2013.10.002 10. Lebda MA, Sadek KM, El-Sayed YS. Aspartame and soft drinkmediated neurotoxicity in rats: implication of oxidative stress, apoptotic signaling pathways, electrolytes and hormonal levels. Metabolic Brain Disease 2017
  11. 32(5): 1639-1647. doi: 10.1007/ s11011-017-0052-y. 11. Abd-Ellah HF, Abou-Zeid NRA, Nasr NM. The possible protective effect of N-acetyl-L-cysteine and folic acid in combination against aspartame-induced cerebral cortex neurotoxicity in adult male rats: a light and transmission electron