Literature DB >> 9714421

Formaldehyde derived from dietary aspartame binds to tissue components in vivo.

C Trocho1, R Pardo, I Rafecas, J Virgili, X Remesar, J A Fernández-López, M Alemany.   

Abstract

Adult male rats were given an oral dose of 10 mg/kg aspartame 14C-labelled in the methanol carbon. At timed intervals of up to 6 hours, the radioactivity in plasma and several organs was investigated. Most of the radioactivity found (>98% in plasma, >75% in liver) was bound to protein. Label present in liver, plasma and kidney was in the range of 1-2% of total radioactivity administered per g or mL, changing little with time. Other organs (brown and white adipose tissues, muscle, brain, cornea and retina) contained levels of label in the range of 1/12 to 1/10th of that of liver. In all, the rat retained, 6 hours after administration about 5% of the label, half of it in the liver. The specific radioactivity of tissue protein, RNA and DNA was quite uniform. The protein label was concentrated in amino acids, different from methionine, and largely coincident with the result of protein exposure to labelled formaldehyde. DNA radioactivity was essentially in a single different adduct base, different from the normal bases present in DNA. The nature of the tissue label accumulated was, thus, a direct consequence of formaldehyde binding to tissue structures. The administration of labelled aspartame to a group of cirrhotic rats resulted in comparable label retention by tissue components, which suggests that liver function (or its defect) has little effect on formaldehyde formation from aspartame and binding to biological components. The chronic treatment of a series of rats with 200 mg/kg of non-labelled aspartame during 10 days resulted in the accumulation of even more label when given the radioactive bolus, suggesting that the amount of formaldehyde adducts coming from aspartame in tissue proteins and nucleic acids may be cumulative. It is concluded that aspartame consumption may constitute a hazard because of its contribution to the formation of formaldehyde adducts.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9714421     DOI: 10.1016/s0024-3205(98)00282-3

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  19 in total

Review 1.  Pharmacological approaches for the treatment of obesity.

Authors:  José-Antonio Fernández-López; Xavier Remesar; Màrius Foz; Marià Alemany
Journal:  Drugs       Date:  2002       Impact factor: 9.546

Review 2.  The role of the gut microbiota in NAFLD.

Authors:  Christopher Leung; Leni Rivera; John B Furness; Peter W Angus
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2016-06-08       Impact factor: 46.802

3.  Cytotoxic effects of aspartame on human cervical carcinoma cells.

Authors:  Muthuraman Pandurangan; Gansukh Enkhtaivan; Doo Hwan Kim
Journal:  Toxicol Res (Camb)       Date:  2015-09-29       Impact factor: 3.524

4.  Effect of aspartame on oxidative stress and monoamine neurotransmitter levels in lipopolysaccharide-treated mice.

Authors:  Omar M E Abdel-Salam; Neveen A Salem; Jihan Seid Hussein
Journal:  Neurotox Res       Date:  2011-08-06       Impact factor: 3.911

Review 5.  Reproductive and developmental toxicity of formaldehyde: a systematic review.

Authors:  Anh Duong; Craig Steinmaus; Cliona M McHale; Charles P Vaughan; Luoping Zhang
Journal:  Mutat Res       Date:  2011-07-20       Impact factor: 2.433

Review 6.  Artificial sweeteners - a review.

Authors:  Sanchari Chattopadhyay; Utpal Raychaudhuri; Runu Chakraborty
Journal:  J Food Sci Technol       Date:  2011-10-21       Impact factor: 2.701

7.  Soft drink consumption linked with fatty liver in the absence of traditional risk factors.

Authors:  Nimer Assy; Gattas Nasser; Iad Kamayse; William Nseir; Zaza Beniashvili; Agness Djibre; Maria Grosovski
Journal:  Can J Gastroenterol       Date:  2008-10       Impact factor: 3.522

8.  The protective effect of N-acetylcysteine on oxidative stress in the brain caused by the long-term intake of aspartame by rats.

Authors:  Isabela A Finamor; Giovana M Ourique; Tanise S Pês; Etiane M H Saccol; Caroline A Bressan; Taína Scheid; Bernardo Baldisserotto; Susana F Llesuy; Wânia A Partata; Maria A Pavanato
Journal:  Neurochem Res       Date:  2014-06-27       Impact factor: 3.996

9.  Association between intake of artificially sweetened and sugar-sweetened beverages and preterm delivery: a large prospective cohort study.

Authors:  Linda Englund-Ögge; Anne Lise Brantsæter; Margareta Haugen; Verena Sengpiel; Ali Khatibi; Ronny Myhre; Solveig Myking; Helle Margrete Meltzer; Marian Kacerovsky; Roy M Nilsen; Bo Jacobsson
Journal:  Am J Clin Nutr       Date:  2012-08-01       Impact factor: 7.045

10.  Methanol may function as a cross-kingdom signal.

Authors:  Yuri L Dorokhov; Tatiana V Komarova; Igor V Petrunia; Vyacheslav S Kosorukov; Roman A Zinovkin; Anastasia V Shindyapina; Olga Y Frolova; Yuri Y Gleba
Journal:  PLoS One       Date:  2012-04-26       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.