scholarly journals Heterocyclic Aromatic Amines in Meat: Formation, Isolation, Risk Assessment and Inhibitory Effect of Plant Extracts

Foods ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 1466
Author(s):  
Hafiz Rehan Nadeem ◽  
Saeed Akhtar ◽  
Tariq Ismail ◽  
Piero Sestili ◽  
Jose Manuel Lorenzo ◽  
...  

Heterocyclic aromatic amines (HAAs) are potent carcinogenic compounds induced by the Maillard reaction in well-done cooked meats. Free amino acids, protein, creatinine, reducing sugars and nucleosides are major precursors involved in the production of polar and non-polar HAAs. The variety and yield of HAAs are linked with various factors such as meat type, heating time and temperature, cooking method and equipment, fresh meat storage time, raw material and additives, precursor’s presence, water activity, and pH level. For the isolation and identification of HAAs, advanced chromatography and spectroscopy techniques have been employed. These potent mutagens are the etiology of several types of human cancers at the ng/g level and are 100- to 2000-fold stronger than that of aflatoxins and benzopyrene, respectively. This review summarizes previous studies on the formation and types of potent mutagenic and/or carcinogenic HAAs in cooked meats. Furthermore, occurrence, risk assessment, and factors affecting HAA formation are discussed in detail. Additionally, sample extraction procedure and quantification techniques to determine these compounds are analyzed and described. Finally, an overview is presented on the promising strategy to mitigate the risk of HAAs by natural compounds and the effect of plant extracts containing antioxidants to reduce or inhibit the formation of these carcinogenic substances in cooked meats.

2005 ◽  
Vol 53 (8) ◽  
pp. 3248-3258 ◽  
Author(s):  
Robert J. Turesky ◽  
Jason Taylor ◽  
Laura Schnackenberg ◽  
James P. Freeman ◽  
Ricky D. Holland

2021 ◽  
Vol 43 (1) ◽  
Author(s):  
Medjda Bellamri ◽  
Scott J. Walmsley ◽  
Robert J. Turesky

AbstractHeterocyclic aromatic amines (HAAs) form during the high-temperature cooking of meats, poultry, and fish. Some HAAs also arise during the combustion of tobacco. HAAs are multisite carcinogens in rodents, inducing cancer of the liver, gastrointestinal tract, pancreas, mammary, and prostate glands. HAAs undergo metabolic activation by N-hydroxylation of the exocyclic amine groups to produce the proposed reactive intermediate, the heteroaryl nitrenium ion, which is the critical metabolite implicated in DNA damage and genotoxicity. Humans efficiently convert HAAs to these reactive intermediates, resulting in HAA protein and DNA adduct formation. Some epidemiologic studies have reported an association between frequent consumption of well-done cooked meats and elevated cancer risk of the colorectum, pancreas, and prostate. However, other studies have reported no associations between cooked meat and these cancer sites. A significant limitation in epidemiology studies assessing the role of HAAs and cooked meat in cancer risk is their reliance on food frequency questionnaires (FFQ) to gauge HAA exposure. FFQs are problematic because of limitations in self-reported dietary history accuracy, and estimating HAA intake formed in cooked meats at the parts-per-billion level is challenging. There is a critical need to establish long-lived biomarkers of HAAs for implementation in molecular epidemiology studies designed to assess the role of HAAs in health risk. This review article highlights the mechanisms of HAA formation, mutagenesis and carcinogenesis, the metabolism of several prominent HAAs, and the impact of critical xenobiotic-metabolizing enzymes on biological effects. The analytical approaches that have successfully biomonitored HAAs and their biomarkers for molecular epidemiology studies are presented.


1996 ◽  
Vol 79 (3) ◽  
pp. 813-816 ◽  
Author(s):  
Gracia A Perfetti

Abstract A liquid chromatographic method for determining heterocyclic aromatic amines (HAAs) was modified so that it can be used to quantitate the following 5 HAAs in complex process flavors: 2-amino-3-methylimidazo[4,5-f]quinoline (IQ); 2-amino-3,4-dimethylimidazo[4,5-f]quinoline (MelQ); 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MelQx); 2-amino-3,4,8-trimethylimidazo[4,5-f]quinoxaline (diMelQx); and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP). By changing the initial extraction procedure, PhIP recovery improved from 35 to 87%. An additional cleanup step using ion-exchange solid-phase extraction reduced the levels of interfering components, thus allowing determination of low levels of the amines. Recoveries from process flavors spiked at 25 ppb averaged 83–90%.


2012 ◽  
Vol 60 (24) ◽  
pp. 6235-6240 ◽  
Author(s):  
Olga Viegas ◽  
L. Filipe Amaro ◽  
Isabel M. P. L. V. O. Ferreira ◽  
Olívia Pinho

2017 ◽  
Vol 98 (5) ◽  
pp. 1988-1994 ◽  
Author(s):  
Bin Zhou ◽  
Yueliang Zhao ◽  
Xichang Wang ◽  
Daming Fan ◽  
Kawing Cheng ◽  
...  

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