Inhibitory effects of cassiae semen extract on the formation of 2-amino-1-methyl-6-phenylimidazo [4,5-b] pyridine (PhIP) in model system
2-Amino-1-methyl-6-phenylimidazole [4,5-b] pyridine (PhIP), a heterocyclic amine (HAA), is found in meat products heated at high temperatures. However, PhIP is a mutagenic and potential carcinogenic compound. Cassiae semen, a type of medicine and food homology plant, is abundant in China and has bee...
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Published in | Frontiers in nutrition (Lausanne) Vol. 11; p. 1407007 |
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Abstract | 2-Amino-1-methyl-6-phenylimidazole [4,5-b] pyridine (PhIP), a heterocyclic amine (HAA), is found in meat products heated at high temperatures. However, PhIP is a mutagenic and potential carcinogenic compound. Cassiae semen, a type of medicine and food homology plant, is abundant in China and has been less applied for inhibiting heterocyclic amines.
To investigate the inhibitory effect of cassiae semen extract on PhIP formation within a model system and elucidate the inhibitory mechanism, an ultrasonic-assisted method with 70% ethanol was used to obtain cassiae semen extract, which was added to a model system (0.6 mmol of phenylalanine: creatinine, 1:1). PhIP was analyzed by LC-MS to determine inhibitory effect. The byproducts of the system and the mechanism of PhIP inhibition were verified by adding the extract to a model mixture of phenylacetaldehyde, phenylacetaldehyde and creatinine.
The results indicated that PhIP production decreased as the concentration of cassiae semen extract increased, and the highest inhibition rate was 91.9%. Byproduct (E), with a mass-charge ratio of m/z 199.9, was detected in the phenylalanine and creatinine model system but was not detected in the other systems. The cassiae semen extract may have reacted with phenylalanine to produce byproduct (E), which prevented the degradation of phenylalanine by the Strecker reaction to produce phenylacetaldehyde.
Cassiae semen extract consumed phenylalanine, which is the precursor for PhIP, thus inhibiting the formation of phenylacetaldehyde and ultimately inhibiting PhIP formation. The main objective of this study was to elucidate the mechanism by which cassiae semen inhibit PhIP formation and establish a theoretical and scientific foundation for practical control measures. |
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AbstractList | Introduction2-Amino-1-methyl-6-phenylimidazole [4,5-b] pyridine (PhIP), a heterocyclic amine (HAA), is found in meat products heated at high temperatures. However, PhIP is a mutagenic and potential carcinogenic compound. Cassiae semen, a type of medicine and food homology plant, is abundant in China and has been less applied for inhibiting heterocyclic amines.MethodsTo investigate the inhibitory effect of cassiae semen extract on PhIP formation within a model system and elucidate the inhibitory mechanism, an ultrasonic-assisted method with 70% ethanol was used to obtain cassiae semen extract, which was added to a model system (0.6 mmol of phenylalanine: creatinine, 1:1). PhIP was analyzed by LC–MS to determine inhibitory effect. The byproducts of the system and the mechanism of PhIP inhibition were verified by adding the extract to a model mixture of phenylacetaldehyde, phenylacetaldehyde and creatinine.ResultsThe results indicated that PhIP production decreased as the concentration of cassiae semen extract increased, and the highest inhibition rate was 91.9%. Byproduct (E), with a mass–charge ratio of m/z 199.9, was detected in the phenylalanine and creatinine model system but was not detected in the other systems. The cassiae semen extract may have reacted with phenylalanine to produce byproduct (E), which prevented the degradation of phenylalanine by the Strecker reaction to produce phenylacetaldehyde.DiscussionCassiae semen extract consumed phenylalanine, which is the precursor for PhIP, thus inhibiting the formation of phenylacetaldehyde and ultimately inhibiting PhIP formation. The main objective of this study was to elucidate the mechanism by which cassiae semen inhibit PhIP formation and establish a theoretical and scientific foundation for practical control measures. 2-Amino-1-methyl-6-phenylimidazole [4,5-b] pyridine (PhIP), a heterocyclic amine (HAA), is found in meat products heated at high temperatures. However, PhIP is a mutagenic and potential carcinogenic compound. Cassiae semen, a type of medicine and food homology plant, is abundant in China and has been less applied for inhibiting heterocyclic amines. To investigate the inhibitory effect of cassiae semen extract on PhIP formation within a model system and elucidate the inhibitory mechanism, an ultrasonic-assisted method with 70% ethanol was used to obtain cassiae semen extract, which was added to a model system (0.6 mmol of phenylalanine: creatinine, 1:1). PhIP was analyzed by LC-MS to determine inhibitory effect. The byproducts of the system and the mechanism of PhIP inhibition were verified by adding the extract to a model mixture of phenylacetaldehyde, phenylacetaldehyde and creatinine. The results indicated that PhIP production decreased as the concentration of cassiae semen extract increased, and the highest inhibition rate was 91.9%. Byproduct (E), with a mass-charge ratio of m/z 199.9, was detected in the phenylalanine and creatinine model system but was not detected in the other systems. The cassiae semen extract may have reacted with phenylalanine to produce byproduct (E), which prevented the degradation of phenylalanine by the Strecker reaction to produce phenylacetaldehyde. Cassiae semen extract consumed phenylalanine, which is the precursor for PhIP, thus inhibiting the formation of phenylacetaldehyde and ultimately inhibiting PhIP formation. The main objective of this study was to elucidate the mechanism by which cassiae semen inhibit PhIP formation and establish a theoretical and scientific foundation for practical control measures. |
Author | Yu, Di Jiang, Donghua Kong, Fanlei Li, Youyou |
AuthorAffiliation | School of Pharmacy, Guangxi University of Chinese Medicine , Nanning , China |
AuthorAffiliation_xml | – name: School of Pharmacy, Guangxi University of Chinese Medicine , Nanning , China |
Author_xml | – sequence: 1 givenname: Di surname: Yu fullname: Yu, Di – sequence: 2 givenname: Youyou surname: Li fullname: Li, Youyou – sequence: 3 givenname: Donghua surname: Jiang fullname: Jiang, Donghua – sequence: 4 givenname: Fanlei surname: Kong fullname: Kong, Fanlei |
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Cites_doi | 10.1021/acs.jafc.1c06842 10.2147/IJN.S79984 10.1016/j.foodchem.2020.128753 10.1016/j.fct.2019.110931 10.1016/j.fochx.2022.100315 10.1016/j.foodchem.2016.01.066 10.1007/s11694-014-9211-6 10.3390/cosmetics4010003 10.1016/j.foodchem.2012.01.089 10.1016/s0278-6915(00)00010-7 10.1016/j.foodchem.2014.01.039 10.1002/ptr.6082 10.1016/s0308-8146(02)00214-5 10.1111/1750-3841.13959 10.1016/j.fct.2009.03.028 10.1021/jf302227b 10.1111/1541-4337.12186 10.1111/1541-4337.12527 10.1016/j.jhazmat.2020.123486 10.14202/vetworld.2017.221-226 10.1016/j.foodchem.2021.131398 10.1016/j.foodchem.2019.126083 10.12161/j.issn.1005-6521.2019.21.022 10.12161/j.issn.1005-6521.2022.16.003 10.1021/jf071820z 10.1111/1750-3841.14035 10.1016/j.foodchem.2010.02.022 10.1021/acs.jafc.2c03122 10.7501/j.issn.0253-2670.2021.09.014 10.3390/cosmetics2040368 10.1016/j.jep.2023.116199 10.1254/jphs.fp0061565 10.1016/s0278-6915(03)00190-x |
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Keywords | model system byproduct cassiae semen inhibiting effect heterocyclic amine |
Language | English |
License | Copyright © 2024 Yu, Li, Jiang and Kong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | He Li, North University of China, China Reviewed by: Lijun Chen, Beijing Sanyuan Foods Co., Ltd., China Edited by: Hock Eng Khoo, Guilin University of Technology, China |
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References | Zhang (ref8) 2020; 312 Khan (ref22) 2015; 2 Dong (ref6) 2020; 19 Zamora (ref9) 2014; 155 Balashanmugam (ref26) 2015; 10 Jing (ref1) 2022; 14 Yu (ref30) 2022; 43 Sahu (ref24) 2017; 10 Cui (ref31) 2019; 40 Zhang (ref2) 2020; 135 Persson (ref13) 2003; 41 Hidalgo (ref7) 2022; 70 Cheng (ref12) 2007; 55 Viegas (ref18) 2012; 60 Wong (ref16) 2012; 133 Jiang (ref4) 2021; 373 (ref5) 1993 Yu (ref32) 2016; 201 Wang (ref3) 2021; 345 Gibis (ref34) 2016; 15 Kim (ref28) 2007; 105 Dong (ref21) 2021; 52 Khan (ref23) 2017; 4 Linghu (ref17) 2017; 82 Balogh (ref14) 2000; 38 Chen (ref20) 2023; 306 Quelhas (ref15) 2010; 122 Kwon (ref25) 2018; 32 Yang (ref10) 2020; 402 Yu (ref19) 2018; 83 Deng (ref11) 2022; 70 Zöchling (ref33) 2002; 79 Hossain (ref27) 2015; 9 Kim (ref29) 2009; 47 |
References_xml | – volume: 70 start-page: 79 year: 2022 ident: ref7 article-title: Carbonyl chemistry and the formation of heterocyclic aromatic amines with the structure of aminoimidazoazaarene publication-title: J Agric Food Chem doi: 10.1021/acs.jafc.1c06842 – volume: 10 start-page: 87 year: 2015 ident: ref26 article-title: Biosynthesis characterization of silver nanoparticles using Cassia roxburghii DC. Aqueous extract, and coated on cotton cloth for effective antibacterial activity publication-title: Int J Nanomedicine doi: 10.2147/IJN.S79984 – volume: 345 start-page: 128753 year: 2021 ident: ref3 article-title: A novel potent inhibitor of 2-amino-1-methyl-6-phenylimidazo[4,5-b] pyridine (PhIP) formation from Chinese chive: identification, inhibitory effect and action mechanism publication-title: Food Chem doi: 10.1016/j.foodchem.2020.128753 – volume: 135 start-page: 110931 year: 2020 ident: ref2 article-title: Heterocyclic aromatic amine concentrations and quality characteristics of traditional smoked and roasted poultry products on the northern Chinese market publication-title: Food Chem Toxicol doi: 10.1016/j.fct.2019.110931 – volume: 14 start-page: 100315 year: 2022 ident: ref1 article-title: Effect of acrolein, a lipid oxidation product, on the formation of the heterocyclic aromatic amine 2-amino-1-methyl-6-phenylimidazo[4,5-]pyridine (PhIP) in model systems and roasted tilapia fish patties publication-title: Food Chem X doi: 10.1016/j.fochx.2022.100315 – volume: 201 start-page: 46 year: 2016 ident: ref32 article-title: Effects of some cations on the formation of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) in a model system publication-title: Food Chem doi: 10.1016/j.foodchem.2016.01.066 – volume: 9 start-page: 68 year: 2015 ident: ref27 article-title: In vitro antioxidant, brine shrimp lethality and antimicrobial activities of methanol and petroleum ether extracts of Cassia renigera fruit publication-title: J Food Meas Charact doi: 10.1007/s11694-014-9211-6 – volume: 4 start-page: 2 year: 2017 ident: ref23 article-title: Relative free radicals scavenging and enzymatic activities of Hippophae rhamnoides and Cassia fistula extracts: importance for cosmetic publication-title: Food Med Appl Cosmetics doi: 10.3390/cosmetics4010003 – volume: 133 start-page: 760 year: 2012 ident: ref16 article-title: Inhibition of heterocyclic amine formation by water-soluble vitamins in Maillard reaction model systems and beef patties publication-title: Food Chem doi: 10.1016/j.foodchem.2012.01.089 – volume: 38 start-page: 395 year: 2000 ident: ref14 article-title: Formation and inhibition of heterocyclic aromatic amines in fried ground beef patties publication-title: Food Chem Toxicol doi: 10.1016/s0278-6915(00)00010-7 – volume: 155 start-page: 74 year: 2014 ident: ref9 article-title: Ammonia and formaldehyde participate in the formation of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine(PhIP) in addition to creati(ni)ne and phenylacetaldehyde publication-title: Food Chem doi: 10.1016/j.foodchem.2014.01.039 – volume: 32 start-page: 1537 year: 2018 ident: ref25 article-title: Aurantio-obtusin, an anthraquinone from cassiae semen, ameliorates lung inflammatory responses publication-title: Phytother Res doi: 10.1002/ptr.6082 – volume: 79 start-page: 125 year: 2002 ident: ref33 article-title: Formation of the heterocyclic aromatic amine PhIP: identification of precursors and intermediates publication-title: Food Chem doi: 10.1016/s0308-8146(02)00214-5 – volume: 82 start-page: 3037 year: 2017 ident: ref17 article-title: Amino acids inhibitory effects and mechanism on 2-Amino-1-Methyl-6-Phenylimidazo [4,5-b]pyridine (PhIP) formation in the Maillard reaction model systems publication-title: J Food Sci doi: 10.1111/1750-3841.13959 – volume: 47 start-page: 1473 year: 2009 ident: ref29 article-title: The neuroprotective effects of the seeds of Cassia obtusifolia on transient cerebral global ischemia in mice publication-title: Food Chem Toxicol doi: 10.1016/j.fct.2009.03.028 – volume: 60 start-page: 6235 year: 2012 ident: ref18 article-title: Inhibitory effect of antioxidant-rich marinades on the formation of heterocyclic aromatic amines in pan-fried beef publication-title: J Agric Food Chem doi: 10.1021/jf302227b – volume: 15 start-page: 269 year: 2016 ident: ref34 article-title: Heterocyclic aromatic amines in cooked meat products: causes, formation, occurrence, and risk assessment publication-title: Compr Rev Food Sci Food Saf doi: 10.1111/1541-4337.12186 – volume-title: Some naturally occurring substances: Food items and constituents, heterocyclic aromatic amines and mycotoxins year: 1993 ident: ref5 article-title: Monographs on the evaluation of carcinogenic risk to humans – volume: 19 start-page: 365 year: 2020 ident: ref6 article-title: Potential carcinogenic heterocyclic aromatic amines (HAAs) in foodstuffs: formation, extraction, analytical methods, and mitigation strategies publication-title: Compr Rev Food Sci Food Saf doi: 10.1111/1541-4337.12527 – volume: 402 start-page: 123486 year: 2020 ident: ref10 article-title: Inhibitory effect of selected hydrocolloids on 2-amino-1-methyl-6-phenylimidazo [4,5-b] pyridine (PhIP) formation in chemical models and beef patties publication-title: J Hazard Mater doi: 10.1016/j.jhazmat.2020.123486 – volume: 10 start-page: 221 year: 2017 ident: ref24 article-title: Attribution of antibacterial and antioxidant activity of Cassia tora extract toward its growth promoting effect in broiler birds publication-title: Vet World doi: 10.14202/vetworld.2017.221-226 – volume: 373 start-page: 131398 year: 2021 ident: ref4 article-title: The inhibitory effects of yellow mustard (Brassica juncea) and its characteristic pungent ingredient allyl isothiocyanate (AITC) on PhIP formation: focused on the inhibitory pathways of AITC publication-title: Food Chem doi: 10.1016/j.foodchem.2021.131398 – volume: 312 start-page: 126083 year: 2020 ident: ref8 article-title: Formation of a creatinine thermal degradation product and its role and participation in the radical pathway of forming the pyridine ring of 2-amino-1-methyl-6-phenylimidazo[4,5-b] pyridine (PhIP) publication-title: Food Chem doi: 10.1016/j.foodchem.2019.126083 – volume: 40 start-page: 126 year: 2019 ident: ref31 article-title: Optimization of ultrasonic assist extracting anthraquinone from semen Cassia by response surface method publication-title: Food Res Dev doi: 10.12161/j.issn.1005-6521.2019.21.022 – volume: 43 start-page: 18 year: 2022 ident: ref30 article-title: Effect of different phenolic acids on inhibition of PhIP formation in the model system reaction publication-title: Food Res Dev doi: 10.12161/j.issn.1005-6521.2022.16.003 – volume: 55 start-page: 10359 year: 2007 ident: ref12 article-title: Inhibitory effect of fruit extracts on the formation of heterocyclic amines publication-title: J Agric Food Chem doi: 10.1021/jf071820z – volume: 83 start-page: 294 year: 2018 ident: ref19 article-title: Dual effects of creatinine on the formation of 2-Amino-1-Methyl-6-Phenylimidazo [4,5-b]pyridine (PhIP) publication-title: J Food Sci doi: 10.1111/1750-3841.14035 – volume: 122 start-page: 98 year: 2010 ident: ref15 article-title: Effect of green tea marinades on the formation of heterocyclic aromatic amines and sensory quality of pan-fried beef publication-title: Food Chem doi: 10.1016/j.foodchem.2010.02.022 – volume: 70 start-page: 10858 year: 2022 ident: ref11 article-title: Synergistic inhibitory effects of selected amino acids on the formation of 2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) in both benzaldehyde- and Phenylacetaldehyde-creatinine model systems publication-title: J Agric Food Chem doi: 10.1021/acs.jafc.2c03122 – volume: 52 start-page: 2719 year: 2021 ident: ref21 article-title: Research progress on chemical composition and pharmacological effects of Cassiae semen and predictive analysis on quality markers publication-title: Chin Tradit Herb Drug doi: 10.7501/j.issn.0253-2670.2021.09.014 – volume: 2 start-page: 368 year: 2015 ident: ref22 article-title: A novel Cassia fistula (L.)-based emulsion elicits skin anti-aging benefits in humans publication-title: Cosmetics doi: 10.3390/cosmetics2040368 – volume: 306 start-page: 116199 year: 2023 ident: ref20 article-title: Cassiae semen: a comprehensive review of botany, traditional use, phytochemistry, pharmacology, toxicity, and quality control publication-title: J Ethnopharmacol doi: 10.1016/j.jep.2023.116199 – volume: 105 start-page: 82 year: 2007 ident: ref28 article-title: The seed extract of Cassia obtusifolia ameliorates learning and memory impairments induced by scopolamine or transient cerebral hypoperfusion in mice publication-title: J Pharmacol Sci doi: 10.1254/jphs.fp0061565 – volume: 41 start-page: 1587 year: 2003 ident: ref13 article-title: Influence of antioxidants in virgin olive oil on the formation of heterocyclic amines in fried beefburgers publication-title: Food Chem Toxicol doi: 10.1016/s0278-6915(03)00190-x |
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Snippet | 2-Amino-1-methyl-6-phenylimidazole [4,5-b] pyridine (PhIP), a heterocyclic amine (HAA), is found in meat products heated at high temperatures. However, PhIP is... Introduction2-Amino-1-methyl-6-phenylimidazole [4,5-b] pyridine (PhIP), a heterocyclic amine (HAA), is found in meat products heated at high temperatures.... |
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SubjectTerms | byproduct cassiae semen heterocyclic amine inhibiting effect model system Nutrition |
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Title | Inhibitory effects of cassiae semen extract on the formation of 2-amino-1-methyl-6-phenylimidazo [4,5-b] pyridine (PhIP) in model system |
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