Keywords:Bioactive Amines; Detection Methods; Toxicity; Acceptable Limits; Food Quality
1. Introduction
Bioactive amines are low molecular weight organic bases produced by the metabolism of plants, animals and microorganisms [1,2]. These amines can be detected in fresh and processed foods and can be formed by transamination of aldehydes and ketones, hydrolysis of nitrogen compounds, thermal decomposition or by decarboxylation of amino acids [2,3].
Amino acid decarboxylation is the main route of biogenic amine formation and consists of the removal of the α-carboxyl group from the amino acid structure forming the correspondent amine [4]. This reaction may occur through two biochemical routes: by the action of endogenous decarboxylase enzymes, i.e. enzymes naturally present in food or by exogenous decarboxylase enzymes produced by microorganisms [5,6]. These microorganisms may constitute the characteristic microbiota of the product or may be introduced before, during or after food processing [7]. The concentration and formation of different types of amines are directly related to the nature of the food and type of microorganism present [8,9].
Biogenic amines are present in low concentrations or are not detected in fresh food; however, in food of animal origin such as fish, meat, eggs, cheese and fermented foods, they can be present in high concentration able to induce a chemical poisoning [6]. In the case of fish, histamine poisoning should be enhanced, historically known as scombroid poisoning for its association with the intake of fish in the Scombridae family which includes tuna and sardines [8].
The accumulation of biogenic amines in food depends on the availability of free amino acids and the presence of microorganisms with decarboxylase activity on amino acids [10]. In addition to the availability of precursor amino acids, amine formation depends on food intrinsic and extrinsic parameters such as: temperature and pH, oxygen tension, availability of carbon sources, presence of vitamins, co-enzymes, concentration of free amino acids and fermentable carbohydrates [11-14]. Thus, the main factors that influence the biosynthesis of these compounds are storage conditions, good manufacturing practices [15,16], the amount of microorganisms with decarboxylase activity [5,17], the quality of the raw material and the availability of free amino acids [18-20].
In this context, the goal of this study is to present a review on the bioactive amines present in food, which included formation, and classification of these metabolites, health related aspects, acceptable limits, detection methods and control methods used in the food industry.
2. Nomeclature, Classification and Biosynthesis of Bioactive Amines
According to their biosynthetic pathway, bioactive amines are classified into [4,21-23]:
1) Biogenic: They are formed by bacterial enzymatic decarboxylation of amino acids (histamine, serotonin, tyramine, phenylethylamine, tryptamine, putrescine, cadaverine and agmatine);
2) Natural: Spermine and spermidine are formed “in situ” in the cells as they are required. It is noteworthy that since histamine is stored in mast cells and basophils, it could be classified as biogenic and natural.
With respect to nomenclature, most amines are named according to their precursor amino acids. The most important biogenic amines found in food are: histamine, tyramine, tryptamine, phenylethylamine and cadaverine, the synthesis of which occurs by decarboxylation of the precursor amino acids histidine, tyrosine, tryptophan, phenylalanine and lysine, respectively. In serotonin synthesis, tryptophan is transformed by tryptophan hydroxylase into 5-hydroxytryptophan, which is enzymatically decarboxylated into 5-hydroxytryptamine or serotonin. Tyrosine is the precursor of phenolic amines such as octopamine and dopamine [24]. Cadaverine and putrescine are associated to products under decomposition or putrefaction like spermine and spermidine are associated to seminal fluids where these amines were found for the first time [2,14,23,24].
Biogenic amines can be classified according to the number of amine groups present in the molecule, the chemical structure, the action in the body, and the biosynthetic pathway.
According to the number of amine groups they are classified into [5,21,5]">25]:
1) Monoamines: Tyramine, phenylethylamine.
2) Diamines: Histamine, serotonin, tryptamine, putrescine, cadaverine.
3) Polyamines: Spermine, spermidine and agmatine.
Regarding their chemical structure, they are classified into three major groups: [3,5]:
1) Aliphatic: Putrescine, cadaverine, spermine and spermidine.
2) Aromatic: Tyramine and phenylethylamine.
3) Heterocyclic: Histamine and tryptamine.
Regarding the action in the body, they are classified into [23,26,27]:
1) Vasoactive: Tyramine, tryptamine, phenylethylamine, isoamylamine, histamine and serotonin.
2) Psychoactive: Norepinephrine, serotonin and dopamine.
Regardless their classification, there is a natural mechanism for bioactive amine catabolism. They are oxidized by monoamine oxidases (MAO) and diamine oxidases (DAO). On the other hand, polyamines are oxidized by DAO and polyamine oxidases (PAO) after acetylation reaction [21]. Thus, these amines do not represent a health hazard unless they are consumed in large quantities or if the natural catabolism mechanism of one or more amines is inhibited [2]. In this case, poisoning occurs and thus it is important to determine amine profile and content in food since these substances can trigger toxicological processes [3,10].
3. Physiological and Toxicological Aspects
Many amines such as histamine, serotonin, dopamine and tyramine play important roles in maintaining the physiology of living organisms [4,28]. Besides, although the bioactive amines spermidine and spermine do not have direct toxicological effects they can potentiate tyramine and histamine toxicity by competing with detoxifying enzymes [29].
The bioactive amines present in food represent a health hazard when consumed in large amount if the natural mechanism for their catabolism is impaired by disease or pharmacological agents or if the individual is genetically deficient [23,30]. Under normal conditions, amines ingested through foods are quickly metabolized by conjugation or by oxidation reactions by amine oxidase enzymes such as monoamine oxidase (MAO), diamine oxidase (DAO), polyamine oxidases (PAO) and N-methyl transferase [21,31-33]. Individuals with respiratory and coronary heart diseases, hypertension problems or vitamin B12 deficiency are at risk because they are sensitive to smaller amounts of amines [4,5,34].
People with gastrointestinal problems (gastritis, irritable bowel syndrome, Crohn’s disease, gastric and colon ulcers) are also at risk since the activity of the oxidases in their bowels is generally lower than in healthy individuals. People using drugs MAO, DAO and PAO activity inhibitors may also be affected because they prevent amine catabolism [33]. These MAO and DAO inhibitors are used to treat stress, depression, Alzheimer and Parkinson, pulmonary tuberculosis, malaria, panic disorder and social phobia. Histamine is the amine most often related to food poisoning [10,20,35].
4. Histamine Poisoning
Histamine poisoning causes an allergic reaction characterized by difficult breathing, vomiting, rash, itching, fever and hypertension. Histamine alone at low levels does not cause poisoning but the presence of other biogenic amines such as putrescine and cadaverine, in concentration five times greater than histamine, enhance its toxicity [36,37]. The amines putrescine and cadaverine can potentiate histamine toxic effect, inhibiting DAO enzymes, increasing its transport through the gastrointestinal wall [38,39]. The presence of these potentiating substances can explain why, in some cases, spoiled fish and aged cheeses are more toxic than the same amount of histamine ingested alone [14].
Usually bioactive amines are absent or in minimum concentration, below 10 µg/g, in fresh foods. However, in fish, fish products, cheese, meat, egg and fermented food they can be present in significant amounts, above 50 µg/g, capable of inducing a chemical intoxication [4,6,8]. The symptoms can appear within minutes or up to an hour after ingestion and they include strange taste, headache, dizziness, nausea, facial swelling and flushing, abdominal pain, rapid, weak pulse besides diarrhea. It is worthy to note that once histamine is formed, it is not destroyed by cooking [40]. The concentration of histamine capable of producing poisoning varies in accordance with the susceptibility of each individual. In susceptible individuals, values between 5 and 10 mg/100g will cause symptoms [23]. Histamine exerts its effects by binding to cell membrane receptors of skin and respiratory, cardiovascular, gastrointestinal and immunologic systems [4]. Clinical signs are more severe in people taking drugs that inhibit histamine detoxifying enzymes in the intestine, in immunosuppressed individuals and individuals that use drugs and/or alcohol and the symptoms of histamine poisoning usually appear shortly after the ingestion of food, lasting approximately 24 hours [41].
5. Physiological and Toxicological Effects of Other Amines
High levels of tyramine can lead to poisoning known as cheese reaction caused by the concomitant consumption of food containing this amine [1]. Its intake is associated to headache, decreased movement of the gastrointestinal tract and action on the hunger center promoting hunger satiety sensation [42].
The amines tryptamine, tyramine and phenylethylamine can cause headache, migraine, increased blood pressure due to constriction of the vascular system and increased heart rate [14]. Theses amines are potent vasoconstrictors of both arteries and veins, with tyramine and tryptamine more potent in veins that in arteries, i.e. they are selective vasoconstrictors [43]. Putrescine and cadaverine cause hypotension and bradycardia, besides potentiating the toxicity of other amines [4]. These amines together with tyramine, can potentiate the action of histamine, because they inhibit DAO and N-HMT (N-methyl transferase) increasing its intestinal absorption [35, 38].
Putrescine, cadaverine, tyramine, tryptamine, phenylethylamine, spermine and spermidine are present in fish, aged cheese, red wine and meat products [44].
The amine putrescine has an importance as cell protector against oxidative stress and modulator in gene expression [45].
Cadaverine is a volatile amine, associated to spoiled food. Cadaverine is also associated to halitosis in patients with periodontal disease, and is found in tongue and saliva samples [46].
Polyamines as spermidine and spermine are essential components of living cells, universally occurring in animals and plants and present in most bacteria. These amines are important in regulating nucleic acid function and protein synthesis, as well as in membrane stabilization [14]. These two amines are part of muscles in normal physiological conditions, where they act as hormone or growth factor, essential for cells [14,47]. All cells require such amines for growth, regeneration and metabolism [21]. In addition, spermine, spermidine and putrescine, can accelerate the development of tumors, because they are found in tissues with high growing rate, and thus, their ingestion is forbidden to patients under treatment for cancer [23].
Serotonin, formed from the amino acid tryptophan is synthesized in the central nervous system and enteric cells. It acts as neurotransmitter in the central nervous system and it is an endogenous vasoconstrictor involved in the regulation of several physiological functions such as sleep, thirst, hunger, mood and sexual activity, acting on the regulatory system of emotions [48,49].
Agmatine derives from the amino acid arginine and acts as antidepressant [50]. This amine is present in the brain and is widely distributed in tissues and particularly in the stomach and blood, but also in the spinal cord, suggesting that it could be an endogenous modulator of pain regulation, i.e. a neurotransmitter/neuromodulator of the central nervous system [50-52].
6. Toxic Levels
The toxic levels of bioactive amines in humans are still uncertain and the toxic dose depends on the efficiency of individual metabolism. The toxic dose of histamine is 10 mg/100g of food; however susceptible individuals, asthma and ulcer patients are more susceptible to the toxic effects of this amine. The toxic dose of tyramine is 10 mg/100g in normal individuals and 6 mg/100g in those under treatment with monoamine oxidase inhibitors. The toxic dose of phenylethylamine is 3 mg/100g [2].
Acute and sub-acute toxicity levels were investigated in rats, the approximate values of lethal dose (LD50) for tyramine and cadaverine are higher than 2000 mg/kg of body weight, and thus their acute toxicity is low. The approximate LD50 for putrescine is 2000 mg/kg, while spermine and spermidine present higher acute toxicity with lethal dose of 600 mg/kg of body weight. Doses that do not cause adverse effects are 2000 ppm (180 mg/kg/ day) for tyramine, cadaverine and putrescine; 1000 ppm (83 mg/kg/day) for spermidine and 200 ppm (19 mg/kg/ day) for spermine [14,53].
In Brazil, the Regulation of Industrial and Sanitary Inspection of Animal Products—RIISPOA does not mention the amine maximum level allowed in products of animal origin [54]. However, MERCOSUR Resolution and the Technical Regulation on the Identity and Quality of Fresh Fish (whole and gutted) establish a maximum level of 100 ppm (10 mg/100g) of histamine in the muscles of species of the Scombridae, Scomberesocidae, Clupeidae, Coryphaenidae and Pomatomidae families [55,56].
Control of histamine levels was not previously included in the technical norms. The maximum acceptable histamine levels in fish were also established in other countries. In the European Union the regulatory limit is 100 mg/kg and in USA, the Food and Drug Administration, established a maximum limit of 5 mg histamine/ 100g product (50 ppm) at the port and 10 mg histamine/ 100g product (100 ppm) in pickled fish for species susceptible to form histamine [41,57]. There are no established standards for cadaverine, putrescine or other biogenic amines with the exception of histamine.
7. Toxic Analytical Methods for Amine Detection in Food
From the analytical point of view, bioactive amine detection in food is not simple, because these substances have different chemical structures and variable concentration range which sometimes is very low [58].
Bioactive amine detection and quantification is a complex analytical operation due to factors such as: strong polar character of the compounds, which results in a greater solubility in water rather than in the organic solvents frequently used; absence of intrinsic properties of the compounds, which could enable their detection by usual physico-chemical methods as spectrophotometric, fluorometric or electrochemical methods; sample complexity; low concentration in food; presence of potentially interfering substances such as amino acids with structural similarities with the amines; simultaneous presence of structurally very different amines in the same extract [4].
7.1. Chromatographic Methods
The analytical methods are generally based on amine extraction and derivation followed by separation and quantification. Extraction refers to the removal of the amines from the sample (food matrix). It depends on factors such as: type of food and amine present. This step is performed using different solvents according with the sample under study. Amine detection in food matrix is complex, because they are usually present in low concentrations. Besides, most amines do not present absorption in the ultraviolet spectrum nor fluorescence; then a derivation process is needed to increase absorbance and consequently increase detection sensitivity and selectivity [58,59]. The reagents most frequently used in amine analysis are: dansyl chloride, fluorescein and orto-phtalaldehyde [60].
Several methods are used for amine separation and quantification in food, among which thin layer chromatography, gas chromatography, high performance liquid chromatography, spectrofluorometry, PCR, ELISA, and electrophoresis.
Chromatographic techniques are the most frequently used, mainly High Performance Liquid Chromatography (HPLC). They provide high resolution, sensitivity and versatility, besides simple sample handling [60]. However, other techniques have been researched aiming at quantifying amines in food in a simple, sensitive and more affordable way.
1) High Performance Liquid Chromatography (HPLC): This analytical method is more advantageous than other methods because it detects other amines along with histamine. Thus, it became the official method for histamine detection in food in several countries. The method enables separations and quantitative analysis of a wide variety of compounds present in various types of samples in a few minutes with high resolution, efficiency and detectability [61]. The European Union (EU) requires the use of HPLC for histamine determination in fishery products with regulation purpose [57]. In Brazil, HPLC is the analytical method for the quantification of histamine and other amines (cadaverine, putrescine, spermidine, spermine) in fish and fishery product control [62]. By establishing this analytical method, Brazil expanded its consumer market, exporting fishery products to the EU and other countries that demand histamine quantification by HPLC.
2) Thin layer chromatography: This is a simple, effective and accurate method for bioactive amine separation and detection in all types of food [4]. It is a screening technique used for some time in industries and warehouses and consists in the separation of the components of a mixture through differential migration on a thin layer of adsorbent placed on a plane surface. It is a method of simple execution and low cost [63,64].
3) Gas chromatography: This technique is less expensive and demands less time than high performance liquid chromatography. It analyzes tens of substances in the same sample and has low detection limits. However, if the substance is thermally unstable, it is necessary to obtain a thermally stable derivative which is not always possible. The preparation stage, before analysis, is long and complex. Besides, gas chromatography is not an efficient qualitative technique and many times auxiliary techniques are necessary for reliable identification of the substances present in the sample [65]. The fact that bioactive amines have low molecular weight, high solubility in water and low volatility is another obstacle in using this technique [66]. The aforementioned author reports that it is necessary to perform derivatization of these amines to reduce polarity, improving the selectivity, volatility, sensitivity and separation of these amines. This process is characterized by conducting baths at 60˚C for about two hours [67,68]. Hydrogen is the carrier gas most frequently used [66].
7.2. Fluorometric Method
The Technical Regulation on the Identity and Quality of Fresh Fish (whole and gutted) defines the fluorometric method as the official technique for histamine detection in fish in Brazil [56]. Currently, even after the HPLC entered in force, the fluorometric method was not revoked. The fluorometric method consists in histamine extraction with methanol, extract purification on ion exchange resin and subsequent chemical reaction with ortophtalaldehyde, in alkaline medium adding phosphoric acid. The reaction forms a fluorescent compound which is analyzed in a device called fluorometer [69]. Other simple method form was developed to measurement of polyamine as indicator of food decomposition with fluorometer by using 4-(1-Pyrene)butyric acid N-hydroxysuccinimide ester (PSE), it was detected in linear polyamines such putrescine, cadaverine, spermidine and spermine. They also demonstrated here the increase of fluorescence in decomposed sardine and mackerel fish by PSE derivatization just by removing proteins or debris with trichloroacetic acid, which is simpler that ortophtalaldehyde method [70].
7.3. Enzymatic Kits
Currently there is an interest for portable, fast screening procedures for field analyses that can be applied for fishery products on the quay, which led to the development of commercial test kits used in Hazard Analysis and Critical Control Point (HACCP) [71]. With the use of HACCP, by many food companies including those that process fishery products, histamine determination was included as critical control point depending on the processed product. The detection of this biogenic amine during food processing led several industries to develop portable kits for histamine analyses which do not require solvents as methanol and can be easily applied in the industries [71].
This is a fast, simple, low cost method for histamine detection capable of promoting accurate results. The kits available in the market are usually classified into qualitative, quantitative or semi quantitative in the range from one to 500 ppm [72].
The tests can be based in two methods, the ELISA method that assesses the direct competition of a substance with the enzyme-linked for a limited number of antibodies, and the chemical colorimetric analysis where an enzyme catalyzes a color change in the reaction with the substrate [72,73].
8. Bioactive Amines as Quality Index and Control Methods Used in the Food Industry
Amine formation in foods rich in protein and amino acids may be inherent to the product or due to the action of added microorganisms (starter cultures) and/or contaminants (inadequate sanitary conditions). Thus, amine quantification may be used as quality parameter or index, because it can reflect poor quality of the raw materials and/or sanitary conditions during the manufacture of certain products [2,14,23,74].
The analyses used to determine food quality include sensory and microbiological methods. The first are fast, well accepted but depend on trained panelists and do not detect specific food contamination. On the other hand, microbiological analyses are usually slow, requiring 2 - 5 days to obtain results. For this reason, alternative methods involving chemical changes caused by microbial activity are being studied [75-78].
The presence of chemical metabolites, the biogenic amines, produced by the microbiological spoilage of food is suggested as quality indicator of food in addition to routine analyses [7,78,79]. High content of histamine and other amines can be used as quality indicators and also as indicators of potential food poisoning [1,26]. This is due to the fact that microbial deterioration can be accompanied by an increase of decarboxylase production [2, 80]. It should be highlighted that these substances are reported as heat stable compounds and, cooking or prolonged exposure to heat do not eliminate the toxin [4, 81,82]. Thus, an advantage in using biogenic amines as quality index is that they are thermo resistant and thus, they remain in the food even after heat treatment [23].
Chemical quality indices, through the relation between the bioactive amines histamine, putrescine, cadaverine, spermine and spermidine, were characterized and suggested by some authors for fish and poultry meat [47,83- 85].
Prevention of the formation of bioactive amines in food has been mainly performed through production and storage temperature control, quality of the raw material, good manufacturing practices, use of starter cultures for fermentation, use of enzymes to oxidize amines, use of microbial modeling to assess favorable conditions to delay amine formation, use of adequate packaging techniques and food irradiation [37,68,86,87].
9. Conclusion
Bioactive amines are chemical components of a variety of foods, which call attention for different reasons since, and they cause positive biological effects. Being essential for maintaining the physiological activities, they can have adverse effects mainly toxicological in concentrations higher than 100 ppm of histamine. However, more studies to determinate toxic levels to other biogenic amines are necessary. Amine identification and quantification is also an important indicator of the sanitary condition of both the raw material and the final product. Its control is important to reduce damages to the production chain and improve commercial relations with other countries reducing export barriers. Thus, further studies are necessary to establish safety limits for bioactive amines in animal products, vegetables and beverages.
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