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Processed fruit juice ready to drink: screening acute toxicity at the cellular level/Sucos de frutas industrializados prontos para consumo: screening da toxicidade aguda em nivel celular.

Introduction

Because of rapid pace of life, the manual preparation of fruit juices has become an inconvenience to daily life. Thus, the world consumption of processed juices has tripled in the last twenty years, which strengthened the attachment of various trademarks in domestic and international market of processed fruit juices ready for consumption (Biral, Taddei, Passoni, & Palma, 2013, Longo-Silva et al., 2015). In addition to the convenience in consumption, ready juices have excellent sensory properties such as color, odor and attractive flavor, are available in various fruit flavors and sold in compact packages, which facilitates storage (Ferrarezi, Santos, & Monteiro, 2010).

However, in order to achieve the organoleptic properties currently offered, the composition of these beverages has undergone several changes over nearly two decades, among which the significant incorporation of food synthetic additives or micro ingredients with acidifying, antioxidant, flavoring, coloring, anti-wetting, acidity regulators, foaming and sweetening actions (Ferrarezi et al., 2010, Longo-Silva et al., 2015). These changes were approved and standardized by the Ministry of Agriculture, Livestock and Supply and the National Health Surveillance Agency (Anvisa) through Ordinance 544 of November 16th, 1998 approving the technical regulations for setting of identity and quality standards of processed juices and refreshments marketed in liquid form (Brasil, 2000, Ferrarezi et al., 2010).

Meanwhile, there are studies that relate the micro ingredients to harmful effects to the health of consumers, especially to children. The consequences described include the development or enhancement of chronic allergies and changes in the functioning of the digestive tract (Gomes, Oliveira, Carvalho, Menezes, & Peron, 2013, Oliveira, Alves, Lima, Castro, & Peron, 2013, Moura, Santana, Ferreira, Sousa, & Peron, 2016). Thus, food surveillance agencies, such as the European Food Safety Authority (EFSA) and Anvisa, point out in their technical regulations the constant need for cytotoxicological studies on the acute effect of food additives in general and especially processed food containing such substances. They also emphasize that the results of these analyzes are the basis of preparation or modification of strategies of food safety agencies and, consequently, the work of professionals responsible for food and nutrition surveillance of the population (Brasil, 2007, Moura et al., 2016, Carvalho, Sales, & Peron, 2017). However, a comprehensive analysis of the scientific literature indicated the lack of studies on the toxicity of processed juices sold in liquid form.

The meristem tissue of roots of Allium cepa L. (onion) is regarded in the scientific community as an effective bioassay for the assessment of acute toxicity at the cellular level of chemical compounds, due to low chromosome number (2n = 16), which facilitates the detection of chromosomal abnormalities and mitotic spindle changes (Neves, Ferreira, Lima, & Peron, 2014, Bianchi, Mantovani, & Marin-Morales, 2015). This test system is internationally accepted by research agencies as an assessment tool with accurate sensitivity for initial analysis of cytotoxicity, genotoxicity and mutagenicity of the substance of interest, as the results obtained show satisfactory similarity to those observed with animal test systems and cell cultures (Turkoglu, 2007, Herrero et al., 2011, Tabrez et al., 2011, Gomes et al., 2013, Oliveira et al., 2013, Lacerda, Malaquias, & Peron, 2014, Campos Ventura & Marin-Morales, 2016, Moura et al., 2016, Santana et al., 2016, Campus-Pereira, Gongalves, Hara, & Marin-Morales, 2016).

As described by Zilifdar et al. (2014) and Valavanidis, Vlachogianni, Fiotakis, and Loridas (2013), cytotoxic, genotoxic and mutagenic substances can damage vital cellular mechanisms, such as gene duplication and transcription, changing dramatically the cell division of tissue through cellular aberrations, such as mitotic spindle changes and chromosome breaks, which can trigger and/or potentiate cancerous processes. According to Zaineddin et al. (2012), the development of the most common types of cancer results from the interaction between endogenous and environmental factors, remarkably the diet, especially when made of processed foods in excess.

Based on the discussed context, the goal of this study was to evaluate cytotoxicity, genotoxicity and mutagenicity of processed liquid preparations ready for consumption, Orange and Grape flavors, of five relevant food companies in the Brazilian market, through the meristematic cells of A. cepa roots. The Orange and Grape juices were selected for analysis based on studies conducted by Ferrarezi et al. (2010) and Pontes, Santiago, Szabo, Toledo, and Gollucke (2010), which point them as the most appreciated by the population.

Material and methods

Study samples

Samples of processed juices ready for consumption, Orange and Grape flavors, from five different food companies--referred to in this study as A, B, C, D and E- were acquired in the retail market in the city of Picos, state of Piauf, Brazil. We were careful to check whether the samples were within the shelf life and the packaging were intact. Analyses of toxicity were carried out directly with the marketed solutions.

Obtaining root meristem cells of A. cepa and cytogenetic analysis

Onion bulbs were placed in aerated bottles with distilled water at room temperature ([+ or -] 27[degrees]C) to obtain 2.0 cm long roots. For analysis of each treatment group, we established an experimental group with five onion bulbs. Before placing the roots in contact with their respective samples ofjuices (treatments), some roots were collected and fixed to serve as control of the bulb it self. The remaining roots were placed in their respective solutions for 24 hours, a procedure called exposure time of 24 hours.

After 24 hours, some roots were collected and fixed. The remaining roots of each bulb were returned to their respective solutions, where they remained for more 24 hours, which is termed exposure time of 48 hours. Subsequently, again, roots were collected and fixed. The exposure times 24 and 48 hours were chosen to evaluate the effect of treatments on more than one cell cycle. Roots were fixed in Carnoy 3: 1 (ethanol: acetic acid) for 24 hours. We collected on average three roots per bulb in each collection. In all exposure times considered, the bottles with the treatments under study remained under gentle and constant stirring. This procedure was carried out to prevent the precipitation of solutions.

Slide preparation and analysis, and statistical analysis

On average, 3 slides per bulb were prepared following the protocol proposed by Guerra and Souza (2002), and analyzed under an optical microscope at 400x magnification. For each onion bulb, we analyzed 1,000 cells, totaling 5,000 cells for each control, exposure time 24 and 48 hours of each treatment group. Cells were observed in interphase, prophase, metaphase, anaphase and telophase. For calculation of the mitotic index (MI), we used the following equation: (total number of cells in mitosis total number of cells analyzed) x 100.

It was also assessed the action of juice samples by the frequency of micronuclei, colchicine metaphase, anaphase and telophase bridges, gene amplifications, cells with adhesions, nuclear buds and multipolar anaphases. For statistical analysis, we used the chisquare test ([[chi].sup.2]) at a probability level < 0.05.

Results and discussion

Considering the results in Table 1, it was observed that the Orange and Grape juices of the company A significantly reduced the cell division index at the 24 hours exposure time compared to the mitotic index observed for its respective control. This result is more pronounced at the 48 hours exposure time, in which the cell division index was statistically lower than those observed for the respective controls and 24 hours exposure time. In turn, Orange and Grape juices of the companies B, C, D and E caused a significant reduction in cell division of the meristem tissue, in both exposure times considered, compared to the mitotic index observed for the respective controls. However, there were no significant differences in the cell division index between the respective exposure times of 24 and 48 hours.

These results show that all juice samples tested, under the conditions established, were cytotoxic to root meristem cells of Allium cepa, because they have caused marked anti proliferative effect to root meristems. According to Gomes et al. (2013), Moura et al. (2016) and Carvalho et al. (2017), the reduction in mitotic index caused by chemical compounds in tissues without any mutation and/or cellular change is harmful to the organism in which they occur, as it does not allow or limit the replacement of cells, altering the production of proteins and therefore resulting in malfunction of the organ where it is located.

With respect to the results listed in Table 2, the orange and grape juices of the five food companies, at both exposure times considered, induced significant formation of mitotic spindle changes, represented in this study by colchicine metaphase and anaphase and telophase bridges, proving to be genotoxic, and chromosome breaks, characterized by the formation of micronuclei.

Mitotic spindle changes, at significant frequency, provoke nuclear instability by inducing structural chromosome damage, giving rise to acentric fragments, which therefore form micronuclei at the end of cell division. The significant presence of micro nucleated cells, as observed herein with ready juices, classifies substances, compounds or solutions tested as mutagenic (Corcuera et al., 2015). This condition with the liquid preparations indicates that they should be evaluated in animal test systems, since, according to Queiroz, Matias, Cunha and Schwarz (2013), the occurrence of cell changes, though not considered a carcinogenicity measurement, are often associated with the appearance of cancer, as there is a positive correlation between increased mitotic spindle aberrations, as well as micro nucleated cells, and detection of neoplasms.

Also, the frequency of cell changes observed in Table 2 confirms the results of reduced cell division in Table 1. Aissa et al. (2012) report that metaphases with misalignment of chromosomes on the equatorial plate or colchicine metaphase, as well as delayed chromosomes in anaphase and/or telophase, or anaphase and telophase bridges, result in formation of cells with different chromosome numbers, and chromosome structural changes. Whereas the principle of the cell cycle is the formation of identical cells, cells with discrepant variations in structure and in chromosome number tend to be eliminated in tissues with normal functioning.

As mentioned above, there is no toxicological evaluation in the scientific literature to date, at the cellular level regarding processed juices sold in liquid form. However, there are cytotoxicity assessments of some of the chemical constituents of the food additive classes in the formulation of these beverages, as described in the technical document that regulates these liquid preparations (Brasil, 2007). Nevertheless, it is very important to mention that the chemical composition of processed fruit juices ready for consumption, such as those from the five companies evaluated here in, is allowed and guaranteed by Brazilian law (Brasil, 2007, Ferrarezi et al., 2010; Pontes et al., 2010).

Artificial food dyes found in orange juice ready for consumption are the Twilight Yellow and Tartrazine. As for the grape, one of the dyes used is the Red 40. The dyes Sunset Yellow, Tartrazine and Red 40 are classified as azo food additives, because they have an azo group in their formulation, which is a nitrous derivative property to produce aromatic amine and sulfanilic acid (Sardi et al., 2010). These color additives have the potential to alter the turnover of cells during interphase and the regenerative hyperplasia process, contributing significantly to the development of digestive tract cancers in rodents (Polonio & Peres, 2009, Mpountoukas et al., 2010). These three azo dyes were also significantly cytotoxic, mutagenic and genotoxic to meristematic cells of Allium cepa roots (Gomes et al., 2013).

The diluents present in taste and flavor additives include benzoic alcohol and diacetyl (2,3-butadione), compounds which promote significant changes in the mitotic spindle and cell division of human peripheral blood cells (Demir, Kocaoglu, & Kaya, 2010) and significant damage to the chromosome 11 locus of rodents, causing loss of expression of essential genes controlling cell division (Whittaker, Clarke, San, Begley, & Dunkel, 2008), respectively. Furthermore, More, Raza, and Vince (2012) found that the diluent diacetyl had the potential to replace thymine with guanine in euchromatin regions, resulting in the disruption of hydrogen and disulfide bonds in the tertiary structure of enzymes important for mitosis. Among the preservatives stand out potassium benzoate, sodium benzoate, potassium nitrate, cytotoxic and genotoxic effects to normal cells of human peripheral blood (Mpountoukas et al., 2010, Zequin, Yuzbagioglu, Unal, Yilmaz, & Aksoy, 2011), boric acid, citric acid, potassium citrate and sodium citrate, cytotoxic and genotoxic to root meristem cells of A. cepa (Turkoglu, 2007).

The sweeteners used in liquid preparations ready to drink comprise aspartame, sodium cyclamate, acesulfame potassium and sodium saccharin, with the exception of juices ready for consumption of Ambev, which have no sweeteners in their chemical composition, according to the site of presentation of the products. Van Eyk (2015) found that, through the cell lines Caco-2 (colon cells), HT-29 (colon cells) and HEK-293 (kidney cells), these sweeteners were cytotoxic, genotoxic and mutagenic to the studied cells. Corroborating the results of these researchers, Sasaki et al. (2002), using the comet assay, observed that sodium saccharin and sodium cyclamate were genotoxic and mutagenic to rodent colonic cells.

Conclusion

All juice samples analyzed were cytotoxic, genotoxic and mutagenic to root meristematic cells of A. cepa.

The results of this study, combined with the toxicity data at the cellular level of some of the food additives present in the basic formulation of juices ready to drink, signal the need for more detailed assessments, intest systems with higher complexity, to then safely establish the toxicity at the cellular level of these foods.

Doi: 10.4025/actascibiolsci.v39i2.33699

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Received on October 4, 2016.

Accepted on March 2, 2017.

Erick Leal da Silva (1), Ila Monize Sousa e Sales (1), Fabelina Karollyne Silva dos Santos (1) and Ana Paula Peron (2) *

(1) Curso de Ciencias Biologicas, Universidade Federal do Piaui, Picos, Piaui, Brazil. (2) Programa de Pos-Graduacao em Genetica e Melhoramento, Centro de Ciencias Agrarias, Universidade Federal do Piaui, Campus Ministro Petronio Portella, s/n., 64049-550, Teresina, Piaui, Brazil.

* Author for correspondence. E-mail: anapaulaperon@ufpi.edu.br
Table 1. Number of cells observed in each phase of the cell cycle
of the root meristem tissue of Allium cepa treated with processed
juices ready for consumption, orange and grape flavors, of the food
companies A, B, C, D and E, at the exposure times of 24 and 48
hours.

                               Orange Processed Juice

Company      ET      TCII    P     M     A     T    TCD    MI (%)

             CO      4136   319   146   267   132   864    17.3 (a)
A         24 hours   4645   130   84    72    69    355     7.1 (b)
          48 hours   4849   56    30    41    24    151     3.0 (c)
             CO      3971   481   207   179   162   1029   20.6 (a)
          24 hours   4744   177   23    18    38    256     5.1 (b)
          48 hours   4846   93    29    16    36    174     3.5 (b)
             CO      4322   232   158   136   152   678    13.6 (a)
C         24 hours   4806   101   54    12    17    194     3.9 (b)
          48 hours   4828   58    52    12    10    172     3.4 (b)
             CO      4201   251   119   246   183   799    15.9 (a)
D         24 hours   4745   98    71    50    36    255     5.1 (b)
          48 hours   4823   83    34    31    29    177     3.5 (b)
             CO      4076   302   292   187   143   924    18.4 (a)
E         24 hours   4633   99    97    82    89    367     7.3 (b)
          48 hours   4678   83    79    79    81    322     6.4 (b)

                               Grape Processed Juice

Company      ET      TCII    P     M     A     T    TCD    MI (%)

             CO      4282   534   80    43    61    718    14.4 (a)
A         24 hours   4685   274   12    09    20    315     6.3 (b)
          48 hours   4847   96    20    06    31    153     3.1 (c)
             CO      4298   499   93    47    63    702    14.4 (a)
B         24 hours   4159   71    21    07    42    141     2.8 (b)
          48 hours   2971   71    11    00    47    129     2.6 (b)
             CO      4422   232   158   136   52    578    11.6 (a)
C         24 hours   4806   101   54    12    17    194     3.9 (b)
          48 hours   4838   78    60    02    22    162     3.2 (b)
             CO      4305   189   191   117   198   695    13.9 (a)
D         24 hours   4704   44    57    13    22    196     3.9 (b)
          48 hours   4817   89    71    17    06    183     3.7 (b)
             CO      4399   178   176   176   71    601    12.0 (a)
E         24 hours   4750   78    86    53    33    250     5.0 (b)
          48 hours   4824   69    45    41    21    176     3.5 (b)

TCII--Total number of cells in interphase and undifferentiated cells;
ET--Exposure Time; CO--Control; MI--Mitotic Index; TCD-Total number of
dividing cells. MI values followed by different letters within the
same treatment are significantly different at 5% by [chi square] test.

Table 2. Cell changes observed in root meristem cells of Allium cepa
treated with water and with processed juice ready for consumption,
orange and grape flavors, of the food companies A, B, C, D and E, at
the exposure times of 24 and 48 hours.

Company       ET      Colchicine    Anaphase
                       metaphase      bridge

             CO           00           00
A         24 hours        32           11
          48 hours        13           17
             CO           00           01
B         24 hours        12           02
          48 hours        08           17
             CO           00           01
C         24 hours        09           04
          48 hours                     01
             CO           01           00
D         24 hours        23           17
          48 hours        19           19
             CO           01           00
E         24 hours        24           07
          48 hours        09           09

Company       ET      Colchicine    Anaphase
                       metaphase     bridge

             CO           01           00
A          24 hours       19           13
          48 hours        17           13
             CO           01           00
B         24 hours        22           09
          48 hours        13           13
             CO           01           00
C         24 hours        04           13
          48 hours        17           01
             CO           01           00
D         24 hours        23           19
          48 hours        11           27
             CO           01           00
E         24 hours        14           09
          48 hours        03           19

Company   Telophase    Micronuclei     TAC
            bridge

              00            01        01 (a)
A             09            37        89 (b)
              11            32        73 (b)
              00            00        01 (a)
B             03            25        42 (b)
              07            21        53 (b)
              00            00        01 (a)
C             04            32        49 (b)
              08            30        41 (b)
              00            00        01 (a)
D             02            44        86 (b)
              00            23        71 (b)
              00            00        01 (a)
E             03            42        76 (b)
              11            44        73 (b)

Company   Telophase    Micronuclei     TAC
            bridge

              00            00        01 (a)
A             13            32        77 (b)
              19            22        71 (b)
              00            00        01 (a)
B             09            32        72 (b)
              04            40        70 (b)
              00            00        01 (a)
C             09            22        48 (b)
              09            24        51 (b)
              00            00        01 (a)
D             03            24        69 (b)
              00            29        67 (b)
              00            00        01 (a)
E             13            33        69 (b)
              02            41        65 (b)

ET--Exposure Time; CO--Control; TAC--Total Cellular Alterations.
MI values followed by different letters within the same treatment
are significantly different at 5% by [chi square] test.
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Author:da Silva, Erick Leal; Sales, Ila Monize Sousa; dos Santos, Fabelina Karollyne Silva; Peron, Ana Paul
Publication:Acta Scientiarum. Biological Sciences (UEM)
Article Type:Ensayo
Date:Apr 1, 2017
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