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Toxicology Reports
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In vitro mutagenicity assay (Ames test) and phytochemical characterization of seeds oil of Helianthus annuus Linné (sunflower)
Nelma de Mello Silva Oliveiraabc, Marielly Reis Resendea, Daniel Alexandre Morales3, Gisela de ragäo Umbuzeiroa, Marcelo Fabiano Gomes Boriollob c d *
a Laboratorio de Ecotoxicologia e Microbiología Ambiental, Faculdade de Tecnología, Universidade Estadual de Campinas (FT/UNICAMP), Limeira, SP, Brazil b Laboratorio de Farmacogenética e Biologia Molecular, Faculdade de Ciencias Médicas, Universidade José do Rosário Vellano (UNIFENAS), Alfenas, MG, Brazil
c Centro de Pesquisa e Pós-graduacao em Ciencia Animal, Área de Patologia e Farmacología Animal, Universidade José do Rosário Vellano (UNIFENAS), Alfenas, MG, Brazil
d Laboratorio de Microbiologia e Imunologia & Laboratorio de Genética Molecular, Departamento de Diagnóstico Oral, Faculdade de Odontologia de Piracicaba, Universidade Estadual de Campinas (FOP/UNICAMP), Piracicaba, SP, Brazil
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ARTICLE INFO
Article history:
Received 22 July 2016
Received in revised form 9 September 2016
Accepted 12 September 2016
Available online 13 September 2016
Chemical compounds studied in this article: a-Linolenic Acid (PubChem CID: 5280934) Arachidic Acid (PubChem CID: 10467) Behenic Acid (PubChem CID: 8215) Lignoceric Acid (PubChem CID: 11197) Linoleic Acid (PubChem CID: 5280450) Myristic Acid (PubChem CID: 11005) Oleic Acid (PubChem CID: 445639) Palmitic Acid (PubChem CID: 985) Palmitoleic Acid (PubChem CID: 445638) Stearic Acid (PubChem CID: 5281)
Keywords:
Helianthus annuus L. Sunflower oil Genetic toxicity Gas chromatography
ABSTRACT
The objective of this research was to investigate the genotoxic potential of the oil of H. annuus L. (sunflower) seeds via the Ames test as well as its oxidative properties and lipid composition. The preincubation method, system metabolic activation (S9 fraction) and five S. typhimurium strains (TA97, TA98, TA100, TA1535 andTA102) were employed for the Ames test. The oxidative stability and fatty acid composition were analyzed by standard methods and gas chromatography. A revertant analysis showed no significant differences between the treatment doses (10-200 ^l/plate) and the negative controls, regardless of S9+ and S9-, and included all of the S. typhimurium strains. Chromatographic analysis showed high levels of polyunsaturated fatty acids, followed by monounsaturated, saturated and total trans-isomers. Among the polyunsaturated, monounsaturated and saturated fatty acids, linoleic, oleic and palmitic acids predominated. The results suggest that the sunflower oil is not genotoxic as indicated by frameshift mutations and base pair substitutions regardless of the treatment dose, but shows dose-dependent toxicity. The oxidative properties of the sunflower oil were consistent with the requirements of national and international standards. However, its composition could also indicate phytotherapeutic properties.
© 2016 The Author(s). Published by Elsevier Ireland Ltd. This is an open access article under the CC BY
license (http://creativecommons.org/licenses/by/4.0/).
1. Introduction
The cultivated sunflower (Helianthus annuus L.) is one of the 67 species of the genus Helianthus and is a dicotyledonous plant and member of the Compositae (Asteraceae) family, having a typical composite flower [1]. Sunflower seed oils are high in saturated
* Corresponding author at.: Laboratorio de Farmacogenómica e Biologia Molecular, Faculdade de Ciencias Médicas & Centro de Pesquisa e Pós-graduacao, Universidade José do Rosário Vellano (UNIFENAS, Rod. MG 179, Km 0, Campus Universitário, CEP: 37130-000, Alfenas, MG, Brazil.
E-mail address: marcelo.boriollo@unifenas.br (M.F.G. Boriollo).
fatty acids (lauric acid C12:0, maristic C14:0 palmitic C16:0 and stearic C18:0), monounsaturated fatty acids (oleic acid C18:1, n-9), and poly-unsaturated fatty acids (linoleic acid C18:2, n-6, and a-linolenic C18:3, n-3) [2]. The unsaturated fatty acids are the most abundant, especially linoleic acid. In turn, linoleic acid makes vegetables oil more susceptible to lipid oxidation [3] and therefore favors the formation of substances (e.g., peroxides, hydroperoxides and free radicals) that cause spoilage [4] in addition to the geno-toxicity caused by the reaction between these substances and DNA molecules [5]. In addition, linoleic acid is a precursor of arachidonic acid [6], which participates in the synthesis of biologically active mediators, such as prostaglandins, thromboxanes and leukotrienes. These substances act as inflammatory mediators [7,8], stimulating
http://dx.doi.org/10.1016/j.toxrep.2016.09.006
2214-7500/© 2016 The Author(s). Published by Elsevier Ireland Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
local neovascularization, cell migration, proliferation and the differentiation of fibroblasts, along with extracellular matrix synthesis that acts directly on healing [9,10].
Sunflower seed oil has potential phytotherapeutic properties [10], and some research also supports the phytotherapeutic effectiveness of the oil and an aqueous or alcoholic extract of sunflower seeds for the relief of asthmatic symptoms and other diseases [11], gastric protection [12,13], healing properties [14], anti-inflammatory action [15-17] and antimicrobial properties [12,14,18,19]. In addition, a limited number of investigations that investigated the genotoxic action of various oils, including sunflower seed oil, have gone unnoticed. For example, vegetable oils for human consumption showed high (linseed oil) and weak (sesame oils, wheat germ and soybean) genotoxic responses or even the absence of genotoxicity (sunflower oil, olive oil and refined olive oil extra-virgin) according to a mutation and somatic recombination test (SMART) in Drosophila melanogaster [20]. In another study, lymphocytes incubated with an aqueous extract of sunflower oil submitted to thermal stress exhibited high rates of chromosomal breakage and were significantly different from those of lymphocytes incubated with the same concentrations of the aqueous extract of sunflower oil in the absence of heat. Furthermore, in tests with HepG2 or HUVEC cells, sunflower oil subjected to heat stress was clastogenic and showed dose-dependent cytotoxicity [21]. The absence of clastogenicity and/or aneugenicity in two sources of oil and a tincture of H. annuus L. (sunflower) seeds was also confirmed by in vivo micronucleus assays in mouse bone marrow and was dose-independent, time-independent and sex-independent, except for the oil. However, systemic toxicity of sunflower oil might be dependent on its origin and dose [22].
Thus, further studies on the genotoxicity of sunflower extracts and oils (seeds, flowers and leaves) must be conducted to determine their effects and potential genotoxic mechanisms, especially for setting limits for human use. The Ames test (Salmonella/Microsome test) has been employed as an indicator of the carcinogenic potential in mammals and uses bacterial strains of S. typhimurium that are auxotrophic for histidine (his-) (i.e., are unable to grow in a minimal culture medium without histidine) because of the presence of mutations in the histidine operon. These strains are used to detect gene mutations, base pair substitutions and frameshift types. However, revertant colonies (i.e., histidine prototrophs) can be quantified after exposure to test substances in the presence or absence of an exogenous metabolic activation system, which indicates the occurrence of gene mutations by the restoration of bacterial metabolism and growth in minimal culture medium [23-25]. Thus, this in vitro assay can be used in the screening of new chemicals and drugs as well as to provide a high predictiv-ity of carcinogenicity due to mutagenesis [24]. Some vegetable oils (Ocimum selloi [26], Melaleuca alternifolia and Lavandula angustifolia [27], Azadirachta indica [28], Curcuma longa L. [29]) have been previously evaluated by the Ames test.
To contribute to the information on the genotoxic potential of vegetable oils, this study evaluated the mutagenic effects of the pharmaceutical oil of H. annuus L. seeds (sunflower) in the Ames test using S. typhimurium strains TA97a, TA98, TA100, TA102 and TA1535. The oxidative properties and lipid composition of this oil were also assayed in oxidative stability tests (iodine, peroxide and acidity index) and by gas chromatography (GC).
2. Material and methods
2.1. Phytotherapeutic sunflower oil
The pharmaceutical oil of H. annuus L. (sunflower) seeds (CAS
# 8001-21-6) was purchased commercially and stored according
to the manufacturer's recommendations (Fagron Farmacêutica do Brasil, Sao Paulo, SP, Brazil, lot 14010155B: relative density equal to 0.923 g/cm3, iodine index equal to 126g/100g, acidity index equal to 0.03% and peroxide index equal to 0.03 mequiv. O2/kg).
2.2. Ames test (Salmonella/Microsome test)
Bacterial strains of S. typhimurium TA97a, TA98, TA100, TA102 and TA1535 were kindly provided by Companhia Ambiental do Estado de Sao Paulo (CETESB, SP, Brazil) to Laboratorio de Ecotoxi-cologia e Microbiologia Ambiental of Prof. Dr. Abílio Lopes - LEAL, stored and maintained as provided in the standard protocol [25]. The test was performed with the pre-incubation method according Mortelmans and Zeiger (2000) [24] and Guideline for testing of chemicals [25]. Initially, each bacterial strain was grown in 20 ml of nutrient broth (Nutrient Broth Oxoide no. 2, code # CM0067, Thermo Fisher Scientific Inc.) at 37°C for 16 h (overnight) under constant shaking at 160-170 r.p.m (Incubator with Orbital Agitation Platform - Shaker model 430, Nova Ética, Vargem Grande Paulista, SP, Brazil). Then, 100-|il aliquots of each freshly grown bacterial culture (1-2x109 CFU/ml) were added to assay tubes containing (i) a known volume of sunflower oil (10, 20, 50, 100 and 200 |il/plate) and 500 |il of the S9 mixture [phosphate buffer, NADPH glucose-6-phosphate, solution of salts (MgCl2 and KCl), and the S9 fraction (S9 microsomal fraction of homogenized rat liver: post-mitochondrial fraction supplemented with a cofactor, prepared from the liver of rodents treated with an agent enzyme inducer, arocloror 1254, MOLTOX®, Molecular Toxicology, USA)] -system with metabolic activation - or (ii) known volumes of sunflower oil (10, 20, 50, 100 e 200 |l/plate) and 500 |l of phosphate buffer (Na2HPO4 and NaH2PO4-H2O) - system without metabolic activation -, and pre-incubated at 37°C for 30min.
Prior to testing, aliquots of the S9 fraction were prepared according to the manufacturer's specifications and stored in 2-ml sterile Eppendorf-type tubes at -20°C. The reagent 2-Aminoanthracene (2.5 |g/plate; CAS Number 613-13-8, Cat. #A38800 Aldrich, Sigma-Aldrich Chemical Co.) was used as a positive control in analysis systems with metabolic activation of all of the S. typhimurium strains. For analysis systems without metabolic activation and as a positive control, 4-Nitroquinoline N-oxide (0.5 |g/plate; CAS Number 56-57-5, Cat. #N8141 Aldrich, Sigma-Aldrich Chemical Co.) was used in the assays with the TA97a, TA98 and TA100 strains and sodium azide (5 | g/plate; CAS Number 26628-22-8, Cat. #V000494 Vetec, Sigma-Aldrich Chemical Co.) and hydrogen peroxide (50 |g/plate; CAS Number 7722-84-1, Cat. #H1009 Sigma, Sigma-Aldrich Chemical Co.) were employed in the assays with strains TA1535 and TA102, respectively. Phosphate buffer was used as a negative control of analysis systems with and without metabolic activation with all S. typhimurium strains [24,25].
After the pre-incubation period, 2 ml of surface agar (top agar) adjusted to 45 °C [10.3 mM NaCl, 0.5 mM biotidine solution (histidine and biotin) and bacteriological agar 0.6% (w/vol)] were added to each test tube, vortexed for 30 s and dispensed on Petri dishes (90 mm x 150 mm) containing 20 ml of minimal Vogel Bonner medium [20 ml of 50 x (10g of MgSO4-7H20,100gofC6H8O7-H2O, 500g of K2HPO4, 175 g of NaNH4HPO4-4H2O, 1000 ml of H2O type 1 q.s.p.); 200 ml ofglucose solution 10% (w/vol); 780 ml ofbacterio-logical agar 1.92% (w/vol)] for the TA98, TA100, TA102 and TA1535 strains, and minimal agar with added glucose at 0.4% (w/vol) for strain TA97a. These plates were kept at room temperature until the complete solidification of the top agar. Revertants (his+) were counted after incubation at 37°C for 66 h [24] and Guideline for testing of chemicals [25].
2.3. Identity standard and quality and lipid characterization of oil
The sunflower oil was characterized by chemical analysis of its oxidative stability, such as the acidity index (mg KOH/g) Iodine (g/100g oil) and peroxide (mequiv. O2/kg) according to standard methods [30]. These analyses provide information about the identity and quality of the oil after processing and marketing. The fatty acid profile was determined as previously described [30-33] employing a Perkin Elmer Clarus 500 gas chromatograph (Norwalk, CT) with an automatic injector and flame ionization detector. Conditions: A 50 m x 0.25 mm WCOT fused silica column (CAPILLARY CP-Sil 88, CP6173, Agilent Technologies, CA, USA), with the injector at 270 °C and a flame ionization detector at 310 °C. Initial oven temperature was 140°C for 2min and was increased in 2°C increments for 60 s to 235 °C, held at 235 °C for 10 min, and finally raised to 270°C. Hydrogen was used as the carrier gas at a flow of 30 ml per min. Individual fatty acids were identified by comparing their retention times with those of purified standards (fatty acid esters). The peak area was calculated using the chromatographic integrator and chromatography software and expressed as a relative percentage of each fatty acid in relation to the total fatty acids.
2.4. Statistical analysis
The Ames test data were subjected to one-way analysis of variance (ANOVA) and medium comparison with Scott-Knott's test (a = 0.05) [34] using the SISVAR computer software [35]. Also the mutagenic ratio was calculated according to the following equation: RM = where RM, xfe X2 correspond to the mutagenicity
ratio, the mean number of revertant colonies on the test plate and the mean number of revertant colonies on the negative control plate, respectively. A compound is considered to be genotoxic when (i) RM >2 was noted in at least one dose tested and (ii) >1 strain showed a significant dose-response (p<0.05) among the tested concentrations or spontaneous revertants (negative control) [36,37].
3. Results and discussion
3.1. Mutagenicity ofsunflower oil
This study indicated that there was no significant increase (p <0.05) in the number of revertant colonies of the S. typhimir-ium strains TA97a, TA98, TA100, TA102 and TA1535 for any of the tested doses of sunflower oil (10-200 |il/plate) compared to the negative controls with and without exogenous metabolic activation system (Table 1). Also any dose tested of the sunflower oil (10-200 |il/plate) presented RM >2 (data not shown).
The Ames test has been previously used for mutagenicity evaluation of some vegetable oils. For example, Ocimum selloi oil was analyzed at concentrations of 500-700 mg/plate using
S. typhimurium strains TA 97a, TA98 e TA100 in the presence or absence of metabolic activation (S9 fraction) [26]. The essential oils of Melaleuca alternifolia and Lavandula angustifolia were also analyzed at concentrations of 0.28, 0.88 and 2 mg/plate with S. typhimurium strains TA98 and TA100 and E. coli WP2 uvrA, respectively, in the presence or absence of metabolic activation (S9 fraction) [27]. Neem oil was studied at concentrations of 0.01-10 mg/plate using S. typhimurium strains TA98, TA100, TA102, TA1535 and TA1537, as well as at concentrations of 0.1-100 |g/plate, diluted in DMSO, using strains TA98, TA100 and TA102 in the presence or absence of metabolic activation (S9 fraction) [28]. The essential oil of Curcuma longa L. was analyzed at concentrations of 0.1-3 mg/plate with S. typhimurium strains TA98,
TA100, TA102 and TA1535 in the presence or absence of metabolic activation (S9 fraction) [29]. All of these Ames test results showed that these oils were not genotoxic regarding frameshift mutations (TA97, TA98 and TA1537) and base pair substitutions (TA100, TA102, TA1535 and E. coli WP2 uvrA) [24].
Recently, a micronucleus test in mouse bone marrow showed no clastogenic and/or aneugenic effects of the tincture and H. annuus L. seed (sunflower) oils from two sources regardless of the dose (0.25-2 g/kg) and treatment time (24 and 48 h), but the results were sex-independent (sunflower tincture) or sex-dependent (sunflower oils) [22]. Differently, in lymphocytes incubated with a water extract of heated sunflower oil containing 0.075 or 0.15 | M thio-barbituric acid-reactive substances (this extract had a high content of polar aldehydes), the rate of chromosomal breakage was 18.4% and 23.1% compared to 8.7% and 6.6% or 8.1% and 9.2%, respectively, in lymphocytes incubated with the same volume of a water extract from a non-heated oil or distilled water [21]. In HepG2 or HUVEC cells, the cytotoxic properties of heated sunflower oil were found to be dose dependent, and cytotoxicity occurred at concentrations as low as 0.25 | M. In contrast, the same volume of non-heated oil or distilled water was non-toxic in these cells [21]. These results showed that the water extract obtained from heated oil is clasto-genic and, in higher doses, cytotoxic. These data also suggested that the water extract obtained from heat-stressed cooking oils that had a high aldehyde content was clastogenic. It was speculated that the ingestion of large amounts of these products could impact human health, especially for diseases resulting from chromosomal breakage, such as certain congenital malformations and certain types of cancer. This last fact can be corroborated by previous reports indicating that the administration of heat-stressed sunflower oil to rats is teratogenic [21].
In this study, a significantly lower number (p <0.05) of rever-tant colonies was observed in sunflower oil treatments with strain TA100 (20-200 |l/plate S9-), as well as strains TA97a (200 |l/plate S9+), TA98 (20-200 |l/plate S9+) and TA102 (50-200 |l/plate S9+), compared with their negative controls (Table 1), suggesting that the dose-dependent toxicity of sunflower oil started from 200 | l/plate for S. typhimurium strain TA97a, 50 | l/plate for TA102 and 20 |l/plate for TA98 and TA100 under the conditions tested. The analysis obtained from the PCE/NCE ratio (PCE: polychromatic erythrocyte; NCE: normochromatic erythro-cyte) during the micronucleus assay in mouse bone marrow also suggested that the systemic toxicity of sunflower oil might be source-dependent on the highest dose used [22]. However, the Ames test indicated no mutagenic responses of sunflower oil at the tested conditions: (10 |l/plate S9+: TA98; 10-20 |l/plate S9+: TA102; 10-100|l/plate S9+: TA97a; 10-200|l/plate S9+: TA100 andTA1535; 10|l/plate S9-:TA100; 10-200|l/plate S9-:TA97a, TA98, TA102 and TA1535). These results could be explained by the Brazlian standards of the identity and quality of sunflower oil, which are established by ANVISA [38]. This norm requires the verification of the identity and minimum quality of vegetable oils, vegetable fats and vegetable creams. The specific requirements are an acidity in refined oils and fats equal to 0.6 mg KOH/g at most and a peroxide index equal to 10 mequiv. O2/kg at most in refined oils and fats. These standards are in accordance with the international standards proposed by the Codex Alimentarius [39], which established the same standards for acidity and peroxides.
3.2. Identity, quality and lipid characterization of sunflower oil
The chemical analyses of the oxidative stability for the characterization of sunflower seed oil showed an acidity index equal to 0.16 mg KOH/g, iodine equal to 124g/100g, and oil and peroxide equal to 6.23 mequiv. O2/kg. According to the RDC 270 [38]
Table 1
Mean number of revertant colonies (TA97a, TA98, TA100, TA102 andTA1535) observed on experimental treatment with sunflower oil including the reference mutagens and the negative control in the Ames test (pre-incubation).
Dose (|xl/plate)
TA1535
S9 (-)
Negative control 10 20 50 100 200
Positive control1
S9 (+)
Negative control 10 20 50 100 200
Positive control2 CV(%)
Sunflower oil
Sunflower oil
144.67 ±5.86 145.67 ±8.33 151.33 ±24.01 126.50 ±4.95 129.00 ±8.54 125.00 ±6.56 1025 ± 102.40a
190.67 ±13.01 155.00 ±0.58 168.33 ±5.51 178.00 ±16.52 165.67 ±16.50 137.67 ± 24.01a 3200 ± 202.23a
27.33 ±5.03 27.33 ±8.08 28.00 ±10.58 29.33 ± 8.96 31.00 ±10.82 25.67 ± 49.93 426.00 ± 33.31a
38.33 ±4.73 37.33 ±7.64 25.33 ± 5.86a 22.00 ± 3.46a 15.00 ± 1.73a 22.33 ± 2.89a 1510.33 ± 222.46a
180.00 ±27.00 172.33 ± 36.12 125.33 ± 13.05a 124.00 ± 20.88a 132.00 ± 5.29a 107.00 ± 18.36a 4061.00 ± 547.85a
185.67 ± 33.38 147.67 ±14.05 166.67 ± 3.51 152.67 ±21.08 153.67 ±16.62 137.33 ±19.66 7932.66 ± 267.4a
463.33 ± 43.25 421.00 ±53.7 462.67 ±51.39 456.67 ± 35.57 477.67 ±55.97 469.00 ±18.00 892.00 ± 181a
611.00 608.50 610.33 519.67 475.67 479.67 912.66
± 28.28 ± 3.54 ± 18.15
± 29.02a ± 30.75a ± 90.75a ± 33.50a
27.00 ±1.73 21.67 ±2.31 21.33 ±2.08 22.00 ±5.57 19.67 ±4.93 20.67 ± 0.58 2707.00 ± 99.71a
16.67 ±4.51 16.33 ±1.15 17.33 ±0.58 14.00 ±3.61 14.00 ±2.00 17.00 ±6.56 244.66 ± 26.63a
The numbers indicate the means and standards deviation values of CFU in triplicate assay systems. CV=coefficient of variation.
Without (-) and with (+) S9 microsomal fraction of homogenized rat liver (post-mitochondrial fraction supplemented with a cofactor, prepared from the liver of rodents treated with an enzyme inducer agent arocloror 1254, MOLTOX®, Molecular Toxicology, USA). Negative control: phosphate buffer.
Positive control1: 4-Nitroquinoline N-oxide (CAS Number 56-57-5, Cat. #N8141 Aldrich, Sigma-Aldrich Chemical Co.) forTA97a, TA98 and TA100; Sodium azide (CAS Number 26628-22-8, Cat. #V000494 Vetec, Sigma-Aldrich Chemical Co.) forTA1535; Hydrogen peroxide (CAS Number 7722-84-1, Cat. #H1009 Sigma, Sigma-Aldrich Chemical Co.) forTA102.
Positive control2: 2-Aminoanthracene (CAS Number 613-13-8, Cat. #A38800 Aldrich, Sigma-Aldrich Chemical Co.). a Significantly different from the corresponding negative control values (ANOVA and Scott-Knott test, p < 0.05).
and the Codex Alimentarius [39] the determinations are within the nationally and internationally required standards.
The identity and quality parameters evaluated in this study were compared with the results previously reported for Citrullus colo-cynthis (L.) Schrad seed oil and Helianthus annuus (sunflower) seed oil [40]. In this study, the peroxide value (ISO 3960), acidity (the percentage of free fatty acids was calculated as oleic acid) (ISO 660) and saponification number (ISO 3657) of the seed oil were determined according to the International Organisation for Standardisation (ISO) standards. The seed oils showed the following properties: acid value of 3.14 ± 0.11 (C. colocynthis) and 2.80 ± 0.08 (H. annuus); free fatty acid - FFA (as oleic%) of 1.57 ±0.11 (C. colocynthis) and 1.40 ±0.08 (H. annuus); saponification value (mg KOH/g) of 204.63 ±0.73 (C. colocynthis) and 197.45 ±0.68 (H. annuus); iodine number (g/100g oil) of 123.31 ±1.32 (C. colocynthis) and 118.56 ± 0.98 (H. annuus); peroxide value (mequiv. O2/kg) of 9.42 ±0.18 (C. colocynthis) and 6.07 ±0.05 (H. annuus). These findings agree with our results for sunflower oil for iodine and peroxide, except for the saponification value, which was significantly lower. It also suggests that the sunflower oil tested for genotoxicity had characteristics that made it less susceptible to lipid oxidation and therefore more resistant to rancidity, which potentially ensured the integrity and preservation of the sunflower oil without interfering with the levels of liposoluble vitamins and essential fatty acids.
The FFA content of both oils (C. colocynthis and H. annuus) was low and found to be well correlated with the moisture values (7.51% and 3.75%, respectively) because FFAs are the result of the hydrolysis of the oil. Furthermore, it is well known that free fatty acids are more susceptible to lipid oxidation, which can explain their relatively high peroxide value (9.42 mequiv. O2/kg) of C. colocynthis seed oil compared to sunflower oil (6.07 mequiv. O2/kg) [40]. In addition, the low peroxide and FFA values and the absence of a disagreeable flavor and odor in C. colocynthis seed oil indicated that this seed is not susceptible to oxidation when intact [41] and can be stored for a long period of time without deterioration until further
use in both the food and oleo-chemical industry. C. colocynthis seed oil had higher saponification and iodine values than sunflower seed oil [40]. A high saponification value is associated with the presence of shorter chain fatty acids, such as palmitic (C16) or stearic (C18) acids [42]. However, the high iodine value indicated that the oil is rich in double bonds [41]. Unsaturated fatty acids tend to be more reactive toward atmospheric oxygen and undergo oxidation. Consequently, the oxidation of an oil can result in changes that affects its integrity and security, such as the generation of potentially toxic polymeric compounds (e.g., peroxides) [40].
The lipid characterization of sunflower seed oil revealed that a specific invariant profile was usually found [43-46]. Initially, our chromatographic analysis (GC) showed a fatty acid content consisting mainly of poly-unsaturated chains (54.05 g/100g), such as omega 6 (50.68 g/100g) and omega 3 (3.37g/100g), and monounsaturated (27.73 g/100g), such as omega 9 (27.27g/100g), and saturated (13.39g/100g) and total trans-isomers (0.45g/100g) (Fig. 1A, Table 2), suggesting that it originated from a sunflower species that had not been genetically modified [3]. Among the saturated fatty acids, palmitic acid (C16:0 ^ 8.58 g/100 g) predominated, followed by stearic (C18:0^ 3.69g/100g), behenic (C22:0^ 0.52g/100g), arachidic (C20:0^ 0.33 g/100g), lignoceric (C24:0 ^ 0.19g/100 g) and myristic (C14:0 ^ 0.8 g/100 g) acids. Among the monounsaturated fatty acids, oleic acid (C18:1 ^ 27.27g/100g) predominated, followed by palmitoleic acid (C16:1 ^ 0.9g/100g), and among the poly-unsaturated fatty acids, linoleic acid (C18:2^ 50.68g/100g) predominated, followed by a-linolenic (C18:2^ 3.37g/100g), trans T-linoleic (C18:2^ 0.27g/100g) and trans T-linolenic acids (C18:3 ^ 0.18 g/100 g) (Fig. 1B, Table 2).
The high amount of linoleic acid (C18:2) present in sunflower seed oil can make it more susceptible to oxidation and consequently cause higher cytotoxicity due to the production of free radicals, which might explain our findings on sunflower oil toxic-ity usingS. typhimurium strainsTA98 (20-200 |l/plate S9+),TA100 (20-200 |il/plate S9-) and TA102 (50-200 |l/plate S9+). On the
Fig. 1. Gas chromatograph (GC) for pharmaceutical oil of H. annuus L. (sunflower) seeds (CAS #8001-21-6). Fatty acids profile: (A) polyunsaturated (total, omega 6 and omega 3), monounsaturated (total and omega 9) saturated and total trans-isomers; (B) saturated fatty acids (palmitic, stearic, behenic, arachidic, lignoceric and myristic acids), monounsaturated fatty acids (oleic and palmitoleic acids), polyunsaturated fatty acids (linoleic and a-linolenic acids), and trans-isomers (trans T-linoleic and trans T-linolenic acids).
other hand, the fatty acid composition also contributes to the phytotherapeutic properties, such as in healing and inflammatory processes [6,8,10,47]. Therefore, any change in the chemical composition due to selective breeding, which is spurred by a worldwide demand for more stable varieties of sunflower oil with a reduced risk of fatty acid oxidation (i.e., | linoleic versus f oleic acid) [3], could directly change the phytotherapeutic properties of sunflower oil. The therapeutic properties of some oils are closely related to its constitution. Similar to the oil of H. annuus seeds used in this study, the C. colocynthis and H. annuus oil previously studied [40] had high levels of oleic monounsaturated fatty acids (C18:1 ^14, 20g/100gand C18:1 ^ 37, 73g/100g, respectively) and polyunsaturated linoleic acid (C18:2^ 66, 78g/100g and C18:2^ 45.49 g/100g, respectively). Due to the linoleic acid, these oils may have an important role in restoring the structure
and function of the permeable barrier of the stratum corneum of the skin [48]. Still, inadequate levels of linoleic acid may result in abnormal barrier functions, such as an increased trans-epidermal water loss [49].
4. Conclusion
The present research has contributed to the toxicological profile of sunflower oil (pharmaceutical quality) by presenting the results from a well conducted Ames test. The results obtained from the Ames test (Salmonella/microsome test), which was used to indicate the carcinogenic potential, suggest that there is no dose-independent mutagenicity of sunflower oil but it was observed a dose-dependent cytotoxicity. The oxidative properties of sunflower oil were found to be in accordance with the require-
Table 2
Fatty acids profile (polyunsaturated, monounsaturated, saturated and total trans-isomers) of pharmaceutical oil of H. annuus L. (sunflower) seeds (CAS #8001-21-6) obtained by gas chromatograph (GC).
Fatty acids Values (g/100g)
Polyunsaturated 54.05
Linoleic acid (C18:2) (omega 6) 50.68
a-Linolenic acid (C18:2) (omega3) 3.37
Monounsaturated 27.73
Oleic acid (C18:1) (omega 9) 27.27
Palmitoleic acid (C16:1) 0.9
Saturated 13.39
Palmitic acid (C16:0) 8.58
Stearic acid (C18:0) 3.69
Behenic acid (C22:0) 0.52
Arachidic acid (C20:0) 0.33
Lignoceric acid (C24:0) 0.19
Myristic acid (C14:0) 0.8
Total trans-isomers 0.45
Trans T-linoleic acid (C18:2) 0.27
Trans T-linolenic acid (C18:3) 0.18
ments of national and international standards [i.e., acidity index (mgKOH/g), iodine (g/100 g oil) and peroxide (mequiv. O2/kg)]. Gas chromatography (GC) revealed high levels of polyunsaturated fatty acids, followed by monounsaturated, saturated and trans-isomers. Among these, the highest were linoleic (50.68 g/100 g), oleic (27.27 g/100 g) and palmitic acids (8.58 g/100 g). The chemical composition might explain the cytotoxicity of sunflower oil to the strains of S. typhimurium used in the Ames test. However, the chemical characteristics of these fatty acids might also contribute to the phytotherapeutic properties of oil seeds of H. annuus L. (sunflower).
Conflict of interest
The authors have declared that there is no conflict of interest. Acknowledgements
This research was supported by Rede Mineira de Ensaios Toxi-cológicos e Farmacológicos de Produtos Terapéuticos (REDE MINEIRA TOXIFAR), Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG RED 00008-14), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Coordenacao de Aperfeicoamento de Pessoal de Nível Superior (CAPES). The authors thank the Language Services of Elsevier for help in English language editing.
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