ABSTRACT:
This research was carried out to evaluate the effect of mycotoxins on the performance of horses through physiological parameters, and hematology and serum biochemistry analyses. The essay lasted 40 days, with 12 days for adaptation and 28 days of experimentation. In the experimental stage, the horses were distributed in a completely randomized design, with three treatments with four animals each. The treatments used were 0 (control), 50 ppb and 100 ppb of Aflatoxin B1 (AFB1) added to a concentrate in a basal diet. The basal diet contained mycotoxins from feedstuffs naturally contaminated. The exercise test was performed over the 21th day of the experimental stage. The exercise consisted in an interval training test with a warm-up of 17 mins at a trot followed by three gallops of 450m/min. The heart rate was monitored between the gallops. Before the exercise test and immediately after the third gallop, the physiological and blood parameters were evaluated, and continued up to 48 hours after the exercise. The results of the physiological, hematological and biochemical parameters were submitted to analysis of variance (ANOVA) and compared by the Tukey test at 5% of significance. The presence of AFB1 in the diet influenced the alkaline phosphatase activity, which presented higher values in horses fed diet with inclusion of 100 ppb AFB1, suggesting a hepatotoxic activity associated with the others mycotoxins naturally present in the feedstuffs.
INDEX TERMS:
Horses; contaminated meal; short-term exercises; alkaline phosphatase; exercise; mycotoxins; morphology
RESUMO:
Esta pesquisa foi conduzida para avaliar o efeito de micotoxinas no desempenho de equinos com avaliações fisiológicas e análises hematológicas e da bioquímica sérica. O ensaio durou 40 dias, com 12 dias de adaptação e 28 dias de experimentação. Na fase experimental, os equinos foram distribuídos em delineamento inteiramente casualizado em três tratamentos, com quatro animais cada. Os tratamentos utilizados foram 0 (controle), 50 ppb e 100 ppb de Aflatoxina B1 (AFB1) adicionada ao concentrado de uma dieta basal. A dieta basal continha alimentos naturalmente contaminados por micotoxinas. O teste de desempenho foi executado no 21º dia da fase experimental por meio de teste intervalado consistindo em aquecimento ao trote por 17 minutos, seguido de três galopes de 450m/min. A frequência cardíaca (FC) foi monitorada entre os galopes. Antes do exercício e imediatamente após o terceiro galope, os parâmetros fisiológicos e sanguíneos foram avaliados e continuaram sendo monitorados até 48 horas após o exercício. Os resultados dos parâmetros fisiológicos, hematológicos e bioquímicos foram submetidos à análise de variância (ANOVA) e comparados pelo teste de Tukey a 5% de significância. A presença de AFB1 na dieta influenciou a atividade da fosfatase alcalina, que apresentou valores mais elevadas na dieta com inclusão de 100 ppb de AFB1, sugerindo uma atividade hepatotóxica associada às outras micotoxinas naturalmente presentes nos alimentos.
TERMOS DE INDEXAÇÃO:
Micotoxinas; equinos; exercícios de curta duração; fosfatase alcalina; micotoxinas; morfologia
Introduction
Several mycotoxins have been identified in foods and diets for humans and animals in Brazil. The importance of aflatoxins (AF), fumonisins (FB), ochratoxins (OTA), zearalenone (ZEA) and trichothecenes should be emphasized due to their occurrence and also their high toxigenic potential for farm animals (Baldissera et al. 1993Baldissera M.A., Santurio J.M., Canto S.H., Pranke P.H., Almeida C.A.A. & Schimidt C. 1993. Aflatoxinas, ocratoxina e zearalenona em alimentos para consumo animal no sul do Brasil - Parte II. Revta Instituto Adolfo Lutz 53(1/2):5-10., Franco et al. 2019Franco L.T., Petta T., Rottinghaus G.E., Bordin K., Gomes G.A. & Oliveira C.A.F. 2019. Co-occurrence of mycotoxins in maize food and maize-based feed from small-scale farms in Brazil: a pilot study. Mycotoxin Res. 35(1):65-73. <http://dx.doi.org/10.1007/s12550-018-0331-4> <PMid:30242616>
https://doi.org/10.1007/s12550-018-0331-...
). In addition, the additive or synergistic effect between different toxins, which increase or alter their effects on animals, should be considered. Although mycotoxins have several adverse effects on animal health, little is known about their impacts in the horse nutrition (Liesener et al. 2010Liesener K., Curtui V., Dietrich R., Märtlbauer E. & Usleber E. 2010. Mycotoxins in horse feed. Mycotoxin Res. 26(1):23-30. <http://dx.doi.org/10.1007/s12550-009-0037-8> <PMid:23605238>
https://doi.org/10.1007/s12550-009-0037-...
, Schumann et al. 2016Schumann B., Winkler J., Mickenautsch N., Warnken T. & Dänicke S. 2016. Effects of deoxynivalenol (DON), zearalenone (ZEN), and related metabolites on equine peripheral blood mononuclear cells (PBMC) in vitro and background occurrence of these toxins in horses. Mycotoxin Res. 32(3):153-161. <http://dx.doi.org/10.1007/s12550-016-0250-1> <PMid:27255919>
https://doi.org/10.1007/s12550-016-0250-...
). Raymond et al. (2005)Raymond S.L., Smith T.K. & Swam H.V.L.N. 2005. Effects of feeding a blend of grains naturally contaminated with Fusarium mycotoxins on feed intake, metabolism, and indices of athletic performance of exercised horses. J. Anim. Sci. 83(6):1267-1273. <http://dx.doi.org/10.2527/2005.8361267x>
https://doi.org/10.2527/2005.8361267x...
pointed out that, especially for sport horses, chronic intake of low mycotoxin levels in diets can affect performance without animals showing typical clinical signs of mycotoxicosis.
Aflatoxins are a class of carcinogenic mycotoxins produced by Aspergillus fungi and are widely distributed in nature, especially in a variety of food commodities. Aflatoxin B1 (AFB1) is confirmed to be the most toxic of all the aflatoxins and has been well-characterized to lead to the development of hepatic cellular carcinoma (HCC) in humans and animals. The occurrence of these mycotoxins, alone and in combination, representes a real risk for human and animal health (Bertero et al. 2018Bertero A., Moretti A., Spicer L.J. & Caloni F. 2018. Fusarium molds and mycotoxins: potential species-specific effects. Toxins 10(6):244. <http://dx.doi.org/103390/toxins10060244> <PMid:29914090>
https://doi.org/103390/toxins10060244...
, Rushing & Selim 2019Rushing B.R. & Selim M. 2019. AflatoxinB1: a review on metabolism,toxicity,occurrence in food occupational exposure, and detoxification methods. Food Chem. Toxicol. 124:81-100. <http://dx.doi.org/10.1016/j.fct.2018.11.047> <PMid:30468841>
https://doi.org/10.1016/j.fct.2018.11.04...
).
Although the importance of mycotoxins in public and animal health is recognized, there is no uniform regulation of mycotoxin limits in foods in the different countries, particularly in Mercosur countries (Brazil/Argentina), (Mercosul/GMC 2002Mercosul/GMC 2002. Resolução nº 25, Regulamento Técnico Mercosul sobre limites máximos de aflatoxinas admissíveis no leite, amendoim e milho. Mercado Comum do Cone Sul/Grupo Mercado Comum <http://portal.anvisa.gov.br/legislacao#/>
http://portal.anvisa.gov.br/legislacao#/...
). The Brazilian legislation (Brasil 1988Brasil 1988. Portaria MA/SNAD/SFA nº 07, de 09/11/88. Diário Oficial da União Seção I, Ministério da Agricultura, Pecuária e Abastecimento (MAPA), Brasília, DF, p.21.968.) establishes the maximum limit of 50μg/kg for aflatoxins in any feedstuffs used directly or as an ingredient in diets for animals but does not specify limits for other mycotoxins. This research was carried out to evaluate the inclusion of aflatoxin B1 (AFB1) in the diet and to verify the effects on metabolism and performance of horses.
Materials and Methods
The experiment was conducted at the Army Sergeant School (ESA), latitude 21°42’15.6’’ South and longitude 45°15’18.9’’ West, of the Brazilian Army, in Três Corações, Minas Gerais State. The assay was performed in accordance with the principles of ethics in experimentation approved by the committee on ethics in animal experimentation from the University: CEUA-UFRRJ Number 1212031017.
Experimental period. The total experimental period was 40 days, divided into two stages: one was the pre-experimental or adaption stage of 12 days and the other was the experimental stage of 28 days. A total of 12 adult Brazilian Sport Horses (9 females and 3 males), aged between 5 and 8 years old with an average body weight of 458.02±22.09kg were used. The research was conducted in a completely randomized design, with three treatments with four animals each, and the animal was the experimental unit. The experimental treatments used were: Treatment I = control diet (0μg/kg of AFB1); Treatment II = diet with 50μg/kg of AFB1; and Treatment III = diet with 100μg/kg AFB1. The AFB1 was added to the basal diet (Table 1). The experimental basal diet was composed by Tifton hay (Cynodon spp.) and alfafa (Medicago sativa), commercial concentrate (S Line -280, Royal Horse®), mineral salt and water ad libitum, elaborated according to the NRC (2007)NRC 2007. Nutrient Requirements of Horses. 6th ed. National Academies Press, Washington, D.C. 341p. for mature horses. The horses remained free in their paddocks during the day and were housed in individual stalls at night. The animals were fed according to the schedule of the Military Unit, which is 2kg of concentrate meal at 05:00 a.m. and 2kg at 17:00 p.m., alfafa hay at 10:00 a.m., and tifton hay at 13:00 p.m. and 20:00 p.m. Every day during the experimental period at the 17:00 p.m. feeding time, 1kg of concentrate feed with AFB1 was prepared and given to the animals, according to the treatment. Before the adaptation period, all feedstuffs were analyzed, and the concentrations of mycotoxins in the basal diet were: 5.620μg/kg of DON, 708μg/kg of ZEA and 560μg/kg of FB1.
The average composition (g or μg /kg on dry matter basis) of the experimental diets with different inclusions of AFB1
Clinical conditions. Before, during and after the experimental period, clinical, hematological and biochemical analyzes of the horses were carried out to check the health conditions, especially regarding the presence of liver damage. Throughout the experimental period, the clinical conditions of the animals were monitored, daily, by a veterinarian.
Aflatoxin production and estimation. The aflatoxin B1 was produced by the Mycology Laboratory of Federal University Rural of Rio de Janeiro from fermenting rice with a spore suspension of Aspergillus parasiticus (NRRL 2999), according to Shotwell et al. (1966)Shotwell O.L., Hesseltine C.V., Stubblefield R.D. & Sorenson W.G. 1966. Production of aflatoxina on rice. Appl. Microbiol. 14(3):425-428. <PMid:5970829>. The AFB1 content was extracted and purified through a Mycosep® Aflazon column (Romer Labs Diagnostic GmbH., Tulln, Austria) as per the manufacturer’s instructions and an aliquot (200μl) was derivatized with 700 μl trifluoroacetic acid-acetic acid-water (20:10:70, v/v). The derivatized aflatoxin was quantified by High Performance Liquid Chromatography (HPLC), at the “Laboratório de Micologia e Micotoxinas” of “Universidade Federal de Minas Gerais”, following the methodology proposed by Trucksess et al. (1994)Trucksess M.W., Stack M.E., Nesheim S., Albert R. & Romer T. 1994. Multifunctional column coupled with liquid chromatography for determination of aflatoxins B1, B2, G1 and G2 in corn, almonds. Brazil nuts, peanuts, and pistachio nuts: collaborative study. J. AOAC Int. 77(6):1512-1521. <PMid:7819761>.
Aflatoxins were quantified by injecting 20μL of extract from each vial into an HPLC system consisting of a JASCO model LC-2000 pump (Tokyo, Japan) connected to a JASCO model FP-2020 programmable fluorescence detector and a data module JASCO model 6937-J041A (ChromNAV). Chromatographic separations were performed on a stainless steel, C18 reversed-phase column (Supelcosil™ LC-ABZ, 150 x 4.6mm, 5μm particle size) connected to a precolumn (Supelguard™ LC-ABZ, 20 x 4.6mm, 5μm particle size). The mobile phase was water:methanol:acetonitrile (4:1:1, v/v/v) at a flow rate of 1.0ml min-1. Fluorescence of aflatoxin derivatives was recorded at excitation and emission wavelengths of λ 360nm and λ 460nm, respectively. Standard curves were constructed with different levels of AFB1. This toxin was quantified by correlating peak heights of sample extracts with those of standard curves. The detection limit of the analytical method was 0.4ng g-1.
The concentration of AFB1 yielded was 4.25mg/kg and it was diluted daily in the concentrate feed to obtain the desired concentrations according to the equation: Ci xVi = Cf x Vf, (where Ci and Cf are the initial and final concentrations and Vi and Vf, the initial and final volumes).
Performance evaluation. The performance was assessed through an exercise test at the 21th day of the experimental stage. The average temperature during the day was 21.5°C, with a minimum of 12.2°C and maximum of 28.1°C and the relative humidity was 62.4%. The animals performed standard exercise training for 50 minutes, 5 days per week, during three weeks of the experimental stage. The training program of walking and trotting had been intercalated with flexion movements. For the exercise test, the animals were randomly split into 3 groups with 4 animals each. The test started at 9:00 a.m. and finished at 12:06 a.m. on the same day; they were performed sequentially for each group. The test consisted of a 17 min warm-up of walking and trotting followed by three sets of gallops at a speed of 450m/min for three minutes each. In the intervals between the gallops, the horses were monitored for heart rate (HR), and when the heart rate returned to 60-70bpm the animals moved on to the next gallop. In order to evaluate the performance of the animals in the test, the heart rate, the respiratory frequency was recorded. Blood samples were taken to analyze the globular volume, glucose, lactate and blood biochemistry. These variables were obtained before the exercise test, and after the third gallop and continued up to 48 hours after the test as described: M0 (Pre-exercise), M1 (Immediately after the exercise test), M2 (10min), M3 (20min), M4 (60min), M5 (3h), M6 (6h), M7 (12h), M8 (24h) and M9 (48h).
Heart rate and respiratory rate were recorded with a stethoscope (Mod LittmannMR). Blood samples were collected using a vacuum collection needle (BD®) and vacuum tubes with EDTA (BD Vacutainer®) for the complete blood count (CBC). Vacuum tubes with sodium fluoride (BD Vacutainer®) were used to determine glucose and lactate measures and vacuum tubes without anticoagulant (BD Vacutainer®) were used to obtain blood serum samples, for biochemical determination of enzymatic activity, total proteins and fractions, cholesterol, urea and creatinine measures. After collection, the samples were centrifuged at 7.000rpm for 10 minutes to separate the plasma and serum. Aliquots of both plasma and serum of 1.0mL were pipetted automatically and stored at -20oC in 1.5mL polypropylene tubes until required for analysis. Subsequently, the analyzes were performed by the enzymatic/colorimetric method in a spectrophotometer SB 190 (CELM® Cia Equipadora de Laboratórios Modernos - CELM. Brazil). Labtest® kits were used for all analyzes.
Statistical analysis. The results were evaluated for normality by Lilliefors test and the homogeneity by Cochran and Bartlett test. Data of the hematological, biochemical and physiological variables were submitted to analysis of variance (ANOVA) in a split-plot scheme with the levels of inclusions of AFB1 in the diets evaluated in the parcels and the exercise test times evaluated in sub-parcels. The means were compared by the Tukey test, at 0.05 significance level, using the Statistical and Genetic Analysis System (SAEG 2007SAEG 2007. Sistema de análises estatísticas e genéticas (SAEG), Versão 9.1. Universidade Federal de Viçosa (UFV), Viçosa, MG. 301p.).
Results
Occurrence of mycotoxins in feedstuffs
The mycotoxins observed in the feedstuffs of basal diet were: DON, 5.620μg/kg, in Tifton and alfalfa hay and commercial concentrate; ZEA, 708μg/kg, in alfalfa hay and commercial concentrate; and FB1, 560μg/kg, in commercial concentrate. The intake of mycotoxins by the horses according to the treatments are given in Table 2.
Means of the mycotoxin intake per kg of dry matter (Kg DM) and per kg of body weight (kg BW), according to the treatments
Physiological parameters
The intake of aflatoxin B1 did not affect the respiratory rate (RR) and heart rate (HR) values of horses in the exercise test (P>0.05), however, there was a simple effect of the time of evaluation (P<0.05) (Table 3).
Blood and biochemical parameters
The inclusion of aflatoxin B1 in the diets did not affected the blood parameters of the horses in the exercise test, except the enzyme alkaline phosphatase (ALP) (Table 4) (P<0.05). The globular volume (GV), total protein (TP), albumin (ALB) and cholesterol (COL) were evaluated at M0 through to M3 of the exercise test, and the results have been influenced by the exercise (P<0.05), with any effect from aflatoxin B1 inclusion to the diets (P>0.05) (Table 5).
The serum concentrations of urea and creatinine were evaluated at many times of the exercise test. The results showed that these parameters were not influenced by the aflatoxin B1 inclusion in the diets (P>0.05). However, a simple effect of the exercise test was observed (Table 6).
The enzymes aspartate transferase (AST), lactate desidrogenase (LDH) and gama glutamil transferase (GGT) activities were evaluated from M0 to M9 of the exercise test, while the enzyme creatine quinase (CK) was evaluated from M0 to M7 of the exercise test. The activities of the enzymes were not affected by aflatoxin B1 inclusion to the diets (P>0.05). However, the AST, LDH, GGT and CK activities were influenced by the exercise (P<0.05) (Table 7). The alkaline phosphatase (ALP) activity was affected by the inclusion of aflatoxin in the diets (P<0.05), presenting a higher value in horses fed diet with 100μg/kg of AFB1, (Table 8).
The serum concentration of glucose was evaluated from M0 to M9 of the exercise test, while the lactate concentration was evaluated from M0 to M7 of the exercise test. Serum glucose and lactate concentrations were not influenced by the inclusion of aflatoxin B1 in the diets (P>0.05) (Table 9).
Discussion
The AFB1 was not detected in the feedstuffs of the basal diet. The AFB1 produced in our laboratory and added to the commercial concentrate at concentrations of 50μg/kg and 100μg/kg, according to the treatments, which was the maximum amount intake by the horses, regardless of weight. Keller et al. (2007)Keller K.M., Queiroz B.D., Keller L.A.M., Ribeiro J.M.M., Cavaglieri L.R., González-Pereyra M.L., Dalcero A.M. & Rosa C.A.R. 2007. The mycobiota and toxicity of equines feeds. Vet. Res. Commun. 31(8):1037-1045. <http://dx.doi.org/10.1007/s11259-007-0028-1> <PMid:17285246>
https://doi.org/10.1007/s11259-007-0028-...
observed in horse’s feedstuffs concentrations of AFB1 ranging from 0.01 to 99.4μg/kg. Franco et al. (2019)Franco L.T., Petta T., Rottinghaus G.E., Bordin K., Gomes G.A. & Oliveira C.A.F. 2019. Co-occurrence of mycotoxins in maize food and maize-based feed from small-scale farms in Brazil: a pilot study. Mycotoxin Res. 35(1):65-73. <http://dx.doi.org/10.1007/s12550-018-0331-4> <PMid:30242616>
https://doi.org/10.1007/s12550-018-0331-...
observed in maize food and maize-based feed from small-scale farms that median levels of total AF, total FB, ZEN, and DON were 100μg/kg, 680μg/kg, 160μg/kg, and 200μg/kg, in feed samples, respectively, and that co-occurrence of two or more mycotoxins was confirmed in 51% of feed samples.
Caloni & Cortinovis (2011)Caloni F. & Cortinovis C. 2011. Toxicological effects of aflatoxins in horses. Vet. J. 188(3):270-273. <http://dx.doi.org/10.1016/j.tvjl.2010.06.002> <PMid:20619706>
https://doi.org/10.1016/j.tvjl.2010.06.0...
in a review of experimental AFB1 intoxication in horses reported that, although inconclusive, aflatoxicosis can occur with AFB1 concentrations between 0.5 and 1.0mg/kg in the diet, which induce clinical signals and hepatic damages, depending on the exposure time. The liver is a target organ in all affected animals, where the toxin induces centrilobular necrosis. Horses with aflatoxicosis show nonspecific clinical signs, such as cough, inappetence, depression, fever, tremor and ataxia. However, the blood and physiological alterations of horses in this research are resulting from the exercise test itself, with no effects from aflatoxin, except for the alkaline phosphatase activity. Dedar et al. (2019)Dedar R.K., Virmani N., Bala P.A., Singh J., Vaid R.K., Legha R.A. & Tripathi B.N. 2019. Clinicopathological findings of an episode of mycotoxicosis in horses. Equine Vet. Educ. 31(5):236-241. <http://dx.doi.org/10.1111/eve.12856>
https://doi.org/10.1111/eve.12856...
observed growth retardation in foals, weight loss and deaths in horses ingesting millet forage contaminated with levels of 24μg of aflatoxins/kg to 70μg of aflatoxins/kg of forage. For the authors, monitoring serum/plasma GGT levels was found to be a sensitive biochemical indicator to identify liver damage caused by mycotoxins. The daily intake of horses of diet in treatment III (100μg/kg of AFB1), corresponding a 9.4μg AFB1 by kg DM, did not result in any clinical signs in the horses.
The simultaneous occurrence of DON, ZEA and FB1 in the feedstuffs of basal diet is related to the 25 to 30% of corn in the diet. The concentration of mycotoxins in feedstuffs for horses is a serious problem, and the weather in Brazil is favorable to fungi multiplication and mycotoxins production (Keller et al. 2007Keller K.M., Queiroz B.D., Keller L.A.M., Ribeiro J.M.M., Cavaglieri L.R., González-Pereyra M.L., Dalcero A.M. & Rosa C.A.R. 2007. The mycobiota and toxicity of equines feeds. Vet. Res. Commun. 31(8):1037-1045. <http://dx.doi.org/10.1007/s11259-007-0028-1> <PMid:17285246>
https://doi.org/10.1007/s11259-007-0028-...
, Schulz et al. 2015Schulz A-K., Kersten S., Dänicke S., Coenen M. & Vervuert I. 2015. Effects of deoxynivalenol in naturally contaminated wheat on feed intake and health status of horses. Mycotoxin Res. 31(4):209-216. <http://dx.doi.org/10.1007/s12550-015-0234-6> <PMid:26420605>
https://doi.org/10.1007/s12550-015-0234-...
). Schumann et al. (2016)Schumann B., Winkler J., Mickenautsch N., Warnken T. & Dänicke S. 2016. Effects of deoxynivalenol (DON), zearalenone (ZEN), and related metabolites on equine peripheral blood mononuclear cells (PBMC) in vitro and background occurrence of these toxins in horses. Mycotoxin Res. 32(3):153-161. <http://dx.doi.org/10.1007/s12550-016-0250-1> <PMid:27255919>
https://doi.org/10.1007/s12550-016-0250-...
and Franco et al. (2019)Franco L.T., Petta T., Rottinghaus G.E., Bordin K., Gomes G.A. & Oliveira C.A.F. 2019. Co-occurrence of mycotoxins in maize food and maize-based feed from small-scale farms in Brazil: a pilot study. Mycotoxin Res. 35(1):65-73. <http://dx.doi.org/10.1007/s12550-018-0331-4> <PMid:30242616>
https://doi.org/10.1007/s12550-018-0331-...
pointed out that the simultaneous occurrence of Fusarium mycotoxins, such as DON and ZEA, is an important issue to be observed due to its implications on animal health and welfare.
The concentration of DON in the basal diet was 5.6mg/kg, with similar concentrations in alfafa hay and in the concentrate. Caloni & Cortinovis (2011)Caloni F. & Cortinovis C. 2011. Toxicological effects of aflatoxins in horses. Vet. J. 188(3):270-273. <http://dx.doi.org/10.1016/j.tvjl.2010.06.002> <PMid:20619706>
https://doi.org/10.1016/j.tvjl.2010.06.0...
and Cortinovis et al. (2012)Cortinovis C., Battini M. & Caloni F. 2012. Deoxynivalenol and T-2 Toxin in raw feeds for horses. J. Equine Vet. Sci. 32(2):72-74. (Short Communication). <http://dx.doi.org/10.1016/j.jevs.2011.08.002>
https://doi.org/10.1016/j.jevs.2011.08.0...
observed that horses fed naturally DON contaminated barley between 36 and 44mg/kg during 40 days they did not show any negative effects, such as refusing feed or alteration of blood biochemistry and hematology, suggesting that like ruminants, horses are relatively resistant to the adverse effects of DON.
The ZEA concentration in feedstuffs were 446.5μg/kg and 261.5μg/kg for concentrate and alfafa, respectively. Gimeno & Quintanilla (1983)Gimeno A. & Quintanilla J.A. 1983. Analytical and mycological study of a natural outbreak of Zearalenone mycotoxicosis in horses. Proceedings of the International Symposium of Mycotoxins, Cairo, p.387-392. reported natural outbreaks from feedstuffs containing approximately 2.7mg/kg of ZEA in horses. Intoxicated mares refused the diet, and presented vulvar edema, vaginal prolapse and internal hemorrhage, and severe sagging of the genitalia. In this research, no clinical symptoms were observed in the horses, suggesting that the amount of ZEA present in the basal diet was not enough to cause clinical alterations. It should be noted that the concentration of ZEA was lower than the European Union (2006)European Union 2006. Recomendação da Comissão, de 17 de agosto de 2006, sobre a presença de desoxinivalenol, zearalenona, ocratoxina A, toxinas T-2 e HT-2 e fumonisinas em produtos destinados à alimentação animal. Off. J. Eur. Union L229:7-9. of 3mg/kg for corn by-products.
The FB1 concentration in feedstuffs was 560μg/kg. Horses are the most sensitive specie to FB1 toxicity, and FB1 concentrations of 20μg/kg and 120μg/kg in feed are already able to cause outbreak in this specie (Bertero et al. 2018Bertero A., Moretti A., Spicer L.J. & Caloni F. 2018. Fusarium molds and mycotoxins: potential species-specific effects. Toxins 10(6):244. <http://dx.doi.org/103390/toxins10060244> <PMid:29914090>
https://doi.org/103390/toxins10060244...
). Ross et al. (1991)Ross P.F., Rice L.G., Reagor J.C., Osweiler G.D., Wilson T.M., Nelson H.A., Owens D.L., Plattner R.D., Harlin K.A., Richard J.L., Colvin B.M. & Banton M.I. 1991. Fumonisin B1 Concentrations in Feeds from 45 Confirmed Equine Leukoencephalomalacia Cases. J. Vet. Diagn. Invest. 3(3):238-241. <http://dx.doi.org/10.1177/104063879100300310> <PMid:1911996>
https://doi.org/10.1177/1040638791003003...
analyzed feedstuffs associated with an equine leukoencephalomalacea outbreaks observed contamination with FB1 with levels ranging from 1 to 126mg/kg. Most samples presented levels above 10mg/kg. According to Reed et al. (2004)Reed S.M, Bayly W.M. & Sellon D.C. 2004. Equine Internal Medicine. 2a ed. W.B. Saunders, Philadelphia. 1.650p. feedstuffs containing concentrations greater than 10mg/kg of fumonisin are fatal to horses. In this research, no clinical signs compatible with equine leukoencephalomalacea were observed, however the hematological and enzymatic alterations should be evaluated as they may be related to the simultaneous presence of several mycotoxins, especially aflatoxin B1.
The physiological parameters Respiratory rate (RR) and Heart rate (HR) were evaluated at pre-exercise (M0), immediately after the exercise (M1) and at the times of 10 (M2) and 20 minutes after exercise (M3) (Table 3). There were no effects of AFB1 inclusion in the diets in the respiratory (RR) and heart rate (HR) of the horses (P>0.05). The results showed the response of horses to exercise, with an increase of both RR and HR immediately after exercise (M1), and with a tendency to return to basal levels at 20 min (M3) after exercise. The values differed from those observed by Paludo et al. (2002)Paludo G.R., McManus C., Melo R.Q., Cardoso A.G., Mello F.PS., Moreira M. & Fuck B.H. 2002. Efeito do estresse térmico e do exercício sobre os parâmetros fisiológicos de cavalos do Exército Brasileiro. Revta Bras. Zootec. 31(3):1130-1142. <http://dx.doi.org/10.1590/S1516-35982002000500009>
https://doi.org/10.1590/S1516-3598200200...
for Brazilian Sport Horses that showed mean values of heart rates of 40.8±4.7, and respiratory rate of 16.7±3.1, in the pre-exercise and of 53.7±8.2 and 37.3±11.5, for heart and respiratory rates, respectively, in the post-exercise period.
The inclusion of AFB1 in the diets did not affected the blood parameters (Table 4), except for the alkaline phosphatase activity. The presence of aflatoxin together with other mycotoxins, especially FB, could be expected to cause changes in the blood profile during exercise due to hepatotoxicity. The intake of low doses of mycotoxins for long periods can influence the health and the performance of horses (Raymond et al. 2005Raymond S.L., Smith T.K. & Swam H.V.L.N. 2005. Effects of feeding a blend of grains naturally contaminated with Fusarium mycotoxins on feed intake, metabolism, and indices of athletic performance of exercised horses. J. Anim. Sci. 83(6):1267-1273. <http://dx.doi.org/10.2527/2005.8361267x>
https://doi.org/10.2527/2005.8361267x...
, Broom 2015Broom L. 2015. Mycotoxins and the intestine. Anim. Nutr. 1(4):262-265. <http://dx.doi.org/10.1016/j.aninu.2015.11.001>
https://doi.org/10.1016/j.aninu.2015.11....
). Thus, hepatotoxic mycotoxins could be expected to impair hepatic metabolism, influencing the results of this research. However, the alterations observed were those resulting from the exercises on the horse, as a simple effect of time, with no effect to AFB1 in the diets.
As expected, immediately after exercise (M1), the Globular volume presented a higher value; about 39% higher than the baseline value. The elevation of globular volume is related to spleen contraction. According to Kingston (2008)Kingston J.K. 2008. Hematologic and serum biochemical responses to exercise and training, p.939-948. In: Hinchcliff K.W., Kaneps A.J., Geor R.J. (Eds), Equine Exercise Physiology: the science of exercise on athletic horse. Philadelphia Saunders, Philadelphia. and McGowan (2008)McGowan C. 2008. Clinical pathology in the racing horse: the role of clinical pathology in assessing fitness and performance in the racehorse. Vet. Clin. N. Am., Equine Pract. 24(2):405-421 <http://dx.doi.org/10.1016/j.cveq.2008.03.001> <PMid:18652962>.
https://doi.org/10.1016/j.cveq.2008.03.0...
the spleen has the capacity to store about 50% of the body’s erythrocytes in horses. The release of the erythrocytes in the body occurs in response to sympathetic stimulation or increased circulation of adrenaline during exercise. The values for total protein and albumin in response to exercise were not influenced by the inclusion of AFB1 in the diets, and only a simple effect of time was observed (P<0.05).
The increase of protein concentration immediately after exercise was observed, and its remained for 10 and 20 minutes (M3 and M4) as a consequence of blood concentration, redistribution of fluids and electrolytes from the vascular compartment to the extracellular spaces, and increased plasma viscosity (Kingston 2008Kingston J.K. 2008. Hematologic and serum biochemical responses to exercise and training, p.939-948. In: Hinchcliff K.W., Kaneps A.J., Geor R.J. (Eds), Equine Exercise Physiology: the science of exercise on athletic horse. Philadelphia Saunders, Philadelphia.). Fluid loss is related to the duration and intensity of exercise and returns to basal levels within 30 minutes of the exercise (Kowal et al. 2006Kowal R.J., Almosny N.R.P., Cascardo B., Summa R.P. & Cury L.J. 2006. Avaliação dos valores hematológicos em cavalos (Equus caballus) da raça Puro Sangue Inglês (PSI), submetidos a teste do esforço físico em esteira ergométrica. Revta Bras. Ciênc. Vet. 13(1):25-31. <http://dx.doi.org/10.4322/rbcv.2014.261>
https://doi.org/10.4322/rbcv.2014.261...
). Cholesterol plasma concentration was not influenced by AFB1 inclusion in the diets (P>0.05). The highest concentration of cholesterol immediately after exercise may be due to the increase in plasma viscosity arising from blood concentration (Kingston 2008Kingston J.K. 2008. Hematologic and serum biochemical responses to exercise and training, p.939-948. In: Hinchcliff K.W., Kaneps A.J., Geor R.J. (Eds), Equine Exercise Physiology: the science of exercise on athletic horse. Philadelphia Saunders, Philadelphia.). However, the values observed are within the reference levels for horses (Gonzalez & Silva 2006Gonzalez F.H.D. & Silva S.C. 2006. Introdução a Bioquímica Clínica Veterinária. 2ª ed. Editora UFRGS, Porto Alegre, 364p.).
Plasma levels of urea and creatinine were evaluated during 48 hours post exercise (M0 to M9). As expected, the urea levels were little influenced by exercise. Snow et al. (1982)Snow D.H., Kerr M. & Nimmo M. 1982. Alterations in blood, sweat, urine and muscle composition during prolonged exercise in the horse. Vet. Rec. 110(16):377-384. <http://dx.doi.org/10.1136/vr.110.16.377> <PMid:7080430>
https://doi.org/10.1136/vr.110.16.377...
stated that the main route of energy generation used by horses is glycolytic and anaerobic, compatible with the exercise test in the experiment: warm-up followed by three sets of gallops at a speed of 450m/min for three minutes each. Also, changes in urea concentration over time may be due to the catabolism of nitrogen from the diets. On the other hand, the serum creatinine concentrations during exercise were lower than the baseline value, which was not expected. According to Fazio et al. (2011)Fazio F., Assenza A., Tosto F., Casella S., Piccione G. & Caola G. 2011. Training and haematochemical profile in thoroughbreds and standardbreds: a longitudinal study. Livest. Sci. 141(2/3):221-226. <http://dx.doi.org/10.1016/j.livsci.2011.06.005>
https://doi.org/10.1016/j.livsci.2011.06...
there is an increase in plasma creatinine concentrations during exercise due to the greater use of phosphocreatine for the generation of muscular energy. Castejón et al. (2006)Castejón F., Rubio M.D., Agüera E.I., Escribano B.M., Requena F. & Vivo R. 2007. Respuesta hematológica y plasmática al ejercicio en cinta rodante, p.169-196. In: López G.E.V. (Ed.), Valoración Morfofuncional e la Selección de Reproductores del Caballo de Pura Raza Española. Caja Rural, Córdoba. observed that this increase is directly proportional to the intensity of the exercise. The values of creatinine concentration in this work were below those observed by Santiago et al. (2013)Santiago J.M., Almeida F.Q., Silva L.L.F., Miranda A.C.T., Azevedo J.F., Oliveira C.A.A. & Carrilho S.S. 2013. Hematologia e bioquímica sérica de equinos de concurso completo de equitação em treinamento. Arq. Bras. Med. Vet. Zootec. 65(2):383-392. <http://dx.doi.org/10.1590/S0102-09352013000200013>
https://doi.org/10.1590/S0102-0935201300...
evaluating eventing horses at training, and Godoi et al. (2009)Godoi F.N., Almeida F.Q., Guarienti G.A., Santiago J.M., Júnior D.G., Nogueira Y.C. & Brasileiro L.S. 2009. Perfil hematológico e características das fezes de equino consumindo dietas hiperlipidêmicas. Ciência Rural 39(9):2571-2577. <http://dx.doi.org/10.1590/S0103-84782009000900029>
https://doi.org/10.1590/S0103-8478200900...
who evaluated eventing horses feeding hyperlipidemic diets. The values of urea and creatinine concentrations were below the reference values for the horses according to Rose & Hodgson (1994)Rose R.J. & Hodgson D.R. 1994. Hematology and biochemistry, p.63-79. In: Hodgson D.R. & Rose R.J. (Eds), The Athletic Horse: principles and practice of equine sports medicine. W.B. Saunders, Philadelphia..
The peak of CK activity was observed at 20 minutes after exercise (M3), with a tendency to return to baseline three hours after the exercise (M5). Harris et al. (1990)Harris P.A., Snow D.H., Greet T.R. & Rossdale P.D. 1990. Some factors influencing plasma AST/CK activities in Thoroughbred racehorses. Equine Vet. J. 9:66-71. <http://dx.doi.org/10.1111/j.2042-3306.1990.tb04738.x> <PMid:9259810>
https://doi.org/10.1111/j.2042-3306.1990...
reported that some animals may have high physiological enzymatic levels of CK, or even that these enzymes are removed more slowly from the circulation, or some animals may be more sensitive as to the permeability of the cellular muscular membrane compared to a similar stimulus in other animals. According to Sloet van Oldruitenborgh-Oosterbaan (1998)Sloet van Oldruitenborgh-Oosterbaan M. 1998. Appropriate blood variables helpful in diagnosing (sub)clinical disease in the horse, p.14-33. Lindner A. (Ed.), Conference on Equine Sports Medicine and Science. Cordoba, Spain. Wageningen Pers, Wageningen., the plasma half-life of CK is very short, around 2 hours, which is compatible with the results observed in this experiment. The mean values of CK were higher than those observed by Oliveira et al. (2014)Oliveira C.A.A., Azevedo J.F., Miranda A.C.T., Souza B.G., Ramos M.T., Costa A.P.D., Baldani C.D., Silva V.P. & Almeida F.Q. 2014. Hematological and blood gas parameters’ response to treadmill exercise test in eventing horses fed different protein levels. J. Equine Vet. Sci. 34(11/12):1279-1285. <http://dx.doi.org/10.1016/j.jevs.2014.09.007>
https://doi.org/10.1016/j.jevs.2014.09.0...
in Brazilian Sport Horses on treadmill exercise tests, but result of CK 12 hours after exercise (M7) was similar those found by Padilha et al. (2017)Padilha F.G.F., Dimache L.A.G., Almeida F.Q. & Ferreira A.M.R. 2017. Blood biochemical parameters of Brazilian sport horses under training in tropical climate. Revta Bras. Zootec. 46(8):678-682. (Short Communication). <http://dx.doi.org/10.1590/s1806-92902017000800008>
https://doi.org/10.1590/s1806-9290201700...
in the same breed, a 48-h rest by training.
The AST serum activity shows a standard exercise profile (Thomassian et al. 2007Thomassian A., Carvalho F., Watanabe M.J., Silveira V.F., Alves A.L.G., Hussni C.A. & Nicoletti J.L.M. 2007. Atividades séricas da aspartato aminotransferase, creatina quinase e lactato desidrogenase de equinos submetidos a teste padrão de exercício progressivo em esteira. Braz. J. Vet. Res. Anim. Sci. 44(3):183-190.). The peak of AST activity was observed immediately after exercise (M1) and a tendency to increase 6 hours post exercise (M6). The high concentrations of AST immediately after exercise are related to the physiological process of fluid transfer to the extravascular space during exercise, increasing the AST activity in plasma, with a return to the 30-minute-baseline (Kingston 2008Kingston J.K. 2008. Hematologic and serum biochemical responses to exercise and training, p.939-948. In: Hinchcliff K.W., Kaneps A.J., Geor R.J. (Eds), Equine Exercise Physiology: the science of exercise on athletic horse. Philadelphia Saunders, Philadelphia.). The results of AST 48 h post exercise (M9) are very similar to those found by Padilha et al. (2017)Padilha F.G.F., Dimache L.A.G., Almeida F.Q. & Ferreira A.M.R. 2017. Blood biochemical parameters of Brazilian sport horses under training in tropical climate. Revta Bras. Zootec. 46(8):678-682. (Short Communication). <http://dx.doi.org/10.1590/s1806-92902017000800008>
https://doi.org/10.1590/s1806-9290201700...
in adult Brazilian sport horses a 48-h rest after training.
Differently from AST, the LDH activity did not present a standard profile in response to exercise, and the LDH peak was observed 12 hours post exercise (M7). The results observed were higher than the values reported by Oliveira et al. (2014)Oliveira C.A.A., Azevedo J.F., Miranda A.C.T., Souza B.G., Ramos M.T., Costa A.P.D., Baldani C.D., Silva V.P. & Almeida F.Q. 2014. Hematological and blood gas parameters’ response to treadmill exercise test in eventing horses fed different protein levels. J. Equine Vet. Sci. 34(11/12):1279-1285. <http://dx.doi.org/10.1016/j.jevs.2014.09.007>
https://doi.org/10.1016/j.jevs.2014.09.0...
in horses on treadmill exercise tests. The large variation of LDH plasma activity can be explained by the distribution of this enzyme in several different tissues. The values of LDH plasma activity refer to the sum of several isoenzymes, so the interpretation of elevated LDH values may be compromised (Harris et al. 1990Harris P.A., Snow D.H., Greet T.R. & Rossdale P.D. 1990. Some factors influencing plasma AST/CK activities in Thoroughbred racehorses. Equine Vet. J. 9:66-71. <http://dx.doi.org/10.1111/j.2042-3306.1990.tb04738.x> <PMid:9259810>
https://doi.org/10.1111/j.2042-3306.1990...
). In addition, non-pathological states may also cause increase in AST activity like LDH, as well as the collection methods, processing and equipment used for the analyzes (Sloet van Oldruitenborgh-Oosterbaan M. 1998Sloet van Oldruitenborgh-Oosterbaan M. 1998. Appropriate blood variables helpful in diagnosing (sub)clinical disease in the horse, p.14-33. Lindner A. (Ed.), Conference on Equine Sports Medicine and Science. Cordoba, Spain. Wageningen Pers, Wageningen., Thomassian et al. 2007Thomassian A., Carvalho F., Watanabe M.J., Silveira V.F., Alves A.L.G., Hussni C.A. & Nicoletti J.L.M. 2007. Atividades séricas da aspartato aminotransferase, creatina quinase e lactato desidrogenase de equinos submetidos a teste padrão de exercício progressivo em esteira. Braz. J. Vet. Res. Anim. Sci. 44(3):183-190.).
The GGT activity was not influenced by the inclusion of AFB1 in the diets (P>0.05). The increase of the enzyme is indicative of liver damage, cholestasis and proliferation of bile ducts in all animal species (Kerr 2002Kerr M.M. 2002. Veterinary Laboratory Medicine. 2ª ed. Blackwell Science Ltd., Oxford, 392p., Kingston 2008Kingston J.K. 2008. Hematologic and serum biochemical responses to exercise and training, p.939-948. In: Hinchcliff K.W., Kaneps A.J., Geor R.J. (Eds), Equine Exercise Physiology: the science of exercise on athletic horse. Philadelphia Saunders, Philadelphia., Dedar et al. 2019Dedar R.K., Virmani N., Bala P.A., Singh J., Vaid R.K., Legha R.A. & Tripathi B.N. 2019. Clinicopathological findings of an episode of mycotoxicosis in horses. Equine Vet. Educ. 31(5):236-241. <http://dx.doi.org/10.1111/eve.12856>
https://doi.org/10.1111/eve.12856...
). Horses submitted to exercise conditioning for a prolonged period may present an increase of GGT (Balarin et al. 2005Balarin M.R.S., Lopes R.S., Kohayagawa A., Laposy C.B. & Fonteque J.H. 2005. Avaliação da glicemia e da atividade sérica da aspartato aminotransferase, creatinoquinase, gama-glutamiltransferase e lactato desidrogenase em equinos puro sangue inglês (PSI) submetidos a exercício de diferentes intensidades. Semina, Ciênc. Agrárias, 26(2):211-218.). In this experiment, the GGT activity had a peak at about 60 minutes after exercise (M4), oscillating for up to 24 hours (M8). The pre-exercise physical training period in this work during three weeks, was very short, when compared with the 12 months of training cited by Balarin et al. (2005)Balarin M.R.S., Lopes R.S., Kohayagawa A., Laposy C.B. & Fonteque J.H. 2005. Avaliação da glicemia e da atividade sérica da aspartato aminotransferase, creatinoquinase, gama-glutamiltransferase e lactato desidrogenase em equinos puro sangue inglês (PSI) submetidos a exercício de diferentes intensidades. Semina, Ciênc. Agrárias, 26(2):211-218.. However, the values observed are within the basal levels for horses, ranging from 4.3 to 13UL-1 (Thomassian 2005Thomassian A. 2005. Enfermidade dos Cavalos. 4ª ed. Ed. Varela, São Paulo. 573p.).
The Alkaline phosphatase (ALP) activity was affected by the AFB1 inclusion in the diets (P<0.05), and ALP activity increased in horses fed diet with the 100μg/kg of AFB1. ALP is an enzyme widely distributed in the body, and the hepatic isoform predominates in the serum, and the higher values of ALP activity is indicative of liver damage in horses (Kerr 2002Kerr M.M. 2002. Veterinary Laboratory Medicine. 2ª ed. Blackwell Science Ltd., Oxford, 392p.). Kingston (2008)Kingston J.K. 2008. Hematologic and serum biochemical responses to exercise and training, p.939-948. In: Hinchcliff K.W., Kaneps A.J., Geor R.J. (Eds), Equine Exercise Physiology: the science of exercise on athletic horse. Philadelphia Saunders, Philadelphia. reported ALP increases in horse serum due to prolonged exercise; however, it is not clear whether this increase is from bone or hepatic origin. Hank et al. (1993)Hank A.M., Hoffmann W.E., Sanecki R.K., Schaeffer D.J. & Dorner J.L. 1993. Quantitative determination of equine alkaline phosphatase lsoenzymes in foal and adult serum. J. Vet. Intern. Med. 7(1):20-24. <http://dx.doi.org/10.1111/j.1939-1676.1993.tb03164.x>
https://doi.org/10.1111/j.1939-1676.1993...
observed that about 17.9% of serum ALP in mature horses is from the bones. Trueman et al. (1983)Trueman K.F., Lumsden J.H. & McSherry B.J. 1983. Examination of the origin of increased equine serum alkaline phosphatase concentrations. Can. Vet. J. 24(4):108-111. <PMid:17422242> stated that increases in ALP are often unexplained and that concentrations between 0-599IU/L can be considered normal. In this work, the horses were submitted to exercise conditioning during three weeks and the ALP activity in horses fed diet with 50μg/kg of AFB1 was higher than ALP activity in horses fed basal diet. The ALP activity in horses fed diet with 100μg/kg of AFB1 was higher than the ALP activity in horses feeding the other two diets. All the animals were submitted the same exercise intensity, and ALP was monitored up to 20 minutes after the test (M3).
Liver damage and gastrointestinal disorders may occur in horses feeding diets containing from 2 to 50μg/kg of AFB1 (Reed et al. 2004Reed S.M, Bayly W.M. & Sellon D.C. 2004. Equine Internal Medicine. 2a ed. W.B. Saunders, Philadelphia. 1.650p.). Kaneko et al. (2008)Kaneko J.J., Harvey J.W. & Bruss M.L. 2008. Clinical Biochemistry of Domestic Animals. 6th ed. San Diego, Academic Press, 932p. reported that chronic intoxication of pigs with fumonisins is associated with increases of ALP, AST and GGT. Thus, the potential interaction and synergism of AFB1 with FB1 (CAST 2003CAST 2003. Mycotoxins: risks in plant, animal and human systems. Report no. 139, Council for Agricultural Science and Technology (CAST), Ames, IA.) which may have influenced the ALP results and should be considered. Thus, it appears that the results of ALP activity were from hepatic tissue and its activity is directly influenced by the increased AFB1 concentration of the diets. However, the results observed are within the clinical values considered normal for the horses, according to Trueman et al. (1983)Trueman K.F., Lumsden J.H. & McSherry B.J. 1983. Examination of the origin of increased equine serum alkaline phosphatase concentrations. Can. Vet. J. 24(4):108-111. <PMid:17422242>.
The serum glucose and lactate concentrations (Table 9) were not affected by the AFB1 inclusion in the diets (P>0.05). Glucose and lactate concentrations reflect the energy metabolism and performance. The mycotoxins were expected to affect the hepatic metabolism and animal response to exercise since the liver plays a central role in metabolism, synthesizing and distributing nutrients to the peripheral organs through blood circulation (Gonzalez & Silva 2006Gonzalez F.H.D. & Silva S.C. 2006. Introdução a Bioquímica Clínica Veterinária. 2ª ed. Editora UFRGS, Porto Alegre, 364p.), however, did not occur. Higher glucose concentration was observed during the rest period (pre-exercise). According to Kerr (2002)Kerr M.M. 2002. Veterinary Laboratory Medicine. 2ª ed. Blackwell Science Ltd., Oxford, 392p., the glucose concentration increases during exercises due to the adrenaline. In this work, a decrease in glucose levels was observed, which glucose levels were restored after feeding. According to Pösö et al. (2004)Pösö A.R., Hyyppä S. & Geor R.J. 2004. Metabolic responses to exercise and training. In: Hinchcliff K.W., Kaneps A.J., Geor R.J. (Eds), Equine Sports Medicine and Surgery. W.B. Saunders, Philadelphia, p.771-792., changes in glucose concentration depend on the type of exercise, and may increase or decrease in short-term exercises. The serum values for glucose in this work were higher than those observed by Santiago et al. (2013)Santiago J.M., Almeida F.Q., Silva L.L.F., Miranda A.C.T., Azevedo J.F., Oliveira C.A.A. & Carrilho S.S. 2013. Hematologia e bioquímica sérica de equinos de concurso completo de equitação em treinamento. Arq. Bras. Med. Vet. Zootec. 65(2):383-392. <http://dx.doi.org/10.1590/S0102-09352013000200013>
https://doi.org/10.1590/S0102-0935201300...
in eventing horses in the initial phase of training as observed up to the moment M4. However, the glucose values reported here are within the serum levels of the horses (Rose & Hodgson 1994Rose R.J. & Hodgson D.R. 1994. Hematology and biochemistry, p.63-79. In: Hodgson D.R. & Rose R.J. (Eds), The Athletic Horse: principles and practice of equine sports medicine. W.B. Saunders, Philadelphia.).
The peak in lactate concentration occurred immediately after exercise (M1). Lactate is an intermediate product of the metabolism of carbohydrates during anaerobic glycolysis. Under anaerobic conditions, such as in intense or prolonged physical activity, pyruvic acid is converted to lactic acid, in a reaction mediated by the Lactate dehydrogenase (Kaneko et al. 2008Kaneko J.J., Harvey J.W. & Bruss M.L. 2008. Clinical Biochemistry of Domestic Animals. 6th ed. San Diego, Academic Press, 932p.). The time to return lactate concentration to a baseline is a measure of the fitness of horses (Evans et al. 1995Evans D.L., Rainger J.E., Hodgson D.R., Eaton M.D. & Rose R.J. 1995. The effects of intensity and duration of training on blood lactate concentrations during and after exercise. Equine Vet. J. 27(supl.18):422-425. http://dx.doi.org/10.1111/j.2042-3306.1995.tb04965.x
https://doi.org/10.1111/j.2042-3306.1995...
). The values observed in this study are similar to those observed by Santiago et al. (2013)Santiago J.M., Almeida F.Q., Silva L.L.F., Miranda A.C.T., Azevedo J.F., Oliveira C.A.A. & Carrilho S.S. 2013. Hematologia e bioquímica sérica de equinos de concurso completo de equitação em treinamento. Arq. Bras. Med. Vet. Zootec. 65(2):383-392. <http://dx.doi.org/10.1590/S0102-09352013000200013>
https://doi.org/10.1590/S0102-0935201300...
working with horses that were beginners in eventing training.
Conclusion
The mycotoxins in the diets during 28 days doesn’t influence the physiological, hematological and blood biochemical responses of the horses, except for the alkaline phosphatase activity, which presented higher activity in the diet with 100μg/kg of AFB1, suggesting a hepatotoxic action and synergistic effect with the others mycotoxins naturally present in the feedstuffs.
Acknowledgements
The authors are grateful to the “Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro” (FAPERJ). To the members of the research team of “Laboratório de Pesquisa em Saúde Eqüina” (EQUILAB). To the members of the “Escola de Sargentos das Armas” (ESA), especially to the Cavalry Section, Veterinary and Clinical Laboratory areas due to their unconditional support in the accomplishment of this research.
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Publication Dates
-
Publication in this collection
20 Nov 2020 -
Date of issue
Sept 2020
History
-
Received
25 May 2020 -
Accepted
02 July 2020