Expression analysis of transcription factors in sugarcane during cold stress / Análise de expressão de fatores de transcrição em cana-de-açúcar sob estresse por frio

Transcription factors (TF) are a wide class of genes in plants, and these can regulate the expression of other genes in response to various environmental stresses (biotic and abiotic). In the current study, transcription factor activity in sugarcane was examined during cold stress. Initially, RNA transcript reads of two sugarcane cultivars (ROC22 and GT08-1108) under cold stress were downloaded from SRA NCBI database. The reads were aligned into a reference genome and the differential expression analyses were performed with the R/Bioconductor edgeR package. Based on our analyses in the ROC22 cultivar, 963 TF genes were significantly upregulated under cold stress among a total of 5649 upregulated genes, while 293 TF genes were downregulated among a total of 3,289 downregulated genes. In the GT08-1108 cultivar, 974 TF genes were identified among 5,649 upregulated genes and 283 TF genes were found among 3,289 downregulated genes. Most transcription factors were annotated with GO categories related to protein binding, transcription factor binding, DNA-sequence-specific binding, transcription factor complex, transcription factor activity in RNA polymerase II, the activity of nucleic acid binding transcription factor, transcription corepressor activity, sequence-specific regulatory region, the activity of transcription factor of RNA polymerase II, transcription factor cofactor activity, transcription factor activity from plastid promoter, transcription factor activity from RNA polymerase I promoter, polymerase II and RNA polymerase III. The findings of above results will help to identify differentially expressed transcription factors during cold stress. It also provides a comprehensive analysis of the regulation of the transcription activity of many genes. Therefore, this study provides the molecular basis for improving cold tolerance in sugarcane and other economically important grasses.

Fatores de transcrição (FT) são uma ampla classe de genes em plantas e podem regular a expressão de outros genes em resposta a vários estresses ambientais (estresses bióticos e abióticos). No presente estudo, a atividade do fator de transcrição na cana-de-açúcar foi examinada durante o estresse pelo frio. Inicialmente, as leituras de transcrição de RNA de duas cultivares de cana-de-açúcar (ROC22 e GT08-1108) sob estresse frio foram baixadas do banco de dados SRA NCBI. As leituras foram alinhadas em um genoma de referência e as análises de expressão diferencial foram realizadas com o pacote R / Bioconductor edgeR. Com base em nossas análises no cultivar ROC22, 963 genes TF foram significativamente regulados positivamente sob estresse pelo frio entre um total de 5.649 genes regulados positivamente, enquanto 293 genes TF foram regulados negativamente entre um total de 3.289 genes regulados negativamente. No cultivar GT08-1108, 974 genes TF foram identificados entre 5.649 genes regulados positivamente e 283 genes TF foram encontrados entre 3.289 genes regulados negativamente. Os fatores de transcrição, em sua maioria, foram anotados com categorias GO relacionadas à ligação de proteína, ligação de fator de transcrição, ligação específica de sequência de DNA, complexo de fator de transcrição, atividade de fator de transcrição em RNA polimerase II, atividade de fator de transcrição de ligação de ácido nucleico, atividade de corepressor de transcrição, sequência específica da região reguladora, atividade do fator de transcrição da RNA polimerase II, atividade do cofator do fator de transcrição, atividade do fator de transcrição do promotor do plastídio, atividade do fator de transcrição do promotor da RNA polimerase I, polimerase II e RNA polimerase III. As descobertas dos resultados acima ajudarão a identificar fatores de transcrição expressos diferencialmente durante o estresse pelo frio. Ele também fornece uma análise abrangente da regulação da atividade [...].

Expression analysis of transcription factors in sugarcane during cold stress / Análise de expressão de fatores de transcrição em cana-de-açúcar sob estresse por frio

Transcription factors (TF) are a wide class of genes in plants, and these can regulate the expression of other genes in response to various environmental stresses (biotic and abiotic). In the current study, transcription factor activity in sugarcane was examined during cold stress. Initially, RNA transcript reads of two sugarcane cultivars (ROC22 and GT08-1108) under cold stress were downloaded from SRA NCBI database. The reads were aligned into a reference genome and the differential expression analyses were performed with the R/Bioconductor edgeR package. Based on our analyses in the ROC22 cultivar, 963 TF genes were significantly upregulated under cold stress among a total of 5649 upregulated genes, while 293 TF genes were downregulated among a total of 3,289 downregulated genes. In the GT08-1108 cultivar, 974 TF genes were identified among 5,649 upregulated genes and 283 TF genes were found among 3,289 downregulated genes. Most transcription factors were annotated with GO categories related to protein binding, transcription factor binding, DNA-sequence-specific binding, transcription factor complex, transcription factor activity in RNA polymerase II, the activity of nucleic acid binding transcription factor, transcription corepressor activity, sequence-specific regulatory region, the activity of transcription factor of RNA polymerase II, transcription factor cofactor activity, transcription factor activity from plastid promoter, transcription factor activity from RNA polymerase I promoter, polymerase II and RNA polymerase III. The findings of above results will help to identify differentially expressed transcription factors during cold stress. It also provides a comprehensive analysis of the regulation of the transcription activity of many genes. Therefore, this study provides the molecular basis for improving cold tolerance in sugarcane and other economically important grasses.(AU)

Fatores de transcrição (FT) são uma ampla classe de genes em plantas e podem regular a expressão de outros genes em resposta a vários estresses ambientais (estresses bióticos e abióticos). No presente estudo, a atividade do fator de transcrição na cana-de-açúcar foi examinada durante o estresse pelo frio. Inicialmente, as leituras de transcrição de RNA de duas cultivares de cana-de-açúcar (ROC22 e GT08-1108) sob estresse frio foram baixadas do banco de dados SRA NCBI. As leituras foram alinhadas em um genoma de referência e as análises de expressão diferencial foram realizadas com o pacote R / Bioconductor edgeR. Com base em nossas análises no cultivar ROC22, 963 genes TF foram significativamente regulados positivamente sob estresse pelo frio entre um total de 5.649 genes regulados positivamente, enquanto 293 genes TF foram regulados negativamente entre um total de 3.289 genes regulados negativamente. No cultivar GT08-1108, 974 genes TF foram identificados entre 5.649 genes regulados positivamente e 283 genes TF foram encontrados entre 3.289 genes regulados negativamente. Os fatores de transcrição, em sua maioria, foram anotados com categorias GO relacionadas à ligação de proteína, ligação de fator de transcrição, ligação específica de sequência de DNA, complexo de fator de transcrição, atividade de fator de transcrição em RNA polimerase II, atividade de fator de transcrição de ligação de ácido nucleico, atividade de corepressor de transcrição, sequência específica da região reguladora, atividade do fator de transcrição da RNA polimerase II, atividade do cofator do fator de transcrição, atividade do fator de transcrição do promotor do plastídio, atividade do fator de transcrição do promotor da RNA polimerase I, polimerase II e RNA polimerase III. As descobertas dos resultados acima ajudarão a identificar fatores de transcrição expressos diferencialmente durante o estresse pelo frio. Ele também fornece uma análise abrangente da regulação da atividade [...].(AU)

Expression analysis of transcription factors in sugarcane during cold stress / Análise de expressão de fatores de transcrição em cana-de-açúcar sob estresse por frio

Abstract Transcription factors (TF) are a wide class of genes in plants, and these can regulate the expression of other genes in response to various environmental stresses (biotic and abiotic). In the current study, transcription factor activity in sugarcane was examined during cold stress. Initially, RNA transcript reads of two sugarcane cultivars (ROC22 and GT08-1108) under cold stress were downloaded from SRA NCBI database. The reads were aligned into a reference genome and the differential expression analyses were performed with the R/Bioconductor edgeR package. Based on our analyses in the ROC22 cultivar, 963 TF genes were significantly upregulated under cold stress among a total of 5649 upregulated genes, while 293 TF genes were downregulated among a total of 3,289 downregulated genes. In the GT08-1108 cultivar, 974 TF genes were identified among 5,649 upregulated genes and 283 TF genes were found among 3,289 downregulated genes. Most transcription factors were annotated with GO categories related to protein binding, transcription factor binding, DNA-sequence-specific binding, transcription factor complex, transcription factor activity in RNA polymerase II, the activity of nucleic acid binding transcription factor, transcription corepressor activity, sequence-specific regulatory region, the activity of transcription factor of RNA polymerase II, transcription factor cofactor activity, transcription factor activity from plastid promoter, transcription factor activity from RNA polymerase I promoter, polymerase II and RNA polymerase III. The findings of above results will help to identify differentially expressed transcription factors during cold stress. It also provides a comprehensive analysis of the regulation of the transcription activity of many genes. Therefore, this study provides the molecular basis for improving cold tolerance in sugarcane and other economically important grasses.

Resumo Fatores de transcrição (FT) são uma ampla classe de genes em plantas e podem regular a expressão de outros genes em resposta a vários estresses ambientais (estresses bióticos e abióticos). No presente estudo, a atividade do fator de transcrição na cana-de-açúcar foi examinada durante o estresse pelo frio. Inicialmente, as leituras de transcrição de RNA de duas cultivares de cana-de-açúcar (ROC22 e GT08-1108) sob estresse frio foram baixadas do banco de dados SRA NCBI. As leituras foram alinhadas em um genoma de referência e as análises de expressão diferencial foram realizadas com o pacote R / Bioconductor edgeR. Com base em nossas análises no cultivar ROC22, 963 genes TF foram significativamente regulados positivamente sob estresse pelo frio entre um total de 5.649 genes regulados positivamente, enquanto 293 genes TF foram regulados negativamente entre um total de 3.289 genes regulados negativamente. No cultivar GT08-1108, 974 genes TF foram identificados entre 5.649 genes regulados positivamente e 283 genes TF foram encontrados entre 3.289 genes regulados negativamente. Os fatores de transcrição, em sua maioria, foram anotados com categorias GO relacionadas à ligação de proteína, ligação de fator de transcrição, ligação específica de sequência de DNA, complexo de fator de transcrição, atividade de fator de transcrição em RNA polimerase II, atividade de fator de transcrição de ligação de ácido nucleico, atividade de corepressor de transcrição, sequência específica da região reguladora, atividade do fator de transcrição da RNA polimerase II, atividade do cofator do fator de transcrição, atividade do fator de transcrição do promotor do plastídio, atividade do fator de transcrição do promotor da RNA polimerase I, polimerase II e RNA polimerase III. As descobertas dos resultados acima ajudarão a identificar fatores de transcrição expressos diferencialmente durante o estresse pelo frio. Ele também fornece uma análise abrangente da regulação da atividade de transcrição de muitos genes. Portanto, este estudo fornece base molecular para melhorar a tolerância ao frio em cana-de-açúcar e outras gramíneas economicamente importantes.

Broiler behavior: influence of thermal stress, age, and period of the day

This study evaluated the behavior of broiler chickens subjected to thermal stress during different periods of the day and age of birds. A total of 180 one-day-old male broiler chicks were allocated to three chambers. Each chamber contained five boxes, with 12 chicks/box. Birds were assigned to a completely randomized design. The birds were filmed, and the images recorded every minute during the two periods: morning (from 08:00 to 09:00 h) and afternoon (from 17:00 to 18:00 h), at 7, 14, and 35 d of age. The frequency of the behavioral category (water intake, feed intake, resting, exploration, and comfort) was determined. Data were subjected to variance analysis for mixed models with rearing temperatures (cold, usual, and hot) and age of birds (7, 14, and 35 d) as subdivided plot, and periods of the day (morning and afternoon) as sub-subdivided plot. Birds at cold and usual temperatures showed higher feed intake than those at hot temperature in the morning. Birds exposed to cold and usual temperatures explored the environment less frequently at 35 d when compared with 14 d. However, chickens at hot temperature showed decreased exploration according to the increase of age. Birds spent more time feeding during the morning, regardless of age and rearing temperature. Also, during this period of the day, chickens spent most of the time exploring the environment. The frequency of feed intake and exploration decreases with the increase of age. The similarity of behavior between chickens reared at cold and usual temperatures may be due to a change in the thermal comfort zone of the birds. It suggests that the real thermal comfort temperature is between the two temperature ranges studied (cold and usual).

Avaliação de tolerância a baixas temperaturas em genótipos de arroz irrigado (Oryza sativa L) na fase reprodutiva em experimento a campo, durante evento climático espontâneo na safra 2019/2020 / Evaluation of low temperature tolerance in irrigated rice (Oryza sativaL) genotypes at reproductive phase in a field experiment, during a spontaneous climatic event in the 2019/2020 cropseason

Aproveitando-se a ocorrência de um evento espontâneo de baixas temperaturas (<17oC) em experimento de campo de arroz irrigado, coincidente com a fase reprodutiva da cultura, foram avaliados a produtividade, a porcentagem de esterilidade de espiguetas e o número de panículas por metro quadrado. O experimento foi conduzido no sul de Santa Catarina, na safra 2019/2020, em delineamento de blocos ao acaso com trêsrepetições no sistema pré-germinado. Do total de genótipos que compunham o experimento, 13 foram selecionados para comporem a análise principal, de esterilidade.Baseado numa série de estudos anteriores para estresse por baixas e altas temperaturas, a hipótese era de que a linhagem SC 806 se destacaria como resiliente. De fato, a SC 806 apresentou níveis de esterilidade significativamente menores que as testemunhas comerciais SCS116 Satoru, SCS122 Miura e SC 790 (SCS125), ao mesmo tempo que foi competitiva com as mesmas no tocante à produtividade. Assim, a SC 806 foi validada como resiliente abaixastemperaturas, confirmando o bom desempenho verificado em experimentos anteriores, e com isso demonstrando ser promissora como linhagem candidata à lançamento na forma de variedade.(AU)

Concerning the occurrence of a spontaneous event of low temperatures (<17oC), in an irrigated rice field experiment, during the reproductive phase of the crop, yield was evaluated as well as percentage of grain sterility and number of panicles. The experiment was conducted in the southof Santa Catarina, in the 2019/2020 crop season, having been water-seeded in randomized blocks with threereplications. Of the total number of genotypes that made up the experiment, 13 were selected to make up the main analysis, of sterility. Based on a series of previous studies for stress due to low and high temperatures, the hypothesis was that the SC 806 line would stand out as resilient. Based on a series of previous studies for low and high temperature stress, the hypothesiswas that the SC 806 inbreed line would stand out as resilient. In fact, SC 806 showed significantly lower sterility levels than the commercial controls, SCS116 Satoru, SCS122 Miura and SC 790 (SCS125), while remaining competitive in terms of yield. Thus, SC 806 confirmed its resilience to low temperatures, what was a behavior showed in previous experiments, proving to be promising as a candidate for release as cultivar soon.(AU)

Evaluation of the effect of phenolic pigments on rice germination under low temperature conditions / Avaliação do efeito de pigmentos fenólicos na germinação de arroz sob condições de baixa temperatura

In Rio Grande do Sul, the main rice producer State in Brazil, low temperatures can occur during germination and seedling establishment, and in some cases, during the reproductive stage. When low temperatures occur in the early developmental stages cause delay in germination, resulting in a non-homogeneous growing. In reproductive stage, low temperatures cause spikelet sterility, directly interfering with plant yield. Researchers have shown that some phenolic compounds such as proanthocyanidins and anthocyanin are associated with low temperature tolerance in plants due to their antioxidant capacity. The red and black color in the seeds of some rice genotypes is conferred by the phenolic compounds proanthocyanidins and anthocyanin, respectively. Therefore, tis study aimed to verify whether rice genotypes with red or black seeds are more tolerant to low temperatures during germination. In this study, five rice genotypes were tested, two present seeds without pigmentation and with contrasting response to low temperature tolerance (BRS Bojuru - tolerant and BRS Pampeira - sensitive), two genotypes with red seeds (BRS 902, SCS 119 Rubi) and one black seed genotype (SCS 120 Ônix). As expected, the genotypes with pigmented seeds had a greater total phenolic compounds content. However, under low temperature conditions, the genotypes with pigmented seed showed a similar response to the sensitive genotype. Therefore, the presence of proanthocyanidins and anthocyanin in the seed of the studied genotypes does not provide tolerance to low temperatures during germination.(AU)

No Rio Grande do Sul, principal estado produtor de arroz do Brasil, baixas temperaturas podem ocorrer durante a germinação e estabelecimento de plântulas, e em alguns casos, durante o estádio reprodutivo. Quando baixas temperaturas ocorrem no estádio inicial de desenvolvimento causam atraso da germinação, resultando em um crescimento não homogêneo. No estádio reprodutivo, baixas temperaturas podem ocasionar esterilidade das espiguetas, interferindo diretamente na produtividade da planta. Pesquisas têm mostrado que alguns compostos fenólicos como as proantocianidinas e antocianinas estão associadas com tolerância a baixa temperatura em plantas devido sua capacidade antioxidante. A coloração vermelha e preta nas sementes de alguns genótipos de arroz é conferida pelos compostos fenólicos proantocianidinas e antocianinas, respectivamente. Portanto, o objetivo desse estudo foi verificar se os genótipos de arroz com sementes vermelhas ou pretas são mais tolerantes a baixas temperaturas durante a germinação. Neste trabalho, cinco genótipos foram testados, dois com sementes sem pigmentação e com resposta contrastante para tolerância a baixa temperatura (BRS Bojuru - tolerante e BRS Pampeira - sensível), dois genótipos com sementes vermelhas (BRS 902, SCS 119 Rubi) e um genótipo com sementes pretas (SCS 120 Ônix). Como esperado, os genótipos com sementes pigmentadas têm maior conteúdo de compostos fenólicos totais. Entretanto, sob condições de baixa temperatura, os genótipos com semente pigmentada mostraram resposta similar ao genótipo sensível. Dessa forma, a presença de proantocianidinas e antocianinas nas sementes dos genótipos estudados não confere tolerância a baixas temperaturas durante a germinação.(AU)

Effect of In Ovo Ascorbic Acid Injection and Thermal Manipulation During Incubation on Intestine Morphology of Broilers Reared under Cold and Heat Stress

It was investigated if pre-incubation ascorbic acid (AA) injection in fertile eggs incubated at high temperature impacts the performance, the yield of carcass and parts, and the intestine morphology of broilers reared under heat stress. Three thousand Cobb® fertile broiler eggs were randomly distributed according to weight into three incubations treatments (eggs not injected with AA and incubated at 37.5°C; eggs not injected with AA and incubated at 39°C; and eggs injected with 6 µg AA/100 µL water prior to incubation and incubated at 39ºC). The hatched birds were reared at thermoneutral, cold, and hot house temperatures. Broilers reared under hot temperature presented lower feed intake and weight gain than the broilers of the different rearing temperatures. Egg incubation at 39.0 ºC and 39.0 ºC + AA reduced broiler viability. Carcass and cut yields were not influenced by incubation and rearing procedures. Duodenal goblet cell count was lower in broilers from eggs of the treatment 39ºC + AA than in broilers from the other incubation treatments and in broiler rearing in hot temperature. In the jejunum, the goblet cell counts were higher in broilers that were reared under hot than thermoneutral temperatures. The incubation treatment of 39 ºC+AA increased the goblet cell counts in the ileum of broilers reared under cold temperatures. Rearing temperature influenced the duodenal villi counts, which were lower under cold rearing conditions than in the two other rearing temperatures. The results showed that egg incubation at 39°C, independently of ascorbic acid injection, did not produce an effective epigenetic heat adaptation in broilers.(AU)

Interactive effects of digestible protein levels on thermal and physical stress responses in Nile tilapia

The effects of dietary digestible protein (DP) levels (22, 26, 29, 32, and 34%) and different stressors (cold-induced stress, CIS; heat/dissolved oxygen-induced stress, HDOIS; transport-induced stress, TIS; and size-sorting-induced stress, SSIS) on hemato-biochemical parameters were evaluated. Four hundred and forty Nile tilapia fingerlings were distributed into 40-250 L aquaria and fed experimental diets for 110 days, and fed each of the five experimental diets, that were randomly distributed to eight replicates per treatment. Then, different groups of fish were subjected to one type of stress. Groups of 40 fish were used on CIS (17 °C), HDOIS (32 °C), and TIS (4 h), and a group of 140 fish on SSIS (15 min air exposure and 60 s handling). There was no effect on hemato-biochemical profile when DP levels were compared, neither before nor after stress; however, there was a significant stress effect. Digestible protein did not mitigate stress response under SSIS and CIS; lymphopenia and neutrophilia were the main cell-mediated immune response; dietary 22 and 26% DP impaired oxygenation on SSIS and TIS; fish under HDOIS and SSIS demanded more energy using triglycerides as an energy source; the diet formulated to contain 22% DP was not adequate to keep homeostasis under temperature stress. Cluster analysis showed that, for DP levels below the requirement for growth, SSIS and CIS were considered the most stressful conditions. At 34% DP level, HDOIS response was comparable to that of non-stressing conditions.(AU)

Quality assessment of amazonian fish from fish farming stored on ice / Avaliação da qualidade de pescados amazônicos provenientes de piscicultura armazenados em gelo

The cultivation of natives Amazonian fish such as tambaqui (Colossoma macropomum), pirapitinga (Piaractus brachypomus), tambatinga (female, Colossoma macropomum X Piaractus brachypomus, male) and Pintando da Amazônia (female, Pseudoplatystoma sp. X Leiarius marmoratus, male) temmoratus, increased in recent years, making studies related to the validity of these foods after processing necessary. Therefore, the aimed of the study was to evaluate the sensory, microbiological (Staphylococcus coagulase positive count and presence of Salmonella spp.) and chemical (pH and Total Volatile Bases (TVB) quality of fresh gutted fish stored on ice. Nine specimens of each species were used, all cultivated in an excavated tanks. The fasting time ranged from 16 to 48 hours, depending on the species, the fish was slaughtered by means of cold shock. The fish was gutted and stored in the fish fridge. Sensory analysis was performed by a trained team available. For other analyses, it was sent to a laboratory specializing in food analysis. The sensory analysis of fresh eviscerated tambaqui was characteristic of the species until the 15th day of storage. Fresh eviscerated pirapitinga presented until the 16th day. The fresh eviscerated tambatinga hybrid was kept until the 14th day of storage. And for the Pintado da Amazônia, the organoleptic characteristics were presentable until the 12th day of storage. The microbiological and physical-chemical analyzes were in accordance with Brazilian legislation in all specimens of the analyzed species. It was observed that the longer the fasting period, there was a numerical increase in the pH of the fish meat.(AU)

O cultivo de peixes nativos da Amazônia como tambaqui (Colossoma macropomum), pirapitinga (Piaractus brachypomus), tambatinga (fêmea, Colossoma macropomum X Piaractus brachypomus, macho) e o pintado da Amazônia (fêmea, Pseudoplatystoma sp. X Leiarius marmoratus, macho) tem aumentado nos últimos anos, fazendo com que estudos relacionados a validade desses alimentos após o processamento sejam necessários. Por isso, o objetivo do estudo foi avaliar os parâmetros de qualidade senso-rial, microbiológica (contagem de Staphylococcus coagulase positiva e presença de Salmonella spp.) e química (pH e Bases Voláteis Totais (BVT)) deses pescados eviscerados frescos armazenados em gelo. Foram utilizados 9 exemplares de cada espécie, todos de origem de cultivo em viveiro escavado. O tempo de jejum variou de 16 a 48 horas, dependendo da espécie, o abate do pescado foi por meio de choque térmico. O pescado foi eviscerado e armazenado no frigorifico de pescado. Analise sensorial foi realizada por uma equipe treinada disponível. Para as demais análises foi enviado para um laboratório especializado em análises de alimentos. A análise sensorial do tambaqui eviscerado fresco estava característica da espécie até o 15°dia de estocagem. A pirapitinga evisce-rado fresco apresentou até o 16°dia. O hibrido tambatinga eviscerado fresco foi até o 14°dia de estocagem. E para o pintado da Amazônia as características organolépticas estavam apresentáveis até o dia 12° dia de armazenamento. As analises microbiológicas e físico químicas estavam de acordo com a legislação brasileira em todos os exemplares das espécies analisadas. Foi observado que quanto maior o tempo de jejum, houve um aumento numérico no pH da carne dos pescados.(AU)

Effect of quercetin or butylated hydroxytoluene on cooled or frozen-thawed ram sperm quality / Efeito da inclusão de quercetina ou butil-hidroxitolueno na qualidade do sêmen de carneiro resfriado ou congelado

Cooling and freezing processes cause physical and chemical damage to sperm by cold shock and oxidative stress. This study aimed to evaluate the effect of two antioxidants on sperm parameters of cooled and frozen-thawed ram semen diluted in an egg yolk-based extender. Semen was collected from 30 rams and processed in two consecutive experiments to test the inclusion of different concentrations of quercetin and butylated hydroxytoluene (BHT) in an egg yolk-based semen extender. Dimethyl sulfoxide (DMSO) was added as a solvent to the semen extender in a ratio of 1 mL DMSO for 90 mg of quercetin and 1 mL DMSO for 880 mg of BHT. After collection, semen was diluted at 200 × 106 motile sperm/mL (control) and split into different groups in each experiment. In experiment 1, semen was diluted with the extender containing quercetin (Q5, 5 µg/mL; Q10, 10 µg/mL; Q15, 15 µg/mL) or DMSO alone (DMSO1, 0.055 µL DMSO per mL; DMSO2, 0.165 µL DMSO per mL). In experiment 2, semen was diluted with the extender with BHT (BHT1, 0.5 µg/mL; BHT2, 1 µg/mL; BHT3, 1.5 µg/mL) or DMSO alone (DMSO3, 0.375 µL DMSO per mL; DMSO4, 1.125 µL DMSO per mL). After dilution, the semen was divided into two aliquots. Treated ram sperm samples were also subjected to different storage methods. The first set of samples was cooled at 5 °C for 24 h, whereas the second set of samples was frozen-thawed. Sperm motility parameters and plasma membrane integrity (PMI) were evaluated immediately after dilution (0h) and 24 h after cooling and in the frozen-thawed samples via computer-assisted sperm analysis and epifluorescence microscopy, respectively. The inclusion of quercetin or BHT did not affect sperm motility parameters or PMI of fresh, cooled, or frozen-thawed sperm in this study (P < 0.05). However, further studies are needed to test the effects of these antioxidants on the fertility of cryopreserved ram semen.(AU)

O resfriamento e o congelamento causam danos físicos e químicos aos espermatozoides por choque térmico e estresse oxidativo. Portanto, este estudo teve como objetivo avaliar o efeito da inclusão de dois antioxidantes em um diluente à base de gema de ovo sobre os parâmetros espermáticos do sêmen ovino resfriado e congelado. Trinta carneiros tiveram o sêmen coletado e processado em dois experimentos consecutivos para testar a inclusão de diferentes concentrações de quercetina e hidroxitolueno butilado (BHT) em diluente de sêmen à base de gema de ovo. O DMSO foi adicionado como solvente ao diluente de sêmen em uma proporção de 1 mL de DMSO parra 90 mg de quercetina e 1 Ml de DMSO para 880 mg de BHT. Após a coleta, o sêmen foi diluído a 200 × 106 espermatozoides móveis/mL (Controle) e dividido em diferentes grupos em cada experimento. Experimento 1, Quercetina (Q5, 5 µg / mL; Q10, 10 µg / mL; Q15, 15 µg / mL) ou DMSO (DMSO1, 0,055 µL de DMSO por ml; DMSO2, 0,165 µL de DMSO / mL) foram adicionados ao extensor. Experimento 2, BHT (BHT1, 0,5 µg / mL; BHT2, 1 µg / mL; BHT3, 1,5 µg / mL) ou DMSO (DMSO3, 0,375 µL de DMSO por ml; DMSO4, 1,125 µL de DMSO / mL) foram adicionados à o extensor. Após a diluição, o sêmen foi dividido em duas alíquotas. O primeiro foi resfriado a 5 ° C por 24h, enquanto o segundo foi congelado. Os parâmetros de motilidade espermática e integridade da membrana plasmática (PMI) foram avaliados, imediatamente após a diluição (0h) e 24h após o resfriamento e nas amostras congeladas, pelo CASA e microscopia de epifluorescência, respectivamente. A inclusão de quercetina ou BHT não afetou os parâmetros de motilidade espermática e PMI de espermatozoides frescos, resfriados ou congelados (P < 0,05). Portanto, a inclusão de quercetina e BHT não beneficiou os parâmetros espermáticos do sêmen ovino submetido a armazenamento líquido a 5 ° C por 24h ou protocolo de congelamento no presente estudo. No entanto, mais estudos são necessários para testar o efeito desses antioxidantes na fertilidade do sêmen ovino criopreservado.(AU)

Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa

Abstract This study was conducted to investigate the effect of different levels of seminal plasma (SP) and cold-shock on ram spermatozoa during 36 h storage at 5°C. In both ejaculated spermatozoa coated with egg yolk (second ejaculate; coated spermatozoa) and epididymal spermatozoa, samples were treated with 0, 50 and 100% seminal plasma. Different levels of seminal plasma were added on the basis of ram spermatocrit (32%). Then half of aliquots were suddenly put on ice water (cold-shock) and other half were gradually (0.25°C/min) chilled (non- cold shock). Sperm motility, viability and functional membrane integrity were determined in both aliquots at 0, 12, 24 and 36 h storage at 5°C. Under non- cold shock and cold-shock conditions, coated spermatozoa treated with 0% SP showed the highest motility compared to ejaculated spermatozoa (first ejaculate; uncoated spermatozoa) after 12, 24 and 36 h of storage at 5°C (P<0.05). Under non- cold shock and cold-shock conditions, viability and functional membrane integrity was higher in the coated spermatozoa treated with 0% SP than in the uncoated spermatozoa during 36 h storage (P<0.05). There was no significant difference between coated spermatozoa treated with 0 and 50% SP in the percentage of motility and viability after 24 and 36 h of storage (P>0.05). Under non- cold shock and cold-shock conditions, the percentage of motility of epididymal spermatozoa treated with 0% SP was significantly (P<0.05) higher than those treated with 100% SP after 36 h of storage at 5°C. In conclusion, removal of seminal plasma and/or reduction (up to 50%) of its concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa.

Reduction of seminal plasma concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa

This study was conducted to investigate the effect of different levels of seminal plasma (SP) and cold-shock on ram spermatozoa during 36 h storage at 5°C. In both ejaculated spermatozoa coated with egg yolk (second ejaculate; coated spermatozoa) and epididymal spermatozoa, samples were treated with 0, 50 and 100% seminal plasma. Different levels of seminal plasma were added on the basis of ram spermatocrit (32%). Then half of aliquots were suddenly put on ice water (cold-shock) and other half were gradually (0.25°C/min) chilled (non- cold shock). Sperm motility, viability and functional membrane integrity were determined in both aliquots at 0, 12, 24 and 36 h storage at 5°C. Under non- cold shock and cold-shock conditions, coated spermatozoa treated with 0% SP showed the highest motility compared to ejaculated spermatozoa (first ejaculate; uncoated spermatozoa) after 12, 24 and 36 h of storage at 5°C (P<0.05). Under non- cold shock and cold-shock conditions, viability and functional membrane integrity was higher in the coated spermatozoa treated with 0% SP than in the uncoated spermatozoa during 36 h storage (P<0.05). There was no significant difference between coated spermatozoa treated with 0 and 50% SP in the percentage of motility and viability after 24 and 36 h of storage (P>0.05). Under non- cold shock and cold-shock conditions, the percentage of motility of epididymal spermatozoa treated with 0% SP was significantly (P<0.05) higher than those treated with 100% SP after 36 h of storage at 5°C. In conclusion, removal of seminal plasma and/or reduction (up to 50%) of its concentration can decrease detrimental effects of seminal plasma on chilled ram spermatozoa.(AU)

Environmental temperature and broiler age on corn energy value / Temperatura ambiente e idade do frango de corte sobre o valor energético do milho

This study aimed to assess the effects of environmental temperature and age of broilers on the energy value of corn. A total of 288 Cobb 500 chicks were distributed in a complete randomized design with a split-plot arrangement and six replications of six chicks each. The main plot consisted of three temperatures (cold: 18 ºC; thermoneutral: 25 ºC; and hot: 33 ºC), while the secondary plot consisted of age (initial: 11 to 14 days; growing: 25 to 28 days; and final: 39 to 42 days). The basal diet was based on corn and soybean meal. The test diet was produced by replacing the basal diet for test food: 40% corn + 60% basal diet. The mean values of AMEn observed for broiler chicks under cold, thermoneutral, and hot temperatures were 3322, 3279, and 3233 kcal/kg of natural matter, respectively, and 3215, 3218, and 3400 kcal/ kg of natural matter for the initial, growing, and final phases, respectively. Overall, the metabolizable energy values of corn and the balance and coefficients of metabolizability of nutrients in the test diet increased with the broiler age, but the true metabolizable energies of corn were not affected by environmental temperature. The balance and coefficients of metabolizability of nutrients in the test diet decreased due to heat exposure during the growing and final phases.

O objetivo deste trabalho foi determinar o efeito da temperatura ambiente e da idade da ave sobre o valor energético do milho. Foram utilizados 288 pintos de corte, da linhagem Cobb 500, distribuídos em delineamento experimental inteiramente casualizado em esquema de parcelas subdivididas no tempo, sendo as parcelas as três temperaturas de criação (fria: 18 ºC; termoneutra: 25 ºC e quente: 33 ºC) e as subparcelas as três idades de avaliação (inicial: 11 a 14; crescimento: 25 a 28 e final: 39 a 42 dias), com seis repetições de seis aves cada. A dieta basal foi composta por milho e farelo de soja. A dieta teste foi produzida substituindo a dieta basal pelo alimento teste: 40% de milho + 60% da dieta basal. Encontraram-se valores médios de energia metabolizável aparente, corrigida pelo balanço de nitrogênio (EMAn) do milho, para aves criadas em 18 ºC; 25 ºC e 33 ºC de 3322, 3279 e 3233 kcal/kg de matéria natural, respectivamente, e para as fases de 11 a 14; 25 a 28 e 39 a 42 dias de 3215, 3218 e 3400 kcal/kg de matéria natural, respectivamente. De um modo geral, os valores de energia metabolizável do milho, os balanços e os coeficientes de metabolizabilidade dos nutrientes da dieta teste aumentam com a idade do frango de corte, porém as energias metabolizáveis verdadeiras do milho não foram afetadas pela temperatura ambiente. Os balanços e os coeficientes de metabolizabilidade dos nutrientes da dieta teste foram reduzidos em estresse por calor para aves na fase de crescimento e final.

Efficiency of cooling systems in broiler houses during hot days / Eficiência dos sistemas de resfriamento em aviários durante dias quentes

This study evaluated: (1) the vulnerability of broiler houses with different cooling systems, and (2) the spatial distribution of environmental variables during hot days. Four potentially vulnerable commercial broiler houses in southern Brazil were selected according to the following parameters: absence or presence of different cooling systems, broilers older than 28 days, and outside air dry-bulb temperature over 30°C. Broiler house vulnerability was classified according to the cooling and mechanical ventilation system: cellulose pad cooling (CPC), sprinkling (SPK), fogging (FOG), and mechanical ventilation without evaporative cooling system (VTL). The air dry-bulb temperature (Tdb, °C) and relative humidity (RH, %) were recorded every 10 min. For each broiler house, we evaluated: (1) relative cooling efficiency (RCE) and (2) inside spatial distribution of microclimate variables using a geostatistical technique. The CPC and SPK did not differ (P<0.05) in RCE (81.6% and 80.7%, respectively), but both differed from FOG (23.8%) and VLT (1.87%) systems. The highest variations in indoor Tdb were recorded in the FOG (7 °C), followed by the SPK (4 °C) and CPC (3 °C). In the CPC, there was an increase in RH from the middle to the end of the broiler house near the exhaust fans. In conclusion, the relative cooling efficiency and the inside spatial distributions of environmental variables in the broiler houses were influenced by the existing cooling system.

Os objetivos deste estudo foram (1) comparar a vulnerabilidade de aviários com diferentes sistemas de resfriamento, e (2) avaliar a distribuição espacial interna das variáveis ambientais durante dias quentes. Quatro aviários comerciais potencialmente vulneráveis no sul do Brasil foram selecionados de acordo com os seguintes parâmetros de elegibilidade: ausência ou presença de diferentes sistemas de resfriamento; frangos de corte com mais de 28 dias de idade; e temperatura de bulbo seco do ar externa acima de 30 °C. A vulnerabilidade do aviário foi classificada de acordo com o sistema de resfriamento e ventilação mecânica, sendo: resfriamento por pad cooling (CPC), aspersão (SPK), nebulização (FOG) e ventilação mecânica sem sistema de resfriamento evaporativo (VTL). A temperatura de bulbo seco do ar (Tbs, °C) e a umidade relativa do ar (UR, %) foram coletadas por registradores de dados autônomos a cada 10 min. Para cada aviário foram avaliados: (1) eficiência relativa de resfriamento (RCE) e (2) distribuição espacial interna das variáveis ambientais por técnica de geoestatística. O CPC e SPK não diferiram (P>0,05) na RCE (81,6% e 80,7% respectivamente), mas ambos diferiram do FOG (23,8%) e VLT (1,87%). As maiores variações na Tbs do ar interno foram registradas no FOG (7 °C), seguido pelo SPK (4 °C) e CPC (3 °C). No CPC, houve um aumento da umidade relativa do meio para o final do aviário, próximo aos exaustores. Em conclusão, a eficiência relativa de resfriamento, assim como a distribuição espacial das variáveis ambientais internas foram influenciadas pelo sistema de resfriamento de cada aviário.

Efficiency of cooling systems in broiler houses during hot days / Eficiência dos sistemas de resfriamento em aviários durante dias quentes

This study evaluated: (1) the vulnerability of broiler houses with different cooling systems, and (2) the spatial distribution of environmental variables during hot days. Four potentially vulnerable commercial broiler houses in southern Brazil were selected according to the following parameters: absence or presence of different cooling systems, broilers older than 28 days, and outside air dry-bulb temperature over 30°C. Broiler house vulnerability was classified according to the cooling and mechanical ventilation system: cellulose pad cooling (CPC), sprinkling (SPK), fogging (FOG), and mechanical ventilation without evaporative cooling system (VTL). The air dry-bulb temperature (Tdb, °C) and relative humidity (RH, %) were recorded every 10 min. For each broiler house, we evaluated: (1) relative cooling efficiency (RCE) and (2) inside spatial distribution of microclimate variables using a geostatistical technique. The CPC and SPK did not differ (P<0.05) in RCE (81.6% and 80.7%, respectively), but both differed from FOG (23.8%) and VLT (1.87%) systems. The highest variations in indoor Tdb were recorded in the FOG (7 °C), followed by the SPK (4 °C) and CPC (3 °C). In the CPC, there was an increase in RH from the middle to the end of the broiler house near the exhaust fans. In conclusion, the relative cooling efficiency and the inside spatial distributions of environmental variables in the broiler houses were influenced by the existing cooling system.(AU)

Os objetivos deste estudo foram (1) comparar a vulnerabilidade de aviários com diferentes sistemas de resfriamento, e (2) avaliar a distribuição espacial interna das variáveis ambientais durante dias quentes. Quatro aviários comerciais potencialmente vulneráveis no sul do Brasil foram selecionados de acordo com os seguintes parâmetros de elegibilidade: ausência ou presença de diferentes sistemas de resfriamento; frangos de corte com mais de 28 dias de idade; e temperatura de bulbo seco do ar externa acima de 30 °C. A vulnerabilidade do aviário foi classificada de acordo com o sistema de resfriamento e ventilação mecânica, sendo: resfriamento por pad cooling (CPC), aspersão (SPK), nebulização (FOG) e ventilação mecânica sem sistema de resfriamento evaporativo (VTL). A temperatura de bulbo seco do ar (Tbs, °C) e a umidade relativa do ar (UR, %) foram coletadas por registradores de dados autônomos a cada 10 min. Para cada aviário foram avaliados: (1) eficiência relativa de resfriamento (RCE) e (2) distribuição espacial interna das variáveis ambientais por técnica de geoestatística. O CPC e SPK não diferiram (P>0,05) na RCE (81,6% e 80,7% respectivamente), mas ambos diferiram do FOG (23,8%) e VLT (1,87%). As maiores variações na Tbs do ar interno foram registradas no FOG (7 °C), seguido pelo SPK (4 °C) e CPC (3 °C). No CPC, houve um aumento da umidade relativa do meio para o final do aviário, próximo aos exaustores. Em conclusão, a eficiência relativa de resfriamento, assim como a distribuição espacial das variáveis ambientais internas foram influenciadas pelo sistema de resfriamento de cada aviário.(AU)

Thermal biology in river buffalo in the humid tropics: neurophysiological and behavioral responses assessed by infrared thermography

The present review aims to analyze the effect of extremely hot climates on the neurophysiological responses of thermal control and behavior in the river buffalo. Understanding thermal neuromodulation and its effects on the buffalo's behavior is of central importance, for this will allow us to make better decisions in terms of improving the level of welfare of buffaloes living in environments characterized by extreme heat, such as the humid tropics. The thermoregulation process involves a complex mechanism that begins with the integration of peripheral signals that are sent to the lateral parabrachial nucleus of the brainstem and then to the preoptic nucleus of the hypothalamus to generate physiological variations such as vasodilatation to dissipate heat under conditions of thermal stress, or vasoconstriction to conserve heat upon the perception of cold stimuli. The thermal biology of the river buffalo is based on several different adaptation mechanisms. The infrared thermography (IRT) technique will be of great help in this area because it permits the detection of vascular microcirculation changes in different thermal windows under adverse climatic conditions. Although buffaloes are classified as rustic animals, it is important to take into account their morpho-physiology and thermoregulation mechanisms to prevent thermal stress and the resulting poor welfare and reduced productivity. However, if appropriate thermoregulation facilities are provided (i.e., ponds, pools, potholes, or swampy areas), buffaloes can properly thermoregulate and tolerate high ambient temperatures. Therefore, they may represent a good option and an appropriate animal-based enterprise under climate change and global warming conditions.(AU)

Thermal biology in river buffalo in the humid tropics: neurophysiological and behavioral responses assessed by infrared thermography

The present review aims to analyze the effect of extremely hot climates on the neurophysiological responses of thermal control and behavior in the river buffalo. Understanding thermal neuromodulation and its effects on the buffalo's behavior is of central importance, for this will allow us to make better decisions in terms of improving the level of welfare of buffaloes living in environments characterized by extreme heat, such as the humid tropics. The thermoregulation process involves a complex mechanism that begins with the integration of peripheral signals that are sent to the lateral parabrachial nucleus of the brainstem and then to the preoptic nucleus of the hypothalamus to generate physiological variations such as vasodilatation to dissipate heat under conditions of thermal stress, or vasoconstriction to conserve heat upon the perception of cold stimuli. The thermal biology of the river buffalo is based on several different adaptation mechanisms. The infrared thermography (IRT) technique will be of great help in this area because it permits the detection of vascular microcirculation changes in different thermal windows under adverse climatic conditions. Although buffaloes are classified as rustic animals, it is important to take into account their morpho-physiology and thermoregulation mechanisms to prevent thermal stress and the resulting poor welfare and reduced productivity. However, if appropriate thermoregulation facilities are provided (i.e., ponds, pools, potholes, or swampy areas), buffaloes can properly thermoregulate and tolerate high ambient temperatures. Therefore, they may represent a good option and an appropriate animal-based enterprise under climate change and global warming conditions.

Addition of Aurantiochytrium sp. meal in the diet affects immunity and thermal shock resistance of the pacific white shrimp / Adição de farinha de Aurantiochytrium sp. na dieta afeta a imunidade e resistência ao choque térmico do camarão-branco-do-pacífico

This paper reports the evaluation of digestibility, immunological parameters, and resistance to thermal shock at low temperature in Litopenaeus vannamei fed diets with diferent Aurantiochytrium sp. meal additions (0; 0.5; 1 and 2%). First, the apparent digestibility coefficient of the ingredient was determined. The digestibility of the microalgae meal was high for protein (74.90%); around 60% for lipids, and for docosahexaenoic fatty acid (DHA) it was 55.61%. After, shrimp rearing with the feed additive was carried out in a clear water system, containing 25 shrimp (initial weight: 4.89 ± 0.27g) per 400 L tank. Feeding occurred four times a day. After a three-week period, immunological parameters were evaluated and thermal shock was performed. Animals fed 0.5% and 2% of the microalgae Aurantiochytrium sp. showed higher survival to thermal shock. In immunological analyses, the serum agglutiniting titer was higher (p <0.05) in the 0.5 and 2% additions of the microalgae meal, and the phenoloxidase activity (PO) was higher in the 1% addition (p <0.05). It is concluded that there is good utilization of the nutrients of Aurantiochytrium sp. meal by L. vannamei and its addition to the diet (0.5 and 1%) increased shrimp resistance to thermal shock.

Avaliou-se a digestibilidade, os parâmetros imunológicos e a resistência ao choque térmico a baixa temperatura em Litopenaeus vannamei alimentado com dietas contendo diferentes proporções de farinha da microalga Aurantiochytrium sp. (0; 0,5; 1 e 2%). Inicialmente, foi determinado o coeficiente de digestibilidade aparente do ingrediente. A digestibilidade da farinha da microalga foi alta para proteína (74,9%), e em torno no 60% para lipídeos em geral, sendo que para o ácido graxo docosahexaenóico (DHA) foi de 55,61%. Posteriormente, o cultivo com o aditivo alimentar foi realizado em sistema de água clara, contendo 25 camarões (peso inicial 4,89 ± 0,27 g) por tanque de 400 L, alimentados quatro vezes ao dia. Após o período de três semanas, foram avaliados os parâmetros imunológicos e realizado o choque térmico. Os animais alimentados com 0,5% e 1% da microalga na dieta apresentaram melhor sobrevivência ao choque térmico. Nas análises imunológicas, o título aglutinante do soro foi significativamente superior (p <0,05) nas adições de 0,5 e 2% da farinha da microalga, e a atividade da fonoloxidade (PO) na adição de 1% (p <0,05). Conclui-se que a farinha de Aurantiochytrium sp. tem bom aproveitamento de seus nutrientes por L. vannamei e sua adição na dieta (0,5 e 1%) aumentou a resistência dos camarões à variação térmica.

Addition of Aurantiochytrium sp. meal in the diet affects immunity and thermal shock resistance of the pacific white shrimp / Adição de farinha de Aurantiochytrium sp. na dieta afeta a imunidade e resistência ao choque térmico do camarão-branco-do-pacífico

This paper reports the evaluation of digestibility, immunological parameters, and resistance to thermal shock at low temperature in Litopenaeus vannamei fed diets with diferent Aurantiochytrium sp. meal additions (0; 0.5; 1 and 2%). First, the apparent digestibility coefficient of the ingredient was determined. The digestibility of the microalgae meal was high for protein (74.90%); around 60% for lipids, and for docosahexaenoic fatty acid (DHA) it was 55.61%. After, shrimp rearing with the feed additive was carried out in a clear water system, containing 25 shrimp (initial weight: 4.89 ± 0.27g) per 400 L tank. Feeding occurred four times a day. After a three-week period, immunological parameters were evaluated and thermal shock was performed. Animals fed 0.5% and 2% of the microalgae Aurantiochytrium sp. showed higher survival to thermal shock. In immunological analyses, the serum agglutiniting titer was higher (p <0.05) in the 0.5 and 2% additions of the microalgae meal, and the phenoloxidase activity (PO) was higher in the 1% addition (p <0.05). It is concluded that there is good utilization of the nutrients of Aurantiochytrium sp. meal by L. vannamei and its addition to the diet (0.5 and 1%) increased shrimp resistance to thermal shock.(AU)

Avaliou-se a digestibilidade, os parâmetros imunológicos e a resistência ao choque térmico a baixa temperatura em Litopenaeus vannamei alimentado com dietas contendo diferentes proporções de farinha da microalga Aurantiochytrium sp. (0; 0,5; 1 e 2%). Inicialmente, foi determinado o coeficiente de digestibilidade aparente do ingrediente. A digestibilidade da farinha da microalga foi alta para proteína (74,9%), e em torno no 60% para lipídeos em geral, sendo que para o ácido graxo docosahexaenóico (DHA) foi de 55,61%. Posteriormente, o cultivo com o aditivo alimentar foi realizado em sistema de água clara, contendo 25 camarões (peso inicial 4,89 ± 0,27 g) por tanque de 400 L, alimentados quatro vezes ao dia. Após o período de três semanas, foram avaliados os parâmetros imunológicos e realizado o choque térmico. Os animais alimentados com 0,5% e 1% da microalga na dieta apresentaram melhor sobrevivência ao choque térmico. Nas análises imunológicas, o título aglutinante do soro foi significativamente superior (p <0,05) nas adições de 0,5 e 2% da farinha da microalga, e a atividade da fonoloxidade (PO) na adição de 1% (p <0,05). Conclui-se que a farinha de Aurantiochytrium sp. tem bom aproveitamento de seus nutrientes por L. vannamei e sua adição na dieta (0,5 e 1%) aumentou a resistência dos camarões à variação térmica.(AU)

Conjugated linoleic acid as a potential bioactive molecule to modulates gamete and embryo cryotolerance / Ácido linoleico conjugado como potencial bioativo para modulação e criotolerância de gametas e embriões

Conjugated linoleic acid (CLA) is a mixture of positional isomers of linoleic acid found in meat and dairy products from ruminants. It is a trans fat widely used by athletes as a food supplement, due to a supposed effect of maximizing the use of body fat reserves. The interest in diet and culture media supplementation with CLA is an emerging area, demanding studies in order to elucidate its benefits in the reproductive parameters, as well as in cryopreservation. Therefore, the aim of this review was to discuss the effects of CLA on the oocytes, sperm and embryos cryotolerance. Some studies have already demonstrated its use in cryopreservation of germline. Among those, it was observed that CLA supplementation during oocyte in vitro maturation can increase their viability post-freezing and developmental capacity. Regarding the use of CLA on sperm, there are few studies and their results are still inconclusive. Finally, studies about CLA supplementation on embryo culture media have shown promising results, indicating that this bioactive molecule is able to modulate lipid uptake on blastomeres. Altogether, these findings demonstrate the potential use of CLA as a bioactive molecule to improve germline and embryo cryotolerance and open new perspectives on human and animal reproduction field.

O ácido linoleico conjugado (CLA) é uma mistura de isômeros posicionais do ácido linoleico encontrado em carne e laticínios de ruminantes. É um tipo de gordura trans muito utilizada por atletas para como suplemento alimentar devido a um suposto efeito de maximizar a utilização das reservas de gordura corporal. O interesse na suplementação de dietas e meios de cultura com o CLA é uma área emergente, exigindo estudos para elucidar seus benefícios nos parâmetros reprodutivos e na criopreservação. Dessa forma, o objetivo dessa revisão foi discutir os efeitos do CLA na criotolerância de oócitos, espermatozóides e embriões. Alguns estudos já demonstraram seu uso na criopreservação da linhagem germinativa. Entre esses, foi observado que a suplementação de CLA durante a maturação in vitro de oócitos pode aumentar sua viabilidade pós-congelamento e capacidade de desenvolvimento. Em relação ao uso de CLA no esperma, existem poucos estudos e seus resultados ainda são inconclusivos. Por último, estudos sobre a suplementação de CLA em meios de cultura de embriões mostraram resultados promissores, indicando que essa molécula bioativa é capaz de modular a captação de lipídios em blastômeros. No total, essas descobertas demonstram o potencial uso do CLA como uma molécula bioativa para melhorar a linha germinativa e a criotolerância ao embrião e abrir novas perspectivas no campo da reprodução humana e animal.