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Aristolochia plants are emblematic from an ethnopharmacological viewpoint and are know to possess numerous biological properties, including antiseptic. However, the medicinal potential of these species is debatable because of their representative chemical constituents, aristolochic acids (AAs) and aristolactams (ALs), which are associated, for instance, with nephropathy and cancer. These contrasting issues have stimulated the development of approaches intended to detoxification of aristoloquiaceous biomasses, among which is included the bioconversion method using larvae of the specialist phytophagous insect Battus polydamas, previously shown to be viable for chemical diversification and to reduce toxicity. Thus, eleven Aristolochia spp. were bioconverted, and the antimicrobial activities of the plant methanolic extracts and its respective bioconversion products were evaluated. The best results were found for Aristolochia esperanzae, Aristolochia gibertii, and Aristolochia ringens against Bacillus cereus, with MIC ranging from 7.8 to 31.25 µg/mL. These three species were selected for chemical, antioxidant, cytotoxic, hemolytic, and mutagenic analyses. Chemical analysis revealed 65 compounds, 21 of them possible bioconversion products. The extracts showed potential to inhibit the formation and degradation of B. cereus biofilms. Extracts of A. gibertii and its bioconverted biomass showed antioxidant activity comparable to dibutylhydroxytoluene (BHT) standard. Bioconversion decreased the hemolytic activity of A. esperanzae and the cytotoxicities of A. esperanzae and A. gibertii. None of the extracts was found to be mutagenic. The bioactivities of the fecal extracts were maintained, and biocompatibility was improved. Therefore, the results obtained in this study reveal positive expectations about the natural detoxification process of the Aristolochia species.

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In this comprehensive study, we delved into the capabilities of five fungal strains: Aspergillus flavus, Aspergillus niger, Penicillium chrysogenum, Penicillium glabrum, and Penicillium rubens (the latter isolated from heavy crude oil [HCO]) in metabolizing HCO as a carbon source. Employing a meticulously designed experimental approach, conducted at room temperature (25 °C), we systematically explored various culture media and incubation periods. The results unveiled the exceptional resilience of all these fungi to HCO, with A. flavus standing out as the top performer. Notably, A. flavus exhibited robust growth, achieving a remarkable 59.1% expansion across the medium's surface, accompanied by distinctive macroscopic traits, including a cottony appearance and vibrant coloration. In an effort to further scrutinize its biotransformation prowess, we conducted experiments in a liquid medium, quantifying CO2 production through gas chromatography, which reached its zenith at day 30, signifying substantial bioconversion with a 38% increase in CO2 production. Additionally, we monitored changes in surface tension using the Du Noüy ring method, revealing a reduction in aqueous phase tension from 72.3 to 47 mN/m. This compelling evidence confirms that A. flavus adeptly metabolizes HCO to fuel its growth, while concurrently generating valuable biosurfactants. These findings underscore the immense biotechnological potential of A. flavus in addressing challenges related to HCO, thereby offering promising prospects for bioremediation and crude oil bioupgrading endeavors.

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BACKGROUND: Spodoptera frugiperda (J. E. Smith) is a widespread agricultural pest with several records of resistance to different insecticides and Bt proteins, including the neurotoxic insecticides chlorpyrifos (organophosphate) and lambda-cyhalothrin (pyrethroid). Here, we (i) characterized and monitored the susceptibility of field populations of S. frugiperda to chlorpyrifos (194 populations) and lambda-cyhalothrin (197 populations) collected from major maize-growing regions of Brazil from 2003 to 2016, and (ii) compared gene expression levels of laboratory-selected, chlorpyrifos- and lambda-cyhalothrin-resistant strains to a susceptible reference strain (Sf-ss) of S. frugiperda. RESULTS: The susceptibility monitoring detected average survival ranging from 29.3% to 36.0% for chlorpyrifos, and 23.1% to 68.0% for lambda-cyhalothrin. The resistance ratio of the chlorpyrifos-resistant strain (Clo-rr) was 25.4-fold and of the lambda-cyhalothrin-resistant strain (Lam-rr) was 21.5-fold. We identified 1098 differentially expressed genes (DEGs) between Clo-rr and Sf-ss, and 303 DEGs between Lam-rr and Sf-ss. Functional analyses of the DEGs revealed the up-regulation of several detoxification enzymes, mainly cytochrome P450 belonging to CYP3 and CYP6 clans. Genes associated with regulatory processes, such as the forkhead box class O (FoxO) transcription factor were also up-regulated. Variant analysis of target-site mutations for both pesticides identified the A201S and F290V mutations in acetylcholinesterase-1, both occurring in heterozigosis in the Clo-rr S. frugiperda strain. CONCLUSION: Our data show that the overexpression of the enzymatic detoxification machinery is the main difference to explain the resistance of Clo-rr and Lam-rr strains of S. frugiperda to chlorpyrifos and lambda-cyhalothrin, although a target-site mutation also contributes to the Clo-rr resistance to chlorpyrifos. © 2023 Society of Chemical Industry.

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BACKGROUND: Some herbicides are commercially formulated with safeners to increase crop selectivity. Fenoxaprop-p-ethyl is formulated with the safener isoxadifen-ethyl for Echinochloa crus-galli control in rice. Safeners act on crops by increasing herbicide metabolism, but this effect may also occur in weeds. The objective of this study was to investigate the effect of the safener isoxadifen-ethyl on the resistance to fenoxaprop-p-ethyl in a biotype of E. crus-galli. RESULTS: A screening of 52 biotypes identified lack of control in the biotype SANTPAT-R treated with the recommended dose of 69 g ha-1 of the commercial formulation of fenoxaprop-p-ethyl with the safener isoxadifen-ethyl. While this biotype survived doses greater than 2208 g ha-1 of the formulation fenoxaprop-p-ethyl + isoxadifen-ethyl, it was killed with 69 g ha-1 of fenoxaprop-p-ethyl without the safener. A glutathione-s-transferase (GST) enzymes inhibitor reduced the resistance factor in two dose-response curves. A minor effect of a CytP450 inhibitor was observed. The previous spraying of the safener isoxadifen-ethyl followed by fenoxaprop-p-ethyl induced survival in the resistant but not in the susceptible biotype. The GST1 and GSTF1 genes were up-regulated in the resistant biotype. ACCase gene mutations were not found, and no cross-resistance to other ACCase inhibitors was identified. CONCLUSION: The safener isoxadifen-ethyl present in the commercial herbicide formulation of fenoxaprop-p-ethyl is associated with resistance in the E. crus-galli SANTPAT-R biotype. This resistance is related with herbicide metabolization mediated by GST pathways. This is the first field-selected weed biotype with herbicide resistance due to safener presence in the sprayed formulation. © 2022 Society of Chemical Industry.

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11C-PK11195 is a positron emitter tracer used for Positron Emission Tomography (PET) imaging of innate immune cell activation in studies of neuroinflammatory diseases. For the image quantitative analysis, it is necessary to quantify the intact fraction of this tracer in the arterial plasma during imaging acquisition (plasma intact fraction). Due to the complexity and costs involved in this analysis it is important to evaluate the real necessity of individual analysis in each 11C-PK11195 PET imaging acquisition. The purpose of this study is to compare 11C-PK11195 plasma metabolization rate between healthy controls and multiple sclerosis (MS) patients and evaluate the interference of sex, age, treatment, and disease phenotype in the tracer intact fraction measured in arterial plasma samples. 11C-PK11195 metabolization rate in arterial plasma was quantified by high performance liquid chromatography in samples from MS patients (n = 50) and healthy controls (n = 23) at 20, 45, and 60 minutes after 11C-PK11195 injection. Analyses were also stratified by sex, age, treatment type, and MS phenotype. The results showed no significant differences in the metabolization rate of healthy controls and MS patients, or in the stratified samples. In conclusion, 11C-PK11195 metabolization has the same rate in patients with MS and healthy controls, which is not affected by sex, age, treatment, and disease phenotype. Thus, these findings could contribute to exempting the necessity for tracer metabolization determination in all 11C-PK11195 PET imaging acquisition, by using a population metabolization rate average. The study procedures were approved by the Ethics Committee for Research Projects Analysis of the Hospital das Clinicas of the University of Sao Paulo Medical School (approval No. 624.065) on April 23, 2014.

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Aquatic animals are vulnerable to arsenic (As) toxicity. However, rarely does a contaminant occur alone in the aquatic environment. For this reason, this study was conducted to evaluate whether titanium dioxide nanoparticles (nTiO2) can interfere with the effects induced by As in Litopenaeus vannamei. Arsenic accumulation and metabolic capacity; expression and enzymatic activity of GSTΩ (glutathione-S-transferase omega isoform); antioxidant responses such as GSH, GR, and GST (reduced glutathione levels, glutathione reductase, and glutathione-S-transferase activity, respectively); and lipid peroxidation in the gills and hepatopancreas of shrimp were evaluated. The results are summarized as follows: (1) higher accumulation of As occurred in both tissues after exposure to As alone; (2) co-exposure to nTiO2 affected the capacity to metabolize As; (3) GSTΩ gene expression was not modified, but its activity was decreased by co-exposure to both contaminants; (4) As alone increased the GSH levels in the hepatopancreas, and co-exposure to nTiO2 reduced these levels in both tissues; (5) a decrease in the GST activity in the gills occurred with all treatments; (6) in the gills, GR activity was increased by As, and nTiO2 reversed this increase, whereas in the hepatopancreas co-exposure inhibited enzyme activity; (7) only in the hepatopancreas lipid damage was observed when animals were exposed to As or nTiO2 but not in co-exposure. The results showed that the As induces toxic effects in both tissues of shrimp and that co-exposure to nTiO2 can potentiate these effects and decrease the capacity to metabolize As, favoring the accumulation of more toxic compounds.

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AIMS: Silibinin is the major component of flavonolignans complex mixture (Silymarin), which is obtained from Silybum marianum (L.) Gaertn. Despite several reports about silibinin, little is known about its effects on gastric diseases. Then, the present study aims to evaluate the silibinin effect against Helicobacter pylori infection, gastric tumor cells and immunomodulation. MAIN METHODS: The anti-H. pylori effect was performed on 43504 and 43629 strains by minimum inhibitory concentration (MIC) determination, observing morphological alterations by scanning electron microscopy and in silico evaluation by molecular docking. Immunomodulatory activity (Interleukins-6 and 10, TNF-α and NO inhibition) was determined in H. pylori-stimulated macrophages and the cytotoxic activity on gastric adenocarcinoma cells prior and after metabolization by S9 fraction. KEY FINDINGS: Silibinin showed anti-H. pylori activity with MIC of 256 µg/mL, promoted important morphological changes in the bacterial cell wall, as blebs and clusters, suggesting interaction with Penicillin Binding Protein (PBP) subunits. Immunomodulatory potential was observed at 50 µg/mL with the inhibition of produced cytokines and NO by H. pylori-stimulated macrophages of 100% for TNF-ɑ, 56.83% for IL-6, and 70.29% for IL-10 and 73.33% for NO. Moreover, silibinin demonstrated significant cytotoxic activity on adenocarcinoma cells (CI50: 60.17 ± 0.95 µg/mL) with a higher selectivity index (SI: 1.52) compared to cisplatin. After metabolization silibinin showed an increase of cytotoxicity with a CI50 six-fold decrease (10.46 ± 0.25). SIGNIFICANCE: The use of silibinin may become an important alternative tool in the prevention and treatment of H. pylori infection and, consequently, in gastric cancer.

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Con posterioridad al anuncio efectuado por investigadores suecos, en Abril del año 2002, sobre la detección de acrilamida (AA) en un amplio grupo de alimentos, se han originado trabajos de investigación en diferentes partes del mundo. Se estudiaron diversas temáticas de gran importancia, entre las que se pueden mencionar la cinética de la formación y degradación de la acrilamida; los mecanismos propuestos para su reducción; los métodos instrumentales empleados para su determinación y los resultados generados tanto en modelos experimentales in vitro como in vivo. En este trabajo se revisan los distintos estudios de la Organización de las Naciones Unidas para la Agricultura y la Alimentación (FAO), Organización Mundial de la Salud (OMS), Agencia Internacional para Investigación en Cáncer (IARC), Swedish National Food Administración (SNFA), Asociación Oficial de Químicos Analíticos (AOAC), European Food Safety Authority (EFSA) sobre la formación de la acrilamida en los alimentos, metabolización, neurotoxicidad, carcinogenicidad, toxicidad aguda y reproductiva, exposición alimentaria, métodos de análisis y mitigación. (AU)

Subsequent to the announcement made by Swedish researchers in April 2002 about the detection of acrylamide (AA) in a wide group of foods, researchs papers have originated in different parts of the world. Various topics of great importance are studied, among which that the kinetics of acrylamide formation and degradation can be specified; the mechanisms proposed for its reduction; the instrumental methods used for its determination and the results generated in both in vitro and in vivo experimental models. This work reviews the different studies of the Food and Agriculture Organization of the United Nations (FAO), World Health Organization (WHO), International Agency for Research on Cancer (IARC), Swedish National Food Administration (SNFA)), Official Association of Analytical Chemists (AOAC), European Food Safety Authority (EFSA) on the formation of acrylamide in food, metabolization, neurotoxicity, carcinogenicity, acute and reproductive toxicity, dietary exposure, analysis methods and mitigation. (AU)

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BACKGROUND: the CYP2D6 gene is clinically important and is known to have a number of variants. This gene has four distinct metabolization profiles that are determined by the different allelic forms present in the individual. The relative frequency of these profiles varies considerably among human populations around the world. Populations from more isolated regions, such as Native Americans, are still relatively poorly studied, however. Even so, recent advances in genotyping techniques and increasing interest in the study of these populations has led to a progressive increase in publication rates. Given this, the review presented here compiled the principal papers published on the CYP2D6 gene in Amerindian populations to determine the metabolic profile of this group. METHODS: a systematic literature review was conducted in three scientific publication platforms (Google Scholar, Science Direct, and Pubmed). The search was run using the keywords "CYP2D6 Amerindians" and "CYP2D6 native Americans". RESULTS: a total of 13 original papers met the inclusion criteria established for this study. All the papers presented frequencies of the different CYP2D6 alleles in Amerindian populations. Seven of the papers focused specifically on Amerindian populations from Mexico, while the others included populations from Argentina, Chile, Costa Rica, Mexico, Paraguay, Peru, and the United States. The results of the papers reviewed here showed that the extensive metabolization profile was the most prevalent in all Amerindian populations studied to date, followed by the intermediate, slow, and ultra-rapid, in that order. CONCLUSION: the metabolization profiles of the Amerindian populations reviewed in the present study do not diverge in any major way from those of other populations from around the world. Given the paucity of the data available on Amerindian populations, further research is required to better characterize the metabolization profile of these populations to ensure the development of adequate therapeutic strategies.

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Conyza bonariensis (hairy fleabane) is one of the most problematic and widespread glyphosate-resistant weeds in the world. This highly competitive weed species significantly interferes with crop growth and substantially decreases crop yield. Despite its agricultural importance, the molecular mechanisms of glyphosate resistance are still unknown. The present RNA-Seq study was performed with the goal of identifying differentially expressed candidate transcripts (genes) related to metabolism-based non-target site glyphosate resistance in C. bonariensis. The whole-transcriptome was de novo assembled from glyphosate-resistant and -sensitive biotypes of C. bonariensis from Southern Brazil. The RNA was extracted from untreated and glyphosate-treated plants at several timepoints up to 288 h after treatment in both biotypes. The transcriptome assembly produced 90,124 contigs with an average length of 777 bp and N50 of 1118 bp. In response to glyphosate treatment, differential gene expression analysis was performed on glyphosate-resistant and -sensitive biotypes. A total of 9622 genes were differentially expressed as a response to glyphosate treatment in both biotypes, 4297 (44.6%) being up- and 5325 (55.4%) down-regulated. The resistant biotype presented 1770 up- and 2333 down-regulated genes while the sensitive biotype had 2335 and 2800 up- and down-regulated genes, respectively. Among them, 974 up- and 1290 down-regulated genes were co-expressed in both biotypes. In the present work, we identified 41 new candidate target genes from five families related to herbicide transport and metabolism: 19 ABC transporters, 10 CYP450s, one glutathione S-transferase (GST), five glycosyltransferases (GT), and six genes related to antioxidant enzyme catalase (CAT), peroxidase (POD), and superoxide dismutase (SOD). The candidate genes may participate in metabolic-based glyphosate resistance via oxidation, conjugation, transport, and degradation, plus antioxidation. One or more of these genes might 'rescue' resistant plants from irreversible damage after glyphosate treatment. The 41 target genes we report in the present study may inform further functional genomics studies, including gene editing approaches to elucidate glyphosate-resistance mechanisms in C. bonariensis.

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OBJECTIVES: To investigate the significance of "subtherapeutic" vs "therapeutic" antiepileptic drug (AED) plasma levels with respect to treatment adherence. MATERIAL AND METHODS: One hundred and seventy patients with refractory temporal lobe epilepsy who underwent video-EEG monitoring in view of a surgical indication had their AEDs (carbamazepine, phenobarbital, phenytoin, and valproate) rapidly withdrawn following a standardized schedule. Plasma levels were measured at admission, and during the 2 days of drug withdrawal. Adherence and nonadherence were identified by the development of plasma levels from day 1 through day 3. Frequencies of an initial level below the reference range in both groups were compared. RESULTS: Adherence was found in 73.2% of cases, and nonadherence in 26.8%. Low levels were seen equally often (about 1/4 of cases) in adherent and nonadherent cases. The vast majority (73.7%) of low levels had another explanation than nonadherence (eg low-dose treatment or enzyme induction). Of 42 nonadherent cases, the vast majority of 76.2% had unsuspicious plasma levels at admission. CONCLUSIONS: "Subtherapeutic" AED plasma levels only rarely are caused by nonadherence whereas levels in the "therapeutic range" by no means prove that the patient is adherent to treatment. For meaningful interpretation, any level needs to be compared with other levels of the same patient. Our findings strongly emphasize the principle of individualized therapeutic AED monitoring as promoted by the Therapeutic Strategies Commission of the ILAE.

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Objetivou-se avaliar os efeitos do óleo ácido de soja (OAS) sobre coeficientes de extinção específica da oxidação (K232 e K270) e a metabolizabilidade das dietas e o desempenho produtivo em codornas. Um total de 80 codornas de duplo propósito foram usadas num experimento com duração de 56 dias. Foi utilizado um delineamento completamente ao acaso com cinco níveis de tratamentos para OAS (0, 25, 50, 75 e 100%), com oito repetições de duas aves cada, como substituto ao óleo de soja refinado (OS) incluído até um nível máximo de 8% na formulação da dieta. O índice de acidez e os coeficientes K232 e K270 mostraram um efeito linear crescente (P<0,001) com o aumento dos níveis de inclusão de OAS na formulação das dietas. Os coeficientes K232 e K270 não foram alterados com o armazenamento das rações durante 7 dias. A suplementação com OAS durante 56 dias não afetou o desempenho produtivo das codornas. Os resultados não mostraram efeitos do OAS sobre a metabolizabilidade de ingredientes, exceto para gordura bruta que exibiu um efeito quadrático decrescente até o nível de 50% de substituição do óleo de soja por OAS (y= 94,31-1,186x+0,018x2, R2= 0,28, P= 0,02). Em conclusão, a inclusão de até 8% de OAS na dieta durante um período curto de tempo (56 dias) não produz efeitos adversos no desempenho produtivo de codornas.(AU)

This study evaluated the effects of soybean acid oil (OAS) on oxidation products specific extinctions coefficients (K232 and K270) and metabolizability of diets and productive performance in quails. A total of 80 dual-purpose quails were used in a 56-days experiment. A completely randomised design with five treatment levels of OAS (0, 25, 50, 75 and 100%) as a dietary replacer for soybean oil (OS) included up to 8% in the diet formulation were used, with eight replicates of two birds each. The acidity index and K232 and K270 coefficients showed a crescent linear effect (P<0.001), with increasing levels of OAS in the diet formulation. There were no changes in K232 and K270 values during 7-days of diet storage. Supplementation with OAS during 56 days has no effect on quail's productive performance. The results showed no effects of OAS on metabolizability of ingredients except for crude fat that exhibited a quadratic effect that was decrescent to the level of 50% of OAS supplementation as soybean oil replacer (y= 94.31-1.186x+0.018x2, R2= 0.28, P= 0.02). In conclusion, dietary inclusion of OAS up to 8% in the diet during a short period of time (56-days) produce no adverse effects on productive performance of quails.(AU)

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Objetivou-se avaliar os efeitos do óleo ácido de soja (OAS) sobre coeficientes de extinção específica da oxidação (K232 e K270) e a metabolizabilidade das dietas e o desempenho produtivo em codornas. Um total de 80 codornas de duplo propósito foram usadas num experimento com duração de 56 dias. Foi utilizado um delineamento completamente ao acaso com cinco níveis de tratamentos para OAS (0, 25, 50, 75 e 100%), com oito repetições de duas aves cada, como substituto ao óleo de soja refinado (OS) incluído até um nível máximo de 8% na formulação da dieta. O índice de acidez e os coeficientes K232 e K270 mostraram um efeito linear crescente (P<0,001) com o aumento dos níveis de inclusão de OAS na formulação das dietas. Os coeficientes K232 e K270 não foram alterados com o armazenamento das rações durante 7 dias. A suplementação com OAS durante 56 dias não afetou o desempenho produtivo das codornas. Os resultados não mostraram efeitos do OAS sobre a metabolizabilidade de ingredientes, exceto para gordura bruta que exibiu um efeito quadrático decrescente até o nível de 50% de substituição do óleo de soja por OAS (y= 94,31-1,186x+0,018x2, R2= 0,28, P= 0,02). Em conclusão, a inclusão de até 8% de OAS na dieta durante um período curto de tempo (56 dias) não produz efeitos adversos no desempenho produtivo de codornas.(AU)

This study evaluated the effects of soybean acid oil (OAS) on oxidation products specific extinctions coefficients (K232 and K270) and metabolizability of diets and productive performance in quails. A total of 80 dual-purpose quails were used in a 56-days experiment. A completely randomised design with five treatment levels of OAS (0, 25, 50, 75 and 100%) as a dietary replacer for soybean oil (OS) included up to 8% in the diet formulation were used, with eight replicates of two birds each. The acidity index and K232 and K270 coefficients showed a crescent linear effect (P<0.001), with increasing levels of OAS in the diet formulation. There were no changes in K232 and K270 values during 7-days of diet storage. Supplementation with OAS during 56 days has no effect on quail's productive performance. The results showed no effects of OAS on metabolizability of ingredients except for crude fat that exhibited a quadratic effect that was decrescent to the level of 50% of OAS supplementation as soybean oil replacer (y= 94.31-1.186x+0.018x2, R2= 0.28, P= 0.02). In conclusion, dietary inclusion of OAS up to 8% in the diet during a short period of time (56-days) produce no adverse effects on productive performance of quails.(AU)

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Nutrition is one of the main factors affecting reproductive efficiency by influencing the growth, maturation and ovulatory capacity of the follicle and metabolic status of the animal, leading to scenarios that impair or corroborate the development and establishment of pregnancy. Different levels of dry matter intake (DMI, providing gain, loss or maintenance of body weight, for example) greatly affect the physiology of the estrous cycle and reproductive performance. The DMI level is also correlated with hepatic blood flow, resulting in a greater or lower metabolization of steroid hormones, which explains part of the reproductive problems that affects high-producing dairy cows. Insulin is one of the main factors that mediate the relationship between nutrition and reproduction. Thus, this review aims to clarify the key points of the relationship between nutrition and reproduction in relation to DMI and insulin action.

A nutrição é um dos principais fatores que afetam a eficiência reprodutiva por influenciar o crescimento, maturação e capacidade ovulatória do folículo bem como o perfil e estado metabólico do animal, gerando cenários que prejudicam ou corroboram o desenvolvimento e estabelecimento da prenhez. Diferentes níveis de ingestão de matéria seca (IMS; proporcionando ganho, perda ou manutenção de peso corporal, por exemplo) afetam consideravelmente a fisio-logia do ciclo estral e o desempenho reprodutivo. O nível de IMS também está correlacionado com o fluxo sanguíneo hepático, determinando maior ou menor metabolização de hormônios esteroides, fato que explica parte dos problemas reprodutivos apresentados por vacas leiteiras de alta produção. A insulina é um dos principais fatores que medeiam a relação da nutrição com a reprodução. Assim, essa revisão tem como objetivo esclarecer os pontos-chave da relação entre a nutrição e reprodução no que diz respeito aos níveis de ingestão de alimento e a ação da insulina.

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Nutrition is one of the main factors affecting reproductive efficiency by influencing the growth, maturation and ovulatory capacity of the follicle and metabolic status of the animal, leading to scenarios that impair or corroborate the development and establishment of pregnancy. Different levels of dry matter intake (DMI, providing gain, loss or maintenance of body weight, for example) greatly affect the physiology of the estrous cycle and reproductive performance. The DMI level is also correlated with hepatic blood flow, resulting in a greater or lower metabolization of steroid hormones, which explains part of the reproductive problems that affects high-producing dairy cows. Insulin is one of the main factors that mediate the relationship between nutrition and reproduction. Thus, this review aims to clarify the key points of the relationship between nutrition and reproduction in relation to DMI and insulin action.(AU)

A nutrição é um dos principais fatores que afetam a eficiência reprodutiva por influenciar o crescimento, maturação e capacidade ovulatória do folículo bem como o perfil e estado metabólico do animal, gerando cenários que prejudicam ou corroboram o desenvolvimento e estabelecimento da prenhez. Diferentes níveis de ingestão de matéria seca (IMS; proporcionando ganho, perda ou manutenção de peso corporal, por exemplo) afetam consideravelmente a fisio-logia do ciclo estral e o desempenho reprodutivo. O nível de IMS também está correlacionado com o fluxo sanguíneo hepático, determinando maior ou menor metabolização de hormônios esteroides, fato que explica parte dos problemas reprodutivos apresentados por vacas leiteiras de alta produção. A insulina é um dos principais fatores que medeiam a relação da nutrição com a reprodução. Assim, essa revisão tem como objetivo esclarecer os pontos-chave da relação entre a nutrição e reprodução no que diz respeito aos níveis de ingestão de alimento e a ação da insulina.(AU)

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Avaliaram-se os efeitos da protease sobre o coeficiente de metabolizabilidade dos nutrientes em dietas contendo farinha de penas (2,0% na fase inicial e 3,0% na fase de crescimento) para frangos de corte machos, Cobb(r), de um a 32 dias de idade. Foram alojadas 336 aves em gaiolas metálicas equipadas com bandeja para coleta total de excretas. Foi utilizado delineamento inteiramente ao acaso, em arranjo fatorial 2x2 (com e sem adição da enzima protease 0,05% e duas valorizações da matriz nutricional da enzima), sendo sete repetições por tratamento, de 12 aves cada. Observou-se, na fase inicial, maior CMPB (P≤0,05) para as aves que, independentemente da adição de protease, consumiram ração com valorização da matriz nutricional da enzima. Não houve efeito dos tratamentos sobre o CMMS e o CMEE (P>0,05). Na fase de crescimento, houve interação entre os tratamentos para as variáveis CMPB e CMEE. Os frangos alimentados com dieta valorizada sem adição de enzima (controle negativo) apresentaram melhores resultados (P≤0,05) para CMPB e CMEE. Nos tratamentos com enzima, o melhor CMEE (P≤0,05) foi obtido com o tratamento sem valorização da matriz nutricional (over the top). Conclui-se que níveis reduzidos e enzima sem valorização melhoram os coeficientes de metabolizabilidade dos nutrientes na fase adulta de frangos de corte.(AU)

This experiment aimed to evaluate the effects of protease on metabolization coefficient of nutrients, performance and slaughter yield from male Cobb(r) broilers fed diets with feather meal. Two experiments were carried out in a completely randomized design in a 2x2 factorial arrangement - with (0.05%) or without enzyme addition x considering or not the improvement of the nutritional value by protease, with seven replicates per treatment group. In experiment 1 the metabolization coefficient of dry matter (MCDM), crude protein (MCCP) and ether extract (MCEE) in initial (9-12-d-old) and growth (29-32-d-old) phase was evaluated. In the initial phase it was observed that regardless of enzyme addition, broiler chickens fed a diet considering improvement in nutritional value had higher MCCP (P≤0.05). However, MCDM and MCEE were not affected (P>0.05). In the growth phase, there were interactions between treatments for the variables MCCP and MCEE. The birds fed diets considering the improvement in nutritional value without enzyme (negative control) showed better results (P≤0.05) for MCCP and MCEE. In the treatments with enzyme, the best MCEE (P≤0.05) was observed in the treatment not considering the improvement in the nutritional value (over the top). Therefore, considering the improvement in the nutritional value and enzyme without considering the improvement in the nutritional value improves the coefficients of metabolization of nutrients in broiler chickens.(AU)

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Avaliaram-se os efeitos da protease sobre o coeficiente de metabolizabilidade dos nutrientes em dietas contendo farinha de penas (2,0% na fase inicial e 3,0% na fase de crescimento) para frangos de corte machos, Cobb(r), de um a 32 dias de idade. Foram alojadas 336 aves em gaiolas metálicas equipadas com bandeja para coleta total de excretas. Foi utilizado delineamento inteiramente ao acaso, em arranjo fatorial 2x2 (com e sem adição da enzima protease 0,05% e duas valorizações da matriz nutricional da enzima), sendo sete repetições por tratamento, de 12 aves cada. Observou-se, na fase inicial, maior CMPB (P≤0,05) para as aves que, independentemente da adição de protease, consumiram ração com valorização da matriz nutricional da enzima. Não houve efeito dos tratamentos sobre o CMMS e o CMEE (P>0,05). Na fase de crescimento, houve interação entre os tratamentos para as variáveis CMPB e CMEE. Os frangos alimentados com dieta valorizada sem adição de enzima (controle negativo) apresentaram melhores resultados (P≤0,05) para CMPB e CMEE. Nos tratamentos com enzima, o melhor CMEE (P≤0,05) foi obtido com o tratamento sem valorização da matriz nutricional (over the top). Conclui-se que níveis reduzidos e enzima sem valorização melhoram os coeficientes de metabolizabilidade dos nutrientes na fase adulta de frangos de corte.(AU)

This experiment aimed to evaluate the effects of protease on metabolization coefficient of nutrients, performance and slaughter yield from male Cobb(r) broilers fed diets with feather meal. Two experiments were carried out in a completely randomized design in a 2x2 factorial arrangement - with (0.05%) or without enzyme addition x considering or not the improvement of the nutritional value by protease, with seven replicates per treatment group. In experiment 1 the metabolization coefficient of dry matter (MCDM), crude protein (MCCP) and ether extract (MCEE) in initial (9-12-d-old) and growth (29-32-d-old) phase was evaluated. In the initial phase it was observed that regardless of enzyme addition, broiler chickens fed a diet considering improvement in nutritional value had higher MCCP (P≤0.05). However, MCDM and MCEE were not affected (P>0.05). In the growth phase, there were interactions between treatments for the variables MCCP and MCEE. The birds fed diets considering the improvement in nutritional value without enzyme (negative control) showed better results (P≤0.05) for MCCP and MCEE. In the treatments with enzyme, the best MCEE (P≤0.05) was observed in the treatment not considering the improvement in the nutritional value (over the top). Therefore, considering the improvement in the nutritional value and enzyme without considering the improvement in the nutritional value improves the coefficients of metabolization of nutrients in broiler chickens.(AU)

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RESUMO

The possible benefits of some bioactive flavones and xanthones present in plants of the genus Syngonanthus prompted us to screen them for estrogenic activity. However, scientific research has shown that such substances may have undesirable properties, such as mutagenicity, carcinogenicity and toxicity, which restrict their use as therapeutic agents. Hence, the aim of this study was to assess the estrogenicity and mutagenic and antimutagenic properties. We used recombinant yeast assay (RYA), with the strain BY4741 of Saccharomyces cerevisiae, and Ames test, with strains TA100, TA98, TA97a and TA102 of Salmonella typhimirium, to evaluate estrogenicity, mutagenicity and antimutagenicity of methanolic extracts of Syngonanthus dealbatus (S.d.), Syngonanthus macrolepsis (S.m.), Syngonanthus nitens (S.n.) and Syngonanthus suberosus (S.s.), and of 9 compounds isolated from them (1=luteolin, 2=mix of A-1,3,6-trihydroxy-2-methoxyxanthone and B-1,3,6-trihydroxy-2,5-dimethoxyxanthone, 3=1,5,7-trihydroxy-3,6-dimethoxyxanthone, 4=1,3,6,8-tetrahydroxy-2,5-dimethoxyxanthone, 5=1,3,6,8-tetrahydroxy-5-methoxyxanthone, 6=7-methoxyluteolin-8-C-ß-glucopyranoside, 7=7-methoxyluteolin-6-C-ß-glucopyranoside, 8=7,3'-dimethoxyluteolin-6-C-ß-glucopyranoside and 9=6-hydroxyluteolin). The results indicated the estrogenic potential of the S. nitens methanol extract and four of its isolated xanthones, which exhibited, respectively, 14.74±1.63 nM; 19.54±6.61; 7.20±0.37; 6.71±1.02 e 10.01±4.26 nM of estradiol-equivalents (EEQ). None of the extracts or isolated compounds showed mutagenicity in any of the test strains and all of them showed antimutagenic potential, in particular preventing mutations caused by aflatoxin B1 (AFB1) and benzo[a]pyrene (B[a]P). The results show that the xanthones, only isolated from the methanol extract of S. nitens capitula, probably were the responsible for its estrogenic activity and could be useful as phytoestrogens, providing a new opportunity to develop hormonal agents. In addition, flavones and xanthones could also be used as a new antimutagenic agent. Since, the mutagens are involved in the initiation and promotion of several human diseases, including cancer, the significance of novel bioactive phytocompounds in counteracting these pro-mutagenic and carcinogenic effects is now gaining credence.

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RESUMO

We performed a sequestration study of aristolactams (ALs) from Aristolochia chilensis in Battus polydamas archidamas (Lepidoptera: Papilionidae) by examining the AL content of the plant, fifth instar larvae, osmeterial secretion, pupae, exuviae and feces. Aristolactam-I (AL-I) and aristolactam-II (AL-II) present in A. chilensis are sequestered by fifth instar larvae of B. polydamas archidamas. There is a preferential sequestration of AL-II, or a more efficient metabolization and excretion of AL-I, by the larva. No ALs were found in the osmeterial secretion, pupae and exuviae; in addition, little AL-I and no AL-II were found in larval frass. The two lactams, particularly AL-I, are extensively metabolized to other products in the larva. A reasonable hypothesis is that the ingested ALs are oxidized to their respective aristolochic acids.