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      Alimentação de suínos em terminação com dietas contendo ractopamina e extratos cítricos: desempenho e características de carcaça Translated title: Pigs fed containing ractopamine and citrus extracts: performance and carcass characteristics

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          Abstract

          Um experimento avaliou a adição de ractopamina e extratos cítricos a dietas de suínos em terminação. Foram utilizados 108 suínos (54 machos e 54 fêmeas) em um delineamento de blocos completos ao acaso, sendo o sexo o fator de bloqueamento e nove os tratamentos: T1. controle (C) (0ppm de ractopamina e 0ppm de extratos cítricos), T2. C+10RAC (ractopamina, em ppm), T3. C+20RAC, T4. C+250EC (extratos cítricos, em ppm), T5. C+500EC, T6. C+250EC+10RAC, T7. C+250EC+20RAC, T8. C+500EC+10RAC e T9. C+500EC+20RAC. O peso vivo final (109,9±3,6kg), consumo de ração (2,6±0,2kgd-1), ganho de peso (1,0±0,1kgd-1), conversão alimentar (2,7±0,2), comprimento de carcaça (97,0±2,7cm), profundidade de músculo (56,1±5,6mm) e pH (5,9±0,3) não foram influenciados pelos tratamentos. Sobre o peso de carcaça, o efeito foi somente do tratamento com 20ppm de ractopamina em relação a 10ppm de ractopamina, sendo 5,7% superior. A espessura de toucinho do grupo controle foi 35% superior aos níveis de ractopamina, e a interação foi 500ppm de extratos cítricos e 10ppm de ractopamina. A carne magra do controle foi 5,3% inferior em relação aos níveis de ractopamina. A alimentação de suínos em terminação com dietas contendo ractopamina, extratos cítricos e suas interações não altera o desempenho, mas influencia algumas características de carcaça.

          Translated abstract

          This study was carried out to evaluate the effect of the addition of the citrus extracts and ractopamine in finishing pig diets. A Hundred eight pigs were used (54 males and 54 females) in a completely randomized design, blocked by sex and distributed in nine treatments: T1. control (C) (0ppm of the ractopamine e 0ppm of the citrus extracts), T2. C+10RAC (ractopamine, ppm), T3. C+20RAC, T4. C+250EC (citrus extracts, ppm), T5. C+500EC, T6. C+250EC+10RAC, T7. C+250EC+20RAC, T8. C+500EC+10RAC and T9. C+500EC+20RAC. The final body weight (109.9±3.60kg), feed intake (2.6±0.24kg d-1), body weight gain (1.01±0.09kg d-1), feed conversion ratio (2.7±0.25), carcass length (97±2.71cm), depth muscle (56.1±5.63mm), and pH (5.9±0.33) were not affected by treatments. There was a significant effect for the treatment with 20ppm of ractopamine, which was 5.7 higher, in relation to the treatment with 10ppm of ractopamine. The backfat thickness of control group was 35% higher than the ractopamine levels and the interaction was of 10ppm of ractopamine and 500ppm of citrus extracts. The lean meat in the control group was on average, 5.3% lower in relation to the ractopamine levels. Feeding of finishing pigs with diets containing ractopamine, citrus extracts and their interactions didn't affect performance, however affected some carcass characteristics.

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          Most cited references27

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          Antimicrobial activity of flavonoids

          Flavonoids are ubiquitous in photosynthesising cells and are commonly found in fruit, vegetables, nuts, seeds, stems, flowers, tea, wine, propolis and honey. For centuries, preparations containing these compounds as the principal physiologically active constituents have been used to treat human diseases. Increasingly, this class of natural products is becoming the subject of anti-infective research, and many groups have isolated and identified the structures of flavonoids possessing antifungal, antiviral and antibacterial activity. Moreover, several groups have demonstrated synergy between active flavonoids as well as between flavonoids and existing chemotherapeutics. Reports of activity in the field of antibacterial flavonoid research are widely conflicting, probably owing to inter- and intra-assay variation in susceptibility testing. However, several high-quality investigations have examined the relationship between flavonoid structure and antibacterial activity and these are in close agreement. In addition, numerous research groups have sought to elucidate the antibacterial mechanisms of action of selected flavonoids. The activity of quercetin, for example, has been at least partially attributed to inhibition of DNA gyrase. It has also been proposed that sophoraflavone G and (−)-epigallocatechin gallate inhibit cytoplasmic membrane function, and that licochalcones A and C inhibit energy metabolism. Other flavonoids whose mechanisms of action have been investigated include robinetin, myricetin, apigenin, rutin, galangin, 2,4,2′-trihydroxy-5′-methylchalcone and lonchocarpol A. These compounds represent novel leads, and future studies may allow the development of a pharmacologically acceptable antimicrobial agent or class of agents.
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            Flavonoids: a review of probable mechanisms of action and potential applications.

            The aim of this review, a summary of the putative biological actions of flavonoids, was to obtain a further understanding of the reported beneficial health effects of these substances. Flavonoids occur naturally in fruit, vegetables, and beverages such as tea and wine. Research in the field of flavonoids has increased since the discovery of the French paradox,ie, the low cardiovascular mortality rate observed in Mediterranean populations in association with red wine consumption and a high saturated fat intake. Several other potential beneficial properties of flavonoids have since been ascertained. We review the different groups of known flavonoids, the probable mechanisms by which they act, and the potential clinical applications of these fascinating natural substances.
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              Vitamin C as an antioxidant: evaluation of its role in disease prevention.

              Vitamin C in humans must be ingested for survival. Vitamin C is an electron donor, and this property accounts for all its known functions. As an electron donor, vitamin C is a potent water-soluble antioxidant in humans. Antioxidant effects of vitamin C have been demonstrated in many experiments in vitro. Human diseases such as atherosclerosis and cancer might occur in part from oxidant damage to tissues. Oxidation of lipids, proteins and DNA results in specific oxidation products that can be measured in the laboratory. While these biomarkers of oxidation have been measured in humans, such assays have not yet been validated or standardized, and the relationship of oxidant markers to human disease conditions is not clear. Epidemiological studies show that diets high in fruits and vegetables are associated with lower risk of cardiovascular disease, stroke and cancer, and with increased longevity. Whether these protective effects are directly attributable to vitamin C is not known. Intervention studies with vitamin C have shown no change in markers of oxidation or clinical benefit. Dose concentration studies of vitamin C in healthy people showed a sigmoidal relationship between oral dose and plasma and tissue vitamin C concentrations. Hence, optimal dosing is critical to intervention studies using vitamin C. Ideally, future studies of antioxidant actions of vitamin C should target selected patient groups. These groups should be known to have increased oxidative damage as assessed by a reliable biomarker or should have high morbidity and mortality due to diseases thought to be caused or exacerbated by oxidant damage.
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                Author and article information

                Journal
                cr
                Ciência Rural
                Cienc. Rural
                Universidade Federal de Santa Maria (Santa Maria, RS, Brazil )
                0103-8478
                1678-4596
                November 2010
                : 40
                : 11
                : 2343-2349
                Affiliations
                [03] Santa Maria RS orgnameUniversidade Federal de Santa Maria Brasil
                [02] Santa Maria RS orgnameUniversidade Federal de Santa Maria orgdiv1Departamento de Zootecnia Brasil
                [01] Santa Maria RS orgnameUniversidade Federal de Santa Maria Brasil
                Article
                S0103-84782010001100015 S0103-8478(10)04001115
                1e7424d9-fed5-4ec7-bb64-8bf71ce89c85

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 01 June 2010
                : 22 September 2010
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 27, Pages: 7
                Product

                SciELO Brazil

                Categories
                Biologia

                bioflavonóides,ascorbic acid,bioflavonoids,ß-adrenergic agonist,nutrition,ácido ascórbico,agonista ß-adrenérgico,nutrição

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