https://doi.org/10.52973/rcfcv-e35581 Revista Científica, FCV-LUZ / Vol. XXXV Recibido: 26/11/2024 Aceptado: 08/02/2025 Publicado: 16/04/2025 1 of 7 Antioxidant activity in dorsal fat and Longissimus dorsi muscle of post-weaned Pelon piglets fed with arboreal leaves meal Actividad antioxidante en la grasa dorsal y en el músculo Longissimus dorsi de lechones Pelones post-destetados alimentados con hojas de arbóreas Claudia Teresita Castellón-Moya¹ * , Clemente Lemus-Flores² Dany Alejandro Dzib-Cauich³ , Julio Enrique Oney-Montalvo³ , Fernando Grageola-Núñez² , Job Oswaldo Bugarín-Prado² ¹*Autonomous University of Nayarit, Master's Program in Biological Agricultural Sciences in the Area of Animal and Veterinary Sciences, Mexico. ²Autonomous University of Nayarit, Graduate Program in Biological Agricultural Sciences, Academic Units of Agriculture and Veterinary Medicine and Animal Science. Mexico. ³Calkiní Higher Technological Institute, Campeche, Mexico. Corresponding Author: 22000242@uan.edu.cu ABSTRACT RESUMEN El presente estudio tuvo como objetivo comparar el efecto de la inclusión al 10% de las harinas de hojas de las arbóreas Morus alba (Morera), Moringa oleifera (Moringa) y Cnidoscolus aconitifolius (Chaya), en la dieta convencional maíz – pasta de soya, sobre la actividad antioxidante (ensayos de DPPH, ABTS y polifenoles totales) en grasa dorsal (GD) y en LD del lechón post destetado de raza Pelón. Para el experimento se utilizaron 28 lechones, con una edad de 24 días de nacidos en etapa post-destete, los cuales se dividieron en cuatro grupos experimentales, cada uno con siete lechones homogenizados por sexo y peso. Después de siete días de adaptación a las jaulas experimentales y a la dieta, los cerdos fueron alimentados ad libitum durante 28 días y se sacrificaron con una edad de 59 días con un peso final de 6,8 ± 0,3 kg. Se empleó un modelo estadístico bajo un diseño de bloques completamente al azar, para determinar si existían diferencias entre las medias de las variables analizadas. Se realizaron correlaciones, regresiones y un análisis de componentes principales para agrupar las variables en cada tratamiento. La dieta con harina de Chaya presentó la mayor actividad antioxidante medida en los ensayos de DPPH, ABTS y polifenoles totales en GD y en LD. También se demostró que la actividad antioxidante en GD y en LD, así como el EE en LD fue mayor (P˂0,0001) en los lechones alimentados con Chaya y Moringa. Las correlaciones y regresiones estadísticas demostraron que a mayor consumo de antioxidantes, incrementa el porcentaje de EE en el LD; y a mayor actividad antioxidante en GD y en LD, mayor es el porcentaje de EE en LD. La inclusión al 10 % de la harina de Moringa y Chaya en la dieta convencional Maíz – pasta de Soya eleva la actividad antioxidante en GD y en LD del lechón Pelón post-destetado. The objective of this study was to compare the effect of a 10% inclusión of leaf meal from the arboreal species Morus alba (Mulberry), Moringa oleifera (Moringa), and Cnidoscolus aconitifolius (Chaya) in a conventional maize-soy bean meal diet on the antioxidant activity (DPPH, ABTS assays, and total polyphenols) in dorsal fat (DF) and Longissimus dorsi (LD) of post-weaned Pelon (hairless) piglets. A total of 28 piglets, 24 days old at weaning, were divided in to four experimental groups, each consisting of seven piglets homogenized by sex and weight. After a seven-day adaptation to the experimental cages and diet, the pigs were fed ad libitum for 28 days and were slaughtered at 59 days of age, with a final weight of 6.8 ± 0.3 kg. A statistical model under a completely randomized block design was employed to determine if there were differences between the means of the analyzed variables. Correlations, regressions and a principal component analysis were performed to group the results obtained from the variables in each treatment. The diet with Chaya meal exhibited the highest antioxidant activity measured in the DPPH, ABTS assays, and total polyphenols in both DF and LD. It was also demonstrated that the antioxidant activity in DF (dorsal fat) and LD, as well as the ether extract (EE) in LD, was greater (P˂0.0001) in piglets fed with Chaya and Moringa. The statistical correlations and regressions showed that increased consumption of antioxidants correlates with a higher percentage of EE in LD; and that greater antioxidant activity in both GD and LD corresponds to a higher percentage of EE in LD. The 10% inclusion of Moringa and Chaya meal in the conventional maize-soybean meal diet enhances antioxidant activity in both DF and LD of post-weaned Pelon piglets. Palabras clave: Compuestos fenólicos; plantas forrajeras; cerdos pelones Key words: Phenolic compounds; forage plants; pelón pigs
2 of 7 Feeding of post-weaning peel pig with tree leaf meal/Castellón-Moya et al. INTRODUCTION Swine (Sus scrofa domesticus) a highly nutritions food but is susceptible to lipid oxidation and microbial contamination, compromising its quality and safety [1]. Some authors, such as Hadidi et al. [2], report that synthetic preservatives like butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), and tert-butylhydroquinone (TBHQ) reduce the oxidation of fats and proteins in meat but pose health risks such as food poisoning, liver damage, carcinogenesis, and mutagenesis. To improve the quality of pork, extend its shelf life, and provide consumers with health hire meat products and by- products, it is necessary to enhance its antioxidant profile through feeding. Antioxidants significantly reduce the development of spoilage and pathogenic microorganisms, prevent lipid oxidation and rancidity, preserve or reduce the loss of sensory attributes such as color, odor, flavor, and texture, and increase shelf life [3]. Serra et al. [4] report numerous publications demonstrating that consuming a variety of antioxidant compounds presenting natural plant-based foods can decrease the risk of serious health disorders due to their antioxidant activities. Additionally, these compounds may reduce lipid oxidation, potentially decreasing the need for synthetic antioxidants, as consumers have expressed a preference for natural alternatives. Some authors [5, 6, 7] , have studied the use of natural antioxidants to reduce lipid oxidation in pork and demonstrated that utilizing forage tree species in the diets of these animals could be considered an alternative to modify their antioxidant profile through their feeding, given that pigs are omnivores. The authors [8, 9] note that various methods can be used to evaluate the antioxidant capacity of a compound or diet, based on quantifying the reaction product between an unstable chemical species and the antioxidant in question. Among the free radical scavenging assays are the DPPH method (1,1-diphenyl- 2-picrylhydrazyl), the ABTS decolorization assay (2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid)), and total polyphenols using the Folin-Ciocalteureagent. The percentages of inhibition determined by the aforementioned assays are generally converted to equivalents of caffeic acid, gallicacid, or trolox [10]. Various researchers affirm that certain arboreal species, such as Morus alba (Mulberry), Moringa oleifera (Moringa), and Cnidoscolus aconitifolius (Chaya), could be valued as alternatives to meet the nutritional needs of Pelon pigs. Besides being rich in proteins, minerals, and vitamins, albeit with a high fiber content, these plants contain bioactive phytochemical components like flavonoids and carotenoids, which can enhance the quality of pork regarding its antioxidant profile [11, 12, 13]. This study was conducted to demonstrate that incorporating 10% leaf meal from the arboreal species Morera, Moringa, and Chaya as an ingredient in the conventional maize-soybean meal diet for post-weaned Pelon piglets increases antioxidant activity (DPPH, ABTS, and total polyphenols) in dorsal fat and Longissimus dorsi muscle. MATERIALS AND METHODS The animal rearing was carried out at the pig farm of the Laboratory of Nutritional Physiology and Experimental Surgery, located at the Academic Unit of Agriculture of the Autonomous University of Nayarit (21º 26' N, 104º 54' W). The lipid and antioxidant analyses of the dorsal fat and Longissimus dorsi muscle of post-weaning Pelon (hairless) piglets were conducted at the Instrumental-Analytical Laboratory Unit of the Higher Technological Institute of Calkiní, Campeche, Mexico (20º 20' N, 90º 2' W). Twenty-eight post-weaning piglets, 24 days old (d), with a weaning weight of 5 ± 0.3 kg were used . They were divided into four experimental groups, each consisting of seven Pelón piglets, homogenized by sex and weight (scale digital Advance, Model I-PCA (±1 g)). After a seven-d adaptation period to the experimental cages and diet, the pigs were fed ad libitum for 28 d. The piglets were housed in individual pens following the recommendations of the Mexican Official Standards (NOM-051- ZOO-1995) [14]. Transportation was carried out according to NOM-062-ZOO-1999 [15] for technical specifications in the production, care, and use of laboratory animals. The animals were slaughtered following the guidelines of the Mexican Official Standard NOM-033-SAG/ZOO-2014 [16], methods for the slaughter of domestic and wild animals. This project was registered by the Graduate Committee of the Autonomous University of Nayarit under identification SIP 21-106-2023. The four experimental groups were: Treatment 1 (Control): Base diet of corn-soybean meal, ad libitum. Treatment 2 (Mulberry): Base diet of corn-soybean meal, ad libitum, plus the inclusion of 10% Mulberry leaf meal. Treatment 3 (Moringa): Base diet of corn-soybean meal, ad libitum, plus the inclusion of 10% Moringa leaf meal. Treatment 4 (Chaya): Base diet of corn-soybean meal, ad libitum, plus the inclusion of 10% Chaya leaf meal. The diet composition (TABLE I) was balanced according to the nutritional requirements of post-weaning piglets, using the Brazilian tables for poultry and swine as a reference [17]. The nutritional content of the diets was calculated based on the nutritional values of the ingredients, and metabolizable energy was calculated using McDowell et al . [18] methodology. The arboreal leaves were dried in shaded mesh screens and ground in a mill to produce the leaf meal. The diets were formulated with the ingredients and pelleted (PELLET MACHINE, model KL150B/ C, made in China), with pellet sizes of 2 cm. Location Animals Experimental desing
3 of 7 Revista Científica, FCV-LUZ / Vol. XXXV ME: Metabolizable Energy; CP: Crude Protein At the time of slaughter, 50 g samples of the Longissimus dorsi and 20 g of dorsal fat (DF) were collected from each animal. These samples were vacuum-packed and stored at -20°C in a Torrey horizontal freezer, model CHTC -145 D made in Mexico, until analyzed (DPPH, ABTS, and total polyphenols assays). Determination of antioxidant activity in dorsal fat and Longissimus dorsi muscle: For the preparation of extracts, 1 g of freeze-dried meat was mixed with 10 mL of distilled water and placed in an ultrasonic bath for 20 minutes (min). The resulting extract was centrifuged (Centrifugue Eppendorf, model 5702 R, Germany) at 35,000 x g for 15 min at 4°C and filtered using Whatman No. 42 paper. The filtrate was stored at -20°C Torrey horizontal freezer, model CHTC -145 D, Mexico) until analysis. DPPH and ABTS radical scavenging activity and the antioxidant activity of polyphenols were determined using a spectrophotometer (Lambda 25, UV/ VIS Spectrometer). The DPPH (2,2-diphenyl-1-picrylhydrazyl) radical scavenging activity was determined using the method of Brand-Williams et al. [19]. The stock solution was prepared by mixing 2.5 mg of DPPH radical with 100 mL of methanol, and the mixture was left to stand at room temperature for 30 min. The absorbance reduction was measured at 515 nm using spectrophotometry (UV/VIS, model Lambda 25, CompanyPerkin Elmer, USA). The calibration curve was prepared using different concentrations of Trolox, and the results were expressed as Trolox equivalents in µM per 100 g of dry weight. The ABTS (2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)) radical scavenging activity was carried out according to the methodology of Miller et al . [20]. The ABTS+ cation was generated through the interaction of 19.2 mg of ABTS dissolved in 5 mL of HPLC-grade water and 88 µL of potassium persulfate 0.0378 g/mL (K2S2O8). The cation was incubated in the dark at room temperature for 16 hours. The activated ABTS radical was diluted with ethanol to obtain an absorbance of 0.70 ± 0.02 at 734 nm. After adding 30 µL of antioxidant extract plus 2970 µL of diluted ABTS solution, the absorbances were recorded Measured variables Sample collection Statistical analysis 6 min after the reaction. The calibration curve was prepared using different concentrations of Trolox, and the results were expressed as Trolox equivalents in µM per 100 g of dry weight. For the determination of total phenol content, 50 µL of each extract was mixed with 3 mL of water, 250 µL of Folin-Ciocalteu reagent (1 N). After 8 min of rest, 750 µL of 20% Na2CO3 and 950 µL of water were added to the extracts; after incubation for 30 min at room temperature, the absorbance was read at 765 nm using a spectrophotometer. The concentration of total soluble phenolic compounds was calculated using a standard curve of aqueous gallic acid solutions (0-10 ppm) and expressed as mg gallic acid equivalents (GAE) per 100 g of fresh weight (Moo- Huchin et al. [21]). Ether Extract of the Longissimus dorsi Muscle: For the ether extract analysis of the Longissimus dorsi muscle, 5 g samples from each piglet were analyzed according to AOAC methods [22]. For the statistical analysis of the variables associated with antioxidant activity (DPPH, ABTS, and total polyphenols), a completely randomized block design statistical model was employed to determine if there were statistical differences between the least squares means of the analyzed parameters. Y=μ+T+B+e The statistical model comprises the variable μ which is the overall mean; T: treatments according to the different diets, B: indicates the blocks, and e: experimental error which were related to the birth litter. Correlations and regressions were also performed using the MINITAB15 program to evaluate the effect of antioxidant consumption on the percentage of ether extract in the Longissimus dorsi (LD), and a principal component analysis was conducted to group the analyzed variables for each treatment. TABLE II presents an analysis of the variables associated with antioxidant activity (DPPH, ABTS, and polyphenols) for each treatment, with the purpose of determining if there are differences between the diets (P<0.0001). These results demonstrate that the antioxidant activity (DPPH, ABTS, and total polyphenols) of each treatment was different (P<0.0001), with the diet containing Chaya presenting the highest results compared to the other diets. This finding may be justified by the research results from Godínez-Santillán et al. [23], who identified and quantified 11 phenolic compounds in the species Cnidoscolus aconitifolius (Chaya): gallic acid, vanillic acid, vanillin, chlorogenic acid, caffeic acid, ferulic acid, rosmarinic RESULTS AND DISCUSSION *P<0.0001; se: standard error; ABTS: 2,2'-azino-bis (3-ethylbenzothiazoline-6- sulfonate), DPPH: 2,2-diphenyl-1-picrylhydrazyl
4 of 7 Feeding of post-weaning peel pig with tree leaf meal/Castellón-Moya et al. acid, p-coumaric acid, resveratrol, luteolin, and apigenin, which enhance the content and antioxidant activity of this plant. TABLE III presents an analysis of the variables associated with the percentage of ether extract and antioxidant activity (DPPH, ABTS, and polyphenols) of the dorsal fat (DF) and the Longissimus dorsi (LD) muscle of Pelon piglets fed with the treatments: Control, Mulberry, Moringa, and Chaya, to determine if there are differences (p<0.0001). *P<0.0001; se: standard error; EE: ether extract; DF: dorsal fat; LD: Longissimus dorsi; ABTS: 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonate), DPPH: 2,2-diphenyl-1-picrylhydrazyl *P<0.0001; x: antioxidant consumption; y: percent of ether extract in Longissimus dorsi; ABTS: 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonate), DPPH: 2,2-diphenyl-1-picrylhydrazyl The obtained results indicated that antioxidant activity (DPPH, ABTS, and polyphenols) in DF and LD was different for each treatment (P<0.0001), where piglets fed with Chaya and Moringa showed the highest values compared to those that consumed the Control and Mulberry treatments. This is related to what was reported by researchers Godínez-Santillán et al. [23], Moo Huchin et al. [24], Dzib-Cauich et al. [6] and Alcívar et al. [12] who demonstrated that the flours from these arboreal forrage present an antioxidant potential with a high phenolic content, influencing the high values of DPPH, ABTS, and total polyphenols, particularly highlighting Chaya and Moringa. The highest percentage of ether extract (EE) in the Longissimus dorsi (LD) was different in the Control and Mulberry treatments, with their values being lower than those of Chaya and Moringa. This may be due to the EE content from the leaf meal these arboreal forrage, which contain oils that, when consumed by the animal, lead to an increase in the percentage of ether extract in the muscle tissue, in agreement with the findings of researchers Alcívar et al. [12], who showed that Chaya and Moringa leaf flours have a higher EE content than Mulberry. TABLE IV presents a correlation analysis between the antioxidant activity (DPPH, ABTS, and polyphenols) of the dorsal fat (DF) and the Longissimus dorsi (LD) muscle and the percentage of ether extract (EE) in LD of post-weaning Pelón piglets. The analysis in TABLE IV demonstrates that there are high and significant correlations between the percentage of EE (%) in LD and the antioxidant activity (DPPH, ABTS, and polyphenols) in DF and LD, indicating that as antioxidant activity in LD and GD increases, the percentage of EE in LD also rises. Piglets supplemented with Chaya and Moringa presented higher EE values in LD and antioxidant activity in DF and LD compared to animals fed the Control and Mulberry treatments. Several authors have reported that animals fed with grasses and green diets may exhibit higher antioxidant content and ether extract percentage in their meat. Furthermore, the fat percentage in meat is accompanied by a greater content and activity of antioxidants, which help delay the oxidative degradation of lipids [25, 26]. TABLE V presents a regression analysis between the percentage of ether extract (EE) in the Longissimus dorsi (LD) muscle and the consumption of antioxidants (flavonoids, carotenoids, and polyphenols) in post-weaning Pelón piglets, according to the results obtained in the DPPH, ABTS, and total polyphenol assays. The previous analyses indicate significant differences (P<0.0001) between the consumption of antioxidants (flavonoids, carotenoids, and polyphenols) corresponding to the values obtained in the DPPH, ABTS, and total polyphenol assays and the percentage of EE (LD), where it is observed that higher antioxidant consumption (x) increases the percentage of EE in the Longissimus dorsi. These results coincide with the search conducted by Benítez et al. [5], who noted that some scientists and the food industry are modifying the nutritional composition of feed intended for livestock, as it has been demonstrated that the diets with which pigs are fed can alter their fat content, antioxidants, and gene expression. In FIG. 1, a principal component analysis was conducted, associating the percentage of ether extract (EE) in the Longissimus dorsi (LD) muscle and the antioxidant activity (DPPH, ABTS, and polyphenols) in the dorsal fat (DF) and in (LD) of post- weaning Pelon piglets fed with the treatments: Control, Mulberry, Moringa, and Chaya. The principal component analysis reveals that Pelon (hairless) piglets fed the Chaya treatment exhibited the highest percentages of ether extract (EE) in LD and antioxidant activity (DPPH, ABTS, and total polyphenols) in both LD and DF, aligning with the data presented in TABLE II. This may be attributed to the high antioxidant content and percentage of EE found in this plant compared to Mulberry and Moringa. *P<0.0001; EE: ether extract; DF: dorsal fat; LD: Longissimus dorsi; g: grams; µm: micromole; ABTS: 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate), DPPH: 2,2-diphenyl-1-picrylhydrazyl
5 of 7 Revista Científica, FCV-LUZ / Vol. XXXV CONCLUSION FIGURE 1. Principal Component analysis for each treatment. DF: dorsal fat; LD: Longissimus dorsi; ABTS: 2,2´- azino – bis – 3etil benzotiazolin – 6-sulfonato de amonio, DPPH: 2,2 –difenil– 1 – picrilhidracilo Some researchers as Godínez-Santillán et al. [23], Us-Medina et al . [27] , and Alcívar et al . [12] demonstrated through the same methods of antioxidant activity determination that Chaya leaves are rich in flavonones, dihydroflavonoids, carotenoids, and polyphenols, and they also exhibit higher EE compared to the other plants used to supplement Pelon piglets. In FIGS. 2, 3, and 4, a principal component association analysis was conducted between antioxidant consumption based on the results of the ABTS, DPPH, and total polyphenol assays, and the average values of EE (%) in the Longissimus dorsi muscle of post-weaning piglets fed the Control, Mulberry, Moringa, and Chaya treatments. The Chaya diet presented the highest antioxidant activity (DPPH, ABTS, and total polyphenols) compared to the Control, Mulberry, and Moringa treatments. The Chaya and Moringa treatments increased antioxidant Post-weaning Pelon (hairless) piglets fed the Chaya and Moringa diets showed the highest antioxidant consumption and the greatest percentage of EE in LD, coinciding with the results in Table 4 and with researchers Vargas et al. [28] and Alcívar et al. [12], who demonstrated a high and significant correlation between the antioxidant content (LD and DF) and the percentage of EE in LD, indicating that higher antioxidant contents associated with a greater percentage of EE in LD. This may be due to the FIGURE 2. Association between the ether extract of Longissimus dorsi and antioxidant consumption reported by the DPPH assay for each treatment. EE: ether extract; LD: Longissimus dorsi, DPPH: 2,2 –difenil– 1 – picrilhidracilo FIGURE 3. Association between the ether extract of Longissimus dorsi and antioxidant consumption reported by the ABTS assay for each treatment. EE: ether extract; LD: Longissimus dorsi ; ABTS: 2,2'-azinobis (3-ethylbenzothiazoline-6-sulfonate) FIGURE 4. Association between the ether extract of Longissimus dorsi and antioxidant consumption reported in the total polyphenols count assay for each treatment. EE: ether extract; LD: Longissimus dorsi organism's need to delay cellular stress processes. According to the results obtained in this research work and those reported by Castellón et al. [29], the inclusion of leaf flours from these arboreal in the conventional corn-soybean meal diet could be valued as an alternative in pig feeding that satisfies the nutritional needs of these animals and, in turn, participates as free radical scavengers, increasing the antioxidant activity in DF and LD of pigs that consume these diets (DPPH, ABTS and total polyphenols), thus prolonging the storage period and quality of their meat. Related to the above, there are a series of investigations in which different extracts of natural plants with antioxidant properties have been tested in the ration of productive animals, including fattening pigs, where it is shown that the consumption of forage plants produces a low transfer of unpleasant odors and flavors to the meat, which indicates that the oxidation process of the meat is reduced (Ranucci et al. [30]).
6 of 7 Feeding of post-weaning peel pig with tree leaf meal/Castellón-Moya et al. ACKNOWLEDEGEMENTS This project was supported by the Graduate Committee of the Autonomous University of Nayarit under identification SIP 21- 106-2023. The authors declare no conflict of interest Conflict of interest Echegaray N, Pateiro M, Munekata PES, Lorenzo JM, Chabani Z, Farag MA, Domínguez R. Measurement of antioxidant capacity of meat and meat products: Methods and Applications. Molecules. [Internet]. 2021;26(13):3880. doi: https://doi.org/gscz33 Hadidi M, Orellana-Palacios JC, Aghababaei F, González- Serrano DJ, Moreno A, Lorenzo JM. Plant by-product antioxidants: Control of protein-lipid oxidation in meat and meat products. Food Sci. Technol. [Internet]. 2022;169:1- 114003. doi: https://doi.org/pgscb Islas RP, Márquez JM, Amaya CA, Gallardo CT, Galindo SA, Treviño MZ. Avances recientes en el desarrollo de recubrimientos comestibles aplicados en productos cárnicos. Inv. Des. Cienc. Tecnol. Aliment. [Internet]. 2024; 9(1):32–42. doi: https://doi.org/pgsd BIBLIOGRAPHICS REFERENCES [1] [2] [3] Serra JJ, Melero J, Martínez G, Fagoaga C. Especies vegetales como antioxidantes de alimentos. Nereis. [Internet]. 2020; 12:71–90. doi: https://doi.org/pgsf [4] Benítez R, Fernández A, Isabel B, Núñez Y, de Mercado E, Gómez-Izquierdo E, García-Casco J, López-Bote C, Óvilo C. Modulatory effects of breed, feeding status, and diet on adipogenic, lipogenic, and lipolytic gene expression in growing Iberian and Duroc pigs. Int. J. Mol. Sci. [Internet]. 2018; 19(1):22. doi: https://doi.org/gtd7z2 [5] Graciano MJ, Rodríguez JG, Sumaya MT, Balois R, Jiménez EI, Bautista PU. Efecto de extractos naturales sobre la estabilidad oxidativa de hamburguesas de carne de cerdo durante el almacenamiento refrigerado. Rev. Mex. Cienc. Pecu. [Internet]. 2022; 13(2):323-339. doi: https://doi. org/g7hdpd [7] Cuapio-Rodriguez MA, López Y, Moreno JA, Sánchez L, García-Barrientos R, Santacruz E, Santiago-Santiago LA. Determinación de la actividad antioxidante por el método DPPH y ABTS en hongos comestibles. Rev. Politécnica Aguascalientes. [Internet]. 2024 [cited 12 November 2024]; 3(3):1-6. Available in: https://goo.su/Xp0Zc Hurtado NH, Charfuelan C. Contribución a la Caracterización y Evaluación de la Actividad Antioxidante de las Antocianinas del Fruto de Ivilan ( Monnina Obtusifolia H.B.K). Inf. Tecnol. [Internet]. 2019; 30(5):81- 90. doi: https://doi.org/pgsh [8] [9] Mendoza-Isaza NA, Hoyos-Arbeláez JA, Peláez-Jaramillo CA. Capacidad antioxidante y contenido de polifenoles totales de extractos de tallo de Stevia rebaudiana en varios modelos in vitro. Rev. EIA. [Internet]. 2020; 17(34):1-9. doi: https://doi.org/pgsj Mejía H. La morera ( Morus sp ) como alternativa en sistemas silvopastoriles. Rev. Ibero. Bioecon. Camb. Clim. [Internet]. 2019; 5(9):1157-1163. doi: https://doi.org/ pgsk Alcívar EH, Fernández Y, Vivas WF, Cusme KE, Verduga CD, Heredia JD. Evaluación del potencial nutritivo de especies arbustivas tropicales para la alimentación de cerdos de traspatio. Cienc. Tecnol. Agropecu. [Internet]. 2023; 24(3):e2991. doi: https://doi.org/pgsm [10] [11] [12] Dzib-Cauich DA, Moo-Huchin VM, Lemus-Flores C, Sierra- Vásquez ÁC. Productive Performance and carcass quality of mexican hairless pig breed castrated males fed with Moringa oleífera and Brosimum alicastrum. J. Anim. Plant Sci. [Internet]. 2022; 32(3):638-644. doi: https://doi.org/ pgsg [6] Rubio-Sanz L. Comparativa nutricional del cultivo de Moringa oleífera en España. Rev. Cienc. Tecnol. [Internet]. 2020; 13(2):17-22. doi: https://doi.org/pgsp Norma Oficial Mexicana NOM-051-ZOO-1995. Trato humanitario en la movilización de animales. Revista Diario Oficial de la Federación. [Internet]. 1995 [cited 16 nov. 2024]; 23p. Available in: https://goo.su/Z7qbs [13] [14] Norma Oficial Mexicana NOM-062-ZOO-1999. Especificaciones técnicas para la producción, cuidado y uso de los animales de laboratorio. Revista Diario Oficial de la Federación. [Internet]. 1999[cited 19 nov. 2024]. 59p. Available in: https://goo.su/BB2UO [15] activity in both the dorsal fat (DF) and the Longissimus dorsi (LD) muscle of Pelón piglets compared to animals fed the Control and Mulberry diets. The Chaya and Moringa diets elevated the percentage of ether extract (EE) in the Longissimus dorsi (LD) of the piglets that consumed them. Higher consumption of antioxidants (flavonoids, carotenoids, and polyphenols) is associated with a greater percentage of ether extract (EE) in the Longissimus dorsi (LD); similarly, a higher antioxidant content in dorsal fat (DF) and in LD correlates with an increased percentage of EE in LD. Norma Oficial Mexicana NOM-033-SAG/ZOO-2014. Métodos para dar Muerte a los Animales Domésticos y Silvestres. Revista Diario Oficial de la Federación. [Internet]. 2014 [cited 11 jul. 2024]. 48p. Available in: https://goo.su/ds6zz [16]
7 of 7 Revista Científica, FCV-LUZ / Vol. XXXV Ahmad S, Gokulakrishnan P, Giriprasad R, Yatoo M. Fruit based natural antioxidants in meat and products: A review. Crit. Rev. Food Sci. Nutr. [Internet]. 2015; 55(11):1503- 1513. doi: https://doi.org/gnkj9w [25] Santiago H, Teixeira LF, Izabel M, Lopes J, Kazue N, Guilherme F, Márvio AS, Teixeira L, Borges P, Flávia R, de Toledo SL, de Oliveira C. Tablas brasileñas para aves y cerdos. [Internet]. 2017 [cited 23 Nov. 2024]; 4(1):488. Available in: https://goo.su/lzt3fU Valenzuela C, Pérez P. Actualización en el uso de antioxidantes naturales derivados de frutas y verduras para prolongar la vida útil de la carne y productos cárneos. Rev. Chil. de Nutr. [Internet]. 2016; 43(2):188-195. doi: https://doi.org/c3c4 McDowell LR, Conrad JE, Thomasn JE, Harris LE. Latin American tables of feed composition. University of Florida, Florida, U.S.A. 1974. 2:552p. Us-Medina U, Millán-Linares MC, Arana-Argaes VE, Segura- Campos MR. Actividad antioxidante y antiinflamatoria in vitro de extractos de chaya (Cnidoscolus aconitifolius (Mill.) I.M. Johnst). Rev. Nutr. Hosp. [Internet]. 2019; 37(1):46- 55. doi: https://doi.org/pgsv Brand-Williams W, Cuvelier ME, Berset C. Use of a Free Radical Method to Evaluate Antioxidant Activity. Food Sci. Technol. [Internet]. 1995;28(1):25-30. doi: https://doi. org/fgbszk Vargas ML, Figueroa H, Tamayo JA. Toledo VM, Moo VM. Aprovechamiento de cáscaras de frutas: análisis nutricional y compuestos bioactivos. CIENCIA ergo-sum. [Internet]. 2019; 26(2):e52. doi: https://doi.org/pgsw Miller WR, Benefield RG, Tonigan JS. Enhancing motivation for change in problema drinking: A controlled comparison of two therapist styles. J. Consult. Clin. Psychol. [Internet]. 1993;61(3):455–461. doi: https://doi.org/dc75fr Castellón-Moya CT, Lemus-Flores C, Bugarín-Prado JO, Grageola-Nùñez F, Dzib-Cauich DA, Àngel-Hernández A, García AA. Evaluación nutricional química proximal de árboles de Morera (Morus alba), Moringa (Moringa oleifera) y Chaya ( Cnidoscolus aconitifolius) como alternativa nutricional para cerdos. Braz. J. Anim. Environ. Res. [Internet]. 2023; 6(3): 2550-2556. doi: https://doi.org/ pgsx Moo-Hunchin VM, Estrada-Mota I, Estrada-León R, Cuevas-Glory L, Ortíz- Vázquez E, Vargas ML, Betancourt- Ancona D, Sauri-Druch E. Determination of somephy sicochemical characterist bioactive compounds and antioxidant activity of tropical fruits from Yucatan, México. Food Chem. [Internet]. 2014;152:508-515. doi: https:// doi.org/gmpk7d Ranucci D, Beghelli D, Trabalza-Marinucci M, Branciari R, Forte C, Olivieri O, Badillo G, Cavallucci C, Acuti G. Dietary effect of a mix derived from oregano (Origanum vulgare L.) essential oil and sweet chesnut (Castanea sativa Mill.) wood extract on pig performance, oxidative status and pork quality traits. Meat Sci. [Internet]. 2015; 100:319- 326. doi: https://doi.org/pgsz [17] [26] [18] [27] [19] [28] [20] 29] [21] [30] Feldsine P, Abeyta C, Andrews WH; AOAC International Methods Committee. AOAC International methods committee guidelines for validation of qualitative and quantitative food microbiological official methods of analysis. J AOAC Int. 2002; 85(5):1187-1200. doi: https:// doi.org/gkdw7d Godínez-Santillán RI, Chávez-Servín JL, García-Gasca T, Guzmán-Maldonado SH. Caracterización fenólica y capacidad antioxidante de extractos alcohólicos de hojas crudas y hervidas de Cnidoscolus aconitifolius (Euphorbiaceae). Acta Bot. Mex. [Internet]. 2019; (126):1493. doi: https://doi.org/pgss Moo-Huchin VM Canto-Pinto JC, Cuevas-Glory LF, Sauri- Duch E, Pérez-Pacheco E, Betancur D. Effect of extraction solvent on the phenolic compounds content and antioxidant activity of Ramon nut (Brosimum alicastrum). Chem. Pap. [Internet]. 2019; 73(7):1647-1657. doi: https://doi.org/pgst [22] [23] [24]