Abstract
We evaluated the influence of the substitution of soybean meal by detoxified castor cake on performance, digestibility of nutrients, nitrogen balance, hepatic and renal functions of pregnant goats fed with diets containing detoxified castor cake by alkaline solutions during the stages (first two-thirds and final third) of pregnancy. Three diets were provided: one based on soybean meal and the other two based on castor cake detoxified with whit calcium hydroxide or sodium hydroxide. Goats fed detoxified castor cake sodium hydroxide had lower consumption. Was no effect (P>0.05) of diets or stages on the digestibility of dry matter and nutrients. The goats that received the diets based on soybean meal and detoxified castor cake calcium hydroxide consumed larger amounts of nitrogen. The goats fed with diet the basis of SM had greater weight in the parturition day. The average levels of enzymes for hepatic and renal functions were within normal patterns. Of enzymes related to liver metabolism, only the gamma-glutamyl transferase increased in the final third of pregnancy. The present study demonstrated that detoxified castor by sodium hydroxide reduces the consumption of goats during gestation, but did not affect negatively the renal and hepatic parameters.
Key words
Anglo Nubian; byproducts of biodiesel; final third; ricin; Saanen
INTRODUCTION
In the production of goats milk, as in any animal production system, barriers are found in the nutritional management of animals, being essential the use of balanced diets, thus avoiding financial waste, especially when it comes to confined animals, given that the costs are higher (Araújo et al. 2020ARAÚJO RA, NEIVA JNM, ROGÉRIO MCP, CÂNDIDO MJD, EGITO AS, PEREIRA PL, LUCAS RC & POMPEU RCFF. 2020. Detoxification and nutritional profile of the detoxified castor by different alkaline solutions. Arq Bras de Med Vet e Zootec 72: 1947-1958.). The ideal is to use diets appropriate to the physiological stage and the level of production of the animals. However, the high cost of some foods hinders the productivity of these systems, often making them inefficient from a nutritional and economic point of view.
There has been a growing interest in the use of alternative food and regional (Menezes et al. 2012MENEZES DR, COSTA RG, ARAÚJO GGL, PEREIRA LGR, OLIVEIRA PTL, SILVA AEVN, VOLTOLINI TV & MORAES SA. 2012. Blood, liver and rumen parameters of sheep fed diets containing detoxified castor bean meal. Pesq Agropecu Bras 47: 103-110., Pompeu et al. 2012POMPEU RCFF, CANDIDO MJD, PEREIRA ES, BOMFIM MAD, CARNEIRO MSS, ROGÉRIO MCP, SOMBRA WA & LOPES MN. 2012. Performance and carcass traits of sheep in feedlot and fed diets containing detoxified castor cake replacing soybean meal. Rev Bras de Zootec 41: 726-733., Gionbelli et al. 2014GIONBELLI TRS ET AL. 2014. Utilization of castor bean meal treated with calcium hydroxide fed wet or dry by lambs. Livest Scien 168: 76-783.) in the diets of ruminants, aiming at the reduction of costs with food supplies, among which we can highlight the castor cake, with its high protein content. However, the presence of antinutritional factors, such as the ricin, ricinina, ricinus agglutinin and complex allergenic renders it unfit for animal feed. However, after detoxification process (Anandan et al. 2005ANANDAN S, ANIL KUMAR GK, GHOSH J & RAMACHANDRA KS. 2005. Effect of different physical and chemical treatments on detoxification of ricin in castor cake. Anim Feed Scien and Techn 120: 159-168.), this problem can be circumvented requiring, therefore, studies proving its use effectively in the diet of ruminants in different physiological situations.
In this sense, the pregnant goats require special attention, because the nutrients required by the body of the female at this stage do not meet only the maintenance of the body, but mainly will be directed to the pregnant uterus and mammary gland, being that during pregnancy. There is a great variation in the metabolism of pregnant goats, in virtue of fetal growth (Konyali et al. 2007KONYALI A, TÖLÜ C, DAS G & SAVAS T. 2007. Factors affecting placental traits and relationships of placental traits with neonatal behaviour in goat. Anim Reprod Scien 97: 394-401.).
During the first and second third of gestation, which begins with the design, the requirements of protein, energy, minerals and vitamins may be similar to the requirements of maintenance for the goats (NRC 2007NRC - NATIONAL RESEARCH COUNCIL. 2007. Nutrient Requirements of Small Ruminants. Washington, DC: National Academy Press, 362 p.). Already in the final third of the pregnancy is observed reduction in the relative rate of growth of the fetus, possibly because the fetus is entering the linear phase of growth (Greenwood & Bell 2003GREENWOOD PL & BELL AW. 2003. Prenatal nutrition influences on growth and development of ruminants. Rec Adv in Anim Nutr in Austr 14: 57-73., Hafez & Hafez 2004HAFEZ ESE & HAFEZ B. 2004. Reprodução Animal. Tradução: original Renato Campanarut Barnabé - Barueri, SP. 7ª ed, 513 p.), at the same time, at this stage there is a strong mobilization of body tissues and the goats are more susceptible to the occurrence of metabolic diseases. In addition, the nutrition of the female during the gestation period will affect the production of milk, the composition and weight gain of their descendants (Liden et al. 2009LIDEN DS, KEMYON PR, BLAIR HT, LOPEZ-VILLALOBOS N, JENKINSONS CMC, PETERSON SW & MACKENZIE DDS. 2009. Effects of ewe size and nutrition on fetal mammary gland development and lactational performance of offspring at their first lactation. Jour Anim Scien 87: 3944-3954.), and highlighted the importance of adequate nutritional plans the goats.
On the basis of claims raised and considering the importance of diet on the pregnancy period, the aim of this research was to evaluate the possibility of use of the detoxified castor by two alkaline solutions in lactating Saanen goats and Anglo Nubian and in confinement during stages of pregnancy and observe the effects on intake and digestibility of dry matter and nutrients, nitrogen balance and hepatic and renal functions.
MATERIALS AND METHODS
All animal procedures were conducted according to the regulations of the Ethics Committee on the Use of Animals of the Brazilian Agricultural Research Corporation, National Center for Research with goats, protocol no. 005/2015. The experiment was conducted at the Technological Center of production of goat milk from Embrapa Goats and Sheep (3°44’57.42”S, 40°20’43.50’W) located in the town of Sobral-CE, Brazil.
Were used 24 goats, being 12 of the Saanen goats and 12 Anglo Nubian, staying in each treatment, with body weight of 42.08 ± 5.33 kg of body condition score of 3.6 ± 0.3 according to the classification of Morand-Fehr (2005)MORAND-FEHR P. 2005. Recent developments in goat nutrition and application: A review. Small Rumin Res 60: 25-43., consisting of four goats with double gestation and two with single gestation in each treatment. All tests were performed on two occasions, the first when the goats were between 30 and 100 days of gestation (first and second third) and the second between 110 and 140 days of pregnancy, representing the final third of pregnancy.
The experimental design was completely randomized, in plots subdivided in time, getting in the gestational phase plots and subplots the diets. Before the trial period, the goats were evaluated in another study where it was analyzed the performance in the growth phase with the use of the detoxified castor, therefore, the goats were already adapted to the foods used, changing only the proportion of ingredients due to the demands of the category in assessment.
In pre-experimental conditions, the reproductive management adopted involved “ natural, with an average duration of breeding season of 30 days. Once identified the estro, the coverage was performed by natural mounts directed. For both, were used for breeding of the same breed, without any degree of kinship with the arrays. From the coverage, the goats were placed in individual stalls, suspended and with floor ripped of 5.06 m², being 2.87 m² solarium area composed of beaten floor, provided with drinkers, feeders and salt shakers. The 35 days of gestation of the latest coverage, was held the confirmation of pregnancy all the goats, with the use of ultrasound device KX 5000®. The 96 days of gestation, the access to the solarium was closed with screens of protection due to the large slope of the ramp access, staying with 2.19 m2 per bay.
The measurement of live weight was performed fortnightly. The animals were weighed always at the same time and in fasting. The treatments consisted of three diets, a formulated with corn and soybean meal (SM) and the others were formulated with detoxified castor cake (DCC) by calcium hydroxide [Ca(OH)2] and another composed by detoxified castor by sodium hydroxide (NaOH), both in total substitution of soybean meal, was used as roughage hay Tifton 85 (Cynodon spp.). The goats began to receive the diets on the day of coverage.
The diets were formulated to meet the needs of pregnant goats with two fetuses, according to the NRC (2007)NRC - NATIONAL RESEARCH COUNCIL. 2007. Nutrient Requirements of Small Ruminants. Washington, DC: National Academy Press, 362 p. for goats with body weight of 42 kg and in early pregnancy. The chemical composition of foods is presented in Table I and the proportion of the ingredients and the chemical composition of diets are shown in Table II.
The castor cake used in this study was obtained after collecting oil, by mechanically pressing castor bean seeds at temperatures between 90 and 100 °C. After mixing the cakes, reagents and water for 3 h (mixing for 10 min and resting for 30 min, alternately), the cake was placed outdoors on a plastic canvas for a period of 48 h and constantly rolled with a squeegee manual adapted for homogeneous drying. After drying, the cake was chopped using a forage machine to reduce the material size (5 mm) and to facilitate its homogenization with the other ingredients.
The concentrations of alkaline products (calcium hydroxide and sodium hydroxide) used for 100% detoxification of ricin in crude castor cakes were 90 g Ca(OH)2 and 60 g NaOH, respectively, per kilogram, which were diluted in 2 L of water using a stationary mixer (Fischer® MOB 400 G2) equipped with a three-phase motor, according to the methodology described by Araújo et al. (2020)ARAÚJO RA, NEIVA JNM, ROGÉRIO MCP, CÂNDIDO MJD, EGITO AS, PEREIRA PL, LUCAS RC & POMPEU RCFF. 2020. Detoxification and nutritional profile of the detoxified castor by different alkaline solutions. Arq Bras de Med Vet e Zootec 72: 1947-1958.. No hemagglutinating activity was observed at those concentrations; i.e., ricinus agglutinin was no longer active. Therefore, these two concentrations were used to formulate the diets.
Diets were supplied daily at 8h00 and 16h00, allowing a 10% leftover. Samples were collected from the bulk, concentrate, and also leftovers during the entire experimental period, then duly packaged in identified plastic bags and stored in a freezer at −18 °C.
At the end of the trial, the samples were thawed and separated between the two stages of pregnancy (first two-thirds and final third) and submitted to pre-drying in forced ventilation oven at 55 °C for 24 h. The dried samples were ground in knife mills (Wiley mill, Arthur H. Thomas, Philadelphia, PA, USA). Feed and leftovers were screened using a 1.0-mm sieve for chemical analyses, and a 2.0-mm sieve was used for evaluating apparent digestibility (Nocek, 1988NOCEK JE. 1988. In situ and other methods to estimate ruminal protein and energy digestibility: a review. J of Dairy Scien 71: 2051-2069.).
Apparent digestibility coefficients were estimated indirectly using the internal iADF indicator. To do so, feces were collected directly from the rectal bulb for five days at different times (0, 3, 6 and 9 h after the first feeding), aiming for greater daily representativeness. Next, they were identified and stored in a freezer at − 18 °C. At the end of data collection, composite samples were made and then dried in a forced ventilation oven at 55 °C until constant weight was reached. The feces (2.0-mm) and feed samples (2.0-mm) were incubated in situ for a period of 240 h, according to the methodology described by Casali et al. (2008)CASALI AO, DETMANN E, VALADARES FILHO SC, PEREIRA JC, HENRIQUES LT, FREITAS SG & PAULINO MF. 2008. Influence of incubation time and particles size on indigestible compounds contents in cattle feeds and feces obtained by in situ procedures. R Bras de Zootec 37: 335-342..
For evaluating nitrogen balance, total urine production was estimated by the concentration of creatinine in the urine. Spot urine samples were obtained approximately 4 h after feeding, from spontaneous urination in colostomy bags (Medsonda®) with a capacity of 200 mL. Samples were prepared according to the methodology of Valadares et al. (1999)VALADARES RFD, BRODERICK GA, VALADARES FILHO SC & CLAYTON MK. 1999. Effect of replacing alfalfa with high moisture corn on ruminal protein synthesis estimated from excretion of total purine derivatives. Jour of Dairy Scien 8: 2686-2696. and immediately frozen. Urine production was estimated by the equation proposed by Fonseca et al. (2006)FONSECA CEM, VALADARES RFD, VALADARES FILHO SC, LEÃO MI, CECON, PR, RODRIGUES MT, PINA DS, MARCONDES MI, PAIXÃO ML & ARAÚJO AM. 2006. Microbial protein synthesis in lactating goats fed diets with increasing levels of dietary protein. Rev Bras de Zootec 35: 1169-1177., where:
Feces were collected directly from the rectal bulb for five days at different times (0, 3, 6 and 9 hours after the first feeding) for a representative sampling. Furthermore, the feces samples used for digestibility tests were collected on different days, so two samplings were performed. Due to the small amount of feces collected per day, we chose to make two separate collections.
Blood samples were collected using 9.0 mL vacutainer tubes (Grainer Bio-One, Vacuette® Americana, SP, BRA), by puncturing the jugular vein, and 4 h after the morning feed. Two blood samples were collected from each animal; one in a tube containing an anticoagulant (EDTA) and another in a tube without the anticoagulant. The tubes with the anticoagulant were used for analyzing urea and total protein concentration, while samples without the anticoagulant were used for analyzing creatinine, total and direct bilirubin, albumin, alkaline phosphatase, alanine aminotransferase (ALT), aspartate aminotransferase (AST), and gamma-glutamyltransferase (GGT) levels. To determine urea and total protein concentration, serum was obtained by centrifuging the tubes at 3,293 × g for 15 min, identified and stored in Eppendorf® mini-tubes, and frozen for analysis. Blood parameters and urine creatinine were analyzed with commercial Labtest® kits using colorimetric procedures. Blood collections were made on two occasions, the first when the goats were 60 days pregnant and the second at 120 days.
Dry matter (DM) (method no. 934.01), organic matter (method no. 942.05), CP (method no. 954.01) and ether extract (EE) (method no. 920.39) levels were determined in the feed samples (leftovers and supplied) according to AOAC (2003)AOAC - ASSOCIATION OF ANALYTICAL CHEMISTS. 2003. Official Methods of Analysis, 17th 2nd rev. ed. Association of Analytical Chemists - AOAC, Gaithersburg, M. D, p. 1094.. The samples were treated with thermostable alpha-amylase for neutral detergent fiber (NDF) analysis, without the use of sodium sulfite (Mertens 2002MERTENS DR. 2002. Gravimetric determination of amylase-treated neutral detergent fiber in feeds with refluxing in beakers or crucibles: Collaborative study. Journ of AOAC Internat 85: 1217-1240.).
The concentration of NDF was corrected for ash as proposed by Mertens (2002)MERTENS DR. 2002. Gravimetric determination of amylase-treated neutral detergent fiber in feeds with refluxing in beakers or crucibles: Collaborative study. Journ of AOAC Internat 85: 1217-1240., and for proteins (NDFan) according to Licitra et al. (1996)LICITRA G, HERNANDEZ TM & VAN SOEST PJ. 1996. Standartization of procedures for nitrogen fractionation of ruminant feeds. Anim Feed Scien and Technol 57: 347-358.. The ADL fraction was extracted with 72% sulfuric acid (Van Soest et al. 1991VAN SOEST PJ, ROBERTSON JB & LEWIS BA. 1991. Methods for extraction fiber, neutral detergent fiber and nonstarch polysaccharides in relation to animal nutrition. Jour of Dairy Scien 74: 3583-3597.). Non-fibrous carbohydrate content (NFC) was calculated with an adaptation of the method proposed by Hall (2003)HALL MB. 2003. Challenges with non-fiber carbohydrate methods. J Anim Scien 81: 3226-3232. and NDF corrected for ashes and protein. Total carbohydrate (TC) content was obtained using the equation proposed by Sniffen et al. (1992)SNIFFEN CJ, O’CONNOR JD, VAN SOEST PJ, FOX DG & RUSSELL JB. 1992. A net carbohydrate and protein system for evaluating cattle diets: carbohydrate and protein availability. Jour Anim Scien 70: 3562-3577..
The quantity of total digestible nutrients (TDN) was calculated according to Weiss (1999)WEISS WP. 1999. Energy prediction equations for ruminant feeds. In: Proc. Cornell Nutrition Conference for Feed Manufacturers. Cornell University, Ithaca, USA, p. 176-185.. The total digestible nutrient values were converted into net energy (NE) for production (maintenance and growth) and digestible energy (DE), according to the equations suggested by the NRC (2001)NRC - NATIONAL RESEARCH COUNCIL. 2001. Nutrient Requirements of Dairy Cattle, 7th ed., Washington, DC: National Academy Press, 381 p.. The intake of TDN (TDNI) was calculated according to the methodology described by Sniffen et al. (1992)SNIFFEN CJ, O’CONNOR JD, VAN SOEST PJ, FOX DG & RUSSELL JB. 1992. A net carbohydrate and protein system for evaluating cattle diets: carbohydrate and protein availability. Jour Anim Scien 70: 3562-3577., as follows: TDNI = (CPI-CPf)+2.25(EEi-EEf)+(TCi-TCf). Where, CPI, EEI, and TCI correspond to the intakes of CP, EE, and TC, respectively; and CPf, EEf, and TCf represent the respective excretion of CP, EE, and TC in the feces. In the conversion of TDNI into metabolizable energy (ME), 1 kg of TDN was assumed to be equivalent to 4.409 Mcal DE, and ME = 0.82 × DE (NRC 2001NRC - NATIONAL RESEARCH COUNCIL. 2001. Nutrient Requirements of Dairy Cattle, 7th ed., Washington, DC: National Academy Press, 381 p.).
Nitrogen intake (NI), faecal nitrogen excretion (FN), and urinary nitrogen excretion (UN) were determined using the micro Kjeldahl technique (method no. 954.01) of the AOAC (2003)AOAC - ASSOCIATION OF ANALYTICAL CHEMISTS. 2003. Official Methods of Analysis, 17th 2nd rev. ed. Association of Analytical Chemists - AOAC, Gaithersburg, M. D, p. 1094.. Nitrogen balance (NB) was calculated according to the equation:
Retained nitrogen (RN) was calculated as:
Where BEN (basal endogenous nitrogen) = 0.35 × BW0.75, and dermal losses = 0.018 × BW0.75, according to the recommendations of the AFRC (1993)AFRC - AGRICULTURAL AND FOOD RESEARCH COUNCIL. 1993. Energy and Protein Requirements of Ruminants. Wallingford. CAB International, 159 p..
Data were initially subjected to normality tests (Shapiro-Wilks) and homoscedasticity tests (Levene), and to analysis of variance by the F test when the presuppositions were met, using the following model:
Where Yijk is the dependent variable corresponding to the experimental observation; μ is the overall mean; αi is the fixed effect of the diets; βj is the fixed effect of stages of pregnancy; (αβ)ij is the interaction effect; and eijk is the random error, assuming an independent normal distribution. Interaction between stages of pregnancy and diet was only deployed when significant at 5% probability by Tukey test. Statistical analyses were performed using the GLM procedure of SAS software version 9.4 (SAS INSTITUTE 2005SAS INSTITUTE. 2005. SAS system for Windows: versão 9.4. SAS Institute, Cary.).
RESULTS
There was effect (P<0.05) of diets and the stages of pregnancy on dry matter intake (DMI) and nutrients (Table III). The DMI was greater for the goats fed with SM and DCC Ca(OH)2, for both the values expressed in g/day and for those expressed in % of body weight (% BW), but the goats fed diets based on SM also did not differ from those who consumed a diet with DCC NaOH, when expressed in % BW. As well as the DMI, the intake of CP, EE, NDF and NDT were higher for the goats fed the diets based on SM and DCC Ca(OH)2. In relation to the effect of the stages of pregnancy, it was observed that, with the passing of the stages, the intake decreased significantly. Similarly, the intake of CP, EE, NDF and TDN decreased in 73.55; 42.11; 235.81 and 404.43 g/day, respectively.
Dry matter intake and nutrients of goats fed with detoxified castor cake (DCC) at different stages of pregnancy.
It has been observed that during pregnancy, the weight of the goats was amended by the diets (P<0.05). The goats fed with diet the basis of SM had greater weight in the parturition day. However, the postpartum weight was equal to the other (P>0.05). In addition, the weight of the goats generated was not influenced by the diets, nor was the body condition score in the pre and postpartum period and the weight of the young goats (Table IV).
Weight and body condition score of pregnant goats fed diets containing detoxified castor (DCC) by different alkali replacing soybean meal during gestation and weight of goats generated.
There was no effect (P>0.05) of diets or stage of pregnancy on the digestibility of DM and nutrients during the gestational period of goats (Table V).
Digestibility of dry matter and nutrients of goats fed with detoxified castor cake (DCC) at different stages of pregnancy.
The diets influenced (P<0.05) the consumption of nitrogen and the amount of nitrogen retained (Table VI). The goats fed the diets based on SM and DCC Ca(OH)2 consumed larger amounts of nitrogen, with average values of 17.13 and 16.78 g/day, respectively, while the goats fed with diet containing DCC NaOH consumed less quantity (15.01 g/day). Similarly, the content of nitrogen retained was lower for latter (10.28 g/day). The stages of pregnancy influenced (P<0.05) all the variables related to the nitrogen balance. In summary, during the first two-thirds of pregnancy, the goats presented larger values, with reductions of 42.56, 49.55, 49.74 and 39.14% for the nitrogen consumed, faeces, urine and nitrogen retained, respectively.
Nitrogen balance of goats fed with detoxified castor cake (DCC) at different stages of pregnancy.
We observed effect (P<0.05) of diets on the values of total protein, albumin, urea and gamma-glutamyl transferase (Table VII). The total protein and albumin content was in the goats that consumed the DCC NaOH diet (6.72 and 2.44 g/dL), but it did not differ from the goats fed with a diet based on DCC Ca(OH)2 (6.49 and 2.32 g/dL), which in turn were the values of goats that consumed the soybean meal diet. Urea showed an opposite behavior values of total protein and albumin, where the goats that consumed the diet the basis of SM showed higher content (31.16 mg/dL) and those who consumed the diet DCC NaOH lower content (27.70 mg/dL), however, the goats fed with DCC Ca(OH)2 did not differ from both diets (28.81 mg/dL). On another hand, the latter presented a higher amount of gamma-glutamyl transferase (65.78 IU/L).
Blood Parameters of goats fed with detoxified castor cake (DCC) at different stages of pregnancy.
In relation to stages of pregnancy, we observed effect (P<0.05) of the same on all blood parameters evaluated, with the exception of the aspartate aminotransferase (P>0.05). In summary, we observed a significant reduction in the levels of protein metabolites, which were: 18.95; 32.74; 17.06; 30.26; 17.34 for total proteins, direct bilirubin, albumin, urea, alkaline phosphatase, alanine aminotransferase, respectively, since the content of gamma-glutamyl transferase increased by approximately 30.74% in the final third of pregnancy.
DISCUSSION
The smallest DMI by goats fed with DCC NaOH may be related to the sodium content of the detoxified castor by this alkaline product (Table I), because according Yousfi et al. (2016)YOUSFI I, BEN SALEM H, AOUADI D & ABIDI S. 2016. Effect of sodium chloride, sodium sulfate or sodium nitrite in drinking water on intake, digestion, growth rate, carcass traits and meat quality of Barbarine lamb. Small Rumin Res 143: 43-52., the greater inclusion of sodium in the diet of ruminants provides a self-adjusting effect of voluntary intake by the animals. It should be noted that the quantity of sodium in the NaOH DCC (Table I) was 32.4 times higher than that in DCC Ca(OH)2, which highlights even more this effect in the control of DMI.
The DMI recommended by NRC (2007)NRC - NATIONAL RESEARCH COUNCIL. 2007. Nutrient Requirements of Small Ruminants. Washington, DC: National Academy Press, 362 p. for non-lactating goats with 42 kg of body weight is of 1593,24 g DM/day for the dual pregnancies. Taking the average of consumption throughout the gestational period, without taking into account the type of pregnancy, it was found that the average DMI was 1166,34 g DM/day. This result is 26.79% lower than the recommended intake by that system. With the passing of the pregnancy, DMI decreases due to factors such as compression of the digestive tract caused by the growth of pregnant uterus and increased serum levels of estrogen (Forbes 2007FORBES JM. 2007. Voluntary food intake diet selection in farm animals. 2nd ed. CAB International, Cambridge, p. 453.). On the other hand, in absolute terms, the coefficient of digestibility of diets increases, because the passage rate tends to be lower (Lu et al. 2005LU CD, KAWAS JR & MAHGOUB OG. 2005. Fibre digestion and utilization in goats. Small Rumin Res 60: 45-52.). Therefore, despite the diets did not have influenced the digestibility in both periods of pregnancy, there is a slight increase of values in the final third of pregnancy (Table IV).
The effect to DMI influenced the results of consumption of EE, NDF and TDN. This result was expected, since the intake of these nutrients is directly related to the amount of DM ingested. In relation to the consumption of TDN, the highest values observed in goats fed with SM and Ca(OH)2 TDN are justified by the greater amount of EE consumed (Danieli & Ronchi 2018DANIELI PP & RONCHI B. 2018. Developing a predictive model for the energy content of goat milk as the basis for a functional unit formulation to be used in the life cycle assessment of dairy goat production systems. Animal 12: 408-416.) and higher non-fiber carbohydrates.
The NRC (2007)NRC - NATIONAL RESEARCH COUNCIL. 2007. Nutrient Requirements of Small Ruminants. Washington, DC: National Academy Press, 362 p. recommends that the consumption of TDN for goats in this category is 1,089.25 g TDN/day, which indicates that all diets smite TDN requirements during the initial two-thirds of the pregnancy, even the goats fed the diet containing DCC NaOH (1107,78 g TDN/day). The consumption of TDN is directly the energy consumed and destined to the development of the mammary gland and of fetuses (Greenwood et al. 1998GREENWOOD PL, HUNT AS, HERMANSON JW & BELL AW. 1998. Effects of birth weight and postnatal nutrition on neonatal sheep: I. body growth and composition, and some aspects of energetic efficiency. J Anim Scien 76: 2354-2367.). In this way, it can be inferred that the replacement of soybean meal by DCC has not reduced the development of fetuses, considering that the weights of the goats at birth were not affected (Table IV), despite the significant reduction in the consumption of TDN in the final third of pregnancy. However, the same conclusion cannot be attributed to the development of the mammary gland, because milk production was not measured.
The consumption of CP was changed with the replacement of the SM by DCC NaOH. The NRC (2007)NRC - NATIONAL RESEARCH COUNCIL. 2007. Nutrient Requirements of Small Ruminants. Washington, DC: National Academy Press, 362 p. recommends that the consumption of CP for goats in this category is 172.41 g/day. In this way, the consumption of CP observed in this experiment has met the requirements of goats fed with diets containing SM and NaOH DCC during the initial two-thirds of pregnancy, being contrary to the goats fed with diets containing DCC NaOH (162.30 g CP/day). On the other hand, the absence of effect on the amount of nitrogen retained (Table VI) demonstrates greater efficiency in the use of this nutrient by goats fed with DCC NaOH, where it can be observed that the amount of nitrogen excreted in feces and urine were lower. In addition, the content of total protein and albumin was greater in the circulation of these goats (Table VII), which may be related to the greater utilization of nitrogen consumed. Under another perspective, it is important to note that in spite of the content of nitrogen retained have decreased in the final third of gestation, in percentage terms the content was higher in this phase (31.08%) that during the initial two-thirds (26.97%).
It is interesting to observe the efficiency of nitrogen use by goats fed with DCC NaOH, as they had the lowest nitrogen consumption, however the excretion of this nutrient, both in urine and faeces, was the same as goats fed with soybean meal and DCC Ca(OH)2 (Table VI). According to Araújo et al. 2020ARAÚJO RA, NEIVA JNM, ROGÉRIO MCP, CÂNDIDO MJD, EGITO AS, PEREIRA PL, LUCAS RC & POMPEU RCFF. 2020. Detoxification and nutritional profile of the detoxified castor by different alkaline solutions. Arq Bras de Med Vet e Zootec 72: 1947-1958., the DCC NaOH has a higher protein content of fraction A. Thus, it can be inferred that the DCC NaOH diet presents greater degradation of soluble proteins, favoring the availability of non-protein nitrogen, which justifies the positive nitrogen balance.
The largest proportion of nitrogen retention is derived from the intense protein metabolism of the fetus in the final third of the pregnancy, because according to Härter et al. (2017)HÄRTER CJ, SILVA HGO, LIMA LD, CASTAGNINO D, RIVERA AR, RESENDE KT & TEIXEIRA IAMA. 2017. Energy and protein requirements for maintenance of dairy goats during pregnancy and their efficiencies of use. J Anim Scien 95: 4181-4193.. The growth of the fetus in this period of gestation can match up to 93.6% of the total weight of the fetus, absorbing large quantities of proteins that are in circulation (Bell et al. 2005BELL AW, GREENWOOD PL & EHRHARDT RA. 2005. Regulation of metabolism and growth during prenatal life. In. Burrin, D.G. and Mersmann H.J. Biology of Metabolism in Growing Animals 3: 3-34.), which may be related, including, in does not change the content of total proteins in the circulation of goats fed with DCC NaOH (Table VII), despite the smaller intake of CP (Table III) during the final third of pregnancy.
The average levels of enzymes for hepatic and renal functions are within the standards for species, according to Smith & Sherman (2009)SMITH MC & SHERMAN DM. 2009. Goat Medicine. 2nd ed. Lea and Febiger, Philadelphia, 871 p.. It is interesting to observe that, in spite of the diets did not affect the levels of these enzymes, there was a decrease in the final third of gestation, except the aspartate aminotransferase, which was not altered (Table VII).
The reduction of these enzymes in the final third of pregnancy is common, because Huy (2005)HUY A. 2005. Biochemical tests in pregnancy. Austral Prescr 28: 98-101., says that all the enzymes related to liver function are usually reduced in the course of the pregnancy of mammals, due to the expansion of the extracellular fluid. This author affirms that only exception is for alkaline phosphatase, which is high during this period due to same be of placental origin, but the values observed, besides not having been influenced by the diets (Table VII) decreased in the final third of pregnancy. Despite this, the values were within the reference range for the species (Contreras et al. 2000CONTRERAS P, WITTWER F & BÖHMWALD H. 2000. Indicadores sanguíneos do metabolismo mineral em ruminantes. In: Perfil metabólico em ruminantes: seu uso em nutrição e doenças nutricionais. Porto Alegre, Brasil, Gráfica da Universidade Federal do Rio Grande do Sul, p. 75-88.), thus discarding a possible deficit in protein metabolism, which is common due to increased metabolic demand during pregnancy (Radin et al. 2015RADIN L, ŠIMPRAGA M, VINCE S, KORTELÍC A & MILINKOVIC-TUR S. 2015. Metabolic and oxidative status of Saanen goats of different parity during the peripartum period. Jour of Dairy Scien 82: 426-433.), which could be observed with the greatest concentration of urea in the blood, but the amount of this metabolite decreased with the passage of the pregnancy (Table VII).
In relation to the effect of the stages of pregnancy, Kalhan (2000)KALHAN SC. 2000. Protein metabolism in pregnancy. Amer Journ of Clin Nutrit 71: 1249-1255. asserts that it is common for decrease of the concentration of urea in pregnant, because this reduction is not only a result of increased glomerular filtration, but also due to a reduction in the hepatic synthesis. With the increase of progesterone and estrogen concentrations, the activity of the enzymes decreases the urea cycle (Ismail et al. 2008ISMAIL ZA, AL-MAJALI AM, AMIREH F & AL-RAWASHDEH OF. 2008. Metabolic profiles in goat does in late pregnancy with and without subclinical pregnancy toxemia. Veter Clin Pathol 37: 434-437.), otherwise you may be related to pregnancy toxemia. Since the reduction of albumin in the final third is related to the effect of dilution, due to the increase of other plasma proteins near the delivery (Rodríguez et al. 2009RODRÍGUEZ C, CASTRO N, CAPOTE J, MORALES-DELANUEZ A, MORENO-INDIAS I, SÁNCHEZ-MACÍAS D & ARGÜELLO A. 2009. Effect of colostrum immunoglobulin concentration on immunity in Majorera goat kids. Jour of Dairy Scien 92: 1696-1701.).
The enzymes related to liver metabolism, only the gamma-glutamyl transferase increased in the final third of the pregnancy. According to Radin et al. (2017)RADIN L, VUGROVEČKI AS, HLEDE JP, VINCE S, LJUBIČIĆ I & ŠIMPRAGA M. 2017. Blood metabolites of extensively reared Croatian multi-coloured goats during early lactation and early gravidity. Veterin Arhiv 87: 273-280., the levels of this enzyme increase physiologically next to childbirth. This behavior can be explained by fact that in ruminants there is transfer of this enzyme to fetuses. Therefore, there is an increase of this compound in maternal blood concentration, so that this enzyme is transferred to their offspring, mainly through the colostrum (Kaneko 2008KANEKO JJ, HARVEY JW & BRUSS ML. 2008. Clinical Biochemistry of Domestic Animals, 6th Academic Press, San Diego, p. 916.). In this way, you can also that diet with DCC Ca(OH)2 presented higher content of gamma-glutamyl transferase, which can passive immunity in calves (Silva et al. 2007SILVA SL, FAGLIARI JJ, BAROZA PFJ, CESCO FTRS & JORGE RLN. 2007. Evaluation of passive immunity in newborn goats feeding with goat and cow colostrum. ARS Veterin 23: 81-88.).
CONCLUSION
During the final third of gestation, the Saanen goats and Anglo Nubian diminish considerably the intake. The detoxified castor cake by alkaline solutions in replacement of soybean meal proved to be a viable alternative in the feeding of goats in pregnancy, because it does not affect the functionality of the liver and kidney function and the nitrogen balance. Diets formulated with detoxified castor by sodium hydroxide decrease the intake of dry matter and nutrients, but without negatively affecting the weight of the offspring.
ACKNOWLEDGMENTS
The authors thank the Dr. Ricardo Alves de Araújo (in memoriam) for his indispensable dedication and collaboration for the successful publication of this article; to the Coordenação de aperfeiçoamento de Pessoal do Nível Superior (CAPES) for financing the project and for post-graduate scholarships; to Embrapa Caprinos e Ovinos for all the technical and installation/infrastructure support; to the Fundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico (Funcap) and to the Conselho Nacional de Pesquisa (CNPq) for the grants; and to Agroindústria OLVEq Ltda. for donating the castor cake for conducting the research.
REFERENCES
- AFRC - AGRICULTURAL AND FOOD RESEARCH COUNCIL. 1993. Energy and Protein Requirements of Ruminants. Wallingford. CAB International, 159 p.
- ANANDAN S, ANIL KUMAR GK, GHOSH J & RAMACHANDRA KS. 2005. Effect of different physical and chemical treatments on detoxification of ricin in castor cake. Anim Feed Scien and Techn 120: 159-168.
- AOAC - ASSOCIATION OF ANALYTICAL CHEMISTS. 2003. Official Methods of Analysis, 17th 2nd rev. ed. Association of Analytical Chemists - AOAC, Gaithersburg, M. D, p. 1094.
- ARAÚJO RA, NEIVA JNM, ROGÉRIO MCP, CÂNDIDO MJD, EGITO AS, PEREIRA PL, LUCAS RC & POMPEU RCFF. 2020. Detoxification and nutritional profile of the detoxified castor by different alkaline solutions. Arq Bras de Med Vet e Zootec 72: 1947-1958.
- BELL AW, GREENWOOD PL & EHRHARDT RA. 2005. Regulation of metabolism and growth during prenatal life. In. Burrin, D.G. and Mersmann H.J. Biology of Metabolism in Growing Animals 3: 3-34.
- CASALI AO, DETMANN E, VALADARES FILHO SC, PEREIRA JC, HENRIQUES LT, FREITAS SG & PAULINO MF. 2008. Influence of incubation time and particles size on indigestible compounds contents in cattle feeds and feces obtained by in situ procedures. R Bras de Zootec 37: 335-342.
- CONTRERAS P, WITTWER F & BÖHMWALD H. 2000. Indicadores sanguíneos do metabolismo mineral em ruminantes. In: Perfil metabólico em ruminantes: seu uso em nutrição e doenças nutricionais. Porto Alegre, Brasil, Gráfica da Universidade Federal do Rio Grande do Sul, p. 75-88.
- DANIELI PP & RONCHI B. 2018. Developing a predictive model for the energy content of goat milk as the basis for a functional unit formulation to be used in the life cycle assessment of dairy goat production systems. Animal 12: 408-416.
- FONSECA CEM, VALADARES RFD, VALADARES FILHO SC, LEÃO MI, CECON, PR, RODRIGUES MT, PINA DS, MARCONDES MI, PAIXÃO ML & ARAÚJO AM. 2006. Microbial protein synthesis in lactating goats fed diets with increasing levels of dietary protein. Rev Bras de Zootec 35: 1169-1177.
- FORBES JM. 2007. Voluntary food intake diet selection in farm animals. 2nd ed. CAB International, Cambridge, p. 453.
- GIONBELLI TRS ET AL. 2014. Utilization of castor bean meal treated with calcium hydroxide fed wet or dry by lambs. Livest Scien 168: 76-783.
- GREENWOOD PL & BELL AW. 2003. Prenatal nutrition influences on growth and development of ruminants. Rec Adv in Anim Nutr in Austr 14: 57-73.
- GREENWOOD PL, HUNT AS, HERMANSON JW & BELL AW. 1998. Effects of birth weight and postnatal nutrition on neonatal sheep: I. body growth and composition, and some aspects of energetic efficiency. J Anim Scien 76: 2354-2367.
- HAFEZ ESE & HAFEZ B. 2004. Reprodução Animal. Tradução: original Renato Campanarut Barnabé - Barueri, SP. 7ª ed, 513 p.
- HALL MB. 2003. Challenges with non-fiber carbohydrate methods. J Anim Scien 81: 3226-3232.
- HÄRTER CJ, SILVA HGO, LIMA LD, CASTAGNINO D, RIVERA AR, RESENDE KT & TEIXEIRA IAMA. 2017. Energy and protein requirements for maintenance of dairy goats during pregnancy and their efficiencies of use. J Anim Scien 95: 4181-4193.
- HUY A. 2005. Biochemical tests in pregnancy. Austral Prescr 28: 98-101.
- ISMAIL ZA, AL-MAJALI AM, AMIREH F & AL-RAWASHDEH OF. 2008. Metabolic profiles in goat does in late pregnancy with and without subclinical pregnancy toxemia. Veter Clin Pathol 37: 434-437.
- KALHAN SC. 2000. Protein metabolism in pregnancy. Amer Journ of Clin Nutrit 71: 1249-1255.
- KANEKO JJ, HARVEY JW & BRUSS ML. 2008. Clinical Biochemistry of Domestic Animals, 6th Academic Press, San Diego, p. 916.
- KONYALI A, TÖLÜ C, DAS G & SAVAS T. 2007. Factors affecting placental traits and relationships of placental traits with neonatal behaviour in goat. Anim Reprod Scien 97: 394-401.
- LICITRA G, HERNANDEZ TM & VAN SOEST PJ. 1996. Standartization of procedures for nitrogen fractionation of ruminant feeds. Anim Feed Scien and Technol 57: 347-358.
- LIDEN DS, KEMYON PR, BLAIR HT, LOPEZ-VILLALOBOS N, JENKINSONS CMC, PETERSON SW & MACKENZIE DDS. 2009. Effects of ewe size and nutrition on fetal mammary gland development and lactational performance of offspring at their first lactation. Jour Anim Scien 87: 3944-3954.
- LU CD, KAWAS JR & MAHGOUB OG. 2005. Fibre digestion and utilization in goats. Small Rumin Res 60: 45-52.
- MENEZES DR, COSTA RG, ARAÚJO GGL, PEREIRA LGR, OLIVEIRA PTL, SILVA AEVN, VOLTOLINI TV & MORAES SA. 2012. Blood, liver and rumen parameters of sheep fed diets containing detoxified castor bean meal. Pesq Agropecu Bras 47: 103-110.
- MERTENS DR. 2002. Gravimetric determination of amylase-treated neutral detergent fiber in feeds with refluxing in beakers or crucibles: Collaborative study. Journ of AOAC Internat 85: 1217-1240.
- MORAND-FEHR P. 2005. Recent developments in goat nutrition and application: A review. Small Rumin Res 60: 25-43.
- NOCEK JE. 1988. In situ and other methods to estimate ruminal protein and energy digestibility: a review. J of Dairy Scien 71: 2051-2069.
- NRC - NATIONAL RESEARCH COUNCIL. 2007. Nutrient Requirements of Small Ruminants. Washington, DC: National Academy Press, 362 p.
- NRC - NATIONAL RESEARCH COUNCIL. 2001. Nutrient Requirements of Dairy Cattle, 7th ed., Washington, DC: National Academy Press, 381 p.
- POMPEU RCFF, CANDIDO MJD, PEREIRA ES, BOMFIM MAD, CARNEIRO MSS, ROGÉRIO MCP, SOMBRA WA & LOPES MN. 2012. Performance and carcass traits of sheep in feedlot and fed diets containing detoxified castor cake replacing soybean meal. Rev Bras de Zootec 41: 726-733.
- RADIN L, ŠIMPRAGA M, VINCE S, KORTELÍC A & MILINKOVIC-TUR S. 2015. Metabolic and oxidative status of Saanen goats of different parity during the peripartum period. Jour of Dairy Scien 82: 426-433.
- RADIN L, VUGROVEČKI AS, HLEDE JP, VINCE S, LJUBIČIĆ I & ŠIMPRAGA M. 2017. Blood metabolites of extensively reared Croatian multi-coloured goats during early lactation and early gravidity. Veterin Arhiv 87: 273-280.
- RODRÍGUEZ C, CASTRO N, CAPOTE J, MORALES-DELANUEZ A, MORENO-INDIAS I, SÁNCHEZ-MACÍAS D & ARGÜELLO A. 2009. Effect of colostrum immunoglobulin concentration on immunity in Majorera goat kids. Jour of Dairy Scien 92: 1696-1701.
- SAS INSTITUTE. 2005. SAS system for Windows: versão 9.4. SAS Institute, Cary.
- SILVA SL, FAGLIARI JJ, BAROZA PFJ, CESCO FTRS & JORGE RLN. 2007. Evaluation of passive immunity in newborn goats feeding with goat and cow colostrum. ARS Veterin 23: 81-88.
- SMITH MC & SHERMAN DM. 2009. Goat Medicine. 2nd ed. Lea and Febiger, Philadelphia, 871 p.
- SNIFFEN CJ, O’CONNOR JD, VAN SOEST PJ, FOX DG & RUSSELL JB. 1992. A net carbohydrate and protein system for evaluating cattle diets: carbohydrate and protein availability. Jour Anim Scien 70: 3562-3577.
- VALADARES RFD, BRODERICK GA, VALADARES FILHO SC & CLAYTON MK. 1999. Effect of replacing alfalfa with high moisture corn on ruminal protein synthesis estimated from excretion of total purine derivatives. Jour of Dairy Scien 8: 2686-2696.
- VAN SOEST PJ, ROBERTSON JB & LEWIS BA. 1991. Methods for extraction fiber, neutral detergent fiber and nonstarch polysaccharides in relation to animal nutrition. Jour of Dairy Scien 74: 3583-3597.
- WEISS WP. 1999. Energy prediction equations for ruminant feeds. In: Proc. Cornell Nutrition Conference for Feed Manufacturers. Cornell University, Ithaca, USA, p. 176-185.
- YOUSFI I, BEN SALEM H, AOUADI D & ABIDI S. 2016. Effect of sodium chloride, sodium sulfate or sodium nitrite in drinking water on intake, digestion, growth rate, carcass traits and meat quality of Barbarine lamb. Small Rumin Res 143: 43-52.
Publication Dates
-
Publication in this collection
10 Oct 2022 -
Date of issue
2022
History
-
Received
13 Nov 2020 -
Accepted
1 May 2021