Next Article in Journal
Prevalence of Shiga Toxin-Producing Escherichia coli O157 in Wild Scottish Deer with High Human Pathogenic Potential
Previous Article in Journal
Reliability Associated with the Measurement of Continuous Variables in Veterinary Medicine: What the Different Possible Indicators Tell, and How to Use and Report Them
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Capsaicin and 1,25-Dihydroxyvitamin D3 Glycoside: Effects on the Reproductive Performance of Hyper-Prolific Sows

by
Julie Gabriela Nagi Dario
1,
Eduardo Raele de Oliveira
2,
Rodrigo Pereira de Souza
2,
Sabrina Theodorovicz
1,
Giovana Chimentão Bernini
1,
Gabriela Ruiz
1,
Rafael Humberto de Carvalho
1 and
Caio Abércio da Silva
1,*
1
Animal Science Program, Center of Agrarian Sciences, State University of Londrina, Londrina 86057-970, PR, Brazil
2
Project Coordinator and Assistant at NutriQuest TechnoFeed, São Paulo 13025-320, SP, Brazil
*
Author to whom correspondence should be addressed.
Animals 2023, 13(17), 2794; https://doi.org/10.3390/ani13172794
Submission received: 20 June 2023 / Revised: 26 August 2023 / Accepted: 27 August 2023 / Published: 2 September 2023
(This article belongs to the Section Pigs)

Abstract

:

Simple Summary

To investigate the potential benefits of phytogenic additives in improving the reproductive performance of sows, we evaluated the effects of capsaicin (CAP) and vitamin D3 [1,25-(OH)2D3], obtained from Capsicum spp. and Solanum glaucophyllum, respectively. Our experiments examined the effects of these additives when used in combination or individually. The results of our study indicate that supplementing diets with vitamin 1,25-(OH)2D3 can reduce the duration of farrowing, stillbirths, and dystocia rate. Colostrum production was also significantly higher in sows that received Vit 1,25-(OH)2D3 supplementation. Furthermore, the use of these additives contributed to litter growth and reduced the incidence of diarrhea in piglets. These findings suggest that CAP and Vit 1,25-(OH)2D3 could serve as valuable tools to improve the reproductive performance of sows.

Abstract

This study evaluated the effect of a natural source of vitamin D3 [1,25-(OH)2D3] and capsaicin (CAP) in the dietary supplementation of sows in the final phase (85–114 days) of gestation (Gest) and lactation (Lact) on the reproductive performance of the sows and health of piglets through two experiments (Exp I and II). In Exp I, 120 sows were subjected to four treatments: T1—control (without [1,25-(OH)2D3] and supplemental CAP); T2—3.5 µg 1,25-(OH)2D3/Gest/day and 7.0 µg Vit 1,25-(OH)2D3/Lact/day; T3—7.0 µg CAP/Gest/day and 14.0 µg CAP/Lact/day; T4—1.75 µg Vit 1,25-(OH)2D3 + 3.5 µg CAP/Gest/day and 3.5 µg 1,25-(OH)2D3 + 7.0 µg CAP/Lact/day. In Exp II, 200 sows were randomly blocked, factorial 2 × 2 (without or with Vit 1,25-(OH)2D3 and without or with CAP): T1—control (without Vit 1,25-(OH)2D3 and CAP); T2—3.5 µg Vit 1,25-(OH)2D3/Gest/day and 7.0 µg Vit 1,25-(OH)2D3/Lact/day; T3—7.0 µg CAP/Gest/day and 14.0 µg CAP/Lact/day; T4—3.5 µg Vit 1,25-(OH)2D3 + 7 µg CAP/Gest/day; and 7.0 µg Vit 1,25-(OH)2D3 + 14.0 µg CAP/Lact/day. The duration of delivery (3:48 vs. 4:57 h) and the percentage of stillbirths (5.37% vs. 7.61%) were improved (p < 0.05) in the group that received Vit 1,25-(OH)2D3 (Exp II) compared to the control group. Moreover, the dystocia rate decreased (p < 0.05) in Exp II, which received Vit 1,25-(OH)2D3 (4.21 vs. 27.63%), and in Exp I, which received the combination of Vit 1,25-(OH)2D3 + CAP (12 vs. 40%) compared to the respective control groups. Colostrum production was greater (p < 0.05) in sows that received Vit 1,25-(OH)2D3 supplementation compared to the control group, consequently resulting in higher colostrum intake (p < 0.05) of the piglets (330 vs. 258 g/piglet). The additives reduced the incidence of diarrhea (p < 0.05) in piglets (Exp I and II). Thus, the use of additives improved the reproductive performance of sows and contributed to litter growth.

1. Introduction

The high reproductive rate of commercial sows results in lower birth weight and less uniform piglets at birth [1]. Additionally, these sows have a prolonged farrowing duration, necessitating increased physical effort and energy demands [2]. This leads to variations in plasma glucose levels, consequently contributing to an elevated stillborn rate and reduced piglet vitality [3].
Longer farrowing lengths in sows may increase the calcium demand of the sow, which might exhibit hypocalcemia [4]. In line with this finding, hyper-prolific sows present electrolyte homeostasis deficiencies (Ca, Mg, and P) around and during parturition, reflecting the large number of dystocic farrowings [5]. Large litters also have limited colostrum intake, impairing passive and active immuno-protection and predisposing them to diseases and poor performance [6].
Hyper-prolific sows have recognized high and specific nutritional requirements [7], and some recent experiments with the use of phytogenic additives aimed at meeting these demands have shown good results. In this group of additives, capsaicin obtained from pepper (Capsicum spp.) has known flavoring properties with effective gastroprotective and antioxidant activities [8]. It also stimulates the production and secretion of bile acids by the liver [9].
Capsaicin, when combined with other plant extracts, has been associated with the replacement of growth-promoting antibiotics in animal production, stimulating appetite, improving digestion, and acting as a modulator of the intestinal microbial ecosystem [10]. The use of these compounds increases immune status through the control of intestinal intraepithelial lymphocytes and via potent anti-inflammatory effects that reduce gastrointestinal challenges [8].
Conversely, vitamin D, whose main role is calcium and phosphorus homeostasis involved in several metabolic processes [11], has an extremely limited presence in plants; however, with some exceptions, vitamin D is found in the species Solanum glaucophyllum, Solanum malacoxylon, Cestrum diurnum, and Trisetum flavescens [12] in the form of glycosylated 1,25-dihydroxyvitamin D3 (vitamin D3) [13], a water-soluble molecule with high stability and bioactivity, compared with calcitriol [14].
In animals, the concentrations of vitamin 1,25-(OH)2D3 in tissues depend on its content in the diet and/or exposure to sunlight. During gestation and lactation, there is a significant increase in calcidiol in the blood plasma (the main circulating form of vitamin D). This condition indicates a high demand for calcium in these important moments involving reproduction [15], highlighting the role of vitamin D3.
Identifying natural additives that can meet the demands of the reproductive phases of sows is compatible with trends in the segment. This confers greater welfare and productive efficiency to sows and their litters. Several previous studies have highlighted the individual effects of capsaicin and vitamin D3 [1,25-(OH)2D3] supplementation in sow diets, suggesting that these phytogenic additives have the potential to improve reproductive performance. Based on these findings, we hypothesize that the use of these additives, either individually or in combination, can lead to positive outcomes in sow reproductive performance. Therefore, the objective of this study was to evaluate two plant-based dietary additives, capsaicin and vitamin 1,25-(OH)2D3, administered via feed, combined or not, to sows from day 85 of gestation to weaning, on reproductive performance and piglet health.

2. Materials and Methods

This experiment was conducted under the approval protocol of the Ethics Committee on Animal Use of the State University of Londrina (Universidade Estadual de Londrina—CEUA/UEL), number 060/2020.
The source of 1,25-dihydroxyvitamin D3 glycoside used in this study was the commercial product Panbonis® (10 mg of 1,25-dihydroxyvitamin D3 glycoside/kg), which is the base of the Solanum glaucophyllum plant. Capsaicin, an active ingredient extracted from Malagueta pepper (Capscicum frutescens), originated from the commercial product Capsin®.
The evaluations were conducted in two commercial farms, with capacities of 2000 (Experiment I) and 6000 sows (Experiment II). Both farms did not have air conditioning systems in the gestation and lactation phases.
The farms were free of Porcine Reproductive and Respiratory Syndrome (PRRS) and Porcine Epidemic Disease (PEDv), and the sows received the vaccine Porcilis® Ery+Parvo+Lepto (MSD Animal Health) 30 days before mating.
The evaluation in both experiments started at 85 days of gestation and ended at weaning of piglets (21 days old), with an average of 50 days of trial.
For the first test, 120 sows were used, subjected to an experimental design in randomized blocks in three groups by parity order (parity 1 and 2, parity 3 and 4, parity 5–6) of 40 sows per block. Within each block, sows were randomly distributed among the 4 treatments, with 30 replicates (sows), with the sow and its respective litter being the experimental units. In Experiment II, 200 sows were subjected to a 2 × 2 factorial design, divided into randomized blocks per parity order (parity 1 and 2, parity 3 and 4, parity 5–6), with the use of capsaicin and vitamin 1,25-(OH)2D3 as factors. There were 50 replicates per treatment in this experiment, with the sow and its litter being the experimental units.
In Experiment I, 120 sows were subjected to a randomized block design with four treatments: T1—control (without Vit 1,25-(OH)2D3 and supplemental capsaicin); T2—3.5 µg Vit 1,25-(OH)2D3/gestation/day and 7.0 µg Vit 1,25-(OH)2D3/lactation/day; T3—7.0 µg capsaicin/gestation/day and 14.0 µg capsaicin/lactation/day; T4—1.75 µg Vit 1,25-(OH)2D3 + 3.5 µg capsaicin/gestation/day and 3.5 µg Vit 1,25-(OH)2D3 + 7.0 µg capsaicin/lactation/day.
In Experiment II, 200 sows were randomly blocked, factorial 2 × 2 (without or with inclusion of Vit 1,25-(OH)2D3; and without or with inclusion of capsaicin), as follows: T1—control (without Vit 1,25-(OH)2D3 and supplemental capsaicin); T2—3.5 µg Vit 1,25-(OH)2D3/gestation/day and 7.0 µg Vit 1,25-(OH)2D3/lactation/day; T3—7.0 µg capsaicin/gestation/day and 14.0 µg capsaicin/lactation/day; T4—3.5 µg Vit 1,25-(OH)2D3 + 7 µg capsaicin/gestation/day; and 7.0 µg Vit 1,25-(OH)2D3 + 14.0 µg capsaicin/lactation/day.
In both experiments, during the gestation phase, the sows were housed individually in crates and fed once a day. In the lactation phase, the sows were housed at 110 days of gestation in individual farrowing crates and kept there until weaning. From farrowing to weaning, the dose of additives offered during the gestation phase was doubled, being administered at the first meal of the day at 7:30 a.m. In total, four food treatments were practiced daily, characterizing ad libitum food management in the lactation phase. The gestation and lactation feeds used in Experiments I and II are shown in Table 1.
From the beginning to the end of the farrowing, the following variables regarding the reproductive performance of the sows were analyzed: (1) duration and type of delivery (normal or dystocic), (2) use of oxytocin, (3) total born, (4) percentage of born alive, (5) percentage of stillbirths, (6) percentage of mummified, (7) percentage of piglets born weighing less than 0.900 kg, (8) total litter weight at birth, (9) individual weight of the piglet at birth, (10) daily feed intake of the lactating sow, and (11) amount of colostrum produced. Farrowing progress was considered normal or dystocic. Normal was defined as a farrowing process taking place without obstetrical intervention. Dystocic was defined as when no piglet was delivered for more than 60 min and a manual obstetric intervention was carried out. In this case, fetuses accessible by hand were carefully pulled out. When no piglets were in the birth canal during manual obstetric interventions and there was no uterine contraction, the use of oxytocin during farrowing was allowed. In order to predict the colostrum produced through the weight of the piglets at birth and 24 h later, the equation described by Devillers et al. [16] was used:
CI = −217.4 + 0.217 × t + 1861019 × BW/t + BWb × (54.80 − 1861019/t) × (0.9985 − 3.7 × 10−4 × tFS + 6.1 × 10−7 × tFS2),
where CI = colostrum intake from t0 (g); BW = actual body weight (kg); BWb = body weight at birth (kg); t = time elapsed from t0 (min); tFS = interval between birth and first sucking (min).
For the analyses of the reproductive performance, the piglets were identified individually with ear tags and weighed at the following times: (1) birth, (2) 24 h after birth, (3) after litter standardization, 2nd day of age, (4) at 10 days of age, and (5) at weaning. The results of this weighing were expressed as the mean piglet weight, litter weight, and daily weight gain (DWG). The percentage of mortality 24 h after birth and the amount of colostrum ingested were also observed.
Immediately after the movement of the piglets for the uniformity of the litters, the presence or absence of diarrhea was observed and classified, according to the protocol of Liu [17], into 1—liquid feces, 2—creamy feces, 3—pasty feces, and 4—normal stools. For data analysis, the stall was considered the experimental unit, and if at least one animal had a score below 3, the stall was considered positive for diarrhea. The same evaluation was performed at the time of weaning.
In both experiments, 40 sows (10 per treatment), six hours after the beginning of parturition, were submitted to blood collection by puncture (5.0 mL syringe, 40 × 10 mm needle) of the vessels in the neck region to determine the levels of serum calcium, phosphorus, C-reactive protein, and cortisol. The samples were collected in vacutainer tubes without anticoagulant for biochemical analysis and subsequently centrifuged (1000 rpm, 15 min). Calcium and phosphorus levels were evaluated using colorimetric biochemical methodology in a semiautomatic reader (Mindray BA-88A, Londrina, Paraná, Brazil). C-reactive protein was determined using the agglutination methodology (Gold Analise, Londrina, Paraná, Brazil), and for cortisol the chemiluminescence method (Immulite 2000 Immunoassay System) was used.
The trial design of Experiment I involved casual blocks, and data were analyzed with ANOVA (GLM) with the block and treatment with Tukey’s test for mean comparison. The trial design of experiment II was a full factorial design with blocks (2 × 2), with two additives as factors in experiment II. The assumption of data normality was tested using the Ryan–Joiner test (a test similar to Shapiro–Wilk), and the null hypothesis expressed that the residual data presented a normal distribution and that data not normally distributed were transformed (X2 + 1 or logx) before analysis. For diarrhea and other parameters related to frequency (percentage of dystocia rate, oxytocin use, and piglets below 900 g), a Chi2 test was applied. Statistical analysis was performed using Minitab (Version 21.2.0). The differences were considered significant with a probability level of 95% (p < 0.05) and as a trend with a probability level of 90% (p ≤ 0.10). The parity order was considered a block for the statistical design. ANCOVA (analysis of covariance) was used to determine the reproductive performance of sows (Experiment I), adjusting/controlling for piglet number and weight (kg) variables (covariates).

3. Results

3.1. Reproductive Performance of Sows

For Experiment I, there was a difference in the dystocia rate (p = 0.017), where vitamin 1,25-(OH)2D3 + capsaicin treatment (both at half dose) resulted in a lower occurrence of complications. Compared to the control group, there was an increase of approximately 233.33% in the incidence of dystocia births (Table 2).
Sows fed diets based on vitamin 1,25-(OH)2D3 + capsaicin had a lower percentage of piglets with body weights (p = 0.044) below 900 g at birth, which reflected a higher individual body weight at birth (1.360 kg), differing from the other treatments (Table 2). The sows that received the treatments supplemented with vitamin 1,25-(OH)2D3 and vitamin 1,25-(OH)2D3 + capsaicin had higher colostrum production (p = 0.003), reflecting the higher consumption of this supplement by the piglets (p = 0.001), with a positive effect on weight gain 24 h after birth (p = 0.001) (Table 2).

3.2. Reproductive Performance of Sows after Litter Standardization

In Experiment I (Table 3), the average number of piglets per sow after uniformity of litters favored the control group (p = 0.024). However, piglets from sows that received vitamin 1,25-(OH)2D3 showed higher body weight 10 days after the litter standardization compared to the other treatments (p = 0.001), with a daily weight gain higher than the treatment that associates vitamin 1,25-(OH)2D3 and capsaicin.
At weaning, the highest weight was maintained for those from sows that received vitamin 1,25-(OH)2D3, which was higher than the control group (p = 0.033).
During lactation, sows with capsaicin supplementation had a higher feed intake (7.938 kg) than sows that consumed diets supplemented with vitamin 1,25-(OH)2D3 (Table 3), but there was no difference in the feed efficiency between the treatments.

3.3. Incidence of Diarrhea

In Experiment I, piglets born to sows that consumed diets supplemented with the evaluated additives had a lower (p = 0.001) incidence of diarrhea in the first week of life (Table 4).

3.4. Blood Analyses

The results of blood analysis of the sows in Experiment I did not differ between treatments (Table 5).

3.5. Reproductive Performance of Sows

Considering the total number of piglets born, in Experiment II (Table 6), vitamin 1,25-(OH)2D3 supplementation resulted in faster births (with 1 h less duration) compared to the control group (p = 0.001). For dystocia, the group supplemented with vitamin 1,25-(OH)2D3, with or without capsaicin, showed better results. Thus, when associated with capsaicin, a ratio of 8.16 versus 20.65% dystocia was observed, whereas, for the condition not associated with capsaicin, there was a ratio of dystocia of 8.60 versus 19.58%. With the shorter delivery time, the percentage of stillborn was also lower for the group of sows that received vitamin 1,25-(OH)2D3 (p = 0.026) (Table 6).

3.6. Reproductive Performance of Sows after Litter Standardization

For Experiment II (Table 7), the individual weights of piglets from sows that received capsaicin were better at the time of standardization (p = 0.001), a result that persisted until the 10th day of life, indicating better DWG in the period. However, there was interaction between the vitamin and capsaicin factors for piglet weight at 10 days of age and for piglet DWG in this interval (2nd to 10th day of life).
Piglets from sows that did not receive capsaicin but were supplemented with vitamin D3 had a better DWG (p = 0.018) and weight at this age (p < 0.001) in relation to piglets born from sows not supplemented with vitamin 1,25-(OH)2D3, respectively, 0.220 versus 0.232 kg, and 3.357 versus 3.444. Similarly, piglets born to sows that did not receive vitamin 1,25-(OH)2D3 and that were supplemented with capsaicin had better DWG (p < 0.001) and better weight at this age (p < 0.014) in relation to piglets born from sows not supplemented with capsaicin, respectively, 0.220 versus 0.232 kg, and 3.357 versus 3.503 kg. Considering the entire lactation period, the feed consumption was similar between the factors, but the feed efficiency was better for sows that received capsaicin. At weaning, there was no interaction between factors or significant differences between capsaicin and vitamin 1,25-(OH)2D3 supplementation for all parameters evaluated.

3.7. Incidence of Diarrhea

In Experiment II, the frequency of diarrhea was significantly lower in the first week of life in piglets born of sows that received capsaicin (Table 8), and the supplementation with capsaicin and vitamin 1,25-(OH)2D3 resulted in lower frequencies of weaning diarrhea. There was an interaction of vitamin and capsaicin factors in this digestive disorder in the first week (p = 0.025) and at weaning (p < 0.001). Regarding the weaning week, piglets from sows that received vitamin 1,25-(OH)2D3, associated (3.18 versus 9.52%) or not associated (3.67 versus 8.76%) to capsaicin, showed minor clinical signs of diarrhea.

3.8. Blood Analyses

In Experiment II, compared to sows in the control group, sows that received 1,25-(OH)2D3 showed a trend of higher serum calcium levels (p = 0.07) (Table 9). The other blood parameters did not differ among the treatments (p > 0.05).

4. Discussion

The use of vitamin 1,25-(OH)2D3 and capsaicin in combination, either with a half dose or higher doses, was effective regarding the reproductive performance in both experiments. The positive results of vitamin 1,25-(OH)2D3, administered alone or in combination with capsaicin, regardless of the dose, on the frequency of dystocic births are promising, considering that modern sows are, due to hyper-prolificity [18], more likely to experience birth dystocia [5].
These results are attributed to the mechanism of the direct action of vitamin 1,25-(OH)2D3 on the homeostasis of calcium and phosphorus, minerals that are associated with uterine contraction [19]. Blim et al. [5] found an increased calcium level at the onset of the fetal expulsion stage. Immediately after the end of parturition, there was a sustained increase in Ca, which was clearly above the levels prior to farrowing. These findings show that calcium is a crucial electrolyte for the parturition process and an important messenger in the myometrial contraction mechanism [5]. In addition, vitamin D3 plays an important role in binding to the vitamin D receptor and activating several interaction pathways, which results in an increase in calcium in the circulation [20]. These effects are confirmed by muscle strength during parturition, which is influenced by the vitamin D receptor, which is capable of modulating hormones involved in uterine contraction [5,21].
The anti-inflammatory and analgesic properties of capsaicin may also have contributed to the reduction in dystocia births. Pepper extract is one of the main TRPV1 receptor agonists, causing desensitization via nociceptor dysfunction, resulting in decreased pain perception [22], a common framework during the calving process.
Although the serum calcium level in this study did not differ in both experiments, the tendency towards a higher level of the circulating mineral may be related to better absorption and metabolism than vitamin D3 (cholecalciferol) provides [23]. In another study, an increase in calcium levels was reported when using vitamin 1,25-(OH)2D3 in monogastric diets [13].
The decrease in the parturition time of sows supplemented with vitamin 1,25-(OH)2D3 supports the hypothesis of an increase in circulating Ca2+ at the time of parturition, which provides a more potent contraction of the myometrium and a lower number of stillborn [24]. This discussion on the increase in serum calcium level is also corroborated by the results found in Experiment II (Table 6), in which sows treated with vitamin 1,25-(OH)2D3 and vitamin 1,25-(OH)2D3 + capsaicin had a lower incidence of complicated parturition, shorter duration of parturition, and lower incidence of stillbirths. These results are consistent with the findings of Elrod et al. [25]; in that study, sows that received a supplement based on calcium chloride in the diet had a shorter delivery time and a lower rate of stillbirths than those in sows who did not receive this supplement. In this scenario, Blim et al. [5] observed that a large proportion of sows have previously unknown deficiencies in electrolyte homeostasis (Ca, Mg, and P) around and during parturition, which is reflected by the large number of dystocic farrowings and the deficiencies in electrolyte concentrations during dystocia. Borges et al. [18] suggested that the longer the calving time, the greater the number of stillborn, and the main reason for this is the interruption of blood flow in the placenta, resulting in hypoxia in the later animals, which, even if they do not die, may become lethargic and nonviable.
In Experiment I, the lower rate of piglets born weighing less than 900 g from sows that received vitamin 1,25-(OH)2D3 + capsaicin in the diet (Table 2) may indicate a better efficiency of these diets in the final period of gestation. According to Yuan [25], birth weight depends on the amount of nutrients available in the body, which are transferred to piglets via the placenta. Thus, the benefits of this active ingredient, which is related to improving enzyme secretion and intestinal integrity through inhibiting gastrin release and stimulation of somatostatin [9], may support these results.
Such effects may also support the best results for the feed intake of sows (Experiment I) when they received capsaicin, reaching an average intake of 7.938 kg feed/day. This result is also important for lactating sows due to their high catabolism, which can lead to greater mobilization of their body reserves, with losses in the subsequent cycle [26]. This finding can be attributed to the effect of tolerance to endogenous heat sensation by the sow, which this alkaloid provides from the desensitization of TRPV receptors responsible for the sensation of pain and heat in the body [27]. A higher feed intake during lactation or attenuation of catabolism during this phase improves reproductive performance in the subsequent cycle [28].
The mechanism of action of vitamin 1,25-(OH)2D3 on the digestive response is attributed to the activation of sensors of the gastrointestinal tract, such as transient member 1 of subfamily V of the cation channel, in the potential of the transient receptor [22]. In Experiment I, the sows that received only vitamin D3 supplementation had a lower feed intake. However, because vitamin 1,25-(OH)2D3 promotes better intestinal absorption of Ca2+, which contributes to the promotion of the plasma level of the mineral [29], the improvement in the zootechnical performance of the piglets observed in this treatment is probably due to the effects of the increased vitamin level in the milk fat and protein contents [30].
The results indicate that the performance of the piglets (Experiments I and II) was effectively influenced by the dietary supplementation of the sows with vitamin 1,25-(OH)2D3 and the association of this supplementation with capsaicin. These gains may be attributed to higher colostrum intake and lower occurrence of diarrhea compared to animals in the control group. The higher intake of colostrum (evaluated only in Experiment I) is justified by the higher production of colostrum by sows fed vitamin 1,25-(OH)2D3) (Table 2). Vitamin receptors are present in more than 90% of body tissues and play an important role in regulating hormones, such as oxytocin, which plays an intrinsic role during delivery and in the ejection of colostrum [12].
In Experiment I, the best results found in the daily weight gain of the piglets in the first 24 h after birth (Table 2), in the weight at the time of uniformity, and at 10 days of life, persisting until weaning (Table 4), are identified with the observations of Devillers et al. [6], which demonstrated that satisfactory colostrum intake can have positive effects on piglet growth up to three weeks after weaning.
The reason why piglets from sows that consumed the control diet or were supplemented with capsaicin alone had a lower colostrum intake than piglets from sows treated with vitamin 1,25-(OH)2D3 and vitamin 1,25-(OH)2D3 + capsaicin (observed in Experiment I) is attributed to the greater duration of delivery and higher percentage of stillbirths within the control group, which led to losses in colostrum synthesis, an approach advocated by Langendijk and Plush [31].
Specifically, related to capsaicin and Vit 1,25-(OH)2D3, the best weights found after animal standardization and at 10 days of life observed in Experiment II (Table 7) correspond to the findings of Matysiak et al. [32], who worked with different plant extracts (carvacrol, cinnamaldehyde, and capsaicin) in the diets of lactating sows and observed an increased lactose concentration in milk, with positive effects on the performance and survival rate of piglets. It is possible that the greater body weight gain of the piglets that we observed is attributed to the higher milk production determined by this capsaicinoid, possibly due to the higher feed intake and use of dietary nutrients. Related to this effect, capsaicin positively influenced feed efficiency, showing a synergistic relationship with litter weight gain and sow feed consumption.
Capsaicin also has recognized antioxidant and anti-inflammatory activity, intervening beneficially in the course of enteric diseases, thus contributing to intestinal health [33] and the production of inflammatory molecules in peritoneal macrophages stimulated by lipopolysaccharides (LPS), showing significant inhibitory activity in the production of prostaglandin E2 (PGE-2) induced by LPS by peritoneal macrophages [8].
The beneficial effects of additives in pig diets have been widely verified in terms of reducing the occurrence of diarrhea and promoting the health of the gastrointestinal tract [34], as observed in both experiments. Along these lines, Liu et al. [35] evaluated different plant extracts (oleoresin capsicum, botanical garlic, and turmeric oleoresin) in pig diets and found effective activation of immune responses and expression of genes involved in tight junctions, indicating that both effects may increase intestinal mucosal immunity and function of the intestinal barrier. This finding is in line with the results of the present study, where we observed a reduction in the occurrence of diarrhea in piglets from sows that received capsaicin in their diet.
Capsaicin exerts recognized pharmacological effects with modulatory properties in the activation or inhibition of several biochemical and immunological pathways [36]; however, the piglets kept with sows that received vitamin 1,25-(OH)2D3 showed a similar response (Experiments I and II). This finding is attributed to the effect of vitamin 1,25-(OH)2D3 in relieving intestinal injury and inhibiting the intestinal immune response induced by pathogens, with an effect on the expression of tight junction proteins to maintain the integrity of the intestinal barrier [37].
Concomitantly, vitamin 1,25-(OH)2D3 has a potential physiological role in the regulation of immune responses, along with the vitamin D receptor, which is induced after the activation of pathogen recognition receptors and can induce the synthesis of antibacterial proteins [38], which promotes improvements in the general health of animals through various nongenomic mechanisms, such as protein expression, inflammation, oxidative stress, and cellular metabolism [19].
Dietary supplementation with plant extracts, vitamin 1,25-(OH)2D3, and capsaicin during the final third of gestation and lactation reduced the occurrence of dystocic births and decreased the incidence of diarrhea in litters. The isolated use of natural vitamin 1,25-(OH)2D3 increased colostrum production, decreased the calving time and number of stillbirths, and maintained the best piglet weight until weaning. The unique use of capsaicin led to higher feed intake and was also positive in the litter evolution. Thus, the use of additives improved the reproductive performance of sows and contributed to litter growth.

5. Conclusions

Vitamin 1,25-(OH)2D3 and capsaicin can be used as additives to improve the farrowing efficiency and colostrum production, with positive consequences for the performance of piglets until weaning, representing resources to improve the performance of high-prolific sows. Additionally, these additives are capable of minimizing diarrhea in suckling piglets. The evaluated doses and the association of additives must be considered in their use while considering the magnitude of their actions and the cost–benefit results.

Author Contributions

Conceptualization, J.G.N.D., E.R.d.O. and C.A.d.S.; methodology, J.G.N.D., E.R.d.O., R.P.d.S., S.T., G.R. and G.C.B.; formal analysis, C.A.d.S., E.R.d.O. and R.H.d.C.; investigation, J.G.N.D., S.T., G.R. and G.C.B.; resources, E.R.d.O., R.P.d.S. and C.A.d.S.; data curation, C.A.d.S. and E.R.d.O., writing—original draft preparation, J.G.N.D. and R.H.d.C.; writing—review and editing, C.A.d.S. and R.H.d.C.; supervision, C.A.d.S., E.R.d.O. and J.G.N.D.; project administration, C.A.d.S. and E.R.d.O. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

This study was conducted according to the recommendations of the National Council for the Control of Animal Experimentation (Conselho Nacional de Controle de Experimentação Animal—CONCEA). This study was approved by the Ethics Committee on Animal Use of the State University of Londrina (Universidade Estadual de Londrina—CEUA/UEL), number 060/2020.

Informed Consent Statement

Not applicable.

Data Availability Statement

The datasets generated during and/or analyzed during the current study are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Zotti, E.; Resmini, F.A.; Schutz, L.G.; Volz, N.; Milani, R.P.; Bridi, A.M.; Alfieri, A.A.; da Silva, C.A. Impact of Piglet Birthweight and Sow Parity on Mortality Rates, Growth Performance, and Carcass Traits in Pigs. Rev. Bras. Zootec. 2017, 46, 856–862. [Google Scholar] [CrossRef]
  2. Van Kempen, T. Supplements to facilitate parturition and reduce perinatal mortality in pigs. In Recent Advances in Animal Nutrition 2007, Proceedings of the 41st University of Nottingham Feed Conference, Sutton Bonington Campus, Nottingham, UK, 4–6 September 2007; Nottingham University Press: Nottingham, UK, 2008; pp. 317–330. [Google Scholar]
  3. Feyera, T.; Højgaard, C.K.; Vinther, J.; Bruun, T.S.; Theil, P.K. Dietary Supplement Rich in Fiber Fed to Late Gestating Sows during Transition Reduces Rate of Stillborn Piglets. J. Anim. Sci. 2017, 95, 5430–5438. [Google Scholar] [CrossRef]
  4. Feyera, T.; Pedersen, T.F.; Krogh, U.; Foldager, L.; Theil, P.K. Impact of Sow Energy Status during Farrowing on Farrowing Kinetics, Frequency of Stillborn Piglets, and Farrowing Assistance1. J. Anim. Sci. 2018, 96, 2320–2331. [Google Scholar] [CrossRef]
  5. Blim, S.; Lehn, D.; Scheu, T.; Koch, C.; Thaller, G.; Bostedt, H. Evaluation of the Electrolyte Status in Hyperprolific Sows on the Farrowing Process under Different Housing Conditions. Theriogenology 2022, 193, 37–46. [Google Scholar] [CrossRef]
  6. Devillers, N.; Le Dividich, J.; Prunier, A. Influence of Colostrum Intake on Piglet Survival and Immunity. Animal 2011, 5, 1605–1612. [Google Scholar] [CrossRef]
  7. Ferreira, S.V.; Rodrigues, L.A.; Ferreira, M.A.; Alkmin, D.V.; Dementshuk, J.M.; Almeida, F.R.C.L.; Fontes, D.O. Plane of Nutrition during Gestation Affects Reproductive Performance and Retention Rate of Hyperprolific Sows under Commercial Conditions. Animal 2021, 15, 100153. [Google Scholar] [CrossRef]
  8. Kim, C.S.; Kawada, T.; Kim, B.S.; Han, I.S.; Choe, S.Y.; Kurata, T.; Yu, R. Capsaicin Exhibits Anti-Inflammatory Property by Inhibiting IkB-a Degradation in LPS-Stimulated Peritoneal Macrophages. Cell. Signal. 2003, 15, 299–306. [Google Scholar] [CrossRef]
  9. Srinivasan, K. Biological Activities of Red Pepper (Capsicum annuum) and Its Pungent Principle Capsaicin: A Review. Crit. Rev. Food Sci. Nutr. 2016, 56, 1488–1500. [Google Scholar] [CrossRef]
  10. Manzanilla, E.G.; Perez, J.F.; Martin, M.; Kamel, C.; Baucells, F.; Gasa, J. Effect of Plant Extracts and Formic Acid on the Intestinal Equilibrium of Early-Weaned Pigs. J. Anim. Sci. 2004, 82, 3210–3218. [Google Scholar] [CrossRef]
  11. Endres, D.B.; Rude, R.K. Mineral and bane metabolism. In Textbook of Clinical Chemistry; Burtis, C.A., Ashwood, E.R., Tietz, N.W., Eds.; W. B. Saunders: Philadelphia, PA, USA, 1994; pp. 1887–1973. [Google Scholar]
  12. Combs, G.F.; McClung, J.P. Chapter 3—General Properties of Vitamins. In The Vitamins, 5th ed.; Combs, G.F., McClung, J.P., Eds.; Academic Press: Cambridge, MA, USA, 2017; pp. 33–58. ISBN 978-0-12-802965-7. [Google Scholar]
  13. Bachmann, H.; Autzen, S.; Frey, U.; Wehr, U.; Rambeck, W.; McCormack, H.; Whitehead, C.C. The Efficacy of a Standardised Product from Dried Leaves of Solanum Glaucophyllum as Source of 1,25-Dihydroxycholecalciferol for Poultry. Br. Poult. Sci. 2013, 54, 642–652. [Google Scholar] [CrossRef]
  14. Jäpelt, R.B.; Jakobsen, J. Vitamin D in Plants: A Review of Occurrence, Analysis, and Biosynthesis. Front. Plant Sci. 2013, 4, 136. [Google Scholar] [CrossRef]
  15. Zhou, H.; Chen, Y.; Lv, G.; Zhuo, Y.; Lin, Y.; Feng, B.; Fang, Z.; Che, L.; Li, J.; Xu, S.; et al. Improving Maternal Vitamin D Status Promotes Prenatal and Postnatal Skeletal Muscle Development of Pig Offspring. Nutrition 2016, 32, 1144–1152. [Google Scholar] [CrossRef]
  16. Devillers, N.; van Milgen, J.; Prunier, A.; Le Dividich, J. Estimation of Colostrum Intake in the Neonatal Pig. Anim. Sci. 2004, 78, 305–313. [Google Scholar] [CrossRef]
  17. Liu, P.; Piao, X.S.; Kim, S.W.; Wang, L.; Shen, Y.B.; Lee, H.S.; Li, S.Y. Effects of chito-oligosaccharide supplementation on the growth performance, nutrient digestibility, intestinal morphology, and fecal shedding of Escherichia coli and Lactobacillus in weaning pigs. J. Anim. Sci. 2008, 86, 2609–2618. [Google Scholar] [CrossRef]
  18. Borges, V.F.; Bernardi, M.L.; Bortolozzo, F.P.; Wentz, I. Stillbirth pattern according to birth order, birth weight, and gender of piglets. Arq. Bras. Med. Veterinária Zootec. 2008, 60, 1234–1240. [Google Scholar] [CrossRef]
  19. Jeong, J.H.; Hong, J.S.; Han, T.H.; Fang, L.H.; Chung, W.L.; Kim, Y.Y. Effects of Dietary Vitamin Levels on Physiological Responses, Blood Profiles, and Reproductive Performance in Gestating Sows. J. Anim. Sci. Technol. 2019, 61, 294–303. [Google Scholar] [CrossRef]
  20. Rosen, C.J.; Adams, J.S.; Bikle, D.D.; Black, D.M.; Demay, M.B.; Manson, J.E.; Murad, M.H.; Kovacs, C.S. The Nonskeletal Effects of Vitamin D: An Endocrine Society Scientific Statement. Endocr. Rev. 2012, 33, 456–492. [Google Scholar] [CrossRef]
  21. Muszkat, P.; Camargo, M.B.R.; Griz, L.H.M.; Lazaretti-Castro, M. Evidence-Based Non-Skeletal Actions of Vitamin D. Arq. Bras. Endocrinol. Metabol. 2010, 54, 110–117. [Google Scholar] [CrossRef]
  22. Schumacher, M.A. Transient Receptor Potential Channels in Pain and Inflammation: Therapeutic Opportunities. Pain Pract. 2010, 10, 185–200. [Google Scholar] [CrossRef]
  23. Nelson, D.L.; Cox, M.M. Lipídios. In Princípios de Bioquímica de Lehninger; Nelson, D.L., Cox, M.M., Eds.; Sartmed: Porto Alegre, Brazil, 2014; pp. 357–384. [Google Scholar]
  24. Wray, S. Uterine Contraction and Physiological Mechanisms of Modulation. Am. J. Physiol. 1993, 264, C1–C18. [Google Scholar] [CrossRef]
  25. Elrod, N.D.; Harp, R.M.; Bryan, K.G. Effect of Calcium Ion Supplementation on Swine Parturition. Tex. J. Agric. Nat. Resour. 2015, 28, 12–17. [Google Scholar]
  26. Bloemhof, S.; van der Waaij, E.H.; Merks, J.W.M.; Knol, E.F. Sow Line Differences in Heat Stress Tolerance Expressed in Reproductive Performance Traits. J. Anim. Sci. 2008, 86, 3330–3337. [Google Scholar] [CrossRef]
  27. Santoni, G.; Cardinali, C.; Morelli, M.B.; Santoni, M.; Nabissi, M.; Amantini, C. Danger- and Pathogen-Associated Molecular Patterns Recognition by Pattern-Recognition Receptors and Ion Channels of the Transient Receptor Potential Family Triggers the Inflammasome Activation in Immune Cells and Sensory Neurons. J. Neuroinflamm. 2015, 12, 21. [Google Scholar] [CrossRef]
  28. Gourley, K.M.; Nichols, G.E.; Sonderman, J.A.; Spencer, Z.T.; Woodworth, J.C.; Tokach, M.D.; DeRouchey, J.M.; Dritz, S.S.; Goodband, R.D.; Kitt, S.J.; et al. Determining the Impact of Increasing Standardized Ileal Digestible Lysine for Primiparous and Multiparous Sows during Lactation1,2. Transl. Anim. Sci. 2017, 1, 426–436. [Google Scholar] [CrossRef]
  29. Schlegel, P.; Guggisberg, D.; Gutzwiller, A. Tolerance to 1,25 Dihydroxyvitamin D3 Glycosides from Solanum Glaucophyllum by the Growing Pig. Res. Vet. Sci. 2017, 112, 119–124. [Google Scholar] [CrossRef]
  30. Thayer, M.T.; Nelssen, J.L.; Langemeier, A.J.; Morton, J.M.; Gonzalez, J.M.; Kruger, S.R.; Ou, Z.; Makowski, A.J.; Bergstrom, J.R. The Effects of Maternal Dietary Supplementation of Cholecalciferol (Vitamin D(3)) and 25(OH)D(3) on Sow and Progeny Performance. Transl. Anim. Sci. 2019, 3, 692–708. [Google Scholar] [CrossRef]
  31. Langendijk, P.; Plush, K. Parturition and Its Relationship with Stillbirths and Asphyxiated Piglets. Animals 2019, 9, 885. [Google Scholar] [CrossRef]
  32. Matysiak, B.; Jacyno, E.; Kawecka, M.; Kołodziej-Skalska, A.; Pietruszka, A. The Effect of Plant Extracts Fed before Farrowing and during Lactation on Sow and Piglet Performance. S. Afr. J. Anim. Sci. 2012, 42, 15–21. [Google Scholar] [CrossRef]
  33. Ogiso, Y.; Hosoda-Yabe, R.; Kawamoto, Y.; Kawamoto, T.; Kato, K.; Yabe, T. An Antioxidant of Dried Chili Pepper Maintained Its Activity through Postharvest Ripening for 18 Months. Biosci. Biotechnol. Biochem. 2008, 72, 3297–3300. [Google Scholar] [CrossRef]
  34. Pluske, J.R.; Turpin, D.L.; Kim, J.C. Gastrointestinal Tract (Gut) Health in the Young Pig. Anim. Nutr. 2018, 4, 187–196. [Google Scholar] [CrossRef]
  35. Liu, Y.; Song, M.; Che, T.M.; Bravo, D.; Maddox, C.W.; Pettigrew, J.E. Effects of Capsicum Oleoresin, Garlic Botanical, and Turmeric Oleoresin on Gene Expression Profile of Ileal Mucosa in Weaned Pigs. J. Anim. Sci. 2014, 92, 3426–3440. [Google Scholar] [CrossRef] [PubMed]
  36. Choi, J.H.; Jin, S.W.; Choi, C.Y.; Kim, H.G.; Lee, G.H.; Kim, Y.A.; Chung, Y.C.; Jeong, H.G. Capsaicin Inhibits Dimethylnitrosamine-Induced Hepatic Fibrosis by Inhibiting the TGF-Β1/Smad Pathway via Peroxisome Proliferator-Activated Receptor Gamma Activation. J. Agric. Food Chem. 2017, 65, 317–326. [Google Scholar] [CrossRef] [PubMed]
  37. Yang, J.; Tian, G.; Chen, D.; Zheng, P.; Yu, J.; Mao, X.; He, J.; Luo, Y.; Luo, J.; Huang, Z.; et al. Dietary 25-Hydroxyvitamin D3 Supplementation Alleviates Porcine Epidemic Diarrhea Virus Infection by Improving Intestinal Structure and Immune Response in Weaned Pigs. Animals 2019, 9, 627. [Google Scholar] [CrossRef] [PubMed]
  38. Hewison, M. Vitamin D and the Immune System: New Perspectives on an Old Theme. Endocrinol. Metab. Clin. N. Am. 2010, 39, 365–379. [Google Scholar] [CrossRef] [PubMed]
Table 1. Dietary ingredients (%) and calculated nutritional values of the gestation and lactation diets used in Experiments I and II.
Table 1. Dietary ingredients (%) and calculated nutritional values of the gestation and lactation diets used in Experiments I and II.
IngredientsExperiment IExperiment II
GestationLactationGestationLactation
Corn grain (7.85%)62.9853.4960.8553.87
Soybean meal (45%)13.5227.6812.0425.48
Soybean hull19.01-22.07-
Meat meal (77.1%)3.675.003.505.00
Wafer bran-5.00-5.00
Energy concentrate 1-7.500.40-
Limestone (35.8%)0.32-0.140.90
Sugar-- 5.00
Dicalcium phosphate (17% Ca/21%P)---1.50
L-Lisina 78.4%-0.40-0.40
DL-Methionine 99%-0.19-0.19
L-Tryptophan 99%-0.05-0.06
L-Threonine 98%-0.19--
Salt0.400.40-0.50
Soybean oil---2.00
Premix 20.100.101.000.10
Nutrients per kg of feed
Metabolizable energy, kcal3008368330073353
Crude protein, %14.6921.0114.4219.28
Extract ethereal, %3.665.73.244.88
Crude fiber, %9.183.2510.432.69
Calcium, %1.001.010.870.95
Total phosphorus, %0.450.620.450.56
Available phosphorus, %0.400.510.400.36
Digestible lysine, %0.571.200.641.06
Digestible threonine, %0.740.670.460.68
Digestible methionine, %0.330.370.230.26
Digestible tryptophan, %0.160.230.140.20
Met + digestible cys, %0.500.610.430.56
1 Energy Farms® (De Heus Animal Nutrition). 2 Premix, guaranteed levels per kg of product: Choline: 75,000 mg/kg−1, Vitamin A: 50,000 IU, Vitamin D3: 75,000 IU, Vitamin E: 9000 mg/kg−1, Vitamin K3: 975 mg kg−1, Vitamin B1: 500 mg/kg−1, Vitamin B2: 1200 mg/kg−1, Vitamin B6: 750 mg/kg−1, Vitamin B12: 8000 mg/kg−1, Vitamin D: 3900 IU/kg; Niacin: 5000 mg/kg−1, Pantothenic acid: 3000 mg/kg−1, Folic acid: 500 mg/kg−1, Biotin: 20,000 mg/kg−1, Iron: 30,000 mg/kg−1, Copper: 3000 mg/kg−1, Manganese: 17,500 mg/kg−1, Zinc: 30,000 mg/kg−1, Iodine: 200 mg/kg−1, Selenium: 150 mg/kg−1, Phytase: 25,000 U kg−1.
Table 2. Reproductive performance of sows supplemented with vitamin D3, capsaicin, or both (in half dosage) at 85 days of gestation until the end of lactation (Experiment I).
Table 2. Reproductive performance of sows supplemented with vitamin D3, capsaicin, or both (in half dosage) at 85 days of gestation until the end of lactation (Experiment I).
ParametersTreatmentsCV (%) *p-Value
ControlVitamin 1,25-(OH)2D3CapsaicinVit. 1,25-(OH)2D3 + Capsaicin
Time of delivery, hours5:455:005:405:0563.610.843
Dystocia rate, %40 a23 ab23 ab12 b-0.017 2
Oxytocin use, %23101007-0.310
Total births, %17.317.316.716.221.120.563
Live births, n15.415.515.514.521.630.679
Stillbirths, %7.55.94.63.3123.840.120
Mummification, %3.64.82.66.4144.470.261
Piglets below 900 g, %14.9 a13.9 ab14.4 ab10.3 b-0.044 2
Litter weight, kg19.020.819.719.822.970.557
Average weight at birth, kg1.28 b1.33 a1.27 b1.36 a16.220.001 1
CV at birth, % *20.7721.2221.8718.3231.210.196
Piglet weight at 24 h, kg1.37 b1.45 a1.36 b1.47 a16.550.001 1
Weight litter at 24 h, kg19.321.620.820.876.050.344
Piglet daily weight gain 24 h, g95 b139 a95 b121 a96.970.001 1
Colostrum intake, g *258 b330 a254 b312 a36.540.001 1
Colostrum production, kg *3772 b4906 a3810 b4402 a33.690.003 1
Mortality to 24 h, %5.14.75.24.212.420.534
¹ a, b Distinct letters in the rows indicate differences (p < 0.05) and trends (p < 0.10) determined using Tukey’s test. 2 a, b Means followed by different letters in the rows indicate differences determined using the chi-square test (p < 0.05). * CV: coefficient of variation.
Table 3. Reproductive performance of sows supplemented with vitamin 1,25-(OH)2D3, capsaicin, or both (in half dosage) from 85 days of gestation until the end of lactation, according to the evaluation time (days) (Experiment I).
Table 3. Reproductive performance of sows supplemented with vitamin 1,25-(OH)2D3, capsaicin, or both (in half dosage) from 85 days of gestation until the end of lactation, according to the evaluation time (days) (Experiment I).
AgeParametersTreatmentsCV (%) *p-Value
ControlVitamin 1,25-(OH)2D3CapsaicinVit. 1,25-(OH)2D3 + Capsaicin
2 daysNumber of piglets, n14.77 a14.03 b14.63 a14.58 a6.890.024
Average birth weight, kg1.55 b1.68 a1.49 b1.54 b28.520.001
Average litter weight, kg22.7223.7421.9022.6320.420.509
10 daysAverage piglet weight, kg2.974 b3.192 a3.043 b2.997 b24.080.001
Average litter weight, kg41.543.1042.4840.8719.800.758
Daily weight gain, g216 ab227 a218 ab206 b33.660.001
WeaningNumber of piglets, n13.8713.4813.8313.540.0700.102
Average birth weight, kg6.10 b6.36 a6.20 ab6.167 ab21.200.033
Average litter weight, kg81.1483.2281.7978.6716.480.656
Daily weight gain, g25326126226024.710.161
Mortality rate, %5.944.805.657.1638.080.535
Daily feed intake during the lactation, kg/d7.68 ab6.92 b7.94 a7.01 ab13.350.038
Feed efficiency, kg piglet/kg feed0.4390.4900.4430.43827.860.679
a,b Means followed by different letters in the rows indicate differences according to Tukey’s test (p < 0.05). * CV: coefficient of variation.
Table 4. Percentage of diarrhea in piglets of sows supplemented with vitamin D3, capsaicin, or both (in half dosage) at 85 days of gestation until the end of lactation (Experiment I).
Table 4. Percentage of diarrhea in piglets of sows supplemented with vitamin D3, capsaicin, or both (in half dosage) at 85 days of gestation until the end of lactation (Experiment I).
AgesTreatmentsp-Value
ControlVitamin 1,25-(OH)2D3CapsaicinVit. 1,25-(OH)2D3 + Capsaicin
First week, %15.09 b6.99 a6.95 a6.71 a0.001
Weaning, %3.211.403.212.520.503
a,b Means followed by different letters in the rows indicate differences determined using the chi-square test (p < 0.05).
Table 5. Blood analysis of sows supplemented with 1,25-dihydroxyvitamin D3, capsaicin, or both (half dosage) at 85 days gestation until the end of lactation (Experiment I).
Table 5. Blood analysis of sows supplemented with 1,25-dihydroxyvitamin D3, capsaicin, or both (half dosage) at 85 days gestation until the end of lactation (Experiment I).
ParameterTreatmentsCV (%) *p-Value
ControlVitamin 1,25-(OH)2D3CapsaicinVit. 1,25-(OH)2D3 + Capsaicin
Calcium, mg/dL90.298.892.194.914.200.276
Phosphorus, mg/dL69.476.575.676.120.390.344
C-reactive protein, mg/dL8.811.19.69.451.500.792
Cortisol, mg/dL75.745.938.346.769.910.183
* CV: coefficient of variation.
Table 6. Reproductive performance of sows supplemented with vitamin D3, capsaicin, or both at 85 days of gestation until the end of lactation (Experiment II).
Table 6. Reproductive performance of sows supplemented with vitamin D3, capsaicin, or both at 85 days of gestation until the end of lactation (Experiment II).
ParametersWithout Vit 1,25-(OH)2D3 and CapsaicinVit 1,25-(OH)2D3 without
Capsaicin
Capsaicin without
Vit 1,25-(OH)2D3
Vit 1,25-(OH)2D3 + CapsaicinCV (%) *p-Value
VitaminCapsaicinV × C **
Delivery, hours 4:57 3:48 4:24 4:26 52.81 0.001 0.857 0.550 1
Dystocia, %27.634.2113.4611.95-0.0010.7520.002 2
Oxytocin use, %6.593.126.813.37-0.2870.3160.592 2
Total births, n 16.55 16.00 16.03 16.54 26.16 0.273 0.542 0.882 1
Live births, n14.6014.5114.1615.0726.810.6150.1380.519 1
Stillbirths, %7.615.376.925.92124.110.0260.3060.168 1
Mummification, %3.583.274.062.74184.210.7060.1620.565 1
Litter weight, kg19.5219.7019.0220.2724.740.8780.0800.290 1
Average weight at birth, kg1.361.361.371.3515.120.8420.5870.208 1
CV at birth, %20.0919.7019.7620.0529.640.5750.7160.578 1
1 Means followed by different letters in the rows indicate differences according to Tukey’s test (p < 0.05). 2 Means followed by different letters in the rows indicate differences found using the chi-square test (p < 0.05). * CV: coefficient of variation. ** V × C represents the vitamin 1,25-(OH)2D3 × capsaicin interaction.
Table 7. Reproductive performance of sows supplemented with vitamin 1,25-(OH)2D3, capsaicin, or both at 85 days of gestation until the end of lactation, according to the evaluation time (days) (Experiment II).
Table 7. Reproductive performance of sows supplemented with vitamin 1,25-(OH)2D3, capsaicin, or both at 85 days of gestation until the end of lactation, according to the evaluation time (days) (Experiment II).
AgeParametersWithout Vit 1,25-(OH)2D3 and CapsaicinVit 1,25-(OH)2D3 without
Capsaicin
Capsaicin without
Vit 1,25-(OH)2D3
Vit 1,25-(OH)2D3 + Capsaicinp-Value
CV (%) *VitaminCapsaicinV × C **
2 daysNumber of piglets, n13.6413.5413.4313.7812.610.7850.3070.471
Average birth weight, kg1.621.611.59 b1.64 a19.730.6060.0010.519
Average litter gain, kg21.8321.9121.3922.4123.920.9400.2750.758
10 daysAverage piglet weight, kg3.443.453.40 b3.49 a16.280.1750.0040.025
Average litter weight, kg44.0644.6043.1345.7121.290.8070.1150.407
Daily weight gain, g238229232b235a29.530.0620.0020.003
WeaningNumber of piglets, n12.6412.6212.5212.7613.870.9760.4500.390
Average piglet weight, kg6.056.106.016.1415.140.9770.3420.968
Average litter weight, kg76.1976.6874.8878.1717.940.8610.2350.655
Daily weight gain, g24724824425128.200.9440.3300.942
Mortality rate, %9.486.508.477.3450.780.1000.6150.336
Daily feed intake, kg/d6.416.426.456.3714.820.2940.6250.400
Feed efficiency, kg piglet/kg feed0.550.530.520.5633.840.3800.0460.410
a,b Means followed by different letters in the rows indicate differences according to Tukey’s test (p < 0.05). * CV: coefficient of variation. ** V × C represents the interaction vitamin 1,25-(OH)2D3 × capsaicin.
Table 8. Percentage of diarrhea in piglets of sows supplemented with vitamin D3, capsaicin, or both at 85 days of gestation until the end of lactation (Experiment II).
Table 8. Percentage of diarrhea in piglets of sows supplemented with vitamin D3, capsaicin, or both at 85 days of gestation until the end of lactation (Experiment II).
AgesWithout 1,25-(OH)2D3 and CapsaicinVit 1,25-(OH)2D3 without
Capsaicin
Capsaicin without
Vit 1,25-(OH)2D3
Vit 1,25-(OH)2D3 + Capsaicinp-Value
VitaminCapsaicinV × C *
First week, %11.6310.0312.109.500.2840.0390.025
Weaning, %3.601.553.611.540.0010.0010.001
* V × C represents the interaction vitamin 1,25-(OH)2D3 × capsaicin.
Table 9. Blood analysis of sows supplemented with 1,25-dihydroxyvitamin D3, capsaicin, or both (half dosage) at 85 days gestation until the end of lactation (Experiment II).
Table 9. Blood analysis of sows supplemented with 1,25-dihydroxyvitamin D3, capsaicin, or both (half dosage) at 85 days gestation until the end of lactation (Experiment II).
ParameterWithout Vit D3 and CapsaicinVit D3 without
Capsaicin
Capsaicin without
Vit D3
Vit D3 + Capsaicinp-Value
CV (%) *VitaminCapsaicinV × C **
Calcium, mg/dL93.188.591.690.710.390.070.620.96
Phosphorus, mg/dL68.967.467.268.811.200.620.710.29
C-reactive protein, mg/dL6.46.66.36.534.070.820.570.56
Cortisol, mg/dL53.243.252.843.664.600.560.570.24
* CV: coefficient of variation. ** V × C represents the interaction vitamin 1,25-(OH)2D3 × capsaicin.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Dario, J.G.N.; de Oliveira, E.R.; de Souza, R.P.; Theodorovicz, S.; Bernini, G.C.; Ruiz, G.; de Carvalho, R.H.; da Silva, C.A. Capsaicin and 1,25-Dihydroxyvitamin D3 Glycoside: Effects on the Reproductive Performance of Hyper-Prolific Sows. Animals 2023, 13, 2794. https://doi.org/10.3390/ani13172794

AMA Style

Dario JGN, de Oliveira ER, de Souza RP, Theodorovicz S, Bernini GC, Ruiz G, de Carvalho RH, da Silva CA. Capsaicin and 1,25-Dihydroxyvitamin D3 Glycoside: Effects on the Reproductive Performance of Hyper-Prolific Sows. Animals. 2023; 13(17):2794. https://doi.org/10.3390/ani13172794

Chicago/Turabian Style

Dario, Julie Gabriela Nagi, Eduardo Raele de Oliveira, Rodrigo Pereira de Souza, Sabrina Theodorovicz, Giovana Chimentão Bernini, Gabriela Ruiz, Rafael Humberto de Carvalho, and Caio Abércio da Silva. 2023. "Capsaicin and 1,25-Dihydroxyvitamin D3 Glycoside: Effects on the Reproductive Performance of Hyper-Prolific Sows" Animals 13, no. 17: 2794. https://doi.org/10.3390/ani13172794

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop