Next Article in Journal
Effect of Tunicamycin on Viability, Motility, Reactive Oxygen Species, Nitric Oxide, and Lipid Peroxidation in Boar Sperm
Previous Article in Journal
Microplastics in Cronius ruber: Links to Wastewater Discharges
Previous Article in Special Issue
Dietary Arginine Supplementation Modulates the Proteome of Boar Seminal Plasma
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Selenium + Vitamin E Supplementation in Anestrus Goats: A Strategy to Enhance Reproductive Outcomes Under a Semi-Arid Production System

by
Raquel Santos-Silva
1,
Cesar A. Meza-Herrera
1,*,
Brenda Castro-Roque
1,
Guadalupe Calderón-Leyva
2,*,
Cayetano Navarrete-Molina
3,
Oscar Angel-García
2,
Jessica M. Flores-Salas
2,
Angeles De Santiago-Miramontes
2,
Fernando Arellano-Rodriguez
2 and
Cesar A. Rosales-Nieto
4
1
Graduate Program—Natural Resources and Environment in Arid Lands, Regional Universitary Unit on Arid Lands, Chapingo Autonomous University, Bermejillo, Durango 35230, Mexico
2
Graduate Program—Agricultural and Livestock Sciences, Antonio Narro Agricultural Autonomous University, Laguna Unit, Torreon Coahuila 27054, Mexico
3
Department of Chemistry, Environmental Technology Area, Rodeo Technological University, Rodeo, Durango 35760, Mexico
4
Department of Agricultural Sciences, Texas State University, San Marcos, TX 78666, USA
*
Authors to whom correspondence should be addressed.
Animals 2025, 15(10), 1421; https://doi.org/10.3390/ani15101421
Submission received: 28 March 2025 / Revised: 3 May 2025 / Accepted: 10 May 2025 / Published: 14 May 2025
(This article belongs to the Special Issue Nutrition and Reproduction Relationships in Animals)

Simple Summary

Seasonal reproduction in goats leads to production seasonality, presenting physiological and economic challenges for producers who aim to extend the reproductive season to ensure a more consistent supply of products and year-round economic returns. Within this complex biological, physiological, and economic context, precision nutritional supplementation to enhance out-of-season ovarian activity in females appears to be a promising strategy. This study evaluated the possible effect of selenium (5 mg) plus vitamin E (350 IU) supplementation (i.e., SeVE) on ovarian activity, embryo implantation, and pregnancy rates in estrus-induced anestrous goats. SeVE supplementation increased (p < 0.05) estrus induction, ovulatory rate, embryo implantation, and pregnancy rates compared to the control group, without affecting (p > 0.05) corpus luteum diameter or left and right ovary diameters.

Abstract

Goats are primarily raised in marginal, arid, and semi-arid production systems and exhibit a seasonal reproductive pattern. Extending their reproductive season would enhance food security and improve the economic viability of goat production. Therefore, the objective of this study was to assess the effects of SeVE supplementation during the anestrus season on ovarian activity in anestrous goats subjected to an estrus synchronization protocol. The response variables included estrus induction (EI), ovulatory rate (OR), corpus luteum diameter (CLD), left and right ovary diameters (LOD and ROD), embryo implantation (EMBRYO), and pregnancy rates (PREG). Adult, anestrous, crossbred dairy goats (n = 32) from northern semi-arid Mexico (i.e., Comarca Lagunera, 26° N) were randomly assigned to two homogeneous groups based on age, live weight (LW), and body condition score (BCS): (1) the supplemented group (SeVE; n = 16), received 5 mg selenium plus 350 IU vitamin E, and (2) the control group (CONT; n = 16), received physiological saline. Estrus was induced using a combination of progesterone (P4, 20 mg), equine chorionic gonadotropin (eCG, 400 IU), and exposure to the male effect. While no differences (p > 0.05) were observed between the groups for LW and BCS, the variables EI, OR, EMBRYO, and PREG rates were higher (p < 0.05) in the SeVE group than the CONT group. No differences (p > 0.05) were observed between the groups for CLD, LOD, or ROD. Thus, SeVE-targeted supplementation improved reproductive outcomes without affecting ovarian structure size (i.e., a non-dimensional ovarian SeVE action), suggesting that this precision supplementation strategy certainly enhances reproductive efficiency. This was possibly related to selenium-induced increases in P4 synthesis, and the antioxidant effects on follicular development correlate with improved endometrial development, conceptus survival, embryo growth, and pregnancy maintenance. Such improvements could contribute to the sustainability of marginal production systems in the semi-arid regions of northern Mexico, supporting food security and increasing economic returns for goat producers and their families.

1. Introduction

Goat production is a vital agricultural activity that has contributed significantly to human development, particularly in marginal, arid, and semi-arid ecosystems and rural communities facing poverty. In these regions, goats provide employment opportunities and a critical source of animal protein for families, often representing their primary or sole source of income [1,2,3,4]. Goats exhibit remarkable adaptability across diverse agroecological zones, owing to their ability to withstand droughts and extreme climates, combined with desirable traits such as high prolificacy, rapid growth rates, and efficient utilization of low-quality plant resources [2,3]. In northern arid Mexico, goat production remains a cornerstone of rural economies, accounting for a substantial proportion of farmers’ income [5]. As of 2023, Mexico reported a goat population of approximately 9 million head, with the Comarca Lagunera (i.e., CL; 26° N) standing out as the leading goat-producing agroecological region, housing 404,414 goats [6]. The CL, a semi-arid region, is recognized nationally for its high goat milk production. However, pronounced seasonal fluctuations in vegetation and crop residue availability have resulted in a seasonal reproductive pattern, subsequently driving a seasonal production cycle for both milk and meat [7].
This reproductive seasonality imposes biological constraints that limit the sustainability of marginal goat production systems [8]. Goat reproduction is primarily regulated by photoperiodic variations, with a period of reproductive quiescence—marked by the absence of estrus and ovulatory activity—extending from January to early June. Reproductive activity typically resumes in late June and continues through December [9]. This pattern presents a significant physiological challenge for goat farmers seeking to extend the reproductive season to ensure more continuous production [10]. In this complex biological framework, the strategic use of socio-sexual cues (i.e., the male effect) combined with precision nutritional supplementation can enhance the metabolic status of females and facilitate the reactivation of the hypothalamic–pituitary–gonadal axis, thereby inducing out-of-season ovarian activity [10]. Consequently, there is an urgent need to identify targeted supplementation strategies to boost reproductive efficiency [11].
The use of vitamins and minerals has emerged as a promising supplementation strategy to enhance animal productivity and reproductive performance, given their role as enzymatic cofactors in multiple metabolic pathways [12]. Selenium (Se) and vitamin E (VE), in particular, act synergistically to exert antioxidant effects through independent biochemical mechanisms [13]. These antioxidants protect cellular membranes from oxidative damage induced by reactive oxygen species and lipid hydroperoxides [14], thereby preserving the integrity of DNA, RNA, and proteins, and preventing cell death by reducing oxidative stress [15]. Improvements in growth, reproductive performance, immune competence, hormone synthesis, and tissue integrity have been associated with adequate Se and VE status [14]. Specifically, sufficient blood Se levels have been linked to enhanced progesterone secretion [16], improved corpus luteum development [17], and reduced lipoperoxide concentrations [18]. Moreover, Se and selenoproteins (i.e., SeProt) are involved in lipid metabolism (i.e., cholesterol-to-progesterone) due to their ability to modulate redox homeostasis. In the last processes, some SeProt encoding genes (i.e., GPX1, GPX4, SELENOP, and SELENOF) and the redox-related gene (i.e., SOD2) were involved [19]. Additionally, SeVE supplementation has been shown to improve ovarian function, mitigate morphological changes, and minimize oxidative damage to ovaries and follicles [20,21,22,23]. SeVE has also been associated with a shortened postpartum estrus interval [17] and plays a crucial role in the activation of key enzyme systems such as glutathione peroxidase (GSH-Px) and deiodinases, both essential for optimal embryonic development [24]. These effects collectively contribute to higher pregnancy rates and increased kidding percentages [25]. Given that oxidative stress during seasonal anestrus may further suppress ovarian activity, the antioxidant properties of SeVE could mitigate this constraint by enhancing both follicular resilience and pregnancy rates. Besides, and from a social and environmental standpoint, enhancing goat reproductive efficiency aligns with several Sustainable Development Goals (SDGs), notably contributing to food security (SDG 2) and promoting responsible production practices (SDG 12) [2,26,27]. Building on these previous findings, we hypothesized that precision supplementation with SeVE would improve out-of-season reproductive performance in adult anestrus crossbred dairy goats in northern semi-arid Mexico, leading to increased ovarian activity, embryo implantation, and pregnancy rates. The present study was designed to test this hypothesis.

2. Materials and Methods

2.1. General

All experimental procedures, animal handling, and management practices in this study were conducted strictly within international [28] and national [29] guidelines for the ethical treatment, care, and welfare of research animals. While all the reported procedures were aligned with conventional veterinary practices, the study received institutional approval under the reference number UAAAN-UL-38111-425501002-2876.

2.2. Location and Environmental Conditions

The study was conducted in the ejido Lázaro Cárdenas, San Pedro, Coahuila de Zaragoza, Mexico (25°45′50″ N, 103°11′03″ W; altitude 1111 m above sea level). The region is characterized by a very dry, semi-warm climate, with rainfall concentrated between May and October; the annual precipitation ranges from 200 to 300 mm [30,31]. Average annual temperatures are approximately 24 °C, with summer highs reaching 41 °C and winter lows dropping to −1 °C. The study was carried out in two phases: (1) the male-to-female interaction phase during April and May, corresponding to the natural seasonal anestrus period, and (2) the implantation, embryogenesis, and early gestation phase during June and July.

2.3. Animal Management and Rangeland Conditions

Multiparous, non-lactating, non-pregnant, anestrous, crossbred goats (i.e., Criollo × Alpine–Saanen–Nubian; n = 32) of known fertility were selected from a 160-goat herd managed under a interesting semi-intensive production system subdivided according to their stage of lactation. In this peculiar production system, those goats that had just given birth and those in the 1/3 and 2/3 lactation (i.e., ≈9 months on lactation) were kept under an intensive management scheme (i.e., zero grazing) with free access to alfalfa hay, mineral salts, and water, while receiving 200 g day−1 goat−1 of a commercial concentrate (14% CP) (see Table 1). On the other hand, the goats in the 3/3 period of lactation, or all through their dry period, were kept under a semi-intensive management approach consisting of a diurnal grazing scheme with evening confinement with reduced nutritional support. In both corrals/groups, the goats were hand-milked daily in the morning; in the second group, milking was carried out before grazing. Grazing was allowed from 1000 to 1800 h in the grazing areas surrounding the production unit, with the guidance of a herdsman. The rangeland has flora characterized as Chihuahuan desert rangeland; while creosote bush (Larrea tridentata (DC. Cov)) dominates the grazing area, different key species consist of lechuguilla (Agave lechuguilla Torr), mesquite (Prosopis glandulosa v. glandulosa), and blue gramma (Bouteloua gracilis (Wild). Ex Kunth Lag. Ex Griffiths). Goats walk approximately 5–8 km daily from the pen to diverse sites of the available rangeland, thus grazing restraints can be considered negligible. Once in the pen, after the grazing period, all 32 goats received 200 g of alfalfa hay and 100 g of a commercial concentrate (14% CP), day−1 goat−1, with free access to mineral salts and water (see Table 1), during the whole experimental period. Since all the goats received such nutritional support on an individual basis and grazed the same rangeland, the goats were considered the experimental unit. The selected goats were homogeneous regarding live weight (LW; 39.4 ± 1.3 kg), body condition score (BCS 1.7 ± 0.0 units, scale: 1 = very thin to 4 = very fat), and age (2.4 ± 0.3 years old) to ensure balanced groups before randomization. To confirm anovulatory status during the increasing photoperiod (April, Northern Hemisphere; Figure 1), ovarian activity was evaluated by an expert using two transrectal ultrasound examinations (Aloka SSD 500, Tokyo, Japan, 7.5 MHz transducer) conducted seven days apart [32,33].

2.4. Experimental Procedures, Experimental Groups, and Treatment Design

Goats showing no evidence of follicular development (n = 32) were selected for estrus induction. Estrus was induced via intramuscular injection of 20 mg progesterone (P4; Progestelas “E”, Lab Aranda, Mexico City, Mexico), followed 24 h later by 400 IU equine chorionic gonadotropin (eCG; Foligon, MSD, Animal Health, Mexico City, Mexico) administered intramuscularly. This was designated as Day 0 of the experimental protocol. Then, goats were randomly assigned to two experimental groups: Supplemented group (SeVE; n = 16) received three intramuscular applications of 5 mg selenium plus 350 IU vitamin E (i.e., SELEBEN-B, Maymo Lab., S.A., Madrid, Spain) administered at 7-day intervals. Control group (CONT; n = 16), received three intramuscular applications of 1 mL physiological saline solution at 7-day intervals. Following treatments, sexually active males were introduced to both experimental groups for 10 days to induce estrus via the “male effect” (Figure 1) [35,36].

2.5. Measurements and Response Variables

2.5.1. Corporal Measurements

Live weight (LW) and body condition score (BCS) were recorded at three points: at the beginning of the experiment, 12 days after initiation, and one day after the third ultrasound evaluation. Body condition was assessed by palpating the lumbar region and scoring on a scale from 1 (very thin) to 4 (very fat).

2.5.2. Determination of Ovarian Size, Structures, and Activity

Thirteen days after male introduction, a transrectal ultrasound (Aloka SSD 500, Tokyo, Japan, 7.5 MHz transducer) was performed to assess ovarian structures in each goat. Estrus induction was determined by calculating the percentage of goats presenting a corpus luteum (i.e., CL) relative to the total number of goats per group. Additionally, the number and diameter of corpora lutea and the left and right ovary diameters were recorded.

2.5.3. Embryonic Rate and Pregnancy Percentage

At 28 days post-male introduction, a fourth ultrasound (Aloka SSD 500, Tokyo, Japan, 7.5 MHz transducer) examination was conducted to detect embryonic vesicles and quantify the number of embryos per female. Embryo implantation rate was calculated as the number of embryos divided by the number of ovulated females per group. Pregnancy confirmation was performed at 56 days post-male introduction via a fifth ultrasound evaluation.

2.6. Statistical Analyses

At enrollment, goats were blocked based on LW and BCS. The response variables of attributes such as LW and BCS were analyzed by a completely random design split-plot analysis of variance for repeated samples in the same animal across time. Response variables included estrus induction response (EI), corpus luteum number (OR) and diameter (CLD), left and right ovary diameter (LOD and ROD), embryonic implantation rate (EMBRYO), and pregnancy rate (PREG). Since both treatment application and response variable quantification were individually collected in both experimental groups, the goat was considered the experimental unit. Thus, the fixed effects treatments as well as sampling date were assessed using a MIXED model for repeated measures across time, with time as the repeated measure and treatment as the repeated subject, regarded as the random error term. Estrus induction (i.e., induced or not) as well as pregnancy rate (i.e., pregnant or not) were analyzed using the generalized linear mixed model procedures with a binomial distribution and logit link function (PROC-GLIMMIX); treatment was the fixed effect. Least-squares means and standard errors for each class of treatments, sampling time, and their interaction were computed; mean comparisons were solved by means of Fisher’s least significant difference. All statistical analyses were done using the procedures of the SAS statistical package version 9.2; a significant difference between means was set at p < 0.05.

3. Results

Table 2 summarizes both experimental groups’ corporal, ovarian, and reproductive responses. No differences (p > 0.05) were found between groups for initial live weight (LW; 41.78 ± 1.08 kg) and body condition score (BCS; 1.69 ± 0.04 units) at the beginning of the breeding period. Similarly, no differences (p > 0.05) were observed for corpus luteum diameter (CLD; 9.1 ± 1.5 mm), left ovary diameter (LOD; 16.6 ± 1.4 mm), or right ovary diameter (ROD; 16.3 ± 1.3 mm). However, key reproductive variables—estrus induction (%), ovulation rate (units), number of embryos (units), and pregnancy rate (%)—were higher (p < 0.05) in the SeVE-supplemented group compared to the control group. Specifically, the SeVE group exhibited increases of 43.75%, 35.00%, 28.50%, and 41.33% over the control group values, respectively. These results indicate that SeVE supplementation improved ovarian activity (i.e., ovulation rate) and enhanced reproductive outcomes (i.e., estrus induction, embryo implantation, and pregnancy rate), without affecting ovarian structure size, suggesting a non-dimensional morphological SeVE’s action.

4. Discussion

Globally, goat production represents a critical source of income and food security for smallholders, particularly in arid and semi-arid regions where other livestock species face significant production constraints. This study tested the hypothesis that SeVE supplementation enhances reproductive performance by increasing ovarian activity, embryo implantation rates, and pregnancy rates in crossbred goats during the anestrus season. The results support this hypothesis: SeVE-supplemented goats exhibited higher values for key reproductive variables without differences in live weight, body condition, or ovarian diameter relative to controls. Therefore, our working hypothesis is not rejected. Interestingly, despite these reproductive enhancements, ovarian structures and corpus luteum diameters remained unaffected. These findings highlight SeVE supplementation as a viable strategy for advancing sustainable livestock production and contributing to global development goals related to responsible production and food security.
At the onset of the experiment, anestrus status was confirmed in all the goats. Following treatment, the SeVE group achieved an 80% estrus induction rate, consistent with previous studies using 10–20 mg P4 and 100 IU eCG administered 24 h after P4 in goats during the anestrus season [37]. The administration of eCG after P4 appears to shorten the time to follicular growth, likely mimicking the luteinizing hormone (LH) surge [38,39,40]. Moreover, a 20 mg P4 dose is sufficient to eliminate short, infertile cycles, enabling effective estrus synchronization and onset of ovarian activity [37]. Females receiving estrus induction protocols supplemented with SeVE achieved 100% induction efficacy [41], likely reflecting an additive or synergistic effect of SeVE on follicular responsiveness and ovulatory outcomes [25,39,42,43].
Regarding ovulation rate—defined as the number of corpora lutea—the SeVE group showed higher values (p < 0.05), suggesting that SeVE supplementation during anestrus enhances follicular development and ovulation even with short-term administration [44]. Selenium supplementation has been reported to stimulate ovarian activity by promoting follicular growth and increasing ovulation rate (i.e., corpus luteum formation) [45]. This effect is partly mediated through enhanced cholesterol availability for progesterone (P4) biosynthesis, with the LRP8 receptor facilitating selenium–protein interactions critical for cholesterol homeostasis [46].
Although no direct link between selenium and GnRH has been identified, selenium may influence LH activity by upregulating GnRH receptor expression in the anterior pituitary, potentially increasing LH synthesis [46]. LH promotes ovarian estrogen release, ovulation, and luteal development [47]. Additionally, selenium may enhance ovarian vascularization, contributing to improved follicular and luteal function [48,49]. In cattle, selenium accumulates in granulosa cells of preovulatory follicles and is associated with corpus luteum development [50]. Furthermore, selenium’s antioxidant role protects corpus luteum function by mitigating oxidative damage [51]. Consistent with prior studies, ovarian size did not differ between groups, suggesting that short-term SeVE supplementation impacts ovarian function rather than structural dimensions [50,51,52].
Embryo implantation and pregnancy rates were also significantly higher in the SeVE-supplemented goats. Selenium is known to promote favorable reproductive tract changes that facilitate sperm transit, fertilization, and implantation [53,54]. Selenium enhances uterine architecture and function by reducing epithelial detachment and increasing myometrial mass [55]. Moreover, selenium-induced increases in P4 synthesis correlate with improved endometrial development, conceptus survival, embryo growth, and pregnancy maintenance [25,56,57]. Synchronization between the embryo and the maternal endometrium prior to implantation is critical. Selenium supplementation has been linked to differential gene expression in maternal recognition of pregnancy, particularly those responsive to INFtau and P4 [53]. Using a blend of organic and inorganic selenium (i.e., 35 ppm) has demonstrated improvements in endometrial and conceptus gene expression [58]. Moreover, preventive SeVE supplementation has improved pregnancy rates post-embryo transfer in heifers (64.7% vs. 41.2%); the latter denotes an interesting cross-species relevance in ruminants [59].
Despite these positive effects, some studies report neutral or negative outcomes of selenium supplementation. For example, no differences in reproductive efficiency were observed in some trials [53,54], possibly due to adequate baseline nutrition, which masks supplementation effects. Similarly, no differences in LW or BCS were observed between groups in this study, aligning with prior findings in goats [60,61] and ewes treated with Se and vitamin E during estrus synchronization [25]. In contrast, excessive or long-term selenium supplementation may impair blastocyst quality and implantation success due to tissue selenium accumulation and embryotoxicity [62]. Therefore, assessing baseline feed mineral content before supplementation is crucial, in addition to tailoring interventions to the physiological stage, timing, dose, and administration route to optimize outcomes [63].
Undeniably, the results obtained represent practical and accessible options for goat producers not only from the biological, productive, and economic perspectives, but also in marginal contexts. In fact, the SeVE group showed a 43.8% improvement in the pregnancy rate, which corresponds to an increase in offspring of 0.7 per goat. If the cost per treatment (i.e., SeVE) is equivalent to USD 1.83 per goat and the selling price for a kid is around USD 51.16 (i.e., MXN 1000), revenues increase up to MXN 35.81 per goat. This means that SeVE treatment shows a cost–benefit ratio of 19.57; if producers invest USD 1, they receive USD 19.57. The above considerations are based on the sale of meat alone; such scenarios can rise significantly if additional revenues are derived from an increasing milk volume in dairy goat production systems.

5. Conclusions

The obtained results support our working hypothesis that short-term precision supplementation with selenium and vitamin E in adult crossbred dairy goats improves key reproductive variables, such as estrus induction, ovulation rate, embryo implantation, and pregnancy rate. Such enhancements occurred with no significant differences between the experimental groups’ live weight or body condition scores. Similarly, no variations occurred in the diameters of the left and right ovaries or the corpus luteum diameters. Thus, a short-term supplementation may not achieve the requested Se level to potentially affect some “long-term response variables” (i.e., live weight, body condition score, and ovarian size–morphology), but it will undoubtedly affect other “short-term response variables” (i.e., estrus induction (i.e., d27), embryo implantation rate (i.e., d42), and pregnancy rate (d70). Improving reproductive outcomes could help not only to stabilize goat producers’ and their families’ year-round income but could also contribute to higher animal protein supply and greater resilience in marginal goat production systems. Undoubtedly, longitudinal studies to evaluate the economic sustainability and scalability of our research findings, are certainly pending assignments.

Author Contributions

Conceptualization, C.A.M.-H., G.C.-L. and O.A.-G.; Data curation, R.S.-S. and C.A.M.-H.; Formal analysis, C.A.M.-H. and G.C.-L.; Funding acquisition, O.A.-G., J.M.F.-S., F.A.-R., A.D.S.-M. and C.A.R.-N.; Investigation, R.S.-S., B.C.-R. and O.A.-G.; Methodology, R.S.-S., C.A.M.-H., B.C.-R., G.C.-L. and C.N.-M.; Project administration, O.A.-G., J.M.F.-S., A.D.S.-M. and F.A.-R.; Resources, C.N.-M., O.A.-G., J.M.F.-S., F.A.-R. and C.A.R.-N.; Software, C.N.-M. and C.A.R.-N.; Supervision, C.A.M.-H., A.D.S.-M. and O.A.-G.; Validation, C.N.-M. and O.A.-G.; Visualization, C.N.-M. and C.A.R.-N.; Writing—original draft, C.A.M.-H. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

All the experimental procedures were completed in accordance with the recommendations for the ethical use, care, and welfare of animals in research at global (USA) and national (Mexico) levels, and they were institutionally authorized by UAAAN; the animal study protocol was authorized by the Institutional Review Board, with approval reference number: UAAAN-UL-38111-425501002-2876.

Informed Consent Statement

Informed consent was obtained from the animal owner involved in the study.

Data Availability Statement

None of the data were deposited in an official repository, yet information can be made available upon request.

Acknowledgments

The authors thank Ricardo Martinez Rangel for providing the goats for this study. We also acknowledge SECIHTI-Mexico for the scholarship awarded to Raquel Santos-Silva for her M.Sc. studies at UACH-URUZA, Bermejillo, Durango, Mexico.

Conflicts of Interest

The authors declare that there are no conflicts of interest that could be perceived as prejudicing the impartiality of the research reported in this manuscript. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

Abbreviations

The following abbreviations are used in this manuscript:
SeVeSelenium and vitamin EP4Progesterone
SeSeleniumeCGEquine chorionic gonadotropin hormone
VEVitamin ECONTControl group
EIEstrus inductionCLComarca Lagunera
OROvulatory rateDNADeoxyribonucleic acid
CLDCorpus luteum diameterRNARibonucleic acid
LODLeft ovary diameterGSH-PxGlutathione peroxidase
RODRight ovary diameterCPCrude protein
EMBRYOEmbryo implantationUsUltrasound
PREGPregnancy percentageSaSoSaline Solution
LWLive weightLHLuteinizing Hormone
BCSBody condition scoreGnRHGonadotropin-releasing hormone

References

  1. Bustamante-Andrade, J.A.; Meza-Herrera, C.A.; Rodríguez-Martínez, R.; Santos-Jimenez, Z.; Ángel-García, O.; Gaytán-Alemán, L.R.; Gutierrez-Guzman, U.N.; Esquivel-Romo, A.; Véliz-Deras, F.G. Luteogenesis and Embryo Implantation Are Enhanced by Exogenous hCG in Goats Subjected to an Out-of-Season Fixed-Time Artificial Insemination Protocol. Biology 2021, 10, 429. [Google Scholar] [CrossRef] [PubMed]
  2. Meza-Herrera, C.A.; Navarrete-Molina, C.; Macias-Cruz, U.; Arellano-Rodriguez, G.; De Santiago-Miramontes, A.; Sariñana-Navarrete, M.A.; Marin-Tinoco, R.I.; Perez-Marin, C. Dairy Goat Production Systems: A Comprehensive Analysis to Reframe Their Global Diversity. Animals 2024, 14, 3717. [Google Scholar] [CrossRef] [PubMed]
  3. Navarrete-Molina, C.; Meza-Herrera, C.A.; De Santiago-Miramontes, A.; Valenzuela-Núñez, L.M.; Marin-Tinoco, R.I.; Soto-Cardenas, M.A.; Sariñana-Navarrete, M.A. Dairy Goat Production: Socioeconomic, Environmental, and Cultural Importance Across Time (1970–2022) and Possible Scenarios (2050). Resources 2024, 13, 177. [Google Scholar] [CrossRef]
  4. Loomis, C.; Kerven, C. The Environmental Impact of Goats: Uprooting the Narrative. Front. Anim. Sci. 2025, 6, 1544366. [Google Scholar] [CrossRef]
  5. Chávez-Espinoza, M.; Cantú-Silva, I.; González-Rodríguez, H.; Montañez-Valdez, O.D. Sistemas de Producción de Pequeños Rumiantes en México y su Efecto en la Sostenibilidad Productiva. Rev. MVZ Córdoba 2022, 27, e2246. [Google Scholar] [CrossRef]
  6. SIAP—Servicio de Informacion Agroalimentaria y Pesquera—Agrifood and Fishery Information System. Avance Mensual de la Producción Pecuaria. 2023. Available online: http://nube.agricultura.gob.mx/avance_pecuario/ (accessed on 13 March 2025). (In Spanish).
  7. Veliz-Deras, F.G.; Meza Herrera, C.A.; De Santiago Miramontes, A.; Santos-Alvarado, A.; Bustamante-Andrade, J.A.; Flores-Salas, J.M.; Arellano-Rodríguez, F.; Mellado, M. An Enhanced Body Condition Improved Sexual Behavior, Ovarian Structure and Function, and Reproductive Fitness in Rangeland-Crossbred Dairy Goats. Agriculture 2023, 13, 1337. [Google Scholar] [CrossRef]
  8. Meza-Herrera, C.A.; Santamaría-Estrada, C.E.; Flores-Hernández, A.; Cano-Villegas, O.; García de la Peña, G.; Macias-Cruz, U.; Calderón-Leyva, G.; Ángel-García, O.; Mellado, M.; Carrillo-Moreno, D.; et al. The Opuntia Effect Upon the Out-of-Season Embryo Implantation Rate in Goats: Corpus Luteal Number, Corpus Luteal Diameter and Serum Progesterone Concentrations. Livest. Sci. 2019, 228, 201–206. [Google Scholar] [CrossRef]
  9. Luna-Garcia, L.A.; Meza-Herrera, C.A.; Perez-Marin, C.C.; De Santiago-Miramontes, A.; Flores-Salas, J.M.; Corona, R.; Calderon-Leyva, G.; Veliz-Deras, F.G.; Navarrete-Molina, C.; Marin-Tinoco, R.I. Targeted Glutamate Supply Boosts Insulin Concentrations, Ovarian Activity, and Ovulation Rate in Yearling Goats during the Anestrous Season. Biology 2023, 12, 1041. [Google Scholar] [CrossRef]
  10. Meza-Herrera, C.A.; Cano-Villegas, O.; Flores-Hernandez, A.; Veliz-Deras, F.G.; Calderon-Leyva, G.; Guillen-Muñoz, J.M.; García-de la Peña, C.; Rosales-Nieto, C.A.; Macias-Cruz, U.; Avendaño-Reyes, L. Reproductive Outcomes of Anestrous Goats Supplemented with Spineless Opuntia megacantha Salm-Dyck Protein-Enriched Cladodes and Exposed to the Male Effect. Trop. Anim. Health Prod. 2017, 49, 1511–1516. [Google Scholar] [CrossRef]
  11. Nava, J.F.; Ángel, G.O.; Rojas, H.S.; Olivares, P.J.; Quiroz, C.F.; Valdés, M.A.D.; Robledo, R.E.E. Efecto de la Pulpa de Café Sobre la Calidad de la Leche en Cabras en Pastoreo en el Norte de México. Arch. Latinoam. Prod. Animal 2023, 31, 169–173. (In Spanish) [Google Scholar] [CrossRef]
  12. Mayasula, V.K.; Arunachalam, A.; Babatunde, S.A.; Naidu, S.J.; Sellappana, S.; Krishnan, B.B.; Rajendran, U.S.; Janardhan, R.I.; Bhatta, R. Trace Minerals for Improved Performance: A Review of Zn and Cu Supplementation Effects on Male Reproduction in Goats. Trop. Anim. Health Prod. 2021, 53, 491. [Google Scholar] [CrossRef]
  13. Morsy, A.S.; El-Zaiat, H.M.; Saber, A.M.; Anwer, M.M.; Sallam, S.M. Impact of Organic Selenium and Vitamin E on Rumen Fermentation, Milk Production, Feed Digestibility, Blood Parameters and Parasitic Response of Lactating Goats. J. Agric. Sci. Technol. 2019, 21, 1793–1806. [Google Scholar]
  14. Barcelos, B.; Gomes, V.; Vidal, A.M.C.; de Freitas Júnior, J.E.; de Araújo, M.L.G.M.L.; Alba, H.D.R.; Netto, A.S. Effect of Selenium and Vitamin E Supplementation on the Metabolic Status of Dairy Goats and Respective Goat Kids in the Peripartum Period. Small Rumin. Res. 2023, 54, 36. [Google Scholar] [CrossRef] [PubMed]
  15. Ziaei, N. Effect of Selenium and Vitamin E Supplementation on Reproductive Indices and Biochemical Metabolites in Raieni Goats. J. Appl. Anim. Res. 2015, 43, 426–430. [Google Scholar] [CrossRef]
  16. Crites, B.R.; Carr, S.N.; Matthews, J.C.; Bridges, P.J. Form of Dietary Selenium Affects mRNA Encoding Cholesterol Biosynthesis and Immune Response Elements in the Early Luteal Phase Bovine Corpus Luteum. J. Anim. Sci. 2022, 100, skac135. [Google Scholar] [CrossRef]
  17. Hosnedlova, B.; Kepinska, M.; Skalickova, S.; Fernandez, C.; Ruttkay-Nedecky, B.; Malevu, T.D.; Sochor, J.; Baron, M.; Melcova, M.; Zidkova, J.; et al. A Summary of New Findings on the Biological Effects of Selenium in Selected Animal Species—A Critical Review. Int. J. Mol. Sci. 2017, 18, 2209. [Google Scholar] [CrossRef]
  18. Talukder, S.; Kerrisk, K.L.; Gabai, G.; Fukutomi, A.; Celi, P. Changes in Milk Oxidative Stress Biomarkers in Lactating Dairy Cows with Ovulatory and An-ovulatory Oestrous Cycles. Anim. Repro. Sci. 2015, 158, 86–95. [Google Scholar] [CrossRef]
  19. Tarhonska, K.; Raimondi, S.; Specchia, C.; Wieczorek, E.; Reszka, E.; Krol, M.B.; Gromadzinska, J.; Wasowicz, W.; Socha, K.; Borawska, M.H.; et al. Association of Allelic Combinations in Selenoprotein and Redox Related Genes with Markers of Lipid Metabolism and Oxidative Stress–Multimarkers Analysis in a Cross-Sectional Study. J. Trace Elem. Med. Biol. 2022, 69, 126873. [Google Scholar] [CrossRef]
  20. Hien, N.T.T. Monitoring Estradiol and Progesterone Content of Saanen Goats During Pregnancy. Int. J. Multidiscip. Res. Anal. 2024, 7, 4636–4642. [Google Scholar] [CrossRef]
  21. Qazi, I.H.; Angel, C.; Yang, H.; Pan, B.; Zoidis, E.; Zeng, C.J.; Han, H.; Zhou, G.B. Selenium, Selenoproteins, and Female Reproduction: A Review. Molecules 2018, 23, 3053. [Google Scholar] [CrossRef]
  22. Safiyeh, F.D.; Mojgan, M.; Parviz, S.; Sakineh, M.A.; Behnaz, S.O. The Effect of Selenium and Vitamin E Supplementation on Anti-Mullerian Hormone and Antral Follicle Count in Infertile Women with Occult Premature Ovarian Insufficiency: Randomized Controlled Clinical Trial. Complement. Ther. Med. 2021, 56, 102533. [Google Scholar] [CrossRef] [PubMed]
  23. Sobiech, P.; Żarczyńska, K. The Influence of Selenium Deficiency on Chosen Biochemical Parameters and Histopathological Changes in Muscles of Goat Kids. Pol. J. Vet. Sci. 2020, 23, 267–279. [Google Scholar] [CrossRef] [PubMed]
  24. Yildiz, A.; Balikçi, E.; Gürdoğan, F. Effect of Injection of Vitamin E and Selenium Administered Immediately Before the Ovsynch Synchronization on Conception Rate, Antioxidant Activity and Progesterone Levels in Dairy Cows. Sağlık Bilim. Vet. Derg. Fırat Üniversitesi 2015, 29, 183–186. [Google Scholar]
  25. Awawdeh, M.S.; Eljarah, A.H.; Ababneh, M.M. Multiple Injections of Vitamin E and Selenium Improved the Reproductive Performance of Estrus-Synchronized Awassi Ewes. Trop. Anim. Health Prod. 2019, 51, 1421–1426. [Google Scholar] [CrossRef]
  26. Hiywotu, A.M. Advancing Sustainable Agriculture for Goal 2: Zero Hunger—A Comprehensive Overview of Practices, Policies, and Technologies. Agroecol. Sustain. Food Syst. 2025, 1–29. [Google Scholar] [CrossRef]
  27. Katherasala, S.; Bheenaveni, R.S.; Venkat, S.R.G.; Thaduru, S.; Rituraj, A.; Sirugumalle, N. The Looming Food Crisis: Exploring the Causes and Consequences—A Comprehensive Analysis and Strategic Recommendations for SDGs 2. J. Lifestyle SDGs Rev. 2024, 5, e02795. [Google Scholar] [CrossRef]
  28. FASS—Federation Animal Science Society. Guide for the Care and Use of Agricultural Animals in Agricultural Research and Teaching, 3rd ed.; Federation Animal Science Society: Champaign, IL, USA, 2010; p. 177. [Google Scholar]
  29. NAM—National Academy of Medicine. Guide for the Care and Use of Laboratory Animals, 1st ed.; National Academy of Medicine: Mexico City, Mexico; Association for Assessment and Accreditation of Laboratory Animal Care International: Harlan, KY, USA, 2002. [Google Scholar]
  30. CONAGUA—Comision Nacional del Agua—National Water Comission. Normales Climatológicas por Estación. Ciudad de México: Servicio Meteorológico Nacional, Comisión Nacional del Agua. 2024. Available online: https://smn.conagua.gob.mx/es/ (accessed on 12 March 2025). (In Spanish).
  31. INEGI—Instituto Nacional de Estadística y Geografía—National Institute of Statistics and Geography. Anuario Estadístico y Geográfico de Coahuila de Zaragoza 2016. 2016. Available online: https://www.inegi.org.mx/contenidos/productos/prod_serv/contenidos/espanol/bvinegi/productos/nueva_estruc/anuarios_2016/702825083632.pdf (accessed on 12 March 2025). (In Spanish).
  32. Karadaev, M. Pregnancy Diagnosis Techniques in Goats—A Review. Bulg. J. Vet. Med. 2015, 18, 183–193. [Google Scholar] [CrossRef]
  33. Urrutia-Morales, J.; Rosales-Nieto, C.A.; Vera-Ávila, H.R.; Villagómez-Amezcua-Manjarres, E. Resumption of Ovarian Activity is Modified by Non-Photoperiodic Environmental Cues in Criollo Goats in Tropical Latitudes. Small Rumin. Res. 2016, 137, 9–16. [Google Scholar] [CrossRef]
  34. Association of Official Analytical Chemists (AOAC). Official Methods of Analysis of AOAC International, 22nd ed.; Latimer, G.W., Jr., Ed.; AOAC: Arlington, VA, USA, 2023. [Google Scholar] [CrossRef]
  35. Delgadillo, J.A.; Duarte, G.; Flore, A.; Vielma, J.; Hernández, H.; Fitz Rodríguez, G.; Bedos, M.; Fernández, I.; Muñoz-Gutiérrez, M.; Retana Márquez, M.S.; et al. Control de la Actividad Sexual de los Caprinos sin Hormonas Exógenas: Uso del Fotoperiodo, Efecto Macho y Nutrición. Trop. Subtrop. Agroecosystems 2012, 15, S15–S27. (In Spanish) [Google Scholar] [CrossRef]
  36. Rosales-Nieto, C.A.; Thompson, A.N.; Cuevas-Reyes, V.; Hérnandez-Arteaga, L.E.; Greeff, J.C.; Ehrhardt, R.; Veiga-Lopez, A.; Martin, G.B. Utilising Male Stimulus to Improve the Reproductive Efficiency of 8-Month-Old Nulliparous Ewes and Adult Parous Ewes. Theriogenology 2024, 217, 143–150. [Google Scholar] [CrossRef]
  37. Veliz-Deras, F.G.; Meza-Herrera, C.A.; Mellado, M.; Contreras-Villareal, V.; Gaytán-Alemán, L.R.; Guillén-Muñoz, J.M. The Effect of P4 + eCG Estrus Induction Protocol during the Deep and the Transition Anestrous Period on the Reproductive Performance of Crossbred Dairy Goats. Biology 2020, 9, 311. [Google Scholar] [CrossRef] [PubMed]
  38. Álvarez, R.L.; Gamboa, B.D. Male Contact can Replace Equine Chorionic Gonadotropin (eCG) Injection in Anestrus Progesterone-Treated Dairy Goats. Spei Domus 2024, 20, 1–14. [Google Scholar] [CrossRef]
  39. Oliveira, C.I.; Alvares, B.m.f.; Martins, S.P.; Ryonosuke, T.A.; Rodrigues, S.J.D.; Sarzedas, R.A.C.; Rigaud, F.B.R.; Campos, P.C.M.M.; Ribeiro, V.B.; Zandonadi, B.F. Influence of eCG and Reproductive Management in the Resynchronization of Ovulation in Dairy Goats. Anim. Reprod. 2022, 19, e20210112. [Google Scholar] [CrossRef]
  40. Sharif, B.; Hassan, M.; Arshad, U.; Tahir, M.Z.; Ahmad, E.; Khan, M.I.; Shahzad, M.; Mohsin, I.; Sosa, F.; Rehman, A. Effect of eCG dose on Ovarian Haemodynamics, Hormonal Profiles and Prolificacy Rate when Oestrus was Induced During Low-Breeding Season in Beetal Goats. Reprod. Domest. Anim. 2023, 58, 48–59. [Google Scholar] [CrossRef]
  41. Mujawar, A.S.; Razzaque, W.A.A.; Ramteke, S.S.; Patil, A.D.; Ali, S.S.; Bhikane, A.U.; Khan, M.A.; Mogal, I.R. Estrus Induction and Fertility Response in Postpartum Anoestrus Marathwadi Buffaloes using Hormonal Protocol Along with Vitamin E and Selenium. Int. J. Livest. Res. 2019, 9, 289–296. [Google Scholar] [CrossRef]
  42. Kolikapongu, R.S.; Namani, S.C.; Shaik, A.; Neha, A.; Chelkapally, S.C.; Perry, C.; Woodard, J.; Schauston, M.; Whitley, N.C.; Kouakou, B.; et al. PSIII-12 The Effects of PGF2 and PGF2 Plus Gnrh on Estrous Behavior and Pregnancy Outcomes in Dairy Goats. J. Anim. Sci. 2023, 101, 390–391. [Google Scholar] [CrossRef]
  43. Mishra, S.K.; Kumar, A.; Anand, M.; Sachan, V.; Saxena, A. Effect of different estrus synchronization protocols on reproductive performance of barbari goats. J. Anim. Res. 2023, 13, 809–813. [Google Scholar] [CrossRef]
  44. Abdel-Raheem, S.M.; Mahmoud, G.B.; Senosy, W.; El-Sherry, T.M. Influence of Vitamin E and Selenium Supplementation on the Performance, Reproductive Indices and Metabolic Status of Ossimi Ewes. Slov. Vet. Res. 2019, 56, 353–363. [Google Scholar] [CrossRef]
  45. Vázquez-Hernández, S.D.; Miranda-Jiménez, L.; Segura-León, O.; Quero Carrillo, A.R. Desarrollo de Folículos y Cuerpo Lúteo en Cabras como Respuesta al Suministro de Selenio. Agroproductividad 2017, 10, 15–18. (In Spanish) [Google Scholar]
  46. Toh, P.; Nicholson, J.L.; Vetter, A.M.; Berry, M.J.; Torres, D.J. Selenium in Bodily Homeostasis: Hypothalamus, Hormones, and Highways of Communication. Int. J. Mol. Sci. 2022, 23, 15445. [Google Scholar] [CrossRef]
  47. Hou, B.; Mao, M.; Dong, S.; Deng, M.; Sun, B.; Guo, Y.; Li, Y.; Liu, D.; Liu, G. Transcriptome Analysis Reveals mRNAs and long Non-coding RNAs Associated with Fecundity in the Hypothalamus of High-And Low-Fecundity Goat. Front. Vet. Sci. 2023, 10, 1145594. [Google Scholar] [CrossRef] [PubMed]
  48. Luo, J.; Wang, W.; Sun, S. Research Advances in Reproduction for Dairy Goats. Asian Australas. J. Anim. Sci. 2019, 32, 1284. [Google Scholar] [CrossRef]
  49. Wang, Y.; Chao, T.; Li, Q.; He, P.; Zhang, L.; Wang, J. Metabolomic and Transcriptomic Analyses Reveal the Potential Mechanisms of Dynamic Ovarian Development in Goats during Sexual Maturation. Int. J. Mol. Sci. 2024, 25, 9898. [Google Scholar] [CrossRef] [PubMed]
  50. Hummitzsch, K.; Kelly, J.E.; Hatzirodos, N.; Bonner, W.M.; Tang, F.; Harris, H.H.; Rodgers, R.J. Expression levels of the selenium-uptake receptor LRP8, the antioxidant selenoprotein GPX1 and steroidogenic enzymes correlate in granulosa cells. Reprod. Fertil. 2024, 5, e230074. [Google Scholar] [CrossRef]
  51. Farahavar, A.; Rostami, Z.; Alipour, D.; Ahmadi, A. The Effect of Pre-Breeding Vitamin E and Selenium Injection on Reproductive Performance, Antioxidant Status, and Progesterone Concentration in Estrus-Synchronized Mehraban Ewes. Trop. Anim. Health Prod. 2020, 52, 1779–1786. [Google Scholar] [CrossRef]
  52. Grazul-Bilska, A.T.; Neville, T.L.; Borowczyk, E.; Sharma, A.; Reynolds, L.P.; Caton, J.S.; Redmer, D.A.; Vonnahme, K.A. Ovarian and Uterine Characteristics and Onset of Puberty in Adolescent Offspring: Effects of Maternal Diet and Selenium Supplementation in Sheep. Theriogenology 2014, 81, 887–895. [Google Scholar] [CrossRef]
  53. Dahlen, C.R.; Reynolds, L.P.; Caton, J.S. Selenium Supplementation and Pregnancy Outcomes. Front. Nutr. 2022, 9, 1011850. [Google Scholar] [CrossRef]
  54. Ortega-Morales, N.B.; Cueto-Wong, J.A.; Velez-Monroy, L.I.; Chavez-Solis, A.U.; Barrientos-Juarez, E.; Duarte-Sustaita, J.J.; Veliz-Deras, F.G.; Calderon-Leyva, G.; Moran-Martinez, J. Counteracting the Toxic Hidroarsenicism Effects upon Reproductive-Physiological Outcomes in Male Goats: The Selenium and Vitamin-E Mitigation Approach. Animals 2023, 13, 2055. [Google Scholar] [CrossRef]
  55. Alalaf, A.S.; Alnuaimy, R. Evaluating the Influence of Vitamin E and Selenium on the Uterine Health of Adult Female Goats: A Histological Study. Egypt. J. Vet. Sci. 2024, 1–9. [Google Scholar] [CrossRef]
  56. Musa, S.I.; Bitto, I.I.; Ayoade, J.A.; Oyedipe, O.E. Effects of Vitamin E and Selenium on Fertility and Lamb Performance of Yankasa Sheep. Open J. Vet. Med. 2018, 8, 167. [Google Scholar] [CrossRef]
  57. Carr, S.; Jia, Y.; Crites, B.; Hamilton, C.; Burris, W.; Edwards, J.L.; Mattews, J.; Bridges, P.J. Form of Supplemental Selenium in Vitamin-Mineral Premixes Differentially Affects Early Luteal and Gestational Concentrations of Progesterone, and Postpartum Concentrations of Prolactin in Beef Cows. Animals 2020, 10, 967. [Google Scholar] [CrossRef] [PubMed]
  58. Crites, R.B. The Effects of Form of Selenium on the Bovine Corpus Luteum, Uterine Endometrium, and Development of the Conceptus. Ph.D. Thesis, University of Kentucky, Lexington, Kentucky, 12 June 2021. [Google Scholar] [CrossRef]
  59. Šmigoc, J.; Vrtač, K.P.; Strajn, B.J.; Stvarnik, M.; Mrkun, J. Preventive Supplementation of Vitamin E and Selenium as a Factor in Improving the Success Rate of Embryo Transfer in Cattle. Acta Vet. 2023, 73, 87–101. [Google Scholar] [CrossRef]
  60. Abdou, A.R. Effect of Selenium and Vitamin E Injection on Digestibility Coefficients and Nutritive Value of Baladi Doe Goats in Southern Sinai. Egypt. J. Nutr. Feeds 2021, 24, 37–47. [Google Scholar] [CrossRef]
  61. Ramadan, S.G.A.; Mahboub, H.D.H.; Helal, M.A.Y.; Sallam, M.A. Effect of Vitamin E and Selenium on Performance and Productivity of Goats. Int. J. Chem. Biomed. Sci. 2018, 4, 16–22. [Google Scholar]
  62. Mamon, M.A.C.; Ramos, G.B. Maternal Selenium-Supplementation at Various Stages of Periconception Period: Influence on Murine Blastocyst Morphology and Implantation Status. J. Anim. Sci. Technol. 2017, 59, 7. [Google Scholar] [CrossRef]
  63. Özar, E.; Kemal, S.M.; Köse, A.M.; Sertkol, R. Effect of Selenium, Vitamin E, and β-Carotene Administration on Fertility of Synchronized Awassi Ewes During Non-Breeding Season. Vet. J. Mehmet Akif Ersoy Univ. 2022, 7, 167–174. [Google Scholar] [CrossRef]
Figure 1. A schematic overview of the experimental timeline is presented. Two ultrasounds (US 1 and 2) were performed before estrus induction (following P4 and eCG administration), and subsequent evaluations (US 3, 4, and 5) assessed ovulation rate, ovarian activity, embryo development, and pregnancy status during the seasonal anestrus period at 25° N latitude.
Figure 1. A schematic overview of the experimental timeline is presented. Two ultrasounds (US 1 and 2) were performed before estrus induction (following P4 and eCG administration), and subsequent evaluations (US 3, 4, and 5) assessed ovulation rate, ovarian activity, embryo development, and pregnancy status during the seasonal anestrus period at 25° N latitude.
Animals 15 01421 g001
Table 1. Chemical composition of alfalfa hay, commercial concentrate, and mineral salts that comprised the basal diet in the adult multibreed goats supplemented with selenium + vitamin E (SeVE; n = 16) or control (CONT; n = 16) under natural photoperiod conditions during the anestrus season in northern Mexico (25° N).
Table 1. Chemical composition of alfalfa hay, commercial concentrate, and mineral salts that comprised the basal diet in the adult multibreed goats supplemented with selenium + vitamin E (SeVE; n = 16) or control (CONT; n = 16) under natural photoperiod conditions during the anestrus season in northern Mexico (25° N).
ItemAlfalfa Hay aCommercial Concentrate bMineral Salts b
Nutrient Composition(%)(%)(%)
Dry matter92.8- -- -
Crude protein15.514.0- -
Neutral detergent fiber56.9- -- -
Acid detergent fiber41.1- -- -
Crude Fat- -6.8- -
Crude Fiber- -2.0- -
Humidity- -10.8- -
Ash- -5.5- -
Nitrogen-Free Extract- -62.9- -
Phosphorus0.26- -9.0
Calcium1.71- -8.5
Magnesium0.20- -1.2
Sodium0.12- -- -
Chlorine0.35- -- -
Potassium2.16- -- -
Iron- -- -740 ppm
Manganese- -- -2030 ppm
Zinc- -- -2600 ppm
Copper- -- -520 ppm
Iodine- -- -96 ppm
Cobalt- -- -12 ppm
Selenium- -- -10 ppm
a Composition values were determined according to the procedures outlined by AOAC, 2023 [34]. b Nutritional values correspond to the guaranteed analysis declared by the manufacturer.
Table 2. Least squares means ± standard error for live weight (LW, kg), body condition score (BCS, units), estrus induction (EI, %), ovulation rate (OR, units), corpus luteum diameter (CLD, mm), left ovary diameter (LOD, mm), right ovary diameter (ROD, mm), embryo number (EMBRYO, units), and pregnancy rate (PREG, %) in adult multibreed goats supplemented with selenium + vitamin E (SeVE; n = 16) or control (CONT; n = 16) under natural photoperiod conditions during the anestrus season in northern Mexico (25° N).
Table 2. Least squares means ± standard error for live weight (LW, kg), body condition score (BCS, units), estrus induction (EI, %), ovulation rate (OR, units), corpus luteum diameter (CLD, mm), left ovary diameter (LOD, mm), right ovary diameter (ROD, mm), embryo number (EMBRYO, units), and pregnancy rate (PREG, %) in adult multibreed goats supplemented with selenium + vitamin E (SeVE; n = 16) or control (CONT; n = 16) under natural photoperiod conditions during the anestrus season in northern Mexico (25° N).
VariablesSeVECONT
LW, kg42.04 ± 1.67 a41.53 ± 1.43 a
BCS, units1.72 ± 0.06 a1.66 ± 0.06 a
Ovarian Size and Activity
EI, %80.0 ± 11 a35.0 ± 12 b
OR, units1.20 ± 0.22 a0.42 ± 0.22 b
CLD, mm9.1 ± 1.1 a9.2 ± 1.9 a
LOD, mm16.5 ± 1.2 a16.8 ± 1.7 a
ROD, mm15.6 ± 1.1 a17.0 ± 1.5 a
Embryo Number and Pregnancy Rate
EMBRYO, units1.23 ± 0.20 a0.35 ± 0.19 b
PREG, %75.0 ± 11.4 a31.2 ± 11.2 b
a,b Values on the same line with different superscripts differ (p < 0.05).
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

Santos-Silva, R.; Meza-Herrera, C.A.; Castro-Roque, B.; Calderón-Leyva, G.; Navarrete-Molina, C.; Angel-García, O.; Flores-Salas, J.M.; De Santiago-Miramontes, A.; Arellano-Rodriguez, F.; Rosales-Nieto, C.A. Selenium + Vitamin E Supplementation in Anestrus Goats: A Strategy to Enhance Reproductive Outcomes Under a Semi-Arid Production System. Animals 2025, 15, 1421. https://doi.org/10.3390/ani15101421

AMA Style

Santos-Silva R, Meza-Herrera CA, Castro-Roque B, Calderón-Leyva G, Navarrete-Molina C, Angel-García O, Flores-Salas JM, De Santiago-Miramontes A, Arellano-Rodriguez F, Rosales-Nieto CA. Selenium + Vitamin E Supplementation in Anestrus Goats: A Strategy to Enhance Reproductive Outcomes Under a Semi-Arid Production System. Animals. 2025; 15(10):1421. https://doi.org/10.3390/ani15101421

Chicago/Turabian Style

Santos-Silva, Raquel, Cesar A. Meza-Herrera, Brenda Castro-Roque, Guadalupe Calderón-Leyva, Cayetano Navarrete-Molina, Oscar Angel-García, Jessica M. Flores-Salas, Angeles De Santiago-Miramontes, Fernando Arellano-Rodriguez, and Cesar A. Rosales-Nieto. 2025. "Selenium + Vitamin E Supplementation in Anestrus Goats: A Strategy to Enhance Reproductive Outcomes Under a Semi-Arid Production System" Animals 15, no. 10: 1421. https://doi.org/10.3390/ani15101421

APA Style

Santos-Silva, R., Meza-Herrera, C. A., Castro-Roque, B., Calderón-Leyva, G., Navarrete-Molina, C., Angel-García, O., Flores-Salas, J. M., De Santiago-Miramontes, A., Arellano-Rodriguez, F., & Rosales-Nieto, C. A. (2025). Selenium + Vitamin E Supplementation in Anestrus Goats: A Strategy to Enhance Reproductive Outcomes Under a Semi-Arid Production System. Animals, 15(10), 1421. https://doi.org/10.3390/ani15101421

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