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Influence of prenatal corticosteroid therapy on neonatal vitality and utility as a labor-inducing agent in Santa Inês ewes

Abstract

Since the 1970s, maternal corticosteroid therapy has been used successfully to induce labor. This allows for better monitoring of parturients and provision of first aid to neonates, improving neonatal viability, as this treatment induces maturation in a variety of fetal tissues, thereby reducing morbidity and mortality. Although the effects of corticosteroids are well known, few studies have investigated the influence of this therapy in Santa Inês sheep. This study aimed to evaluate the efficacy of dexamethasone at two doses (8 and 16 mg) to induce lambing in Santa Inês ewes at 145 days of gestation and assess its effects on neonatal vitality. For this study, 58 ewes raised in an extensive system were investigated. Pregnancy was confirmed after artificial insemination at a set time or after controlled mounting. Ewes were separated into three groups: an untreated control group (G1: 0 mg) and groups treated with two doses of dexamethasone (G2: 8 mg and G3: 16 mg). In total, 79 lambs were born. Their vitality was assessed based on their Apgar score, weight, temperature, and postnatal behavior. SAS v9.1.3 (SAS Institute, Cary, NC) was used to analyze data, considering a 5% significance level for all analyses. The births in the induced groups occurred 48.4 ± 22.1 h after induction, while the ewes that underwent non-induced labor gave birth 131.96 ± 41.9 h after placebo application (p < 0.05), confirming the efficacy of dexamethasone to induce and synchronize labor. The induced and non-induced neonates had similar Apgar scores, temperatures, weights, and postnatal behavioral parameters (p > 0.05). This study showed that inducing labor in Santa Inês ewes at 145 days of gestation with a full (16 mg) or half dose (8 mg) of dexamethasone is an effective technique and does not compromise neonate vitality.

Keywords:
corticosteroid; parturient; reproductive biotechnology; sheep

Introduction

Since the 1970s, many studies have reported on inducing labor in sheep (Adams and Wagner, 1970Adams WM, Wagner C. The role of corticoids in parturition. Biol Reprod. 1970;3(2):223-8. http://dx.doi.org/10.1093/biolreprod/3.2.223. PMid:5522854.
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). This method aims to synchronize parturitions to streamline workers’ labor so that they may provide assistance to sheep and manage neonates, thereby minimizing maternal and neonatal mortality and enhancing breeding efficiency (Özalp et al., 2017Özalp RG, Yavuz A, Orman A, Seker I, Udum Küçükşen D, Rişvanlı A, Demiral ÖO, Wehrend A. Parturition induction in ewes by a progesterone receptor blocker, aglepristone, and subsequent neonatal survival: preliminary results. Theriogenology. 2017;87:141-7. http://dx.doi.org/10.1016/j.theriogenology.2016.08.016. PMid:27658744.
http://dx.doi.org/10.1016/j.theriogenolo...
). Among the currently available drugs capable of inducing labor in ewes, dexamethasone (DEX) is most often used and has shown to be efficient and inexpensive as compared to other labor-inducing drugs. The dose most commonly used is 16 mg (Kastelic et al., 1996Kastelic JP, Cook RB, McMahon LR, McAllister TA, McClelland LA, Cheng KJ. Induction of parturition in ewes with dexamethasone or dexamethasone and cloprostenol. Can Vet J. 1996;37(2):101-2. PMid:8640645.; Ingoldby and Jackson, 2001Ingoldby L, Jackson P. Induction of parturition in sheep. In Pract. 2001;23(4):228-31. http://dx.doi.org/10.1136/inpract.23.4.228.
http://dx.doi.org/10.1136/inpract.23.4.2...
).

Labor is induced through exogenous glucocorticoids that mimic the action of cortisol produced by the fetal adrenal cortex, which acts as an initial trigger to a hormonal cascade that, in turn, triggers labor (Zoller et al., 2015Zoller DK, Vassiliadis PM, Voigt K, Sauter-Louis C, Zerbe H. Two treatment protocols for induction of preterm parturition in ewes: evaluation of the effects on lung maturation and lamb survival. Small Rumin Res. 2015;124:112-9. http://dx.doi.org/10.1016/j.smallrumres.2014.12.015.
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; Barreto et al., 2021Barreto JVP, Pertile SFN, Rego FCA, Patelli THC, Nascimento ST, Lorenzetti E, Cunha LFC Fo. Prediction of vitality and survival of newborn lambs using a modified Apgar score. Appl Anim Behav Sci. 2021;238:105281. http://dx.doi.org/10.1016/j.applanim.2021.105281.
http://dx.doi.org/10.1016/j.applanim.202...
). Corticosteroids also promote fetal maturation, particularly structural pulmonary maturation, thereby stimulating the production of surfactant phospholipids and activating the maturation of brown adipose tissue (Liggins, 1969Liggins GC. Premature delivery of foetal lambs infused with glucocorticoids. J Endocrinol. 1969;45(4):515-23. http://dx.doi.org/10.1677/joe.0.0450515. PMid:5366112.
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; Fowden et al., 1995Fowden AL, Apatu RS, Silver M. The glucogenic capacity of the fetal pig: developmental regulation by cortisol. Exp Physiol. 1995;80(3):457-67. http://dx.doi.org/10.1113/expphysiol.1995.sp003860. PMid:7640010.
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; Ballard et al., 1997Ballard PL, Ning Y, Polk D, Ikegami M, Jobe AH. Glucocorticoid regulation of surfactant components in immature lambs. Am J Physiol. 1997;273(5):L1048 -57. http://dx.doi.org/10.1152/ajplung.1997.273.5.L1048. PMid:9374734.
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; Zaremba et al., 1997Zaremba W, Grunert E, Aurich J. Prophylaxis of respiratory distress syndrome in premature calves by administration of dexamethasone or a prostaglandin F2 alpha analogue to their dams before parturition. Am J Vet Res. 1997;58(4):404-7. http://dx.doi.org/10.2460/ajvr.1997.58.04.404. PMid:9099388.
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; Bispham et al., 2002Bispham J, Budge H, Mostyn A, Dandrea J, Clarke L, Keisler DH, Symonds ME, Stephenson T. Ambient temperature, maternal dexamethasone, and postnatal ontogeny of leptin in the neonatal lamb. Pediatr Res. 2002;52(1):85-90. http://dx.doi.org/10.1203/00006450-200207000-00016. PMid:12084852.
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).

In 1972, in a study by Liggins and Howie (1972)Liggins GC, Howie R. A controlled trial of antepartum glucocorticoid treatment for prevention of the respiratory distress syndrome in premature infants. Pediatrics. 1972;50(4):515-25. http://dx.doi.org/10.1542/peds.50.4.515. PMid:4561295.
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on the artificial induction of fetal lung maturation, premature lambs of mothers who had received antenatal corticosteroid therapy exhibited better vitality than did the lambs of mothers who had not received corticosteroid therapy. Subsequently, new studies were conducted and demonstrated a reduction in pulmonary changes and better rates of neonatal viability for fetuses of ewes that underwent antenatal glucocorticoid therapy (Feitosa et al., 2017Feitosa FLF, Ávila LG, Bovino F, Santos GGF, Mendes LCN, Peiró JR, Perri SHV. Effects of maternal blood gas values corticotherapy of lambs born at term and premature. Pesq Vet Bras. 2017;37(5):521-5. http://dx.doi.org/10.1590/s0100-736x2017000500016.
http://dx.doi.org/10.1590/s0100-736x2017...
; Regazzi et al., 2022Regazzi FM, Justo BM, Vidal ABG, Brito MM, Angrimani DSR, Abreu RA, Lúcio CF, Fernandes CB, Vannucchi CI. Prenatal or postnatal corticosteroids favor clinical, respiratory, metabolic outcomes and oxidative balance of preterm lambs corticotherapy for premature neonatal lambs. Theriogenology. 2022;182:129-37. http://dx.doi.org/10.1016/j.theriogenology.2022.02.006. PMid:35168015.
http://dx.doi.org/10.1016/j.theriogenolo...
).

Assessing neonatal vitality at birth allows for assessment of the neonate’s vital parameters in its first hours of life and the opportunity to implement preventive or corrective methods to the changes found, and to differentiate between healthy and compromised neonates (Garcia, 2001Garcia PCR. The arrival of prognostic indices in neonatology. J Pediatr. 2001;77(6):436-7. http://dx.doi.org/10.2223/JPED.346. PMid:14647819.
http://dx.doi.org/10.2223/JPED.346...
; Vassalo et al., 2014Vassalo FG, Peternelli Silva L, Lourenço MLG, Chiacchio SB. Escore de Apgar: história e importância na medicina veterinária. Rev Bras Reprod Anim [serial on the Internet]. 2014 [cited 2022 Oct 30];38(1):54-9. Available from: http://cbra.org.br/pages/publicacoes/rbra/v38n1/pag54-59%20(RB490%20Vassalo).pdf
http://cbra.org.br/pages/publicacoes/rbr...
). In veterinary medicine, a neonate’s clinical condition is determined by several adaptations of the Apgar score, a method created by a medical anesthesiologist for application in human neonates (Garcia, 2001Garcia PCR. The arrival of prognostic indices in neonatology. J Pediatr. 2001;77(6):436-7. http://dx.doi.org/10.2223/JPED.346. PMid:14647819.
http://dx.doi.org/10.2223/JPED.346...
). In a recent study, Barreto et al. (2021)Barreto JVP, Pertile SFN, Rego FCA, Patelli THC, Nascimento ST, Lorenzetti E, Cunha LFC Fo. Prediction of vitality and survival of newborn lambs using a modified Apgar score. Appl Anim Behav Sci. 2021;238:105281. http://dx.doi.org/10.1016/j.applanim.2021.105281.
http://dx.doi.org/10.1016/j.applanim.202...
found that neonates with a high Apgar score ingested a greater amount of colostrum and had a higher liver enzyme index, which is associated with greater survival likelihood.

Despite prior knowledge of the action of DEX on fetal maturation, relatively few studies have investigated the interaction between corticosteroid-induced labor and parameters associated with neonatal vitality, particularly in Santa Inês lambs. Thus, this study set out to assess the efficacy of two different DEX doses, the full conventional dose (16 mg) and a half dose (8 mg), for inducing labor in Santa Inês ewes at 145 days of gestation, and to analyze the effect of induction on the lambs’ neonatal vitality.

Methods

The study was conducted on two experimental farms, with the following geographical coordinates: altitude of 162 m and 234 m, an average annual rainfall of 1,251 mm and 1,079 mm, and a hot, semi-humid and a hot, humid climate, for the first and second farm, respectively.

The study was conducted based on the ethical precepts recommended by the National Council for the Control of Animal Experimentation (CONCEA), following approval by the Ethics Committee on the Use of Animals (CEUA) under protocol number 23/2018.

In this study, 58 multiparous adult ewes, with an average weight of 43.34 ± 8.49 were observed and average body condition of 3±0,35, based on a scale of 0 to 5 points (from very thin to very fat) devised by Jefferies (1961)Jefferies BC. Body condition scoring and its use in management. Tasman J Agric. 1961;32:19-21.. The animals were initially subjected to clinical, gynecological, and ultrasound examinations with the aid of a multifrequency transrectal linear transducer, used at a frequency of 7.5 MHz (Mindray Z5, Shenzhen, China). Clinically healthy ewes that did not present abnormalities in the reproductive tract and were not pregnant at the time of the examination were considered eligible for inclusion in the study.

The ewes were raised in an extensive farming system on pasture (mixed pasture with Brachiara humidícula and B. decumbens), with water and mineral salt ad libitum, without added concentrates. Before the experiment began, all animals were vaccinated and dewormed.

After the ultrasound examination, the animals were included in an estrus synchronization protocol in October 2016 at both experimental farms. Initially, all animals received an intravaginal device with 0.33 g of progesterone (CIDR®, Pfizer, Guarulhos, Brazil), on a random day of the estrous cycle (Day 0), which remained in place for 8 consecutive days. On day to the removal of the devices, 300 IU of equine chorionic gonadotropin (eCG, Novormon®, MSD Animal Health, São Paulo, Brazil) and 0.125 mg of cloprostenol sodium (PGF2α, Ciosin ®, MSD Animal Health) were administered via intramuscular (IM) injection. Thirty-two hours after CIDR removal, 200 IU of human chorionic gonadotropin (hCG, Chorulon ®, MSD Animal Health, São Paulo, Brazil) was applied (Kiya et al., 2017Kiya CK, Biscarde CEA, Silva LFMC, Campos GA, Garcia VFC, Barbosa LP, Resende MV, Bittencourt TCSBC, Gusmão AL. Different times of administration of eCG with or without hCG in a short protocols for FTAI on wooless ewes of semiarid. Magistra [serial on the Internet]. 2017 [cited 2022 Oct 30];26(4):532. Available from: https://www.cabdirect.org/cabdirect/abstract/20153151256
https://www.cabdirect.org/cabdirect/abst...
). Considering that the average interval between CIDR removal and the end of estrus is 60 h and knowing that ovulation in sheep preferentially occurs at the end of estrus (Gordon, 1997Gordon I. Controlled reproductioninsheep and goats. Cambridge: CAB International; 1997. 450 p.), laparoscopic intrauterine insemination was performed with frozen semen from a reproduction center approximately 56 h after removal of the intravaginal device. The semen parameters exceeded those recommended by the Brazilian College of Animal Reproduction (CBRA) (Henry and Neves, 2013Henry M, Neves JP. Manual for andrological examination and evaluation of animal semen. 3a ed. Belo Horizonte: CBRA; 2013. p. 34-7.).

Between days 16 and 18 after the fixed-time artificial insemination protocol, the ewes under the protocol that had returned to estrus (as observed through their acceptance of mating by the ruffian), were serviced by a Santa Inês breeder ram. The last mounting date was duly recorded for subsequent labor induction at 145 days after being serviced or after artificial insemination, as described in Figure 1.

Figure 1
Schematic diagram of the fixed-time artificial insemination (FTAI) protocol and controlled mounting. D0: The day the protocol is initiated, and the progesterone device is introduced (CIDR®, Pfizer, Guarulhos, Brazil). D8: Eighth day of the protocol, removal of the CIDR and application of 300 IU of equine chorionic gonadotropin (eCG, Novormon ®, MSD Saúde Animal, São Paulo, Brazil) and 0.125mg of cloprostenol sodium (Ciosin ®, MSD Saúde Animal, São Paulo, Brazil). 32 h: Ninth day of the protocol, application of 200 IU of human chorionic gonadotrophin (hCG, Chorulon ®, MSD Saúde Animal, São Paulo, Brazil), 32 h after removal of the CIDR. 52 h: Tenth day of the protocol. FTAI is performed 52 h after removal of the CIDR. D26, 27, and 28: Days 16, 17, and 18 after the protocol, estrus is observed and controlled mounting is allowed.

Prior to initiating the reproductive program, the mating ram underwent clinical and andrological evaluations, and his semen was found to be within the evaluation standards recommended by the CBRA (Henry and Neves, 2013Henry M, Neves JP. Manual for andrological examination and evaluation of animal semen. 3a ed. Belo Horizonte: CBRA; 2013. p. 34-7.). After 30 days of servicing, all ewes underwent an ultrasound to confirm pregnancy and fetal viability, through fetal identification, with observation of heartbeats and fetal movements (Barr, 1988Barr FJ. Pregnancy diagnosis and assessment of fetal viability in the dog: a review. J Small Anim Pract. 1988;29(10):647-56. http://dx.doi.org/10.1111/j.1748-5827.1988.tb02164.x.
http://dx.doi.org/10.1111/j.1748-5827.19...
).

Immediately after the evaluations, the pregnant ewes were kept in closed facilities equipped with drinking fountains and troughs with water, hay, and ad libitum mineral salt during the labor-induction period, to facilitate the division between the groups as well as observation of and assistance to the parturient ewes and neonates.

Pregnant ewes were separated into three groups in a completely randomized design. Group G1 (control) received 0.9% NaCl solution via IM injection (n = 19). Group G2 (n = 20) received 8 mg of DEX (Azium®, MSD), and group G3 (n = 19) received 16 mg of DEX (Azium®, MSD). Starting from 24 h after DEX administration, the animals were monitored full-time until day 11 after induction. No human interference between fetal ejection and maternal recognition were allowed, except in cases of dystocia.

After birth and maternal recognition, the neonates’ vitality was assessed based on the modified Apgar score (Silva et al., 2013Silva LP, Lourenço MLG, Grandi MC, Ulian CM, Sudano MJ, Chiacchio SB. Concentração de lactato sérico em ovelhas e cordeiros mestiços (1/2 Suffolk) nascidos em eutocia. Arq Bras Med Vet Zootec. 2013;65(4):989-94. http://dx.doi.org/10.1590/S0102-09352013000400008.
http://dx.doi.org/10.1590/S0102-09352013...
), postnatal behavior, weight, and temperature, with only one assessment being performed in the first 5 minutes of life.

The following parameters were observed in the Apgar score: heart rate (HR), respiratory rate (RR), mucosa color (MC), general movement (GM), and reflex irritability (RI). The results obtained after adding up the points were interpreted as follows: 7-8 indicated good vitality, 4-6 indicated moderate vitality, and 0-3 indicated low vitality (Silva, 2012Silva LP. Clinical trial carried out under the modified APGAR score method aimed at measuring lactate and blood glucose level in neonate lamb [thesis]. Botucatu: Faculdade de Medicina Veterinária e Zootecnia, Universidade Estadual Paulista “Julio de Mesquita Filho”; 2012 [cited 2022 Oct 30]. Available from: http://hdl.handle.net/11449/89248
http://hdl.handle.net/11449/89248...
). The neonates born in abnormal parturition (dystocia, n = 4) did not undergo neonatal vitality and Apgar evaluation.

For the HR assessment, a score of 0 was assigned when there was no heartbeat, 1 when the frequency was below 100 bpm, and 2 when the frequency was >100 bpm. For RR, a score of 0 was given when the neonates presented with apnea, a score of 1 when RR was under 50 respiratory movements per minute (rpm), and a score of 2 when RR > 50 rpm. MC was assessed by attributing a score of 0, 1, and 2 for cyanotic, pale, and pink mucous membranes, respectively. GM was observed from the moment of birth to the neonate’s contact with the mother: a score of 0 was assigned when there was no movement, 1 when movement was slow, and 2 when movement was vigorous. RI was evaluated through painful stimulus in the interdigital space of the thoracic limb: a score of 0 was given when there was no withdrawal of the limb, a score of 1 for subtle withdrawal, and a score of 2 for quick withdrawal. Table 1 provides the details of the assessment of these parameters.

Table 1
Modified Apgar score for sheep.

Postnatal behavior was assessed by measuring the intervals, in minutes, between birth and the lamb’s adoption of the sternal decubitus (ISD) position, between birth and the lamb’s adoption of the quadrupedal position (IQP), between birth and the lamb’s pursuit of the mammary gland for the first suckle (IFS). A digital thermometer was further used to measure rectal temperature, a digital scale with a 120-kg capacity was used to weigh the neonate, and the sex was observed.

The SAS v9.1.3 (SAS Institute, Cary, NC, USA) software was used to analyze the variables. Data consistency and descriptive analysis (means and standard deviation) of the characteristics of interest to the study were performed using the MEANS procedure (PROC MEANS). The data were initially tested for normality (Shapiro wilk test). The effect of groups (G1: control, G2: 8 mg DEX and G3: 16 mg DEX), location, sex and type of birth (single or multiple) on neonatal vitality characteristics parameters (temperature, weight, ISD, IQP and IFS) were studied using univariate analyses, for variables that presented an abnormal distribution, the Kruskal - Wallis test was used and for those that presented a normal distribution, ANOVA was used. In order to verify whether the APGAR score is related to indices such as ISD, IQP, IFS, temperature and live weight, the Spearman correlation was performed as these variables were not normally distributed. For all analyses, a significance level of 5% was used.

Results

Fifty-eight ewes were enrolled in this study, 39 of which underwent labor induction with DEX. The parturitions in the induced groups occurred on average at 147 days of gestation. The parturitions in the non-induced group occurred on average at 150 days of gestation. A total of 79 lambs were born, including 40 females and 38 males; one lamb’s sex was not recorded. Forty lambs were born as multiple births (two or more) and 39 from single births.

Four ewes presented with dystocia: in these cases, the fetal position was in the anterior longitudinal, dorsal position, and flexed attitude of the carpal joint. All cases of dystocia occurred in single births of male lambs. Therefore, 10.25% of the single births and 10.5% of the males were born in dystocia, with two births each from G1 and G2. In these cases, obstetric interventions were necessary to correct the attitude, and forced traction was performed afterwards. All offspring were born alive.

Farm location, type of birth (multiple or single), and sex had no effect on the parameters studied (P > 0.05). The 8- and 16-mg doses of DEX were both efficient at inducing birth in Santa Inês ewes at 145 days of gestation.

The parameters observed in neonates after birth, such as temperature, Apgar score, weight, and postnatal behavior (assuming the ISD position, the standing position, and first suckle), were similar (P>0.05) between groups (Table 2). When verifying the relationship between the APGAR score and the ISD, IQP, IFS, temperature and live weight indices, no significant correlations were found (P>0.05).

Table 2
Mean and standard deviation of weight, Apgar score, temperature, and postnatal behavior among groups whose labor was induced with dexamethasone.

Discussion

The animals in G1 lambed at an average of 150 days of gestation, which corresponds to the physiological norm for the species. Machado and Simplício (1998)Machado R, Simplício AA. Effect of breed of sire and mating season on the reproductive performance of hairsheep females mated to rams of meat-type breeds. Rev Bras Zootec. 1998;27(1):54-9. and Silva et al. (1995)Silva FLR, Figueiredo EAP, Barbieri ME, Simplício AA. Environmental and sire effects on reproductive and growth traits in Santa Inês sheep in Ceará State. Rev Bras Zootec [serial on the Internet]. 1995 [cited 2022 Oct 30];24(4):559-69. Available from: https://ainfo.cnptia.embrapa.br/digital/bitstream/item/41795/1/API-Efeito-de-ambiente.pdf
https://ainfo.cnptia.embrapa.br/digital/...
respectively found that parturition occurred at an average of 149.80 and 151.66 days of gestation for the Santa Inês breed.

In G3, a 16-mg dose of DEX per animal was chosen based on studies previously conducted by Kastelic et al. (1996)Kastelic JP, Cook RB, McMahon LR, McAllister TA, McClelland LA, Cheng KJ. Induction of parturition in ewes with dexamethasone or dexamethasone and cloprostenol. Can Vet J. 1996;37(2):101-2. PMid:8640645. and Ingoldby and Jackson (2001)Ingoldby L, Jackson P. Induction of parturition in sheep. In Pract. 2001;23(4):228-31. http://dx.doi.org/10.1136/inpract.23.4.228.
http://dx.doi.org/10.1136/inpract.23.4.2...
, which established this as the standard dose for inducing labor in sheep (Sir and Bartlewski, 2010Sir C, Bartlewski PM. Analyses of parental and seasonal influences on the synchrony of dexamethasone-induced lambing and lamb characteristics. Livest Sci. 2010;131(1):119-24. http://dx.doi.org/10.1016/j.livsci.2010.03.011.
http://dx.doi.org/10.1016/j.livsci.2010....
). Animals in G2 and G3 gave birth on average at 147 days of gestation, indicating that both doses of DEX were efficient at inducing and concentrating labor.

Labor induction with DEX simulates natural labor. The glucocorticoid mimics the cortisol produced by the fetal adrenal cortex, acting as a trigger to the hormonal cascade that triggers labor (Silver, 1992Silver M. Parturition: spontaneous or induced preterm labour and its consequences for the neonate. Anim Reprod Sci. 1992;28(1-4):441-9. http://dx.doi.org/10.1016/0378-4320(92)90131-V.
http://dx.doi.org/10.1016/0378-4320(92)9...
). Fetal cortisol induces the transformation of placental progesterone (P4) into estrogen (E2), resulting in a reduction in P4 levels and an increase in E2 levels. Estrogen induces the release of prostaglandins, mainly PGF2α, PGE2, and PGI2, from the uterus. These promote luteolysis, increased placental vascular perfusion, myometrial contractions, and relaxation of the cervix and vaginal canal, triggering parturition (Silver, 1992Silver M. Parturition: spontaneous or induced preterm labour and its consequences for the neonate. Anim Reprod Sci. 1992;28(1-4):441-9. http://dx.doi.org/10.1016/0378-4320(92)90131-V.
http://dx.doi.org/10.1016/0378-4320(92)9...
; Jenkin and Young, 2004Jenkin G, Young IR. Mechanisms responsible for parturition; the use of experimental models. Anim Reprod Sci. 2004;82-83:567-81. http://dx.doi.org/10.1016/j.anireprosci.2004.05.010. PMid:15271480.
http://dx.doi.org/10.1016/j.anireprosci....
).

The fetus releases cortisol naturally from 140 days of gestation. During this period, important processes modulated by cortisol occur, preparing the fetus for post-uterine life (Ingoldby and Jackson, 2001Ingoldby L, Jackson P. Induction of parturition in sheep. In Pract. 2001;23(4):228-31. http://dx.doi.org/10.1136/inpract.23.4.228.
http://dx.doi.org/10.1136/inpract.23.4.2...
; Feitosa et al., 2017Feitosa FLF, Ávila LG, Bovino F, Santos GGF, Mendes LCN, Peiró JR, Perri SHV. Effects of maternal blood gas values corticotherapy of lambs born at term and premature. Pesq Vet Bras. 2017;37(5):521-5. http://dx.doi.org/10.1590/s0100-736x2017000500016.
http://dx.doi.org/10.1590/s0100-736x2017...
). At 146 days of gestation, fetal cortisol expression peaks, suggesting that even a small dose of DEX would be sufficient to reinforce endogenous cortisol and trigger labor soon after (Tsiligianni et al., 2008Tsiligianni T, Ntovolou E, Amiridis GS. Synchronisation of lambing with low doses of dexamethasone in Chios ewes: short communication. Acta Vet Hung. 2008;56(3):393-7. http://dx.doi.org/10.1556/avet.56.2008.3.12. PMid:18828490.
http://dx.doi.org/10.1556/avet.56.2008.3...
), which explains the similar performance between the G2 and G3 groups, even with half the dose.

The weights of the neonates born in the different groups, even in the G2 and G3 groups whose births occurred 2-3 days earlier than that of neonates in G1, did not differ significantly. The weights recorded in the study corroborate reports of the average birthweight of Santa Inês lambs, which is in the range of 3.3-3.6 kg (Castro et al., 2012Castro FAB, Ribeiro ELA, Koritiaki NA, Mizubuti IY, Silva LDF, Pereira ES, Pinto AP, Constantino C, Fernandes F Jr. Performance from birth to weaning of Santa Inês lambs born to ewes fed different levels of energy. Semina: Ciênc Agrár. 2012;33(Suppl 2):3379-88. http://dx.doi.org/10.5433/1679-0359.2012v33Supl2p3379.
http://dx.doi.org/10.5433/1679-0359.2012...
). This parameter is of paramount importance, since birthweight is correlated with neonatal death (Dwyer and Morgan, 2006Dwyer CM, Morgan CA. Maintenance of body temperature in the neonatal lamb: effects of breed, birth weight, and litter size. J Anim Sci. 2006;84(5):1093-101. http://dx.doi.org/10.2527/2006.8451093x. PMid:16612011.
http://dx.doi.org/10.2527/2006.8451093x...
). Lower-weight lambs are less vigorous at birth, take longer to suckle colostrum effectively, and are less able to maintain their body temperature than are heavier lambs (Dwyer, 2008Dwyer CM. Individual variation in the expression of maternal behaviour: a review of the neuroendocrine mechanisms in the sheep. J Neuroendocrinol. 2008;20(4):526-34. http://dx.doi.org/10.1111/j.1365-2826.2008.01657.x. PMid:18266950.
http://dx.doi.org/10.1111/j.1365-2826.20...
). Induction that anticipates labor could negatively influence birthweight.

In this study, lambs born by induced labor presented the same Apgar score classification as non-induced lambs. All the lambs from all groups exhibited good vitality. This finding can be explained by the fact that glucocorticoids such as DEX produce a series of hormonal reactions in the fetus that aid fetal maturation, including maturation of the lungs, liver, kidneys, and intestine (Fowden et al., 1998Fowden AL, Li J, Forhead AJ. Glucocorticoids and the preparation for life after birth: are there long-term consequences of the life insurance? Proc Nutr Soc. 1998;57(1):113-22. http://dx.doi.org/10.1079/PNS19980017. PMid:9571716.
http://dx.doi.org/10.1079/PNS19980017...
; Regazzi et al., 2022Regazzi FM, Justo BM, Vidal ABG, Brito MM, Angrimani DSR, Abreu RA, Lúcio CF, Fernandes CB, Vannucchi CI. Prenatal or postnatal corticosteroids favor clinical, respiratory, metabolic outcomes and oxidative balance of preterm lambs corticotherapy for premature neonatal lambs. Theriogenology. 2022;182:129-37. http://dx.doi.org/10.1016/j.theriogenology.2022.02.006. PMid:35168015.
http://dx.doi.org/10.1016/j.theriogenolo...
). In fact, due to these effects, DEX is widely used to aid fetal maturation in situations where the fetus needs to be born prematurely (Whittle et al., 2001Whittle WL, Patel FA, Alfaidy N, Holloway AC, Fraser M, Gyomorey S, Lye SJ, Gibb W, Challis JR. Glucocorticoid regulation of human and ovine parturition: the relationship between fetal hypothalamic-pituitary-adrenal axis activation and intrauterine prostaglandin production. Biol Reprod. 2001;64(4):1019-32. http://dx.doi.org/10.1095/biolreprod64.4.1019. PMid:11259246.
http://dx.doi.org/10.1095/biolreprod64.4...
).

The lambs’ temperature after birth was within the normal range for the species and did not differ (P > 0.05) among the groups. Thermoregulation is an important factor after birth, and the energy demand to maintain body temperature depends mainly on the heat produced by the oxidation of brown adipose tissue (BAT). Oxidation occurs by controlling triiodothyronine (T3), whose activity increases in the last month of gestation (Bispham et al., 2002Bispham J, Budge H, Mostyn A, Dandrea J, Clarke L, Keisler DH, Symonds ME, Stephenson T. Ambient temperature, maternal dexamethasone, and postnatal ontogeny of leptin in the neonatal lamb. Pediatr Res. 2002;52(1):85-90. http://dx.doi.org/10.1203/00006450-200207000-00016. PMid:12084852.
http://dx.doi.org/10.1203/00006450-20020...
; Dauncey, 1990Dauncey MJ. Thyroid hormones and thermogenesis. Proc Nutr Soc. 1990;49(2):203-15. http://dx.doi.org/10.1079/PNS19900024. PMid:2236086.
http://dx.doi.org/10.1079/PNS19900024...
; Forhead et al., 2007Forhead AJ, Jellyman JK, Gardner DS, Giussani DA, Kaptein E, Visser TJ, Fowden AL. Differential effects of maternal dexamethasone treatment on circulating thyroid hormone concentrations and tissue deiodinase activity in the pregnant ewe and fetus. Endocrinology. 2007;148(2):800-5. http://dx.doi.org/10.1210/en.2006-1194. PMid:17110425.
http://dx.doi.org/10.1210/en.2006-1194...
).

The neonate’s thermoregulatory capacity enhances with administration of corticosteroids to the mother. Even exogenous administration is an important regulator of fetal maturation, as it increases the production of T3, thereby activating BAT oxidation and consequently raising neonatal temperature (Osathanondh et al., 1978Osathanondh R, Chopra IJ, Tulchinsky D. Effects of dexamethasone on fetal and maternal thyroxine, triiodothyronine, reverse triiodothyronine, and thyrotropin levels. J Clin Endocrinol Metab. 1978;47(6):1236-9. http://dx.doi.org/10.1210/jcem-47-6-1236. PMid:263347.
http://dx.doi.org/10.1210/jcem-47-6-1236...
; Bispham et al., 2002Bispham J, Budge H, Mostyn A, Dandrea J, Clarke L, Keisler DH, Symonds ME, Stephenson T. Ambient temperature, maternal dexamethasone, and postnatal ontogeny of leptin in the neonatal lamb. Pediatr Res. 2002;52(1):85-90. http://dx.doi.org/10.1203/00006450-200207000-00016. PMid:12084852.
http://dx.doi.org/10.1203/00006450-20020...
; Forhead et al., 2007Forhead AJ, Jellyman JK, Gardner DS, Giussani DA, Kaptein E, Visser TJ, Fowden AL. Differential effects of maternal dexamethasone treatment on circulating thyroid hormone concentrations and tissue deiodinase activity in the pregnant ewe and fetus. Endocrinology. 2007;148(2):800-5. http://dx.doi.org/10.1210/en.2006-1194. PMid:17110425.
http://dx.doi.org/10.1210/en.2006-1194...
). Furthermore, it enables the neonate to perform thermogenesis without requiring muscle tremors (Bispham et al., 1999Bispham J, Heasman L, Clarke L, Ingleton PM, Stephenson T, Symonds ME. Effect of maternal dexamethasone treatment and ambient temperature on prolactin receptor abundance in brown adipose and hepatic tissue in the foetus and new-born lamb. J Neuroendocrinol. 1999;11(11):849-56. http://dx.doi.org/10.1046/j.1365-2826.1999.00401.x. PMid:10520135.
http://dx.doi.org/10.1046/j.1365-2826.19...
). Thus, all these events explain why the same (P > 0.05) temperature was observed between the lambs in all three groups. After evaluating the influence of sex, number of offspring, and type of birth on the lambs’ neonatal vigor, Fagundes et al. (2019)Fagundes GB, Nascimento DM, Santiago MR, Neves CA, Silva CMG, Oba E, Arrivabene M, Cavalcante TV. Response of vital functions, Apgar and cortisol in the prognosis of vigor against neonatal factors of lambs. Pesq Vet Bras. 2019;39(2):155-62. http://dx.doi.org/10.1590/1678-5150-pvb-5731.
http://dx.doi.org/10.1590/1678-5150-pvb-...
found temperatures of 38-39 °C to be the normothermic range indicating adequate development of homeostasis mechanisms. These results corroborate the neonatal temperatures reported in this study.

In this study, the neonates’ behavioral chronology after birth was to assume the ISD position first, then the IQP position, and finally suckle at 2.8 ± 2.5, 18.63 ± 11, and 50.49 ± 38 min, respectively. These data were similar to those described by Dwyer (2003)Dwyer CM. Behavioural development in the neonatal lamb: effect of maternal and birth-related factors. Theriogenology. 2003;59(3-4):1027-50. http://dx.doi.org/10.1016/S0093-691X(02)01137-8. PMid:12517402.
http://dx.doi.org/10.1016/S0093-691X(02)...
for neonates from eutocic parturitions. The data also corroborated the findings of Barreto et al. (2021)Barreto JVP, Pertile SFN, Rego FCA, Patelli THC, Nascimento ST, Lorenzetti E, Cunha LFC Fo. Prediction of vitality and survival of newborn lambs using a modified Apgar score. Appl Anim Behav Sci. 2021;238:105281. http://dx.doi.org/10.1016/j.applanim.2021.105281.
http://dx.doi.org/10.1016/j.applanim.202...
, who used the modified Apgar score to assess the influence of maternal and neonatal conditions on lambs’ vitality and survival, and who noted averages in minutes between the ISD position and the first suckle that were similar to those found in this study in neonates with moderate to high Apgar scores.

Regardless to which experimental group they belonged, the neonates presented parameters within the normal range for the species immediately after birth (Dwyer, 2003Dwyer CM. Behavioural development in the neonatal lamb: effect of maternal and birth-related factors. Theriogenology. 2003;59(3-4):1027-50. http://dx.doi.org/10.1016/S0093-691X(02)01137-8. PMid:12517402.
http://dx.doi.org/10.1016/S0093-691X(02)...
; Nowak and Poindron, 2006Nowak R, Poindron P. From birth to colostrum: early steps leading to lamb survival. Reprod Nutr Dev. 2006;46(4):431-46. http://dx.doi.org/10.1051/rnd:2006023. PMid:16824451.
http://dx.doi.org/10.1051/rnd:2006023...
). By pursuing the udder within the first hour of life, they obtained colostrum at the proper time for its absorption, considering that the best use of colostrum occurs within the first 8 hours after birth (Nowak and Poindron, 2006Nowak R, Poindron P. From birth to colostrum: early steps leading to lamb survival. Reprod Nutr Dev. 2006;46(4):431-46. http://dx.doi.org/10.1051/rnd:2006023. PMid:16824451.
http://dx.doi.org/10.1051/rnd:2006023...
). Thus, the lambs born by labor induction in this study did not exhibit any type of alteration regarding neonatal vitality, based on postnatal behavior, Apgar score, weight, or rectal temperature.

Conclusions

Neonates born by induced deliveries at 145 days of gestation, using doses of 8 mg or 16 mg of DEX, showed the same vitality as neonates born by non-induced deliveries. Thus, it is concluded that the use of antenatal corticosteroid therapy does not influence the vitality of ovine neonates, implying that these DEX doses can be used safely to induce labor in ewes.

  • Financial support: ESS received funding for this research from the Coordination for the Improvement of Higher Education Personnel - Brasil (CAPES) - Financial Code 001.
  • How to cite: Santos ES, Bittencourt RF, Xavier GM, Biscarde CEA, Carneiro IMB, Santos MMR, Ribeiro Filho AL. Influence of prenatal corticosteroid therapy on neonatal vitality and utility as a labor-inducing agent in Santa Inês ewes. Anim Reprod. 2024;21(1):e20220109. https://doi.org/10.1590/1984-3143-AR2022-0109

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Publication Dates

  • Publication in this collection
    22 Mar 2024
  • Date of issue
    2024

History

  • Received
    30 Oct 2022
  • Accepted
    15 Jan 2024
Colégio Brasileiro de Reprodução Animal Coronel José dias Bicalho, 1224, CEP: , 31275-050, Belo Horizonte, MG - Brasil, Tel.: 55-31-3491 7122 - Belo Horizonte - MG - Brazil
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