Animal Reproduction (AR)
https://www.animal-reproduction.org/article/doi/10.1590/1984-3143-AR2025-0070
Animal Reproduction (AR)
ORIGINAL ARTICLE

Histomorphometric characterization of the uterus and placenta in Piau and Commercial sows during early gestation

Tânia Fernandes Martins; Lívia Maria dos Reis Barbosa; Luiz Otávio Guimarães Ervilha; Mariana Machado Neves; Alysson Saraiva; José Domingos Guimarães; Mateus Guimarães dos Santos; Paula da Fonseca Pereira; Simone Eliza Facioni Guimarães

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Abstract

Pregnancy induces critical physiological adaptations to support embryonic development and fetal survival. This study compared endometrial and placental phenotypic and histomorphometric characteristics of Piau and Commercial sows at two gestational ages (25 and 35 days). Twelve sows (six Piau and six Commercial) were evaluated in a randomized design, with samples collected from three regions of the right uterine horn of each animal. Histomorphometric analyses were performed using microscopy and ImageJ software. Statistical analyses employed linear mixed-effects models, with Shapiro-Wilk and Levene’s tests applied to assess normality and homogeneity of variances, respectively. At 25 days of gestation, Commercial sows showed greater uterine and ovarian weights, a higher number of corpora lutea, and longer uterine horn horns, reflecting genetic selection for reproductive efficiency. Conversely, Piau sows exhibited more advanced embryonic development at this stage, with fetuses of greater size. At 35 days, the phenotypic superiority of Commercial sows persisted, while Piau fetuses maintained greater weight and length, indicating distinct temporal growth dynamics. Histomorphometric analyses at 25 days revealed that Commercial sows had increased placental connective tissue deposition and thicker endometrial epithelium, whereas Piau sows presented larger placental vascular area, as well as enhanced endometrial vascularization and glandular density across all uterine regions. At 35 days, no significant differences were observed in placental vascular area and endometrial vascularization; however, subtle trends in connective tissue development suggested ongoing placental differentiation. These findings highlight distinct reproductive strategies between Piau and Commercial sows, with potential implications for embryonic development and gestational success. Altogether, the results confirm that genetic background influences uterine and placental morphology during early gestation.

Supplementary material accompanies this paper.


Table 1. Normality (Shapiro–Wilk) and homogeneity of variances (Levene’s test) for raw data (pre-transformation) and transformed data (log or square-root) of the traits evaluated in Piau and Commercial genetic groups at 25 days of gestation.


Table 2. Normality (Shapiro–Wilk) and homogeneity of variances (Levene’s test) for raw data (pre-transformation) and transformed data (log or square-root) of the traits evaluated in Piau and Commercial genetic groups at 35 days of gestation.

Keywords

fetal development, endometrium, morphometry, placental vascularization, pig

References

Almeida FRL, Alvarenga Dias ALN. Pregnancy in pigs: the journey of early life. Domest Anim Endocrinol. 2022;78:106656. https://doi.org/10.1016/j.domaniend.2021.106656. PMid:34474228.

Brito EP No, Reis EP, Penitente-Filho JM, Montes JC, Costa KA, Teixeira SA, Silva W, Pinho R, Guimarães JD, Costa EP, Lopes MS, Guimarães SEF. Expression of apoptosis and myogenesis related genes during prenatal life in two divergent breeds of pigs. Theriogenology. 2020;145:67-76. https://doi.org/10.1016/j.theriogenology.2020.01.035. PMid:32004820.

Cagnazzo M, Te Pas MFW, Priem J, De Wit AAC, Pool MH, Davoli R, Russo V. Comparison of prenatal muscle tissue expression profiles of two pig breeds differing in muscle characteristics. J Anim Sci. 2006;84(1):1-10. https://doi.org/10.2527/2006.8411. PMid:16361485.

Costa KA, Saraiva A, Guimaraes JD, Marques DBD, Machado-Neves M, Barbosa LMR, Villadiego FAC, Veroneze R, Oliveira LF, Garcia IS, Teixeira SA, Guimarães SEF. Dietary L-arginine supplementation during early gestation of gilts affects conceptuses development. Theriogenology. 2019;140:62-71. https://doi.org/10.1016/j.theriogenology.2019.08.018. PMid:31445222.

De Faria VR, Pinho RO, Camilo BS, Guimarães JD, Silva FF, Lopes PS, Silva PV, Teixeira SA, Veroneze R, Penitente-Filho JM, Guimarães SEF. Genes expression and phenotypic differences in corpus luteum and cumulus cells of commercial line and piau breed gilts. Theriogenology. 2019;136:111-7. https://doi.org/10.1016/j.theriogenology.2019.06.034. PMid:31254724.

Foxcroft GR, Dixon WT, Dyck MK, Novak S, Harding JC, Almeida FC. Prenatal programming of postnatal development in the pig. Soc Reprod Fertil Suppl. 2009;66:213-31. PMid:19848290.

Guimarães GC, Betarelli RP, Zangeronimo MG, Abreu ML, Almeida FR, Rosa MC, Ferreira LG, Alves LA, Assis CK, Lopes GC. al. Vascularization of broad ligament of uterus and its relationship with fetal and placental development in gilts. Theriogenology. 2014;82(2):232-7. https://doi.org/10.1016/j.theriogenology.2014.03.023. PMid:24810996.

Kridli RT, Khalaj K, Bidarimath M, Tayade C. Placentation, maternal–fetal interface, and conceptuses loss in swine. Theriogenology. 2016;85(1):135-44. https://doi.org/10.1016/j.theriogenology.2015.08.001. PMid:26324112.

Kruskal WH, Wallis WA. Use of ranks in one-criterion variance analysis. J Am Stat Assoc. 1952;47(260):583-621. https://doi.org/10.1080/01621459.1952.10483441.

Linck M, Tsoi S, Wenger II, Plastow GS, Dyck MK. Placental transcriptome analysis in connection with low Litter Birth Weight Phenotype (LBWP) sows. Genes. 2024;15(6):703. https://doi.org/10.3390/genes15060703. PMid:38927639.

Montes JC, Penitente-Filho JM, Guimarães SEF, Lopes PS, Camilo BS, Shiomi HH, Lima DA, Pinho RO, Pereira JVTDN, Okano DS, Costa KA, Guimarães JD. Aspects of sexual precocity and morphometry of uterus, placenta and embryos/fetuses in Piau breed and Commercial line gilts. Theriogenology. 2018;105:75-83. https://doi.org/10.1016/j.theriogenology.2017.09.007. PMid:28930668.

Montes-Vergara JC, Penitente-Filho JM, Machado-Neves M, Machado LCM, Castaño-Villadiego FA, Costa KA, da Costa EP, de Campos CF, Ramírez-López CJ, Guimarães SEF, Lopes PS, Guimarães JD. Influence of Genotype on Endometrial Angiogenesis during Early Pregnancy in Piau and Commercial Line Gilts. Animals. 2022;12(5):553. https://doi.org/10.3390/ani12050553. PMid:35268121.

Reis EPD, Paixão DM, Brustolini OJB, Silva FFE, Silva W, Araújo FMGD, Salim AC, Oliveira G, Guimarães SE. Expression of myogenes in longissimus dorsi muscle during prenatal development in commercial and local Piau pigs. Genet Mol Biol. 2016;39(4):589-99. https://doi.org/10.1590/1678-4685-gmb-2015-0295. PMid:27801482.

Reynolds LP, Caton JS, Redmer DA, Grazul‐Bilska AT, Vonnahme KA, Borowicz PP, Luther JS, Wallace JM, Wu G, Spencer TE. Evidence for altered placental blood flow and vascularity in compromised pregnancies. J Physiol. 2006;572(Pt 1):51-8. https://doi.org/10.1113/jphysiol.2005.104430. PMid:16469783.

Silva PV, Guimarães SEF, Guimarães JD, Nascimento CS, Lopes PS, Siqueira JB, Amorim LS, Fonseca E Silva F, Foxcroft GR. Follicular dynamics and gene expression in granulosa cells, corpora lutea and oocytes from gilts of breeds with low and high ovulation rates. Reprod Fertil Dev. 2014;26(2):316-27. https://doi.org/10.1071/RD12257. PMid:23464354.

Silva CLA, Van Den Brand H, Laurenssen BFA, Broekhuijse MJ, Knol EF, Kemp B, Soede NM. Relationships between ovulation rate and embryonic and placental characteristics in multiparous sows at 35 days of pregnancy. Animal. 2016;10(7):1192-9. https://doi.org/10.1017/S175173111600015X. PMid:26891961.

Stenhouse C, Hogg CO, Ashworth CJ. Associations between fetal size, sex and both proliferation and apoptosis at the porcine feto-maternal interface. Placenta. 2018;70:15-24. https://doi.org/10.1016/j.placenta.2018.08.006. PMid:30316322.

Sollero BP, Guimarães SEF, Rilington VD, Tempelman RJ, Raney NE, Steibel JP, Guimarães JD, Lopes PS, Lopes MS, Ernst CW. Transcriptional profiling during foetal skeletal muscle development of Piau and Yorkshire–Landrace cross‐bred pigs. Anim Genet. 2011;42(6):600-12. https://doi.org/10.1111/j.1365-2052.2011.02186.x. PMid:22035001.

Souza ACF, Bastos DSS, Santos FC, Sertorio MN, Ervilha LOG, Gonçalves RV, Oliveira LL, Machado-Neves M. Arsenic aggravates oxidative stress causing hepatic alterations and inflammation in diabetic rats. Life Sci. 2018;209:472-80. https://doi.org/10.1016/j.lfs.2018.08.054. PMid:30144451.

Tung E, Roberts CT, Heinemann GK, De Blasio MJ, Kind KL, Van Wettere WH, Owens JA, Gatford KL. Increased placental nutrient transporter expression at midgestation after maternal growth hormone treatment in pigs: a placental mechanism for increased fetal growth. Biol Reprod. 2012;87(5):126. https://doi.org/10.1095/biolreprod.112.100222. PMid:23018188.

Wigmore PMC, Stickland NC. Muscle development in large and small pig fetuses. J Anat. 1983;137(Pt 2):235-45. PMid:6630038.
 


Submitted date:
05/24/2025

Accepted date:
11/11/2025

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