Morphometric changes of maternal fetal units due to their location within the uterine horns in the guinea pig

  • Gabriela Sofia Garay Universidad de Cuenca, Facultad de Ciencias Agropecuarias, Carrera de Medicina Veterinaria. Cuenca, Ecuador
  • Gissela Eugenia Gañán Universidad de Cuenca, Facultad de Ciencias Agropecuarias, Carrera de Medicina Veterinaria. Cuenca, Ecuador
  • Fernanda Estefanía Munzón Universidad de Cuenca, Facultad de Ciencias Agropecuarias, Carrera de Medicina Veterinaria. Cuenca, Ecuador
  • Luis Eduardo Ayala Universidad de Cuenca, Facultad de Ciencias Agropecuarias, Carrera de Medicina Veterinaria. Cuenca, Ecuador
Keywords: Maternal-fetal unit, gestational vesicle, progesterone, uterus

Abstract

The objective of this research was to compare the post-mortem macroscopic morphometric characteristics of maternal-fetal units (MFUs) in each uterine horn (CU) and their relationship with progesterone (P4) concentration during the first 35 days of gestation in the guinea pig (Cavia porcellus). Twenty Peruvian line guinea pigs were used, with an average weight of 964.5 ± 33.99 g and a body condition score of 2.6 ± 0.11. The post-mortem evaluation was performed at 5 different times during gestation (days 15, 20, 25, 30 and 35), sacrificing 4 guinea pigs in each one. Blood samples were taken to measure P4 levels and then the reproductive system was removed, identifying the right horn (CUD) and left horn (CUI), which were divided into three sections: caudal, middle, cranial, to describe the site of embryonic implantation. The volume and weight of UMFs were determined, the placental diameter (DPL), gestational sac diameter (DSG) and crown-rump length (CR) were measured. The results showed a higher percentage of implantation in CUD (66.8 %) compared to CUI (33.2%) and a higher frequency of implantations in the caudal part of both horns (CpD = 32.5% and CpIZ = 22.1%). The volume of the UMFs showed a progressive growth, although it decreased on day 30, recovering again on day 35. A similar pattern was recorded in the development of DPL, DSG and CR. The concentration of P4 was 68.4 ± 3.41 ng·mL-1 on day 15 and 63.7 ± 2.20 ng·mL-1 on day 35. In conclusion, pregnancies occurred more frequently in the right horn, with implantations located in the caudal and middle positions of both horns. Embryonic development showed slow but progressive growth in the first 20 days, accelerating on day 30, driven by the functionality of the placenta.

Downloads

References

Lord E, Collins CJ, deFrance SD, LeFebvre MJ, Pigière F, Eeckhout P, Erauw C, Fitzpatrick SM, Healy PF, Martínez-Polanco MF, Garcia JL, Ramos-Roca E, Delgado ME, Sánchez-Urriago A, Peña-Léon GA, Toyne JM, Dahlstedt A, Moore KM, Laguer-Diaz C, Zori C, Matisoo-Smith E. Ancient DNA of Guinea Pigs (Cavia spp.) indicates a probable new center of domestication and pathways of global distribution. Sci. Rep. [Internet]. 2020; 10(1):65784. doi: https://doi.org/gjdr3h

Aguiló Gisbert J. Alteraciones reproductivas en cobayas hembra. Argos [Internet]. 2019 [consultado 15 Ago. 2024]; 201:86-88. Disponible en: https://goo.su/cWnK

Fernández EA, Rosales CA, Garzón JP, Argudo DE, Ayala LE, Guevara GE, Maldonado JE, Perea FP. Morphological and histological characteristics of ovaries from two genetic groups of guinea pigs (Cavia porcellus) from South America. Rev. Investig. Vet. Perú [Internet]. 2022;33(4):1-11. doi: https://doi.org/g8w7b4

Ayala Guanga LE, Rodas Carpio R, Almeida A, Torres Inga CS, Nieto Escandón PE. Espículas peneanas del cobayo (Cavia porcellus), influencia sobre el comportamiento sexual, fertilidad y calidad espermática. Rev. Prod. Anim. [Internet]. 2017 [consultado 15 Ago. 2024]; 29(3):36-42. Disponible en: https://goo.su/aUwyh

Araníbar E, Echevarría L. Número de ovulaciones por ciclo estrual en cuyes (Cavia porcellus) andina y Perú. Rev. Investig. Vet. Perú [Internet]. 2014; 25(1):29-36. doi: https://doi.org/g8w7b5

Candia AA, Jiménez T, Navarrete Á, Beñaldo F, Silva P, García-Herrera C, Sferruzzi-Perri AN, Krause BJ, González-Candia A, Herrera EA. Developmental ultrasound characteristics in Guinea pigs: similarities with human pregnancy. Vet. Sci. [Internet]. 2023; 10(2):144. doi: https://doi.org/g8w7b6

Castellini C, Dal Bosco A, Arias-Álvarez M, Lorenzo PL, Cardinali R, Rebollar PG. The main factors affecting the reproductive performance of rabbit does: a review. Anim Reprod Sci. [Internet]. 2010; 122(3-4):174-182. doi: https://doi.org/c4mtwv

McLaurin KA, Mactutus CF. Polytocus focus: Uterine position effect is dependent upon horn size. Int. J. Dev. Neurosci. [Internet]. 2015; 40(1):85-91. doi: https://doi.org/f6x2r3

Heap RB, Deanesly R. The increase in plasma progesterone levels in the pregnant Guinea-pig and its possible significance. Reproduction [Internet]. 1967; 14(2):339-341. doi: https://doi.org/d6f4gk

Ara M, Jiménez R, Huamán A, Carcelén F, Díaz D. Desarrollo de un índice de condición corporal en cuyes: relaciones entre condición corporal y estimados cuantitativos de grasa corporal. Rev. Investig. Vet. Perú [Internet]. 2012; 23(4):420-428. doi: https://doi.org/g8w7b7

Vivas Tórres JA, Carballo D. Especies alternativas: Manual de crianza de Cobayos (Cavia porcellus) [Internet]. Managua: Universidad Nacional Agraria; 2013 [consultado 12 May. 2024]. 49 p. Disponible en: https://goo.su/GhtIT

Benítez-González EE, Chamba-Ochoa HR, Calderón-Abad ÁE, Cordero-Salazar FB. Evaluación de bloques nutricionales en la alimentación de cobayos (Cavia porcellus) en etapas de crecimiento y engorde. J. Selva Andina Anim. Sci. [Internet]. 2019; 6(2):66-73. https://doi.org/g8w7b8

Garay Peña G, Velesaca Ayala P, Ayala Guanga L. Efecto de diferentes dosis de progesterona oral sobre la sincronización de celo y la ovulación de las cobayas [Internet]. Rev. Prod. Animal. 2023 [consultado 15 Ago. 2024]; 35(2). Disponible en: https://goo.su/OFoh8Qf

Santos J, Fonseca E, van Melis J, Miglino MA. Morphometric analysis of fetal development of Cavia porcellus (Linnaeus, 1758) by ultrasonography—Pilot study. Theriogenology [Internet]. 2014; 81(7):896-900. doi: https://doi.org/f5ww6f

Close B, Banister K, Baumans V, Bernoth EM, Bromage N, Bunyan J, Erhardt W, Flecknell P, Gregory N, Hackbarth H, Morton D, Warwick C. Recommendations for euthanasia of experimental animals: Part 1. Lab Anim. [Internet]. 1996; 30(4):293-316. doi: https://doi.org/fh22hx

Norma Oficial Mexicana. NOM-033-ZOO-1995, Sacrificio humanitario de los animales domésticos y silvestres [Internet]. Ciudad de México: Secretaría de Agricultura, Ganadería y Desarrollo Rural; 1996 [consultado 12 Mar. 2024]. 18 p. Disponible en: https://goo.su/NGhmLs

Grégoire A, Allard A, Huamán E, León S, Silva RM, Buff S, Berard M, Joly T. Control of the estrous cycle in Guinea-pig (Cavia porcellus). Theriogenology [Internet]. 2012; 78(4):842-847. doi: https://doi.org/f346dv

Espinoza M, Carhuaricra D, Maturrano AL, Rosadio R, Luna L. Efecto de la administración oral de estreptomicina en la mortalidad de cuyes inoculados con una cepa virulenta de Salmonella Typhimurium. Rev. Investig. Vet. Perú [Internet]. 2023; 34(1):e24592. doi: https://doi.org/g8w7b9

Turner AJ, Trudinger BJ. Ultrasound measurement of biparietal diameter and umbilical artery blood flow in the normal fetal Guinea pig. Comp. Med. 2000; 50(4):379-384. PMID: 11020155.

Crane MB, Muirhead TL. Evaluation of ovarian volume by transrectal ultrasonography in cattle; effect of the day of the estrous cycle and validation of a method of subtracting of corpora lutea and follicle volume. Anim. Reprod. Sci. [Internet]. 2020; 214:106302. doi: https://doi.org/g8w7cb

Egund N, Carter AM. Uterine and placental circulation in the Guinea-pig: An angiographic study. J. Reprod. Fert. [Internet]. 1974; 40(2):401-410. doi: https://doi.org/fxdtmz

Barr Jr. M, Jensh RP, Brent RL. Prenatal growth in the albino rat: Effects of number, intrauterine position and resorptions. Am. J. Anat. [Internet]. 1970; 128(4):413-427. doi: https://doi.org/cj66pr

Prickett M. The development of the external form of the guinea-pig (Cavia cobaya) between the ages of 11 days and 20 days of gestation [tesis de maestria en Internet]. Kansas city: Kansas State College of Agriculture and Applied Science; 1931. [consultado 15 Ago. 2024]. 40 p. Disponible en: https://goo.su/8TXoiUd

Pijnenborg R, Robertson WB, Brosens I, Dixon G. Review article: Trophoblast invasion and the establishment of haemochorial placentation in man and laboratory animals. Placenta [Internet]. 1981; 2(1):71-91. doi: https://doi.org/c6r5qk

Tam WH, Burgess SM. The developmental changes in the placenta of the guinea-pig. J. Anat. [Internet]. 1977 [consultado 15 Ago. 2024]; 123(3):601-614. PMID: 885778. Disponible en: https://goo.su/FwfZ

Vasconcelos BG, Favaron PO, Miglino MA, Mess AM. Development and morphology of the inverted yolk sac in the guinea pig (Cavia porcellus). Theriogenology [Internet]. 2013; 80(6):636-641. doi: https://doi.org/f484p7

Silva FMdeO, Alcantara D, Carvalho RC, Favaron PO, dos Santos AC, Viana DC, Miglino MA. Development of the central nervous system in guinea pig (Cavia porcellus, Rodentia, Caviidae). Pesq. Vet. Bras. [Internet]. 2016; 36(8):753-760. doi: https://doi.org/g8w7cc

Published
2024-12-31
How to Cite
1.
Garay GS, Gañán GE, Munzón FE, Ayala LE. Morphometric changes of maternal fetal units due to their location within the uterine horns in the guinea pig. Rev. Cient. FCV-LUZ [Internet]. 2024Dec.31 [cited 2025Jul.24];34(3):7. Available from: https://produccioncientificaluz.org/index.php/cientifica/article/view/43183
Section
Veterinary Medicine