The fusion of the male and female gametes results in the zygote. The zygote becomes the blastocyst and embryo after several repeated cell divisions, and organ differentiation results in the fetus. The embryoin viviparous and oviparous vertebrates develop extra-embryonic membranes that perform important functions during embryonic and fetal life. One of these functions is related to nutrient transport. The physiological exchange processes dur- ing this period, such as respiration and nutrition, demand a specific arrangement of maternal and fetal tissues [1] . The intimate connection between the fetal membrane and the endometrium provide these functions, followed by the implantation process. This process forms the placenta, which is comprised of a fetal component and a modi- fied uterine barrier [7] . The fetus and the placenta form the conceptus. The development and attachment of the fetal membrane to the uterine epithelium results in the development of the placenta, i.e., the placentation process [8] . The embryo requires nutrients during its growth and development, and the maternal-fetal exchange may oc- cur in structures other than the chorioallantoic placenta because some species have specialized accessory struc- tures. The subplacenta is an accessory structure in hystricognath rodents [9] . Other accessory structures to the placenta include the placental areola in swine and equines [10] , the hemophagous organ in carnivores [11] , and placental hematomas in ruminants [12] .

The subplacenta as a structure of considerable size, located on the roof of the central excavation of the placental disc. It is composed of giant cells as a result of a peculiar transformation of the peripheral syncytial layer. The term subplacenta was used subsequently to indicate a different structure of the placenta in guinea pigs [2] . The subplacenta is found in rodents of the suborder hystricomorphous, and it has been described in the Brazilian porcupine, Coendou prehensilis [13] ; the guinea pig, Caviaporcellus [4] [14] -[16] , the Coypu, Myocastor coy- pus [17] ; the Mongolian gerbil, Meriones unguiculatus [18] ; the capybara, Hydrochaerus hydrochaeris [19] -[21] ; the rock cavy, Kerodon rupestris [22] ; Spix’s yellow-toothed cavy, Galea spixii [3] ; the common agouti, Dasyprocta aguti; the lowland paca, Agouti paca [23] ; and the Brazilian punaré, Thrichomys laurentinus [24] .

The location of the subplacenta differs between species. It is located in the central and mesometrial portions of the placental disc in the Mongolian Gerbil, M. unguiculatus [25] . However, it is located on the roof of the central excavation in the guinea pig, C. porcellus [4] [15] ; the capybara [19] [20] [23] ; and the rock cavy [22] .

That the subplacenta of the rock cavy corresponds to a large circular lobe encrusted between the main placenta and the decidua basalis, but septa composed of connective tissue separates these structures. The subplacenta is divided internally into small irregular lobes separated by connective tissue containing fetal blood vessels. It is composed of trophoblastic cells of syncytial and cellular natures, which correspond to the syncytiotrophoblast and the cytotrophoblast, respectively [22] .

The subplacenta as having a circulation promoted by maternal vessels until approximately the 20^th day, but this circulation ceases in all regions of the subplacenta around the 28^th day. Few fetal vessels are found in the central excavation at the time of subplacental formation, but these vessels are do not contact the trophoblast. The first fetal vessels penetrate deeper between the trophoblast lobes when the maternal circulation recedes between the 23^rd and 27^th days. Fetal vascularization of the subplacenta is completed on the 32^nd day, but these vessels are obliterated after the 55^th day during the degenerative processes of the subplacenta. Only a few fetal vessels are observed in this region after the 58^th day [14] .

Initially that the subplacenta and main placenta were together and touched the maternal blood channels in its outer border prior to becoming a distinctive organ. The subplacenta has two fetal vessels and maternal blood channels in the beginning of the pregnancy and during the middle of the gestation, but debris obstructs some of the spaces with maternal blood. All other studies of the middle stage of the gestation observed that only fetal vessels supply the subplacenta. The subplacenta is reduced near birth, and only vestiges of its tissue can be found. The subplacenta develops as layers of cellular and syncytial proliferative trophoblasts in the fetal mesen- chyme, similar to the main placenta [3] .

The subplacenta as a specialized zone of the chorion between the placental disc and the decidua basalis [26] . The placental syncytium of the fetal ectoderm and the inversion of the vitelline sac defines the origin of the sub- placenta from the chorionic ectoderm [4] . Minot (1889) [27] used the term “subplacenta” for the first time re- garding the rabbit placenta, and it was later used in guinea pigs [4] .

The subplacenta, or accessory organ to the placenta, in two animals, the C. porcellus (guinea pig) and the Brazilian porcupine (C. prehensilis), both hystrichomorphous rodents [28] . The chorioallantoic placentation of the G. spixii and the subplacenta as a component of the placenta that served as a point of origin of invasive tro- phoblasts [3] . The placenta of the red-rumped agouti Dasyprocta leporina and that the subplacenta is related to the production of hormones secreted in the fetal blood but not on maternal tissues [29] . Evolutionary transfor- mations of the chorioallantoic placenta in hystricognath rodents and found macroscopic changes in these ani- mals, primarily the formation of a ring-shaped arrangement of placental regions with maternal arteries situated centrally with a subplacenta [30] .

Characteristics identified the placenta of rodents as experimental models for humans, such as a prominent vi- telline placenta and fewer placental hormones. The superficial invasion of trophoblasts in the rat and the trans- formation of arteries depend on maternal hormones. These characteristics are ideal for pathogenesis research [31] [32] .

The placental areolae of swine are dome-shaped structures located at the openings of the uterine glands. Their epithelium forms tall columns with long microvilli, tubular systems and vesicles, which indicate a high absorp- tive capacity of the epithelium [33] .

That the placental areolae is formed from a portion of the fetal tissue and maternal tissue surrounding the areolar cavity. These areolae accumulate histotrophic secretions from one uterine gland (regular areola) or sev- eral uterine glands (irregular areola). Regular areolae appear as opaque, circular spots measuring a few millime- ters that are variably translucent and form larger structures when observed through the fetal membranes (cho- rioallantoic/chorioamniotic) [34] .

Miglino et al. (2001) [35] mention that regular areolae can total 7000 per conceptus, but irregular areolae ex- hibit a higher or lower frequency of approximately 1500 per placenta. Other structures are present in the fetal placenta, such as the cysts, hippomanes, and petrifactions.

The fetal surface of swine placenta displays a capillary network that forms papillae with protrusions and areolar cavities or converge into a circle in the direction of the areola’s periphery. Irregular areolae have indis- tinct boundaries and are characterized by the opening of one or more uterine glands. The arrangement of the blood vessels of irregular and regular areolae results in the inflow of blood to the areola at the level of capillaries and arterioles. The capillary flow of the areolae includes the convergence of venules to one or two areolar veins, which leads the venous blood from that areolar area in a distinctive manner and suggests that this architecture favors the control mechanisms for the uterus, placenta, and fetus [35] .

The inter-microvillous attachment in the areolar regions is interrupted in the pig and camel, and the exchange of substances between the mother and the fetus occurs through the areolar cavity. The trophoblast absorbs the histotrophic secretions of the endometrium in swine areola to develop the embryo during the pregnancy [36] .

The calcium and iron pass through the same areolar cell and trophoblast using different paths. Calcium crosses through the cytoplasm, but iron and its carrying protein (uteroferrin) bind to the membrane during ab- sorption through a vesicle or lysosome [37] . Uteroferrin is an important substance in iron transport through the areolar cavity from the mother to the fetus in horses [37] and other species, such as the pig [33] [38] . However, only maternal and fetal microcotyledonary epithelial cells transport glucose [37] .

The areolar glands are subunits specialized in the transfer of maternal-fetal substances [33] . Bazer (1975) [39] , Chen et al. (1975) [40] and Raub et al. (1985) [41] reported that the columnar to cuboidal epithelium of the ute- rine glands is involved in the synthesis of iron-binding proteins, including uteroferrin. Uterine secretions in the areolar cavity contain substances with metabolic enzymatic activity [33] .

Abd-Elnaeim et al. (2003) [36] demonstrated that regular areolae of dromedaries are similar to regular areolae in swine [35] , in which only one uterine gland opens to the inner area of the areolar cavity. However, these are- olae differ from mares, which have more than one uterine gland opening at this location.

The chorionic girdle is observed in mares between days 15 - 47 and 53 - 57 of pregnancy. This structure disap- pears as gestation progresses, which suggests that its function of synthesis and proliferation occurs only at the beginning of pregnancy [42] .

That many aspects of embryogenesis in the mare are unique to the genus Equus, especially the development of the chorionic girdle and its posterior invasion of the endometrium [10] .

Trophoblastic cells form an avascular tissue called the chorionic girdle that surrounds the conceptus between days 25 and 35 of gestation in the mare. These cells invade the uterine endometrium on the 35^th day of gestation and form 0.5- to 1.0-cm structures called endometrial cups in 48 hours. The equine chorionic gonadotrophin (eCG) hormone stimulates the accessory luteal glands that aid in the maintenance of gestation [43] .

The high eCG concentrations appear in the maternal serum at the beginning of gestation. Placental structures, called endometrial cups, secrete the eCG. These structures originate from the trophoblastic cells of the chorionic girdle and are destroyed by the immune system after a certain period of activity [44] .

That eCG binds to follicle-stimulating hormone (FSH) and luteinizing hormone (LH) receptors, and it is the only gonadotropin capable of binding both receptors in mammals, except equines. The eCG is secreted between the 33^rd and 120^th day of gestation, and its concentration remains high until the 90^th day [43] . The concentration of eCG declines after this period, and it is absent at the 150^th day. The eCG secretion peaks at approximately 55 and 70 days of gestation, which corresponds to the maximum size of the endometrial cups [10] . TheeCG also binds to the LH receptors in the corpus luteum [45] . This binding increases progesterone (P4pregn-4-eno-3,20- diona) production, which plays a fundamental role during early gestation and acts on the endometrial epithelium to induce the secretion of factors that are indispensable to embryonic development [46] .

eCG has been largely used in superovulation donor programs and in studies with embryo donors due to its ac- tion on FSH [47] . Therefore, the use of eCG in protocols of ovulation synchronization for fixed-time artificial insemination (FTAI) and fixed-time embryo transfer (FTET) has been growing to increase the efficacy of these programs [48] .

In the first half the hemophagous organ is a tubular structure, followed by an expanded and bulbous characteris- tic in the distal half. This accessory organ to the placenta grows, regresses and almost disappears as gestation approaches [49] . The hemophagous organ as a multi-lobular structure is consisting of two relatively large lobes and several smaller lobes. All of the lobes are round, and the larger lobes bind and extend from the allantoic cavity to the back of the embryo at the end of gestation. The proximal extremities of the lobes gather to form a region attached to the maternal surface of the placenta [11] .

The term hemophagous organ was proposed for a particular structure found on the placenta of the raccoons (Procyonlotorlotor) [49] . This sac-shaped, highly vascularized, macroscopic structure hangs in the interior of the allantoic cavity and emerges from an anti-mesometrial central area of the placental ring in procyonid carni- vores. This structure increases in size and complexity until approximately two-thirds to three-fourths of the ges- tational period, and then it regresses [49] -[51] .

Different placental types in different species address 3 types of iron transfer [8] [52] :

1) Absorption of iron bound to transferrin through the outer surface of the trophoblast in direct contact with the maternal bloodstream (i.e., hemochorial placenta);

2) Absorption of erythrocytes by the chorionic epithelium in direct contact with the accumulation of blood leaked from hematophagous areas (i.e., endotheliochorial and synepitheliochorial placenta); and

3) Absorption of iron by the chorionic epithelium in direct contact with the enriched iron originating from endometrial gland secretions (i.e., diffuse placenta).

Another iron absorption mechanism was described as the leakage of blood in the maternal-fetal relationship followed by the phagocytosis of erythrocytes by trophoblastic cells in ovines, bovines, caprines, carnivores, and chiroptera. This absorption occurs in different areas of the placenta, known as placental hematoma or hemo- phagous areas [53] [54] .

That studies were performed as to elucidate iron transfer to the fetus, and iron deficiency leads to some dis- eases in the newborn, such as high blood pressure, anomalies in the immune system, and compromises in brain function [55] [56] .

One of the main characteristics of carnivore placentas is the presence of placental hematomas. A placental he- matoma is a large, compact mass of red blood cells that is well-adhered to the chorioallantoic membrane, and it is found in the medial surface of the placental girdle. Cuboidal epithelium surrounds placental hematomas on the majority of its margin. The largest area is found between the layer adhered to the junctional zone between the maternal and fetal surfaces and the labyrinth zone. The hematoma invades the space previously occupied by the uterine epithelium and its stroma in some areas of the epithelium [2] .

The hemophagous organ is equivalent to the placental hematoma of certain carnivores and indicates that the term “hematoma”, which has pathological implications, can be replaced with the functional and descriptive term “hemophagous” in hemophagocytic areas of the placenta [50] .

The hematomas are an iron source for embryonic development because trophoblasts phagocytose and digest the maternal red blood cells. Observations in buffalos suggest that these areas also correspond to the iron trans- fer for the fetus during the final stages of pregnancy [57] .

The placental hematomas in buffalos (7 to 10 months of pregnancy) are located exclusively in the base of the chorionic villi. The placental hematomas in these animals are numerous and irregularly distributed along the maternal-fetal interface and contain a variable amount of leaked maternal blood. The authors suggest that an erythrophagocytosis occurs due to the trophoblastic cells from areas adjacent to the hematomas presenting eryt- hrophagosomes [12] .