Abstract in English:
ABSTRACT.- Conceição R.A., Ambrósio C.E., Martins D.S., Carvalho A.F., Franciolli A.L.R., Machado M.R.F., Oliveira M.F. & Miglino M.A. 2008. [Morphological aspects of yolk sac from rodents of Hystricomorpha subordem: paca (Agouti paca) and agouti (Dasyprocta aguti).] Aspectos morfológicos do saco vitelino em dois roedores da subordem Hystricomorpha: paca (Agouti paca) e cutia (Dasyprocta aguti). Pesquisa Veterinária Brasileira 28(5):253-259. Setor de Anatomia dos Animais Domésticos e Silvestres, Departamento de Cirurgia, Faculdade de Medicina Veterinária e Zootecnia. Universidade de São Paulo, Cidade Universitária, Av. Prof. Dr. Orlando Marques de Paiva 87, São Paulo, SP 05508-900, Brazil. E-mail: ceambrosio@usp.br
The study aimed to characterize gross and microscopic features of the yolk sac in paca (Agouti paca) and agouti (Dasyprocta aguti) in early gestation. Fragments of the yolk sac of 3 paca and 3 agouti fetuses at early gestation were taken and processed for histological and ultrastructural analyses. Gross features of the vitelline placenta in both species showed its insertion over the main placenta surface and projections to the embryos/fetuses. Microscopically, the vitelline placenta was constituted by endoderm epithelium and mesenchyme, in which vitelline vessels are abundant. The ultrastructure of the samples showed that the visceral yolk sac of the paca was formed by endodermic cells with nuclei in the median region, and that the visceral yolk sac of the agouti was formed by nuclei arranged apically; other characteristic was the large number of mitochondrias, eletrodense vesicles with microvilosities We conclude that (1) the vitelline placenta of the two species presents insertion in the surface of the main placenta; (2) the vitelline placenta of paca rests on the Reichert’s membrane, whereas the agouti vitelline placenta does not have this membrane; (3) the chorion and allantoic are fusioned; and (4) the chorioallantoic placenta and the yolk sac in both species are reversed and vascularized.
Abstract in Portuguese:
ABSTRACT.- Conceição R.A., Ambrósio C.E., Martins D.S., Carvalho A.F., Franciolli A.L.R., Machado M.R.F., Oliveira M.F. & Miglino M.A. 2008. [Morphological aspects of yolk sac from rodents of Hystricomorpha subordem: paca (Agouti paca) and agouti (Dasyprocta aguti).] Aspectos morfológicos do saco vitelino em dois roedores da subordem Hystricomorpha: paca (Agouti paca) e cutia (Dasyprocta aguti). Pesquisa Veterinária Brasileira 28(5):253-259. Setor de Anatomia dos Animais Domésticos e Silvestres, Departamento de Cirurgia, Faculdade de Medicina Veterinária e Zootecnia. Universidade de São Paulo, Cidade Universitária, Av. Prof. Dr. Orlando Marques de Paiva 87, São Paulo, SP 05508-900, Brazil. E-mail: ceambrosio@usp.br
The study aimed to characterize gross and microscopic features of the yolk sac in paca (Agouti paca) and agouti (Dasyprocta aguti) in early gestation. Fragments of the yolk sac of 3 paca and 3 agouti fetuses at early gestation were taken and processed for histological and ultrastructural analyses. Gross features of the vitelline placenta in both species showed its insertion over the main placenta surface and projections to the embryos/fetuses. Microscopically, the vitelline placenta was constituted by endoderm epithelium and mesenchyme, in which vitelline vessels are abundant. The ultrastructure of the samples showed that the visceral yolk sac of the paca was formed by endodermic cells with nuclei in the median region, and that the visceral yolk sac of the agouti was formed by nuclei arranged apically; other characteristic was the large number of mitochondrias, eletrodense vesicles with microvilosities We conclude that (1) the vitelline placenta of the two species presents insertion in the surface of the main placenta; (2) the vitelline placenta of paca rests on the Reichert’s membrane, whereas the agouti vitelline placenta does not have this membrane; (3) the chorion and allantoic are fusioned; and (4) the chorioallantoic placenta and the yolk sac in both species are reversed and vascularized.
Abstract in English:
ABSTRACT.- Moura C.E.B., Albuquerque J.F.G., Magalhães M.S., Silva N.B., Oliveira M.F. & Papa P.C. 2007. [Comparative analysis of the origin of the brachial plexus of the collared peccary (Tayassu tajacu).] Análise comparativa da origem do plexo braquial de catetos (Tayassu tajacu). Pesquisa Veterinária Brasileira 27(9):357-362. Departamento de Morfologia, Universidade Federal do Rio Grande do Norte, Cx. Postal 1524, Campus Universitário Lagoa Nova, Natal, RN 59072-970, Brazil. E-mail: cadumoura@ufrnet.br
Collared peccary (Tayassu tajacu) belongs to the Tayassuidae family, characterized by a “collar” of white hairs that cross behind the neck and extend bilaterally in front of the shoulders. It can be found from south-western United States to Argentina. In the literature a shortage of data is verified regarding the functional anatomy of the collared peccaries, especially of studies that involve the anatomy of the brachial plexus. To elucidate the behavior of this plexus of collared peccaries and with the purpose to contribute for the development of compared anatomy, this study was accomplished. Thirty animals of different ages were used (17 males and 13 females) coming from the Wild Animal Multiplication Center of the “Universidade Federal Rural do Semi-árido” Mossoró, Rio Grande do Norte, Brazil. After slaughter bilateral dissection of the brachial plexuses took place, and the results were registered in schematic drawings and the dispositions grouped in tables for subsequent statistical analysis based on the percentile frequency. It was found that the Plexus brachialis of collared peccaries is the result of established communications, mainly among the Rami ventrales of the last three cervical nerves and of the first two thoracic nerves, having a contribution of the fourth and fifth cervical nerves in 16.67% and 50.00% of the cases, respectively. In 40.00% of the dissections the most frequent plexus was of the type C6, C7, C8, T1 and T2. The main nerves derived from brachial plexus of the collared peccaries and its respective origins had been: Nervus suprascapularis (C6, C7), Nn. subscapulares (C5, C6 e C7 or C6 e C7), N. axillaris (C6, C7), N. musculocutaneus (C7, C8), N. medianus (C7, C8, T1, T2), N. radialis (C8, T1, T2), N. ulnaris (C8, T1, T2), cranialis (C7), and caudalis (C7, C8) Nn. pectorales, N. thoracodorsalis (C6, C7, C8), N. thoracicus longus (C7, C8), and N. thoracicus lateralis (C8, T1, T2).
Abstract in Portuguese:
ABSTRACT.- Moura C.E.B., Albuquerque J.F.G., Magalhães M.S., Silva N.B., Oliveira M.F. & Papa P.C. 2007. [Comparative analysis of the origin of the brachial plexus of the collared peccary (Tayassu tajacu).] Análise comparativa da origem do plexo braquial de catetos (Tayassu tajacu). Pesquisa Veterinária Brasileira 27(9):357-362. Departamento de Morfologia, Universidade Federal do Rio Grande do Norte, Cx. Postal 1524, Campus Universitário Lagoa Nova, Natal, RN 59072-970, Brazil. E-mail: cadumoura@ufrnet.br
Collared peccary (Tayassu tajacu) belongs to the Tayassuidae family, characterized by a “collar” of white hairs that cross behind the neck and extend bilaterally in front of the shoulders. It can be found from south-western United States to Argentina. In the literature a shortage of data is verified regarding the functional anatomy of the collared peccaries, especially of studies that involve the anatomy of the brachial plexus. To elucidate the behavior of this plexus of collared peccaries and with the purpose to contribute for the development of compared anatomy, this study was accomplished. Thirty animals of different ages were used (17 males and 13 females) coming from the Wild Animal Multiplication Center of the “Universidade Federal Rural do Semi-árido” Mossoró, Rio Grande do Norte, Brazil. After slaughter bilateral dissection of the brachial plexuses took place, and the results were registered in schematic drawings and the dispositions grouped in tables for subsequent statistical analysis based on the percentile frequency. It was found that the Plexus brachialis of collared peccaries is the result of established communications, mainly among the Rami ventrales of the last three cervical nerves and of the first two thoracic nerves, having a contribution of the fourth and fifth cervical nerves in 16.67% and 50.00% of the cases, respectively. In 40.00% of the dissections the most frequent plexus was of the type C6, C7, C8, T1 and T2. The main nerves derived from brachial plexus of the collared peccaries and its respective origins had been: Nervus suprascapularis (C6, C7), Nn. subscapulares (C5, C6 e C7 or C6 e C7), N. axillaris (C6, C7), N. musculocutaneus (C7, C8), N. medianus (C7, C8, T1, T2), N. radialis (C8, T1, T2), N. ulnaris (C8, T1, T2), cranialis (C7), and caudalis (C7, C8) Nn. pectorales, N. thoracodorsalis (C6, C7, C8), N. thoracicus longus (C7, C8), and N. thoracicus lateralis (C8, T1, T2).
Abstract in English:
ABSTRACT.- Parizzi R.C., Miglino M.A., Maia M.O., Souza J.A., Santos J.M., Oliveira M.F. & Santos T.C. 2007. [Morphology of the ovary in rhea (Rhea americana).] Morfologia do ovário da ema (Rhea americana). Pesquisa Veterinária Brasileira 27(3):89-94. Departamento de Cirurgia, Faculdade de Medicina Veterinária e Zootecnia, USP, Av. Prof. Dr. Orlando Marques de Paiva 87, São Paulo, SP 05508-270. E-mail: tcsantos@usp.br
The ovarian morphology of the sexually mature rhea (Rhea Americana) is described. Ovaries from 24 adult rheas in their reproductive age were collected in the slaughterhouse. Follicular diameters (n = 18) were measured and samples (n = 6) were fixed in 10% formaldehyde with 0.1M phosphate buffer at pH 7.4 for light microscopy. Results showed that the left ovary occupied the dorsal portion of the celomatic cavity in contact with the cranial portion of the left kidney and the suprarenal gland, being supported in the cavity through the mesovary. On the free surface of the ovary 72.4±17.09 follicles in different phases of development and 30.4±3.65 atretic follicles were observed. The follicles were linked to the ovarian surface by the follicular stalk and had a wide band surrounding its surface, the Stigma folliculare. Histologically, the ovary is constituted by a medulla, composed by connective tissue and vessels, and by a cortex with oocytes and follicles. The follicular wall is composed by the Theca externa and Theca interna, Stratum granulosum and the Zona radiata. The ovary surface is covered by a cubic epithelium, the germinal epithelium, on the connective tissue of the Tunica albuginea. The morphologic characteristics of the ovary of the rhea are due to the egg size in this species and generally similar to other birds.
Abstract in Portuguese:
ABSTRACT.- Parizzi R.C., Miglino M.A., Maia M.O., Souza J.A., Santos J.M., Oliveira M.F. & Santos T.C. 2007. [Morphology of the ovary in rhea (Rhea americana).] Morfologia do ovário da ema (Rhea americana). Pesquisa Veterinária Brasileira 27(3):89-94. Departamento de Cirurgia, Faculdade de Medicina Veterinária e Zootecnia, USP, Av. Prof. Dr. Orlando Marques de Paiva 87, São Paulo, SP 05508-270. E-mail: tcsantos@usp.br
The ovarian morphology of the sexually mature rhea (Rhea Americana) is described. Ovaries from 24 adult rheas in their reproductive age were collected in the slaughterhouse. Follicular diameters (n = 18) were measured and samples (n = 6) were fixed in 10% formaldehyde with 0.1M phosphate buffer at pH 7.4 for light microscopy. Results showed that the left ovary occupied the dorsal portion of the celomatic cavity in contact with the cranial portion of the left kidney and the suprarenal gland, being supported in the cavity through the mesovary. On the free surface of the ovary 72.4±17.09 follicles in different phases of development and 30.4±3.65 atretic follicles were observed. The follicles were linked to the ovarian surface by the follicular stalk and had a wide band surrounding its surface, the Stigma folliculare. Histologically, the ovary is constituted by a medulla, composed by connective tissue and vessels, and by a cortex with oocytes and follicles. The follicular wall is composed by the Theca externa and Theca interna, Stratum granulosum and the Zona radiata. The ovary surface is covered by a cubic epithelium, the germinal epithelium, on the connective tissue of the Tunica albuginea. The morphologic characteristics of the ovary of the rhea are due to the egg size in this species and generally similar to other birds.
Abstract in English:
The evolution of colostral antibodies to bovine leukemia virus (BLV) was examined by testing serum samples of female calves collected from birth to 270 days of age. To observe the levels of BLV-specific antibodies in dams in the peri-natal period, sérum samples were collected between days 35 pre-partum and days 28 post-partum. The presence of antibodies was examined by agar gel immunodiffusion tests (AGID). One week after ingestion of colostrum 100% (49/49) of the heifers gave positive results for BLV antibodies. The number of antibodiy-positive heifers decreased progressively until animais became sem-negative by day 180 of age. From the 41 sem-positive dams tested during the peri-natal period, three (7.3%) became sem-negative at that time. These data suggest that serologic diagnostic of BLV infectious with AGID should be performed after the 6th month of age in calves in order to avoid false-positive results due to passively acquired maternal antibodies. Moreover, serologic diagnosis in pregnant cows between 2 weeks pre and 4 weeks "post-partum" may give rise to false-negative results.
Abstract in Portuguese:
A presença de anticorpos colostrais contra o vírus da leucose bovina (BLV), foi examinada através de análise de amostras de soro de terneiras coletadas desde o nascimento até 270 dias de idade. Também foram coletadas amostras de soro de vacas entre 35 dias antes do parto até 28 dias após o parto. As amostras foram examinadas pelo teste de imunodifusão em gel de ágar (IDGA). Uma semana após a ingestão de colostro, 100% (49/49) das terneiras apresentaram anticorpos para o BLV. Posteriormente, houve uma queda progressiva do número de animais soropositivos, com o desaparecimento de níveis detectáveis de anticorpos até que todas as terneiras se tornassem soronegativas aos 180 dias de idade. De 41 vacas analisadas durante o período peri-parto, 3 (7,3%) apresentaram- se sorologicamente negativas neste período. Nas terneiras, os testes deverão ser realizados após o 6 mês de idade a fim de evitar resultados falso-positivos devido a anticorpos maternos passivamente adquiridos. Sugere-se também que para diagnóstico de infecções pelo BLV, a prova de IDGA seja realizada, nas vacas prenhes, somente até duas semanas antes do parto ou após 1 mês do parto.