Impact of high-fat diet consumption during prolonged period of pregnancy on placenta structures and umbilical vascular growth in goats

This study aimed to verify the impact of high-fat diet consumption for a prolonged period on oxidative stress, fetal growth, umbilical vascular system, and placental structures in pregnant goats. Twenty-two pregnant goats were grouped into the control diet (n= 11) and fat diet (n = 11). Flaxseed meal was added to the fat diet, replacing the corn grain of concentrate, from gestational day 100 to delivery date. Diets were isonitrogenous and isoenergetic, differing in fat content (2.8% vs. 6.3% dry matter). The fat group showed higher feed intake and total plasma lipid levels than the control group (P < 0.001). No difference was found in placentome, and umbilical vascular development. Fat diet-fed goats exhibited a lower systolic peak in the umbilical artery. At delivery, placental traits were similar with the exception of the cotyledon width (P = 0.0075), which was smaller in the fat group and cotyledon surface (P = 0.0047) for multiple pregnancy of fat diet. Cotyledonary epithelium showed more intense staining of lipid droplets and a greater area for lipofuscin staining in the fat group compared to control group (P < 0.001). The mean live weight of the kids was lower in the fat group in the first week after delivery than in control group. Thus, in goats, the continuous administration of a high-fat diet during pregnancy does not appear to modify the fetal-maternal vascular structures but has an impact on a part of the placental structure; therefore, its use must be carefully evaluated.(AU)

Objective lameness assessment in horses used for equine-assisted therapy in Rio Grande do Sul state, Brazil / Avaliação objetiva da claudicação em cavalos de equoterapia no Rio Grande do Sul, Brasil

Equine-assisted therapy is a method used since ancient times to rehabilitate individuals. The biomechanics provided by horses and the friction between their back and the riders' saddle generate impulses that are transmitted to riders' central nervous system; thus, these horses must be healthy enough to enable the desired therapeutic effect. The aim of the current study is to investigate lameness prevalence and intensity in equine-assisted therapy horses in Rio Grande do Sul State. The adopted methodology consisted of the objective evaluation of lameness based on Lameness Locator® wireless inertial sensors, which were placed in the 21 horses assessed in six equestrian centers in Rio Grande do Sul State. Results have shown that 90.1% of the assessed horses presented lameness in the hind (54.2%) and forelimbs (45.8%), as well as that 72% of them with presented mild lameness degree. This outcome has evidenced the need, and significance, of assessing these horses' locomotor system. To support effective therapy and protect equine welfare, it is essential that veterinarians should regularly monitor these animals in order to treat and prevent disease. Even subtle lameness can influence the generated stimuli; thus, it is an important factor to be taken into consideration when selecting equine-assisted therapy.

A equoterapia é um método de terapia, utilizada para reabilitação do praticante desde a antiguidade. A biomecânica proporcionada pelo cavalo e o atrito entre o dorso do cavalo e a sela do praticante geram impulsos que são transmitidos ao sistema nervoso central do mesmo, por isso a importância desse cavalo estar em condições aptas para promover o efeito terapêutico desejado. Nosso objetivo foi identificar a prevalência e intensidade da claudicação em equinos de equoterapia no estado do Rio Grande do Sul. A metodologia utilizada foi a avaliação objetiva da claudicação com base na utilização de sensores inerciais sem fio Lameness Locator® em seis centros equestres do Rio Grande do Sul, totalizando 21 equinos avaliados. Foi constatado que 90,1% dos equinos avaliados apresentavam claudicação, 54,2% do membro pélvico e 45,8% do membro torácico, quanto a intensidade 72% foram leves. A partir desse resultado, verifica-se a necessidade e a importância da avaliação no sistema locomotor destes animais. Para uma terapia eficaz e proteger o bem-estar dos equinos, é essencial o acompanhamento periódico por um médico veterinário para tratamento e prevenção de afecções. Claudicações, mesmo sutis, podem interferir nos estímulos gerados, sendo um importante fator de escolha do cavalo apto para a equoterapia.

Gaining body temperature in horses: mercury, digital and infrared thermometer in different locations / Aferição da temperatura corporal em equinos: avaliações de diferentes métodos e locais

The physical examination has several stages, one of which is the measurement of body temperature, when it exceeds the physiological values is indicative of some disease or hyperthermia, for this in veterinary medicine the mercury or digital thermometer is commonly used. The objective of this work is to compare if there is a difference between the mercury thermometer and the infrared thermometer or digital thermometer, as well as to identify if there is a difference between the measurement locations with the infrared thermometer and the mercury column thermometer and digital thermometer. Infrared temperature was evaluated in three places: oral mucosa, pinna and anal or vaginal mucosa (females), then a digital thermometer, followed by mercury, which was used as a reference standard. There was a statistical difference between the mercury thermometer and the infrared thermometer, when measured on the anal or vaginal mucosa and on the oral mucosa. The infrared thermometer, in the ear, and the digital thermometer did not differ from the mercury thermometer, demonstrating that these present similar values during the temperature measurement. The infrared thermometer proved to be little invasive and fast when compared to the others. However, some limitations were observed in the measurement of body temperature with the infrared thermometer measured in the ear.(AU)

O exame físico tem várias etapas, uma delas é a aferição da temperatura corporal, quando ultrapassa os valores fisio-lógicos é indicativo de alguma enfermidade ou hipertermia, para isso na medicina veterinária é comumente utilizado o termô-metro de mercúrio ou o digital. O objetivo desse trabalho é comparar se existe diferença entre o termômetro de mercúrio e o termômetro infravermelho ou termômetro digital, bem como identificar se existe diferença entre os locais de aferição com o termômetro infravermelho e o termômetro de coluna de mercúrio e termômetro digital. Realizava-se a avaliação da tempera-tura com o infravermelho, em três lugares: mucosa oral, pavilhão auricular e mucosa anal ou vaginal (fêmeas), depois termô-metro digital, seguido pelo de mercúrio que foi utilizado como padrão de referência. Observou-se diferença estatística entre o termômetro de mercúrio e o termômetro infravermelho, quando aferido na mucosa anal ou vaginal e na mucosa bucal. Já o termômetro infravermelho, no pavilhão auricular, e o digital não diferiram do termômetro de mercúrio, demonstrando que estes apresentam valores semelhantes durante a aferição de temperatura. O termômetro infravermelho se demonstrou pouco invasivo e rápido quando comparados aos demais. Entretanto foram observadas algumas limitações da mensuração da tempe-ratura corporal com o termômetro infravermelho aferido no pavilhão auricular. Conclui-se que o termômetro infravermelho, utilizado no pavilhão auricular, e o termômetro digital se equivalem ao termômetro de mercúrio e podem ser utilizados em equinos, porém ainda é preciso mais estudos sobre esse tema.(AU)

Gaining body temperature in horses: mercury, digital and infrared thermometer in different locations / Aferição da temperatura corporal em equinos: avaliações de diferentes métodos e locais

The physical examination has several stages, one of which is the measurement of body temperature, when it exceeds the physiological values is indicative of some disease or hyperthermia, for this in veterinary medicine the mercury or digital thermometer is commonly used. The objective of this work is to compare if there is a difference between the mercury thermometer and the infrared thermometer or digital thermometer, as well as to identify if there is a difference between the measurement locations with the infrared thermometer and the mercury column thermometer and digital thermometer. Infrared temperature was evaluated in three places: oral mucosa, pinna and anal or vaginal mucosa (females), then a digital thermometer, followed by mercury, which was used as a reference standard. There was a statistical difference between the mercury thermometer and the infrared thermometer, when measured on the anal or vaginal mucosa and on the oral mucosa. The infrared thermometer, in the ear, and the digital thermometer did not differ from the mercury thermometer, demonstrating that these present similar values during the temperature measurement. The infrared thermometer proved to be little invasive and fast when compared to the others. However, some limitations were observed in the measurement of body temperature with the infrared thermometer measured in the ear.

O exame físico tem várias etapas, uma delas é a aferição da temperatura corporal, quando ultrapassa os valores fisio-lógicos é indicativo de alguma enfermidade ou hipertermia, para isso na medicina veterinária é comumente utilizado o termô-metro de mercúrio ou o digital. O objetivo desse trabalho é comparar se existe diferença entre o termômetro de mercúrio e o termômetro infravermelho ou termômetro digital, bem como identificar se existe diferença entre os locais de aferição com o termômetro infravermelho e o termômetro de coluna de mercúrio e termômetro digital. Realizava-se a avaliação da tempera-tura com o infravermelho, em três lugares: mucosa oral, pavilhão auricular e mucosa anal ou vaginal (fêmeas), depois termô-metro digital, seguido pelo de mercúrio que foi utilizado como padrão de referência. Observou-se diferença estatística entre o termômetro de mercúrio e o termômetro infravermelho, quando aferido na mucosa anal ou vaginal e na mucosa bucal. Já o termômetro infravermelho, no pavilhão auricular, e o digital não diferiram do termômetro de mercúrio, demonstrando que estes apresentam valores semelhantes durante a aferição de temperatura. O termômetro infravermelho se demonstrou pouco invasivo e rápido quando comparados aos demais. Entretanto foram observadas algumas limitações da mensuração da tempe-ratura corporal com o termômetro infravermelho aferido no pavilhão auricular. Conclui-se que o termômetro infravermelho, utilizado no pavilhão auricular, e o termômetro digital se equivalem ao termômetro de mercúrio e podem ser utilizados em equinos, porém ainda é preciso mais estudos sobre esse tema.

Efeitos da vitrificação na preservação morfológica do tecido testicular de gato doméstico / Vitrification effects during morphological preservation of testicular tissue from domestic cat

This study aimed to evaluate the effect of domestic cats (Felis Catus) testicular parenchyma vitrification by Ovarian Tissue Cryosystem and conventional straw. Three (n=3) adult cats were submitted to routine orchiectomy. For the vitrification, the samples were exposed to equilibrium solution composed by RPMI, containing 20% of ethylene glycol (EG) and 0,1M of sucrose at 20 °C, for 3 minutes. Subsequently, exposed to vitrification solution, containing RPMI added to 40% of EG and 0,1 M of sucrose at 20 °C, for 2 minutes. After devitrification, 10 seminiferous tubules of each treatment were analyzed by histology assay. The viability of spermatic and Sertolicells were analysed with light histology, as well as the seminiferous tubules morphometry. The vitrified groups were inferior to the control group in the morphologically integral cells analysis. However, the OTC was superior to straw in terms of morphological preservation of the germinative cells. Nevertheless, in morphometric analysis there was no statistical difference between the treatments (control, OTC and straw). Therefore, the vitrification in OTC method showed better results than vitrification in straw based on histological evaluation of germ and Sertoli cells of domestic cats.

Effect of dietary taurine supplementation on the growth and blood physiological parameters of juvenile pirarucu / Efeito da suplementação de taurina sobre o crescimento e parâmetros fisiológicos sanguíneos de juvenis de pirarucu

For some fish species, dietary taurine supplementation has been proven necessary in feeds with considerable utilization of vegetable proteins to substitute fishmeal. Pirarucu, Arapaima gigas feeds mainly on taurine-rich animal items in nature, therefore this study aimed to evaluate the effect of dietary taurine supplementation (0, 0.5, 1, 1.5 and 3%) on the growth and blood physiological parameters of juvenile pirarucu. A commercial feed was utilized as the basal diet for the experimental diets. Three hundred fish (20.8 ± 2.3 g) were randomly distributed in 15 tanks and fed for 28 days. At the end of the trial, dietary taurine supplementation did not affect fish growth, feed consumption and feed efficiency. The original amounts of taurine (0.18%) and methionine (1.13%) in the commercial feed (0% taurine diet) apparently sufficed to promote adequate pirarucu growth, with no variation noted in the main blood physiological parameters. Further studies to assess whether taurine is conditionally essential for the pirarucu fed methionine-deficient diets are needed to elucidate the functionality of this nutrient for the studied species.(AU)

Para algumas espécies de peixe, a suplementação de taurina na dieta tem-se mostrado necessária em dietas com grande utilização de proteínas vegetais em substituição à farinha de peixe. Na natureza, o pirarucu, Arapaima gigas se alimenta de itens animais ricos em taurina, portanto este estudo avaliou o efeito da suplementação de taurina (0; 0,5; 1; 1,5 e 3%) sobre o crescimento e parâmetros fisiológicos sanguíneos de juvenis da espécie. Uma ração comercial foi utilizada como dieta basal para as dietas experimentais. Trezentos peixes (20,8 ± 2,3 g) foram aleatoriamente distribuídos em 15 tanques e alimentados durante 28 dias. Ao final do ensaio, a suplementação de taurina nas dietas não afetou crescimento, consumo de alimento e eficiência alimentar dos peixes. As quantidades iniciais de taurina (0,18%) e metionina (1,13%) da ração comercial (dieta 0% taurina) foram aparentemente suficientes para promover o crescimento adequado do pirarucu sem alteração dos principais parâmetros fisiológicos do sangue. Futuros estudos que avaliem se a taurina é condicionalmente essencial para pirarucu alimentado com dietas deficientes em metionina são necessários para elucidar a funcionalidade deste nutriente para a espécie.(AU)

Efeitos da vitrificação na preservação morfológica do tecido testicular de gato doméstico / Vitrification effects during morphological preservation of testicular tissue from domestic cat

This study aimed to evaluate the effect of domestic cats (Felis Catus) testicular parenchyma vitrification by Ovarian Tissue Cryosystem and conventional straw. Three (n=3) adult cats were submitted to routine orchiectomy. For the vitrification, the samples were exposed to equilibrium solution composed by RPMI, containing 20% of ethylene glycol (EG) and 0,1M of sucrose at 20 °C, for 3 minutes. Subsequently, exposed to vitrification solution, containing RPMI added to 40% of EG and 0,1 M of sucrose at 20 °C, for 2 minutes. After devitrification, 10 seminiferous tubules of each treatment were analyzed by histology assay. The viability of spermatic and Sertolicells were analysed with light histology, as well as the seminiferous tubules morphometry. The vitrified groups were inferior to the control group in the morphologically integral cells analysis. However, the OTC was superior to straw in terms of morphological preservation of the germinative cells. Nevertheless, in morphometric analysis there was no statistical difference between the treatments (control, OTC and straw). Therefore, the vitrification in OTC method showed better results than vitrification in straw based on histological evaluation of germ and Sertoli cells of domestic cats.(AU)

Feeding frequency affects feed intake and growth in juvenile pirarucu (Arapaima gigas) / Frequência alimentar afeta a ingestão alimentar e o crescimento de juvenis de pirarucu (Arapaima gigas)

Pirarucu is one of the main fish species for the development of aquaculture in the Amazon. In this study, the optimal feeding frequency for juvenile pirarucu was assessed based on growth and feed efficiency. Juvenile pirarucu weighing ca. 80 g were fed once, twice, three or four times daily until apparent satiation for 63 days. Fish fed three or four times per day presented higher growth, feed intake, and fat body content than those fed once or twice per day. There was no significant difference for feed conversion ratio, and protein and energy retention rates among treatments, suggesting that increased feeding frequency did not affect feed utilization efficiency. Mean feed intake per meal was higher when fish were fed once per day, possibly causing hyperphagic behavior. Results suggest that feeding three times per day was sufficient to secure adequate feeding and growth of juvenile pirarucu.(AU)

O pirarucu é uma das principais espécies de peixe para o desenvolvimento da aquicultura na região amazônica. Neste trabalho foi avaliada a frequência de alimentação ideal para juvenis de pirarucu com base em crescimento e eficiência alimentar. Juvenis de aproximadamente 80 g foram alimentados uma, duas, três ou quatro vezes ao dia até a saciedade aparente durante 63 dias. Maior crescimento, ingestão alimentar e gordura corporal foram observados nos peixes alimentados três ou quatro vezes ao dia em comparação com aqueles alimentados uma ou duas vezes ao dia. Não houve diferença significativa para as taxas de conversão alimentar, retenção proteica e retenção energética entre os tratamentos, indicando que o aumento da frequência de alimentação não resultou em prejuízo da eficiência de utilização do alimento. O consumo médio de alimento por refeição foi maior nos peixes alimentados apenas uma vez ao dia, que provavelmente desenvolveram comportamento hiperfágico. Os resultados sugerem que três refeições diárias foram suficientes para garantir o consumo de alimento e crescimento adequados nessa fase.(AU)

Criopreservação de tecido ovariano e/ou folículos pré-antrais: uma alternativa para salvaguardar o material genético e a fertilidade de ovelhas e cabras valiosas / Cryopreservation of ovarian tissue and/or preantral follicles: an alternative to safeguard the genetic material and fertility of valuable sheep and goats

A redução da biodiversidade tem levado a uma preocupação emergencial frente a conservação do material biológico de animais geneticamente valiosos. Para tanto, a implantação de bancos de germoplasma, como embriões, gametas e tecido gonadal e somáticos, tem sido uma alternativa para auxiliar na manutenção da biodiversidade. No tocante ao material genético de fêmeas, a criopreservação de folículos pré-antrais isolados ou inclusos no tecido ovariano associada ao uso de tecnologias de reprodução assistida, como cultivo, fertilização in vitro e produção de embriões in vitro, poderá auxiliar na conservação da fertilidade de animais domésticos de interesse econômico com dificuldades reprodutivas ou animais ameaçados de extinção. Além disso, a criopreservação de tecido ovariano seguida de transplante pode ser uma alternativa promissora, uma vez que permite a restauração da função ovariana e reprodutiva. Estudos realizados em humanos relataram o nascimento de 130 indivíduos após o transplante de tecido ovariano previamente criopreservado. Apesar desse sucesso, a criopreservação de ovário ainda é considerada uma técnica experimental. Especialmente em caprinos e ovinos, a grande maioria dos estudos tem usado essas espécies como modelo experimental para a espécie humana. Nessas espécies, o sucesso da criopreservação de folículos ovarianos já foi evidenciado, o que nos dá esperança para o uso dessa tecnologia, vislumbrando, não somente a conservação do material genético, mas a obtenção de embriões e nascimento de crias mesmo após a morte de um animal geneticamente valioso. Assim, todos os esforços atuais estão voltados para a avaliação adequada da qualidade de protocolos de criopreservação que assegurem que esses recursos genéticos permaneçam como parte funcional dos sistemas de produção e conservação das espécies.(AU)

Reducing biodiversity has led to an emergency concern over the conservation of biological material from genetically valuable animals. Therefore, the establishment of gene banks, such as embryos, gametes and somatic and ovarian tissue has been an alternative to assist in maintaining biodiversity. Concerning the genetic material of females, the cryopreservation of preantral follicles isolated or included in the ovarian tissue associated with the use of assisted reproduction technologies, such as culture, in vitro fertilization and in vitro embryo production, may help to preserve the fertility of domestic animals of economic interest with reproductive difficulties or animals threatened with extinction. In addition, cryopreservation of ovarian tissue followed by transplantation may be a promising alternative, since it allows the restoration of ovarian and reproductive function. Studies in humans have reported the birth of 130 individuals after previously cryopreserved ovarian tissue transplantation. Despite this success, ovary cryopreservation is still considered an experimental technique. Especially in goats and sheep, the vast majority of studies have used these species as an experimental model for the human species. In these species, the success of cryopreservation of ovarian follicles has already been shown, which gives us hope for the use of this technology, noting not only the conservation of the genetic material, but the obtaining of embryos and the birth of youngsters even after the death of a genetically valuable animal. Thus, all current efforts are focused on the proper evaluation of the quality of cryopreservation protocols that ensure that these genetic resources remain as a functional part of the systems of production and conservation of the species.(AU)

Criopreservação de tecido ovariano e/ou folículos pré-antrais: uma alternativa para salvaguardar o material genético e a fertilidade de ovelhas e cabras valiosas / Cryopreservation of ovarian tissue and/or preantral follicles: an alternative to safeguard the genetic material and fertility of valuable sheep and goats

A redução da biodiversidade tem levado a uma preocupação emergencial frente a conservação do material biológico de animais geneticamente valiosos. Para tanto, a implantação de bancos de germoplasma, como embriões, gametas e tecido gonadal e somáticos, tem sido uma alternativa para auxiliar na manutenção da biodiversidade. No tocante ao material genético de fêmeas, a criopreservação de folículos pré-antrais isolados ou inclusos no tecido ovariano associada ao uso de tecnologias de reprodução assistida, como cultivo, fertilização in vitro e produção de embriões in vitro, poderá auxiliar na conservação da fertilidade de animais domésticos de interesse econômico com dificuldades reprodutivas ou animais ameaçados de extinção. Além disso, a criopreservação de tecido ovariano seguida de transplante pode ser uma alternativa promissora, uma vez que permite a restauração da função ovariana e reprodutiva. Estudos realizados em humanos relataram o nascimento de 130 indivíduos após o transplante de tecido ovariano previamente criopreservado. Apesar desse sucesso, a criopreservação de ovário ainda é considerada uma técnica experimental. Especialmente em caprinos e ovinos, a grande maioria dos estudos tem usado essas espécies como modelo experimental para a espécie humana. Nessas espécies, o sucesso da criopreservação de folículos ovarianos já foi evidenciado, o que nos dá esperança para o uso dessa tecnologia, vislumbrando, não somente a conservação do material genético, mas a obtenção de embriões e nascimento de crias mesmo após a morte de um animal geneticamente valioso. Assim, todos os esforços atuais estão voltados para a avaliação adequada da qualidade de protocolos de criopreservação que assegurem que esses recursos genéticos permaneçam como parte funcional dos sistemas de produção e conservação das espécies.

Reducing biodiversity has led to an emergency concern over the conservation of biological material from genetically valuable animals. Therefore, the establishment of gene banks, such as embryos, gametes and somatic and ovarian tissue has been an alternative to assist in maintaining biodiversity. Concerning the genetic material of females, the cryopreservation of preantral follicles isolated or included in the ovarian tissue associated with the use of assisted reproduction technologies, such as culture, in vitro fertilization and in vitro embryo production, may help to preserve the fertility of domestic animals of economic interest with reproductive difficulties or animals threatened with extinction. In addition, cryopreservation of ovarian tissue followed by transplantation may be a promising alternative, since it allows the restoration of ovarian and reproductive function. Studies in humans have reported the birth of 130 individuals after previously cryopreserved ovarian tissue transplantation. Despite this success, ovary cryopreservation is still considered an experimental technique. Especially in goats and sheep, the vast majority of studies have used these species as an experimental model for the human species. In these species, the success of cryopreservation of ovarian follicles has already been shown, which gives us hope for the use of this technology, noting not only the conservation of the genetic material, but the obtaining of embryos and the birth of youngsters even after the death of a genetically valuable animal. Thus, all current efforts are focused on the proper evaluation of the quality of cryopreservation protocols that ensure that these genetic resources remain as a functional part of the systems of production and conservation of the species.

Use of platelet-rich plasma in the treatment of desmitis of distal interphalangeal joint collateral ligament in a horse

Background: Platelet-rich plasma (PRP) has been increasingly used to hasten healing of tendonitis and desmitis, allowinghorse athletes to go back to practicing sports in a shorter period of time. However, its use has rarely been reported in thetreatment of desmitis of the collateral ligaments of the distal interphalangeal joint (CL-DIP), which is based on the useof horseshoes and rest for at least six months. This paper describes the use of PRP as an aid in the treatment of CL-DIPin a horse athlete.Case: A male Criollo horse, 450 kg, about 15-year-old, used for paleteada. The animal had a month-long history of lameness, and a visual inspection revealed an increase in volume in the lateral dorsal region of the limb proximal to the coronaryband of the hoof. A specific examination of the locomotive system showed Grade III, Category 5 claudication, which became evident the beginning of the exercise and ceased after a short period. A radiographic evaluation of the distal phalanxrevealed no clinically relevant changes. Therefore, and in view of the location of the increased volume, an ultrasound scanwas performed, which showed an image compatible with an extensive hematoma in the region underlying the periopliccorium, while the CL-DIP presented swelling with large areas of hypoechogenicity. Considering the findings of the image,the physical examination and the history of the horse, desmitis of the collateral ligaments of the distal interphalangeal jointwas diagnosed. The treatment plan consisted of rest, application of a therapeutic horseshoe, and infiltration of the lesionwith platelet-rich plasma (PRP). First, however, warm compresses were applied to reduce the swelling. The PRP wasobtained by collecting whole blood from the external jugular vein, subjecting it to double centrifugation, and separatingthe supernatant blood plasma. The end product was applied to the lesion by ultrasound-guided infiltration. The horseshoewas a model...

Use of platelet-rich plasma in the treatment of desmitis of distal interphalangeal joint collateral ligament in a horse

Background: Platelet-rich plasma (PRP) has been increasingly used to hasten healing of tendonitis and desmitis, allowinghorse athletes to go back to practicing sports in a shorter period of time. However, its use has rarely been reported in thetreatment of desmitis of the collateral ligaments of the distal interphalangeal joint (CL-DIP), which is based on the useof horseshoes and rest for at least six months. This paper describes the use of PRP as an aid in the treatment of CL-DIPin a horse athlete.Case: A male Criollo horse, 450 kg, about 15-year-old, used for paleteada. The animal had a month-long history of lameness, and a visual inspection revealed an increase in volume in the lateral dorsal region of the limb proximal to the coronaryband of the hoof. A specific examination of the locomotive system showed Grade III, Category 5 claudication, which became evident the beginning of the exercise and ceased after a short period. A radiographic evaluation of the distal phalanxrevealed no clinically relevant changes. Therefore, and in view of the location of the increased volume, an ultrasound scanwas performed, which showed an image compatible with an extensive hematoma in the region underlying the periopliccorium, while the CL-DIP presented swelling with large areas of hypoechogenicity. Considering the findings of the image,the physical examination and the history of the horse, desmitis of the collateral ligaments of the distal interphalangeal jointwas diagnosed. The treatment plan consisted of rest, application of a therapeutic horseshoe, and infiltration of the lesionwith platelet-rich plasma (PRP). First, however, warm compresses were applied to reduce the swelling. The PRP wasobtained by collecting whole blood from the external jugular vein, subjecting it to double centrifugation, and separatingthe supernatant blood plasma. The end product was applied to the lesion by ultrasound-guided infiltration. The horseshoewas a model...(AU)

Estimation, morphometry and ultrastructure of ovarian preantral follicle population in agouti (Dasyprocta leporina) / Morfometria, estimativa e ultraestrutura da população folicular ovariana preantral de cutia (Dasyprocta leporina)

The aim of this study was to characterize the preantral ovarian follicular population in agoutis (D. leporina) by estimating the number of follicles at each developmental category, and also describe the morphometry and the specific features of the follicle and the oocyte by using light and transmission electron microscopy. The length of each ovary was measured using a caliper rule, longitudinally sectioned into two halves and both were immediately fixed to perform the estimation of follicular population and ultrastructural analysis. The mean (±S.E.M.) population of follicular per pair of ovary was estimated at 4419.8±532.26 and 5397.52±574.91 for right and left ovaries, respectively, but no differences were observed between them. The diameters for follicles, oocyte and nuclei were: 18.62±3.40µm, 12.28±2.37µm and 6.10±0.93µm for primordial, 23.75±5.70µm, 14.22±3.00µm and 6.70±1.24µm for primary and 88.55±17.61µm, 52.85±17.56µm and 22.33±17.61µm for secondary follicles, respectively. The most of the follicles found belonged to the primordial category (86.63%), followed by primary (13.01%) and secondary (0.35%) one. Additionally, polyovular follicles were observed in all the animals and they represented 7.51% of the total follicles counted. The ultrastructural analysis showed that the oocyte presented a central and regular nuclei, displaying a homogenous mass. Among the organelles, the mitochondria were the most abundant and the oocyte Golgi apparatus was rarely observed. In conclusion, this work shows for the first time the characterization of the population of preantral follicles in the ovary of Dasyprocta leporina. Those information will be useful for further development and adaptation of biotechniques such as germplasm cryopreservation and in vitro gametes manipulation.(AU)

O objetivo deste trabalho foi caracterizar a população folicular ovariana pré-antral em cutias (D. leporina) estimando o número de folículos em cada categoria de desenvolvimento, e também descrever a morfometria e as características específicas do folículo e oócito usando microscopia de luz e eletrônica de transmissão. O comprimento de cada ovário foi medido utilizando um paquímetro, seccionados longitudinalmente em duas metades e ambos foram imediatamente fixados para realizar a estimativa da população folicular e análise ultraestrutural. A média (±S.E.M.) da população folicular por par de ovário foi estimada em 4419,8±532,26 e 5397,52±574,91 nos ovários direito e esquerdo, respectivamente, mas não foram observadas diferenças entre eles. Os diâmetros dos folículos, oócito e núcleos, respectivamente, foram: 18,62±3,40µm, 12,28±2.37µm e 6,10±0,93µm para primordial, 23,75±5,70µm, 14,22±3,00µm e 6,70±1,24µm para primário e 88,55±17,61µm, 52,85±17,56µm e 22,33±17,61µm de folículos secundários. A maioria dos folículos encontrados pertencia à categoria primordial (86,63%), seguido pelo primário (13,01%) e um secundário (0,35%). Adicionalmente, os folículos poliovulares foram observados em todos os animais e representavam 7,51% do total de folículos contados. A análise ultra-estrutural mostrou que o oócito apresentou núcleos centrais e regulares, exibindo uma massa homogênea. Dentre as organelas, as mitocôndrias foram as mais abundantes e o aparelho de Golgi do oócito foi raramente observado. Em conclusão, este trabalho mostra pela primeira vez a caracterização da população de folículos pré-antrais do ovário da Dasyprocta leporina. Essas informações serão úteis para o desenvolvimento e adaptação de biotécnicas, como a criopreservação de germoplasma e manipulação de gametas in vitro.(AU)

Estimation, morphometry and ultrastructure of ovarian preantral follicle population in agouti (Dasyprocta leporina) / Morfometria, estimativa e ultraestrutura da população folicular ovariana preantral de cutia (Dasyprocta leporina)

The aim of this study was to characterize the preantral ovarian follicular population in agoutis (D. leporina) by estimating the number of follicles at each developmental category, and also describe the morphometry and the specific features of the follicle and the oocyte by using light and transmission electron microscopy. The length of each ovary was measured using a caliper rule, longitudinally sectioned into two halves and both were immediately fixed to perform the estimation of follicular population and ultrastructural analysis. The mean (±S.E.M.) population of follicular per pair of ovary was estimated at 4419.8±532.26 and 5397.52±574.91 for right and left ovaries, respectively, but no differences were observed between them. The diameters for follicles, oocyte and nuclei were: 18.62±3.40µm, 12.28±2.37µm and 6.10±0.93µm for primordial, 23.75±5.70µm, 14.22±3.00µm and 6.70±1.24µm for primary and 88.55±17.61µm, 52.85±17.56µm and 22.33±17.61µm for secondary follicles, respectively. The most of the follicles found belonged to the primordial category (86.63%), followed by primary (13.01%) and secondary (0.35%) one. Additionally, polyovular follicles were observed in all the animals and they represented 7.51% of the total follicles counted. The ultrastructural analysis showed that the oocyte presented a central and regular nuclei, displaying a homogenous mass. Among the organelles, the mitochondria were the most abundant and the oocyte Golgi apparatus was rarely observed. In conclusion, this work shows for the first time the characterization of the population of preantral follicles in the ovary of Dasyprocta leporina. Those information will be useful for further development and adaptation of biotechniques such as germplasm cryopreservation and in vitro gametes manipulation.(AU)

O objetivo deste trabalho foi caracterizar a população folicular ovariana pré-antral em cutias (D. leporina) estimando o número de folículos em cada categoria de desenvolvimento, e também descrever a morfometria e as características específicas do folículo e oócito usando microscopia de luz e eletrônica de transmissão. O comprimento de cada ovário foi medido utilizando um paquímetro, seccionados longitudinalmente em duas metades e ambos foram imediatamente fixados para realizar a estimativa da população folicular e análise ultraestrutural. A média (±S.E.M.) da população folicular por par de ovário foi estimada em 4419,8±532,26 e 5397,52±574,91 nos ovários direito e esquerdo, respectivamente, mas não foram observadas diferenças entre eles. Os diâmetros dos folículos, oócito e núcleos, respectivamente, foram: 18,62±3,40µm, 12,28±2.37µm e 6,10±0,93µm para primordial, 23,75±5,70µm, 14,22±3,00µm e 6,70±1,24µm para primário e 88,55±17,61µm, 52,85±17,56µm e 22,33±17,61µm de folículos secundários. A maioria dos folículos encontrados pertencia à categoria primordial (86,63%), seguido pelo primário (13,01%) e um secundário (0,35%). Adicionalmente, os folículos poliovulares foram observados em todos os animais e representavam 7,51% do total de folículos contados. A análise ultra-estrutural mostrou que o oócito apresentou núcleos centrais e regulares, exibindo uma massa homogênea. Dentre as organelas, as mitocôndrias foram as mais abundantes e o aparelho de Golgi do oócito foi raramente observado. Em conclusão, este trabalho mostra pela primeira vez a caracterização da população de folículos pré-antrais do ovário da Dasyprocta leporina. Essas informações serão úteis para o desenvolvimento e adaptação de biotécnicas, como a criopreservação de germoplasma e manipulação de gametas in vitro.(AU)

Estimation, morphometry and ultrastructure of ovarian preantral follicle population in agouti (Dasyprocta leporina)

ABSTRACT: The aim of this study was to characterize the preantral ovarian follicular population in agoutis (D. leporina) by estimating the number of follicles at each developmental category, and also describe the morphometry and the specific features of the follicle and the oocyte by using light and transmission electron microscopy. The length of each ovary was measured using a caliper rule, longitudinally sectioned into two halves and both were immediately fixed to perform the estimation of follicular population and ultrastructural analysis. The mean (±S.E.M.) population of follicular per pair of ovary was estimated at 4419.8±532.26 and 5397.52±574.91 for right and left ovaries, respectively, but no differences were observed between them. The diameters for follicles, oocyte and nuclei were: 18.62±3.40m, 12.28±2.37m and 6.10±0.93m for primordial, 23.75±5.70m, 14.22±3.00m and 6.70±1.24m for primary and 88.55±17.61m, 52.85±17.56m and 22.33±17.61m for secondary follicles, respectively. The most of the follicles found belonged to the primordial category (86.63%), followed by primary (13.01%) and secondary (0.35%) one. Additionally, polyovular follicles were observed in all the animals and they represented 7.51% of the total follicles counted. The ultrastructural analysis showed that the oocyte presented a central and regular nuclei, displaying a homogenous mass. Among the organelles, the mitochondria were the most abundant and the oocyte Golgi apparatus was rarely observed. In conclusion, this work shows for the first time the characterization of the population of preantral follicles in the ovary of Dasyprocta leporina. Those information will be useful for further development and adaptation of biotechniques such as germplasm cryopreservation and in vitro gametes manipulation.

RESUMO: O objetivo deste trabalho foi caracterizar a população folicular ovariana pré-antral em cutias (D. leporina) estimando o número de folículos em cada categoria de desenvolvimento, e também descrever a morfometria e as características específicas do folículo e oócito usando microscopia de luz e eletrônica de transmissão. O comprimento de cada ovário foi medido utilizando um paquímetro, seccionados longitudinalmente em duas metades e ambos foram imediatamente fixados para realizar a estimativa da população folicular e análise ultraestrutural. A média (±S.E.M.) da população folicular por par de ovário foi estimada em 4419,8±532,26 e 5397,52±574,91 nos ovários direito e esquerdo, respectivamente, mas não foram observadas diferenças entre eles. Os diâmetros dos folículos, oócito e núcleos, respectivamente, foram: 18,62±3,40m, 12,28±2.37m e 6,10±0,93m para primordial, 23,75±5,70m, 14,22±3,00m e 6,70±1,24m para primário e 88,55±17,61m, 52,85±17,56m e 22,33±17,61m de folículos secundários. A maioria dos folículos encontrados pertencia à categoria primordial (86,63%), seguido pelo primário (13,01%) e um secundário (0,35%). Adicionalmente, os folículos poliovulares foram observados em todos os animais e representavam 7,51% do total de folículos contados. A análise ultra-estrutural mostrou que o oócito apresentou núcleos centrais e regulares, exibindo uma massa homogênea. Dentre as organelas, as mitocôndrias foram as mais abundantes e o aparelho de Golgi do oócito foi raramente observado. Em conclusão, este trabalho mostra pela primeira vez a caracterização da população de folículos pré-antrais do ovário da Dasyprocta leporina. Essas informações serão úteis para o desenvolvimento e adaptação de biotécnicas, como a criopreservação de germoplasma e manipulação de gametas in vitro.

Vitrification of ovarian tissue from non-human primates

Background: One of the strategies to preserve genetic material from nonhuman primates (NHP) consists in the implementation of germplasm banks, for future application in reproductive biotechniques, as well as for biomedical research. Based on the success rates achieved in human, there is a prominent possibility to succeed also with NHP. However, studies with NHP are still scarce, especially regarding the cryopreservation of ovarian tissue.Review: Neotropical non-human primates, especially males, have been used in research related to reproductive biotechniques in Brazil. Regarding research on female reproduction and ovarian tissue preservation, most studies were performed using domestic animals as models. Current concepts and controversies in the restoration of gametes in adult females does not exclude the needs to preserve ovarian tissue. Importantly, ovarian tissue can be collected and preserved even after the death of the donors, being applied when finding dead females. Furthermore, collection of ovarian biopsies is also feasible and will not affect reproductive function. Among the cryopreservation methods, the vitrification has been indicated due to practical logistic, as well as because it will avoid the formation of large intracellular ice crystals, and it is claimed that ovarian stromal damage will be decreased under vitrification. Considering the number of threatened primate species and the needs to preserve their habitat, but also their gametes, development of preservation protocols are needed. Among the procedures, vitrification appears as a practical method to be applied in the near future. Although a low number of studies is reported, most of them were performed in the recent years. In this context, this article reviews recent information on the vitrification of ovarian tissue of non-human primates. Due to the limited number of studies in these species, observed data are compared with the literature in domestic and human mammals.[...]

Vitrification of ovarian tissue from non-human primates

Background: One of the strategies to preserve genetic material from nonhuman primates (NHP) consists in the implementation of germplasm banks, for future application in reproductive biotechniques, as well as for biomedical research. Based on the success rates achieved in human, there is a prominent possibility to succeed also with NHP. However, studies with NHP are still scarce, especially regarding the cryopreservation of ovarian tissue.Review: Neotropical non-human primates, especially males, have been used in research related to reproductive biotechniques in Brazil. Regarding research on female reproduction and ovarian tissue preservation, most studies were performed using domestic animals as models. Current concepts and controversies in the restoration of gametes in adult females does not exclude the needs to preserve ovarian tissue. Importantly, ovarian tissue can be collected and preserved even after the death of the donors, being applied when finding dead females. Furthermore, collection of ovarian biopsies is also feasible and will not affect reproductive function. Among the cryopreservation methods, the vitrification has been indicated due to practical logistic, as well as because it will avoid the formation of large intracellular ice crystals, and it is claimed that ovarian stromal damage will be decreased under vitrification. Considering the number of threatened primate species and the needs to preserve their habitat, but also their gametes, development of preservation protocols are needed. Among the procedures, vitrification appears as a practical method to be applied in the near future. Although a low number of studies is reported, most of them were performed in the recent years. In this context, this article reviews recent information on the vitrification of ovarian tissue of non-human primates. Due to the limited number of studies in these species, observed data are compared with the literature in domestic and human mammals.[...](AU)

Toxicity effect of Auxemma oncocalyx fraction and its active principle oncocalyxone A on in vitro culture of caprine secondary follicles and in vitro oocyte maturation / Efeito da toxicidade da fração da Auxemma oncocalyx e seu princípio ativo oncocalyxona A no cultivo in vitro de folículos secundários e na maturação in vitro de oócitos de caprinos

The extract of Auxemma oncocalyx (A. oncocalyx) and its main component, oncocalyxone A (onco A), possess anti-tumoral activity that may affect fertility. There is limited literature on the action of these substances regarding caprine folliculogenesis. In this study, we evaluated the effect of A. oncocaly and onco A on the in vitro culture of isolated secondary follicles (Experiment 1) and on the in vitro maturation (IVM) of oocytes from caprine antral follicles grown in vivo (Experiment 2). Isolated secondary follicles were distributed in six groups: the non-cultured control was immediately fixed in 4% paraformaldehyde. The remaining follicles were cultured for 7 days in α-minimal essential medium (α-MEM+ ) alone (control) or with dimethyl sulfoxide (DMSO), doxorubicin (DXR), A. oncocalyx, or onco A. After culture, the follicles were evaluated for antrum formation, growth rate, apoptosis (TUNEL), cellular proliferation (PCNA), as well as the expression of BCL2 and BAX. In addition, cumulus oocyte complexes (COCs) were aspirated and allocated into five treatments for IVM: control, cultured only in maturation base medium (TCM 199+ ); or supplemented with DMSO; DXR; A. oncocalyx or onco A. After IVM, oocyte chromatin configuration and viability were assessed. After 7 days of culture, a reduction was noted in the percent of morphologically intact follicles, antrum formation, growth rate, and numbers of PCNApositive granulosa cells (P < 0.05). After culture, the DXR treatment showed a higher percent of TUNELpositive follicles and relative BAX:BCL2 mRNA ratio’s (P < 0.05). After IVM of the COCs, DXR, A. oncocalyx, and onco A treatments showed a greater percent (P < 0.05) of abnormal oocytes and a lower percent of viable oocytes as compared with the control group (P < 0.05)...

O extrato da Auxemma oncocalyx (A. oncocalyx) e seu componente, Oncocalyxona A (onco A), possui atividade antitumoral, podendo afetar a fertilidade. Entretanto, estudos sobre a ação dessas substâncias em relação à foliculogênese caprina são desconhecidos. O objetivo desse estudo foi avaliar o efeito da A. oncocalyx e onco A no cultivo in vitro de folículos secundários isolados (Experimento 1) e na maturação in vitro (MIV) de oócitos de folículos antrais caprinos crescidos in vivo (Experimento 2). Folículos secundários isolados foram distribuídos em seis grupos, em que o controle não-cultivado foi imediatamente fixado em paraformaldeído 4%. Os folículos restantes foram cultivados durante 7 dias em α-MEM+ sozinho (controle) ou suplementado com DMSO, doxorrubicina (DXR), A. oncocalyx ou onco A. Após o cultivo, os folículos foram avaliados quanto à formação de antro, taxa de crescimento, apoptose (TUNEL) e proliferação celular (PCNA), bem como a expressão dos genes BCL2 e BAX. Além disso, os complexos cumulus-oócitos (CCOs) foram aspirados e distribuídos em cinco tratamentos para MIV: o controle em meio de maturação (TCM 199+), e os demais tratamentos suplementados com DMSO, DXR, A. oncocalyx ou onco A. Depois da MIV, a configuração da cromatina e viabilidade oocitária foram avaliadas. Após 7 dias de cultivo, observou-se redução na percentagem de folículos morfologicamente intactos, na formação de antro, na taxa de crescimento e no número de células PCNA positivas (P < 0,05). Depois do cultivo, no tratamento DXR foi observada maior percentagem de folículos TUNEL positivos (P < 0,05) e também aumento na taxa de RNAm BAX: BCL2 (P < 0,05). Após MIV dos CCOs, nos tratamentos com DXR, A. oncocalyx e onco A, observou-se maior (P < 0,05) percentagem de oócitos anormais e menor de oócitos viáveis quando comparados ao grupo controle (P < 0,05)...

Toxicity effect of Auxemma oncocalyx fraction and its active principle oncocalyxone A on in vitro culture of caprine secondary follicles and in vitro oocyte maturation / Efeito da toxicidade da fração da Auxemma oncocalyx e seu princípio ativo oncocalyxona A no cultivo in vitro de folículos secundários e na maturação in vitro de oócitos de caprinos

The extract of Auxemma oncocalyx (A. oncocalyx) and its main component, oncocalyxone A (onco A), possess anti-tumoral activity that may affect fertility. There is limited literature on the action of these substances regarding caprine folliculogenesis. In this study, we evaluated the effect of A. oncocaly and onco A on the in vitro culture of isolated secondary follicles (Experiment 1) and on the in vitro maturation (IVM) of oocytes from caprine antral follicles grown in vivo (Experiment 2). Isolated secondary follicles were distributed in six groups: the non-cultured control was immediately fixed in 4% paraformaldehyde. The remaining follicles were cultured for 7 days in α-minimal essential medium (α-MEM+ ) alone (control) or with dimethyl sulfoxide (DMSO), doxorubicin (DXR), A. oncocalyx, or onco A. After culture, the follicles were evaluated for antrum formation, growth rate, apoptosis (TUNEL), cellular proliferation (PCNA), as well as the expression of BCL2 and BAX. In addition, cumulus oocyte complexes (COCs) were aspirated and allocated into five treatments for IVM: control, cultured only in maturation base medium (TCM 199+ ); or supplemented with DMSO; DXR; A. oncocalyx or onco A. After IVM, oocyte chromatin configuration and viability were assessed. After 7 days of culture, a reduction was noted in the percent of morphologically intact follicles, antrum formation, growth rate, and numbers of PCNApositive granulosa cells (P < 0.05). After culture, the DXR treatment showed a higher percent of TUNELpositive follicles and relative BAX:BCL2 mRNA ratios (P < 0.05). After IVM of the COCs, DXR, A. oncocalyx, and onco A treatments showed a greater percent (P < 0.05) of abnormal oocytes and a lower percent of viable oocytes as compared with the control group (P < 0.05)...(AU)

O extrato da Auxemma oncocalyx (A. oncocalyx) e seu componente, Oncocalyxona A (onco A), possui atividade antitumoral, podendo afetar a fertilidade. Entretanto, estudos sobre a ação dessas substâncias em relação à foliculogênese caprina são desconhecidos. O objetivo desse estudo foi avaliar o efeito da A. oncocalyx e onco A no cultivo in vitro de folículos secundários isolados (Experimento 1) e na maturação in vitro (MIV) de oócitos de folículos antrais caprinos crescidos in vivo (Experimento 2). Folículos secundários isolados foram distribuídos em seis grupos, em que o controle não-cultivado foi imediatamente fixado em paraformaldeído 4%. Os folículos restantes foram cultivados durante 7 dias em α-MEM+ sozinho (controle) ou suplementado com DMSO, doxorrubicina (DXR), A. oncocalyx ou onco A. Após o cultivo, os folículos foram avaliados quanto à formação de antro, taxa de crescimento, apoptose (TUNEL) e proliferação celular (PCNA), bem como a expressão dos genes BCL2 e BAX. Além disso, os complexos cumulus-oócitos (CCOs) foram aspirados e distribuídos em cinco tratamentos para MIV: o controle em meio de maturação (TCM 199+), e os demais tratamentos suplementados com DMSO, DXR, A. oncocalyx ou onco A. Depois da MIV, a configuração da cromatina e viabilidade oocitária foram avaliadas. Após 7 dias de cultivo, observou-se redução na percentagem de folículos morfologicamente intactos, na formação de antro, na taxa de crescimento e no número de células PCNA positivas (P < 0,05). Depois do cultivo, no tratamento DXR foi observada maior percentagem de folículos TUNEL positivos (P < 0,05) e também aumento na taxa de RNAm BAX: BCL2 (P < 0,05). Após MIV dos CCOs, nos tratamentos com DXR, A. oncocalyx e onco A, observou-se maior (P < 0,05) percentagem de oócitos anormais e menor de oócitos viáveis quando comparados ao grupo controle (P < 0,05)...(AU)

Platelet-derived growth factor-BB (PDGF-BB) improves follicular survival, oocyte and follicular diameters, in a dose-dependent manner, after the in vitro culture of goat preantral follicles enclosed in ovarian tissue fragments

The aims of this study were to investigate the effects of different concentrations of Platelet-derived growth factor-BB (PDGF-BB) on the survival, activation, levels of ROS, and growth of goat preantral follicles enclosed in ovarian tissue. For this, ovarian fragments were cultured for 7 days in Alpha Minimum Essential Medium (α-MEM+ ) with or without PDGF-BB (0, 25, 50 and 100 ng/ml). The results showed that both the 25 ng/ml PDGF and the 50 ng/ml PDGF treatments maintained the percentage of morphologically normal follicles from day 1 to day 7. In addition, the 25 ng/ml PDGF treatment showed a significantly higher percentage of morphologically normal follicles when compared to the other treatments. At day 7, greater (P < 0.05) follicular and oocyte diameters were observed in the 25 ng/ml PDGF and the 50 ng/ml PDGF treatments when compared to the cultured control treatment. On day 7 of culture, all the treatments tested had a significant increase in the percentage of developing follicles when compared to the non-cultured control. However, the percentage of follicle activation, as well as ROS production, were similar (P < 0.05) among the treatments, irrespective of culture time. In conclusion, PDGF-BB improved, in a concentration-dependent manner, follicular survival as well as oocyte and follicular diameter after in vitro culture of goat preantral follicle-enclosed in ovarian tissue fragments.