Full confluency, serum starvation, and roscovitine for inducing arrest in the G0/G1 phase of the cell cycle in puma skin-derived fibroblast lines

The puma population is constantly decreasing, and cloning by somatic cell nuclear transfer can be used to conserve the species. One of the factors determining the success of the development of cloned embryos is the cell cycle stage of the donor cells. We evaluated the effects of full confluency (~100%), serum starvation (0.5% serum), and roscovitine (15 µM) treatments on the cell cycle synchronization in G0/G1 of puma skin-derived fibroblasts by flow cytometric analysis. Also, we assessed the effects of these synchronization methods on morphology, viability, and apoptosis levels using microscopy tools. The results showed that culturing the cells to confluence for 24 h (84.0%), 48 h (84.6%), and 72 h (84.2%) and serum starvation for 96 h (85.4%) yielded a significantly higher percentage of cells arrested in the G0/G1 (P < 0.05) phase than cells not subjected to any cell cycle synchronization method (73.9%). Nevertheless, while serum starvation reduced the percentage of viable cells, no difference was observed for the full confluence and roscovitine treatments (P > 0.05). Moreover, roscovitine for 12 h (78.6%) and 24 h (82.1%) was unable to synchronize cells in G0/G1 (P > 0.05). In summary, full confluency induces puma fibroblast cell cycle synchronization at the G0/G1 stage without affecting cell viability. These outcomes may be valuable for planning donor cells for somatic cell nuclear transfer in pumas.(AU)

Cutaneous myxoma in broiler chicken detected during slaughtering

Background: A cutaneous or superficial myxoma is a benign neoplasm of dermal or subcutaneous fibroblast origin. Although rare, it has been previously described in several species, including poultry. It presents as a single node or soft mass with a gelatinous cut surface. Histopathological analysis is essential for diagnosis and to differentiate it from other mesenchymal neoplasms and inflammatory or degenerative processes. Microscopically, it consists of dermal or subcutaneous lobules of plump, stellate, or spindle-shaped, bland-looking cells embedded in a basophilic myxoid matrix. This report describes the pathological findings in a rare case of cutaneous myxoma in a 42-day-old broiler flock. Cases: During ante mortem inspection of a 42-day-old broiler flock at a slaughterhouse under the authority of the Federal Inspection Service (southern Brazil), nodular lesions or encrusted areas with yellow and black areas were observed in the head skin of less than 1% of animals. These lesions, approximately 0.5 cm in diameter, were observed on the comb, in the periocular skin region, and close to the animals' nostrils. During the breeding period, no health or epidemiological events were observed. Fragments of the lesions in the comb and periocular skin were collected and fixed in buffered 10% formalin. The samples were sent to the laboratory, routinely processed, and stained with hematoxylin and eosin and Alcian blue. Microscopically, the lesions consisted of irregular multifocal proliferation of connective tissue showing spindle cells with poorly demarcated borders and scarce cytoplasm in a slightly basophilic myxoid aspect matrix. The adjacent epidermis is compressed due to neoplastic proliferation. No areas of epithelial hyperplasia or inclusion bodies were observed. According to the pathologic description and considering its descriptive epidemiology, our main clinical suspicion was cutaneous fowl pox, a pathology characterized by the appearance of nodules in regions devoid of feathers. However, the microscopic changes observed were compatible with those described for cutaneous myxomas. In addition, the extracellular matrix was positive for Alcian Blue staining, which is an indicator of myxoma. In the present case, the SIF did not report the same macroscopic lesions in other flocks of the same origin. Discussion: Connective tissue tumors, including myxomas, occur considerably less frequently under field conditions. In addition, these neoplasms are more frequent in mature birds and are not usually described in broilers, as observed in this report. The cutaneous myxoma described in broilers is usually a sporadic neoplasm that does not cause zootechnical losses, as observed in the case report. Its etiology is unknown and has been associated with various factors, such as local trauma and foreign bodies. Some fragments of plant material from the breeding environment were microscopically detected in the encrusted areas, which may indicate previous trauma or a foreign body. Myxoma has been associated with avian leukosis virus (ALV) subgroup A, but SIF did not report the same macroscopic lesions in other flocks of the same breeder hen's origin in the present case. Furthermore, sporadic connective tissue tumors associated with the virus occur in mature chickens but not in broilers. Myxoma lesions should be considered in the differential diagnosis of other connective tissue tumors and infectious agents that cause lesions in the skin and subcutaneous tissue.

Evaluation of the acid-neutralizing and cytotoxicity properties of novel plant mucilage used as an alternative treatment for peptic ulcers and as antacids in Namibia

Hypersecretion of gastric acid damages the stomach lining, causing the formation of peptic ulcers. Mucilage from medicinal plants offers a relaxing and soothing effect to the endodermal lining of the gut and has antacid properties, which can protect the mucosal lining from gastric acidity. This is the first report aimed to evaluate the physicochemical characteristics, acid-neutralizing, and cytotoxicity properties of traditionally used aqueous mucilage from Asparagus exuvialis and Sesamum capense. The physicochemical properties were determined by biochemical methods. Acid neutralizing and buffering capacities were determined by titration methods. Normal mouse embryonic fibroblast cells were used for cytotoxicity evaluation by MTT assay. The physicochemical characterization confirmed the presence of carbohydrates, alkaloids, saponins, proteins, tannins, flavonoids, and glycosides. Sesamum capense mucilage exhibited the most potent artificial gastric juice neutralizing capacity pH of 4.62±0.01, 8.0±0.00 acid neutralization capacity per gram of acid, and 30 minutes duration of acid neutralization. The aqueous mucilage from S. capense did not cause any significant cytotoxicity to 3T3 cell lines showing an IC50 value of 91.5 ± 0.06 µg mL-1, confirming the safe nature of the mucilage. These findings revealed that S. capense has the potential to neutralize gastric acid responsible for ulceration and can be safely consumed.(AU)

ISOLATION AND AMPLIFICATION OF Anaplasma marginale IN CHICKEN EMBRYO FIBROBLAST CELL CULTURE / ISOLATION AND AMPLIFICATION OF Anaplasma marginale IN CHICKEN EMBRYO FIBROBLAST CELL CULTURE

Anaplasma marginale is an important agent for animal livestock, its presence in herds of cattle, sheep and goats leads to losses for Brazilian agribusiness. The present study aimed to describe an isolation technique for A. marginale, using chicken embryo fibroblast (CEF) cell culture. For this, blood and tick samples were collected from 5 calves, between 2 and 3 months of age, which due to anemia, jaundiced mucous membranes and prostration, were considered supposedly infected with A.marginale. For the diagnosis, DNA extraction and PCR was performed from the blood and tick samples collected. All the tick and blood samples were positive in the PCR test. Additionally, ticks were crushed with the aid of a blender for inoculation in CEF cell culture. After inoculation, the cultures were kept at 37ºC and 5% CO2 for 15 days. The cell supernatant of cell cultures were again analyzed by PCR and by the technique Wrighte stain to confirm A. marginale isolation. Cell cultures were positive in PCR and the presence of the agent was demonstrated by Wrighte stain. Therefore, using CEF cell culture was possible to isolate and amplify the A. marginale in a concentration of 1.3 x 107.2 bodies per ml. The CEF cells are undemanding, easy to maintain and they are an option for isolation and production of A. marginale in the laboratory condition.

Anaplasma marginale (A. marginale) is a worldwide pathogen that infects a variety ofruminants, but mostly cattle. The present study aimed to describe an isolation technique for A. marginale, using chicken embryo Þ broblast (CEF) cell culture. Blood and tick samples were collected from 5 calves from 2 to 3 months old, which were considered to be infected with A.marginale due to anemia, jaundiced mucous membranes, and prostration. DNA extractionand PCR were performed for diagnosis using blood and tick samples. All tick and blood samples tested positive in PCR. Additionally,ticks were crushed with the aid of a blender for inoculation in CEF cell culture. After inoculation, the cultures were kept at 37ºC and 5%CO2 for 15 days. The cell supernatant of cell cultures was again analyzed using PCR and Wright stain method to conÞ rm A. marginaleisolation. Cell cultures tested positive in PCR, and the presence of the agent was demonstrated by Wright stain. Therefore, by using CEFcell culture it was possible to isolate and amplify the A. marginale in a concentration of 1.3x 107.2 bodies per mL. The CEF cells are undemanding and easy to preserve; they are anoption for isolation and production of A. marginale under laboratory conditions.

Fibroma cutâneo atípico em uma vaca / Atypical cutaneous fibroma in a cow

Background: Cutaneous fibroma is a benign neoplasm affecting the fibroblasts and collagen matrix that develops in the dermis or subcutaneous tissue. This neoplasm is uncommon in cattle, and few reports have described the treatment and resolution of this neoplasm. Despite its benign character, a veterinarian should consider cutaneous fibroma in the differential diagnosis of skin tumors. This report aims to describe a rare case of large fibroma in the scapular region in a cow, with emphasis on the clinical-surgical and anatomopathological aspects of the condition. Case: A 3-year-old Girolando 3/4 cow was attended to at a rural property in Lagamar-MG, Brazil. According to the owner, the animal presented with a small mass in the right scapular region that grew progressively over 1 year and 6 months. Clinical examination revealed an exuberant and painless increase in volume on palpation in the proximal region of the right thoracic limb, which, in its vertical axis, extended from the proximal end of the scapula to near the olecranon tuberosity, and, in its horizontal axis, extended from the 6th intercostal space to the scapulohumeral joint, reaching the dimensions 66 cm and 62 cm, respectively. It presented with multiple nodules that were firm in consistency with extensive areas of ulceration. Neoplasia was suspected, and surgical excision was decided upon. The cow was sedated and restrained in the left lateral decubitus position. Trichotomy and antisepsis of the operative field were performed followed by an infiltrative anesthetic block around the tumor. The tumor was excised maintaining a safety margin of 1 cm. Dermorrhaphy was not possible, and healing by secondary intention was awaited. In the postoperative period, antibiotic therapy with benzathine penicillin, analgesia with meloxicamand dipyrone and daily dressing of the wound were performed. There were no postoperative complications and complete healing occurred approximately 100 days after surgery. One year after the surgical procedure, the owner reported that the cow did not present with recurrence of the neoplasm. The resected tumor weighed 11.2 kg, and, when cut, presented with solid conformation and whitish coloration. Tumor fragments were harvested, fixed in 10% formalin, and sent for histopathological examination, which revealed neoproliferation of remarkable cellular density composed of dense, well vascularized fibrocollagenous connective tissue arranged in multidirectional bundles and undulating pattern. Mild cellular pleomorphism was identified, and no mitosis figures were observed. Alcian blue staining was negative for mucopolysaccharides, differing from Masson's trichrome staining, which widely stained the fibrocollagenous tissue blue. In view of these findings, the diagnosis of cutaneous fibroma was confirmed. Discussion: Cutaneous fibromas are benign neoplasms of fibrous tissue, and they are uncommon in cattle and may be associated with bovine papillomavirus and/or trauma. Although the origin of cutaneous fibroma is not clear, the present report stands out due to the large size of the tumor mass. The complete healing of the surgical wound, the absence of recurrence one year after surgery and the return of the animal to dairy production demonstrate that the surgical treatment was adequate. The macro- and microscopic characteristics of the cutaneous fibroma in this case corroborate with other cases reported in the literature. Large cutaneous fibroma is uncommon in bovines, and may hinder surgical excision and prolong healing time, as well as the complete recovery of the animal. Moreover, the differential diagnosis with other neoplasms of fibroblastic origin is relevant, especially for those with malignant biological behavior, such as fibrosarcoma and myxosarcoma.

A modified hydrogel production protocol to decrease cellular content

Purpose: To analyze the cytotoxicity and cell in porcine-derived decellularized skin matrix. Methods: We analyzed the effect of multiple decellularization processes by histological analysis, DNA quantification, and flow cytometry. Subsequently, we analyzed the most appropriate hydrogel concentration to minimize cytotoxicity on fibroblast culture and to maximize cell proliferation. Results: After the fourth decellularization, the DNA quantification showed the lowest DNA concentration (< 50 ng/mg). Histological analysis showed no cell components in the hydrogel. Moreover, hematoxylin and eosin showed a heterogeneous structure of collagen fibers. The best hydrogel concentration ranged from 3 to 25%, and there was no significant difference between the 24 hours and seven days. Conclusions: The process of hydrogel production was effective for removing cells and DNA elements. The best hydrogel concentration ranged from 3 to 25%.

El extracto acuoso de la cáscara de Caryocar brasiliense mejora la retracción de heridas / Aqueous extract of stem bark from Caryocar Brasiliense improves the wound retraction / O extrato aquoso da casca de Caryocar brasiliense melhora a retração de feridas

Este estudio fue conducido para verificar el efecto del extracto acuoso y de la pomada basada en cáscara de Caryocar brasiliense sobre la retracción de heridas en conejos. Fueron utilizados 12 conejos Nueva Zelanda Blanco divididos en dos grupos y cuatro lesiones fueron producidas en la región dorsal de cada animal. Las lesiones a la derecha fueron tratadas con extracto acuoso (grupo 1) o con la pomada (grupo 2) y las lesiones a la izquierda fueron tratadas con solución salina 0,9% (grupo control). Los niveles de colágeno y fibroblastos fueron menores (P<0,05) en lesiones tratadas con extracto acuoso, comparado con el grupo control. A los 7 y 14 días después del procedimiento, la retracción de las lesiones era mayor (P<0,05) cuando tratadas con extracto acuoso y en las lesiones tratadas con la pomada, la mejora ocurrió solamente el 7º día, comparado con el grupo control. Se concluyó que el extracto acuoso de la cáscara de Caryocar brasiliense mejoro la retracción de heridas por un período de tiempo mayor do que la pomada. 

This study was carried out to verify the effect of the aqueous extract and the ointment of the stem bark from Caryocar brasiliense on the wound healing in rabbits. Twelve New Zealand rabbits were divided in two groups and four lesions were produced on the back of each animal. The lesions on the right side were treated with aqueous extract (group 1) or with ointment (group 2), while the lesions on the left side were the control group (treated with 0.9% saline solution). Collagen and fibroblast levels were lower (P<0.05) in wounds treated with aqueous extract, compared to the control group. On days 7 and 14 after the procedures, the wound retraction was better (P<0.05) when treated with aqueous extract, while in wounds treated with the ointment, the improvement occurred only on the 7th day. The aqueous extract of stem bark from Caryocar brasiliense improved the wound retraction longer than the ointment. 

Este estudo foi conduzido para verificar o efeito do extrato aquoso e da pomada à base de casca de Caryocar brasiliense sobre a retração de feridas em coelhos. Foram utilizados 12 coelhos Nova Zelândia Branco divididos em dois grupos e quatro lesões foram produzidas na região dorsal de cada animal. As lesões à direita foram tratadas com extrato aquoso (grupo 1) ou com a pomada (grupo 2) e as lesões à esquerda foram tratadas com solução salina 0,9% (grupo controle). Os níveis de colágeno e fibroblastos foram menores (P<0,05) em lesões tratadas com extrato aquoso, comparado com o grupo controle. Aos 7 e 14 dias após o procedimento, a retração das lesões era maior (P<0,05) quando tratadas com extrato aquoso e nas lesões tratadas com a pomada, a melhora ocorreu apenas no 7º dia, comparado com o tratamento controle. Concluiu-se que o extrato aquoso de casca de Caryocar brasiliense melhorou a retração de feridas por um período de tempo maior do que a pomada.   

Viability of fibroblasts from "Curraleiro Pé Duro" cattle after different cryopreservation protocols / Viabilidade de fibroblastos de bovinos da raça Curraleiro Pé Duro submetidos a diferentes protocolos de criopreservação

A raça tropicalmente adaptada Curraleiro Pé Duro (CPD) possui grande rusticidade e capacidade de produção. A técnica de criopreservação de células somáticas permite estocar, por tempo indeterminado, o material genético. O objetivo deste trabalho é avaliar a viabilidade de fibroblastos, pós-criopreservação, em protocolos diferentes. Foi utilizada uma biópsia auricular de um bovino CPD, que passou por antissepsia e anestesia local. Posteriormente o material foi processado e incubado para ser observado quanto à confluência e à morfologia. Em seguida, os fibroblastos foram criopreservados em três tratamentos (T1, T2 e T3). Após serem criopreservados, foram descongelados e analisados quanto à viabilidade celular, à capacidade de crescimento e à morfologia. Na análise de variância e das médias, foram comparados pelo teste de Tukey com significância de 5%. Não foram observadas, nos protocolos, diferenças estatísticas entre a viabilidade celular (T1 = 67,98%, T2 = 71,42% e T3 = 69,93%), a capacidade de confluência (T1 = 80%, T2 = 90%, T3 = 85%) ou a passagem de origem das células. A criopreservação de fibroblastos auriculares de bovinos CPD não mostrou diferença entre os três métodos, sugerindo até que o método que demanda equipamentos menos especializados (T1) é tão eficiente quanto os demais.

Cytotoxicity of iodine-131 radiopharmaceutical in tumor and non-tumor human cells and radioprotection by integral juices of Vitis labrusca L / Citotoxicidade do radiofarmacêutico iodo-131 em células humanas tumorais e não tumorais e radioprotecção por sucos integrais de Vitis labrusca L

Iodine-131 (I-131) radioisotope it causes the formation of free radicals, which lead to the formation of cell lesions and the reduction of cell viability. Thus, the use of radioprotectors, especially those from natural sources, which reduce the effects of radiation to healthy tissues, while maintaining the sensitivity of tumor cells, stands out. The objective of the present study was to evaluate the cytoprotective/radioprotective effects of whole grape juices manufactured from the conventional or organic production systems, whether or not exposed to ultraviolet (UV-C) light irradiation. The results showed that I-131 presented a cytotoxic effect on human hepatocellular cells (HepG2/C3A) at concentrations above 1.85 MBq/mL, after 24 and 48 hours of treatment, though all concentrations (0.0037 to 7.40 MBq/mL) were cytotoxic to non-tumor human lung fibroblast (MCR-5) cells, after 48 hours. However, grape juices (10 and 20 µL/mL) did not interfere with the cytotoxic effect of the therapeutic dose of I-131 on tumor cells within 48 hours of treatment, while protecting the non-tumor cells, probably due to its high antioxidant activity. In accordance with their nutraceutical potential, antioxidant and radioprotective activity, these data stimulate in vivo studies on the use of natural products as radioprotectants, such as grape juice, in order to confirm the positive beneficial potential in living organisms.

O radioisótopo iodo-131 (I-131) causa a formação de radicais livres, que levam à formação de lesões celulares e redução da viabilidade celular. Assim, destaca-se a utilização de radioprotetores, principalmente de origem natural, que reduzem os efeitos da radiação nos tecidos saudáveis, mantendo a sensibilidade das células tumorais. O objetivo do presente estudo foi avaliar os efeitos citoprotetores/radioprotetores de sucos de uva integral fabricados em sistemas de produção convencional ou orgânico, expostos ou não à radiação ultravioleta (UV-C). Os resultados mostraram que o I-131 apresentou efeito citotóxico nas células hepatocelulares humanas (HepG2/C3A) em concentrações acima de 1,85 MBq/mL, após 24 e 48 horas de tratamento, embora todas as concentrações (0,0037 a 7,40 MBq/mL) fossem citotóxicas para células de fibroblasto de pulmão humano não tumoral (MCR-5), após 48 horas. No entanto, os sucos de uva (10 e 20 µL/mL) não interferiram no efeito citotóxico da dose terapêutica de I-131 nas células tumorais em 48 horas de tratamento, protegendo as células não tumorais, provavelmente devido ao seu alto poder antioxidante. atividade. De acordo com seu potencial nutracêutico, atividade antioxidante e radioprotetora, esses dados estimulam estudos in vivo sobre o uso de produtos naturais como radioprotetores, como o suco de uva, a fim de confirmar o potencial benéfico positivo em organismos vivos.

New multienzymatic complex formed between human cathepsin D and snake venom phospholipase A2

Background Cathepsin D (CatD) is a lysosomal proteolytic enzyme expressed in almost all tissues and organs. This protease is a multifunctional enzyme responsible for essential biological processes such as cell cycle regulation, differentiation, migration, tissue remodeling, neuronal growth, ovulation, and apoptosis. The overexpression and hypersecretion of CatD have been correlated with cancer aggressiveness and tumor progression, stimulating cancer cell proliferation, fibroblast growth, and angiogenesis. In addition, some studies report its participation in neurodegenerative diseases and inflammatory processes. In this regard, the search for new inhibitors from natural products could be an alternative against the harmful effects of this enzyme. Methods An investigation was carried out to analyze CatD interaction with snake venom toxins in an attempt to find inhibitory molecules. Interestingly, human CatD shows the ability to bind strongly to snake venom phospholipases A2 (svPLA2), forming a stable muti-enzymatic complex that maintains the catalytic activity of both CatD and PLA2. In addition, this complex remains active even under exposure to the specific inhibitor pepstatin A. Furthermore, the complex formation between CatD and svPLA2 was evidenced by surface plasmon resonance (SPR), two-dimensional electrophoresis, enzymatic assays, and extensive molecular docking and dynamics techniques. Conclusion The present study suggests the versatility of human CatD and svPLA2, showing that these enzymes can form a fully functional new enzymatic complex.

Isolation and amplification of Anaplasma marginale in chicken embryo fibroblast cell culture / Isolamento e amplificação de Anaplasma marginale em cultivos celulares de fibroblastos de embriões de galinhas

Anaplasma marginale (A. marginale) is a worldwide pathogen that infects a variety of ruminants, but mostly cattle. The present study aimed to describe an isolation technique for A. marginale, using chicken embryo Þ broblast (CEF) cell culture. Blood and tick samples were collected from 5 calves from 2 to 3 months old, which were considered to be infected with A.marginale due to anemia, jaundiced mucous membranes, and prostration. DNA extraction and PCR were performed for diagnosis using blood and tick samples. All tick and blood samples tested positive in PCR. Additionally, ticks were crushed with the aid of a blender for inoculation in CEF cell culture. After inoculation, the cultures were kept at 37ºC and 5% CO2 for 15 days. The cell supernatant of cell cultures was again analyzed using PCR and Wright stain method to conÞ rm A. marginale isolation. Cell cultures tested positive in PCR, and the presence of the agent was demonstrated by Wright stain. Therefore, by using CEF cell culture it was possible to isolate and amplify the A. marginale in a concentration of 1.3 x 107.2 bodies per mL. The CEF cells are undemanding and easy to preserve; they are an option for isolation and production of A. marginale under laboratory conditions.(AU)

Anaplasma marginale (A. marginale) é um patógeno mundial que infecta uma variedade de ruminantes, mas principalmente bovinos. O presente estudo teve como objetivo descrever uma técnica de isolamento para A. marginale, utilizando cultivo celular de Þ broblastos de embriões (CFE) de galinhas. Para isso, foram coletadas amostras de sangue e de carrapatos de 5 bezerros, entre 2 e 3 meses de idade, os quais, devido a anemia, icterícia de mucosas e prostração, foram considerados supostamente infectados com A. marginale. Ethics Approval This study was approved by Credenciamento Institucional para Atividades com Animais em Ensino ou Pesquisa (CIAEP: 02.0420.2021). Consent to participate Not applicable Consent to publish Not applicable Data availability Not applicable Para o diagnóstico, realizaram-se extração de DNA e posterior PCR a partir das amostras de sangue e de carrapatos coletados. Todos os carrapatos e amostras de sangue foram positivas para o teste de PCR. Além disso, os carrapatos foram triturados com o auxílio de um liquidiÞ cador para inoculação em CFE. Após a inoculação, as culturas foram mantidas a 37ºC e a 5% de CO2 durante 15 dias. O sobrenadante celular das culturas foi novamente analisado por PCR e pela técnica de coloração de Wright para conÞ rmar o isolamento de Anaplasma marginale. As culturas celulares foram po sitivas por PCR, e a presença do agente foi comprovada por meio da coloração de Wright. Portanto, utilizando CFE, foi possível isolar e ampliÞ car o A. marginale em uma concentração de 1,3x107,2 bactérias por ml. As células da CEF são pouco exigentes, de fácil manutenção e uma boa opção para isolamento e produção de A. marginale em condição laboratorial.(AU)

Hemoperitoneum in a cow with lumbar muscle hemangiosarcoma

Background: Hemangiosarcoma is a malignant neoplasm of endothelial cells with an infiltrative growth pattern. Hemangiosarcomas are frequently reported in canines and rare in felines, sheep, goats, swine, horses and cattle. Few cases of hemangiosarcoma were reported in cattle. In the present report, we describe the clinicopathological findings of a bovine muscle hemangiosarcoma. Case: A 6-year-old, Girolando cow from the Dairy Cattle Sector of the Federal Rural University of Rio de Janeiro (UFRRJ), Seropédica, presented sternal decubitus. Clinical signs were markedly pale mucous membranes, moderate dehydration, respiratory distress, and increased heart rate. The hematological examination revealed intense regenerative anemia. Due to the worsening of the clinical condition, the cow was submitted to euthanasia. The necropsy and collection of various fragments of organs were performed, which were sent to the "Setor de Anatomia Patológica" (SAP-UFRRJ). Tissues were fixed in 10 % buffered formalin, routinely processed for histology and stained with Hematoxylin and Eosin (HE). The external mucous membranes were markedly pale. Multifocal areas of 1.5 x 1.0 cm, irregular and dark red were observed dissecting the quadratus lumborum muscle (hemangiosarcoma) fibers. These neoplasms were associated with an extensive cruoric clot adhered to the muscle fibers. The extensive, red, friable mass measured approximately 76 x 55 x 20 cm on the serous surfaces of the organs of the peritoneal cavity (hemoperitoneum). The spleen was moderately reduced. The bone marrow was markedly pale. Histologically, it was observed that there was an extensive proliferation of endothelial cells in the quadratus lumbar muscle mass dissecting the epimysium and perimysium. Endothelial cells had moderate pleomorphism, organized in vascular channels and forming multifocally solid areas with a significant amount of eosinophilic fibrillar material (fibrin). Sections of muscle neoplasm were subjected to immunohistochemistry with anti-von Willebrand factor primary antibody, which showed a multifocal moderate cytoplasmic immunolabeling of neoplastic endothelial cells. Discussion: There are few reports of striated muscle hemangiosarcoma in cattle. Muscular hemangiosarcomas were reported in a 4-month-old calf in the left cervical trapezius muscle and a 6-year-old Holstein cow with left pelvic limb mass lateral and distal to the knee. Some reports presented hemangiosarcoma in the iliopsoas muscle, left cervical trapezius muscle, pelvic limb muscles and right cervical muscle of the bovine. In the presented report, hemoperitoneum occurred as a result of hemorrhages from muscle hemangiosarcoma. Other studies have demonstrated cavity hemorrhages in joint, pelvic, pleural and cranial cavities associated with hemangiosarcoma. Hemangiosarcoma with regenerative anemia must be distinguished from other diseases that cause anemia. The main differential diagnoses of bovine with anemia are vena cava syndrome, coumarin derivatives poisoning, acute poisoning by Pteridium spp., tick fever, anaplasmosis, babesiosis and trypanosomiasis. Hemangiosarcoma should be differentiated from other lesions as hemangioma, vascular tumor of lymphatic endothelium and perivascular wall tumors. Cases with poorly differentiated morphology should be submitted for immunohistochemistry. In the present hemangiosarcoma case, we have used the von Willebrand factor for immunohistochemistry diagnosis. Expression of angiogenic growth factors such as CD31, vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF) and angiopoietin-1 (Ang-1) have also been used in the diagnosis of vascular proliferation lesions. Hemangiosarcoma in cattle should be included mainly in the differential diagnosis of diseases that cause acute anemia in cattle.

Closure of defects in a geometric figure pattern associated with tumescent anesthesia with lidocaine in rabbits (Oryctolagus cuniculus) / Fechamento de defeitos em padrão de figura geométrica associado ao emprego de anestesia por tumescência com lidocaína em coelhos (Oryctolagus cuniculus)

The use of tumescent anesthesia with lidocaine can provide better intra- and postoperative analgesia that would benefit extensive reconstructive surgery. However, lidocaine can interfere with the healing process. Therefore, this study aimed to assess the local interference of the healing of induced and closed skin defects in a geometric pattern associated with the use of tumescent anesthesia with lidocaine in rabbits. Furthermore, we assessed its influence on cardiorespiratory parameters and postoperative analgesia. This study included 27 rabbits divided into three groups: GC (without the use of tumescence), GS (use of tumescence with 0.9% NaCl solution), and GL (use of tumescent anesthesia with lidocaine). There was no statistically significant intergroup difference in any stage of the wound healing process on macroscopic evaluations, in the angiogenesis process, or in the process of collagenization and fibroblast deposition. There were significant differences in heart rate (lower in GL), respiratory rate (higher in GC), mean arterial pressure (higher in GL), and expired concentration of isoflurane (lower in GL). There was no significant intergroup difference in the von Frey filament test or the visual analog scale score used to evaluate postoperative analgesia. We concluded that tumescent anesthesia with lidocaine does not impair postoperative tissue repair. Its use features benefits such as reducing the volume of inhaled anesthetic, maintaining the anesthesia plan, stable heart and respiratory rates, and lower hypotension during the surgical procedure.

O uso da anestesia por tumescência com lidocaína pode proporcionar melhor analgesia transoperatória e pós-operatória, o que seria um benefício em cirurgias reconstrutivas extensas. Entretanto, a lidocaína pode interferir na cicatrização. Diante disso, delineou-se um estudo a fim de avaliar a interferência local da cicatrização de defeitos cutâneos induzidos e fechados em padrão de figura geométrica, associado ao emprego de anestesia por tumescência com lidocaína em coelhos. Ademais, avaliar sua influência em parâmetros cardiorrespiratórios e na analgesia pós-operatória. Foi realizado um estudo com 27 coelhos, separados em três grupos, compreendidos em GC (sem o emprego de tumescência), GS (emprego de tumescência com solução NaCl 0.9%) e GL (emprego de anestesia por tumescência com lidocaína). Não houve diferença estatística em nenhuma etapa do processo cicatricial da ferida entre os grupos, tampouco nas avaliações macroscópicas, e no processo de angiogênese, ou ainda no processo de colagenização e deposição de fibroblastos. Houve diferença significativa na frequência cardíaca (menor no GL) e na respiratória (maior no GC), na pressão arterial média (maior no GL) e na concentração expirada de isoflurano (menor no GL). Não houve diferença significativa entre os grupos no teste de filamentos de von Frey e na Escala Visual Analógica, utilizados para avaliar a analgesia pós-operatória. Conclui-se que anestesia por tumescência com lidocaína não prejudica a regeneração tecidual após a cirurgia. O seu uso oferece benefícios como a diminuição do volume de anestésico inalatório, manutenção do plano anestésico, estabilidade das frequências cardíaca e respiratória, além de menor hipotensão durante o procedimento cirúrgico.

Tissue healing changes on wounds in rats after treatment with Hancornia speciosa latex in cream-gel formulation

Purpose: Hancornia speciosa latex has shown pharmacological potential in wound healing processes due to its angiogenic, osteogenic, and anti-inflammatory activities. The aims of this study were to carry out a cream-gel formulation with 5, 10 and 25% of H. speciosa serum latex and to evaluate its potential to stimulate the skin regeneration in rats' wounds. Methods: One hundred and twenty rats were divided into five groups: neutral control with saline (G1), cream-gel based on H. speciosa latex serum at 5% m/v (G2), cream-gel at 15% m/v (G3), cream-gel at 25% m/v (G4), and cream-gel (G5). The animals were euthanized at three, seven, 14 and 21 days after the injury induction, and some parameters were analyzed: wound contraction, necrosis, fibrin, polymorphonuclear and mononuclear infiltrates, fibroblast, angiogenesis, hemorrhage, and collagen. Results:The therapeutic treatment with cream-gel at 15 and 25% is beneficial in the inflammatory phase of healing processes since it increased the angiogenesis and proliferation of mononuclear infiltrations in wounds. Regarding wound contraction, the treatment with cream-gel (5 and 15%) induced a higher rate of contraction in the proliferative phase. The 15% cream-gel formulation stimulated a greater production of collagen in the injured tissues. Conclusions: H. speciosa cream-gel is a low-cost herbal medicine which can aid in tissue repair.

O extrato aquoso da casca de pequi Caryocar brasiliense melhora a retração de feridas / Aqueous extract of stem bark from Caryocar Brasiliense improves the wound retraction / El extracto acuoso de la cáscara de Caryocar brasiliense mejora la retracción de heridas

Este estudo foi conduzido para verificar o efeito do extrato aquoso e da pomada à base de casca de Caryocar brasiliense sobre a retração de feridas em coelhos. Foram utilizados 12 coelhos Nova Zelândia Branco divididos em dois grupos e quatro lesões foram produzidas na região dorsal de cada animal. As lesões à direita foram tratadas com extrato aquoso (grupo 1) ou com a pomada (grupo 2) e as lesões à esquerda foram tratadas com solução salina 0,9% (grupo controle). Os níveis de colágeno e fibroblastos foram menores (P<0,05) em lesões tratadas com extrato aquoso, comparado com o grupo controle. Aos 7 e 14 dias após o procedimento, a retração das lesões era maior (P<0,05) quando tratadas com extrato aquoso e nas lesões tratadas com a pomada, a melhora ocorreu apenas no 7º dia, comparado com o tratamento controle. Concluiu-se que o extrato aquoso de casca de Caryocar brasiliense melhorou a retração de feridas por um período de tempo maior do que a pomada.

This study was carried out to verify the effect of the aqueous extract and the ointment of the stem bark from Caryocar brasiliense on the wound healing in rabbits. Twelve New Zealand rabbits were divided in two groups and four lesions were produced on the back of each animal. The lesions on the right side were treated with aqueous extract (group 1) or with ointment (group 2), while the lesions on the left side were the control group (treated with 0.9% saline solution). Collagen and fibroblast levels were lower (P<0.05) in wounds treated with aqueous extract, compared to the control group. On days 7 and 14 after the procedures, the wound retraction was better (P<0.05) when treated with aqueous extract, while in wounds treated with the ointment, the improvement occurred only on the 7th day. The aqueous extract of stem bark from Caryocar brasiliense improved the wound retraction longer than the ointment.

Este estudio fue conducido para verificar el efecto del extracto acuoso y de la pomada basada en cáscara de Caryocar brasiliense sobre la retracción de heridas en conejos. Fueron utilizados 12 conejos Nueva Zelanda Blanco divididos en dos grupos y cuatro lesiones fueron producidas en la región dorsal de cada animal. Las lesiones a la derecha fueron tratadas com extracto acuoso (grupo 1) o con la pomada (grupo 2) y las lesiones a la izquierda fueron tratadas con solución salina 0,9% (grupo control). Los niveles de colágeno y fibroblastos fueron menores (P<0,05) en lesiones tratadas con extracto acuoso, comparado con el grupo control. A los 7 y 14 días después del procedimiento, la retracción de las lesiones era mayor (P<0,05) cuando tratadas con extracto acuoso y en las lesiones tratadas con la pomada, la mejora ocurrió solamente el 7° día, comparado con el grupo control. Se concluyó que el extracto acuoso de la cáscara de Caryocar brasiliense mejoro la retracción de heridas por un período de tiempo mayor do que la pomada.

Walnut ointment promotes full-thickness burning wound healing: role of linoleic acid

Purpose: To investigate the active ingredients of walnut ointment (WO) and its mechanism in repairing wounds. Methods: The ingredients of WO were detected by gas chromatography­mass spectrometry. The effect of linoleic acid (LA) was tested by in vitro Alamar Blue (AB) reagent. Image J software, histological and immunohistochemical analysis were used to confirm the healing effect of LA in the porcine skin model. The animals were euthanized after the experiment by injection of pentobarbital sodium. Results: LA, 24% in WO, promotes keratinocytes and fibroblasts proliferation, which were 50.09% and 15.07% respectively higher than control (p < 0.05). The healing rate of the LA group (96.02% ± 2%, 98.58% ± 0.78%) was higher than the saline group (82.11% ± 3.37%, 88.72% ± 1.73%) at week 3 and week 4 (p < 0.05). The epidermal thickness of the LA was 0.16 ± 0.04 mm greater and the expression of the P63 and CK10 proteins was stronger in the LA group than the control (p < 0.05). Conclusions: LA, which is the main components in WO can promote full-thickness burning wounds (FBWs) by stimulating cell proliferation and differentiation.

Cytotoxicity and the bioconversion strategy of Aristolochia spp

Aristolochia plants are notable from an ethnopharmacological viewpoint, but the relevance of these species for medicinal purposes has been debated because of their inherent toxicity. The convergence of these contrasting realities can be readily achieved using bioconversion methods, which have been shown to be useful tools for numerous applications, including the detoxification of biomass. In this context, methanolic extracts of leaves from Aristolochia triangularis and Aristolochia gibertii, as well as the feces of Battus polydamas larvae fed with leaves from these plants, were prepared, and their cytotoxic activities were evaluated on a human fibroblast cell line (GM07492). The leaf extracts were found to be cytotoxic, leading to reductions of 42.1 and 33.8% on cell viability, respectively, while the fecal extracts were considered inactive. In addition to evidencing the cytotoxicity of A. triangularis and A. gibertii, these findings demonstrated a potential bioconversion strategy for obtaining aristolochiaceous extracts with reduced toxicity using the larvae of a specialist phytophagous insect, thus renewing expectations in relation to the pharmacological importance of Aristolochia spp. The results were also ecologically relevant, as B. polydamas larvae were found to be able to detoxify compounds from host plants.(AU)

Cytotoxicity and the bioconversion strategy of Aristolochia spp

Aristolochia plants are notable from an ethnopharmacological viewpoint, but the relevance of these species for medicinal purposes has been debated because of their inherent toxicity. The convergence of these contrasting realities can be readily achieved using bioconversion methods, which have been shown to be useful tools for numerous applications, including the detoxification of biomass. In this context, methanolic extracts of leaves from Aristolochia triangularis and Aristolochia gibertii, as well as the feces of Battus polydamas larvae fed with leaves from these plants, were prepared, and their cytotoxic activities were evaluated on a human fibroblast cell line (GM07492). The leaf extracts were found to be cytotoxic, leading to reductions of 42.1 and 33.8% on cell viability, respectively, while the fecal extracts were considered inactive. In addition to evidencing the cytotoxicity of A. triangularis and A. gibertii, these findings demonstrated a potential bioconversion strategy for obtaining aristolochiaceous extracts with reduced toxicity using the larvae of a specialist phytophagous insect, thus renewing expectations in relation to the pharmacological importance of Aristolochia spp. The results were also ecologically relevant, as B. polydamas larvae were found to be able to detoxify compounds from host plants.(AU)

Desafios para a reprodução assistida em animais de vida livre / Challenges for assisted reproduction in free-living animals

A reprodução assistida se faz necessária em programas de conservação de espécies ameaçadas de extinção, sendo um facilitador de transporte e troca de material genético. Neste contexto, o acesso ao material de animais de vida livre é essencial para incrementar o banco genético da espécie em questão, no entanto adaptar os métodos possíveis à realidade do campo torna essa área de pesquisa desafiadora. Ainda hoje os espermatozoides são os gametas mais acessados em animais de vida livre, porém com pouco uso efetivo para criopreservação e produção de filhotes. É pungente a necessidade de mais pesquisas nesta área, uma vez que há centenas de espécies brasileiras ameaçadas, com especificidades fisiológicas e que habitam habitats variados, o que demanda adaptações espécie-específicas e hábitat específicas.

Assisted reproduction is necessary for conservation programs for endangered species, facilitating transport and exchange of genetic material. In this context, access to material from free-living animals is essential to increase the genetic bank of the species in question. However, adapting the possible methods to the reality of the fieldwork makes this area of research a challenge. Even today, sperm are the most accessed gametes in free-living animals, but with little effective use for cryopreservation and production of offspring. The need for more research in this area is acute, as there are hundreds of Brazilian species under threat, with physiological specificities, and that inhabit varied habitats, which demand species-specific adaptations and specific habitats.

In vitro and in vivo genotoxicity and cytotoxicity analysis of protein extract from Aplysina fulva sponges

This study evaluated the physicochemical and morphological properties of a marine sponge protein extract (PE) using scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDS), analysis of mass loss and pH and in vitro and in vivo. Scanning electron microscopy showed that PE fibers present a granular aspect and irregular structure and the element carbon followed by oxygen was detected in the EDS analysis. Moreover, a 29% of mass loss was observed after 14 days and the pH slightly modified after 14 days. Cell viability of fibroblast cells (L929) of control and PE at a concentration of 25% demonstrated higher values compared to the groups. Osteoblast cell viability of PE at 25 and 50% was significantly higher. Comet assay on day 1 showed higher values for PE at 25%. In addition, in vivo experiments demonstrated that in the treated animals, the bone defects were filled with biomaterial particles, granulation tissue and some areas of newly formed bone. Furthermore, similar immunoexpression of Runx-2 and Cox-2 was observed. Taken together, all results suggest that PE is biocompatible, present non-citotoxicity in the in vitro studies (at the lower concentration) and in the in vivo studies and it can be considered as an alternative source of collagen for tissue engineering proposals.