Evaluation of the efficacy of hydrated sodium aluminosilicate in the prevention of aflatoxin-induced hepatic cancer in rainbow trout / Avaliação da eficácia do aluminosilicato de sódio hidratado na prevenção de câncer hepático induzido por aflatoxina em truta arco-íris

The use of aluminum silicates for decontaminating animal feed containing aflatoxins has yielded encouraging results in chicken and turkey poults. In contrast, very few studies have tested these substances in aquaculture. In this work, we investigated the efficacy of a trout diet containing 0.5 percent hydrated sodium aluminosilicate (HSAS) in protecting against contamination with aflatoxin B1. Trout were reared on these diets for one year and the experimental groups were examined monthly for hepatic presumptive preneoplastic and neoplastic lesions. Regardless of the presence of HSAS, all of the fish that received aflatoxin in their diet have shown hepatic lesions indicative of a carcinogenic process, presenting also the development of cancer in some fish. The concentration of HSAS used in this study was ineffective in preventing the onset of hepatic lesions induced by aflatoxin B1 in rainbow trout.

Resultados encorajadores têm sido observados com o emprego de aluminosilicatos para descontaminação de ração contendo aflatoxina destinada à avicultura. No entanto, raros estudos têm sido destinados a testar essa substância em aqüicultura. Assim, no presente trabalho, foi investigada a eficácia do aluminosilicato de sódio hidratado (HSAS, 0,5 por cento) em proteger a truta arco-íris dos danos hepáticos causados por ração contaminada com aflatoxina B1. Os grupos experimentais foram alimentados com suas respectivas dietas durante 12 meses, mensalmente cada grupo foi amostrado para análises anatomopatológica e histopatológica para verificação da presença de lesões hepáticas. Apesar da presença de HSAS, todos os grupos que receberam dieta contaminada com aflatoxina B1 apresentaram lesões hepáticas indicativas do processo carcinogênico, sendo que exemplares alimentados com essas dietas por mais longo prazo apresentaram hepatocarcinoma ou colangiocarcinoma. Estes resultados indicaram que a concentração de HSAS usada no presente estudo não foi efetiva em prevenir o desenvolvimento de lesões hepáticas induzidas por aflatoxina B1 em truta arco-íris.

Evaluation of the efficacy of hydrated sodium aluminosilicate in the prevention of aflatoxin-induced hepatic cancer in rainbow trout / Avaliação da eficácia do aluminosilicato de sódio hidratado na prevenção de câncer hepático induzido por aflatoxina em truta arco-íris

The use of aluminum silicates for decontaminating animal feed containing aflatoxins has yielded encouraging results in chicken and turkey poults. In contrast, very few studies have tested these substances in aquaculture. In this work, we investigated the efficacy of a trout diet containing 0.5 percent hydrated sodium aluminosilicate (HSAS) in protecting against contamination with aflatoxin B1. Trout were reared on these diets for one year and the experimental groups were examined monthly for hepatic presumptive preneoplastic and neoplastic lesions. Regardless of the presence of HSAS, all of the fish that received aflatoxin in their diet have shown hepatic lesions indicative of a carcinogenic process, presenting also the development of cancer in some fish. The concentration of HSAS used in this study was ineffective in preventing the onset of hepatic lesions induced by aflatoxin B1 in rainbow trout.(AU)

Resultados encorajadores têm sido observados com o emprego de aluminosilicatos para descontaminação de ração contendo aflatoxina destinada à avicultura. No entanto, raros estudos têm sido destinados a testar essa substância em aqüicultura. Assim, no presente trabalho, foi investigada a eficácia do aluminosilicato de sódio hidratado (HSAS, 0,5 por cento) em proteger a truta arco-íris dos danos hepáticos causados por ração contaminada com aflatoxina B1. Os grupos experimentais foram alimentados com suas respectivas dietas durante 12 meses, mensalmente cada grupo foi amostrado para análises anatomopatológica e histopatológica para verificação da presença de lesões hepáticas. Apesar da presença de HSAS, todos os grupos que receberam dieta contaminada com aflatoxina B1 apresentaram lesões hepáticas indicativas do processo carcinogênico, sendo que exemplares alimentados com essas dietas por mais longo prazo apresentaram hepatocarcinoma ou colangiocarcinoma. Estes resultados indicaram que a concentração de HSAS usada no presente estudo não foi efetiva em prevenir o desenvolvimento de lesões hepáticas induzidas por aflatoxina B1 em truta arco-íris.(AU)

Consensus for the Diagnosis, Prognosis and Treatment of Canine Mammary Tumors

The purpose of this paper is to establish criteria that could guide the diagnosis, prognosis and treatment of canine mammary neoplasias. It was elaborated during the Mammary Pathology Meeting: Diagnosis, Prognosis and Treatment of the Canine Mammary Neoplasm, held on November 6th and 7th, 2010 in Belo Horizonte ­ MG, Brazil, sponsored by the Laboratory of Comparative Pathology ­ UFMG, with the support of the Brazilian Association of Veterinary Pathology (ABPV) and Brazilian Association of Veterinary Oncology (ABROVET). Academics from several regions of Brazil were present and contributed to this work.(AU)

Retrospective study of melanocytic neoplasms in dogs and cats

Melanoma is one of the most lethal skin neoplasms among dogs and cats, and its incidence is increasing worldwide in the last years. The relation between the study of tumor biology and epidemiologic data from melanocytic tumors (melanomas and melanocytomas) can help in the achievement of an earlier and safer clinical diagnosis.However, epidemiologic data for these neoplasms are still rare in Brazil. Thus, we performed a retrospective study of melanocytic neoplasms in dogs and cats registered at the Animal Pathology Service of the School of Veterinary Medicine and Animal Science (SVMAS), University of São Paulo (USP), between January of 2000 and December of 2006. The epidemiological data extracted from pathology records regarded affected population (age, gender, hair color) and tumor characteristics (anatomic location and histological type). Of 2154 histopathological reports analyzed 193 (8.9%) were melanocytic neoplasms, of which 186 cases in dogs (96.4%) and only 7 in cats (3.6%). Male dogs, of

mixed breed, among 8 and 11 years of age and black hair were most affected by melanocytic neoplasms. Histological types most often found were epithelioid cell melanoma mainly located in the buccal cavity, and melanocytomas, located on the skin. Among cats, females between 8 and 11 years of age of mixed breed and black hair were most often affected. Epithelioid melanoma again presented as the most common histological type, located, however, on the skin. In conclusion, this casuistic demonstrated that melanocytic neoplasms develop mostly in middle age dogs with dark hair, in the oral cavity or skin, with histological type of epithelioid cells. Melanocytic tumors are rare in cats when compared to dogs; in our cases, they were diagnosed in middle aged female cats, mostly located in skin, and with epithelioid histological type. Epidemiological data strengthen the importance of early diagnosis of melanocytic tumors in Veterinary Medicine, promoting initiation of the most appropriate therapeutical process, improving diagnosis and promoting animal welfare.

Retrospective study of melanocytic neoplasms in dogs and cats

Melanoma is one of the most lethal skin neoplasms among dogs and cats, and its incidence is increasing worldwide in the last years. The relation between the study of tumor biology and epidemiologic data from melanocytic tumors (melanomas and melanocytomas) can help in the achievement of an earlier and safer clinical diagnosis.However, epidemiologic data for these neoplasms are still rare in Brazil. Thus, we performed a retrospective study of melanocytic neoplasms in dogs and cats registered at the Animal Pathology Service of the School of Veterinary Medicine and Animal Science (SVMAS), University of São Paulo (USP), between January of 2000 and December of 2006. The epidemiological data extracted from pathology records regarded affected population (age, gender, hair color) and tumor characteristics (anatomic location and histological type). Of 2154 histopathological reports analyzed 193 (8.9%) were melanocytic neoplasms, of which 186 cases in dogs (96.4%) and only 7 in cats (3.6%). Male dogs, of

mixed breed, among 8 and 11 years of age and black hair were most affected by melanocytic neoplasms. Histological types most often found were epithelioid cell melanoma mainly located in the buccal cavity, and melanocytomas, located on the skin. Among cats, females between 8 and 11 years of age of mixed breed and black hair were most often affected. Epithelioid melanoma again presented as the most common histological type, located, however, on the skin. In conclusion, this casuistic demonstrated that melanocytic neoplasms develop mostly in middle age dogs with dark hair, in the oral cavity or skin, with histological type of epithelioid cells. Melanocytic tumors are rare in cats when compared to dogs; in our cases, they were diagnosed in middle aged female cats, mostly located in skin, and with epithelioid histological type. Epidemiological data strengthen the importance of early diagnosis of melanocytic tumors in Veterinary Medicine, promoting initiation of the most appropriate therapeutical process, improving diagnosis and promoting animal welfare.(AU)

A novel chronic cirrhosis TAA-induced model in rats

Experimental models for hepatic lesions are necessary so the effectiveness of new drugs in reversing cirrhosis or fibrosis can be tested. This is the case of liver cirrhosis, which requires animal models. Three drugs widely used to induce cirrhosis in animal models are carbon tetrachloride (CCI4), Dimethylnitrosamine (DMN), and Thioacetamide (TAA). TAA has been largely used, but a model that confirms the occurrence of chronic cirrhosis in rats has not yet been well defined. In this study we developed a model of chronic cirrhosis induced by TAA in rats. Our cirrhotic protocol used 200 mg of TAA in 4% aqueous solution per kg of body weight applied intraperitoneally three times per week for 14 weeks in Wistar rats. On the seventh week the dose was increased by 20%. Our protocol caused low mortality rate and represents an alternative and valid model for chronic cirrhosis

A novel chronic cirrhosis TAA-induced model in rats

Experimental models for hepatic lesions are necessary so the effectiveness of new drugs in reversing cirrhosis or fibrosis can be tested. This is the case of liver cirrhosis, which requires animal models. Three drugs widely used to induce cirrhosis in animal models are carbon tetrachloride (CCI4), Dimethylnitrosamine (DMN), and Thioacetamide (TAA). TAA has been largely used, but a model that confirms the occurrence of chronic cirrhosis in rats has not yet been well defined. In this study we developed a model of chronic cirrhosis induced by TAA in rats. Our cirrhotic protocol used 200 mg of TAA in 4% aqueous solution per kg of body weight applied intraperitoneally three times per week for 14 weeks in Wistar rats. On the seventh week the dose was increased by 20%. Our protocol caused low mortality rate and represents an alternative and valid model for chronic cirrhosis(AU)

Expression of Connexins 43, 26 and 32 in normal, hyperplastic and neoplastic perianal dog glands

Connexin (Cx) expression is reportedly altered in neoplasms. This study aimed to investigate the expression of Cx43, 26 and 32 in normal and pathological canine perianal glands. Thirty perianal glands bearing pathological processes and ten normal canine perianal glands were submitted to immunohistochemistry to search for presence of Cx43, Cx26 and Cx32. Both Cx43 and Cx26 expressions were observed in normal, hyperplastic glands, and in well and moderately differentiated adenomas. However, in poorly differentiated adenomas, expressions were reduced, and they were absent in carcinomas. Cx26 was located in the cytoplasm of normal, hyperplastic perianal gland cells, and in well and moderately differentiated adenomas. Cx32 was not observed in any neoplasm neither in normal or hyperplastic glands. Our results show that Cx43 and Cx26 expressions are altered in more aggressive canine perianal gland neoplasms, and we conclude that they may be related to the perianal gland carcinogenesis process

Expression of Connexins 43, 26 and 32 in normal, hyperplastic and neoplastic perianal dog glands

Connexin (Cx) expression is reportedly altered in neoplasms. This study aimed to investigate the expression of Cx43, 26 and 32 in normal and pathological canine perianal glands. Thirty perianal glands bearing pathological processes and ten normal canine perianal glands were submitted to immunohistochemistry to search for presence of Cx43, Cx26 and Cx32. Both Cx43 and Cx26 expressions were observed in normal, hyperplastic glands, and in well and moderately differentiated adenomas. However, in poorly differentiated adenomas, expressions were reduced, and they were absent in carcinomas. Cx26 was located in the cytoplasm of normal, hyperplastic perianal gland cells, and in well and moderately differentiated adenomas. Cx32 was not observed in any neoplasm neither in normal or hyperplastic glands. Our results show that Cx43 and Cx26 expressions are altered in more aggressive canine perianal gland neoplasms, and we conclude that they may be related to the perianal gland carcinogenesis process (AU)

Diminished angiogenesis in the cornea of mice with heterologous deletion of Connexin 43 gene (Gja1)

Angiogenesis is involved in several physiological and pathological processes, and the proliferation of endothelial cells is a central event in the generation of new blood vessels. Gap junctions (GJ) are membrane structures that communicate adjacent cells, contribute to tissue homeostasis, and are important to the control of cell proliferation. Connexins (Cxs) are the proteins that form gap junctions. Endothelial cells may express Cx43, Cx37 and Cx40. In this study, we analyzed the effect of the heterologous deletion of the Gja1 (Cx43 gene) on the development of newly formed blood vessels (NFBV) in the mouse cornea. Heterozygous (Cx43+/-) and wild-type (Cx43+/+) mice were submitted to the silver crystal corneal cauterization model. Two parameters were quantified by image analysis 2 or 6 days after cauterization: NFBV density and length. At days 2 and 6 after corneal cauterization, Cx43+/- mice showed smaller density of NFBV as compared to Cx43+/+ mice. Therefore, deletion of one Gja1 allele (connexin-43 gene) may lead to impaired cell-cell communication in endothelial cells, diminishing angiogenesis after cauterization of the mouse cornea

Diminished angiogenesis in the cornea of mice with heterologous deletion of Connexin 43 gene (Gja1)

Angiogenesis is involved in several physiological and pathological processes, and the proliferation of endothelial cells is a central event in the generation of new blood vessels. Gap junctions (GJ) are membrane structures that communicate adjacent cells, contribute to tissue homeostasis, and are important to the control of cell proliferation. Connexins (Cxs) are the proteins that form gap junctions. Endothelial cells may express Cx43, Cx37 and Cx40. In this study, we analyzed the effect of the heterologous deletion of the Gja1 (Cx43 gene) on the development of newly formed blood vessels (NFBV) in the mouse cornea. Heterozygous (Cx43+/-) and wild-type (Cx43+/+) mice were submitted to the silver crystal corneal cauterization model. Two parameters were quantified by image analysis 2 or 6 days after cauterization: NFBV density and length. At days 2 and 6 after corneal cauterization, Cx43+/- mice showed smaller density of NFBV as compared to Cx43+/+ mice. Therefore, deletion of one Gja1 allele (connexin-43 gene) may lead to impaired cell-cell communication in endothelial cells, diminishing angiogenesis after cauterization of the mouse cornea(AU)

Canine hemangiopericytomas: cell proliferation and apoptosis in the perivascular, storiform and epithelioid histological subtypes and their significance for prognosis

Canine hemangiopericytomas (CHP) are soft tissue neoplasms, originary from pericytes. They are frequently diagnosed in dogs and can be seen more frequently in limbs as circumscribed and firm nodules. The histopathology of CHP reveals the presence of spindle cells around blood vessels, forming whorls. In this study, cases of CHP from the Animal Pathology Service of the Veterinary Hospital of the School of Veterinary Medicine and Animal Science, registered from 1990 to 2003, were studied. All cases were reviewed and classified in the three histological subtypes recently described - perivascular (PVHP), storiform (SHP) and epithelioid (EHP). Immunohistochemical markers (vimentin, S-100 protein, CD34, Factor VIII and glial fibrillary acidic protein - GFAP) were applied to all tumors. Samples were submitted to the immunostaining of PCNA, and the labeling indexes were obtained. The mitotic index was also quantified in each subtype. Apoptosis bodies were morphologically identified in H&E stained sections, subsequently confirmed by fluorescence microscopy and then quantified in the three histological subtypes. Dog owners were contacted by telephone, and asked to inform about the outcome of their dogs. The survey revealed 61 cases of CHP, in which 21 (34.43.%) belonged to the perivascular subtype, 18 cases (29.51.%) belonged to the storiform subtype, and 22 cases (36.06.%) belonged to the epithelioid subtype. PCNA labeling index, mitotic and apoptotic indexes were significantly higher in the epithelioid subtype. Records of the follow-up of each case revealed 59% of recurrence rate in the epithelioid subtype, 55% in the storiform subtype and 17% in the perivascular subtype. According to these results, epithelioid hemangiopericytomas seem to be the most aggressive CHP subtype. Therefore, we conclude that the histopathological analysis with classification in subtypes, as well as the quantification of cell proliferation and apoptosis rates, can help in the establishment of prognosis for CHP.

Gap junctions and communication within the nervous system

Gap junctions are sites on the cellular membrane with intercellular channels build up by twelve protein subunits called connexins. Each connected cell contributes with a hemichannel made up by six connexins subunits. This kind of connection represents and efficient way of intercellular communication in most tissues, including the nervous system. It works as a passage for ions, secondary messenger and metabolites exchange between the cells. In a complex tissue like the nervous tissue they are particularly important because they connect the various cellular types composing a panglial syncytium that performs neuronal protection and tissue homeostasis. The expression of connexins and the intercellular communication through gap junctions are crucial to regulate vital functions as cellular motility, proliferations and survival; changes in the conformational expression of connexins may be involved in diseases as Alzheimer's disease, neoplasms, bacterial and parasitic infections, or even affect cellular groups when they occur as genetic mutations leading to functional defects of the nervous system as demyelination in the PNS (Charcot-Marie-Tooth disease), hereditary epilepsy, non-syndromic deafness and senile cataract.

Compensatory kidney hypertrophy/hyperplasia after nephrectomy in mice: alterations of connexin 43 (Cx43) phosphorylated isoforms

Compensatory kidney hypertrophy/hyperplasia leads to several changes in kidney structure and function, as increased glomeruli filtration. The aim of this study was to evaluate connexin 43 in remnant mouse kidneys after unilateral nephrectomy. The right kidney was surgically removed from BALB/c mice. Groups were euthanized at 24, 48 and 72 hours, and at 7 and 30 days. Kidney sections of the reminiscent kidneys were stained with Periodic Acid/Schiff and additional slides were submitted to BrdU and Cx43 immunohistochemistry. The results demonstrated an increase in kidney weight as early as 24 hours through 30 post-nephrectomy. In addition, BrdU positive epithelial cells increased at 24 and 48 hours post-nephrectomy. Cx43 was detected in the cytoplasm and membrane of epithelial cells and vasculature. Taking into consideration the quantity, intensity and localization of Cx43 immunostaining pattern, we observed that nephrectomized mice presented lower Cx43 expression and a cytoplasmic localization after 24 hours, peaking in 48 hours. Furthermore, western blot revealed that during the first 24 and 48 hours after nephrectomy, PO (unphosphorylated) and P1 (phosphorylated) Cx43 disappeared, and the products of Cx43 degradation were reduced. On the other hand, after 72 hours the PO and P1 state reappeared and the amount of degraded peptides also increased. Seven and thirty days after nephrectomy, a higher intensity of PO and P1 state and a lower P2 (hyperphosphorylated) band were observed. In conclusion, our results suggest that Cx43 phosphorylation results in the retention of Cx43 in cytoplasm and its increased degradation during compensatory renal hyperplasia/hypertrophy.