O objetivo desse estudo foi confirmar a toxidez e caracterizar os aspectos clínicos e patológicos da intoxicação por Trema micrantha em equinos. Três equinos, pôneis, com idade entre 2 e 7 anos consumiram espontaneamente folhas de T. micrantha em doses únicas de 30g/kg, 25g/ kg e 20g/kg. Os três animais adoeceram e evoluíram para morte. Outro equino recebeu 15 e 25g/kg da planta com intervalo de 30 dias entre as doses e não apresentou alteração clínica. Coletas diárias de sangue foram realizadas para análises bioquímicas. Os principais sinais clínicos apresentados foram apatia, desequilíbrios, dificuldade de deglutição, decúbito esternal, decúbito lateral, movimentos de pedalagem, coma e morte. Os três equinos afetados apresentaram elevação da atividade sérica de gama-glutamil transferase, dos níveis séricos de amônia e diminuição da glicemia. Esses animais foram necropsiados e fragmentos de diversos órgãos foram coletados para análise histopatológica e imuno-histoquímica. Os principais achados patológicos foram encontrados no fígado e no encéfalo dos três animais. O fígado apresentava, macroscopicamente, acentuação do padrão lobular; enquanto que, no encéfalo havia áreas amareladas na superfície de corte, mais evidentes na substância branca do cerebelo. Microscopicamente, o fígado apresentava tumefação hepatocelular, necrose de coagulação predominantemente centrolobular e hemorragia associada. No encéfalo, havia edema perivascular generalizado e astrócitos Alzheimer tipo II na substância cinzenta. Esses astrócitos apresentaram marcação fraca ou negativa na imuno-histoquímica anti-GFAP e marcação positiva do antígeno S-100. A dose letal mínima de folhas de T. micrantha estabelecida nesse experimento foi de 20g/kg. A ampla distribuição e palatabilidade desta planta, associadas à alta sensibilidade da espécie equina, constatada nesse experimento, reforçam a importância da planta em casos acidentais de intoxicação em equinos.

INTRODUÇÃOSida carpinifolia L.f. (Malvaceae) ou Sida acuta var. carpinifolia (L.f) K.Schum, popularmente conhecida como guanxuma, vassourinha, malva-brava e relógio-de-vaqueiro é planta nativa do Brasil, onde ocorre em quase todo o território nacional. A planta é invasora de lavouras e pastagens, principalmente em solos mais argilosos, compactados e ricos em matéria orgâni-

Pesq. Vet. Bras. 31(4): 307-312, abril 2011 RESUMO.-A doença granulomatosa sistêmica associada ao consumo de Vicia villosa (Leg. Papilionoideae) foi diagnosticada em 5 bovinos no período de 2005 a 2008. Os bovinos apresentavam alopecia, lesões crostosas na pele, prurido, febre, queda da produção leiteira, anorexia e emagrecimento. O curso clínico médio da doença foi de 2 semanas. Dos bovinos analisados três morreram e dois foram eutanasiados. As lesões macroscópicas de alopecia e crostas na pele eram localizadas principalmente na face e pescoço. Observava-se nódulos multifocais a coalescentes branco-acinzentados que infiltravam vários órgãos especialmente em linfonodos, rins e coração. As lesões microscópicas consistiam na infiltração de linfócitos, macrófagos, células epitelioides, células gigantes multinucleadas, eosinófilos e plasmócitos. Linfonodos, rins, adrenal, baço e fí-gado de todos os bovinos apresentaram infiltrado granulo- Affected cattle showed alopecia, crusted lesions on the skin, had itching, fever, decreased milk yield, anorexia and wasting. Average clinical course was 2 weeks. Three cattle died and two were euthanized in extremis. The main gross changes are alopecic and crusts in the skin, mainly on the face and neck. There also were multifocal to coalescent whitish nodules that infiltrated several organs, but especially lymph nodes, kidneys and hearth. Microscopic changes consisted of infiltration with lymphocytes, macrophages, epithelioid cells, giant multinucleated cells, eosinophils, and plasmocytes. Lymph nodes, kidneys, adrenal gland, spleen and liver from affected cattle showed varying degrees of granulomatous infiltration. Immunohistochemical procedures on samples from affected organs revealed that Tlymphocytes and macrophages/epithelioid cells/giant multinucleated cells were the main components of the inflammatory infiltrates, B-lymphocytes were only rarely seen within. The reduced numbers of cells marked by Ki-67 in the granulomatous lesions would indicate that cell proliferation was not responsible for the hypercellularity in the lesions and that rather the recruitment of macrophages and lymphocytes to the site inflammation probably accounted for the building up of the local cellular inflammatory infiltrate.

A captive fallow deer (Dama dama) in a zoo was spontaneously poisoned after consumption of Sida carpinifolia. The paddock where cervids were kept was severely infested by S. carpinifolia. The deer developed a neurological syndrome characterized by muscular weakness, intention tremors, visual and standing-up deficits, falls, and abnormal behavior and posture. Because a severe mandibular fracture and the consequent deteriorating condition, it was euthanized. Main microscopic findings were swelling and multifocal cytoplasmic vacuolation in the Purkinje cells. The cytoplasm of multiple cells of the cerebellum, especially the Purkinje cells, stained with the lectins Concanavalia ensiformis, Triticum vulgaris, and succinylated Triticum vulgaris. Diagnostic possibilities such as bovine diarrhea virus, rabies, and transmissible spongiform encephalopathy were excluded. The report focuses on the risk of maintaining S. carpinifolia populations in zoo enclosures of wild herbivores.

ABSTRACT.-Panziera W., Gonçalves M.A., Oliveira L.G.S., Lorenzett M.P., Reis M., Hammerschmitt M.E., Pavarini S. Characterization and evolution of liver lesions during the outbreak are also described. Two hundred and six 4-month-old female calves were weaned and placed in a 25-hectare pasture heavily infested by S. brasiliensis at of varying growth stages. The calves remained in this pasture for three months and were later transferred to another area where six calves aged 7-8-month-old developed clinical signs including unthriftiness, diarrhea, and subcutaneous dependent edema in the submandibular region. All these six affected calves died within 15 days from the onset of clinical signs and one of those was necropsied. Grossly the first of three patterns of hepatic lesions described in this report was observed and it was characterized by an enlarged liver, with round borders and an orange hue to the capsular and cut surfaces. Histologically there was marked diffuse vacuolar hepatocellular degeneration, bilestasis, hepatocellular megalocytosis, and mild bile duct proliferation and periportal fibrosis. Two months after the onset of the outbreak, in another visit to the farm, it was observed that an additional 28 calves got sick and 14 died. Affected calves observed in this second on-site visit were 9-10 month-old and their main clinical sign was photosensitization characterized by varying degrees of photophobia, tearing from the eyes, marked drooling, mucopurulent ocular discharge, increased nasal secretion, and ventral diphtheric glossitis. Two of the fourteen calves that died were necropsied and displayed the second pattern of hepatic lesions observed in the outbreak. Liver had smooth and whitish capsular surfaces and a moderate decrease in size. There was moderate irregularity to the cut surface of hepatic parenchyma and pale areas intercalated with red ones. Histologically there was marked periportal fibrosis, marked bile duct proliferation, hepatocellular megalocytosis, focal areas of hepatocellular necrosis, and hemorrhage and veno-occlusive changes. In this second on-site visit, GGT serum activity was determined in 15 affected calves and 13 of them had increased values (26-175 U/L). Seven months after the onset of the outbreak, a third visit was made to the farm when was learned that and additional 27 calves have been affected, 23 of which died within a period of 40 days. At the necropsy of three of these calves the third pattern of hepatic lesions were observed. The liver was decreased in size and markedly firm. The capsular surface was smooth and whitish and the capsular surface 1 Recebido em 1 de junho de 2016.Aceito para publicação em 29 de agosto de 2016.