ABSTRACT
Autumn crocus poisoning of cattle is characterized by severe diarrhea caused by alkaloid colchicine. Previously, we examined pathologically this poisoning in cattle and reported that enterotoxic lesions were closely associated with apoptosis. To examine enterotoxicity of autumn crocus more precisely, a reproductive study was performed using guinea pigs and mice, and pathological findings associated with autumn crocus poisoning were compared with those of colchicine. Each group of guinea pigs given the bulb of autumn crocus or colchicine exhibited severe diarrhea. Histopathological findings in intoxicated guinea pigs were entirely consistent with those in the autumn crocus-poisoned cattle. In contrast, each group of mice administered with the bulb or colchicine did not develop diarrhea. Our results confirmed that the toxicity of autumn crocus bulb is attributable to the toxicity of ingredient colchicine, and revealed that the guinea pig has high reproducibility of autumn crocus poisoning in cattle and colchicine poisoning in humans. It has been reported that the physiological mechanism of the apoptotic process for eliminating the enterocytes in the mouse and rat differs from that of the guinea pig, monkey, cattle and horse. Taking the observation that the former animals do not develop diarrhea, whereas the latter animals do so in the autumn crocus or colchicine poisoning into consideration, it would seem that the species-difference in enterotoxicity of autumn crocus may be closely associated with the physiological mechanism of eliminating the effete enterocytes.
Subject(s)
Cattle Diseases/etiology , Colchicine/toxicity , Colchicum/toxicity , Diarrhea/veterinary , Intestines/drug effects , Plants, Medicinal , Animals , Cattle , Diarrhea/etiology , Disease Models, Animal , Guinea Pigs , Intestines/pathology , Male , Mice , Rats , Species SpecificityABSTRACT
Previously we reported that tissue destruction characterized by the presence of karyopyknotic, karyorrhectic and mitotically arrested cells was seen in alimentary epithelial cells and lymphocytes in the lymphoid and hemopoietic systems of cattle experimentally administered with autumn crocus (Colchicum autumnale L.). This report deals with the mechanism of acute cellular injury following experimental autumn crocus poisoning in cattle as demonstrated by the in situ DNA strand break analysis and electron microscopy. The analyses revealed that cellular injury caused by autumn crocus was closely associated with apoptosis.
Subject(s)
Apoptosis , Cattle Diseases/pathology , Colchicum/toxicity , Digestive System/pathology , Intestinal Mucosa/pathology , Lymphocytes/pathology , Plants, Medicinal , Plants, Toxic , Poisoning/veterinary , Animals , Cattle , Cattle Diseases/physiopathology , Cell Nucleus/drug effects , Cell Nucleus/pathology , Chromatin/drug effects , Chromatin/pathology , Cytoplasm/pathology , Digestive System/drug effects , Digestive System/ultrastructure , In Situ Nick-End Labeling , Intestinal Mucosa/drug effects , Intestinal Mucosa/ultrastructure , Intestine, Small/pathology , Lymphocytes/drug effects , Mitosis , Poisoning/pathology , Poisoning/physiopathology , Spleen/drug effects , Spleen/pathologyABSTRACT
Crude or dehydrated bulbs of autumn crocus (Colchicum autumnale L.) were fed to eleven calves. All the calves developed severe diarrhea and died or euthanized within 63 hr. At necropsy, the gastro-intestinal mucosa was edematous and hemorrhagic. Histologically, necrosis and degeneration with karyopyknosis and karyorrhexis were shown in the basal cell layer of the tongue, esophagus, forestomach, renal pelvis, urinary bladder, neck cell layer of the abomasal gastric glands, and intestinal cryps. These findings were also seen in Kupffer cells, renal tubular epithelial cells, and lymphocytes in the lymphoid and hemopoietic systems. The lesion of the present acute crocus poisoning of cattle closely resembled those reported in humans with colchicine intoxication. Refined acetone extract of organs of poisoned cattle proved to contain colchicine and demecolcine by high performance liquid chromatography.