A pathological study was carried out in different helminth parasite infection organs in 110 animals during the period from 2010 to 2016. Histopathological examination of hydatid cysts in the liver, showed extensive fibrous connective tissue proliferation with eosinophilic and lymphocytic infiltration, in lung, parenchyma showed severe emphysema with infiltration of alveolar macrophages and lymphocytes infiltration. In infection, polymorphonuclear infiltration in the sub-mucosa with hyper activity of goblet cells leading to occlusion of the gland was noted in the tissue sections. In amphistomiasis, intestinal mucosa showed diffuse hyperemia, thickening and ulceration. Petechiae were observed in the anterior part of the duodenum and jejunum. Presence of parasites in the abomasum revealed petechial haemorrhages on the mucousa. In infection, the rectum showed hypertrophy, hyperplasia and hyperactivity of the goblet cells. In some places there is focal aggregation of mononuclear cells.
It is mandatory for all new drugs to be tested for their potential genotoxicity in addition to general toxicity testing. Some old drugs have not been tested adequately for their genotoxic effects because these were in use before the local regulations were enforced. According to the material safety database, the toxicological effect of nimesulide is not yet fully understood. The present study therefore aimed to explore the genotoxic potential of nimesulide in Wistar albino rats. Nimesulide at the dose level of 50 (Gr-50), 100 (Gr-100) and 200 (Gr-200) mg/kg body weight (b.w.) was given orally. Each rat in treated groups (Gr-50 to Gr-200; n = 10) and negative control group (Gr-NC; n = 10) were administered orally (p.o.) with nimesulide and normal saline, respectively, for 14 days. Similarly, rats of positive control (Gr-PC; n = 10) were administered with cyclophosphamide (CPA; 20 mg/kg b.w.) intraperitoneally. CPA served as positive control, whereas normal saline served as as negative control. Approximately 1-2 mL of blood was collected from retro-orbital sinus for comet assay and subsequently rats were sacrificed to aspirate the femoral bone marrow for the micronucleus test. Structural chromosomal aberration, micronucleated polychromatic erythrocytes (MnPCEs), polychromatic erythrocytes (PCEs) and comet tail length were calculated using micronucleus assay and comet assay, respectively, which served as markers of genotoxicity. In the present study, it was observed that a significant increase in (1) different classified structural chromosomal aberrations with increase in nimesulide dose, such as gaps (50 mg/kg), gaps, breaks and pulverizations (100 mg/kg) and gaps, breaks, fragments, rings and pulverizations (200 mg/kg) and (2) % MnPCE and comet tail length was observed in animals treated with CPA (p < 0.001) or 200 mg of nimesulide (p < 0.05), as compared to negative control. In conclusion, nimesulide (200 mg/kg b.w.) produced a potential genotoxicity in rats.
Seasonal outbreaks of swine erysipelas have been reported in back yard pig farms in the Phek district of Nagaland, India. The alpha haemolytic isolate of Erysipelothrix rhusiopathi ae was recovered on blood agar from the clinical samples. The organism s were confirmed microscopically, biochemical analysi s as well as by polymerase chain reaction (PCR) amplification of 16S rRNA gene and sequence analysi s. These Nagaland isolates (KT160358, KT160359) were closely related to the type spp. E. rhusiopathiae in phylogenetic analysi s and form s the same clad with Chineese isolates of swine and murine origin indicating an epidemiological link. The isolates were found to be most sensitive to oxytetracycline and responded to treatment. Swine erysipelas occurred in Phek district in a season due to sudden change of weather and temperature. Pigs exposed to such predi sposing factors probably favoured to propagation of already persi sted organi sm s in pigs. Thi s i s the first confirmed case of E. rhusiopathiae infection from the NE states of Nagaland, India.
In histopathological study, Lung was emphysematous, showed pronounced interstitial pneumonia followed by severe thickening of alveolar septa and bronchial wall, haemorrhages with connective tissue proliferation and infiltration of leucocytes around the bronchial wall. Bulla formation was also evident in some places. Liver showed mild haemorrhages of hepatocytes and congestion in sinusoidal space. In abomasum, adult parasites were embedded in mucousa and sectioning of adult parasites were seen with full of eggs. In large intestine, there was necrosis and degeneration of colonic villi and lost of normal architecture. There was also evidence of hyperactivity of acinar cells, fibrous tissue proliferation with polymorphonuclear cell infiltration. An apical tip shows degenerative changes, adhesion with mild fibrous tissue proliferation. In small intestine, there was congestion, oedema with thickening of sub mucousa as well as erosion of intestinal villi in certain areas, adhesion and fibrous tissue proliferation. In spleen, there was depletion of spleenic venule, congestion of spleenic pulp, haemorrhages surrounding the spleenic venule.
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