Acknowledging the limitations of cytology and the extent of discrepancies between cytologic and histopathologic findings in dogs and cats will help clinicians make better decisions in diagnosing liver disease.
The effects of thermal manipulation (TM) at 38.5°C and 40°C for 6 h at embryonic day (ED) 16, 9 h at ED 17, and 12 h at ED 18 on body weight (BW) and cloacal body temperature (T) during the first wk and later at post-hatch d 10, 14, 21, 28, and 42 were evaluated. Furthermore, chicks' ability to cope with a thermal challenge (TC; 41°C for 6 h) at post-hatch d 14 and 42 was also evaluated. A chick's response to TC was measured by determining the cloacal body temperature; the plasma thyroid hormones (thyroxin (T) and triiodothyronine (T)); the packed cell volume (PCV); the heterophil (H), lymphocyte (L), monocyte, basophil, and eosinophil percentages; and the heterophil-to-lymphocyte ratios (H/L). Thermal manipulation did not affect the hatchability. However, the body weight of TM chicken was higher compared with controls at marketing age (post-hatch d 42). At post-hatch d 14 and 42, no significant changes in T were observed among the different treatment groups. However, during TC at d 14 and 42, the T of TM chicks was lower compared with the controls. During TC, a significant increase in plasma T and a significant decrease in plasma T of TM chicks compared with controls were reported. Furthermore, during TC, a significant increase in the PCV and heterophil, monocyte, and H/L ratios, and a reduction in the lymphocyte percentages also were observed in TM chicks compared with the controls. Results of this study showed that chicks subjected to heat manipulation during late embryogenesis respond better to heat stress later in the growth and development period.
Twenty-seven 9-12 months old healthy male dromedarian camels were used to determine total nucleated leucocyte count (TNCC), absolute and percentages of polymorphonuclear (PMN) and mononuclear leucocytes, and total protein (TP) concentration in synovial fluid from grossly and radiographically normal fetlock joints. Arthrocentesis was performed bilaterally from the fetlock joints of the forelimbs and hindlimbs. Blood contaminated samples and samples obtained from grossly or radiographically abnormal joints were excluded. The mean +/- SD of TNCC in 108 samples of fetlock joint synovial fluids was 500 +/- 400 cells/microl. Monocytes/macrophages were the predominant cell type. There were no significant differences in mean TNCC, absolute numbers and percentages of various leucocytes and TP concentrations between the right and left fetlock joints of the forelimbs and hindlimbs or between the fetlock joints of the forelimbs and hindlimbs. The mean +/- SD of absolute numbers and percentages of various cell types were: PMN leucocytes 1 +/- 2 cells/microl (2%), lymphocytes 116 +/- 167 cells/microl (26%), and monocytes/macrophages 383 +/- 323 cells/microl (72%). The mean +/- SD of TP concentration was 2 +/- 1 g/dl.
Tracheal Wash (TW) and bronchoalveolar lavage (BAL) are not well documented in adult cattle and published studies were undertaken on diseased animals aiming at isolating the causative agent of respiratory diseases. This study was undertaken to establish the normal cytological and microbiological findings of TW and BAL in normal adult cattle and compare between the laboratory analysis findings of both techniques. Eighteen healthy adult cattle were divided into two groups. BAL was completed the first group (n = 10) and TW was completed the second group (n = 8). Normal cytological findings of TW in healthy adult cattle were found to be primarily neutrophils (42.7 ± 35.7)% intermixed with lower numbers of columnar epithelial cells (26.2 ± 34.8)%, alveolar macrophages (14.7 ± 15.4)%, squamous epithelial cells (10 ± 28.6)%, lymphocytes (6.8 ± 16.1)% and rarely seen eosinophils (0.1 ± 0.0)% with a total cell count of 457 ± 310.1 cells/µl. Cytological findings of BAL were found to be mainly alveolar macrophages (94.3 ± 3.9)%, intermixed with lower number of neutrophils (4.3 ± 3.9)% and lymphocytes (1.3 ± 1.2)% and rarely seen eosinophils (0 ± 0.1)% with a total cell count of 238 ± 169 cells/µl. There are remarkable differences in TW and BAL cytological findings and the degree of contamination was higher in TW samples than that seen in BAL lavage.
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