Noboru Machida

ELECTROCARDIOGRAPHY, HEART RATES, AND HEART WEIGHTS OF FREE-LIVING BIRDS

Abstract To examine the waveforms of electrocardiograms, cardiac rhythm, heart rates at rest and during excitement, and the rate of increase of heart rate, electrocardiograms were recorded with standard bipolar limb leads from 79 free-living birds, including 19 species. The heart weights and heart-to-body weight ratios were obtained from an additional 96 free-living birds, including 20 species. In the majority of the electrocardiograms, lead I was of low amplitudes for all waves except the P wave, and leads II and III were very similar to each other with a predominant S wave and a very short or elevated ST segment. The P wave was often superimposed on the T wave when the heart rate increased to 330 beats/min. Four types of arrhythmia were observed in 50 of the 79 birds (63.3%): 48 sinus arrhythmias, four sinus arrests, two atrial premature contractions, and one ventricular premature contraction. The resting heart rate was negatively associated with the rate of increase, suggesting that a bird with a low resting rate might be able to maintain a greater capacity to increase its heart rate than one with a high resting rate. A negative correlation on a bilogarithmic scale was obtained between the heart weight and the resting heart rate, indicating that a bird with a high heart weight had lower resting heart rate than a bird with a low heart weight. When the heart-to-body weight ratios of free-living birds were compared according to their motility, the ratios of more active birds were greater than those of less active ones.

Cardiac Myxoma of the Tricuspid Valve in a Dog

A case of cardiac myxoma arising from the tricuspid valve is described in an 8-year-old dog that had suffered intermittent episodes of syncope. At surgical operation, a large, irregular, gelatinous mass was found attached to the septal leaflet of the tricuspid valve. The excised tumour, measuring 5x4x3.5 cm, had a grey-to-yellow, friable, mucoid, multilobulated and polypoid appearance, with focal haemorrhage. Histologically, the tumour consisted of a hypocellular mass of a myxoid matrix, rich in acid mucopolysaccharides, with a supporting structure of spindle-like, elongated or stellate cells scattered in an abundant stroma. The surface of the mass was covered by a single layer of endothelial-like cells. Immunohistochemistry revealed that the surface cells of the mass were positive for the endothelial marker CD34 and the constituent cells within the mass reacted positively and uniformly with antibodies to vimentin and alpha-smooth muscle actin. The dog died 36 h after the operation and, at necropsy, wide dissemination of myxomatous embolization to the intrapulmonary arteries was found.

Possible mechanisms underlying the testicular toxicity of oxfendazole in rats

To clarify the mechanisms underlying the testicular toxicity of oxfendazole (OX), adult Wistar rats were orally administered a dose of 100 mg/kg/day for 3, 7, or 14 days. Assays of sex-related hormones showed a significant decrease in only the estradiol serum level at days 3 and 7, as compared with the control group. Histopathologically, marked degeneration of meiotic spermatocytes was observed in stage XIV—I seminiferous tubules from day 3 onwards, and these spermatocytes gave positive results on terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end-labeling (TUNEL). Abnormalities of spermiogenesis such as megakaryospermatids and binucleated spermatids were also observed in the testes of OX-treated rats. Under the electron microscope, lipid accumulation and dilatation of the endoplasmic reticulum were frequently found in the cytoplasm of the Sertoli cells on day 3. These results strongly suggest that OX induces both apoptosis of meiotic spermatocytes, most probably due to disruption of the microtubules, and degeneration of the Sertoli cells, characterized by distended endoplasmic reticulum and prominent cytosolic lipid accumulation.

Smooth muscle hamartoma of the abomasum in a calf.

This report describes a case of smooth muscle hamartoma of the abomasum in a 6-month-old steer humanely killed because of severe pneumonia. At necropsy, marked thickening of the abomasal wall in the area of the pylorus was found. On cut section, the thickness of the submucosal layer, extending from the submucosa to the muscularis propria, was seen to be increased to 3 cm. The upper (i.e., nearest to the gut lumen) half of the sectioned thickening was composed mainly of adipose-like tissue and the lower half mainly of muscle-like tissue. Histologically, the submucosal layer was composed of fibroadipose tissue, within which were embedded, to varying degrees, numerous well-defined, haphazardly oriented, thin to thick bundles of smooth muscle fibres. This appears to be the first report of smooth muscle hamartoma of the stomach or abomasum in animals, including man.

Carcinogenic susceptibility to N-bis(2-hydroxypropyl)nitrosamine (DHPN) in rasH2 mice.

To evaluate the susceptibility of rasH2 mice to N-bis(2-hydroxypropyl)nitrosamine (DHPN), a potent carcinogen targeting the lung, liver, thyroid, and kidney, male, 6-week old, rasH2 mice and wild-type littermates (non-Tg mice) were given DHPN in drinking water at 0, 20 or 200 ppm, and 0 or 200 ppm, respectively, for 26 weeks. The experiment using rasH2 mice given 200 ppm DHPN and non-Tg mice given 200 and 0 ppm DHPN was completed at 20 weeks, since mortality in these groups was remarkably increased due to hemangiosarcomas of the liver. Histologically, tumors developed in the lung and liver in both rasH2 and non-Tg mice treated with DHPN. In addition, proliferative lesions were observed in the forestomach, urethra, and excretory duct of salivary glands in rasH2 mice given 200 ppm DHPN. RT-PCR analysis showed no marked difference in expression of mRNAs for the transgene and the endogenous mouse ras gene between the whole lung tissue containing a neoplasm and normal lung tissue. Our results suggest that rasH2 mice are highly susceptible to DHPN, the target organs including the forestomach, salivary gland and urethra, which have not been found to develop tumors in previous long-term carcinogenicity studies of DHPN in rats and mice.