Diurnal rhythms of heart and respiratory rates in donkeys of different age groups during the cold-dry and hot-dry seasons in a tropical savannah.

The aim of this study was to determine the effect of season on diurnal rhythms of heart (HR) and respiratory rates (RespR) in the adult, yearling, and foal donkeys during the cold-dry and hot-dry seasons under natural light/dark cycle. The resting HR and RespR were recorded bihourly for 24 consecutive hours from 06:00 to 06:00 h (GMT +1) in 30, clinically healthy donkeys (10 adults,10 yearlings, and 10 foals). Dry-bulb temperature (DBT), relative humidity (RH), temperature-humidity index (THI) and wet-bulb globe temperature index (WBGT) inside the pen were recorded bihourly from 06:00 to 06:00 h. Values of DBT, THI, and WBGT obtained during the hot-dry season were significantly (P < 0.05) higher than corresponding values recorded during the cold-dry season. Application of single-cosinor procedure showed that HR and RespR exhibited daily rhythmicity in both seasons. The mesors of the HR in adult (41.51 ± 0.34 beats/min [bpm]), yearling (40.80 ± 0.43 bpm), and foal (47.55 ± 0.40 bpm) donkeys during the cold-dry season were significantly (P < 0.01) lower, compared to the corresponding values of 48.4 ± 0.40 bpm, 50.42 ± 0.52 bpm and 58.10 ± 0.50 bpm, respectively during the hot-dry season. The mesors of RespR in adult, yearling, and foal donkeys during the hot-dry season were higher (P < 0.05), when compared to the corresponding values recorded in the cold-dry season. The HR and RespR of foals were significantly (P < 0.05) higher than those of the adult and yearling donkeys. Amplitudes of HR and RespR were higher during the hot-dry season than the cold-dry season. In conclusion, seasonal changes affect diurnal rhythmicity of HR and RespR of adult, yearling, and foal donkeys during the cold-dry and hot-dry seasons. The HR and RespR of donkeys vary with age, with higher values in the foals than the adult and yearling donkeys in both seasons.

Testicular pathology, gonadal and epididymal sperm reserves of Yankasa rams infected with experimental Trypanosoma brucei brucei and Trypanosoma evansi.

AIM: The study was conducted to evaluate the pathological effects of trypanosomosis on the testes, gonadal, and epididymal sperm reserves of Yankasa rams for 98 days. MATERIALS AND METHODS: A total of 16 Yankasa rams, aged between 24 and 30 months and weighed between 22 and 25 kg, were acclimatized for a period of 2-months in a clean fly proof house and were adequately fed and given water ad-libitum. Of the 16 rams, 12 that were clinically fit for the experiment at the end of the acclimatization period were randomly divided into four groups: Groups I, II, III, and IV, each having 3 rams. Groups I and II were each challenged singly with experimental Trypanosoma brucei brucei (Federer strain) and Trypanosoma evansi (Sokoto strain), respectively, while Group III was challenged with mixed T. brucei brucei and T. evansi parasites (50% of each species in the infective inoculum) and Group IV was left as an uninfected control. Each infected ram received 2 mL of the infected blood containing 2×10(6) trypomastigotes via the jugular vein, while the control group received 2 mL each, normal saline. RESULTS: All the infected rams developed clinical signs typical of trypanosomosis at varying pre-patent periods. The gross lesions observed in the infected rams in Group II were moderate and more severe in those of Groups I and III. Histological sections of the testes of infected rams (Groups I, II, and III) showed moderate (T. evansi-infected group) to severe (mixed and T. brucei brucei-infected groups) testicular degenerations with reduction in number of spermatogenic cell layers, degenerated seminiferous tubules, congested interlobular spaces, loss of tissue architecture with significant (p<0.01) depletion, and loss of gonadal and epididymal sperm reserves in Groups I and III in comparison to Group II and the control Group IV. No observable clinical signs and histopathological lesions were found in those rams of the control Group IV. CONCLUSION: The study concluded that trypanosomosis due to experimental T. brucei brucei or T. evansi or mixed infections (of both parasites) caused testicular damage, decreased epididymal and gonadal sperm reserves and an important cause of infertility in Yankasa rams.

Effect of packing on changes in erythrocyte osmotic fragility and malondialdehyde concentration in donkeys administered with ascorbic acid.

Experiments were performed with the aim of investigating the effect of packing on erythrocyte osmotic fragility (EOF) and malondialdehyde (MDA) concentration in donkeys, and the effect of ascorbic acid (AA). Twelve apparently healthy donkeys raised under the traditional extensive system served as experimental subjects. Six donkeys administered orally with AA (200 mg/kg) and subjected to packing were used as experimental animals, whilst six others not administered with AA served as controls. Blood samples were collected pre- and post-packing from all the donkeys for the determination of MDA and EOF. At 0.3% Sodium Chloride (NaCl) concentration, the percentage haemolysis was 93.69% ± 2.21% in the control donkeys and the value was significantly (P < 0.05) higher than the value of 71.31% ± 8.33%, recorded in the experimental donkeys. The post-packing MDA concentration obtained in the control donkeys was 39.62 µmol ± 4.16 µmol, and was not significantly different (P > 0.05) from the value of 35.97 µmol ± 2.88 µmol recorded in the experimental donkeys. In conclusion, the increase in haemolysis obtained in the donkeys suggested that packing induced oxidative stress, which was ameliorated by AA administration.

Effect of ascorbic acid administration on erythrocyte osmotic fragility of pigs transported by road during the hot-dry season.

The experiments were performed in order to determine the effect of 8-h road transportation of pigs on erythrocytes osmotic fragility during the hot-dry season, and the ameliorative role of ascorbic acid. Twenty-three adult pigs comprising of both sexes served as subjects for the study. Thirteen pigs administered ascorbic acid (AA) per os 30 min before transportation, at a dose rate of 100 mg/kg served as experimental animals, while ten pigs administered with distilled water per os served as control, and were transported for 8 h during the hot-dry season. EDTA blood samples collected a day before (pre-transportation), immediately after 8-h transportation and 7 days post-transportation were used to determine erythrocyte osmotic fragility. The ambient temperature (AT) and relative humidity (RH) measured within the vehicle ranged between 30.5-39.0 °C and 40.0-71.0% respectively. These values were outside the thermoneutral zone for the pig, indicating that the season was thermally stressful. Results obtained showed a significant difference (p<0.05) in percent haemolysis recorded at NaCl concentrations of 0.4% and 0.6% immediately after transportation in experimental pigs and at 0.5, 0.6, 0.8 and 0.9% NaCl concentrations in experimental pigs 7 days post-transportation. In conclusion, result from the present study indicated that 8-h road transportation during the hot-dry season could induce stress resulting in haemolysis of erythrocytes and AA administration ameliorated the stress.