Urolithiasis is a nutritional disease that affects domestic carnivores. Past and recent literature on urolithiasis was reviewed for information on anatomical occurrence, physiology of urine formation, prevalence, mineral composition, clinical signs, laboratory findings, dissolution therapy, surgery and prevention of urolithiasis. The acquired knowledge of complexed and multifaceted urolithiasis is a tremendous achievement towards the treatment and control of the disease. However, eradication of the disease is the most challenging as it requires total overhaul of all the factors that are responsible for the formation of uroliths.
SummarySaganuwan, S. A., 2017. Toxicity studies of drugs and chemicals in animals: An overview. Bulg. J. Vet. Med., 20, No 4, Toxicity study is the investigation of either short or long-term toxic effects of a drug or chemical on animals. The toxicity is dose-dependent as asserted by Paracelsus over 500 years ago. However, short-term toxic effect is determined using median lethal dose (LD 50 ) first introduced by Trevan in 1927 and revised many times. Presently there is a growing preponderance of rejection of scientific papers on acute toxicity study, simply because of the belief that in the current hazard and safety assessment of drugs and chemicals, LD 50 values are no longer used. In view of this, literature search was carried out with a view to investigating the relevance of LD 50 in development and assessment of drugs and chemicals. The findings revealed that in the past, many animals had been used for LD 50 determination. OECD has reduced the number of test animals to 5-15 and presently it is further reduced to 2-6. Acute toxicity study is being carried out in medicinal plants research and in the study of patent medicine. Although the application of LD 50 has been drastically reduced, it is still applied and accepted in some parts of the world. Moreover, animals on which LD 50 tests are conducted, should be allowed to die to see the end effect of the test drug or chemical because euthanisia of test animals may mask some toxicity signs of the test agents. Therefore, toxicity study of drugs and chemicals is a scientific process necessary for discovery and development of drugs as well as identification of potential toxicants.
Cases of Stevens-Johnson syndrome have been increasingly reported in Nigeria by individuals who consumed meat products of animals especially goats injected sulfonamides. Hence, tissue distribution and residues of intramuscular sulfadimidine were studied in West African Dwarf (WAD) goats. Twenty goats divided into two groups of 10 each (five males; five females) weighing 10.4 ± 1.63 kg were administered intramuscular sulfadimidine (100 mg/kg body weight), and the second group was coadministered 5 mg/kg of piroxicam via right and left thigh muscle, respectively. Samples of the liver, kidney, spleen, heart, lung, intestine, brain, and skeletal muscle were collected into sterile cellophane bags. Two untreated goats were killed and used for preparation of tissue standards. The tissue samples were stored frozen for analysis. High concentration of sulfadimidine residues was found in all the tissues of goats administered sulfadimidine as well as tissues of goats coadministered sulfadimidine/piroxicam for up to 30 days postdrug administration. Generally, residues of sulfadimidine were observed to be significantly higher than the acceptable limit (0.1 ppm). Hence, consumption of meats from WAD goats administered sulfadimidine may pose very high risk of Stevens-Johnson syndrome in sensitive humans. As such consumption of such meats should be avoided.
Summary: Acute toxicity study of potassium permanganate was carried out in Swiss albino mice. Potassium permanganate was administered at dose rate of 0.0, 500, 1000, 1500, 2000, 2500, 3000 and 3500mg/kg body weight to groups 1, 2, 3, 4, 5, 6, 7 and 8, ten per group for LD 50 determination. The dead animals were posted for gross lesions. A predetermined dose of 160mg/kg of the chemical was administered to experimental group of 12 mice, whereas control group of 12 mice received 16ml/kg body weight of distilled water for a period of 7 days. Grower's marsh and water were provided ad libitum. The animals were weighed daily before administration of potassium permanganate. On the eighth day 1ml of blood sample was collected from both control and experimental mice for haematology and plasma biochemistry into ethylene diamine tetraacetic acid bottles. The median lethal dose (LD 50 ) was estimated at 1449.7mg/kg body weight. There was no significant difference between the mean weight of control and experimental group. Haematological and biochemical parameters of both control and experimental groups did not increase significantly though there was a significant (P<0.05) decrease in chloride ion level in plasma. Toxicity signs observed are rapid and shallow respiration, rough hair coat, dullness, diarrhoea, bloat, gastroenteritis, congestion of liver, paleness of lungs and hypochloraemia.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.