The tissues of the head of honey bees which are kept in the areas with a medium and low level of technogenic burden demonstrate the decrease in the contents of iron, zinc, copper, chromium, nickel, lead and cadmium in comparison with the tissues of the head of honey bees grown in areas with a high level of technogenic burden. Due to the activity of saturated fatty acids with the even and odd number of carbon atoms in chain, monounsaturated fatty acids of n-7 and n-9 families and polyunsaturated fatty acids of n-3 and n-6 families, the contents of anionic fatty acids, which are inaccessible for the bee body, decreases in the tissues of the head of honey bees which are kept in the areas with a medium and low level of technogenic burden in comparison with the tissues of the head of honey bees grown in areas with a high level of technogenic burden. 3. Monounsaturated fatty acids of n-7 and n-9 families and polyunsaturated fatty acids of n-3 and n-6 families in the tissues of the head of honey bees lead to increase of the total number of easily accessible non-esterified fatty acids for the honey bees which are kept in the areas with a medium and low level of technogenic burden in comparison with the tissues of the head of honey bees grown in areas with a high level of technogenic burden. Furthermore, the intensity of transformations of the non-esterified form of linolenic acid in its more long-chain and more unsaturated derivatives rises in the head tissues of the former. This fact indicates that the reduction of technogenic impact on the area results in the increase of the activity of desaturase in the tissues of the head of honey bees. The contents of heavy metals, anionic and non-esterified fatty acids in the tissues of the head of honey bees which are kept in the areas with low level of technogenic burden undergoes the most significant changes.
«Kolidev 8M» (powder for oral use) is a veterinary drug used to treat ornamental birds (pheasants, peacocks) in diseases of the digestive tract caused by microorganisms sensitive to colistin. In the study of the drug «Kolidev 8M» for oral administration, along with the confirmation of therapeutic properties, it is necessary to determine the LD50 obtained in the process of studying acute toxicity. The aim of research. The aim of research was to determine the acute toxicity of the veterinary drug «Kolidev 8M» (powder for oral administration) under the conditions of intragastric administration to white mice. Materials and methods of research. To achieve this aim, an experiment was conducted on 114 males of nonlinear white mice kept under optimal conditions in the vivarium of DEVIE LLC (Rivne, Ukraine). In the first series of experiments on the principle of analogues was formed control and three experimental groups of 6 animals each (n=6). The drug in the form of a solution was administered once orally using a esophageal gastric tube in doses of 500,0; 2000,0 and 4000,0 mg/kg body weight by absolute weight of the drug. The animals of the control group were injected with distilled water. After taking into account the results of the first experiment in the next experiment, 6 experimental groups were formed – mice, which were administered the drug «Kolidev 8M» in the form of a solution in doses (by absolute weight of the drug) – 500,0; 1000,0; 1500,0; 2000.0; 2500,0; 3000,0; 3500 and 4000,0 mg/kg body weight, as well as the control group – animals that were injected with distilled water with a volume of 0.5 cm3 according to similar regulations (Zapadniuk, 1983; Kotsiumbas, 2005; Karkyshchenko & Hrachev, 2010). There were 6 animals in each group (n=6). After their death, a pathological autopsy was performed (Zharov A. et al., 2003). The average lethal dose of LD50 was calculated by the method of probit analysis by Prozorovsky V.B. Research results. According to the results of research, it was found that the LD50 of the drug «Kolidev 8M» (powder for oral administration) under the conditions of its single intragastric administration to male mice is 2024,72±232,45 mg/kg, LD10 – 392,87 mg/kg, LD16 – 751,56 mg/kg, LD84 – 3297,88 mg/kg, LD90 – 3656,57 mg/kg, LD100 – 3934,47 mg/kg body weight, respectively. According to the results of an acute toxicological experiment with intragastric administration of the drug «Kolidev 8M» to white male mice, LD50 was 2024,72±232,45 mg/kg body weight. This allows, according to toxicity, to refer this drug to class IV – low-toxic substances (LD50 501,0-5000,0 mg/kg body weight), and the degree of danger to class III – moderately safe substances (LD50 151,0-5000,0 mg/kg body weight). Conclusions and prospects for further research. The drug «Kolidev 8M» in terms of toxicity belongs to class IV – low-toxic substances, and the degree of danger to class III – moderately safe substances. Further studies will be the next stage of pre-registration trials aimed at studying the subacute toxicity of the drug «Kolidev 8M»
In the 20th century, representatives of the Cervidae family, in particular the red deer (Cervus elaphus) and fallow deer (Dama dama) became relatively popular "farm animals", they began to be bred on farms as semi-domestic animals. In Ukraine (especially in its western region) such opportunities are extremely large, which is due to the large areas of agricultural land, the use of which for agriculture and animal husbandry is impractical. Іn order preserve authenticity wild animals and to maximally improve the quality of the meat obtained from them, it is necessary to carry out veterinary and zootechnical measures in such a farm and they should be of with as little human disturbance as possible to reduce animal stress. The application of veterinary drugs specially developed for aviary complexes to red deer (n=18) and fallow deer (n=18) on the background of a corrected diet twice during three seasons (years) in conditions of semi-free housing did not affect on the organoleptic indicators and moisture content of the meat, but contributed to a more intense increase in its quality due to an increase in the mass fraction of protein by 13.8 and 10.8%, fat – by 7.4 and 15.5%, ash – by 19.1 and 44.2%, as well as enrichment with trace elements: the content of zinc increased by 23.9 and 38.6%, copper – by 6.6 and 13.2%, iron – by 6.4 and 1.9%, manganese – by 20.4 and 19.5%, cobalt – by 30.0 and 50.0%, selenium – by 11.8 and 11.3% respectively.
The study of pharmacological studies of the veterinary medicinal product for external use in the form of ointment – “Dibutalastin Ointment” is a mandatory stage of preclinical research of the drug, which is a new development of PP “Biopharm” and LLC “DEVIE”. In a scientific experiment on laboratory animals, it is possible to assess the drug's safety for different terms of use to determine the zone of toxic action and doses that do not cause harmful effects on health. Therefore, the work aimed to carry out pharmacological studies of the drug with methyl salicylate and dimethyl sulfoxide in the form of an ointment for treating European fallow deer, deer, dogs, and cats with mastitis, arthritis, myositis, and injuries of various origins. The toxicological characteristics of the studied ointment “Dibutalastin” based on methyl salicylate and dimethyl sulfoxide were studied in an "acute" study on warm-blooded animals. The average lethal dose (LD50) for intragastric administration could not be established, as the volume exceeded the permissible level. It was established that according to the “average lethal dose when entering the stomach” indicator, the veterinary medicinal product belongs to relatively non-toxic substances (toxicity class IV). The results of pharmacological studies indicate the absence of resorptive-toxic effects, sensitizing properties, and irritating effects on the mucous membranes of the eyes and skin. Pathomorphological studies of animal organs when studying the acute toxicity of the drug showed that the developed ointment with methyl salicylate and dimethyl sulfoxide does not cause pathological changes in internal organs. From the point of view of veterinary toxicology, this drug is safe. Further studies will be the next stage of pre-registration tests aimed at studying the embryotoxic effect of “Dibutalastin Ointment”, which is mandatory material of the “Safety and residue studies” section of the dossier for this medicinal product.
web/structural-businessstatistics/data/main-tables. 5 Лебедева Л. В. Виклики СOVID-19 для промисловості України та країн ЄС // Електонне наукове фахове видання «Ефективна економіка», №6, 2021.
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