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Uncontrolled and over-intensive training can lead to a decrease in exercise efficiency and health state disorders in dogs. Examinations of sled dogs revealed that prolonged effort induced specific biochemical changes and released indicatory enzymes into peripheral circulation. The purpose of the study was to reveal the efficacy of selected markers of aspartate aminotransferase (AST), creatine kinase (CK), lactate dehydrogenate (LDH) and their isoenzymes, C-reactive protein (CRP), glucose and lactic acid in detecting sub clinical states of skeletal muscles lesions. Examinations were carried out on 17 sled dogs (Siberian Husky, Alaskan Malamut) at the start, during and end of the training season, before and after exercise. Dogs were in good condition before study and did not revealed clinical symptoms of disease. During progressively extended training loads a decrease in the motor activity of some dogs was noted. An increase in the activity of AST, CK and LDH5 in the examined dogs confirmed these changes and testified to skeletal muscle injury. The lack of adaptation of organism efficiency to excessive trainings loads also caused an increase in the concentration of glucose and lactic acid in the plasma of the sled dogs. C-reactive protein and inflammatory state markers were also designated to estimate of health state of the dogs. An increase of CRP concentration, noted in the examined dogs, could testified to inflammatory states of muscles or may have be connected with exercise stress. Clinical symptoms confirmed these changes. A lack of physical adaptation to the intensity of training leads to muscle injuries. Measurements of muscle injury markers during excessive load training facilitate the recognition of hyper-training states and muscles injuries in sled dogs.
The research objective was to determine the effect of supplemental enzymes that break down phytates or hydrolyze non-starch polysaccharide fractions in the diets of pigs under the complete production cycle (sows at gestation and lactation, growers and fatteners) on the activity of blood ALT, AST, AP and LDH. Also analyzed were the interaction between some feed additives (formic acid and its potassium salt, calcitriol) and microbial phytase or a multienzymatic preparation and their impact on the activity of these enzymes. In each of the three experiments, two control groups were formed: positive (PC) with a dicalcium phosphate (10 g kg⁻¹) supplement and negative (NC) with plant feedstuffs as a phosphorus source. Nutrient content (excluding phosphorus and calcium) at each feeding period was consistent with the Standards for Pig Feeding, 1993. In Experiment I, the NC mixture was supplemented with the following: microbial phytase (500 PU kg⁻¹) for group F, enzymes hydrolyzing non-starch polysaccharide fractions for group E, microbial phytase and enzymes hydrolyzing non-starch polysaccharide fractions for group FE, while group W received a multienzymatic preparation which comprised both microbial phytase and enzymes contributing into the non-starch polysaccharide hydrolysis (xylanase, beta-glucanase, cellulase). In Experiment II, the pig groups FM, WM, FK and WK were supplied with a mixture like in group NC with the addition of microbial phytase and a preparation including formic acid and its potassium salt for group FM, a multienzymatic preparation and a preparation with formic acid and salt for group WM, microbial phytase and calcitriol for group FK, as well as a multienzymatic preparation and calcitriol for group WK. In Experiment III, the animals from group FKM and WKM were fed the NC diet supplemented with microbial phytase, calcitriol and a preparation comprising formic acid and its potassium salt for group FKM, with a multienzymatic preparation, calcitriol and a preparation with formic acid and its potassium salt for group WKM. Blood was collected from 8 gilts from each group at 84 days of gestation and 21 days of lactation, from 8 growing pigs from each group at the starter period (56 raising day), the grower period (91 days of age) and finisher period (154 days of age). Blood was examined to establish the activity of ALT, AST, AP and LDH using the colorimetric assay with Cormay monotests. The results of the present research conducted on the pigs at the complete production cycle, fed diets deprived of a calcium phosphate content but supplemented with microbial phytase, enzymes hydrolyzing non-starch polysaccharide fractions, calcitriol or a preparation comprising formic acid and its potassium salt have given evidence of a stimulating effect of the employed additives on the activity of enzymes from the transferase enzyme group, AP and LDH. The animals from group W showed a significant increase in AST, AP and LDH activity, primarily in the fatteners. The activity of AST and LDH in the blood of pigs from the groups FKM, WKM proved to be significantly higher (p ≤ 0.05) during the whole cycle as compared to the animals from the NC group. In none of the groups under study were deviations noted from the reference values for the activity of enzymes analyzed in the present research.
The aim of the study was to evaluate changes in enzymatic activity taking place in the organisms of fattening pigs, located in two different places; with closed and opened runs - with their breeding conditions in accordance with animal husbandry standards (on average: temperature - 21.1°C; 79.2% - humidity; velocity of air movement - 0.3 m/s²; cooling - mWxcm²). The animals were fed with identical mash mixtures ad libitum (with no limits). The increase of body mass and the daily average growth of both sexes of the examined cross-breads during their feeding period proceeded correctly. However, when the animals were located in two different places during the entire feeding period feeding, the most beneficial growth occurred in the animals held in places with opened runs (850 and 895 g). Changes in the activity of the examined enzymes in the blood serum of the animals were also found, especially during the final period of feeding. An increase in the maximum content of LDH enzyme took place in the blood serum of gilts and amounted to 55%. A similar tendency was found in hogs and amounted to 50%. Nevertheless, when this data was compared with the initial statistics the highest activity during the period of feeding was demonstrated by creatine kinase, since gilts had an average increase of that indicator of 112%, and hogs - 101%. The rapid change of the enzymatic profile of both LDH and CK in intensive feeding of fattening pigs has an adverse effect on their health.
A histochemical assay was elaborated to study lactate dehydrogenase activity in the tissues of Fasciola hepatica and in the liver of mice during the course of fasciolosis. LDH activity was determined in the tegument, muscles, parenchyma, oral sucker and the caecum of juvenile and adult liver flukes inhabiting the host liver parenchyma and bile ducts. The most substantial changes in LDH activity were recorded in the tegument outer surface layer. White mice of CFW strain were infected with 10, 30 and 50 doses of F. hepatica metacerkariae administered per os. A dramatic decrease in LDH activity in the experimental mice liver during the course of infection, particularly in the acute fasciolosis was observed.
Badano odczyn histochemiczny na aktywność dehydrogenazy mleczanowej [LDH 1.1.1.27] w wątrobach szczurów poddanych działaniu fluorku sodu (NaF). W wyniku przeprowadzonych badań stwierdzono zmiany w aktywności LDH w wątrobach szczurów po podaniu NaF z wodą do picia.
W dostępnej literaturze krajowej i zagranicznej prezentowane są nieliczne doniesienia na temat aktywności enzymów wskaźnikowych, zwłaszcza markerowych, charakteryzujących pracę konkretnych organelli komórkowych. Ubogie są również informacje na temat zmian aktywności enzymów, jakie zachodzą pod wpływem żywieniowych czynników doświadczalnych. W doświadczeniu założono, że koncentrat białkowo-ksantofilowy PX z lucerny pozytywnie wpłynie na metabolizm, czego efektem będzie poprawa wskaźników produkcyjnych u tuczników. Celem badań było zatem sprawdzenie możliwości wykorzystania niestosowanych dotąd enzymów w ocenie poprawności zachodzących procesów biochemicznych po podaniu PX. Oceniano aktywność enzymów związanych z kluczowymi przemianami biochemicznymi zachodzącymi w komórce, co pozwala na ocenę poprawności zachodzących procesów, jak i reakcji ustroju na czynniki zewnętrzne. Doświadczenie przeprowadzono na 288 tucznikach (loszkach i wieprzkach) mieszańcach (wbp x Neckar), podzielonych na 4 grupy, zróżnicowane pod względem dawki i okresu podawania koncentratu białkowo-ksantofilowego PX z lucerny (Medicago sativa L.). Koncentrat z lucerny wprowadzono do mieszanki paszowej w miejsce poekstrakcyjnej śruty sojowej. Analizowano aktywność wybranych enzymów markerowych: dehydrogenazy mleczanowej (LDH), jabłczanowej (MDH), bursztynianowej (SDH) oraz hydrolazy glukozo-6-fosforanowej (G6PC). Wykazano obniżenie aktywności analizowanych enzymów w komórkach wątroby u zwierząt otrzymujących dodatek koncentratu PX w porównaniu do zwierząt z grupy kontrolnej, co sugeruje korzystny wpływ zastosowanego preparatu na przemiany metaboliczne u badanych zwierząt. Wyniki doświadczenia potwierdzają celowość stosowania w żywieniu świń koncentratu białkowo-ksantofilowego PX z lucerny, zwłaszcza w dawce 3% podawanej w sposób ciągły.
The studies were carried out on 90 male guinea pigs ot which 75 were infected per os with a dose of ca. 5000 invasive eggs of Ascaris lumbricoides suis. At the 1st, 2nd, 4th, 7th and 20th day ot intection blood was taken from experimental and control animals. The activity of LDH and its liver traction (spectrophotometric method), GGTP (circle test method) was determined. The level of glucose (orthotoluidin methhod) and alpha amino nitrogen (ninhydrin method was determined. In the course of larval ascariasis an increase in the values of the studied parameters was noted, especially at the 4th and 7th day of infection. The changes in the activity of the studied enzymes evidence disturbances of the structure and function of the liver of infected animals. The increased level of glucose and alpha amino nitrogen is probably associated with a disturbance of basic energy metabolism of the host organism.
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