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At least 487 records · Page 27Linked to original sources
PubMed2005

Effect of inorganic versus organic selenium on hen production and egg selenium concentration.

A 28-d experiment using 288 Hy-Line W-36 laying hens was conducted to compare sodium selenite (SS) with Se-enriched yeast (SY). The Se from SS or SY was supplemented into a corn-soybean meal basal diet at 0, 0.15, 0.30, 0.60, or 3.00 ppm, and the basal diet was formulated to provide 0.82% lysine and 2,950 kcal/kg of ME. Each treatment was replicated 4 times with 2 cages of 4 hens per cage in each replicate. Hen production was assessed daily, and 2 eggs per replicate were collected every 4 d for whole-egg Se analysis. Albumen quality was assessed at 2 egg storage temperatures (7.2 vs. 22.2 degrees C) with the eggs collected on d 24 and 28, respectively. The percentage of dirty and cracked eggs was greater (P < 0.04) in hens fed SY than in those fed SS. Percentage hen-day production was not affected (P > 0.05) by diet. Albumen quality of eggs stored at 22.2 degrees C was improved (P < 0.04) in eggs from hens fed SS, but there was no difference (P > 0.05) in albumen quality of eggs stored at 7.2 degrees C. Egg weight was linearly increased (P < 0.01) by SY. Whole-egg Se levels were linearly increased (P < 0.01) as dietary Se level increased for both sources of Se, but eggs from hens fed SY had higher (P < 0.01) Se concentrations than those fed SS. The results from this experiment indicate that percentage hen-day production is not affected by Se source, and that SY increases egg Se concentrations more than SS.

Animal Feed↗
PubMed2005

Changes in glutathione peroxidase and tissue selenium concentrations of broilers after consuming a diet adequate in selenium.

Three experiments (EXP) were conducted with commercial broilers to develop a low-Se diet for comparing plasma glutathione peroxidase (pGPX3) concentrations and then to compare pGPX3 and plasma and tissue Se concentrations in broilers fed this low-Se diet after being supplemented with sodium selenite (SS) or Se-enriched yeast (SY). With the exception of Se, all diets were nutritionally adequate. The EXP lasted from 0 to 20 or 22 d posthatching, and treatments were replicated with 6 to 8 pens of 6 to 15 chicks per pen. The results of EXP 1 and 2 indicated that a cornstarch-dextrose diet containing 10% torula yeast and 31% soybean meal (SBM) resulted in similar gain as a corn-SBM (C-SBM) diet, but the cornstarch-dextrose-torula yeast-SBM diet with no added Se reduced pGPX3 activity 6-fold. In EXP 3, the treatments were a C-SBM diet with 0 or 0.30 ppm added Se from SS or SY. These diets were fed from 0 to 10 d posthatching. Beginning on d 10, all broilers were fed the cornstarch-dextrose-torula yeast-SBM, low-Se diet. On d 10, 13, 16, 19, and 22, three broilers per replicate were randomly selected for plasma and tissue collection. Treatment differences were significant at P < 0.05. Daily gain, daily feed intake, and gain:feed were not affected by diet during the 0-to-10-d or 0-to-22-d periods. Plasma GPX3 activity and plasma, liver, and breast Se concentrations were greater in broilers previously fed the diets with added Se, regardless of source, than in those fed the C-SBM diet, except for liver Se concentration on d 19 of broilers previously fed the SS diet. The pGPX3 concentrations were not different in broilers previously fed either Se diet on d 10 and 13 but were greater in broilers previously fed the SY diet on d 16, 19, and 22. Plasma Se concentrations were not different in broilers previously fed diets with SS or SY on d 10 and 22 but were greater in broilers previously fed the SY diet on d 13, 16, and 19. Breast Se concentrations were greater in broilers previously fed the SY diet than in those fed the SS diet on each day. Liver Se concentrations were not different in broilers previously fed SS or SY diets on d 19 and 22 but were greater in those previously fed the SY diet on d 10, 13, and 16. These results indicated that SY supplementation in broiler diets resulted in greater tissue Se concentrations than SS and that pGPX3 and tissue Se concentrations remained greater in birds previously fed a diet with SY than in those fed SS after being fed a low-Se diet.

Animal Feed↗
PubMed2006

Maternal organo-selenium compounds and polyunsaturated fatty acids affect progeny performance and levels of selenium and docosahexaenoic acid in the chick tissues.

The effects of supplementing broiler breeder diets with polyunsaturated fatty acids (PUFA) and organo-Se compounds on the levels of Se and PUFA in chick tissues and on chick performance were assessed. Prepeak (23 wk) and peak (27 wk) production broiler breeders were fed 1 of 4 diets: a wheat-based commercial diet with soybean oil or fish oil but no added Se, and each diet with added Se as Sel-Plex (soybean oil + Se, fish oil + Se; Alltech Inc, Nicholasville, KY). The diets were designed to contain less than 0.1 mg of Se/kg and about 0.5 mg/kg for the nonsupplemented and the supplemented diets, respectively. As-hatched chicks from the 4 parental treatments were fed a nutritionally high quality diet (ME = 12.57 MJ/kg; CP = 228.7 g/kg) or a low quality diet (ME = 10.28 MJ/kg; CP = 182.8 g/kg), resulting in 8 dietary treatments. Performance was better and mortality lower in chicks from 27-wk-old breeders compared with those from 23-wk-old breeders. Fish oil in the maternal diet increased progeny mortality and reduced chick body mass at hatch. Body mass at 7 and 14 d posthatch was lower in chicks fed the low quality diet compared with chicks fed the high quality diet. At hatch, and for up to 14 d posthatch, chicks from hens fed diets high in PUFA had higher concentrations of docosahexaenoic acid (DHA) in the brain and liver compared with chicks hatched from hens fed diets low in PUFA. The DHA content of the tissues of chicks from breeders fed diets supplemented with Se was higher than that in chicks from breeders fed unsupplemented diets. Even after 14 d of being fed a diet with identical levels of Se, chicks hatched from parents fed diets high in Se had higher tissue Se concentrations than those hatched from parents fed diets low in Se. Supplementation of the maternal diet of chicks with organo-Se appears to enhance the DHA concentration of the chick brain, which may improve brain function.

Animal Feed↗
PubMed1972

Effects of selenium compounds on formate metabolism and coincidence of selenium-75 incorporation and formic dehydrogenase activity in cell-free preparations of Escherichia coli.

The effects of selenite, selenocystine, and selenomethionine in a defined growth medium on formic dehydrogenase biosynthesis in aerobically and anaerobically grown Escherichia coli have been studied. Sucrose gradient centrifugation of a partially purified enzyme demonstrated a coincidence of (75)Se incorporation and formic dehydrogenase activity.

Aerobiosis↗
PubMed2006

Selenium bioaccumulation in Chlamydomonas reinhardtii and subsequent transfer to Corbicula fluminea: role of selenium speciation and bivalve ventilation.

The uptake of Se by the freshwater alga Chlamydomonas reinhardtii and the subsequent transfer to the Asiatic clam Corbicula fluminea was investigated. The objective was to investigate the bioavailability of algal-bound Se for C. fluminea while taking into account Se speciation and bivalve ventilation. First, uptake rates of waterborne Se (selenite, selenate, and selenomethionine) in the algae during a 1-h exposure period were determined for a range of concentrations up to 2,000 microg/L. Fluxes for selenite uptake were constant in the range of concentrations tested, whereas fluxes for selenate and selenomethionine uptake decreased with increasing concentrations, suggesting a saturated transport system at high concentrations (approximately 1,000 microg/L for selenate and 100 microg/L for selenomethionine). These data were used to set the algal contamination for the study of trophic transfer to the clam. Three parameters were studied: The Se form, the algal density, and the Se burden in the algae. The results show that for a fixed algal density, an Se-contaminated algal diet does not modify ventilation. In this case, the driving factor for ventilation is the algal density, with ventilation being enhanced for low algal densities. On the basis of ventilatory flow rate measurements and Se burdens in algae, it was found that bioaccumulation of Se in C. fluminea was proportional to the total quantity of Se passing through the whole organism, but with a lesser extraction coefficient for selenomethionine than for the inorganic forms. These results underline the importance of both physiological factors and speciation in understanding the trophic transfer of Se.

Animals↗