Abstract:The selenium nutrition of sheep throughout Victoria was assessed by a survey of the blood glutathione peroxidase activity in 708 flocks. It was shown that the blood glutathione peroxidase activity in sheep had a seasonal variation with lowest levels in the spring. The enzyme activity was correlated with the blood selenium concentration. Areas where blood selenium was less than 0.03 micrograms/ml in spring were defined. Sheep with low selenium nutrition were grazing pastures in the high rainfall areas on acid s… Show more
“…Direct effects of cyanide on Se metabolism have been recorded in sheep (Rudert & Lewis 1978;Gutzwiller 1993), rats (Beilstein & Whanger 1984), and chicks (Elzubeir & Davis 1988). The seasonal occurrence of symptoms of Se deficiency in stock has been associated with periods of active clover growth (Underwood 1966;McDonald & Caple 1977;Caple et al 1980). It is not known if this association is solely the result of the low Se content of clover herbage, which is lower than browntop, cocksfoot, or ryegrass (Davies & Watkinson 1966), or if the cyanide released by clover markedly reduced absorption and utilisation of ingested Se.…”
Hydrogen cyanide (HCN) and iodine (I) concentrations in the herbage were determined for 51 white clover (Trifolium repens L.) cultivars that had been grown under uniform conditions in a glasshouse. HCN contents ranged from 120 to 1110ngHCN/g dry matter (DM). Cultivars that are agronomically successful in New Zealand, and cultivars of New Zealand origin, were mainly highly cyanogenic. There was evidence in 'Grasslands Kopu' and 'Aran' of a decline in cyanide content in plants raised from first generation seed, compared to plants from Breeders or Basic seed. This decline may result in part from contamination of seed crops by low HCN resident clovers. Iodine concentration in the white clovers ranged from 0.08 to 0.21 µg I/g DM with 77% of values being below 0.12 µg I/g DM. There was no correlation between I and HCN concentrations. It seems there is little potential to improve the I nutrition of stock by selecting for increased I content in white clover. The influence of cyanogenic clover on the metabolism of I, selenium (Se), and sulphur (S) in sheep is discussed. It is concluded that these factors, and safety margins against direct cyanide toxicity, warrant further study.
A94090
“…Direct effects of cyanide on Se metabolism have been recorded in sheep (Rudert & Lewis 1978;Gutzwiller 1993), rats (Beilstein & Whanger 1984), and chicks (Elzubeir & Davis 1988). The seasonal occurrence of symptoms of Se deficiency in stock has been associated with periods of active clover growth (Underwood 1966;McDonald & Caple 1977;Caple et al 1980). It is not known if this association is solely the result of the low Se content of clover herbage, which is lower than browntop, cocksfoot, or ryegrass (Davies & Watkinson 1966), or if the cyanide released by clover markedly reduced absorption and utilisation of ingested Se.…”
Hydrogen cyanide (HCN) and iodine (I) concentrations in the herbage were determined for 51 white clover (Trifolium repens L.) cultivars that had been grown under uniform conditions in a glasshouse. HCN contents ranged from 120 to 1110ngHCN/g dry matter (DM). Cultivars that are agronomically successful in New Zealand, and cultivars of New Zealand origin, were mainly highly cyanogenic. There was evidence in 'Grasslands Kopu' and 'Aran' of a decline in cyanide content in plants raised from first generation seed, compared to plants from Breeders or Basic seed. This decline may result in part from contamination of seed crops by low HCN resident clovers. Iodine concentration in the white clovers ranged from 0.08 to 0.21 µg I/g DM with 77% of values being below 0.12 µg I/g DM. There was no correlation between I and HCN concentrations. It seems there is little potential to improve the I nutrition of stock by selecting for increased I content in white clover. The influence of cyanogenic clover on the metabolism of I, selenium (Se), and sulphur (S) in sheep is discussed. It is concluded that these factors, and safety margins against direct cyanide toxicity, warrant further study.
A94090
“…It is principally when Se supplements are fed to Se-deficient cows that production responses can be expected. Witchel et al (1994) suggested cows grazing pasture with less than 30 g of Se/kg of DM would have inadequate Se intakes, whereas Caple et al (1980) considered that pasture with 50 g of Se/kg of DM would provide adequate Se. The Se concentrations in our pastures and supplements were always greater than 60 g of Se/kg of DM, indicating sufficiency of Se in the basal diet.…”
Section: Discussionmentioning
confidence: 99%
“…Binnerts (1979) reported milk Se concentrations of 3 to 5 g of Se/kg of milk from cattle in low-Se areas in the Netherlands and 6 to 11 g/kg for those from high-Se areas. Variations in Se concentrations in pastures (10 to >50 g of Se/kg of DM; Caple et al, 1980) may lead to variations in concentrations in milk, but the effects are likely to be relatively small unless significant amounts of Se are added in fertilizer (Aro et al, 1998). The Se concentrations in concentrate supplements, such as wheat (1 to 117 g/ kg of DM) and lupins (10 to 488 g/kg of DM), vary to a greater degree than those in pasture (White et al, 1981) and are therefore more likely to affect concentrations in milk.…”
Two experiments were conducted to establish responses in milk Se concentrations in grazing dairy cows to different amounts of dietary Se yeast, and to determine the effects of the Se concentration of the basal diet. The hypothesis tested was that the response in milk, blood, and tissue Se concentrations to supplemental Se would not be affected by whether the Se was from the basal diet or from Se yeast. In addition, by conducting a similar experiment in either early (spring; experiment 1) or late (autumn; experiment 2) lactation, we hypothesized that different Se input-output relationships would result. Both 6-wk experiments involved 60 multiparous Holstein-Friesian cows, all of which had calved in spring. They were allocated to 1 of 10 dietary Se treatments that included 2 types of crushed triticale grain (low Se, approximately 165 microg of Se/kg of DM; or high Se, approximately 580 microg/kg of DM) fed at 4 kg of DM/d, and 1 kg of DM/d of pellets formulated to carry 5 quantities of Se yeast (0, 4, 8, 12, or 16 mg of Se). Daily total Se intakes ranged from <2 to >18 mg/cow in both experiments. Milk Se concentrations plateaued after 15 and 7 d of supplementation in experiments 1 and 2, respectively, and then remained at plateau concentrations. Average milk Se concentrations for the plateau period increased as the amount of Se yeast increased, and low- and high-Se grain treatments were different at all quantities of Se yeast, although there was a tendency for this difference to diminish at the greatest concentrations of yeast. There were significant positive, linear relationships between Se intake and the concentrations of Se in milk, which were not affected by the source of Se, and the relationships were similar for both experiments. Therefore, the output of Se in milk in experiment 1 was greater than that in experiment 2 because the milk yield of the cows in early lactation was greater. The estimated proportions of Se partitioned to destinations other than milk and feces increased with the amount of Se in the diet and were greater in experiment 2 than in experiment 1, a result that was supported by Se concentrations in whole blood and plasma and in semitendinosus muscle tissue. If high-Se products are to be produced for human nutrition, it is important to be able to develop feeding systems that produce milk with consistent and predictable Se concentrations so that products can consistently meet specifications. The results indicate that this objective is achievable.
“…The decrease of average GSH-Px activity within the experimental period cannot be explained by an analytical failure as the levels were rechecked later from freezed samples. A seasonal variation in blood GSH-Px activity in sheep has been reported (CAPLE et al, 1980). Thc seasonal variation in the present study could partly arise from changcs in oxidative processes contributed by vitamin E. However, the effect of vitamin E on GSH-Px activity has been reported to vary between species and in lambs it has been shown to have no effect on this selenoenzyme (GODWIN et al, 1975).…”
Address of authors: Department of Biochemistry, College of Veterinary Medicine, Hameentie rat muscle and some effects of selenium deficiency. Aust. J. Biol. Sci., 28, 251-258. animals. Adv. Vet. Sci. Comp. Med., 19, 127-164. methodological study. Acta Vet. Scand., Suppl. 23. 57, Box 6, SF-00551 Helsinki 55.
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