Deep freezing of sheep embryos.

Sheep embryos, collected 1-8 days after oestrus, were placed in Dulbecco's phosphate-buffered saline medium (PBS). After treatment, the viability of the embryos was tested by temporary transfer to ligated rabbit oviducts. In Exp. 1, Days 5-8 embryos survived for at least 15 min at 0 degrees C in the presence of 1-5 M-DMSO. In Exp. 2, 12/14 Days 5-8 embryos survived after being frozen in 1-5 M-DMSO at 0-3 degrees C/min to temperatures ranging between-15 degrees and -60 degrees C and then thawed at 12 degrees C/min. In Exp. 3, Days 5-8 embryos were frozen in 1-5 M-DMSO at 0-3 degrees C/min to below-65 degrees C before being transferred to liquid nitrogen (-196 degrees C), and stored for 12 hr to 1 month. The embryos were thawed at 3 degrees C/min, 12 degrees C/MIN or 360 degrees C/min and, after transfer to rabbit oviducts, 0/4, 10/36 and 1/4, respectively, developed normally. The 11 embryos which were considered normal when recovered from the rabbit oviducts plus 1 slightly retarded embryo were transferred to 7 recipient ewes. Four ewes subsequently lambed, producing 5 lambs. In addition, 8 embryos were transferred to 4 ewes directly after thawing. Three of these ewes subsequently lambed, producing 3 lambs.     

Hip joint forces in sheep.

Testing orthopaedic implants at the proximal femur of sheep requires knowledge of the contact forces acting on this joint. Telemeterized implants were used for long-term measurements of these forces in four sheep, mostly during treadmill walking. Joint forces in the same sheep varied widely from day to day and interindividual differences were also pronounced. Forces during walking were mostly higher than in previous short-term measurements. At medium walking speed, loads in the range of 65-140% of the body weight were typical. Fast walking increased the forces by only 20%, compared to slow speed. Stomping on the ground at the beginning of the stance phase and starting to run freely led to very high forces. The highest values observed were nearly four times the body weight. As in humans, the directions of high forces varied only slightly in the frontal plane throughout the whole stance phase but much more in the transverse plane. With regard to the force magnitudes and their directions, sheep seem to be a good model for testing human implant at the proximal femur.     

Magnesium movement in hypothyroid sheep.

We described magnesium transport in hypothyroid and normal sheep with an eight-compartment biomodel fitted by a least-squares technique to data from multiple compartments and routes of entry of 28-Mg. Isotopic equilibrium was not attained during this period of observation in hypothyroid or control sheep. Hypothyroidism reduced transfer coefficients for absorption (P less than 0.01) of 28-Mg from the GI tract but did not change the rate coefficient for endogenous 28-Mg losses to feces (P less than 0.05). Nutritional balance data indicated higher absorption and retention of Mg in hypothyroid sheep, and the observed decrease in rate of passage of digestive residues suggested that mean retention time of GI tract contents had a definite effect on the availability of Mg.     

Transferrin polymorphism in Herdwick sheep.

The transferrin system in Herdwick sheep, bred at Compton, was investigated with special reference to the susceptibility of the flock to experimentally produced scrapie. No significant correlations were observed between susceptibility and transferrin phenotypes.     

Desulfovibrio of the sheep rumen.

A sulfate-reducing bacterium has been isolated in pure culture from sheep rumen contents. Its properties agree in all respects tested with those ascribed to Desulfovibrio desulfuricans. The populations observed (about 10(8)/ml) are sufficient to account for published rates of ruminal sulfide production.     

Ureolytic bacteria in sheep rumen.

Estimates were made of the numbers of viable bacteria in the rumens of sheep receiving different rations. Representative colonies were isolated and tested for urease production. Some urease-positive isolates were characterized and identified. The ureolytic activities of the urease-producing isolates were determined and compared with the activity of rumen fluid. The rations fed to the sheep did not exert a significant influence on the relative numbers of the urease-producting organisms in the rumen. No obligately anaerobic ureolytic bacteria were found. All urease-positive isolates were facultatively anaerobic, Gram-positive, catalase-positive cocci. Out of ten isolates, nine were identified as Staphylococcus saprophyticus and one as Micrococcus varians. The total urease activity of the different isolates based on the lowest numbers in which they were present in the rumen, compared favourably with the urease activity of rumen fluid. The facultatively anaerobic Gram-positive cocci were probably responsible for a large proportion of the urease activity of the rumen fluid. Conditions prevailing in the rumen were found to be conducive to urease production by the isolates tested.     

Stomach motility in insulin-treated sheep.

The effect of insulin-induced hypoglycaemia on the motility of the reticulum, rumen and abomasum of sheep was investigated using small lightly inflated balloons connected to transducers and a multichannel recorder. The principle response recorded was an inhibition of reticulo-ruminal and abomasal motility, occurring in 'resting' cycles only, and not during eating or rumination. The only hypermotility recorded was that shown by the abomasum just before the onset of inhibition. Ruminating cycles were recorded as frequently during hypoglycaemia as in control periods, and showed no abnormality. The inhibition was reversed by intravenous glucose or adrenaline and by feeding or ruminating.     

Polyclonal B-lymphocyte activation of sheep by Mycobacterium phlei against sheep pox virus.

A trypsinized preparation of Mycobacterium phlei, non specific stimulator of immunity (NSI), and Sheep Pox Virus (SPV) were inoculated in different groups of sheep to activate B-lymphocytes and induce SPV neutralizing substance(s). NSI sensitized sheep B-lymphocytes in the presence of NSI or lymphokine elaborated SPV neutralizing substance(s). The SPV sensitized B-lymphocytes also mediated such neutralizing substance(s). Healthy control sheep B-lymphocytes failed to show any appreciable amount of viral neutralizing substance. However, a significant virus neutralizing substance(s) was detected when healthy sheep B-lymphocytes were cultured in presence of NSI antigen along with lymphokines.     

Fostering in sheep. IV. Use of restraint

Fostering an additional lamb on to a ewe with a single lamb of her own was attempted in Dorset, Corriedale and Merino ewes restrained by the neck in pens for up to 12 days. Fostering occurred more rapidly in Dorsets than in Merinos, and success rates tended to be higher in Dorsets (81%) than the other breeds (73% in Corriedales and 69% in Merinos). The use of screens at the level of the ewe's neck to limit her olfactory examination of the lambs was more successful than when full olfactory contact was allowed. The prevention of any close olfactory contact resulted in an intermediate rate of acceptance, even though acceptance was apparently based on olfaction, as shown by universal rejection of strange alien lambs. Acceptance tests done within a few minutes of release from restraint were found not to reflect accurately the final level of acceptance, since some lambs came to be accepted within a day of being released. Further acceptances, that developed several days after release into a flock of ewes and lambs, emphasize an important role of the lamb in maintaining contact with the ewe. With few exceptions, lambs accepted when released from the pens were still accepted after a week or so in the flock.Dorset ewes given one or two foster lambs in the absence of their own lamb accepted the fosters within 9 days.Restraint fostering had no apparent harmful effects on the ewes or lambs, but had the disadvantages of being laborious and of soiling the ewes' wool. It has the advantage of providing lambs with an assured milk supply, and could prove useful for ewes that have failed to accept lambs under other methods.     

Phosphoinositides of sheep platelets plasma membranes.

Phospholipid composition of sheep blood platelets and its various plasma membrane fractions have been analyzed. Based on their flotation rates in discontinuous sucrose density gradient centrifugation, three membrane fractions were isolated. 5'-Nucelotidase and alkaline phosphatase were distributed nearly equally in all the three membrane fractions. However these membrane fractions showed differences in the distribution of phosphatidyl ethanolamine, phosphatidyl choline and phosphoinositides. Phosphatidyl ethanolamine was predominant in fraction I (11.05 micrograms PLP/mg protein) while phosphatidyl choline was predominant in fractions II and III (110.10 and 68.30 micrograms PLP/mg protein respectively). Phosphatidyl inositol (Ptd-InsP) was equally distributed in all three membrane fractions. However, both Ptd-InsP and phosphatidyl inositol 4,5-bisphosphate were about 4-fold higher in fraction II (73.55 and 89.89 micrograms PLP/mg protein respectively).