The physiological role of placental lactogen (PL; chorionic somatomammotrophin) in the ewe has been investigated by infusion of ewes (n = 3) on day 131 of pregnancy with sufficient ovine PL (oPL) antibody to neutralize circulating oPL for at least 12 h. Effectiveness of the antibody neutralization was defined both in vitro and in vivo according to rigorous criteria. Control ewes (n = 3) were infused simultaneously with an equivalent amount of pooled goat gamma globulin. Since both sets of ewes had previously been catheterized with jugular, utero-ovarian and femoral vein catheters and a femoral arterial catheter, it was possible to measure whole body glucose kinetics as well as muscle and uterine glucose, free fatty acid (FFA) and 3-hydroxybutyrate extraction. In addition, plasma levels of insulin, GH, prolactin, insulin-like growth factor-I (IGF-I), IGF-II, progesterone and cholesterol were determined in femoral arterial samples. Neutralization of maternal oPL did not significantly affect whole body glucose metabolism, uterine and muscle glucose extraction, or 3-hydroxybutyrate extraction by muscle. A trend towards lower plasma FFA levels was observed after prolonged infusion, but was not statistically significant. However, plasma insulin levels rose significantly during antibody infusion after an early fall. These observations are rationalized in terms of the known requirements of ruminant metabolism during pregnancy, and contrasted with the accepted model for the role of human PL in the metabolic adjustments of pregnancy. No change in plasma IGF-I, IGF-II or GH was observed, providing no support for the concept that oPL is responsible for maternal somatomedin generation during pregnancy. Similarly, plasma prolactin did not differ between antibody-treated and control groups. Finally, antibody neutralization had no influence on either plasma progesterone or cholesterol, mitigating against a role for oPL in progesterone production during late pregnancy in the ewe.

No abstract

A rapid method of excising skin biopsies, from skin blebs formed by a subcutaneous injection of anaesthetic, was investigated to determine the effect on wool follicle density measurements. Two biopsies were taken from the midside of 28 sheep using a trephine, one directly over the skin bleb and the second adjacent to it. Biopsy shrinkage as a result of fixation and histological processing was measured. Total follicle densities were determined and adjusted for biopsy shrinkage using a correction factor (area of skin section/area of the trephine). Biopsies taken over blebs had a greater sectional area (c. 9.3%) most likely because of distension of the skin during the collection of the biopsy, in comparison with their paired biopsy. This increase in the area of skin sampled, resulted in inaccurate correction factors A96071Received 18 September 1996; accepted 6 January 1997 and consequently artificially increased (c. 7.3%) follicle density measurements in biopsies sampled over blebs. The results of this study indicate that inaccurate follicle density measurement will occur if skin blebs are biopsied from above sites of subcutaneous anaesthetic injection.

No abstract

The fleece of the Merino sheep is composed predominantly of wool fibres grown from secondary wool follicles. This study investigates the effects of melatonin and prolactin on the development of secondarv follicles in grafted ovine foetal skin. Skin from day 85 ovine foetuses was grafted onto nude mice, developed for 40 days and then excised. Mice received either 30 8g prolactin ip mouse-1 day-1 (P), one melatonin implant (Regulin�) sc mouse -1 (M), commencing at grafting or no further treatment (C). Wool follicle density and development were assessed in grafted skin and compared with day 125 control foetal skin. Cuticle structure of graft fibres was also examined and compared with those of day 125 foetuses. Total follicle density and the rate of follicle initiation were reduced in the grafts compared with control foetal skin. Total follicle density did not vary significantly between treatments, but the number of derived secondary follicles was greater in grafts from mice receiving prolactin (group P). Follicles in grafted skin were larger, produced medullated fibres, and were not grouped, in comparison with follicles in the control foetal skin. Epidermal thickness was greater in grafts than in control foetal skin. The cuticle structure of graft fibres from all groups was similar to the control wool fibres. These findings indicate that prolactin, but not melatonin, may be involved in the regulation of derived secondary follicle development.