Ovarian inhibition of pulsatile luteinizing hormone secretion in prepuberal holstein heifers

Fifteen prepuberal Holstein heifers were utilized to examine pulsatile luteinizing hormone (LH) secretion before and after ovariectomy. Heifers were ovariectornized at 3, 6 or 9 months of age (n=5/group) and scheduled for blood sampling at 1 week before, 1 week after and 4 weeks following ovariectomy. During each 8 hr sampling period (0600–1400 hr), blood samples (10 ml) were collected via indwelling jugular canulae at 10 min intervals. Prior to ovariectomy, mean plasma LH concentration and both number and amplitude of LH pulses per 8 hr sampling period were similar (P>.05) among age groups, and the absence of a pulsatile LH secretion profile was accompanied by a low mean LH concentration. Within 1 week after ovariectomy, both number of LH pulses and mean LH concentrations increased (P<.O1) in all age groups. Between 1 and 4 weeks after ovariectomy, both amplitude of LH pulses and mean LH concentrations increased (P<.O1) when the data from the three age groups were combined. We conclude that ovarian inhibition of pulsatile LH secretion is established by 3 months of age and is maintained through 9 months of age. In addition, the initial elevation mean plasma LH concentration is due to greater pulse frequency, while the subsequent rise in mean LH concentration reflects increased amplitude of LH pulses.     

Effects of various mating stimuli on pituitary release of luteinizing hormone in the gilt

Twenty-four nulliparous crossbred gilts approximately 9 months of age were assigned to either a naturally mated (NM), artificially inseminated (Al) or non-mated control group (C). All gilts were fitted with indwelling cephalic cannulas for collection of blood samples for subsequent hormonal analyses every 10 min for the first 24 hr of the periestrous period. Plasma luteinizing hormone (LH) concentrations were not affected by type of mating. The mean duration of the LH surge for Al group was less than the C or NM groups (44.5 vs 67 and 87 hr (P<.05)). Mean maximal LH concentrations for the Al and NM groups occurred prior to the control group (P> 05). Area under the LH release curve and number of episodic surges were not different for the three treatments. Length of standing estrus and exposure time to back pressure were not different among treatment groups.The results suggest that stimulation of the pelvic region during either natural mating or artificial insemination did not enhance release of LH. Mated gilts did exhibit different secretory patterns of LH release than non-mated gilts.     

Effect of suckling intensity on human growth hormone binding, biochemical composition and histological characteristics of ovine mammary glands

Suckling both, or only one contralateral mammary gland during 15 days postpartum was utilized to study lactogenic hormone binding to mammary microsomal membranes and quantitative mammary morphology in ewes. Binding of radiolabeled human growth hormone was specific for lactogenic hormones. Non-radiolabeled human growth hormone, ovine and bovine prolactin and human placental lactogen effectively competed with radiolabeled human growth hormone for binding sites but ovine and bovine growth hormone were completely ineffective. Specific binding of radiolabeled human growth hormone to 600 μg of membrane protein averaged 23 ± 3% in all lactating glands. Neither days postpartum nor treatment of contralateral mammary glands substantially altered hormone binding in lactating glands. Specific human growth hormone binding (6 ± 0.5%) in non-suckled glands (15 days postpartum both udder halves) was significantly lower (P<0.01) than in lactating tissue but only a moderate and variable reduction in specific binding was measured in membranes from glands non-suckled for 15 days but contralateral to a suckled gland (14 ± 4%). Specific binding was approximately doubled in assays with 600 compared with 300 μg of membrane protein and the pattern of binding among variously suckled glands was not changed by treatment of membranes with 4 M MgCl₂ prior to assay. Most secretory cells from all lactating glands had rounded, basally displaced nuclei, apical fat globules, secretory vesicles and abundant densely stained basal cytoplasm (ergastoplasm). Alveolar lumenal area was maximal (50% of tissue area) and stromal tissue area was minimal. After 15 days of non-suckling (both udder halves) mammary cells were engorged with lipid, ergastoplasm was reduced and nuclei were irregularly shaped and randomly displaced compared with lactating tissue. In addition, lumenal area was reduced and stromal tissue more evident. Lack of suckling for 5 days had little apparent effect on mammary cytology. Like lactogenic hormone binding, mammary tissue morphology was only moderately altered by 15 days of non-suckling when the remaining gland was suckled. RNA concentration was lowest (2.1 ± 0.3 mg/g) in mammary tissue from ewes in which neither gland was suckled for 15 days postpartum but non-suckling interval had no significant effect when contralateral glands were suckled. DNA concentration was not significantly influenced by suckling treatments. Relative lactogenic hormone binding closely corresponded to changes in cytological and biochemical indices of secretory cell function.     

Isolation of Pasteurella haemolytica and correlation with serum antibody response in clinically normal beef calves

Bacteria from the nasal cavity and trachea were cultured, and serum antibody titers determined for Pasteurella haemolytica serotype 1 in 164 beef calves obtained from a closed herd on range pasture. At the first sampling, P. haemolytica serotype 1 was cultured from 16.4% of the calves. Antibody titers were determined by a quantitative fluorimetric method and the mean titer was 9.5 +/- 5.8. Fifty-seven randomly selected calves were used to study the correlation of serum antibody response and positive culture of P. haemolytica under natural conditions. Clinical signs of respiratory disease were not observed in those calves. During the observation periods, there was a two-fold increase in the percentage of calves that were culture positive. There was no significant difference between mean serum antibody titers or frequency distribution of antibody titers from the two samplings. Comparisons between serum antibody titers, rise in titers, and P. haemolytica isolation failed to reveal any significant correlation. Of the 9 calves that had a decline in antibody titer to P. haemolytica, none was culture positive. Seroconversion to respiratory viruses did not correlate with P. haemolytica related variables.     

The recreational and commercial importance of feral swine in Florida: Relevance to the possible introduction of African swine fever into the U.S.A.

Florida has the largest population of feral swine in the U.S.A. Feral swine have recreational and economic importance to hunters, trappers, taxidermists, and also to dealers who sell feral swine to hunting clubs. Hunters spent over 522 00 man-days hunting feral swine during the 1980–1981 hunting year. They killed nearly 103 000 hogs which they valued at over $58 each, for a total value of nearly $6 million. Trappers caught 25 000 head valued at about $ 700 000, and landowners collected about $1.2 million in hunting lease fees. Taxidermists received about $389 000 in gross income from mounting feral swine. Sales of feral swine to hunting clubs amounted to about $81 000.

Sales of feral swine through commercial livestock auctions were limited to 1620 head valued at only $16 800 in 1980. Thus, feral swine are important to Florida from a recreational standpoint, but not from the perspective of commercial agriculture.

If African swine fever were to enter Florida, there are many socio-economic factors associated with feral swine that must be carefully evaluated for eradication to be successful.