The Effect of Lameness on Average Daily Gain in Feedlot Steers

The objective of this study was to test the effects of lameness on average daily gain (ADG) of feedlot steers. We evaluated two feedlot health data sets: 1) 14,798 steers from a 14-year period (1993 to 2006) at the Meat Animal Research Center (USDA MARC) near Clay Center, Neb.; and 2) 16,766 steers from an 8-year period (2002 to 2009) at the University of Nebraska Agricultural Research and Development Center (ARDC) near Mead, Neb. The ADG for USDA MARC steers with lameness late in the feeding period (≥ 60 days) was 0.04 lb./day less than steers without lameness. The ADG for ARDC steers with lameness later in the experimental trial period (≥ 60 days) was 0.2 lb./day less than steers without lameness. Lameness in steers had a significant and meaningful negative effect on ADG later in the feeding period

Neonatal exposure to the D1 agonist SKF38393 inhibits pair bonding in the adult prairie vole.

The monogamous prairie vole displays developmental sensitivity to early pharmacological manipulation in a number of species-typical social behaviors. The long-term consequences of altering the neonatal dopamine system are not well characterized. This study examined whether early manipulation of the dopamine system, a known mediator of adult prairie vole social behavior, during neonatal development would affect adult aggressive and attachment behaviors. Eight-day-old pups were given a single treatment with either 1 mg/kg of SKF38393 (D1 agonist), quinpirole (D2 agonist), SCH23390 (D1 antagonist), eticlopride (D2 antagonist), or saline vehicle. As adults, animals received tests for intrasexual aggression and partner preference. Activation of D1-like receptors in pups impaired partner preference formation, but had no effect on aggression. Other neonatal treatments had no effect on their behavior as adults. To determine whether D1 activation in pups induced changes in dopamine receptor expression, we performed autoradiography on striatal tissue from a second cohort of saline-treated and SKF38393-treated animals. Although sex differences were observed, we found no treatment differences in D1 or D2 receptor binding in any striatal subregion. This study shows that exposure to a single early pharmacological alteration of dopamine receptor activity may have long-term effects on the social behavior of prairie voles

Neonatal exposure to the D1 agonist SKF38393 inhibits pair bonding in the adult prairie vole.

The monogamous prairie vole displays developmental sensitivity to early pharmacological manipulation in a number of species-typical social behaviors. The long-term consequences of altering the neonatal dopamine system are not well characterized. This study examined whether early manipulation of the dopamine system, a known mediator of adult prairie vole social behavior, during neonatal development would affect adult aggressive and attachment behaviors. Eight-day-old pups were given a single treatment with either 1 mg/kg of SKF38393 (D1 agonist), quinpirole (D2 agonist), SCH23390 (D1 antagonist), eticlopride (D2 antagonist), or saline vehicle. As adults, animals received tests for intrasexual aggression and partner preference. Activation of D1-like receptors in pups impaired partner preference formation, but had no effect on aggression. Other neonatal treatments had no effect on their behavior as adults. To determine whether D1 activation in pups induced changes in dopamine receptor expression, we performed autoradiography on striatal tissue from a second cohort of saline-treated and SKF38393-treated animals. Although sex differences were observed, we found no treatment differences in D1 or D2 receptor binding in any striatal subregion. This study shows that exposure to a single early pharmacological alteration of dopamine receptor activity may have long-term effects on the social behavior of prairie voles