Play behavior is a promising welfare indicator in dairy calves because it decreases in negative situations such as pain or hunger and increases in positive contexts such as in appropriate social environments. Directly measuring play is time consuming because it is performed in irregular bouts and can be inconsistent over days. To facilitate automatic recording of play, previous studies fitted triaxial accelerometers to the hind legs of calves and measured the velocity of movements in large arenas; high correlations were reported between vertical axis peak duration and the duration of locomotor play. The current study aimed to validate accelerometers for recording spontaneous locomotor play in calves' home pens over longer periods. Data were collected from 48 Holstein Friesian calves, housed in groups of 3 in pens of 10 m, at either 4 or 8 wk of age. Acceleration at the vertical axis of the hind leg was recorded at a rate of 1 Hz. One active time period for each calf was randomly selected (mean duration ± standard deviation = 34 ± 9 min). From video of the corresponding time period, the frequency of locomotor play events, consisting of run, turn, and buck/buck-kick, was recorded using behavior sampling. Combined counts of play events were highly correlated (Pearson r = 0.91) with counts of acceleration peaks. However, for calves with higher levels of locomotor play, this method underestimated the extent of play. Alternatively, run, turn, and buck events obtained from video were transformed by creating intervals of 10 s and then classifying each 10-s interval as comprising events of play ("play") or not comprising events of play ("no play"). The corresponding accelerometer data for all 10-s periods, equaling 10 consecutive readings each, were classified into play or no play by using quadratic discriminant analysis; 79% of periods with locomotor play were correctly classified. Counts of observed play intervals correlated with the counts of play periods from accelerometers (r = 0.87), but the discriminant analysis consistently overestimated play. In conclusion, accelerometer measurements at 1 Hz (in 1-s intervals) and at the vertical axis cannot be used alone to exactly quantify absolute levels of locomotor play in the home pen. However, counts of peak accelerations can provide a rough estimate of inter-individual differences in play events, and discriminant analysis can be used as a proxy for one-zero sampling of inter-individual differences in locomotor play.
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http://dx.doi.org/10.3168/jds.2019-17005 | DOI Listing |
Neuroscience
January 2025
Institute for Neuroscience, The University of Texas at Austin, Austin, TX, USA; Waggoner Center for Alcohol & Addiction Research, The University of Texas at Austin, Austin, TX, USA; Department of Neuroscience, The University of Texas at Austin, Austin, TX, USA; Department of Neurology, Dell Medical School, The University of Texas at Austin, Austin, TX, USA. Electronic address:
While our understanding of the neurobiological mechanisms underlying cocaine and opiate reward has historically been dopamine-focused, evidence from genetic and pharmacological approaches indicates that µ-opioid receptors (MORs) in the striatum are important contributors. Within the striatum, MORs are expressed in both dopamine D1-receptor and D2-receptor expressing GABAergic medium spiny neurons (MSNs), as well as in interneurons and various afferents. Thus, it remains unclear how these distinct MOR populations regulate drug reward.
View Article and Find Full Text PDFCortical interneurons play an important role in mediating the juvenile critical period for ocular dominance plasticity in the mouse primary visual cortex. Previously, we showed that transplantation of cortical interneurons derived from the medial ganglionic eminence (MGE) opens a robust period of ocular dominance plasticity 33-35 days after transplantation into neonatal host visual cortex. The plasticity can be induced by transplanting either PV or SST MGE-derived cortical interneurons; it requires transplanted interneurons to express the vesicular GABAergic transporter; and it is manifested by changes to the host visual circuit.
View Article and Find Full Text PDFBackground: Bridge-like lipid transfer proteins (BLTPs) mediate bulk lipid transport at membrane contact sites. Mutations in BLTPs are linked to both early-onset neurodevelopmental and later-onset neurodegenerative diseases, including movement disorders. The tissue specificity and temporal requirements of BLTPs in disease pathogenesis remain poorly understood.
View Article and Find Full Text PDFJ Dairy Sci
January 2025
Department of Animal and Veterinary Sciences, Aarhus University, Tjele, Denmark.
Given increasing adoption of social housing for pre-weaned dairy calves, we conducted a systematic review to summarize existing literature describing effects of social housing management factors on behavior, performance, and health of dairy calves. Included articles addressed interventions applied to pre-weaned, socially housed dairy calves, encompassing age at introduction to social housing, group composition (size, stocking density, within-group age range, stability), and housing environment (space allowance, enrichment provision). Outcome measures addressed behavior, including social behavior, locomotor behavior, feeding behavior, abnormal oral behavior, and behavioral responses during tests; performance, including body measurements and weight gain; and health, including clinical health scores and mortality rate.
View Article and Find Full Text PDFChildren (Basel)
November 2024
Department of Neurosurgery, Houston Methodist Hospital/Research, 6565 Fannin St, Houston, TX 77030, USA.
Background And Purpose: activities-based locomotor training (AB-LT) is a restorative therapeutic approach to the treatment of movement deficits in people with non-progressive neurological conditions, including cerebral palsy (CP). Transcutaneous spinal stimulation (TSS) is an emerging tool in the rehabilitation of individuals with sensorimotor deficits caused by neurological dysfunction. This non-invasive technique delivers electrical stimulation over the spinal cord, leading to the modulation of spinal sensorimotor networks.
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