Open-field behavior was compared between untreated, saline-treated, and butoxamine (a beta-2-adrenoceptor antagonist) treated (15 and 5 mg/kg body weight) male golden hamsters (Mesocricetus auratus). Butoxamine-treated males spent significantly more time self-grooming than saline-treated and untreated males. Especially, untreated males and very similar saline control males showed a clear time sequential structure of behavior with two axes: a grooming-grooming sequence and a highly organized flankmark followed by scrape axis. The degree of this organization was markedly decreased in the butoxamine-treated males, showing an increase in organization of the transition between grooming acts. In general, these males displayed a more stereotypic pattern of behavior than the other. To reveal a systematic relation between the flankmark-scrape response and the exposition to butoxamine and to keep the numbers of experimental animals low, mixed samples were created through consecutive summing of the individual transition matrices of six males treated with 5 mg/kg b.wt. butoxamine to the 15 mg/kg b.wt. sample. By analyzing all samples separately, a positive linear relation between the number of low dosed males in the samples and the degree of organization of the flankmark-scrape sequence was found. The results suggest that the analysis of the transitional structure of behavior during short-term challenges can considerably contribute to an estimation of the coping style and seems to be a more sensitive method than comparing frequencies of behavioral indicators of stress.
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http://dx.doi.org/10.1016/s0031-9384(98)00312-6 | DOI Listing |
Naunyn Schmiedebergs Arch Pharmacol
January 2025
Department of Pharmacology and Toxicology, School of Pharmacy, University of Health and Allied Sciences, Ho, Ghana.
Purpose: Major depressive disorder is one of the most common and burdensome psychiatric disorders worldwide. This study evaluated the anxiolytic- and antidepressant-like activity of three semi-synthetic derivatives of xylopic acid (XA) to identify the most promising derivative based on mechanism(s) of action, in vivo pharmacokinetics and in vitro cytotoxicity.
Methods: The anxiolytic potential and the involvement of GABAergic mechanisms were assessed in the elevated plus-maze and open field tests in mice.
Prog Neuropsychopharmacol Biol Psychiatry
January 2025
Laboratory of Molecular Neurobiology and Behavior, Department of Neurobiology, Institute for Biological Research "Siniša Stanković" - National Institute of Republic of Serbia, University of Belgrade, Belgrade, Serbia. Electronic address:
Attention-Deficit/Hyperactivity Disorder (ADHD) is associated with an increased risk of Parkinson's disease (PD) and other synucleinopathies later in life. The severity of the ADHD phenotype may play a significant role in this association. There is no indication that any of the existing animal models can unify these disorders.
View Article and Find Full Text PDFNeuroreport
January 2025
Department of Neurosurgery.
Nowadays, intracerebral hemorrhage (ICH) is the main cause of death and disability, and motor impairment is a common sequel to ICH. Electroacupuncture (EA) has been widely used for functional recovery after ICH. However, its role and associated regulatory mechanisms in rehabilitation after ICH remain poorly understood.
View Article and Find Full Text PDFJ Exp Zool A Ecol Integr Physiol
January 2025
Departamento de Biologia, Faculdade de Ciências, Universidade de Lisboa, Lisboa, Portugal.
The open field test (OFT) is frequently used in research to assess anxiety-like behavior and locomotor activity. Its simple design can lead to the misconception that it is a standardized procedure comparable between laboratories. However, some modifications in the setup can cause changes in behavior.
View Article and Find Full Text PDFRationale: WW domain-containing oxidoreductase ( ) is a gene associated implicated in both neurologic and inflammatory diseases and is susceptible to environmental stressors. We hypothesize partial loss of Wwox function will result in increased sepsis severity and neuroinflammation.
Methods: mice, generated by CRISPR/Cas9, and mice were treated with intraperitoneal PBS vs LPS (10mg/kg) and euthanized 12 hours post-injection.
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