Publications by authors named "Kristen Bushell"

Research concerning Alcohol Use Disorder (AUD) has previously focused primarily on either the behavioral or chemical consequences experienced following ethanol intake, but these areas of research have rarely been considered in tandem. Compared with other drugs of abuse, ethanol has been shown to have a unique metabolic pathway once it enters the body, which leads to the formation of downstream metabolites which can go on to form biologically active products. These metabolites can mediate a variety of behavioral responses that are commonly observed with AUD, such as ethanol intake, reinforcement, and vulnerability to relapse.

View Article and Find Full Text PDF

Dysregulation of TNF-α in lamina propria macrophages (LPM) is a feature of inflammatory bowel diseases (IBD). LPS-Induced-TNF-Alpha-Factor (LITAF) is a transcription factor that mediates TNF-α expression. To determine whether LITAF participates in the mediation of TNF-α expression in acutely inflamed colonic tissues, we first established the TNBS-induced colonic inflammation model in C57BL/6 mice.

View Article and Find Full Text PDF

Primarily, rats have served as subjects in Delta(9)-tetrahydrocannabinol's (THC) discrimination studies although other species such as monkeys and pigeons have been used. While the introduction of the knockout and transgenic mice has vastly stimulated the study of the discriminative stimulus effects of drugs there is only a single published report of mice trained to discriminate THC. Thus, this study extended those results by providing a systematic replication that THC serves as an effective discriminative stimulus in mice and by further investigating the mechanisms of action involved in the THC discrimination model in the mouse.

View Article and Find Full Text PDF

The liver is the most common site for metastasis by colorectal cancer, and numerous studies have shown a relationship between serum carcinoembryonic antigen (CEA) levels and metastasis to this site. CEA activates hepatic macrophages or Kupffer cells via binding to the CEA receptor (CEA-R), which results in the production of cytokines and the up-regulation of endothelial adhesion molecules, both of which are implicated in hepatic metastasis. Since tissue macrophages implicated in the metastatic process can often be difficult to isolate, the aim of this study was to develop an in vitro model system to study the complex mechanisms of CEA-induced macrophage activation and metastasis.

View Article and Find Full Text PDF

Background: The proinflammatory cytokine tumor necrosis factor-alpha (TNF-alpha) plays a key role in the pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC). Recently, a new transcription factor termed LITAF (lipopolysaccharide-induced TNF-alpha factor) was shown to mediate TNF-alpha expression in human macrophages by direct binding to specific sequences in the promoter region of the TNF-alpha gene.

Methods: In this report, we identified LITAF in resected ileal and colonic tissues from patients with CD and UC by immunohistochemistry, real-time polymerase chain reaction, and Western blot analysis.

View Article and Find Full Text PDF

A novel fluorescent assay to continuously monitor fatty acid amide hydrolase (FAAH) activity that is simple, sensitive, and amenable to high-throughput screening (HTS) of compound libraries is described in this article. Stable Chinese hamster ovary (CHO) cell lines expressing either human FAAH or an inactive mutant, FAAH-S241A, were established. Arachidonyl 7-amino, 4-methyl coumarin amide (AAMCA), a novel fluorogenic substrate for FAAH, was designed and synthesized.

View Article and Find Full Text PDF
Article Synopsis
  • A new class of indole compounds with 3-phenylacetyl variations has been created and tested for their binding strength to cannabinoid receptors CB1 and CB2.
  • Compounds featuring a 2-substituted phenylacetyl group show strong binding affinity, while those with 4-substituents show little to no affinity, and 3-substituted compounds have moderate binding.
  • Two specific compounds, JWH-251 and JWH-302, are identified as having a strong preference for the CB1 receptor and demonstrate high efficacy as agonists for that receptor, with partial agonist activity for the CB2 receptor.
View Article and Find Full Text PDF
Article Synopsis
  • Researchers created and tested 47 indole derivatives to enhance ligands for CB(1) and CB(2) cannabinoid receptors, analyzing how various substituents affect receptor affinity.
  • Three new highly selective CB(2) receptor agonists were identified, with distinct activity levels (full or partial agonists) for each compound.
  • Molecular modeling and receptor docking studies revealed that the compounds' affinities for the CB(1) receptor were related to their interactions within the receptor's aromatic microdomain.
View Article and Find Full Text PDF