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Publication : Handling stress impairs learning through a mechanism involving caspase-1 activation and adenosine signaling.

First Author  Towers AE Year  2019
Journal  Brain Behav Immun Volume  80
Pages  763-776 PubMed ID  31108171
Mgi Jnum  J:295521 Mgi Id  MGI:6453915
Doi  10.1016/j.bbi.2019.05.025 Citation  Towers AE, et al. (2019) Handling stress impairs learning through a mechanism involving caspase-1 activation and adenosine signaling. Brain Behav Immun 80:763-776
abstractText  Acute stressors can induce fear and physiologic responses that prepare the body to protect from danger. A key component of this response is immune system readiness. In particular, inflammasome activation appears critical to linking stress to the immune system. Here, we show that a novel combination of handling procedures used regularly in mouse research impairs novel object recognition (NOR) and activates caspase-1 in the amygdala. In male mice, this handling-stress paradigm combined weighing, scruffing and sham abdominal injection once per hr. While one round of weigh/scruff/needle-stick had no impact on NOR, two rounds compromised NOR without impacting location memory or anxiety-like behaviors. Caspase-1 knockout (KO), IL-1 receptor 1 (IL-1R1) KO and IL-1 receptor antagonist (IL-RA)-administered mice were resistant to handling stress-induced loss of NOR. In addition, examination of the brain showed that handling stress increased caspase-1 activity 85% in the amygdala without impacting hippocampal caspase-1 activity. To delineate danger signals relevant to handling stress, caffeine-administered and adenosine 2A receptor (A2AR) KO mice were tested and found resistant to impaired learning and caspase-1 activation. Finally, mice treated with the beta-adrenergic receptor antagonist, propranolol, were resistant to handling stress-induced loss of NOR and caspase-1 activation. Taken together, these results indicate that handling stress-induced impairment of object learning is reliant on a pathway requiring A2AR-dependent activation of caspase-1 in the amygdala that appears contingent on beta-adrenergic receptor functionality.
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