URB597

Effects of different post-encoding stress intensities on short-term recognition memory in rats: The endocannabinoid buffering

Stress-induced changes in corticosterone affect memory. The endocannabinoid system appears as an emotional buffer in stress regulation. We evaluated how different stress intensities after encoding influence rat short-term memory in an object recognition task, whether the effects depend on circadian variation of corticosterone and if exogenous augmentation of anandamide levels could restore any observed impairment.

Endocannabinoid modulation of circadian- and stress-dependent effects on short-term memory in rats

The endocannabinoid system plays a key role in the control of emotional responses to environmental challenges. CB1 receptors are highly expressed within cortico-limbic brain areas, where they modulate stress effects on memory processes. Glucocorticoid and endocannabinoid release is influenced by circadian rhythm.

Integrating endocannabinoid signaling and cannabinoids into the biology and treatment of posttraumatic stress disorder

Exposure to stress is an undeniable, but in most cases surmountable, part of life. However, in certain individuals, exposure to severe or cumulative stressors can lead to an array of pathological conditions including posttraumatic stress disorder (PTSD), characterized by debilitating trauma-related intrusive thoughts, avoidance behaviors, hyperarousal, as well as depressed mood and anxiety.

Cannabinoid modulation of memory consolidation in rats: beyond the role of cannabinoid receptor subtype 1

The effects induced by exogenous manipulation of endocannabinoid neurotransmission on emotion and memory are often contradictory. Among the different factors involved, of particular interest is the binding affinity of endocannabinoids, and their analogs, for other receptor families beyond cannabinoid receptors, such as the peroxisome proliferator-activated receptors (PPARs), and the transient receptor potential cation channel subfamily V member 1 (TRPV1).

Lipid nanoparticles for administration of poorly water soluble neuroactive drugs

This study describes the potential of solid lipid nanoparticles and nanostructured lipid carriers as nano-formulations to administer to the central nervous system poorly water soluble drugs. Different neuroactive drugs, i.e. dimethylfumarate, retinyl palmitate, progesterone and the endocannabinoid hydrolysis inhibitor URB597 have been studied. Lipid nanoparticles constituted of tristearin or tristearin in association with gliceryl monoolein were produced.

Acute administration of Urb597 fatty acid amide hydrolase inhibitor prevents attentional impairments by distractors in adolescent mice

The maturation of attentional control during adolescence might influence later functional outcome or predisposition to psychiatric disorders. During adolescence, the cannabinoid system is particularly sensitive to pharmacological challenges, with potential impact on cognitive functions. Here, we used a recently validated five-choice serial reaction time task protocol to test adolescent C57BL/6J mice.

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