Neuroscience meets salivary bioscience: An integrative perspective.

Advances in salivary bioscience enable unique opportunities to explore individual differences in biological mechanisms related to learning and memory, psychiatric disorders, and more recently neurodegenerative diseases, neurotrauma/stroke, pain, and sleep. Sampling oral fluid is not only minimally invasive, but specimens can be collected easily and quickly in clinical and field settings. Salivary analytes allow neuroscientists to index endocrine, autonomic, immune, metabolic, and inflammatory processes within close proximity of discrete behavioral, biological, and social events, which is particularly important to advancing our understanding of human neuroscience. This review provides an update on the advances in salivary bioscience for specialty fields within neuroscience, presents novel salivary analytes of interest to neuroscience and the status of their development, and outlines a procedural framework to facilitate integration of these concepts and methods into neuroscience. (PsycINFO Database Record

Hormonal contraception use alters stress responses and emotional memory.

Emotionally arousing material is typically better remembered than neutral material. Since norepinephrine and cortisol interact to modulate emotional memory, sex-related influences on stress responses may be related to sex differences in emotional memory. Two groups of healthy women - one naturally cycling (NC women, n=42) and one using hormonal contraceptives (HC women, n=36) - viewed emotionally arousing and neutral images. Immediately after, they were assigned to Cold Pressor Stress (CPS) or a control procedure. One week later, participants received a surprise free recall test. Saliva samples were collected and later assayed for salivary alpha-amylase (biomarker for norepinephrine) and cortisol. Compared to NC women, HC women exhibited significantly blunted stress hormone responses to the images and CPS. Recall of emotional images differed between HC and NC women depending on noradrenergic and cortisol responses. These findings may have important implications for understanding the neurobiology of emotional memory disorders, especially those that disproportionately affect women.

Exercise-induced noradrenergic activation enhances memory consolidation in both normal aging and patients with amnestic mild cognitive impairment.

Post-trial pharmacological activation of the noradrenergic system can facilitate memory consolidation. Because exercise activates the locus coeruleus and increases brain norepinephrine release, we hypothesized that post-trial exercise could function as a natural stimulus to enhance memory consolidation. We investigated this in amnestic mild cognitive impairment (aMCI) and cognitively normal elderly individuals by examining the effects of an acute bout of post-learning, aerobic exercise (6 minutes at 70% VO2 max on a stationary bicycle) on memory for some emotional images. Exercise significantly elevated endogenous norepinephrine (measured via the biomarker, salivary alpha-amylase) in both aMCI patients and controls. Additionally, exercise retrogradely enhanced memory in both aMCI patients and controls. Acute exercise that activates the noradrenergic system may serve as a beneficial, natural, and practical therapeutic intervention for cognitive decline in the aging population.

Norepinephrine-mediated emotional arousal facilitates subsequent pattern separation.

Pattern separation, the process by which similar experiences can be stored as distinct memories, has been ascribed to the dentate gyrus (DG) of the hippocampus. The DG is the target of noradrenergic modulation directly and indirectly via the basolateral amygdala. We tested the hypothesis that noradrenergic activation (tested using salivary alpha-amylase) potentiates DG function, enhancing pattern separation, by showing participants fearful stimuli in a pre-training task and then testing their capacity for pattern separation in a later test. Consistent with our hypothesis, we found that increased levels of salivary alpha-amylase were positively correlated with enhanced pattern separation performance even after accounting for general enhancements in recognition.

Endogenous noradrenergic activation and memory for emotional material in men and women.

A plethora of evidence from the animal and human literature suggests that emotionally arousing material is often remembered better than is neutral material, and that this effect critically involves noradrenergic activation during and soon after exposure to the emotional material. A crucial prediction of this hypothesis is that endogenous adrenergic activation should relate positively and selectively to memory for emotional events in humans. Salivary alpha-amylase (sAA), a biomarker for adrenergic activity was measured in response to viewing a series of mixed emotional and neutral images to test this prediction in healthy men and women. One week after viewing these images subjects returned for a surprise free recall test. Endogenous noradrenergic activation, defined as an increase in sAA immediately after versus before slide viewing, occurred in 24 of 67 subjects. Regression analysis of the data revealed a significant positive correlation between the increase in sAA and the percentage of emotional pictures recalled. No correlation existed in the same subjects between sAA and the percentage of neutral pictures recalled. Additionally, the difference between these two correlations closely approached significance. The findings therefore demonstrate a relationship between a measure of endogenous noradrenergic activation and long-term memory performance in humans. The results support the view that adrenergic activation underlies enhanced memory for emotional material in humans, namely, that endogenous adrenergic activation in response to an emotional event should predict long-term memory for the event. The selectivity of the relationship for emotional, and not neutral, material supports the view derived from earlier research that stress activation does not necessarily enhance memory for all aspects of an emotional event; rather, that it acts disproportionately to influence memory for the more emotional aspects of an event. These findings are the first involving human subjects to indicate that the degree of endogenous noradrenergic activation in response to emotionally arousing stimuli predicts the strength of long-term memory for those stimuli.