Predictive cues and age-related declines in working memory performance.

Older adults, compared to younger adults, do not benefit from predictive information regarding either what type of stimuli they will see or when to expect them, yet it is unclear whether older adults benefit when given both types of predictive information. Here, electroencephalogram recordings of older (aged 62-87 years) and younger (aged 20-32 years) adults were recorded during a working memory task. Each trial contained 2 faces and 2 scenes presented sequentially, followed by a 5-second delay and a probe stimulus. Participants were told what stimuli to remember/ignore and when they would appear. Predictive cues enabled older adults to remember stimuli as accurately as younger adults, although response times were significantly slower, even when corrected for general age-related slowing. Previously observed reductions in P1/N1 amplitude and latency suppression to irrelevant stimuli were not seen. Rather, older adults exhibited lowered P3 amplitudes to relevant stimuli; those with the greatest declines yielded the lowest accuracy and slowest response times. This shows that predictive information can help maintain accuracy, although not response times, which correspond to age-related declines in neural enhancement to relevant stimuli.

Circadian Control of the Female Reproductive Axis Through Gated Responsiveness of the RFRP-3 System to VIP Signaling.

Throughout most of the ovulatory cycle, estrogen negative feedback restrains the GnRH neuronal system. Just before ovulation, however, estrogen negative feedback is removed to permit stimulation of the preovulatory GnRH/LH surge (positive feedback) by the circadian clock in the suprachiasmatic nucleus (SCN). The mammalian ortholog of avian gonadotropin-inhibitory hormone, RFamide-related peptide 3 (RFRP-3), participates in the circadian-timed removal of estrogen negative feedback to permit the LH surge. The present study examined the specific neurochemical means by which the SCN controls RFRP-3 activity and explored whether the RFRP-3 system exhibits time-dependent responsiveness to SCN signaling to precisely time the LH surge. We found that RFRP-3 cells in female Syrian hamsters (Mesocricetus auratus) receive close appositions from SCN-derived vasopressin-ergic and vasoactive intestinal peptide (VIP)-ergic terminal fibers. Central VIP administration markedly suppressed RFRP-3 cellular activity in the evening, but not the morning, relative to saline controls, whereas vasopressin was without effect at either time point. Double-label in situ hybridization for Rfrp-3 and the VIP receptors VPAC1 and VPAC2 revealed that the majority of RFRP-3 cells do not coexpress either receptor in Syrian hamsters or mice, suggesting that SCN VIP-ergic signaling inhibits RFRP-3 cells indirectly. The timing of this VIP-mediated disinhibition is further coordinated via temporally gated responsiveness of RFRP-3 cells to circadian signaling. Together, these findings reveal a novel circadian hierarchy of control coordinating the preovulatory LH surge and ovulation.