小動物におけるEEGとfMRIの同時計測法の確立

Tohoku University川島隆太課

Aerospace Medicine and Biology: A continuing bibliography with indexes, supplement 127, April 1974

This special bibliography lists 279 reports, articles, and other documents introduced into the NASA scientific and technical information system in March 1974

Brain State Dependent Activity in the Lateral Geniculate Nucleus

Brain state dependent thalamocortical (TC) activity plays and important role in sensory coding, oscillations and cognition. The lateral geniculate nucleus (LGN) relays visual information to the cortex, but the state dependent spontaneous and visually evoked activity of LGN neurons in awake behaving animals remains controversial. In awake head-restrained mice, using a combination of pupillometry, extracellular and intracellular recordings from morphologically and physiologically identified LGN neurons we show that TC neurons and putative local interneurons are inversely related to arousal forming two complementary coalitions with TC cells being positively correlates with wakefulness, while local interneuron activity is negatively correlated. Additionally, the orientation tuning of visually evoked thalamic cell responses is altered during various brain states. Intracellular recordings indicated that the membrane potential of LGN TC neurons was tightly correlated to fluctuations in pupil size. Inactivating the corticothalamic feedback by GABAA agonist muscimol applied on the dural surface significantly diminishes the correlation between brain states and thalamic neuronal activity. Additional investigations show that by photostimulating GABAergic axons (expressing Channelrhodopsin-2 in a Cre-dependent manner) that project from the lateral hypothalamus (LH) to the dorsal raphe nucleus (DRN), neurons in the DRN increase their action potential output, presumably through disinhibition. Taken together our results show that LGN neuronal membrane potential and action potential output are dynamically linked to arousal dependent brain states in awake mice and this fact might have important functional implications

Respiratory influences on pupil size dynamics and visual recognition memory

Breathing, a fundamental rhythm of life, has traditionally been associated with the exchange of oxygen and carbon dioxide. However, recent research in both animal models and humans has unveiled additional roles of respiration in modulating cortical neuronal activity, influencing sensory, motor, emotional, and cognitive processes. This dissertation aims to explore the impact of respiration on pupil size dynamics and visual recognition memory in humans. In Study I, we synthesized the research conducted on respiratory influences on pupil size dynamics in humans by conducting a systematic literature review. We discovered that the evidence for respiratory influences on pupil size dynamics in humans is less solid and extensive than previously believed. After more than 50 years of research, only 12 studies have directly investigated this topic. Not only was the underlying evidence for an effect of breathing phase, depth, and rate on pupil size dynamics weak, but the influence of breathing route (oral or nasal breathing) had not been investigated at all. In Study II, we conducted an experimental study to answer the outstanding questions identified in Study I. We collected pupil size data from participants during periods of rest while they breathed through their nose and mouth, on separate occasions. We demonstrated small but significant effects of breathing phase on pupil size and a spurious correlation and phase synchronization between the breathing and the pupil signal that is largely driven by breathing rate. After accounting for this spurious correlation and phase synchronization, we show that a small but significant interaction between the breathing and the pupil signal remains. Importantly, we show that, contrary to common belief, pupil size does not increase during inhalation, but rather during exhalation. Furthermore, we did not find any changes in pupil size in the time around inhalation and exhalation, and our results were not affected by the breathing route. In conclusion, we confirmed the influence of breathing on pupil size dynamics, while uncovering a more complex and intricate relationship than previously conceived. In Study III, we investigated the influence of breathing phase and breathing route on performance in a visual recognition memory task with a within-subject design and with stimuli presentation phase-locked to the inhalation or exhalation onset. We show that neither breathing phase nor breathing route affect memory performance. However, we did find an effect of breathing phase on response bias, with participants using a more conservative response bias during exhalation. Furthermore, we found that breathing route and breathing phase shape the Late Parietal Effect (LPE), but not the Frontal Negative Component (FN400), amplitude during encoding. Additionally, during recognition, both the LPE and FN400 component amplitudes were not, or only to a small extent, affected by breathing route and phase. While we demonstrated that breathing does not shape visual recognition memory performance, we also showed that breathing influences brain activity related to memory functions. Therefore, we highlight the importance of further research to elucidate the extent of respiratory influence on perception, cognition, and behavior. In Study IV, we further investigated the impact of breathing on visual memory performance by investigating the effects of nasal breathing phase on memory of repeated images presented in a rapid serial visual presentation (RSVP) task. In two separate, high-powered experiments, we did not find an effect of breathing phase on task performance. An exploratory analysis in the first experiment discovered a potential performance increase for stimuli presented approximately one second after inhalation. However, this was not replicated in the second, larger, and pre-registered study. Thus, we find no effect of breathing phase on performance in this RSVP task and urge for caution regarding the notion that visual memory is broadly affected by the breathing phase. Finally, in Study V, we investigated whether oral hormonal contraceptives (OC) affect chemosensory sensitivity and perception. Whereas previous research focused nearly exclusively on olfaction, we expanded this to also study the taste and trigeminal sense. Making use of Bayesian statistics, we evaluated the performance differences between a group of women taking OC, and a control group of normal cycling women. Our results indicated that the use of OC does not affect odor, trigeminal, or taste detection thresholds. Furthermore, neither odor nor taste perception were affected, with Bayes factors weighing the evidence in favor of the null hypothesis. We therefore conclude it to be unlikely that OC affect chemosensory perception to a degree that is of behavioral relevance. Collectively, this doctoral thesis challenges prevailing myths while paving the way for a more intricate understanding of the relationship between respiration and pupil size, and perceptual and cognitive processes. Importantly, it underscores the importance of implementing rigorous methodological paradigms in future research