Theory of exciton thermal radiation in semiconducting single-walled carbon nanotubes

Spectral control of thermal radiation is an essential strategy for highly efficient and functional utilization of thermal radiation energy. Among the various proposed methods, quantum confinement in low-dimensional materials is promising because of its inherent ability to emit narrowband thermal radiation. Here, we theoretically investigate thermal radiation from one-dimensional (1D) semiconductors characterized by the strong quantum correlation effect due to the Coulomb interaction. We derive a simple and useful formula for the emissivity, which is then used to calculate the thermal radiation spectrum of semiconducting single-walled carbon nanotubes as a representative of 1D semiconductors. The calculations show that the exciton state, which is an electron–hole pair mutually bound by the Coulomb interaction, causes enhancement of the radiation spectrum peak and significant narrowing of its linewidth in the near-infrared wavelength range. The theory developed here will be a firm foundation for exciton thermal radiation in 1D semiconductors, which is expected to lead to new energy harvesting technologies

Mirror symmetrical transfer of perceptual learning by prism adaptation

AbstractRecent study of [Sugita, Y. (1996) Global plasticity in adult visual cortex following reversal of visual input. Nature, 380, 523–526.] demonstrated that prism adaptation to reversed retinal input generates the transfer of neuronal activities in monkey V1 to the opposite visual cortex. This raises the question if perceptual learning on one side of the visual field can transfer to the other side. We tested this in using the Gabor lateral masking paradigm. Before adaptation, long-range interaction was induced vertically on one side (i.e., the right) of the visual field with training (perceptual learning). Prism adaptation was achieved by wearing right-left reversing goggles. During adaptation period, perceptual learning transferred to a mirror symmetrical region across the vertical meridian. Results in the post adaptation period revealed that both learning and transfer persisted for over three months. These results provide direct evidence of transferred perceptual plasticity across the visual field, the underlying mechanism of which is supported by the mirror symmetrical connection between the right and left cortices

Oral Local Anesthesia Successfully Ameliorated Neuropathic Pain in an Upper Limb Suggesting Pain Alleviation through Neural Plasticity within the Central Nervous System: A Case Report

Neural blockades are considered an alternative to pharmacotherapy for neuropathic pain although these blockades elicit limited effects. We encountered a patient with postbrachial plexus avulsion injury pain, which was refractory to conventional treatments but disappeared temporarily with the administration of the local anesthetic lidocaine around the left mandibular molar tooth during dental treatments. This analgesic effect on neuropathic pain by oral local anesthesia was reproducible. Under conditions of neuropathic pain, cerebral somatotopic reorganization in the sensorimotor cortices of the brain has been observed. Either expansion or shrinkage of the somatotopic representation of a deafferentated body part correlates with the degree of neuropathic pain. In our case, administration of an oral local anesthetic shrank the somatotopic representation of the mouth, which is next to the upper limb representation and thereby expanded the upper limb representation in a normal manner. Consequently, oral local anesthesia improved the pain in the upper limb. This case suggests that pain alleviation through neural plasticity within the brain is related to neural blockade

Network-dependent modulation of brain activity during sleep

AbstractBrain activity dynamically changes even during sleep. A line of neuroimaging studies has reported changes in functional connectivity and regional activity across different sleep stages such as slow-wave sleep (SWS) and rapid-eye-movement (REM) sleep. However, it remains unclear whether and how the large-scale network activity of human brains changes within a given sleep stage. Here, we investigated modulation of network activity within sleep stages by applying the pairwise maximum entropy model to brain activity obtained by functional magnetic resonance imaging from sleeping healthy subjects. We found that the brain activity of individual brain regions and functional interactions between pairs of regions significantly increased in the default-mode network during SWS and decreased during REM sleep. In contrast, the network activity of the fronto-parietal and sensory-motor networks showed the opposite pattern. Furthermore, in the three networks, the amount of the activity changes throughout REM sleep was negatively correlated with that throughout SWS. The present findings suggest that the brain activity is dynamically modulated even in a sleep stage and that the pattern of modulation depends on the type of the large-scale brain networks

音刺激提示後に出現する睡眠紡錘波に関する検討(自然科学篇)

Sleep spindles during sleep stage 2 were measured using the automatic spindle analyzer to examine the effect of the tone stimulus on the appearance of spindle waves. All-night polygraphic sleep recordings were made on six norml human male subjects for four consecutive nights. The fourth night was used as the experimental night, and tone stimuli (62.5 dB(A), 50 msec, 500/1,000Hz) were presented over the night at 30～40 sec ISI. The third night was used as the baseline night, and the tone stimulus was not presented, but only the stimulus marks were recorded on the chart and used as the pseudo-stimulus. There were no significant differences in spindle rate per minute among the baseline night and the experimental night. However, the spindle appearance rate within 2.5 sec after the tone stimulus was significantly elevated in the experimental night compared to the baseline night. And the frequency of spindle waves detedted after the tone stimulus was faster than the other spindles. There were no significant differences in the spindle duration. The relation between the spindle and the K-complex, and the possible function of the spindle appearance in the sleep process were discussed. And some kinds of spindles and/or spindle-wave-like activities were compared and the importance of measuring the frequency of spindle waves was discussed for the study of the sleep spindle activity

The impact of human leukocyte antigen mismatch on recipient outcomes in living‐donor liver transplantation

Donor–recipient human leukocyte antigen (HLA) compatibility has not been considered to significantly affect liver transplantation (LT) outcomes; however, its significance in living-donor LT (LDLT), which is mostly performed between blood relatives, remains unclear. This retrospective cohort study included 1954 LDLTs at our institution (1990–2020). The primary and secondary endpoints were recipient survival and the incidence of T cell–mediated rejection (TCMR) after LDLT, respectively, according to the number of HLA mismatches at all five loci: HLA-A, HLA-B, HLA-C, HLA-DR, and HLA-DQ. Subgroup analyses were also performed in between-siblings that characteristically have widely distributed 0–10 HLA mismatches. A total of 1304 cases of primary LDLTs were finally enrolled, including 631 adults (recipient age at LT ≥18 years) and 673 children (<18 years). In adult-to-adult LDLT, the more HLA mismatches at each locus, the significantly worse the recipient survival was (p = 0.03, 0.01, 0.03, 0.001, and <0.001 for HLA-A, HLA-B, HLA-C, HLA-DR, and HLA-DQ, respectively). This trend was more pronounced when multiple loci were combined (all p < 0.001 for A + B + DR, A + B + C, DR + DQ, and A + B + C + DR + DQ). Notably, a total of three or more HLA-B + DR mismatches was an independent risk factor for both TCMR (hazard ratio [HR] 2.66, 95% confidence interval [CI] 1.21–5.87; p = 0.02) and recipient survival (HR 2.44, 95% CI 1.11–5.35; p = 0.03) in between-siblings. By contrast, HLA mismatch did not affect pediatric LDLT outcomes at any locus or in any combinations; however, it should be noted that all donor–recipient relationships are parent-to-child that characteristically possesses one or less HLA mismatch at each locus and maximally five or less mismatches in total. In conclusion, HLA mismatch significantly affects not only TCMR development but also recipient survival in adult LDLT, but not in children

Japanese Lung Cancer Society Guidelines for Stage IV NSCLC With EGFR Mutations

Patients with NSCLC in East Asia, including Japan, frequently contain EGFR mutations. In 2018, we published the latest full clinical practice guidelines on the basis of those provided by the Japanese Lung Cancer Society Guidelines Committee. The purpose of this study was to update those recommendations, especially for the treatment of metastatic or recurrent EGFR-mutated NSCLC. We conducted a literature search of systematic reviews of randomized controlled and nonrandomized trials published between 2018 and 2019 that multiple physicians had reviewed independently. On the basis of those studies and the advice from the Japanese Society of Lung Cancer Expert Panel, we developed updated guidelines according to the Grading of Recommendations, Assessment, Development, and Evaluation system. We also evaluated the benefits of overall and progression-free survival, end points, toxicities, and patients’ reported outcomes. For patients with NSCLC harboring EGFR-activating mutations, the use of EGFR tyrosine kinase inhibitors (EGFR TKIs), especially osimertinib, had the best recommendation as to first-line treatment. We also recommended the combination of EGFR TKI with other agents (platinum-based chemotherapy or antiangiogenic agents); however, it can lead to toxicity. In the presence of EGFR uncommon mutations, except for an exon 20 insertion, we also recommended the EGFR TKI treatment. However, we could not provide recommendations for the treatment of EGFR mutations with immune checkpoint inhibitors, including monotherapy, and its combination with cytotoxic chemotherapy, because of the limited evidence present in the literature. The 2020 Japanese Lung Cancer Society Guidelines can help community-based physicians to determine the most appropriate treatments and adequately provide medical care to their patients

Down-regulation of GATA1-dependent erythrocyte-related genes in the spleens of mice exposed to a space travel

Secondary lymphoid organs are critical for regulating acquired immune responses. The aim of this study was to characterize the impact of spaceflight on secondary lymphoid organs at the molecular level. We analysed the spleens and lymph nodes from mice flown aboard the International Space Station (ISS) in orbit for 35 days, as part of a Japan Aerospace Exploration Agency mission. During flight, half of the mice were exposed to 1 g by centrifuging in the ISS, to provide information regarding the effect of microgravity and 1 g exposure during spaceflight. Whole-transcript cDNA sequencing (RNA-Seq) analysis of the spleen suggested that erythrocyte-related genes regulated by the transcription factor GATA1 were significantly down-regulated in ISS-flown vs. ground control mice. GATA1 and Tal1 (regulators of erythropoiesis) mRNA expression was consistently reduced by approximately half. These reductions were not completely alleviated by 1 g exposure in the ISS, suggesting that the combined effect of space environments aside from microgravity could down-regulate gene expression in the spleen. Additionally, plasma immunoglobulin concentrations were slightly altered in ISS-flown mice. Overall, our data suggest that spaceflight might disturb the homeostatic gene expression of the spleen through a combination of microgravity and other environmental changes