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Fushimi, M.

Publications and source records attributed to Fushimi, M..

4 recordsLinked to original sources

Luteal-phase resistance training enhances nocturnal heat dissipation and delta power during sleep

Study ObjectivesThis study examined the effects of resistance training on sleep architecture, physiological heat dissipation, and {delta} power in young adult women during the follicular and luteal phases of the menstrual cycle. MethodsNine healthy young women participated in a four-condition crossover protocol comprising (1) follicular phase non-exercise, (2) follicular phase exercise, (3) luteal phase non-exercise, and (4) luteal phase exercise. The exercise condition consisted of 30 minutes of resistance training at 70% of one-repetition maximum performed during the day. During each night, electroencephalography, body temperature, and core body temperature were measured in the home environment. The distal-proximal body temperature gradient (DPG), which is a validated indicator of heat dissipation, was calculated ResultsResistance training enhanced heat dissipation, as reflected by increased DPG values, and increased the proportion of stage N3 sleep during both menstrual cycle phases, with more pronounced effects during the luteal phase. Sleep from bedtime to wake time was divided into four equal segments. Under the luteal phase with exercise, the appearance of stage N3, {delta} power, and the DPG were elevated in the mid-to-late segments of sleep. ConclusionsThese findings suggest that daytime resistance training promotes nocturnal deep sleep and facilitates thermoregulatory heat loss, as indicated by an increased DPG, particularly during the luteal phase when thermoregulation is less stable than the follicular phase. This training may represent a practical intervention to improve sleep quality and physiological recovery in women across different phases of the menstrual cycle. STATEMENT OF SIGNIFICANCEWomen often experience sleep disturbances during the luteal phase of the menstrual cycle, but the physiological mechanisms and effective interventions remain unclear. This study shows that daytime resistance training enhances nighttime heat dissipation and increases slow-wave sleep during this phase. These findings suggest that exercise is a practical approach to alleviate menstrual cycle-related sleep issues. By clarifying how exercise interacts with thermoregulation and sleep across the cycle, this work contributes to understanding female-specific sleep physiology and supports the development of non-pharmacological strategies to improve womens sleep health in women. Future research should examine the long-term effects of daytime resistance training and compare different exercise modalities across diverse populations.

neuroscience↗

Subjective sleep onset latency is influenced by sleep structure and body heat loss in human subjects

ObjectivesThe current study examined the relationship between subjective SOL, sleep structure, changes in skin and body temperature, and subjective evaluation in healthy young adults to elucidate the pathophysiological mechanisms of insomnia. MethodsTwenty-eight participants (mean age: 21.5 {+/-} 0.5 years) with no sleep problems participated in a 1-hour polysomnographic recording that obtained objective sleep parameters during the daytime while skin and body temperatures were recorded. The distal-proximal skin temperature gradient (DPG) was calculated. Subjective parameters, such as subjective SOL, sleep time, and restorative sleepiness, were evaluated before and after sleep. ResultsMost participants estimated their sleep latency as being longer than their actual SOL (13.7 min vs. 7.6 min). Objective SOL was significantly correlated with each sleep stage parameter whereas subjective SOL was negatively correlated with stage N2 sleep duration (Rho = -0.454, p = 0.020), slow-wave activity and delta power (Rho = -0.500, p = 0.011, Rho = -0.432, p = 0.031, respectively), and {Delta}DPG (the degree of reduction of heat loss before and after lights-off). Stepwise regression analysis showed that {Delta}DPG was the strongest predictive factor in explaining the length of subjective SOL. ConclusionsThe degree of heat dissipation before falling asleep contributed most to the sensation of falling asleep in healthy young adults. This finding may be helpful for elucidating the physiological mechanisms of insomnia and its treatment. STATEMENT OF SIGNIFICANCEThe time estimate ability is also activated during sleep. However, some insomniacs have abnormalities in this function and suffer from sleep state misperception, which is a discrepancy between subjective and objective sleep time. They often overestimate the sleep onset latency. We investigated the relationship between subjective sleep onset latency, sleep structure, EEG frequency components, and body temperature during the process of falling asleep in healthy adults. It was suggested that the Stage N2 duration, the amounts of slow wave activity around after lights-out, and the degree of heat dissipation before falling asleep may be related to the perception of falling asleep. These results are expected to contribute to the understanding of the pathophysiological mechanisms and to the treatment of insomnia.

physiology↗

AP2/ERF transcription factor NbERF-IX-33 is involved in the regulation of phytoalexin production for the resistance of Nicotiana benthamiana to Phytophthora infestans.

Plants recognize molecular patterns unique to a certain group of microbes to induce effective resistance mechanisms. Elicitins are secretory proteins produced by plant pathogenic oomycete genera including Phytophthora and Pythium. Treatment of INF1 (an elicitin produced by P. infestans) induces a series of defense responses in Nicotiana species, including reactive oxygen species (ROS) production, transient induction of ethylene production, hypersensitive cell death and accumulation of the sesquiterpenoid phytoalexin capsidiol. In this study, we analyzed the expression profiles of N. benthamiana genes after INF1 treatment by RNAseq analysis. Based on their expression patterns, N. benthamiana genes were categorized into 20 clusters and 4,761 (8.3%) out of 57,140 genes were assigned to the clusters for INF1-induced genes. All genes encoding enzymes dedicated to capsidiol production, 5-epi-aristolochene (EA) synthase (NbEAS, 10 copies) and EA dehydrogenase (NbEAH, 6 copies), and some genes for ethylene production, such as 1-aminocyclopropane 1-carboxylate (ACC) synthase (NbACS) and ACC oxidase (NbACO), were significantly upregulated by INF1 treatment. Analysis of NbEAS1 and NbEAS4 promoters revealed that AGACGCC (GCC box-like motif) is the essential cis-element required for INF1-induced expression of NbEAS genes. Given that the GCC box is known to be targeted by ERF (ethylene-responsive factor) transcription factors, we created a complete list of N. benthamiana genes encoding AP2/ERF family transcription factors, and identified 45 out of 337 AP2/ERF genes in the clusters for INF1-induced genes. Among INF1-induced NbERF genes, silencing of NbERF-IX-33 compromised resistance against P. infestans and INF1-induced production of capsidiol. Recombinant NbERF-IX-33 protein can bind to the promoter sequence of NbEAS4, suggesting that NbERF-IX-33 is a transcription factor directly regulating the expression of genes for phytoalexin production.

plant biology↗

Soluble adenylyl cyclase inhibition prevents human sperm functions essential for fertilization

Soluble adenylyl cyclase (sAC: ADCY10) is essential for activating dormant sperm. Studies of freshly dissected mouse sperm identified sAC as needed for initiating capacitation and activating motility. We now use an improved sAC inhibitor, TDI-10229, for a comprehensive analysis of sAC function in human sperm. Unlike dissected mouse sperm, human sperm are collected post-ejaculation, after sAC activity has already been stimulated. Even in ejaculated human sperm, TDI-10229 interrupts stimulated motility and capacitation, and it prevents acrosome reaction in capacitated sperm. At present, there are no non-hormonal, pharmacological methods for contraception. Because sAC activity is required post-ejaculation at multiple points during the sperms journey to fertilize the oocyte, sAC inhibitors define candidates for non-hormonal, on-demand contraceptives suitable for delivery via intravaginal devices in females.

pharmacology and toxicology↗