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Biology subjects

Miwa, H.

Publications and source records attributed to Miwa, H..

3 recordsLinked to original sources

Respiratory suppression enhances voluntary control of human action

Athletes often regulate their breathing to optimize motor performance, suggesting a close link between respiration and movement control. Previous studies have shown that respiration modulates neuronal oscillations and influences behavior. However, how respiratory control directly affects motor behavior remains unclear. Here, we demonstrate that breath holding during the preparatory period facilitates voluntary movement. We examined respiratory patterns while participants performed two types of eye movement tasks: pro-saccade and anti-saccade tasks. In the anti-saccade task, participants were required to suppress a reflexive saccade toward a visual target and instead generate a voluntary saccade in the opposite direction. To assess whether motivation modulates respiratory control, the tasks were conducted under two motivational conditions. Most participants suppressed their breath during the anticipatory period preceding saccade initiation, regardless of task type, and this tendency was more pronounced under high motivation. In the anti-saccade task, stronger respiratory adjustments were associated with shorter reaction times, whereas no such relationship was observed in the pro-saccade task. Moreover, intentional breath holding during the preparatory period selectively reduced reaction times in the anti-saccade task. These findings indicate that individuals spontaneously hold their breath to facilitate voluntary actions in highly motivated situations, and that this effect can be reproduced through intentional breath holding. We propose that anticipatory breath holding may play a functional role in proactively modulating neural processes underlying voluntary movement control.

neuroscience↗

Improved humoral immunity and protection against influenza virus infection with a 3D porous biomaterial vaccine

New vaccine platforms that properly activate humoral immunity and generate neutralizing antibodies are required to combat emerging and re-emerging pathogens, including influenza virus. Biomaterial scaffolds with macroscale porosity have demonstrated tremendous promise in regenerative medicine where they have been shown to allow immune cell infiltration and subsequent activation, but whether these types of materials can serve as an immunization platform is unknown. We developed an injectable immunization platform that uses a slurry of antigen-loaded hydrogel microparticles that anneal to form a porous scaffold with high surface area for antigen uptake by infiltrating immune cells as the biomaterial degrades to maximize humoral immunity. Antigen-loaded-microgels elicited a robust cellular humoral immune response, with increased CD4+ T follicular helper (Tfh) cells and prolonged germinal center (GC) B cells comparable to the commonly used adjuvant, aluminum hydroxide (Alum). By simply increasing the weight fraction of polymer material, we enhanced material stiffness and further increased antigen-specific antibody titers superior to Alum. Vaccinating mice with inactivated influenza virus loaded into this more highly crosslinked formulation elicited a strong antibody response and provided better protection against a high dose viral challenge than Alum. Thus, we demonstrate that by tuning physical and chemical properties alone, we can enhance adjuvanticity and promote humoral immunity and protection against a pathogen, leveraging two different types of antigenic material: individual protein antigen and inactivated virus. The flexibility of the platform may enable design of new vaccines to enhance innate and adaptive immune cell programming to generate and tune high affinity antibodies, a promising approach to generate long-lasting immunity against specific pathogens.

bioengineering↗

Angiopathy with impaired glucose logistics observed in schizophrenia-like model mice

Metabolic dysfunction is thought to contribute to the severity of psychiatric disorders; however, it has been unclear whether current high-simple-sugar diets contribute to pathogenesis of these diseases. Here we demonstrate that a high-sucrose diet during adolescence induces psychosis-related behavioral endophenotypes, including hyperactivity, poor working memory, impaired sensory gating, and disrupted interneuron function in mice deficient for glyoxalase-1 (Glo1), an enzyme involved in detoxification of sucrose metabolites. Further, the high-sucrose diet induced microcapillary impairments and reduced brain glucose uptake in brains of Glo1 deficient mice. Aspirin protected against this angiopathy, enhancing brain glucose uptake, and preventing abnormal behavioral phenotypes. Similar vascular damage to our model mice was found in the brains of randomly collected schizophrenia and bipolar disorder patients, suggesting that psychiatric disorders are associated with angiopathy in the brain caused by various environmental stresses, including metabolic stress.

neuroscience↗