Haruo Kasai

ORCID: 0000-0003-2327-9027
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About
Contact & Profiles
Research Areas
  • Neuroscience and Neuropharmacology Research
  • Cellular transport and secretion
  • Pancreatic function and diabetes
  • Photoreceptor and optogenetics research
  • Neural dynamics and brain function
  • Neuroscience and Neural Engineering
  • Ion channel regulation and function
  • Lipid Membrane Structure and Behavior
  • Quantum Dots Synthesis And Properties
  • Chalcogenide Semiconductor Thin Films
  • Advanced Fluorescence Microscopy Techniques
  • Receptor Mechanisms and Signaling
  • Advanced Chemical Physics Studies
  • Calcium signaling and nucleotide metabolism
  • Photochromic and Fluorescence Chemistry
  • Ultrasound and Hyperthermia Applications
  • Semiconductor Quantum Structures and Devices
  • Quantum, superfluid, helium dynamics
  • Microwave Imaging and Scattering Analysis
  • Erythrocyte Function and Pathophysiology
  • Spectroscopy and Quantum Chemical Studies
  • Advanced MRI Techniques and Applications
  • Nicotinic Acetylcholine Receptors Study
  • Memory and Neural Mechanisms
  • Advanced Memory and Neural Computing

The University of Tokyo
2015-2024

University of Tsukuba
2023

Tohoku University Hospital
2023

Kyoto University Hospital
2017-2020

University of North Carolina at Chapel Hill
2017

University of Illinois Chicago
2017

King's College London
2017

Scripps Research Institute
2017

Japan Science and Technology Agency
2001-2016

Toyoda Gosei (Japan)
2016

Long-term potentiation (LTP) at glutamatergic synapses is considered to underlie learning and memory associated with the enlargement of dendritic spines. Because consolidation LTP require protein synthesis, it important clarify how synthesis affects spine enlargement. In rat brain slices, repetitive pairing postsynaptic spikes two-photon uncaging glutamate single spines (a spike-timing protocol) produced both immediate gradual phases in CA1 pyramidal neurons. The was strongly dependent on...

10.1126/science.1152864 article EN Science 2008-02-29

Animal behaviors are reinforced by subsequent rewards following within a narrow time window. Such reward signals primarily coded dopamine, which modulates the synaptic connections of medium spiny neurons in striatum. The mechanisms timing detection, however, remain unknown. Here, we optically stimulated dopaminergic and glutamatergic inputs separately found that dopamine promoted spine enlargement only during window (0.3 to 2 seconds) after inputs. temporal contingency was detected rapid...

10.1126/science.1255514 article EN Science 2014-09-25

The neurobiological mechanisms underlying the induction and remission of depressive episodes over time are not well understood. Through repeated longitudinal imaging medial prefrontal microcircuits in living brain, we found that spinogenesis plays a critical role sustaining specific antidepressant behavioral effects maintaining long-term remission. Depression-related behavior was associated with targeted, branch-specific elimination postsynaptic dendritic spines on projection neurons....

10.1126/science.aat8078 article EN Science 2019-04-12

Glucose metabolism in glycolysis and mitochondria is pivotal to glucose-induced insulin secretion from pancreatic β cells. One or more factors derived other than pyruvate appear be required for the generation of mitochondrial signals that lead secretion. The electrons glycolysis-derived reduced form nicotinamide adenine dinucleotide (NADH) are transferred through NADH shuttle system. By abolishing function, increases autofluorescence, membrane potential, adenosine triphosphate content were...

10.1126/science.283.5404.981 article EN Science 1999-02-12

To permit rapid optical control of brain activity, we have engineered multiple lines transgenic mice that express the light-activated cation channel Channelrhodopsin-2 (ChR2) in subsets neurons. Illumination ChR2-positive neurons slices produced photocurrents generated action potentials within milliseconds and with precisely timed latencies. The number light-evoked could be controlled by varying either amplitude or duration illumination. Furthermore, frequency up to 30 Hz. Photostimulation...

10.1073/pnas.0700384104 article EN Proceedings of the National Academy of Sciences 2007-05-02

Long-term potentiation of synapse strength requires enlargement dendritic spines on cerebral pyramidal neurons. depression is linked to spine shrinkage. Indeed, are dynamic structures: they form, change their shapes and volumes, or can disappear in the space hours. Do all such changes result from synaptic activity, do some intrinsic processes? How shrinkage relate elimination generation spines, how these processes contribute stationary distribution volumes? To answer questions, we recorded...

10.1523/jneurosci.0603-08.2008 article EN cc-by-nc-sa Journal of Neuroscience 2008-12-10

We describe a strategy for developing hydrophilic chemical cocktails tissue delipidation, decoloring, refractive index (RI) matching, and decalcification, based on comprehensive profiling. More than 1,600 chemicals were screened by high-throughput evaluation system each process. The profiling revealed important factors: salt-free amine with high octanol/water partition-coefficient (logP) N-alkylimidazole aromatic amide RI protonation of phosphate ion decalcification. strategic integration...

10.1016/j.celrep.2018.07.056 article EN cc-by Cell Reports 2018-08-01

Insulin secretion from intact mouse pancreatic islets was investigated with two-photon excitation imaging. granule exocytosis occurred mainly toward the interstitial space, away blood vessels. The fusion pore unusually stable a lifetime of 1.8 seconds. Opening 1.4-nanometer-diameter preceded by unrestricted lateral diffusion lipids along inner wall pore, supporting idea that this structure is composed membrane lipids. When dilated to 12 nanometers, granules rapidly flattened and discharged...

10.1126/science.1073806 article EN Science 2002-08-23

Mice carrying a null mutation in the glucokinase (GK) gene pancreatic β-cells, but not liver, were generated by disrupting β-cell-specific exon. Heterozygous mutant mice showed early-onset mild diabetes due to impaired insulin-secretory response glucose. Homozygotes severe shortly after birth and died within week. GK-deficient islets isolated from homozygotes defective insulin secretion glucose, while they responded other secretagogues: almost normally arginine some extent sulfonylureas....

10.1074/jbc.270.51.30253 article EN cc-by Journal of Biological Chemistry 1995-12-01
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