医学部
Profile Information
- Affiliation
- Assistant Professor, Department of Physiology, School of Medicine, Fujita Health University助教, (兼任)精神・神経病態解明センター 神経生理学部門
- Degree
- 博士(生命科学)(京都大学)
- Contact information
- kansai.fukumitsu
fujita-hu.ac.jp
- J-GLOBAL ID
- 201201031940878973
- researchmap Member ID
- B000222421
- External link
Research Areas
1Research History
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Apr, 2020 - Feb, 2023
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Apr, 2017 - Mar, 2020
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Jun, 2015 - Mar, 2017
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Apr, 2013 - Mar, 2015
Education
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Apr, 2012 - May, 2015
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Apr, 2010 - Mar, 2012
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Apr, 2006 - Mar, 2010
Awards
1-
Mar, 2023
Papers
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Neuroscience Research, in press, Jan, 2025 Peer-reviewedInvitedLead authorCorresponding author
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International Journal of Molecular Sciences, 25(21) 11365-11365, Oct 22, 2024 Peer-reviewedWhen exposed to X-rays, scintillators emit visible luminescence. X-ray-mediated optogenetics employs scintillators for remotely activating light-sensitive proteins in biological tissue through X-ray irradiation. This approach offers advantages over traditional optogenetics, allowing for deeper tissue penetration and wireless control. Here, we assessed the short-term safety and efficacy of candidate scintillator materials for neuronal control. Our analyses revealed that lead-free halide scintillators, such as Cs3Cu2I5, exhibited significant cytotoxicity within 24 h and induced neuroinflammatory effects when injected into the mouse brain. In contrast, cerium-doped gadolinium aluminum gallium garnet (Ce:GAGG) nanoparticles showed no detectable cytotoxicity within the same period, and injection into the mouse brain did not lead to observable neuroinflammation over four weeks. Electrophysiological recordings in the cerebral cortex of awake mice showed that X-ray-induced radioluminescence from Ce:GAGG nanoparticles reliably activated 45% of the neuronal population surrounding the implanted particles, a significantly higher activation rate than europium-doped GAGG (Eu:GAGG) microparticles, which activated only 10% of neurons. Furthermore, we established the cell-type specificity of this technique by using Ce:GAGG nanoparticles to selectively stimulate midbrain dopamine neurons. This technique was applied to freely behaving mice, allowing for wireless modulation of place preference behavior mediated by midbrain dopamine neurons. These findings highlight the unique suitability of Ce:GAGG nanoparticles for X-ray-mediated optogenetics. The deep tissue penetration, short-term safety, wireless neuronal control, and cell-type specificity of this system offer exciting possibilities for diverse neuroscience applications and therapeutic interventions.
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Parental brain through time: The origin and development of the neural circuit of mammalian parentingAnnals of the New York Academy of Sciences, Mar, 2024 Peer-reviewedAbstract This review consolidates current knowledge on mammalian parental care, focusing on its neural mechanisms, evolutionary origins, and derivatives. Neurobiological studies have identified specific neurons in the medial preoptic area as crucial for parental care. Unexpectedly, these neurons are characterized by the expression of molecules signaling satiety, such as calcitonin receptor and BRS3, and overlap with neurons involved in the reproductive behaviors of males but not females. A synthesis of comparative ecology and paleontology suggests an evolutionary scenario for mammalian parental care, possibly stemming from male‐biased guarding of offspring in basal vertebrates. The terrestrial transition of tetrapods led to prolonged egg retention in females and the emergence of amniotes, skewing care toward females. The nocturnal adaptation of Mesozoic mammalian ancestors reinforced maternal care for lactation and thermal regulation via endothermy, potentially introducing metabolic gate control in parenting neurons. The established maternal care may have served as the precursor for paternal and cooperative care in mammals and also fostered the development of group living, which may have further contributed to the emergence of empathy and altruism. These evolution‐informed working hypotheses require empirical validation, yet they offer promising avenues to investigate the neural underpinnings of mammalian social behaviors.
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Neuroscience Research, 194 36-43, Sep, 2023 Peer-reviewedLead authorCorresponding author
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Brain Nerve, 75(3) 263-268, Mar, 2023 InvitedLead authorCorresponding authorProlonged social isolation has been reported to be one of the risk factors for human health, equivalent to smoking cigarettes. Therefore, some developed countries have recognized prolonged social isolation as a social problem and have started to address this problem. Studies on rodent models are essential to fundamentally clarify the impacts of social isolation on human health mentally and physically. In this review, we conduct an overview of the neuromolecular mechanisms of loneliness, perceived social isolation, and the effects of prolonged social isolation. Finally, we consider the evolutionary development of neural bases of loneliness.
Misc.
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EcoevoRxiv, Dec 5, 2023Mammalian parental care is highly mother-biased, prompting researchers to presume its connection to female reproductive behavior and physiology, not male. However, recent findings in neurobiological studies suggest the opposite. Considering the evolutionary path of mammalian parental care, the ancestral form of vertebrate parental care appears to be male-biased as in living teleosts (bony fish), and originated from egg guarding as an extension of territorial behavior. Phylogenetic analyses suggest that in basal tetrapods, the harsh reproductive environments have facilitated terrestrial adaptation and extensive parental investment in females, and salamander-like basal amniotes exhibited extended egg retention in female bodies. Molecular and fossil evidence indicates that synapsids that have later evolved into mammals have already performed extensive maternal care including egg/offspring hydration in the Carboniferous period. Then the nocturnal adaptation in Jurassic mammaliaforms promoted endothermy and prolonged maternal care for thermal control and lactation. This situation may have added nutritional gate control to the offspring care circuit to balance parental provisioning with maternal homeostatic needs. Combining these paleontological, comparative ecological, and neuromolecular findings, we propose that the mammalian parenting circuit may be derived from MPOA neurons controlling reproductive behaviors during the terrestrial adaptation in anamniotes, either by divergent or parallel evolution. Next, we discuss another long-postulated hypothesis that complex affiliative sociality among adults, including group living, cooperative infant care, empathy, and altruism, may have emerged primarily for extended support of the offspring growth, utilizing the established maternal care circuit in mammals. These evolution-informed working hypotheses may also help dissect the neural basis of the complex cognitive functions in mammals.
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Neuroscience Research, 71 e96-e96, Sep, 2011 Peer-reviewed
Professional Memberships
2Research Projects
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公益信託成茂神経科学研究助成基金, Jul, 2024 - Mar, 2025
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研究助成, 堀科学芸術振興財団, Apr, 2024 - Mar, 2025
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科学研究費助成事業 若手研究, 日本学術振興会, Apr, 2022 - Mar, 2025
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研究助成, ひと・健康・未来研究財団, Aug, 2023
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基礎科学特別研究員研究奨励費, 理化学研究所, Apr, 2020 - Mar, 2023
Media Coverage
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FNN プライムオンライン編集部, いきものディープランド, Feb 17, 2022 Internet