Tohoku University · Chemistry
Professor Seong-Yun Kim's research lab specializes in neurodegenerative disease mechanisms, particularly subcortical vascular dementia and post-ischemic brain repair. The lab investigates microglial activation, white matter damage, and neurogenesis in response to cerebral hypoperfusion and excitotoxic injury, using rodent models and molecular techniques. Additionally, the lab explores actinide and rare earth element separation using functionalized resin materials, focusing on selective adsorption and electrochemical behavior of uranium complexes. These interdisciplinary efforts span neuroscience and materials chemistry with translational relevance to brain disorders and nuclear waste management.
Figures are computed from collected data and may differ slightly.
White matter lesions are thought to result from chronic cerebral ischemia and constitute a core pathology of subcortical vascular dementia. This rarefaction has been known to be associated with microglial activation. We investigated whether minocycline, a microglial inhibitor, attenuates the white matter damage induced by chronic cerebral hypoperfusion that is used as a model of vascular dementia. Male Wistar rats were subjected to bilateral, permanent occlusion of the common carotid arteries (B
The optimal cut-off values of SSTs needed to be individualized according to the type of SST and tested patient population.
A crown ether loaded resin was prepared by successive impregnation and fixing the 4′,4′(5″)-di(tert-butylcyclohexano)-18-crown-6 (DtBuCH18C6) and its molecule modifier, 1-dodecanol, onto the porous silica/polymer composite support (SiO2-P particles). The characterization of DtBuCH18C6 loaded resin was examined by thermal gravimetry and differential thermal analysis and electron probe microanalysis. The adsorption behavior of Sr(II), Cs(I), Ru(III), Pd(II), La(III), Nd(III), Sm(III), Gd(III), Zr(
Neurogenesis in the dentate gyrus occurs throughout life. We observed regional differences in neurogenesis in the dentate gyrus of adult rats following transient forebrain ischemia. Nine days after ischemic-reperfusion or sham manipulation, rats were given 5-bromo-2'-deoxyuridine-5'-monophosphate (BrdU), a marker for dividing cells. They were killed 1 or 28 days later to distinguish between cell proliferation and survival. Neurogenesis was evaluated by BrdU incorporation as well by identifying n
The present study was performed to investigate the spatial and temporal expression of osteopontin (OPN) mRNA in the rat brain after kainic acid-induced seizures, and to determine whether this phenomenon is associated spatiotemporally with the microglial reaction. The expression of OPN mRNA was detected using an in situ hybridization technique and Northern blot analysis. Following intraperitoneal injection of kainic acid (10 mg/kg), OPN mRNA was expressed in selective vulnerable areas, including
Abstract Electrochemical studies on [UO2(DMF)5]2+, UO2(acac)2DMF, and UO2(salen)DMF (DMF=N, N-dimethylformamide, acac=acethylacetonate, and salen=N,N′-disalicylidene-ethylenediaminate) complexes in DMF containing tetrabutylammonium perchlorate as supporting electrolyte have been carried out by using cyclic voltammetry to compare the stabilities of the reduction products of U(Vi) complexes with unidentate or multidentate ligands. The [UO2(DMF)5]2+, UO2(acac)2DMF, and UO2(salen)DMF complexes were
Paragangliomas rarely originate from the pancreas and they are characterized on imaging studies as well-marginated, hypervascular masses with cystic areas. We herein report on a case report of pancreatic paraganglioma in a 57-year-old woman, which was confirmed on pathology. Color Doppler ultrasonography and dynamic CT demonstrated a well-demarcated, extremely hypervascular mass with prominent intratumoral vessels and early contrast filling of the draining veins from the mass. Endoscopic retrogr
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