18 research outputs found

    Neuroprotective Effect of β-Caryophyllene on Cerebral Ischemia-Reperfusion Injury via Regulation of Necroptotic Neuronal Death and Inflammation: In Vivo and in Vitro

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    Necrotic cell death is a hallmark feature of ischemic stroke and it may facilitate inflammation by releasing intracellular components after cell-membrane rupture. Previous studies reported that β-caryophyllene (BCP) mitigates cerebral ischemia-reperfusion (I/R) injury, but the underlying mechanism remains unclear. We explored whether BCP exerts a neuroprotective effect in cerebral I/R injury through inhibiting necroptotic cell death and inflammation. Primary neurons with and without BCP (0.2, 1, 5, 25 μM) treatment were exposed to oxygen-glucose deprivation and re-oxygenation (OGD/R). Neuron damage, neuronal death type and mixed lineage kinase domain-like (MLKL) protein expression were assessed 48 h after OGD/R. Furthermore, mice underwent I/R procedures with or without BCP (8, 24, 72 mg/kg, ip.). Neurologic dysfunction, cerebral infarct volumes, cell death, cytokine levels, necroptosis core molecules, and HMGB1-TLR4 signaling were determined at 48 h after I/R. BCP (5 μM) significantly reduced necroptotic neurons and MLKL protein expression following OGD/R. BCP (24, 72 mg/kg, ip.) reduced infarct volumes, neuronal necrosis, receptor-interaction protein kinase-1 (RIPK1), receptor-interaction protein kinase-3 (RIPK3) expression, and MLKL phosphorylation after I/R injury. BCP also decreased high-mobility group box 1 (HMGB1), toll-like receptor 4 (TLR4), interleukin-1β (IL-1β), and tumor necrosis factor-α (TNF-α) levels. Thus, BCP alleviates ischemic brain damage potentially by inhibiting necroptotic neuronal death and inflammatory response. This study suggests a novel application for BCP as a neuroprotective agent

    Preparation of aromatic polyamide with ultra-high intrinsic breakdown strength via layered stacking structure induced by coplanar monomer

    No full text
    Dielectric polymers with high breakdown strength (Eb) and high retention rate of breakdown strength at elevated temperature have important application potential in advanced electrical insulation devices. Herein, the aromatic heterocyclic diamine monomer, 5-amino-2-(2-hydroxy-4-aminobenzene)-benzoxazole (HBOA), was synthesized. Theoretical calculation and single crystal date demonstrated fully the formation of intramolecular H-bond of OH?N]C between benzoxazole and benzene ring in HBOA, which endows the monomer a coplanar geometry. Moreover, the aromatic polyamide films were prepared by polycondensation of HBOA, and the in -plane orientation of films increases with increasing the coplanar HBOA content, which reduces the orientation confusion and cavity of chains packing. When the HBOA content is over 70%, the films exhibit dense-layered stacking structure with high crystallinity. It is found that the dense-layered stacking structure can prevent the films breakdown and failure effectively, which endows the homopolymerization (HBOA-100) film with Eb of 771 kV/mm. Moreover, the Eb of the HBOA-100 film is still as high as 634 kV/mm at 150 ?C, and its retention rate of Eb reaches 82% in high temperature environment. In addition, tensile strength of the HBOA-100 film is nearly 343 MPa, glass transition temperature is about 334 ?C and the thermal stability up to 487 ?C

    Preparation of aromatic polyamide with ultra-high intrinsic breakdown strength via layered stacking structure induced by coplanar monomer

    No full text
    Dielectric polymers with high breakdown strength (Eb) and high retention rate of breakdown strength at elevated temperature have important application potential in advanced electrical insulation devices. Herein, the aromatic heterocyclic diamine monomer, 5-amino-2-(2-hydroxy-4-aminobenzene)-benzoxazole (HBOA), was synthesized. Theoretical calculation and single crystal date demonstrated fully the formation of intramolecular H-bond of OH?N]C between benzoxazole and benzene ring in HBOA, which endows the monomer a coplanar geometry. Moreover, the aromatic polyamide films were prepared by polycondensation of HBOA, and the in -plane orientation of films increases with increasing the coplanar HBOA content, which reduces the orientation confusion and cavity of chains packing. When the HBOA content is over 70%, the films exhibit dense-layered stacking structure with high crystallinity. It is found that the dense-layered stacking structure can prevent the films breakdown and failure effectively, which endows the homopolymerization (HBOA-100) film with Eb of 771 kV/mm. Moreover, the Eb of the HBOA-100 film is still as high as 634 kV/mm at 150 ?C, and its retention rate of Eb reaches 82% in high temperature environment. In addition, tensile strength of the HBOA-100 film is nearly 343 MPa, glass transition temperature is about 334 ?C and the thermal stability up to 487 ?C
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