In this study, we established a Wistar rat model of right middle cerebral artery occlusion and observed pathological imaging changes （T2-weighted imaging [T2WI], T2FLAIR, and diffusion-weighted imaging [DWI]） follow...In this study, we established a Wistar rat model of right middle cerebral artery occlusion and observed pathological imaging changes （T2-weighted imaging [T2WI], T2FLAIR, and diffusion-weighted imaging [DWI]） following cerebral infarction. The pathological changes were divided into three phases： early cerebral infarction, middle cerebral infarction, and late cerebral infarction. In the early cerebral infarction phase （less than 2 hours post-infarction）, there was evidence of intracellular edema, which improved after reperfusion. This improvement was defined as the ischemic penumbra. In this phase, a high DWI signal and a low apparent diffusion coefficient were observed in the right basal ganglia region. By contrast, there were no abnormal T2WI and T2FLAIR signals. For the middle cerebral infarction phase （2-4 hours post-infarction）, a mixed edema was observed. After reperfusion, there was a mild improvement in cell edema, while the angioedema became more serious. A high DWI signal and a low apparent diffusion coefficient signal were observed, and some rats showed high T2WI and T2FLAIR signals. For the late cerebral infarction phase （4-6 hours post-infarction）, significant angioedema was visible in the infarction site. After reperfusion, there was a significant increase in angioedema, while there was evidence of hemorrhage and necrosis. A mixed signal was observed on DWI, while a high apparent diffusion coefficient signal, a high T2WI signal, and a high T2FLAIR signal were also observed. All 86 cerebral infarction patients were subjected to T2WI, T2FLAIR, and DWI. MRI results of clinic data similar to the early infarction phase of animal experiments were found in 51 patients, for which 10 patients （10/51） had an onset time greater than 6 hours. A total of 35 patients had MRI results similar to the middle and late infarction phase of animal experiments, of which eight patients （8/35） had an onset time less than 6 hours. These data suggest that defining the ＂therapeutic time window＂ as the time 6 hours after infarction may not be suitable for all patients. Integrated application of MRI sequences including T2WI, T2FLAIR, DW-MRI, and apparent diffusion coefficient mapping should be used to examine the ischemic penumbra, which may provide valuable information for identifying the ＂therapeutic time window＂.展开更多
Humans and plants have become enfolded and inseparable.Abiotic stresses in particular oxidative stress caused by heavy-metal ions or high-level salt contamination deleteriously impact plants’growth process and have b...Humans and plants have become enfolded and inseparable.Abiotic stresses in particular oxidative stress caused by heavy-metal ions or high-level salt contamination deleteriously impact plants’growth process and have become a major threat to sustaining food security.Sprouting is the first step in plants’growth process.When plant sprouts endure oxidative stress induced by toxic heavy-metal ions or high-level salt,accelerated generation of reactive oxygen species(e.g.,H_(2)O_(2))occurs inside plant sprouts;hence in-situ H_(2)O_(2) in plant sprouts could serve as the in-vivo biomarker for tracking the oxidative stress in plant sprouts.Herein,we design an activatable probe CT-XA-H_(2)O_(2) to track the oxidative stress in plant sprouts via in vivo NIR-Ⅱ fluorescent imaging.In CT-XA-H_(2)O_(2),cyano-thiazole acts as the electron-accepting moiety and xanthane-aminodiphenyl as the electron-donating moiety,and dioxaborolane as the biomarker-responsive unit and fluorescence quencher.The probe CT-XA-H_(2)O_(2) shows weak fluorescent emission.When H_(2)O_(2) is present,the dioxaborolane in the probe is cleaved,consequently,the dye CT-XA-OH is generated and brings about significant fluorescent signals for detecting and imaging the in-situ biomarker.Moreover,the aminodiphenyl group endues the chromophore(the activated probe)with aggregation-induced emission characteristics,which ensures stronger fluorescence in the aggregated state in the aqueous milieu.The probe CT-XA-H_(2)O_(2) has been employed in the Cd^(2+)-ion or high-level salt(NaCl)induced oxidative stress models of soybean sprouts and peanut sprouts,and the experimental results evidently reveal the probe’s ability for in-situ biomarker-activatable in-vivo detection and imaging in the plants’sprouts.展开更多
基金supported by the National Natural Science Foundation of China,No.30960399,and No.81160181
文摘In this study, we established a Wistar rat model of right middle cerebral artery occlusion and observed pathological imaging changes （T2-weighted imaging [T2WI], T2FLAIR, and diffusion-weighted imaging [DWI]） following cerebral infarction. The pathological changes were divided into three phases： early cerebral infarction, middle cerebral infarction, and late cerebral infarction. In the early cerebral infarction phase （less than 2 hours post-infarction）, there was evidence of intracellular edema, which improved after reperfusion. This improvement was defined as the ischemic penumbra. In this phase, a high DWI signal and a low apparent diffusion coefficient were observed in the right basal ganglia region. By contrast, there were no abnormal T2WI and T2FLAIR signals. For the middle cerebral infarction phase （2-4 hours post-infarction）, a mixed edema was observed. After reperfusion, there was a mild improvement in cell edema, while the angioedema became more serious. A high DWI signal and a low apparent diffusion coefficient signal were observed, and some rats showed high T2WI and T2FLAIR signals. For the late cerebral infarction phase （4-6 hours post-infarction）, significant angioedema was visible in the infarction site. After reperfusion, there was a significant increase in angioedema, while there was evidence of hemorrhage and necrosis. A mixed signal was observed on DWI, while a high apparent diffusion coefficient signal, a high T2WI signal, and a high T2FLAIR signal were also observed. All 86 cerebral infarction patients were subjected to T2WI, T2FLAIR, and DWI. MRI results of clinic data similar to the early infarction phase of animal experiments were found in 51 patients, for which 10 patients （10/51） had an onset time greater than 6 hours. A total of 35 patients had MRI results similar to the middle and late infarction phase of animal experiments, of which eight patients （8/35） had an onset time less than 6 hours. These data suggest that defining the ＂therapeutic time window＂ as the time 6 hours after infarction may not be suitable for all patients. Integrated application of MRI sequences including T2WI, T2FLAIR, DW-MRI, and apparent diffusion coefficient mapping should be used to examine the ischemic penumbra, which may provide valuable information for identifying the ＂therapeutic time window＂.
基金NSFC,Grant/Award Numbers:21788102,21875069the Fund of Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates,Grant/Award Number:2019B030301003。
文摘Humans and plants have become enfolded and inseparable.Abiotic stresses in particular oxidative stress caused by heavy-metal ions or high-level salt contamination deleteriously impact plants’growth process and have become a major threat to sustaining food security.Sprouting is the first step in plants’growth process.When plant sprouts endure oxidative stress induced by toxic heavy-metal ions or high-level salt,accelerated generation of reactive oxygen species(e.g.,H_(2)O_(2))occurs inside plant sprouts;hence in-situ H_(2)O_(2) in plant sprouts could serve as the in-vivo biomarker for tracking the oxidative stress in plant sprouts.Herein,we design an activatable probe CT-XA-H_(2)O_(2) to track the oxidative stress in plant sprouts via in vivo NIR-Ⅱ fluorescent imaging.In CT-XA-H_(2)O_(2),cyano-thiazole acts as the electron-accepting moiety and xanthane-aminodiphenyl as the electron-donating moiety,and dioxaborolane as the biomarker-responsive unit and fluorescence quencher.The probe CT-XA-H_(2)O_(2) shows weak fluorescent emission.When H_(2)O_(2) is present,the dioxaborolane in the probe is cleaved,consequently,the dye CT-XA-OH is generated and brings about significant fluorescent signals for detecting and imaging the in-situ biomarker.Moreover,the aminodiphenyl group endues the chromophore(the activated probe)with aggregation-induced emission characteristics,which ensures stronger fluorescence in the aggregated state in the aqueous milieu.The probe CT-XA-H_(2)O_(2) has been employed in the Cd^(2+)-ion or high-level salt(NaCl)induced oxidative stress models of soybean sprouts and peanut sprouts,and the experimental results evidently reveal the probe’s ability for in-situ biomarker-activatable in-vivo detection and imaging in the plants’sprouts.
