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Nafamostat mesylate attenuates the pathophysiologic sequelae of neurovascular ischemia 被引量:4
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作者 george zaki ghali Michael george zaki ghali 《Neural Regeneration Research》 SCIE CAS CSCD 2020年第12期2217-2234,共18页
Nafamostat mesylate,an apparent soi-disant panacea of sorts,is widely used to anticoagulate patients undergoing hemodialysis or cardiopulmonary bypass,mitigate the inflammatory response in patients diagnosed with acut... Nafamostat mesylate,an apparent soi-disant panacea of sorts,is widely used to anticoagulate patients undergoing hemodialysis or cardiopulmonary bypass,mitigate the inflammatory response in patients diagnosed with acute pancreatitis,and reverse the coagulopathy of patients experiencing the commonly preterminal disseminated intravascular coagulation in the Far East.The serine protease inhibitor nafamostat mesylate exhibits significant neuroprotective effects in the setting of neurovascular ischemia.Nafamostat mesylate generates neuroprotective effects by attenuating the enzymatic activity of serine proteases,neuroinflammatory signaling cascades,and the endoplasmic reticulum stress responses,downregulating excitotoxic transient receptor membrane channel subfamily 7 cationic currents,modulating the activity of intracellular signal transduction pathways,and supporting neuronal survival brain-derived neurotrophic factor/TrkB/ERK1/2/CREB,nuclear factor kappa B.The effects collectively reduce neuronal necrosis and apoptosis and prevent ischemia mediated disruption of blood-brain barrier microarchitecture.Investigational clinical applications of these compounds may mitigate ischemic reperfusion injury in patients undergoing cardiac,hepatic,renal,or intestinal transplant,preventing allograft rejection,and treating solid organ malignancies.Neuroprotective effects mediated by nafamostat mesylate support the wise conduct of randomized prospective controlled trials in Western countries to evaluate the clinical utility of this compound. 展开更多
关键词 apoptosis cerebrovascular EXCITOTOXICITY infarction ISCHEMIA nafamostat mesylate necrosis neuroprotection serine protesae subarachnoid hemorrhage
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Spinal genesis of Mayer waves 被引量:1
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作者 george zaki ghali Michael george zaki ghali Emil zaki ghali 《Neural Regeneration Research》 SCIE CAS CSCD 2020年第10期1821-1830,共10页
Variability in cardiovascular spectra was first described by Stephan Hales in 1733.Traube and Hering initially noted respirophasic variation of the arterial pressure waveform in 1865 and Sigmund Mayer noted a lower fr... Variability in cardiovascular spectra was first described by Stephan Hales in 1733.Traube and Hering initially noted respirophasic variation of the arterial pressure waveform in 1865 and Sigmund Mayer noted a lower frequency oscillation of the same in anesthetized rabbits in 1876.Very low frequency oscillations were noted by Barcroft and Nisimaru in 1932,likely representing vasogenic autorhythmicity.While the origins of Traube Hering and very low frequency oscillatory variability in cardiovascular spectra are well described,genesis mechanisms and functional significance of Mayer waves remain in controversy.Various theories have posited baroreflex and central supraspinal mechanisms for genesis of Mayer waves.Several studies have demonstrated the persistence of Mayer waves following high cervical transection,indicating a spinal capacity for genesis of these oscillations.We suggest a general tendency for central sympathetic neurons to oscillate at the Mayer wave frequency,the presence of multiple Mayer wave oscillators throughout the brainstem and spinal cord,and possible contemporaneous genesis by baroreflex and vasomotor mechanisms. 展开更多
关键词 Mayer waves GENESIS origins CENTRAL sympathogenesis spinal cord CERVICAL TRANSECTION
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