简介:摘要:目的:研究急性心力衰竭的重症护理干预措施及效果分析;方法:本次研究选取2020年5月至2021年5月于我院治疗急性心力衰竭的66例患者作为本次研究对象,并选用抽样法将其分为对照组与研究组,每组各33例,对照组应用常规护理方式,研究组以常规护理为基础进行重症护理干预措施,在护理完成后对两组患者的生活质量评分、护理满意度进行对比。结果:研究组生活质量评分显著高于对照组,且再入院率低于对照组。同时研究组服药依从性及满意度显著优于对照组,差异较大,存在统计学意义(P<0.05)。结论:将重症护理应用至急性心力衰竭患者治疗中可有效提升抢救成功率,提高患者生活质量,值得在临床中推广应用。
简介:像使用费的受体(TLR)是主人防卫系统的哨兵,它认出很多微生物引起的病原体。主机防卫系统可能是低效的或如果由TLR和随后的被触发TLR的cytokine生产的微生物引起的识别是deregulated,煽动性的疾病可以发展。激活抄写因素4(ATF4),ATF/CREB抄写因素家庭的一个成员,是参予几个pathophysiological过程的一个重要因素。在这份报告,我们发现ATF4也涉及调停TLR的天生的有免疫力的反应,它参予TLR4信号transduction并且调停许多cytokines的分泌物。我们观察到ATF4被激活并且translocates到经由TLR4-MyD88-dependent小径跟随lipopolysaccharide(LPS)刺激的原子核。另外,cytokine数组试金证明某关键煽动性的cytokines例如IL-6,IL-8和RANTES,被ATF4断然调整。我们也证明c6月直接绑在ATF4,从而支持煽动性的cytokines的分泌物。一起拿,这些结果显示ATF4在被触发TLR4的cytokine充当一个积极管理者生产。
简介:AbstractLeucine-rich repeats containing 4 (LRRC4, also named netrin-G ligand 2 [NGL-2]) is a member of the NetrinGs ligands (NGLs) family. As a gene with relatively high and specific expression in brain, it is a member of the leucine-rich repeat superfamily and has been proven to be a suppressor gene for gliomas, thus being involved in gliomagenesis. LRRC4 is the core of microRNA-dependent multi-phase regulatory loops that inhibit the proliferation and invasion of glioblastoma (GB) cells, including LRRC4/NGL2-activator protein 2 (AP2)-microRNA (miR) 182-LRRC4 and LRRC4-miR185-DNA methyltransferase 1 (DNMT1)-LRRC4/specific protein 1 (SP1)-DNMT1-LRRC4. In this review, we demonstrated LRRC4 as a new member of the partitioning-defective protein (PAR) polarity complex that promotes axon differentiation, mediates the formation and plasticity of synapses, and assists information input to the hippocampus and storage of memory. As an important synapse regulator, aberrant expression of LRRC4 has been detected in autism, spinal injury and GBs. LRRC4 is a candidate susceptibility gene for autism and a neuro-protective factor in spinal nerve damage. In GBs, LRRC4 is a novel inhibitor of autophagy, and an inhibitor of protein-protein interactions involving in temozolomide resistance, tumor immune microenvironment, and formation of circular RNA.
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