曲美他嗪对冠心病合并左心功能不全的效果

目的 探讨冠心病合并左心功能不全患者行曲美他嗪治疗的临床效果.方法 选择医院于2016年3月—2017年4月期间接收的老年冠心病合并左心功能不全患者60例,采用随机数字表法形式均分为研究组和对照组,每组均30例.对照组行基础治疗,研究组在此基础上口服曲美他嗪,记录两组心功能指标以及不良反应发生率.结果 研究组治疗后LVEDD、LVESD指标低于对照组,左心室射血分数高于对照组(P<0.05);研究组和对照组在用药过程中均未出现严重的反应,研究组出现3例转氨酶上升,2例胃肠道不适;对照组出现2例转氨酶上升,组间对比P<0.05.结论 曲美他嗪行冠心病合并左心功能不全治疗效果明显,心肌功能以及血脂水平有所改善.     

Resveratrol improves the therapeutic efficacy of bone marrow-derived mesenchymal stem cells in rats with severe acute pancreatitis

ObjectiveBone marrow-derived mesenchymal stem cells (BMSCs) are effective in the treatment of severe acute pancreatitis (SAP), but their therapeutic effects could still be improved. In order to optimize the clinical application of BMSCs, we adopted the strategy of resveratrol (Res) pretreatment of BMSCs (Res-BMSCs) and applied it to a rat model of sodium taurocholate (NaT)-induced acute pancreatitis.MethodsSAP was induced by injection of 3% NaT into the pancreatic duct and successful induction of SAP occurred after 12 h. Rats were treated with BMSCs, Res or BMSCs primed with Res at 40 mmol/L, Vandetanib (ZD6474) daily oral dosages of 50 mg/kg vandetanib.ResultsRes stimulated BMSCs to secrete vascular endothelial growth factor A (VEGFA), activated the downstream phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K)/protein kinase B (AKT) signaling pathway, and inhibited pancreatic cell apoptosis. In addition, conditioned medium (CM) from Res-BMSCs enhanced the proliferation of human umbilical vein endothelial cells (HUVECs) in vitro, increased resistance to apoptosis and promoted the expression of angiogenesis-related proteins CD31, VEGF and VEGFR2 in pancreatic tissue, but Vandetanib partly abolished these effects by blocking the VEGFA- mediated pathway.ConclusionResveratrol-preprocessed BMSCs can activate the PI3K/AKT signaling pathway in pancreatic cells and HUVECs through paracrine release of VEGFA; thus, achieving the therapeutic effect of resisting apoptosis of pancreatic cells and promoting regeneration of damaged blood vessels. Res pretreatment may be a new strategy to improve the therapeutic effect of BMSCs on SAP.     

Role and mechanism of angiotensin-converting enzyme 2 in acute lung injury in coronavirus disease 2019

Coronavirus disease 2019 is a major threat to public health globally. Though its pathogenesis has not been fully elucidated, angiotensin-converting enzyme 2 (ACE2) has been recently identified as a receptor for the entry of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) into the cell. Here, we aimed to clarify the potential role of ACE2 in SARS-CoV-2-induced acute lung injury and its underlying mechanism. As a receptor for coronavirus, ACE2 mediates the entry of SARS-CoV-2 into cells in a similar way as for severe acute respiratory syndrome coronavirus (SARS-CoV). The high binding affinity of SARS-CoV-2 to ACE2 correlates with its efficient spread among humans. On the other hand, ACE2 negatively regulates the renin-angiotensin-aldosterone system (RAAS) primarily by converting angiotensin II to angiotensin 1–7, which exerts a beneficial effect on coronavirus-induced acute lung injury. Human recombinant ACE2 has been considered as a potential therapy for SARS-CoV-2 by blocking virus entry and redressing the imbalance of RAAS in SARS-CoV-2 infection. The level of ACE2 expression can be upregulated by treatment with an ACE inhibitor (ACEI) or angiotensin Ⅱ type 1 receptor blocker (ARB). To date, no evidence shows that ACEIs or ARBs increase the susceptibility and mortality of patients infected with SARS-CoV-2, and hence, it is not advisable to discontinue such drugs in patients with cardiovascular disease.     

血管紧张素转换酶2对儿童2019冠状病毒病的作用研究进展

随着严重急性呼吸综合征冠状病毒2（SARS-CoV-2）在全球的肆虐，儿童感染者人数也越来越多。血管紧张素转换酶2（ACE2）是SARS-CoV-2感染人体的结合位点之一，可以与病毒尖峰蛋白结合，使得跨膜丝氨酸蛋白酶（TMPRSS2）启动S蛋白触发感染，引起白细胞介素-1、干扰素-γ、肿瘤坏死因子等多种炎性因子的产生。与成人相比，儿童的ACE2及TMPRSS2的表达水平较低，推测儿童症状较成人轻，发病人数较成人少均与此有关。该综述对SARS-CoV-2感染过程中ACE2的作用研究进展进行总结，有助于了解SARS-CoV-2的致病机制，为更好地开发药物及疫苗，防治儿童2019冠状病毒病提供参考。     

Patent ductus arteriosus and cerebral,cardiac, and gut hemodynamics in premature neonates

Patent ductus arteriosus is associated with multiple comorbidities in premature infants, however a causal link or strategy to decrease these morbidities has not been found. The association between the patent ductus arteriosus and morbidities has biologic plausibility as, like any cardiac mixing lesion, a significant systemic to pulmonic shunt may lead to pulmonary over-circulation and systemic hypoperfusion. Understanding the underlying pathophysiology of associated morbidities in the setting of a patent ductus arteriosus may aid in risk stratifying infants and offer a patient targeted approach to infants with a pathological ductal shunt. While the deleterious impact of increased pulmonary blood flow maybe easier to identify, the impact on end-organ perfusion is more challenging. In this review, we will discuss the pathophysiology of a hemodynamically significant patent ductus arteriosus in premature infants, impact on end-organ perfusion and associated morbidities, and novel modalities to assess shunt volume and effect on end-organ perfusion.     

经皮肺动脉瓣植入术在肺动脉瓣反流患者中的临床应用

经皮肺动脉瓣植入术(PPVI)在我国作为一种新兴的技术,开展相对较晚,但随着我国医疗水平的不断提高以及临床对于右心室流出道梗阻的先天性心脏病患者术后出现重度肺动脉瓣反流的不断重视,PPVI在我国得到了飞速发展。近十几年来,欧美国家已在临床成熟应用PPVI,相对于传统外科手术而言其具有微创、可重复性、术后疗效好等优点。现对PPVI在肺动脉瓣反流患者中的临床应用进行叙述。     

奥曲肽和垂体后叶素治疗肝硬化上消化道出血的疗效对比

目的对比奥曲肽和垂体后叶素治疗肝硬化上消化道出血的疗效。方法选取我院2017年8月至2019年2月收治的肝硬化上消化道出血患者100例,随机分为对照组和观察组各50例。对照组采用垂体后叶素治疗,观察组采用奥曲肽治疗,比较两组的止血时间、住院时间、不良反应发生率及治疗前后的血清胰高血糖素水平。结果观察组的止血时间、住院时间均明显短于对照组(P<0.05)。治疗后,观察组的血清胰高血糖素水平明显低于对照组(P<0.05)。观察组的不良反应发生率为14.00%,明显低于对照组的50.00%(P<0.05)。结论与垂体后叶素比较,采用奥曲肽治疗肝硬化上消化道出血患者可更加快速止血,降低机体胰高血糖素水平及不良反应发生率,值得临床推广。