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Gut-derived endotoxin translocation is the main aggravating mechanism of acute severe pancreatitis

机译:肠源性内毒素易位是急性重症胰腺炎的主要加重机制

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Severe acute pancreatitis (SAP) is a serious systemic disease. It exacerbates when complicated with multiple organ dysfunction syndrome or failure (MODS or MOF). However, the aggravating mechanism of SAP is still unknown up to now. Study showed that maintaining integrity of intestinal mucosal barrier function by given effective antibiotics, selective digestive decontamination (SDD) and enteral nutrition therapy to the patients with SAP could significantly reduce infection of pancreatic necrotic tissue and improve the patient's outcome. Combining the findings of gut-derived bacteria in animals' pancreas, liver, spleen, mesenteric lymph nodes with increasing concentration of inflammatory cytokines and endotoxin in plasma with SAP, we hypothesize thatgut-derived endotoxin translocation is the main aggravating mechanism of SAP. The hypothesis holds potential as a target for therapeutic intervention.
机译:重症急性胰腺炎(SAP)是一种严重的全身性疾病。当并发多器官功能障碍综合征或衰竭(MODS或MOF)时,病情恶化。但是,到目前为止,SAP的加重机制仍然未知。研究表明,通过对SAP患者给予有效的抗生素,选择性消化净化(SDD)和肠内营养疗法来维持肠道粘膜屏障功能的完整性,可以显着减少胰腺坏死组织的感染并改善患者的预后。结合动物血浆中胰腺,肝脏,脾脏,肠系膜淋巴结中肠源性细菌的发现与血浆中炎症细胞因子和内毒素浓度的增加,我们推测肠源性内毒素易位是SAP的主要加重机制。该假设具有作为治疗干预目标的潜力。

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