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Dai-Huang-Fu-Zi-Tang alleviates pulmonary and intestinal injury with severe acute pancreatitis via regulating aquaporins in rats

机译:戴黄附子汤通过调节水通道蛋白减轻大鼠重症急性胰腺炎的肺肠损伤

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Background Dai-Huang-Fu-Zi-Tang (DHFZT) is a famous traditional Chinese prescription with intestinal obstruction, acute pancreatitis and cholecystalgia for thousands of years. Our previous work found that DHFZT could act against pulmonary and intestinal pathological injury in rats with severe acute pancreatitis (SAP). But the underlying mechanism has not been fully elucidated. The aim of present study was to investigate whether DHFZT could relieve pulmonary and intestinal injury by regulating aquaporins after SAP induced by sodium taurocholate in rats. Methods Forty of SD rats were used for dose dependant experiments of DHFZT.Accurate-mass Time-of-flight liquid chromatography-mass spectrometry was used for qualitative screening of chemical compositions of DHFZT. Twenty-four rats were randomly divided into 3 groups: sham group ( n =?8), model group (SAP, n =?8), DHFZT group (SAP with DHFZT treatment, n =?8). SAP models were established by retrograde injections of 5% sodium taurocholate solutions into rat pancreaticobiliary ducts. Blood samples were taken at 0, 12, 24, 48?h post-operation for detecting serum amylase, lipase, endotoxin, TNF-α, IL-6 and IL-10. Protein expression and location of aquaporin (AQP)1, 5, 8 and 9 were assessed by immunohistochemistry, western blot and immunofluorescence respectively. Results The study showed that 27 kinds of chemical composition were identified, including 10 kinds in positive ion mode and 17 kinds in negative ion mode. The results showed that AQP1, AQP5 of lung, and AQP1, AQP5, AQP8 of intestine in model group were significantly lower than that of sham group ( P Conclusions DHFZT ameliorated the pulmonary and intestinal edema and injury induced by SAP via the upregulation of different AQPs in lung and intestine, and suppressed TNF-α, IL-6 expression and enhanced IL-10 expression.
机译:背景大黄附子汤(DHFZT)是一种著名的中医处方,具有肠梗阻,急性胰腺炎和胆囊痛已有数千年的历史。我们以前的工作发现,DHFZT可以预防重症急性胰腺炎(SAP)大鼠的肺和肠道病理损伤。但是尚未完全阐明其潜在机制。本研究的目的是研究DHFZT是否可以通过调节牛磺胆酸钠引起的SAP后水通道蛋白的表达来减轻肺和肠损伤。方法40只SD大鼠用于DHFZT的剂量依赖性实验,准确质量飞行时间液相色谱-质谱法定性筛选DHFZT的化学成分。 24只大鼠随机分为3组:假手术组(n =?8),模型组(SAP,n =?8),DHFZT组(SAP DHFZT治疗,n =?8)。通过向大鼠胰胆管逆行注射5%牛磺胆酸钠溶液来建立SAP模型。术后0、12、24、48小时采血,以检测血清淀粉酶,脂肪酶,内毒素,TNF-α,IL-6和IL-10。通过免疫组织化学,蛋白质印迹和免疫荧光分别评估水通道蛋白(AQP)1、5、8和9的蛋白表达和位置。结果研究表明,共鉴定出27种化学成分,其中正离子模式为10种,负离子模式为17种。结果表明,模型组的肺AQP1,AQP5和肠的AQP1,AQP5,AQP8明显低于假手术组(P结论DHFZT通过上调不同的AQPs减轻了SAP引起的肺和肠水肿和损伤。可以抑制肺和肠中的TNF-α,IL-6表达并增强IL-10表达。

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