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先天性心脏病并肺动脉高压患者血清MMP-2,TIMP-2水平变化及其意义 被引量:2
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作者 樊芳 赵延恕 +2 位作者 吕晓玲 段纬喆 聂赛 《医学临床研究》 CAS 2009年第11期2074-2077,共4页
【目的】探讨先天性心脏病(CHD)并肺动脉高压(PH)患者血清基质金属蛋白酶(MMP-2)、金属蛋白酶组织抑制物(TIMP-2)水平的变化及其意义。[方法]40例左向右分流型CHD患者按肺动脉主干收缩压(SPAP)分为4组:非PH组11例(SPAP〈4.... 【目的】探讨先天性心脏病(CHD)并肺动脉高压(PH)患者血清基质金属蛋白酶(MMP-2)、金属蛋白酶组织抑制物(TIMP-2)水平的变化及其意义。[方法]40例左向右分流型CHD患者按肺动脉主干收缩压(SPAP)分为4组:非PH组11例(SPAP〈4.0 kPa)、轻度PH纽11例(4.0 kPa≤SPAP〈5.33 kPa)、中度PH组11例(5.33kPa≤SPAP〈9.33kPa)、重度PH组7例(SPAP≥9.33kPa)。选8例同期心内科行射频消融术患者为健康对照组。用ELISA检测其血清MMP-2和TIMP-2水平,并计算MMP-2/TIMP-2比值。【结果】①与对照组比较,CHD组MMP一2、TIMP一2和MMP-2/TIMP-2均显著增高(P〈0.01)。②非PH、轻和中、重度PH组MMP-2与对照组比较均显著增高(P〈0.01)。轻和中、重度PH组TIMP-2与对照组比较均显著增高。非PH、轻和中度PH组MMP-2/TIMP-2与对照组比较均显著增高③与非PH组比较,PH组MMP-2、TIMP-2(P〈0.01)与MMP-2/TIMP-2(P〈0.05)均增高④MMP-2与TIMP-2呈显著正相关(r=0.38,P〈0.01),TIMP-2与MMP-2/TIMP-2呈显著负相关(r=0.38,P〈0.01)。⑤CHD组下腔静脉的血清MMP-2、TIMP-2和MMP-2/TIMP-2与肺动脉相比,差异没有统计学意义(P〉0.05)。【结论】①左向右分流型CHD血清MMP-2的显著增高,且并PH患者血清TIMP-2显著升高,TIMp-2与MMP-2/TIMP-2呈显著负相关,提示MMP-2和TIMP-2参与肺血管重构全过程。②本实验将为延缓肺动脉高压形成或肺动脉高压逆转的深入研究提供一定的理论根据。 展开更多
关键词 心脏缺损 先天性/病理学 心脏缺损 先天性/并发症 高血压 肺性/病理学 高血压 肺性/并发症 金属蛋白酶类/血液 金属蛋白酶1组织抑制剂/血液
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先天性肾积水组织的超微结构及CTGF表达定位的电镜观察 被引量:2
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作者 窘产信 刘永东 +4 位作者 李俊峰 张传光 张广平 商希峰 胡强 《中国医师杂志》 CAS 2016年第9期1393-1395,共3页
目的研究肾盂输尿管连接部梗阻(UPJO)引起的先天性肾积水组织的超微结构变化及结缔组织生长因子(CTGF)在先天性肾积水中的表达定位。方法分别留取肾积水患儿5例、对照组2例组织标本,先用透射电镜观察超微结构的变化,再用胶体金做... 目的研究肾盂输尿管连接部梗阻(UPJO)引起的先天性肾积水组织的超微结构变化及结缔组织生长因子(CTGF)在先天性肾积水中的表达定位。方法分别留取肾积水患儿5例、对照组2例组织标本,先用透射电镜观察超微结构的变化,再用胶体金做示踪物对病变组织进行免疫电镜观察,观察标记物所在位置,了解其在不同组织表达的差异性。结果透射电镜:积水肾实质细胞核间隙局部增宽,滤过膜的基质局部变薄、裂孔膜部分缺如、细胞核核型、核仁不规则,有较多自噬体。免疫电镜:CTGF在患肾的肾实质、肾盂、肾盂输尿管连接处狭窄段中的表达均明显增高,成纤维细胞细胞超微结构清晰,金颗粒呈团状、点灶状分布,特异性强,CTGF蛋白阳性标记主要位于粗面内质网、细胞核、核膜、线粒体等部位。结论先天性肾积水的形成与组织纤维化密切相关,CTGF与先天性肾积水的形成之间有相关性,在其发病过程中可能发挥重要作用。 展开更多
关键词 肾盂积水/先天性/代谢/病理学 胞间信号肽类和蛋白质类/代谢 显微镜检查 电子
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Antiviral innate immunity pathways 被引量:49
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作者 Rashu B Seth Lijun Sun Zhijian J Chen 《Cell Research》 SCIE CAS CSCD 2006年第2期141-147,共7页
Recent studies have uncovered two signaling pathways that activate the host innate immunity against viral infection. One of the pathways utilizes members of the Toll-like receptor (TLR) family to detect viruses that... Recent studies have uncovered two signaling pathways that activate the host innate immunity against viral infection. One of the pathways utilizes members of the Toll-like receptor (TLR) family to detect viruses that enter the endosome through endocytosis. The TLR pathway induces interferon production through several signaling proteins that ultimately lead to the activation of the transcription factors NF-kB, IRF3 and IRFT. The other antiviral pathway uses the RNA helicase RIG-Ⅰ as the receptor for intracellular viral double-stranded RNA. RIG-Ⅰ activates NF-kB and IRFs through the recently identified adaptor protein MAVS, a CARD domain containing protein that resides in the mitochondrial membrane. MAVS is essential for antiviral innate immunity, but it also serves as a target of Hepatitis C virus (HCV), which employs a viral protease to cleave MAVS off the mitochondria, thereby allowing HCV to escape the host immune system. 展开更多
关键词 INTERFERON Toll-like receptor RIG-Ⅰ MAVS MITOCHONDRIA NF-KB IRF
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Enteric neuropathology of congenital intestinal obstruction:A case report 被引量:4
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作者 Giovanni Di Nardo Vincenzo Stanghellini +12 位作者 Salvatore Cucchiara Giovanni Barbara Gianandrea Pasquinelli Donatella Santini Cristina Felicani Gianluca Grazi Antonio D Pinna Rosanna Cogliandro Cesare Cremon Alessandra Gori Roberto Corinaldesi Kenton M Sanders Roberto De Giorgio 《World Journal of Gastroenterology》 SCIE CAS CSCD 2006年第32期5229-5233,共5页
Experimental evidence indicates that chronic mechanical sub-occlusion of the intestine may damage the enteric nervous system (ENS), although data in humans are lacking. We here describe the first case of enteric deg... Experimental evidence indicates that chronic mechanical sub-occlusion of the intestine may damage the enteric nervous system (ENS), although data in humans are lacking. We here describe the first case of enteric degenerative neuropathy related to a congenital obstruction of the gut. A 3-year and 9-mo old girl began to complain of vomiting, abdominal distension, constipation with air-fluid levels at plane abdominal radiology. Her subsequent medical history was characterized by 3 operations: the first showed dilated duodeno-jejunal loops in the absence of occlusive lesions; the second (2 years later) was performed to obtain full-thickness biopsies of the dilated intestinal loops and revealed hyperganglionosis at histopathology; the third (9 years after the hyperganglionosis was identified) disclosed a Ladd's band which was removed and the associated gut malrotation was corrected. Repeated intraoperative full-thickness biopsies showed enteric degenerative neuropathy along with reduced interstitial cells of Cajal network in dilated loops above the obstruction and a normal neuromuscular layer below the Ladd's band. One year after the latest surgery the patient tolerated oral feeding and did well, suggesting that congenital (partial) mechanical obstruction of the small bowel in humans can evoke progressive adaptive changes of the ENS which are similar to those found in animal models of intestinal mechanical occlusion. Such ENS changes mimic neuronal abnormalities observed in intestinal pseudoobstruction. 展开更多
关键词 Enteric neuropathy Chronic intestinal pseudo-obstruction Congenital intestinal obstruction Ladd's band Enteric nervous system
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A rare case of duodenal duplication treated surgically 被引量:1
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作者 Mehmet Ali Uzun Neset Koksal +3 位作者 Munire Kayahan Atilla Celik Gamze Kilicoglu Selvinaz Ozkara 《World Journal of Gastroenterology》 SCIE CAS CSCD 2009年第7期882-884,共3页
Duodenal duplication,a rare congenital malformation,can also be observed in adulthood.Although it can be cystic or tubular,communicating or non-communicating,cystic and non-communicating forms are the most common.Seve... Duodenal duplication,a rare congenital malformation,can also be observed in adulthood.Although it can be cystic or tubular,communicating or non-communicating,cystic and non-communicating forms are the most common.Several complications,such as obstruction,bleeding,perforation and pancreatitis,may result.Optimal treatment is total excision,although endoscopic procedures have also been described in appropriate cases.If total excision is not possible,subtotal excision and internal derivation can be performed.The 38-year-old woman presented here had occasional attacks of abdominal pain and obstruction,and we considered the diagnosis of duodenal duplication by abdominal computerized tomography.As we confirmed the diagnosis with operative findings and histopathological signs,we treated her with subtotal excision and intraduodenal cystoduodenostomy. 展开更多
关键词 DUODENUM DUPLICATION Subtotal excision Intraduodenal cystoduodenostomy
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