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Relationship between chronic rhinosinusitis and lower airway diseases: An extensive review 被引量:3
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作者 Shin Kariya Mitsuhiro Okano Kazunori Nishizaki 《World Journal of Otorhinolaryngology》 2015年第2期44-52,共9页
Signifcant links between allergic rhinitis and asthma have been reported, and the united airway disease hypothesis is supported by numerous findings in epidemiologic, physiologic, pathologic, and immunologic studies. ... Signifcant links between allergic rhinitis and asthma have been reported, and the united airway disease hypothesis is supported by numerous findings in epidemiologic, physiologic, pathologic, and immunologic studies. The impact of allergic rhinitis on asthma has been esta-blished. On the other hand, the relationship between chronic rhinosinusitis and lung diseases has been under investigation. Chronic rhinosinusitis is a common disease, and the high prevalence of chronic rhinosinusitis in some kinds of lung diseases has been reported. Recent studies suggest that the treatment of chronic rhinosinusitis has beneficial effects in the management of asthma. Here, we present an overview of the current research on the relationship between chronic rhinosinusitis and lower airway diseases including asthma, chronic obstructive pul-monary disease, cystic fibrosis, diffuse panbronchiolitis, primary ciliary dyskinesia, idiopathic bronchiectasis, and allergic bronchopulmonary aspergillosis. 展开更多
关键词 Chronic rhinosinusitis SINUSITIS Asthma Chronic obstructive pulmonary disease Cystic fbrosis Diffuse panbronchiolitis Primary ciliary dyskinesia Idiopathic bronchiectasis Allergic bronchopulmonary aspergillosis
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Antimicrobial lipids:Emerging effector molecules of innate host defense
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作者 Edith Porter Daniel C Ma +1 位作者 Sandy Alvarez Kym F Faull 《World Journal of Immunology》 2015年第2期51-61,共11页
The antimicrobial properties of host-derived derived lipids have become increasingly recognized and evidence is mounting that antimicrobial lipids (AMLs), like antimicrobial peptides, are effector molecules of the i... The antimicrobial properties of host-derived derived lipids have become increasingly recognized and evidence is mounting that antimicrobial lipids (AMLs), like antimicrobial peptides, are effector molecules of the innate immune system and are regulated by its conserved pathways. This review, with primary focus on the human body, provides some background on the biochemistry of lipids, summarizes their biological functions, expands on their antimicrobial properties and site-specifc composition, presents modes of synergism with antimicrobial peptides, and highlights the more recent reports on the regulation of AML production as well as bacterial resistance mechanisms. Based on extant data a concept of innate epithelial defense is proposed where epithelial cells, in response to microbial products and proinflammatory cytokines and through activation of conserved innate signaling pathways, increase their lipid uptake and up-regulate transcription of enzymes involved in antimicrobial lipid biosynthesis, and induce transcription of antimicrobial peptides as well as cytokines and chemokines. The subsequently secreted antimicrobial peptides and lipids then attack and eliminate the invader, assisted by or in synergism with other antimicrobial molecules delivered by other defense cells that have been recruited to the site of infection, in most of the cases. This review invites reconsideration of the interpretation of cholesteryl ester accumulation in macrophage lipid droplets in response to infection as a solely proinflammatory event, and proposes a direct antimicrobial role of lipid droplet- associated cholesteryl esters. Finally, for the interested, but new- to- the-feld investigator some starting points for the characterization of AMLs are provided. Before it is possible to utilize AMLs for anti-infectious therapeutic and prophylactic approaches, we need to better understand pathogen responses to these lipids and their role in the pathogenesis of chronic infectious disease. 展开更多
关键词 Atopic dermatitis CHOLESTEROL Infectious disease Cystic fbrosis MUCOSA
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Protective effect of fu-qi granule on carbon tetrachloride-induced liver fibrosis in rats
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作者 Lin Zhong Yan-Ling Sun +8 位作者 Wen-Li Shi Xiao Ma Zhe Chen Jia-Bo Wang Rui-Sheng Li Xue-Ai Song Hong-Hong Liu Yan-Ling Zhao Xiao-He Xiao 《World Journal of Pharmacology》 2015年第2期227-235,共9页
AIM: To investigate the effcacy of fu-qi granule (FQG) on carbon tetrachloride (CCl4) induced liver fbrosis in rats and the underlying mechanisms. METHODS: Sixty rats were randomly divided into six groups: norm... AIM: To investigate the effcacy of fu-qi granule (FQG) on carbon tetrachloride (CCl4) induced liver fbrosis in rats and the underlying mechanisms. METHODS: Sixty rats were randomly divided into six groups: normal control group, CCl4 induced liver fbrosis group, AnluoHuaxianWan group and three treatment groups of FQG. Treatment of rats with intraperitoneal injection of carbon tetrachloride solution at 0.3 mL per 100 g body weigh twice a week for 8 wk. The normal control group the rats were given the media (olive oil) at the same time. In the frst 2 wk, rats were raised with feedstuff (80% corn meal, 20% lard, 0.5% cholesterol). Serum samples were collected for alanine transaminase, aspartate aminotransferase, alkaline phosphatase, albumin, total protein assay and typical histopathological changes was observed in Hematoxylin-eosin staining sections. Smooth muscle alpha actin (α-SMA) was analyzed with immunohistochemistry. Mammalian target of rapamycin (mTOR) and hypoxia-inducible factor-1 (HIF-1α) expressions were detected by Western blot-ting. Tissue inhibitor of matrix metalloproteinases-1 (TIMP-1) and matrix metalloproteinases-9 (MMP-9) were measured with semi-quantitative reverse transcriptase-polymerase chain reaction.RESULTS: FQG significantly reduced the serum levels of alanine transaminase, aspartate aminotransferase, alkaline phosphatase and increased the serum contents of albumin, total protein in rats with liver fibrosis. Moreover, FQG promoted extracellular matrix degradation by increasing MMP-9 and inhibiting TIMP-1 and α-SMA. mTOR and HIF-1α expression in liver significantly decreased in the rats treated with FQG. CONCLUSION: The results indicated that FQG signi-fcantly reverse fbrosis induced by CCl4, which should be developed as a new and promising preparation for the prevention of liver fbrosis. 展开更多
关键词 Protective effect Fu-qi granule Carbon tetrachloride Mammalian target of rapamycin/p70S6K signal pathway Liver fbrosis
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Effects of Electroacupuncture on Serum Indexes of Rats with Hepatic Fibrosis
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作者 闵友江 马晓芃 +5 位作者 赵天平 吴焕淦 安彩萍 杨玲 杨珊 崔学军 《Journal of Acupuncture and Tuina Science》 2008年第3期145-149,共5页
Objective: To observe the effects of electroacupuncture on the histopathological changes and serum indexes of rats' liver, and to investigate the mechanism of electroacupuncture in treating hepatic fibrosis of rats.... Objective: To observe the effects of electroacupuncture on the histopathological changes and serum indexes of rats' liver, and to investigate the mechanism of electroacupuncture in treating hepatic fibrosis of rats. Methods: The rat model of hepatic fibrosis was induced with carbon tetrachloride. Then, the rats were divided into electroacupuncture group, medicine group, and model group. The collagen of liver, and serum hyaluronic acid (HA), laminin (LN), procollagen Ⅲ (PⅢNP), and collagen Ⅳ (C-Ⅳ) were detected with morphologic methods and radioimmunoassay. Results: Compared with normal rats, the collagen was hyperplasia in the liver tissue, and the contents of the serum HA, LN, and PⅢ NP were higher in the model group. The collagen area of liver tissue, and the contents of the serum HA, and LN were lower in rats treated with electroacupuncture than model rats. The contents of serum of PⅢ NP, and C-Ⅳ changed little. Conclusion: Electroacupuncture had some effects of prevention and treatment, and the mechanism may relate to the effects of electroacupuncture in protecting liver cells, inhibiting synthesis of extracellular matrix, and promoting the breakup of collagen. 展开更多
关键词 ELECTROACUPUNCTURE Hpatic fbrosis Hyaluronic Acid LAMININ Precollagen Collagen RATS
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