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Nonpeptide somatostatin analogs:recent advances in its application and research 被引量:1
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作者 Wang Song Liang Qingmo Liao Duanfang 《Journal of Medical Colleges of PLA(China)》 CAS 2008年第6期364-376,共13页
Along with its wide anatomical distribution, somatostatin (SST) acts on multiple targets via a family of 5 receptors to produce a broad spectrum of biological effects. Therefore, a variety of peptide analogs have been... Along with its wide anatomical distribution, somatostatin (SST) acts on multiple targets via a family of 5 receptors to produce a broad spectrum of biological effects. Therefore, a variety of peptide analogs have been produced and are widely used in clinical treatment. However, because of their flaws in the structure of peptide, the clinical efficacy is limited. In this review, we summarize the structure, pharmacological effects and the potential clinical value of non-peptide SST analogs. We focus on the research and development of non-peptide SST analogs since 1998, and discuss the problems and potential prospects for non-peptide SST analogs. We believe that as more non-peptide somatostatin analogs are successfully developed, the extensive clinical application of SSTs will contribute a great deal to medical science. 展开更多
关键词 nonpeptide somatostatin STRUCTURE Pharmacological study Potential clinical value
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Effect of nonpeptide NK1 receptor antagonist L-703,606 on the edema formation in rats at early stage after deep partial-thickness skin scalding
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作者 Ke Tao Hong-Tao Wang +5 位作者 Bi Chen Bo-Tao Wang Zhi-Yuan Li Xiong-Xiang Zhu Chao-Wu Tang Da-Hai Hu 《Asian Pacific Journal of Tropical Medicine》 SCIE CAS 2013年第5期387-394,共8页
Objective:To investigate the effect and the relevant potential mechanism of nonpeptide neurokinin 1(NK1) receptor antagonist L-703,606 in the edema formation after burn injury. Method:1.-703,606 treatment was performe... Objective:To investigate the effect and the relevant potential mechanism of nonpeptide neurokinin 1(NK1) receptor antagonist L-703,606 in the edema formation after burn injury. Method:1.-703,606 treatment was performed in Sprague-Dawley(SD) rats at early stage after deep partial-thickness skin scalding.One hundred and fifty two adult male SI) rats were used in the study and randomly divided into sham scald(SS,n=8),scald control(SC,n=48),and L-703,606 treatment(IT,n=48) groups.The rats in SC and LT groups were subjected to 20%total body surface area(TBSA) deep partial-thickness skin scalding.Modified Evans blue extravasation, tracing electron microscopy by lanthanum nitrate and mean water content assay were employed to observe and detect the changes of vascular permeability,ultrastructure and edema formation in adjacent tissue to the wounds and in the jejuna of rats at early stage(72 h) after scald.Results: The pathological increase of vascular permeability in the periwound tissue and jejunum of rats in LT group were significantly lower than that in SC group(P【0.01),and recuperated earlier. Meanwhile,the changes of water contents of corresponding tissues in LT group were lighter than those in SC group(P【0.01).The ultrastructural changes of the microvessels in the peri-wound tissue of LT group showed that the junctions between microvascular endothelium cells were more narrow than those of SC group,moreover,and the number of opening and the engorgement and cavitation of the vascular endothelium cells decreased,the areosis and edema in perivascular tissue lightened,and the precipitation of the high eletron density lanthanum tracing agent in the interspace of the tissue decreased significantly in LT group.Conclusions:It is concluded that nonpeptide NK1-receptor antagonist L-703,606 could lighten the vascular permeability and edema formation in the periwound tissue and jejunum,and accelerate the normalization process of pathological changes in the tissues of rats after scald. 展开更多
关键词 nonpeptide NK1-receptor ANTAGONIST L-703 606 SCALD EDEMA Vascular permeability ULTRASTRUCTURE Substance P
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促代谢型谷氨酸受体激活的分子开关调节LTP的诱导
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《Neuroscience Bulletin》 SCIE CAS CSCD 1994年第3期15-15,共1页
促代谢型谷氨酸受体激活的分子开关调节LTP的诱导已知在海马CAI区突触激活NMDA受体与促代谢型谷氨酸受体(mGluR)是诱导LTP所必不可少的。英国的Lollingridey实验室最近报道:在LTP的形成过程中NM... 促代谢型谷氨酸受体激活的分子开关调节LTP的诱导已知在海马CAI区突触激活NMDA受体与促代谢型谷氨酸受体(mGluR)是诱导LTP所必不可少的。英国的Lollingridey实验室最近报道:在LTP的形成过程中NMDA受体与mG1uR的基本作用是不... 展开更多
关键词 substance P electroacupuncture ANALGESIA spinal cord RP67580 nonpeptide ANTAGONIST INTRATHECAL injection
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