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Effects of highly potent atrial natriuretic peptide on circulating reninangiotensin-aldosterone system and cardiac function in dogs with ischemic heart failure
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作者 吴宏超 钱学贤 +3 位作者 冯常森 王佳勇 张勇 施傅涛 《Journal of Medical Colleges of PLA(China)》 CAS 1997年第2期136-139,共4页
The effects of highly-potent atrial natriuretic peptide (HPANP) on circulating re nin-angiotensin-aldos-terone system (RAAS) and cardiac function were studied in an acute ischemic heart failure model. HPANP (6 μg/kg ... The effects of highly-potent atrial natriuretic peptide (HPANP) on circulating re nin-angiotensin-aldos-terone system (RAAS) and cardiac function were studied in an acute ischemic heart failure model. HPANP (6 μg/kg and 3 μg/kg) was infused intracoronarily. It was found that both doses of HPANP could cause significant decrease in plasma renin activity (PRA), angiotensin II (AII) and aldosterone (Ald). After the administraticn of HPANP, PRA, AII and Ald in the coronary sinus were decreased by 73. 2% (P<0.01), 68. o% (P<0.01) and 73. 6% (P<0.01), and the hormones in peripheral venous blood by 63. 3% (P<0.01), 53. 3% (P<0.01) and 64. 9% (P<0.01), respectively at the dose of 6 μg/kg. While PRA, AII and Ald in the coronary sinus and in peripheral venous blood decreased by 55. 9%, 55. 3%, 61. 9%, and 54. 0%, 42. 3%, 53, 3%, respectively at the 3μg/kg dose level. At the higher dose, HPANP increased left ventricular systolic pressure (LVSP, +13. 1%, P<0. 05), +dP/dtmax(+24.1 %, P<0.01), -dp/dtmax (+35.9%, P<0.01), and VCE(+28.9%, P<0.05). Mean arterial pressure and left ventricular end-diastolic pressure (LVEDP) were decreased (-15.0%, P<0.01, and 29. 6%, P<0.01, respectively). In contrast, the lower dose caused no significant changes of LVSP, +dp/dtmex,dp/dtmax and VCE(not including LVEDP, - 20. 5 %, P<0.05). Neither of the doses caused significant changes in heart rate and T value- Normal saline infusion has no effects on cardiac function and circulating RAAS- We conclude that in ischemic heart failure, intracoronary administration of HPANP can significantly suppress the activity of circulating RAAS, and improve cardiac function by reducing pre- and after-load of the heart, but has no direct myocardial effects. 展开更多
关键词 highly POTENT ATRIAL NATRIURETIC peptide renin-angiotensin-aldosterone system myocardial ischemia heart failure
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人GM-CSF受体β链胞膜外区域与GM-CSF结合位点的研究
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作者 黄传书 金伯泉 +5 位作者 汪美先 鞠躬 陈常庆 梁卫平 朱剑峰 施傅涛 《中国科学(C辑)》 CSCD 1996年第5期420-427,共8页
研究了抗人GM-CSF受体β链胞膜外区域4种人工合成多肽D1(9~114),D2(115~225),D3(226~325)和D4(326~422)4个多肽片段多克隆抗血清和McAb对GM-CSF生物学活性的阻断作用,结果首次发现抗D1多克隆抗血清和抗D1McAb 2A_9对 GM-CSF促进的 D... 研究了抗人GM-CSF受体β链胞膜外区域4种人工合成多肽D1(9~114),D2(115~225),D3(226~325)和D4(326~422)4个多肽片段多克隆抗血清和McAb对GM-CSF生物学活性的阻断作用,结果首次发现抗D1多克隆抗血清和抗D1McAb 2A_9对 GM-CSF促进的 DMSO诱导的 HL60细胞、正常人胎儿骨髓细胞以及人GM-CSF依赖的TF-1细胞增殖有显著的阻断效应,抗D2McAb 1C_(12)对GM-CSF诱导的 TF-1细胞增殖也有显著的阻断效应,阻断抑制率均可达 90%以上,而其它抗受体 β链 McAb和无关对照 McAb E_7均无阻断活性.此结果表明:抗 D1 McAb2A_9和抗D2 McAb 1C_(12)所识别的表位则可能为受体β链与 GM-CSF的结合位点依据受体β链二级结构预测,受体与细胞因子结合部位的结构理论,设计和合成了受体β链45~75,56~75和 66~75 3个人工合成多肽片段,用间接ELISA结合试验分析表明,McAb 2A_9识别表位位于第 45~55位氨基酸内.应用受体与细胞因子结合部位的结构理论推测 McAb 1C_(12)识别表位可能位于β链内 216~220位氨基酸.此结果对于深入了解受体β链的结构与功能以及细胞因子与受体的相互作用均有十分重要的意义. 展开更多
关键词 粒细胞巨噬细胞 集落刺激因子 受体 β链胞膜区
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ENKEPHALIN ANALOGS AND STEPPING AUTOMATISM IN GUINEA-PIGS
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作者 刘世熠 李金翠 +3 位作者 张茂斌 戴秀菊 施傅涛 曲淑敏 《Chinese Science Bulletin》 SCIE EI CAS 1983年第10期1418-1421,共4页
Stepping automatism is a widely adopted model for investigating the central control of movements. Traditionally stepping automatism was performed in the mesen-cephalic or spinal cats and induced electrically with a tr... Stepping automatism is a widely adopted model for investigating the central control of movements. Traditionally stepping automatism was performed in the mesen-cephalic or spinal cats and induced electrically with a treadmill. We have recently reported that regular stepping automatism could be evoked chemically by 4-R-2, 2, 5,5-tetrakis(trifluoromethyl)-imidazoline derivatives. It appears, however, that 展开更多
关键词 evoked electrically guinea chemically STEPPING dissolved NALOXONE TREMOR administration attenuation
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