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细辛与verapamil镇痛协同作用的实验研究 被引量:26
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作者 陈超 郑卫红 +1 位作者 熊素兵 钱京萍 《中国药理学通报》 CAS CSCD 北大核心 2003年第3期337-339,共3页
目的 研究细辛与verapamil的镇痛协同作用 ,为临床联合用药提供理论依据。方法 采用醋酸扭体实验及热板法致痛实验观测其镇痛作用 ,并用神经盒、多媒体MS 30 2系统观察其对蟾蜍坐骨神经动作电位的影响。结果 细辛及A V复方制剂对醋... 目的 研究细辛与verapamil的镇痛协同作用 ,为临床联合用药提供理论依据。方法 采用醋酸扭体实验及热板法致痛实验观测其镇痛作用 ,并用神经盒、多媒体MS 30 2系统观察其对蟾蜍坐骨神经动作电位的影响。结果 细辛及A V复方制剂对醋酸致小鼠腹痛、热板法致小鼠足痛均有明显的镇痛作用并能抑制蟾蜍坐骨神经动作电位的传导。verapamil有弱的镇痛作用 ,无坐骨神经动作电位阻滞作用。A V复方制剂的镇痛及抑制神经动作电位传导作用均大于其组分细辛和维拉帕米。 展开更多
关键词 细辛 verapamil 镇痛作用 联合用药
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顺铂及增敏剂Verapamil、SDZ PSC 833诱导卵巢癌细胞凋亡的研究 被引量:3
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作者 廖美焱 陈惠祯 +3 位作者 杨庆忆 邱慧玲 刘诗权 候流英 《肿瘤》 CAS CSCD 北大核心 2000年第2期93-95,共3页
目的 探讨顺铂及 Verapam il、SDZ PSC 833作用机制 ,探讨获得性耐药机制。方法 以人卵巢癌亲代细胞株COC1 及其耐药亚株 COC1 /DDP为材料 ,计算细胞生长抑制率、细胞凋亡率及进行细胞周期分析。结果 顺铂联用Verapamil或 SDZ PSC83... 目的 探讨顺铂及 Verapam il、SDZ PSC 833作用机制 ,探讨获得性耐药机制。方法 以人卵巢癌亲代细胞株COC1 及其耐药亚株 COC1 /DDP为材料 ,计算细胞生长抑制率、细胞凋亡率及进行细胞周期分析。结果 顺铂联用Verapamil或 SDZ PSC833可提高细胞生长抑制率 ;顺铂引起 S期细胞比例增高 ,大剂量顺铂造成 S期细胞大量凋亡 ;COC1 、COC1 /DDP凋亡率不同 ,PSC833能明显增强顺铂诱导 COC1 /DDP细胞凋亡。结论  Verapamil、PSC833有增敏作用 ,PSC833能增强顺铂诱导 COC1 /DDP细胞凋亡 ;诱导细胞凋亡是顺铂作用机制之一 ,获得性耐药与凋亡耐受有关 ;顺铂引起 S期细胞增多 ,凋亡细胞为 展开更多
关键词 卵巢癌 细胞凋亡 顺铂 增敏剂 verapamil
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CP-154,526和verapamil对促肾上腺皮质激素释放因子分泌水平的影响 被引量:2
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作者 董静 祝益民 +6 位作者 周文武 袁发 张川 董春艳 肖政辉 桂永浩 陈超 《医学研究杂志》 2011年第9期66-68,共3页
目的探讨促肾上腺皮质激素释放因子Ⅰ型受体(CRF-R1)拮抗剂CP-154,526(CP)和钙离子通道拮抗剂vera-pamil(VP)对幼年大鼠在缺氧缺血(HI)后并放置1天后血浆中促肾上腺皮质激素释放因子分泌水平的影响。方法 80只幼年大鼠随机分成8组,即对... 目的探讨促肾上腺皮质激素释放因子Ⅰ型受体(CRF-R1)拮抗剂CP-154,526(CP)和钙离子通道拮抗剂vera-pamil(VP)对幼年大鼠在缺氧缺血(HI)后并放置1天后血浆中促肾上腺皮质激素释放因子分泌水平的影响。方法 80只幼年大鼠随机分成8组,即对照组、假手术组、CP对照组、VP对照组、模型组(HI组)、HI+CP组、HI+VP组和HI+CP+VP组。用放射免疫法测定各组幼年大鼠血浆中CRF水平。结果与对照组比较,HI组、HI+CP组和HI+CP+VP组血浆CRF水平都显著降低(P<0.001、P<0.001、P<0.001);与假手术组比较,HI组、HI+CP组和HI+CP+VP组血浆CRF水平都显著降低(P<0.001、P<0.001、P<0.001);与CP对照组比较,HI组、HI+CP组和HI+CP+VP组血浆CRF水平都显著降低(P<0.001、P<0.001、P<0.001);与VP对照组比较,HI组、HI+CP组和HI+CP+VP血浆CRF水平都显著降低(P<0.001、P<0.001、P<0.001);与HI组比较,HI+CP组和HI+VP组血浆CRF水平显著增加(P<0.05、P<0.001);与HI+CP比较,HI+VP组血浆CRF水平显著增加(P<0.001);与HI+VP组比较,HI+CP+VP组血浆CRF水平显著降低(P<0.001)。结论幼年大鼠在HI后并放置1天后血浆CRF水平都显著减少;可是,当幼年大鼠用CP或者VP预处理后,血浆CRF分泌水平在缺氧缺血下的减少能被逆转;当用CP和VP同时预处理后,血浆CRF分泌水平在缺氧缺血下的减少没有被改变。 展开更多
关键词 缺氧缺血脑损伤促肾上腺皮质激素释放因子 CP-154 526 verapamil幼年SD大鼠
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Verapamil和Mn^(2+)对缺氧及缺氧复氧心肌细胞内pH的影响 被引量:1
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作者 王军 张佩瑾 +4 位作者 章鲁 齐建华 魏丕敬 顾培坤 金正均 《中国药理学通报》 CAS CSCD 北大核心 1996年第1期68-70,共3页
采用荧光探针BCECF/AM结合计算机图像处理技术测定不同时间的缺氧和缺氧复氧单心肌细胞内pH的变化以及Ca2+通道阻滞剂Verapamil和Na+-Ca2+交换抑制剂Mn2+对其的影响。结果显示随着缺氧时间的延长,... 采用荧光探针BCECF/AM结合计算机图像处理技术测定不同时间的缺氧和缺氧复氧单心肌细胞内pH的变化以及Ca2+通道阻滞剂Verapamil和Na+-Ca2+交换抑制剂Mn2+对其的影响。结果显示随着缺氧时间的延长,细胞内pH也逐渐降低。复氧开始40min内,细胞内pH并未恢复正常。Verapamil能减轻缺氧细胞内酸化程度并使其接近正常水平(P>0.05),却未能减轻缺氧复氧细胞内的酸化。无论是缺氧或缺氧复氧心肌细胞,Mn2+均未能减轻细胞内的酸化程度。本实验结果提示缺氧和缺氧复氧时细胞内酸化途径并非完全一致。VeraPamil抑制缺氧细胞内pH下降是其保护缺氧心肌作用的机制之一。 展开更多
关键词 verapamil 钙拮抗剂 心肌缺氧 细胞内PH 缺氧
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HTK液与Verapamil配伍对供心保存效果的实验研究 被引量:2
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作者 黄健 周云 《四川医学》 CAS 2013年第1期15-17,共3页
目的通过建立Langendorff离体鼠心灌流模型,研究HTK液与Verapamil配伍对供心的保护效果。方法30只SD大鼠(200~400g/只),随机分为实验组与对照组,实验组予以HTK液与Verapamil(5mg/L)配伍、对照组予以单纯HTK液作为停搏液,建立标准的Lang... 目的通过建立Langendorff离体鼠心灌流模型,研究HTK液与Verapamil配伍对供心的保护效果。方法30只SD大鼠(200~400g/只),随机分为实验组与对照组,实验组予以HTK液与Verapamil(5mg/L)配伍、对照组予以单纯HTK液作为停搏液,建立标准的Langendorff离体心脏灌注模型,4℃低温下保存大鼠心脏6h,予以37℃K-H液复灌,心脏复跳,生理仪记录缺血前、复灌20min、40min、60min、80min时血流动力学标值,检测心脏复灌45min时冠脉流出液中心肌酶学指标,实验结束后各组留取样本以行常规病理切片及电镜切片观察微观结构变化。结果实验组LVSP平均恢复率高于对照组,对照组LVEDP持续上升,实验组LVEDP相对稳定;对照组心肌酶均明显高于实验组(P<0.05);病理切片显示对照组损伤较实验组明显。结论 HTK液联合Verapamil较单独使用HTK液作为心肌保护液,对心肌具有更明显的保护作用。 展开更多
关键词 HTK液 verapamil 心肌保护 缺血再灌注
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硫氮酮(diltlazem)和异扑定(Verapamil)治疗高血压时的血脂变化
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作者 王宪衍 邱慧丽 +1 位作者 范明昌 龚蓝生 《中国临床药理学杂志》 CAS CSCD 北大核心 1990年第S1期38-38,共1页
本文对53例原发性高血压患者,用随机、双盲法分为两组,分别用硫氮酮和异扑定治疗,疗程4周。两组均显示明显的降压效果,前者的降压幅度又明显大于后者,治疗后的血脂改变为:(1)HDL-C,(HDL-C)/TC比值和(HDL-C)/(LDL-C)比值升高。... 本文对53例原发性高血压患者,用随机、双盲法分为两组,分别用硫氮酮和异扑定治疗,疗程4周。两组均显示明显的降压效果,前者的降压幅度又明显大于后者,治疗后的血脂改变为:(1)HDL-C,(HDL-C)/TC比值和(HDL-C)/(LDL-C)比值升高。(2)APOA<sub>1</sub>升高。这些改变均有利于防止动脉粥样硬化。从而认为。 展开更多
关键词 血脂变化 verapamil diltlazem 降压幅度 钙离子拮抗剂 双盲法 心动过速 脂血症
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Verapamil和Propranolol对非胰岛素依赖型糖尿病透析患者物质代谢的影响
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作者 尹良红 《暨南大学学报(自然科学与医学版)》 CAS CSCD 1998年第6期120-122,共3页
比较Verapamil和Propranolol对患有胰岛素非依赖型糖尿病及轻度至中度高血压的透析患者的血糖和物质代谢的影响。方法:46例患有非胰岛素依赖型糖尿病及轻度至中度高血压的透析患者,为德国福尔达市KfH血透中... 比较Verapamil和Propranolol对患有胰岛素非依赖型糖尿病及轻度至中度高血压的透析患者的血糖和物质代谢的影响。方法:46例患有非胰岛素依赖型糖尿病及轻度至中度高血压的透析患者,为德国福尔达市KfH血透中心和柏林KfH血透中心的透析病人。分别经Verapamil和Propranolol治疗三个月后测空腹血糖、血红蛋白A1c、果酸、胰岛素、胆固醇和甘油三脂,同时记录透析前心率和血压。结果:Verapamil对血糖及物质代谢无不良影响,Propranolol可引起血糖、果酸和血红蛋白A1c升高。结论:在糖尿病透析患者。 展开更多
关键词 糖尿病 透析 物质代谢 verapamil PROPRANOLOL
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异搏定(verapamil)对急性缺氧复合失血性休克狗的心泵功能的影响
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作者 罗德成 王俊元 +2 位作者 夏一阳 王仕军 田景亮 《四川生理科学杂志》 1991年第Z1期79-79,共1页
本文观察了Ca<sup>2+</sup>通道阻断剂——异搏定(verapamil)对急性缺氧复合失血性休克狗,回输血后心泵功能的影响。健康雄性家犬13只,体重8.5~16kg,戊巴比妥钠麻醉,在低压舱内(模拟高度4000m,大气压460mmHg)按wigger... 本文观察了Ca<sup>2+</sup>通道阻断剂——异搏定(verapamil)对急性缺氧复合失血性休克狗,回输血后心泵功能的影响。健康雄性家犬13只,体重8.5~16kg,戊巴比妥钠麻醉,在低压舱内(模拟高度4000m,大气压460mmHg)按wigger法自股动脉快速放血,在5min内使平均动脉压降至5. 展开更多
关键词 verapamil 急性缺氧 异搏定 失血性休克 心泵功能 阻断剂 低压舱 平均动脉压 心肌耗氧量 细胞代谢
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细辛与Verapamil镇痛协同作用的实验研究
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作者 陈超 郑卫红 《中国药理通讯》 2003年第1期4-5,共2页
关键词 细辛 verapamil 镇痛协同作用 实验研究 中药
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Verapamil inhibits scar formation after peripheral nerve repair in vivo 被引量:4
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作者 A-chao Han Jing-xiu Deng +4 位作者 Qi-shun Huang Huai-yuan Zheng Pan Zhou Zhi-wei Liu Zhen-bing Chen 《Neural Regeneration Research》 SCIE CAS CSCD 2016年第3期508-511,共4页
The calcium channel blocker,verapamil,has been shown to reduce scar formation by inhibiting fibroblast adhesion and proliferation in vitro.It was not clear whether topical application of verapamil after surgical repai... The calcium channel blocker,verapamil,has been shown to reduce scar formation by inhibiting fibroblast adhesion and proliferation in vitro.It was not clear whether topical application of verapamil after surgical repair of the nerve in vivo could inhibit the formation of excessive scar tissue.In this study,the right sciatic nerve of adult Sprague-Dawley rats was transected and sutured with No.10-0 suture.The stoma was wrapped with gelfoam soaked with verapamil solution for 4 weeks.Compared with the control group(stoma wrapped with gelfoam soaked with physiological saline),the verapamil application inhibited the secretion of extracellular matrix from fibroblasts in vivo,suppressed type I and III collagen secretion and increased the total number of axons and the number of myelinated axons.These findings suggest that verapamil could reduce the formation of scar tissue and promote axon growth after peripheral nerve repair. 展开更多
关键词 nerve regeneration nerve injury verapamil SCAR sciatic nerve type I collagen type III collagen neural regeneration
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Protective effects of verapamil on myocardial mitochondrial respiratory function after combined radiation-burn injury in rats 被引量:2
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作者 熊业 陈宗荣 程天民 《Journal of Medical Colleges of PLA(China)》 CAS 1996年第1期11-13,共3页
Protectiveeffectsofverapamilonmyocardialmitochondrialrespiratoryfunctionafter combinedradiation-burninjuryin... Protectiveeffectsofverapamilonmyocardialmitochondrialrespiratoryfunctionafter combinedradiation-burninjuryinratsXiongYe(熊业);C... 展开更多
关键词 MITOCHONDRION ionizing radiation BURNS verapamil RATS
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稀土离子的跨膜内流及Verapamil影响的研究 被引量:1
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作者 莫尚武 陈恒留 +2 位作者 刘宁 余燕萍 金建南 《四川大学学报(自然科学版)》 CAS CSCD 北大核心 1998年第5期756-758,共3页
用放射性核素141Ce作示踪剂,通过对稀土Ce3+在大鼠主动脉上的跨膜内流的研究表明,去甲肾上腺素(1.2μmol/L)和KCl(100mol/L)都可引起Ce3+跨膜内流量的增加,并以KCl(100mol/L)引起... 用放射性核素141Ce作示踪剂,通过对稀土Ce3+在大鼠主动脉上的跨膜内流的研究表明,去甲肾上腺素(1.2μmol/L)和KCl(100mol/L)都可引起Ce3+跨膜内流量的增加,并以KCl(100mol/L)引起的增加量较多.钙拮抗剂Verapamil(1μmol/L)对去甲肾上腺素(1.2μmol/L)和KCl(100mol/L)引起的Ce3+跨膜内流无明显的阻滞作用. 展开更多
关键词 稀土元素 生物效应 跨膜内流 verapamil
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HPLCASSAY FOR INTRACELLULAR ACCUMULATION OF VERAPAMIL IN VER-RESISTANT HUMAN LEUKEMIC CELL SUSLINES AND THEIR PARENTAL CELL LINES
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作者 谢佐福 林贤东 +1 位作者 周冬梅 林声 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 1998年第3期37-39,共3页
Verapamil(VER),acalciumchannelblocker,hasbenfoundtoefectivelyreversemultidrugresistanceintumorcelsthroughcom... Verapamil(VER),acalciumchannelblocker,hasbenfoundtoefectivelyreversemultidrugresistanceintumorcelsthroughcompetitivecombinati... 展开更多
关键词 HPLC verapamil INTRACELLULAR accumu lation Leukemic cells.
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Dose calcium channel blocker verapamil decrease urinary VMA levels in sympathoadrenal hyperactive patients with posttraumatic stress disorder?
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作者 Munawar Alam Ansari Shahida P.Ahmed Zahida Memon 《Asian Pacific Journal of Tropical Medicine》 SCIE CAS 2008年第4期36-39,共4页
Objective:The majority of the patients with posttraumatic stress disorders(PTSD) embrace augmented urinary flow of Vanillylmandelic Acid(VMA) than normal subjects owing to superior sympathetic doings,which steer to ca... Objective:The majority of the patients with posttraumatic stress disorders(PTSD) embrace augmented urinary flow of Vanillylmandelic Acid(VMA) than normal subjects owing to superior sympathetic doings,which steer to cardiovascular catastrophe.Urinary flow of VMA was evaluated as sympathoadrenal bustle marker in patients with posttraumatic stress disorder.Calcium ion shows a noteworthy dependability in nervousness owing to its special effects on brain synaptosomes.So this study was conducted to explore the effects of Verapamil on sympathoadrenal motion in patients with PTSD.Methods:Placebo controlled clinical tryout was conducted. At first hundred(100) PTSD patients were chosen and enrolled in the study,from department of Psychological Medicine Dow University of Health Sciences,Karachi.Verapamil 120 mg/day was specified in divided doses to group-Ⅰ(n=50)patients and group-Ⅱ(n =50) patients received placebo therapy on a daily basis for nine weeks.Each and every patient was monitored weekly,all the way through extent of study.Results:Underneath the posttraumatic stress disorder,urinary excretion of VMA was greater.Calcium channel blocker verapamil additionally abolished the embellished retort in urinary flow of VMA appreciably in patients with PTSD. Conclusion:Verapamil was experiential to be exceedingly effectual treatment.It reduces VMA levels in urine, and on the whole cardiovascular threat in PTSD patients. 展开更多
关键词 PTSD SYMPATHETIC activity URINARY VMA and verapamil
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INDEPENDENT AND SYNERGIC INHIBITION OF VERAPAMIL AND ELECTRIC BEAM RADIATION ON CLONOGENIC GROWTH IN K562 AND K562/ADM CELL L
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作者 谢佐福 沈世仁 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 1995年第1期24-27,共4页
INDEPENDENTANDSYNERGICINHIBITIONOFVERAPAMILANDELECTRICBEAMRADIATIONONCLONOGENICGROWTHINK562ANDK562/ADMCELLLI... INDEPENDENTANDSYNERGICINHIBITIONOFVERAPAMILANDELECTRICBEAMRADIATIONONCLONOGENICGROWTHINK562ANDK562/ADMCELLLINESINVITRO¥XieZuo... 展开更多
关键词 verapamil RADIATION K562 CELL LINE K562/ADM CELL line.
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Effect of captopril or verapamil on intracellular sodium in cultured vascular smooth muscle cells
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作者 QI JIAN HUA LU ZHANG +3 位作者 JUN WANG MIN LU XIN MING WANG ZHENG JUN JIN(Shanghai Institute of Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China.)(Department of Pharmacology, Shanghai Second Medical University, Shanghai 200025, China.) 《Cell Research》 SCIE CAS CSCD 1996年第1期47-53,共7页
The effects of captopril (Cap) and verapamil (Ver)alone and in combination on intracellular Na+ concentration ([Na+]i) in cultured aortic smooth muscle cells (ASMC) of rabbits was evaluated by a direct measurement of ... The effects of captopril (Cap) and verapamil (Ver)alone and in combination on intracellular Na+ concentration ([Na+]i) in cultured aortic smooth muscle cells (ASMC) of rabbits was evaluated by a direct measurement of [Na+]i with fluorescent dye sodium-binding benzofuran isophthalate (SBFI) combined with digital image. [Na+]i in resting cells was found to be 11.9 ± 0. 7 mmol/L. Angiotensin II (Ang-II, 0.1-10μmol/L) induced an increase of [Na+]i in concentration-dependent manner. Ver (0.1-10μmol/L) inhibited Ang-II (1 μmol/L)-induced increase in [Na+]i, while Cap enhanced Ang-II-induced increase in [Na+]i at 10μmol/L but not at 0.1-1μmol/L. Ver (0.1-1μmol/L)abolished enhancement of Ang-II-induced increase in [Na+]i by Cap. Thus, the inhibition of Capenhanced [Na+]i by Ver may provide a new hypothesis for the underlying molecular mechanism of synergistic effect of the combination of Ca2+ antagonists and angiotensinconverting enzyme inhibitors in controlling blood pressure. 展开更多
关键词 CAPTOPRIL verapamil 血管平滑肌细胞 细胞钠 钠通道 异博喧 钙拮抗剂 卡托普利 血管紧张素转换酶抑制剂
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Repurposing verapamil for prevention of cognitive decline in sporadic Alzheimer's disease
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作者 Heba A.Ahmed Tauheed Ishrat 《Neural Regeneration Research》 SCIE CAS CSCD 2022年第5期1018-1019,共2页
Dementia is currently the only leading cause of death that is still on the rise,with its overall costs already surpassing those of cancer and heart disease combined,it has developed into a worldwide crisis.In response... Dementia is currently the only leading cause of death that is still on the rise,with its overall costs already surpassing those of cancer and heart disease combined,it has developed into a worldwide crisis.In response to its serious and far-reaching effects,the US government has established the"National Alzheimer's Project Act"(Public Law 111-375). 展开更多
关键词 ALZHEIMER PREVENTION DEATH verapamil
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Design and preparation of press-coated tablets for pulsed release of verapamil
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作者 邹豪 马伯良 蒋雪涛 《Journal of Medical Colleges of PLA(China)》 CAS 1999年第4期266-269,共4页
Objective: To achieve pulsed release system of verapamil on the basis of circadian rhythms of hypertensive patients. Methods: Factors affecting the lag time of the system were tested. Three swelling disintegrates (L-H... Objective: To achieve pulsed release system of verapamil on the basis of circadian rhythms of hypertensive patients. Methods: Factors affecting the lag time of the system were tested. Three swelling disintegrates (L-HPC,CMS-Na, CMC-Ca) of different contents were used- Various compositions of out shell were tested throughthe uniform design and dealt with multipleregression. Two basic formulations whose lag time is 3 and 5 h were decided- Results: The lag time 5 h formulation: CMS-Na was the preferable disintegrate with content 15 mg/tablet,out shell composition were chosen as PEG 6000 110 mg, HCO 105 mg, EVA 25 mg each tablet. Hardness 5 kg/cm2. Conclusion: A new press-coated tablets for the pulsed release of drug after a programmable period of time isachieved in the in vitro dissolution test. 展开更多
关键词 verapamil PULSED RELEASE system CIRCADIAN RHYTHMS lag time
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Controlled release tablets of verapamil hydrochloride
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作者 Treephu Kimlek Tossaporn Prasertporn +2 位作者 Jiramet Sawantranon Chaisan Sriwichupong Garnpimol Ritthidej 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2016年第1期219-220,共2页
Verapamil is a calcium channel blocker drug which reduces heart rhythm and blood pressure in high blood pressure patient.The steady state of this drug has to be continually controlled to obtain optimal efficacy.In add... Verapamil is a calcium channel blocker drug which reduces heart rhythm and blood pressure in high blood pressure patient.The steady state of this drug has to be continually controlled to obtain optimal efficacy.In addition,patient compliance needs to be considered.Therefore,controlled release tablet of verapamil hydrochloride was essentially developed using hydrophilic matrix polymer,namely hydroxypropylmethyl cellulose(HPMC)and sodium alginate,and compared to marketed product[1].HPMC,a pH-independent polymer,hydrates to form a gel layer at the surface of the tablet to sustain the drug release.Sodium alginate,a pH-dependent gelling polymer,converts to insoluble alginic acid after exposure to acidic condition in stomach. 展开更多
关键词 verapamil CONTROLLED RELEASE HPMC SODIUM ALGINATE
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Inhibiting effects of verapamil on respiratory burst of polymorphonuclear leucocytes
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作者 刘雪芬 陈树元 廖锡麟 《Journal of Medical Colleges of PLA(China)》 CAS 1995年第1期39-41,共3页
Chemiluminescence method was used to measure the effect of verapamil on the active oxygen generation in respiratory burst of human blood polymorphonuclear leucocytes (PMNs) stimulated with phorbol myristate acetate(PM... Chemiluminescence method was used to measure the effect of verapamil on the active oxygen generation in respiratory burst of human blood polymorphonuclear leucocytes (PMNs) stimulated with phorbol myristate acetate(PMA) (a) . on superoxide anion (O_2 ̄-) p 展开更多
关键词 CHEMILUMINESCENCE NEUTROPHILS verapamil oxygen free RADICALS
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