期刊文献+
共找到672篇文章
< 1 2 34 >
每页显示 20 50 100
Calcium channel blockers and Alzheimer's disease 被引量:2
1
作者 Yi Tan Yulin Deng Hong Qing 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第2期137-140,共4页
Alzheimer's disease is characterized by two pathological hallmarks: amyloid plaques and neurofibrillary tangles. In addition, calcium homeostasis is disrupted in the course of human aging Recent research shows that ... Alzheimer's disease is characterized by two pathological hallmarks: amyloid plaques and neurofibrillary tangles. In addition, calcium homeostasis is disrupted in the course of human aging Recent research shows that dense plaques can cause functional alteration of calcium signals in mice with Alzheimer's disease. Calcium channel blockers are effective therapeutics for treating Alzheimer's disease. This review provides an overview of the current research of calcium channel blockers involved in Alzheimer's disease theraov. 展开更多
关键词 Alzheimer's disease caic-ium channel calcium homeostasis Alzheimer's diseasepathogenesis Β-AMYLOID calcium channel blocker
下载PDF
Effect of Calcium Ionophore and Calcium Channel Blockers on Immediate Hypersensitivity Reactions
2
作者 黄钦田 陈丙莺 孙爱民 《The Journal of Biomedical Research》 CAS 1994年第1期26-28,共3页
The release of mediators from mast cells is a model for cell secretion and is an in-vitro index for immediate hypersensitivity reactions. Calcium influx is generally accepted to be the primary biochemicalevent in mast... The release of mediators from mast cells is a model for cell secretion and is an in-vitro index for immediate hypersensitivity reactions. Calcium influx is generally accepted to be the primary biochemicalevent in mast cell activation.We studied the effect of the calcium ionophore A 23187 and calcium channelblockers,nifedipine and verapamil, in triggering the activation of rat peritoneal mast cells.At suitableconcentration nifedipine and verapamil have had the inhibition effect in the IgE-dependent roaction. 展开更多
关键词 calcium ionophore A23187 calcium channel blocker NIFEDIPINE VERAPAMIL mediator Histamine
下载PDF
Argemone mexicana extract alleviates gastrointestinal disorders by stimulating muscarinic receptors and blocking voltage-gated L-type calcium channels
3
作者 Rabia Iqbal Irfan Hamid +7 位作者 Khalid Hussain Janbaz Muhammad Furqan Akhtar Ammara Saleem Ali Sharif Sohaib Peerzada Bushra Akhtar Kashif Sohail Sajid Ali 《Asian Pacific Journal of Tropical Biomedicine》 SCIE CAS 2021年第5期214-221,共8页
Objective:To investigate the pharmacological potential of Argemone mexicana in treating constipation and emesis by using in vitro and in vivo models.Methods:The spasmogenic and spasmolytic effects were evaluated on is... Objective:To investigate the pharmacological potential of Argemone mexicana in treating constipation and emesis by using in vitro and in vivo models.Methods:The spasmogenic and spasmolytic effects were evaluated on isolated rabbit jejunum fragments loaded in a tissue organ bath.The response was recorded with an isotonic transducer attached with Power Lab Data Acquisition System.The laxative and antiemetic activities were assessed in BALB-c mice and poultry chicks challenged with carbamylcholine and copper sulphate stimulated emesis,respectively.Results:The total phenolic and total flavonoids contents of the extract were(267.75±5.77)mg GAE/g and(73.86±6.01)mg QE/g,respectively.Argemone mexicana extract exerted spasmogenic effect on isolated rabbit jejunum segments with an EC_(50)value of 0.016 mg/m L,which was blocked by atropine(0.3μM).Argemone mexicana extract exerted spasmolytic effect in atropine treated jejunum fragments with an EC_(50)value of 2.185 mg/mL.Furthermore,Argemone mexicana extract relaxed potassium(80 mM)-induced contractions(EC_(50):9.07 mg/mL),similar to a standard drug verapamil.The calcium channel blocker activity was confirmed by a rightward shift of concentration-response curve of calcium in the presence of Argemone mexicana extract(1-5 mg/mL)and verapamil(0.1-1μM).In addition,the extract increased the distance travelled by a charcoal in the gastrointestinal tract and exhibited antiemetic effect on copper sulphate induced emesis in chicks.Conclusions:Argemone mexicana shows cholinergic agonist and calcium channel blocker activities,as well as antiemetic effect.It may be used as a potential agent for treating gastrointestinal disorders. 展开更多
关键词 Argemone mexicana Muscarinic agonist calcium channel blocker CONSTIPATION EMESIS
下载PDF
Calcium Channel Blockers《钙离子阻断剂》
4
作者 苏定冯 《中国药理学通报》 CAS CSCD 北大核心 2005年第2期140-140,共1页
关键词 阻断剂 钙通道 对抗药 慢通道 凝血因子Ⅳ 钙离子 calcium Channel blockers
下载PDF
CCB及RAAS抑制剂降压治疗预防脑血管事件差异的真实世界研究
5
作者 宁丽晔 曾六仔 +6 位作者 陈春晖 刘香 傅宴 郑国燕 黎智森 贾国良 曾广民 《中国实用医药》 2023年第8期101-104,共4页
目的研究钙通道阻滞剂(CCB)及肾素-血管紧张素-醛固酮系统(RAAS)抑制剂降压治疗预防脑血管事件差异的真实世界。方法对915例高血压患者进行资料查看、筛选、分析,观察患者血压控制及终点事件发生情况,比较用药CCB、RAAS抑制剂对减少心... 目的研究钙通道阻滞剂(CCB)及肾素-血管紧张素-醛固酮系统(RAAS)抑制剂降压治疗预防脑血管事件差异的真实世界。方法对915例高血压患者进行资料查看、筛选、分析,观察患者血压控制及终点事件发生情况,比较用药CCB、RAAS抑制剂对减少心脑血管事件效果的真实世界情况。结果随访时间2.0~6.5年,平均随访时间4.5年。915例高血压患者中,482例患者采用单一CCB治疗,433例患者采用单一RAAS抑制剂治疗。用药CCB患者收缩压降低幅度略大于用药RAAS抑制剂患者,舒张压降低幅度略小于用药RAAS抑制剂患者,但差异无统计学意义(P>0.05);随访至终点时,用药CCB患者脑卒中发生率为5.60%(27/482),低于用药RAAS抑制剂患者的6.47%(28/433),经R语言生存分析差异具有统计学意义(P=0.016<0.05)。用药CCB患者心肌梗死发生率为2.90%(14/482),高于用药RAAS抑制剂患者的2.31%(10/433),经R语言生存分析差异无统计学意义(P=0.920>0.05)。用药CCB患者总死亡率为4.56%(22/482),用药RAAS抑制剂患者总死亡率为4.62%(20/433),经R语言生存分析差异无统计学意义(P=0.872>0.05)。结论CCB降压治疗预防脑卒中的效果优于RAAS抑制剂,显示CCB对脑卒中的一级预防具有更多的优势。 展开更多
关键词 高血压 钙通道阻滞剂 肾素-血管紧张素-醛固酮系统抑制剂 脑卒中 心肌梗死
下载PDF
ACEI/ARB与CCB防治高血压病伴慢性肾功能不全患者发生造影剂肾病的效果比较 被引量:7
6
作者 陈彩玲 黄铮 +3 位作者 赖雯苑 滕树恩 洪承路 赵新军 《心脏杂志》 CAS 2015年第6期703-707,共5页
目的 比较血管紧张素转换酶抑制剂(ACEI)/血管紧张素受体阻断剂(ARB)和钙离子通道阻断剂(CCB)对高血压病伴慢性肾功能不全(CKD)患者在介入术后发生造影剂肾病(CIN)的防治效果。方法 回顾分析近6年南方医院内科病房180例高血... 目的 比较血管紧张素转换酶抑制剂(ACEI)/血管紧张素受体阻断剂(ARB)和钙离子通道阻断剂(CCB)对高血压病伴慢性肾功能不全(CKD)患者在介入术后发生造影剂肾病(CIN)的防治效果。方法 回顾分析近6年南方医院内科病房180例高血压病伴CKD 2-3期患者,所有患者均接受了冠脉介入术,并在术前术后使用了水化治疗,术前至少使用了7 d的ACEI/ARB或CCB药物,另设单纯水化对照组;观察3组患者发生CIN的例数,以及术后24、48、72 h及 7d的血清肌酐(SCr)、肌酐清除率(CCr)的变化水平,并记录肾功能恢复的时间。结果 ACEI/ARB组术后发生CIN 20例(占37%),CCB组术后发生CIN 16例(占20%),单纯水化组发生28例(占61%);与单纯水化组比较,两组术后CIN发生率均较低(P〈0.05,P〈0.01);CCB组和ACEI/ARB组比较,CCB组的CIN发生率较低(P〈0.05)。3组患者介入术后24、48、72 h及7 d的SCr、CCr水平均有明显升高,差异有显著性;与单纯水化组相比,ACEI/ARB组和CCB组的血清SCr、CCr水平在24、48、72 h及7 d的时间点均有所降低,差异有显著性;CCB组与ACEI/ARB组相比,48、72 h及7 d的SCr降低较明显(均P〈0.05)。术后14 d,ACEI/ARB组有14例(占70%)CIN患者肾功能恢复至术前水平,CCB组有12例(占75%),单纯水化组有16例(占62%),ACEI/ARB组和CCB比较差异无统计学意义。结论 使用ACEI/ARB 和CCB类药物均可对高血压病并发CKD患者发生CIN有预防作用;CCB类药物优于ACEI/ARB类药物。 展开更多
关键词 高血压病 慢性肾功能不全 造影剂肾病 血管紧张素转换酶抑制剂 血管紧张素受体阻断剂 钙离子通道阻断剂
下载PDF
钙通道阻滞剂1,4-二氢吡啶类药物的绿色合成
7
作者 谢建武 刘俊男 谢玄升 《陕西科技大学学报》 北大核心 2024年第1期65-72,共8页
心脏及心脑血管疾病是发达国家人群的第一死因,也是中国人死亡的首位原因.L-型钙通道是目前临床上主要使用选择性钙通道阻滞剂1,4-二氢吡啶类药物.文章研究了在非均相催化剂离子交换树脂Amberlyst 15的催化以及无溶剂条件下,高效的合成... 心脏及心脑血管疾病是发达国家人群的第一死因,也是中国人死亡的首位原因.L-型钙通道是目前临床上主要使用选择性钙通道阻滞剂1,4-二氢吡啶类药物.文章研究了在非均相催化剂离子交换树脂Amberlyst 15的催化以及无溶剂条件下,高效的合成了钙通道阻滞剂1,4-二氢吡啶类药物.该反应体系具有原料便宜、反应时间短、操作及后处理简单、催化剂可回收利用、反应可放大等优良特点. 展开更多
关键词 药物合成 钙通道阻滞剂 1 4-二氢吡啶 绿色合成 非均相催化
下载PDF
钙通道阻滞剂对未破裂颅内动脉瘤影响的研究进展
8
作者 万子豪 李爱民 《中国医药》 2024年第7期1091-1095,共5页
未破裂的颅内动脉瘤是一颗埋在患者体内的定时炸弹,这类患者往往伴有高血压病。除去多数研究已证实的促破裂危险因素以外,复杂的血流动力学、炎症因素以及未控制的高血压也增加了其破裂风险。作为临床常用的抗高血压药物,钙通道阻滞剂... 未破裂的颅内动脉瘤是一颗埋在患者体内的定时炸弹,这类患者往往伴有高血压病。除去多数研究已证实的促破裂危险因素以外,复杂的血流动力学、炎症因素以及未控制的高血压也增加了其破裂风险。作为临床常用的抗高血压药物,钙通道阻滞剂被发现在促破裂进程中可以发挥保护作用,但也有研究发现了不同甚至矛盾的结果。本文就动脉瘤破裂的危险因素、钙通道阻滞剂使用对瘤体破裂的影响以及发挥的双重效应作一综述。 展开更多
关键词 未破裂颅内动脉瘤 钙通道阻滞剂 血流动力学 慢性炎症 高血压
下载PDF
钙离子通道阻滞剂在慢性疼痛患者中临床应用的研究进展
9
作者 王翼华 王前 +1 位作者 张立贇 梁元 《系统医学》 2024年第4期191-194,共4页
现代医学将疼痛列为继呼吸、脉搏、血压、体温后的第五生命体征,足见其在人体健康中的重要性。慢性疼痛是指超过正常愈合时间(一般指3个月)持续存在的自觉疼痛感,相对于急性疼痛而言,慢性疼痛一般会涉及生理或神经系统,并可能会影响身... 现代医学将疼痛列为继呼吸、脉搏、血压、体温后的第五生命体征,足见其在人体健康中的重要性。慢性疼痛是指超过正常愈合时间(一般指3个月)持续存在的自觉疼痛感,相对于急性疼痛而言,慢性疼痛一般会涉及生理或神经系统,并可能会影响身体的多个方面。由于受到发病机制复杂、个体差异大以及神经可塑性等因素的影响,慢性疼痛的治疗难度相对较大。药物治疗是慢性疼痛管理中的常用手段,关于药物的选择或配伍也一直是临床研究的热点。本文综述了钙离子通道阻滞剂在慢性疼痛中的应用,旨在为疾病的治疗提供参考。 展开更多
关键词 慢性疼痛 钙离子通道阻滞剂 研究进展
下载PDF
Antineoplastic Effect of Calcium Channel Blocker-Verapamil and 5-Fluorouracil Intraperitoneal Chemotherapy on Hepatocarcinoma-Bearing Rats
10
作者 曹天生 史海安 周亚魁 《The Chinese-German Journal of Clinical Oncology》 CAS 2002年第2期84-87,共4页
Objective To study the antineoplastic effect of the calcium channel blocker verapamil and 5-fluorouracil intraperitoneal chemotherapy on hepatocarcinoma-bearing rats,and examine the action between calcium channel bloc... Objective To study the antineoplastic effect of the calcium channel blocker verapamil and 5-fluorouracil intraperitoneal chemotherapy on hepatocarcinoma-bearing rats,and examine the action between calcium channel blockers and cytotoxic drugs. Methods We adopted the method of subcapsular implantation of carcinoma tissues of walker-256 in the left liver lobe as a model of liver carcinoma-bearing rats.All experimental animals were divided into four groups.On the sixth day post implantation,in group A (control group) 6ml of saline was injected intraperitoneally once a day for 3 days.In group B(single chemotherapy group) 6ml of 5-Fu 75 mg/kg was injected intraperitoneally once a day for 3 days.In group C(combination of treatment group)both 5-Fu(75mg/kg) and verapamil (25mg/kg) were administered simultaneously as in A and B.In group D(simple verapamil group)only 6ml of verapamil(25mg/kg)was administered as above. Results Compared with groups A, B and D,The volume of cancer and the contents of liver cancer DNA and protein were significantly reduced.The rates of inhibiting cancer(89.9% in group C and 35.4% in group B)were significantly increased in groupC. Group C had significantly long survival time compared to groups A, B and D(P<0.05).By light microscopy, a number of focal necroses were found in cancer tissue in group C.Conclusion Calcium channel blockers can enhance the antineoplastic effect of 5-Fu intraperitonea chemotherapy to liver cancer;The use of verapamil can not increase the toxicity of 5-Fu. 展开更多
关键词 钙通道阻滞剂 5-氟尿嘧啶 维拉帕米 肝细胞癌 荷瘤大鼠 腹腔内化疗 抗肿瘤作用
下载PDF
Effects of Tetrandrine on Cytosolic Free Calcium in Cultured Bovine Aortic Smooth Muscle Cells 被引量:1
11
作者 李新天 王幼林 《Journal of Chinese Pharmaceutical Sciences》 CAS 1998年第2期38-41,共4页
利用Fura2技术和ARCMMIC阳离子系统研究了粉防己碱对传代培养牛主动脉血管平滑肌细胞内游离钙的影响。粉防己碱(1~100μmol·L-1)不影响血管平滑肌细胞的静息钙,但在有胞外钙存在时,对高钾,5... 利用Fura2技术和ARCMMIC阳离子系统研究了粉防己碱对传代培养牛主动脉血管平滑肌细胞内游离钙的影响。粉防己碱(1~100μmol·L-1)不影响血管平滑肌细胞的静息钙,但在有胞外钙存在时,对高钾,5羟色胺,ATP,血管紧张素I,去甲肾上腺素引起的胞内钙升高有抑制作用;在无胞外钙存在时,粉防己碱对苯肾上腺素引起的胞内钙升高也有一定的抑制作用。粉防己碱对高钾升高内钙的抑制作用呈剂量依赖性,IC50值为9.2(95%可信限:5.7~14.9)μmol·L-1。上述结果提示粉防己碱对血管平滑肌细胞的电压依赖性钙通道和受体调控性钙通道均有阻滞作用,对受体调控性钙通道阻滞作用主要表现为阻滞钙离子内流。 展开更多
关键词 粉防己碱 血管平滑肌细胞 FURA-2 钙通道阻滞剂
全文增补中
缬沙坦/氨氯地平复方制剂与ARB+CCB联用治疗高血压的药物经济学比较 被引量:21
12
作者 李海燕 胡宇千 于智杰 《中国药房》 CAS 北大核心 2018年第17期2398-2402,共5页
目的:比较缬沙坦/氨氯地平复方制剂与血管紧张素Ⅱ受体阻滞药(ARB)+钙通道阻滞药(CCB)联用治疗高血压的有效性和经济性。方法:检索Medline、Pub Med、Cochrane Library等3个英文期刊数据库,以及中国知网、维普网、万方数据等3个中文期... 目的:比较缬沙坦/氨氯地平复方制剂与血管紧张素Ⅱ受体阻滞药(ARB)+钙通道阻滞药(CCB)联用治疗高血压的有效性和经济性。方法:检索Medline、Pub Med、Cochrane Library等3个英文期刊数据库,以及中国知网、维普网、万方数据等3个中文期刊数据库,检索范围设定为"题目/摘要(Title/Abstract)",检索词为"缬沙坦/氨氯地平(Valsartan/Amlodipine)""高血压(Hypertension)",检索时限均为建库起至2018年5月。运用Markov模型,基于中国2017年的药品价格与医疗费用,对纳入文献中缬沙坦/氨氯地平复方制剂组与ARB+CCB组患者的有效性和经济性进行对比分析。结果:从医疗卫生系统角度分析,缬沙坦/氨氯地平复方制剂组在Markov模型中非致死性心肌梗死和非致死性卒中状态的人均治疗成本低于ARB+CCB组。与ARB+CCB组比较,缬沙坦/氨氯地平复方制剂组患者治疗的增量效用是质量调整生命年(QALY)每增加0.067 8个单位所需的增量成本为2 916.63元,其增量成本-效果比为42 988.44元/QALY。结论:与ARB+CCB联用相比,缬沙坦/氨氯地平复方制剂治疗高血压可显著降低患者非致死性心肌梗死和非致死性卒中等不良事件的发生,且可为患者节省医疗费用,更具经济性。 展开更多
关键词 缬沙坦/氨氯地平 血管紧张素Ⅱ受体阻滞药 钙通道阻滞药 高血压 经济性
下载PDF
Calcium Signaling is Involved in Negative Phototropism of Rice Seminal Roots 被引量:5
13
作者 CHEN Juan MO Yi-wei XU Hua-wei 《Rice science》 SCIE 2014年第1期39-46,共8页
Calcium ions (Ca2+) act as an intracellular second messenger and affect nearly all aspects of cellular life. They are functioned by interacting with polar auxin transport, and the negative phototropism of plant roo... Calcium ions (Ca2+) act as an intracellular second messenger and affect nearly all aspects of cellular life. They are functioned by interacting with polar auxin transport, and the negative phototropism of plant roots is caused by the transport of auxin from the irradiated side to the shaded side of the roots. To clarify the role of calcium signaling in the modulation of rice root negative phototropism, as well as the relationship between polar auxin transport and calcium signaling, calcium signaling reagents were used to treat rice seminal roots which were cultivated in hydroculture and unilaterally illuminated at an intensity of 100-200 pmol/(m2.s) for 24 h. Negative phototropism curvature and growth rate of rice roots were both promoted by exogenous CaCI2 lower than 100 pmol/L, but inhibited by calcium channel blockers (verapamil and LaCI3), calcineurin inhibitor (chlorpromazine, CPZ), and polar auxin transport inhibitor (N-l-naphthylphthalamic acid, NPA). Roots stopped growing and negative phototropism disappeared when the concentrations increased to 100 pmol/L verapamil, 12.500 ~Jmol/L LaCI3, 60 pmol/L CPZ, and 6 pmol/L NPA. Moreover, 100 pmol/L CaCI2 could relieve the inhibition of LaCI3, verapamil and NPA. The enhanced negative phototropism curvature was caused by the transportation of more auxin from the irradiated side to the shaded side in the presence of exogenous Ca2+. Calcium signaling plays a key role as a second messenger in the process of light signal regulation of rice root growth and negative phototropism. 展开更多
关键词 calcium signaling polar auxin transport calcium channel blocker second messenger negative phototropism
下载PDF
Calcium channel blocker monotherapy versus combination with reninangiotensin system inhibitors on the development of new-onset diabetes mellitus in hypertensive Korean patients 被引量:3
14
作者 Yong Hoon Kim Ae-Young Her +16 位作者 Seung-Woon Rha Byoung Geol Choi Se Yeon Choi Jae Kyeong Byun Yoonjee Park Dong Oh Kang Won Young Jang Woohyeun Kim Woong Gil Choi Tae Soo Kang Jihun Ahn Sang-Ho Park Ji Young Park Min-Ho Lee Cheol Ung Choi Chang Gyu Park Hong Seog Seo 《Journal of Geriatric Cardiology》 SCIE CAS CSCD 2019年第6期439-447,共9页
Background In real practice, two or more antihypertensive drugs are needed to achieve target blood pressure. We investigated the comparative beneficial actions of combination therapy of renin-angiotensin system inhibi... Background In real practice, two or more antihypertensive drugs are needed to achieve target blood pressure. We investigated the comparative beneficial actions of combination therapy of renin-angiotensin system inhibitors (RASI), with calcium channel blockers (CCB) over CCB monotherapy on the development of new-onset diabetes mellitus (NODM) in Korean patients during four-year follow-up periods. Methods A total of 3208 consecutive hypertensive patients without a history of diabetes mellitus who had been prescribed CCB were retrospectively enrolled from January 2004 to December 2012. These patients were divided into the two groups according to the additional use of RASI (the RASI group, n = 1221 and the no RASI group, n = 1987). Primary endpoint was NODM, defined as a fasting blood glucose ≥ 126 mg/dL or hemoglobin A1c ≥ 6.5%. Secondary endpoint was major adverse cardiac events (MACE) defined as total death, myocardial infarction (MI) and percutaneous coronary intervention (PCI). Results After propensity score-matched (PSM) analysis, two propensity- matched groups (939 pairs, n = 1878, C-statistic = 0.743) were generated. The incidences of NODM (HR = 1.009, 95% CI: 0.700–1.452, P = 0.962), MACE (HR = 0.877, 95% CI: 0.544–1.413, P = 0.589), total death, MI, PCI were similar between the two groups after PSM during four years. Conclusions The use of RASI in addition to CCB showed comparable incidences of NODM and MACE compared to CCB monotherapy in non-diabetic hypertensive Korean patients during four-year follow-up period. However, large-scaled randomized controlled clinical trials will be required for a more definitive conclusion. 展开更多
关键词 calcium channel BLOCKER Diabetes mellitus RENIN-ANGIOTENSIN system INHIBITORS
下载PDF
The effect of calcium-antagonist on Bcl-2 and Bax mRNA expression following ischemic brain injury 被引量:4
15
作者 周瑞祥 刘昌勤 孙圣刚 《中国临床康复》 CSCD 2003年第4期672-673,共2页
AIM:In order to explore whether the member of Bcl-2 gene family,for example,B cl-2 and Bax,are induced after cerebral ischemia,and whether expression of gene s can be modulated by calcium-antagonist.METHODS:The rat ce... AIM:In order to explore whether the member of Bcl-2 gene family,for example,B cl-2 and Bax,are induced after cerebral ischemia,and whether expression of gene s can be modulated by calcium-antagonist.METHODS:The rat cerebral ischemic mode ls were made by Nagasawa and Zea Longa improvement method,by occluding left midd le cerebral artery;the expression of Bcl-2 and Bax mRNA were measured by RT-PC R method.RESULTS:After administration of nimodipine, Bcl-2 mRNA was up-regulat ed in the hippocampus at 6 and 24 h after ischemia,while Bax mRNA was down-regu lated at 6 and 24h after ischemia.CONCLUSION:Calcium-antagonist can up-regulat e Bcl-2 mRNA and down-regulate Bax mRNA.Increasing the ratio of Bcl-2 and Bax mRNA may contribute to the anti-apoptic effect of nimodipine. 展开更多
关键词 钙拮抗剂 缺血性脑损伤 BCL-2 Bax 基因表达
下载PDF
ACEI与长效CCB对高血压脑卒中二级预防的效果分析 被引量:10
16
作者 刘国韬 王艾 +5 位作者 刘小红 严利南 曾广民 欧阳学逸 刘世芳 邓东明 《中国当代医药》 2015年第12期102-105,共4页
目的:探讨ACEI与长效CCB对高血压合并脑卒中二级预防的效果。方法回顾性分析2009年6月~2014年6月社区健康档案中高血压合并脑卒中存活跃2个月的患者863例,以ACEI为降压基础治疗的408例,长效CCB为降压基础治疗的455例,主要观察脑卒... 目的:探讨ACEI与长效CCB对高血压合并脑卒中二级预防的效果。方法回顾性分析2009年6月~2014年6月社区健康档案中高血压合并脑卒中存活跃2个月的患者863例,以ACEI为降压基础治疗的408例,长效CCB为降压基础治疗的455例,主要观察脑卒中的复发、脑卒中死亡、心肌梗死发生及死亡、总死亡等,观察时间6~70个月,平均39个月。结果两组患者血压下降幅度比较差异无统计学意义(P〉0.05);两组危险因素干预情况比较差异无统计学意义(P〉0.05);ACEI组联合利尿剂的患者多于CCB组,差异有统计学意义(P〈0.05);两组≥2种联合用药率相比,差异无统计学意义(P〉0.05);ACEI组与CCB组所有脑卒中复发分别为111例(27.2%)、107例(23.5%),差异有统计学意义(P〈0.05);两组其他心血管事件发生率比较,差异无统计学意义(P〉0.05)。结论降压药对高血压合并脑卒中二级预防的效果与脑卒中一级预防相同,长效CCB优于ACEI。 展开更多
关键词 高血压 脑卒中 二级预防 规范治疗 长效钙拮抗剂 血管紧张素转换酶抑制剂
下载PDF
Pharmacological Investigation of Voltage-dependent Ca^(2+) Channels in Human Ejaculatory Sperm in vitro
17
作者 李路 刘继红 +1 位作者 李家贵 叶章群 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2006年第5期607-609,共3页
The types of the voltage-dependent calcium channels (VDCCs) in human ejaculatory sperm and the effects of calcium channel blocker (CCB) on human sperm motility parameters in vitro were investigated. The human sper... The types of the voltage-dependent calcium channels (VDCCs) in human ejaculatory sperm and the effects of calcium channel blocker (CCB) on human sperm motility parameters in vitro were investigated. The human sperm motility parameters in vitro in response to the pharmacological agents nifedipine (NIF, inhibitor of L-type VDCC) and ω-conotoxin (GVIA, inhibitor of N-type VDCC) were compared and analyzed statistically. The results showed that NIF (1, 5, 10 μmol/L) could not only significantly affect human sperm's shape but also spermatozoa motility after incubated at least 10 rain in vitro (P〈0.001). GVIA (0.1, 0.5 and 1 μmol/L) could just only significantly affect human sperm's progressive motility (a %+b %) after incubated for 20 min in vitro (P〈0.01), but they both could not significantly affect spermic abnormality rate. It is suggested that L-type VDCC, non L-type VDCCs and isoform of L-type VDCC exist in the cell membrane of human sperm solely or together, and they participate in the spermic physiological processes especially the spermic motility. 展开更多
关键词 voltage-dependent calcium channels calcium channel blocker human sperm motility in vitro
下载PDF
Exploiting MCF-7 Cells’ Calcium Dependence with Interlaced Therapy
18
作者 Jonathan Pottle Chengrong Sun +1 位作者 Lloyd Gray Ming Li 《Journal of Cancer Therapy》 2013年第7期32-40,共9页
The purpose of this study is to demonstrate MCF-7 cells’ dependence on calcium for growth and to exploit that dependence to improve chemotherapy efficacy. Fura-2 fluorescence imaging shows that MCF-7 cells maintain a... The purpose of this study is to demonstrate MCF-7 cells’ dependence on calcium for growth and to exploit that dependence to improve chemotherapy efficacy. Fura-2 fluorescence imaging shows that MCF-7 cells maintain a higher basal intracellular calcium concentration than non-tumorigenic MCF-10A cells. Blocking T-type calcium channels with mibefradil reduced MCF-7 intracellular calcium concentration. Flow cytometry shows that knocking down T-type calcium channel expression with siRNA caused an increase in MCF-7 cells in G1 phase and a decrease in cells in S phase. Proliferation assays of MCF-7 cells treated with EGTA and thapsigargin reveal the dependence of MCF-7 cell growth on extracellular and intracellular calcium sources, respectively. In vitro, interlaced treatment that alternated the T-type calcium channel blocker NNC-55-0396 with paclitaxel more effectively reduced MCF-7 cell number than chemotherapy alone. In a mouse in vivo model, interlaced mibefradil and paclitaxel more effectively reduced MCF-7 xenograft size than chemotherapy alone. These findings indicate that MCF-7 cells are dependent on calcium for proliferation, particularly in passing the G1/S cell cycle checkpoint. Further, this dependence on calcium can be exploited by alternating treatment with T-type calcium channel blockers with paclitaxel in an interlaced therapy scheme that increases the efficacy of the chemotherapy. 展开更多
关键词 BREAST Cancer calcium calcium Channel blockers Ion channels Interlaced THERAPY
下载PDF
急性钙通道阻滞剂中毒的临床特征研究 被引量:1
19
作者 李辉 任珍 郭治国 《中国全科医学》 CAS 北大核心 2023年第14期1758-1765,共8页
背景 钙通道阻滞剂(CCBs)是我国最常用的一类降压药物,严重CCBs中毒死亡率高,但目前关于其临床特征的相关报道少。目的 通过总结11例急性CCBs中毒患者的临床表现及诊疗结果,分析急性CCBs中毒的临床特点以及血液净化治疗的价值。方法 回... 背景 钙通道阻滞剂(CCBs)是我国最常用的一类降压药物,严重CCBs中毒死亡率高,但目前关于其临床特征的相关报道少。目的 通过总结11例急性CCBs中毒患者的临床表现及诊疗结果,分析急性CCBs中毒的临床特点以及血液净化治疗的价值。方法 回顾性分析2019年1月至2022年6月因CCBs急性中毒就诊于北京大学第三医院急诊科的11例患者的临床表现、症状评分、治疗经过及预后。结果 11例CCBs急性中毒患者中女3例,男8例;平均年龄(39.8±18.0)岁;服药至就诊的中位间隔时间为2.25(6.58)h;来诊时主要临床表现为休克9例(9/11),恶心、呕吐5例(5/11),头晕4例(4/11),乏力3例(3/11),心率增快3例(3/11),心率减慢2例(2/11),晕厥1例(1/11),昏睡1例(1/11)。10例(10/11)患者到达急诊时意识清楚[格拉斯哥昏迷量表(GCS)评分15分]。除了常规治疗,其中6例患者接受血液净化治疗,包括血液灌流联合血浆置换和连续性静脉-静脉血液滤过(CVVH)2例、血液灌流联合CVVH 2例、单独血液灌流2例。此6例中4例患者接受体外膜肺氧合(ECMO)治疗。接受首次血液净化治疗后复查CCBs血药浓度均有下降,硝苯地平下降比例(40.00%~63.64%)高于氨氯地平和维拉帕米(9.09%~26.67%)。11例患者出院时存活9例(9/11)。入院24 h中位急性生理及慢性健康状况评分Ⅱ(APACHEⅡ)评分为10(25)分。入院时中位中毒严重度评分(PSS)为3(1)分。入院时PSS评分为3分的8例患者中死亡2例(2/8),入院时APACHEⅡ评分≥15分的5例患者中死亡2例(2/5)。结论 休克早期意识清晰是急性CCBs中毒较常见表现。在降低血药浓度方面,血液灌流在急性硝苯地平中毒中的作用可能优于在急性氨氯地平和维拉帕米中毒中的作用。APACHEⅡ评分在预测CCBs急性中毒的死亡预后方面可能优于PSS评分。 展开更多
关键词 钙通道阻滞药 中毒 血药浓度 血液净化 临床评分 休克 体外膜肺氧合
下载PDF
多棘蜈蚣钙通道毒素多肽CaTX-Ssmd1原核表达及功能鉴定
20
作者 尹世金 肖敏 +3 位作者 向琪琳 李昱烨 刘柯驿 赵倩茹 《中南民族大学学报(自然科学版)》 CAS 北大核心 2023年第3期313-318,共6页
为了检测广西多棘蜈蚣毒腺转录组文库新基因CaTX-Ssmd1编码的多肽是否具有阻断钙离子通道蛋白的生物活性,将构建的pGEX-4T-1-CaTX-Ssmd1原核表达载体转化Escherichia coli Rosetta(DE3),诱导表达产物经酶切和RP-HPLC分离后得到CaTX-Ssmd... 为了检测广西多棘蜈蚣毒腺转录组文库新基因CaTX-Ssmd1编码的多肽是否具有阻断钙离子通道蛋白的生物活性,将构建的pGEX-4T-1-CaTX-Ssmd1原核表达载体转化Escherichia coli Rosetta(DE3),诱导表达产物经酶切和RP-HPLC分离后得到CaTX-Ssmd1成熟多肽.质谱检测显示CaTX-Ssmd1多肽分子量与理论值一致;钙成像实验表明CaTX-Ssmd1多肽能有效减弱高钾外液灌流激发的小鼠背根神经节(dorsal root ganglion,DRG)细胞[Ca^(2+)]i信号.结论:初步验证了原核表达纯化的CaTX-Ssmd1多肽为新发现的电压门控性钙通道(voltage gated calcium channels,VGCC)阻断剂,丰富了多棘蜈蚣生物活性多肽资源库. 展开更多
关键词 多棘蜈蚣 多肽CaTX-Ssmd1 原核表达 钙通道阻断剂
下载PDF
上一页 1 2 34 下一页 到第
使用帮助 返回顶部