prazosin
英
美
网络 哌唑嗪; 脉宁平; 派唑嗪; 呱唑嗪; 盐酸哌唑嗪
双语例句
- OBJECTIVE: To determine the content of main component in prazosin hydrochloride tablets by non-aqueous capillary electrophoresis ( NACE).
目的：建立以非水毛细管电泳法快速测定盐酸哌唑嗪片中主药含量的方法。 - With prazosin, the average cardiac index increased ( by) 20 percent and systemic vascular resistance decreased ( by) 20 percent.
使用哌唑嗪，平均心脏指数增加20%，全身血管阻力下降20%。 - Sustained release and biocompatibility of prazosin hydrochloride Preparation and in vitro drug release behavior study of the sustained-release hydrogel based on sulfate chitosan
盐酸哌唑嗪缓释贴片的释药行为及其生物相容性评价SCS药物缓释凝胶的制备及其体外释药研究 - OBJECTIVE To develop a simplified preparative method for osmotic pump tablet using prazosin hydrochloride as a model drug.
目的以盐酸哌唑嗪为模型药物研究单层芯渗透泵片简化的制备方法。 - OBJECTIVE To determine prazosin hydrochloride in human plasma by HPLC-MS method, and to investigate its pharmacokinetics and bioequivalance.
目的：采用高效液相-荧光色谱法测定人血清中拉呋替丁药物浓度，研究临床推荐剂量下的健康人体药动学。 - Studies on Monolithic Core Osmotic Pump Tablets of Prazosin Hydrochloride and Oleanolic Acid
盐酸哌唑嗪和齐墩果酸单层芯渗透泵片的研究 - Evaluation of the therapeutic effect of medroxyprogesterone acetate and prazosin on benign prostatic hypertrophy
甲孕酮与哌唑嗪治疗良性前列腺增生症的疗效评价 - These responses were abolished or diminished by prazosin ( 1 μ M) or calcium channel blocker Mn_ ( 2+) ( 1 mM).
这些慢反应动作电位可被哌唑嗪（1μM）或钙通道阻断剂Mn~（++）（1mM）所取消或抑制。 - Objective To investigate the changes of α 1-adrenergic receptor(α 1-AR) in lung tissues after smoke inhalation injury and the protective effects of prazosin on pulmonary smoke inhalation injury in rats.
目的探讨α1肾上腺素受体（α1-AR）在烟雾吸入伤大鼠肺组织变化与哌唑嗪对烟雾吸入伤的保护作用。 - OBJECTIVE To establish a method for the determination of content and related substances of Prazosin Hydrochloride Tablets by RP-HPLC.
目的以HPLC法测定盐酸哌唑嗪片的含量及有关物质。 - AIM: To evaluate the effects of carvedilol, bisoprolol and prazosin on collage synthesis of cultured rat cardiac fibroblast ( CFs) derived from SHR ( CFs SHR) and Wistar rats ( CFs Wis).
目的：探讨卡维地洛、比索洛尔、哌唑嗪对培养的SHR和Wistar大鼠心脏成纤维细胞（CFs）胶原合成的影响。 - We suggested that prazosin Co might be an effective drug of first choice for chronic hypertensive patients.
所以，复方哌唑嗪可作为肾性高血压和原发性高血压患者的首选降压药物。 - CONCLUSION The solubility and dissolution rate of prazosin hydrochloride are increased by HP-β-CD inclusion complexation evidently.
结论HP-β-CD能大幅度地提高盐酸哌唑嗪的溶解度和溶出度。 - The inhibition of ICV of prazosin also occurred after the cannulation of the Aqueduct of Sylvius.
中脑导水管插管后，侧脑室注射哌唑嗪，抑制RAS的升压作用同样有效； - Prazosin can decrease the pressure of portal vein and the recurrence rate of EVB and increase survival rate after ligation ( P < 0.01).
EVL术后服用哌唑嗪可降低门静脉压力，降低食管静脉曲张复发、EVB再发率，提高生存率（P＜0.01）。 - From the above, it may be suggested that prazosin can prevent and delay the development of liver fibrosis induced by CCl4 in rats.
表明哌唑嗪有预防和延缓鼠肝纤维化发生、发展的作用。 - Prazosin and β antagonist propranolol had no effect on C and A δ units.
哌唑嗪和β受体拮抗剂心得安不影响SS对C和Aδ单位的作用； - α 1 agonist phenylephrine and α 1 antagonist prazosin had no effect on the activity of C and A δ units.
α1受体激动剂苯肾上腺素和拮抗剂哌唑嗪不影响C和Aδ单位的电活动。 - The effects of atenolol with prazosin on physiological characters were studied in rabbit papillary muscles and guinea pig left atria.
本文研究了氨酰心安和哌唑嗪合用对兔乳头肌和豚鼠心房生理特性的作用。 - Conclusion The mechanisms of pulmonary smoke inhalation injury in rats are related to the elevation of the density of α 1-AR in lung tissues, and prazosin has some protective effects on pulmonary smoke inhalation injury.
结论大鼠烟雾吸入性肺损伤的发病机制与α1-AR密度升高有关，哌唑嗪对烟雾吸入伤具有一定保护作用。 - Bilateral microinjection of prazosin into paraventricular nucleus of the hypothalamus greatly attenuated the pressor responses to RAS.
两侧室旁核微量注射哌唑嗪可明显抑制RAS的升压反应。 - Antiarrhythmic effects of prazosin on several experimental models
哌唑嗪在不同实验模型上的抗心律失常作用 - A study of prazosin hydrochloride for prevention of recurrent esophageal or gastric varices bleeding
哌唑嗪预防食管胃静脉曲张破裂再出血的临床对照研究 - Effects of prazosin hydrochloride on rabbits plasma digoxin levels
盐酸哌唑嗪对家兔地高辛血药浓度的影响 - The number of binding sites, association constant and influencing of immobilization alpha 1A-adrenocepters with prazosin and terazosin were determinated by the methods of frontal analysis and zonal elution.
分别采用前沿分析法和竞争置换法研究了固载化α1A-AR与盐酸哌唑嗪.盐酸特拉唑嗪作用的结合位点数、结合常数及其影响因素。