...
首页> 外文期刊>Journal of biomedical science. >In vitro study of the tocolytic effect of oroxylin A from Scutellariabaicalensis root
【24h】

In vitro study of the tocolytic effect of oroxylin A from Scutellariabaicalensis root

机译:黄cut根中催产素A的宫缩作用的体外研究

获取原文
获取原文并翻译 | 示例
           

摘要

Scutellariae Radix is one of the well-known tocolytic Chinese herbs. Oroxylin A is isolated fromthe root of Scutellaria baicalensis. The main syndrome of preterm birth is caused by uteruscontractions from excitatory factors. Administration of tocolytic agents is a strategy to prevent theoccurrence of preterm births. The aim of this study was to investigate the effects of oroxylin A oncontractions of uterine strips isolated from non-pregnant female Wistar rats (250~350 g).Contractions of the uterus were induced with acetylcholine (Ach) (1muM), PGF2alpha (0.1muM),oxytocin (10-3 mu/ml), KCl (56.3 mM), tetraethylammonium (TEA; 1 and 10 mM), 4-aminopyridine(4-AP; 5 mM), glipizide (30muM), a nitric oxide synthase (NOS) inhibitor (LNNA; 10-3M), a beta?-receptor blocker (propranolol; 10muM), and a cyclooxygenase inhibitor (indomethacin; 60muM). Theinhibitory effects of the amplitude and frequency of spontaneous contractions by oroxylin A wereantagonized with Ach (IC50 22.85muM), PGF2? (IC5027.28muM), oxytocin (IC50 12.34muM), TEA; 1 and10 mM (IC_50 52.73 and 76.43muM), 4-AP (IC50 67.16muM), and glipizide (IC5027.53muM), but oroxylinA was not influenced by Ca2+-free medium, LNNA, propranolol, or indomethacin. Otherwise,oroxylin A-mediated relaxation of the rat uterus might occur through opening of uterine calciumdependentpotassium channels or adenosine triphosphate potassium channel activation. Thissuggests that oroxylin A is the tocolytic principle constituent of Scutellariae Radix, and oroxylin Amay provide a lead compound for new tocolytic drug development in the future.
机译:黄cut是著名的安胎中草药之一。从木黄S的根中分离出奥昔林A。早产的主要综合征是由兴奋性因素引起的子宫收缩引起的。服用宫缩抑制剂是一种预防早产发生的策略。这项研究的目的是研究木犀草素A对从未怀孕的Wistar雌性大鼠(250〜350 g)分离出的子宫条的收缩作用。乙酰胆碱(Ach)(1μM),PGF2alpha(0.1 μM),催产素(10-3μm/ ml),氯化钾(56.3 mM),四乙铵(TEA; 1和10 mM),4-氨基吡啶(4-AP; 5 mM),格列吡嗪(30μM),一氧化氮合酶(NOS)抑制剂(LNNA; 10-3M),β-受体阻滞剂(普萘洛尔;10μM)和环氧合酶抑制剂(吲哚美辛;60μM)。用Ach(IC5022.85μM),PGF2β拮抗了羟甲氧基胆红素A对自发性收缩的幅度和频率的抑制作用。 (IC5027.28μM),催产素(IC5012.34μM),TEA; 1和10 mM(IC_50 52.73和76.43μM),4-AP(IC5067.16μM)和格列吡嗪(IC5027.53μM),但oroxylinA不受无Ca2 +培养基,LNNA,普萘洛尔或消炎痛的影响。否则,可能通过打开子宫钙依赖性钾通道或三磷酸腺苷钾通道的激活而发生奥洛西林A介导的大鼠子宫松弛。这表明,草木素A是黄cut的宫缩抑制剂的主要成分,而草木素A可为未来新的宫缩药开发提供先导化合物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号