首页> 外文期刊>Journal of herbal pharmacotherapy >The ingestion of Ginkgo biloba extract (EGb 761) inhibits arachidonic acid-mediated platelet aggregation and thromboxane B2 production in healthy volunteers.
【24h】

The ingestion of Ginkgo biloba extract (EGb 761) inhibits arachidonic acid-mediated platelet aggregation and thromboxane B2 production in healthy volunteers.

机译:摄入银杏叶提取物(EGb 761)可以抑制健康志愿者体内花生四烯酸介导的血小板聚集和血栓烷B2的产生。

获取原文
获取原文并翻译 | 示例
           

摘要

Twelve non-diabetic volunteers (age = 39 +/- 13 years, BMI = 23.5 +/- 3.5) undertook a randomized double-blind placebo-controlled crossover study in which they ingested either 120 mg of EGb 761 or a placebo daily for 3 months and then switched to the other test capsules for the next 3 months. Platelet aggregation in platelet-rich plasma (PRP) was performed at the end of each 3-month arm, with or without 1-min incubation with graded doses of EGb 761. In the placebo cycles, AA-stimulated TXB2 production was 2581 +/-1337 pg/10(6) platelets (range 897-5485) compared to 1668 +/- 992 pg/10(6) platelets (range 6-1668) in the EGb 761 cycles (p < 0.005). Incubation of PRP with EGb 761 (150 microg/ml) completely inhibited platelet aggregation accompanied by inhibition of TXB2 synthesis in all subjects both in the placebo (<200 pg TXB2/10(6) platelets) and EGb 761 cycles (< 120 TXB2/10(6) platelets) (p < 0.0001). These results support EGb 761-mediated inhibition of platelet TXB2 synthesis in vivo.
机译:12名非糖尿病志愿者(年龄= 39 +/- 13岁,BMI = 23.5 +/- 3.5)进行了一项随机双盲安慰剂对照交叉研究,他们每天摄入120 mg EGb 761或安慰剂3几个月,然后在接下来的3个月内改用其他测试胶囊。在每个3个月组的末尾进行富血小板血浆(PRP)中的血小板聚集,无论是否使用分级剂量的EGb 761孵育1分钟。在安慰剂周期中,AA刺激的TXB2产生为2581 + / EGB 761周期中-1337 pg / 10(6)血小板(范围897-5485)与1668 +/- 992 pg / 10(6)血小板(范围6-1668)相比(p <0.005)。在EPG 761(<200 pg TXB2 / 10(6)血小板)和EGb 761周期(<120 TXB2 /)中,在所有受试者中将ERP 761(150 microg / ml)与PRP孵育完全抑制了血小板凝集,同时抑制了TXB2的合成。 10(6)个血小板)(p <0.0001)。这些结果支持了EGb 761介导的体内血小板TXB2合成的抑制。

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