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DA-9701(一种由牵牛子和延胡索制成的新型促动力剂)的胃促动力作用

Gastroprokinetic effects of DA-9701, a new prokinetic agent formulated with Pharbitis Semen and Corydalis Tuber.

作者信息

Lee Tae Ho, Choi Jeong June, Kim Dong Hee, Choi Seok, Lee Kang Ro, Son Miwon, Jin Mirim

机构信息

Dong-A Pharm. Co., Ltd., R&D Center, Yongin, Gyeonggi-do 449-905, Republic of Korea.

出版信息

Phytomedicine. 2008 Oct;15(10):836-43. doi: 10.1016/j.phymed.2008.02.019. Epub 2008 May 19.

Abstract

To develop a therapeutic for functional dyspepsia (FD), a prokinetic agent, DA-9701 has been newly formulated with Pharbitis Semen and Corydalis Tuber and we evaluated the gastroprokinetic effects of DA-9701 in comparison with conventional prokinetics. Oral administration with DA-9701 not only significantly accelerated gastric emptying in normal rats but also restored the delayed gastric emptying caused by apomorphine and cisplatin up to almost normal levels. For gastrointestinal transit, DA-9701 caused FITC-dextran to travel a significantly longer distance than the control, and in the delayed GI transit models induced by laparotomy and atopine, DA-9701 considerably increased the values of mean geometric center (MGC), while the conventional prokinetics rarely showed significant effects. Furthermore, DA-9701 drastically increased the gastric accommodation in Beagle dogs, shifting the pressure-volume curve toward considerably higher volume compared to the control, which was comparable to that of cisapride. These results indicate that DA-9701 has potential as a safe and effective therapeutic for FD patients with abnormalities in GI motor function.

摘要

为开发一种用于功能性消化不良(FD)的治疗药物,一种促动力剂DA - 9701已与牵牛子和延胡索重新配制,我们评估了DA - 9701与传统促动力剂相比的胃促动力作用。给正常大鼠口服DA - 9701不仅显著加速了胃排空,还将阿扑吗啡和顺铂引起的胃排空延迟恢复到几乎正常水平。对于胃肠传输,DA - 9701使异硫氰酸荧光素标记的葡聚糖传输的距离比对照组显著更长,并且在剖腹术和阿托品诱导的胃肠传输延迟模型中,DA - 9701显著增加了平均几何中心(MGC)值,而传统促动力剂很少显示出显著效果。此外,DA - 9701显著增加了比格犬的胃容纳能力,与对照组相比,压力 - 容积曲线向显著更高的容积偏移,这与西沙必利相当。这些结果表明,DA - 9701有潜力成为治疗胃肠运动功能异常的FD患者的安全有效药物。

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