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桂枝的引药作用机制及其对环丙沙星在小鼠体内分布的影响 被引量:4

The drug-guide mechanism of Guizhi and its effect on the distribution of ciprofloxacin in mice
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摘要 研究了桂枝和桂皮醛对环丙沙星在小鼠体内分布的影响,并基于此探讨了桂枝作为引药使用的作用机制.实验中将小鼠分为三组,分别灌胃生理盐水、桂枝(50gkg-1)和桂皮醛(0.25mLkg-1),然后对三组小鼠尾静脉注射环丙沙星(20mgkg-1),并以荧光法测定不同时间点小鼠体内各组织中环丙沙星的浓度.结果显示桂枝、桂皮醛均促进了环丙沙星在四肢的分布,桂枝与桂皮醛组相对于生理盐水组可将环丙沙星在四肢的含量提高约40%~200%,证实了桂枝引药到达肢节的作用.桂枝与桂皮醛组对环丙沙星分布情况的影响没有显著性差异,说明桂皮醛很可能是发挥桂枝引药作用的主要物质. The drug-guide mechanism of Guizhi and its effect on the distribution of ciprofloxacin in mice were investigated in detail. Three groups of mice were administrated with physiological saline, Guizhi (50 g kg?1) and cinnamaldehyde (0.25 mL kg?1), respectively. Then ciprofloxacin was injected into tail intravenous of the mice. Afterward the concentrations of ciprofloxacin in the mice various tissues were determined by fluorospectrophotometry after different time. The results showed that Guizhi and cinnamaldehyde improved the concentrations of ciprofloxacin in the limbs. Compared to the "physiological saline" group, the levels of ciprofloxacin increased 40%~200% after administrating Guizhi or cinnamaldehyde. These results confirmed that Guizhi could deliver drug to limbs, and the performance of Guizhi and cinnamaldehyde was very similar. Therefore, it is concluded that cinnamaldehyde is the key substance for Guizhi as drug-guide.
出处 《中国科学:化学》 CAS CSCD 北大核心 2011年第5期856-862,共7页 SCIENTIA SINICA Chimica
基金 国家自然科学基金(21035005) 西南大学本科生科技创新基金项目(0929001)资助
关键词 桂枝 桂皮醛 引药 环丙沙星 药物分布 荧光分光光度法 Guizhi cinnamaldehyde drug-guide ciprofloxacin drug distribution fluorospectrophotometry
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  • 1周硕,霍海如,郭建友,梁鸿,蔡少青,赵玉英.桂枝汤对体温整合调节作用的活性成分研究[J].中国中药杂志,2007,32(9):865-867. 被引量:17
  • 2Ushiroyarna T, lkeda A, Sakuma K, Ueki M. Comparing the effects of estrogen and an herbal medicine on peripheral blood flow in post-menopausal women with hot flashes: hormone replacement therapy and Gui-Zhi-Fu-Ling-Wan, a Kampo medicine. Am J Chin Med, 2005, 33: 259-267. 被引量:1
  • 3Park WH, Kim KS, Kim KH, Kim DS, Kim CH. The antiplatelet activity of Geiji-Bokryung-Hwan, Korean traditional formulation, is mediated through inhibition of phospholipase C and inhibition of TxB(2) synthetase activity, Int J Immunopharm, 2003, 3:971-978. 被引量:1
  • 4Sekiya N, Kainuma M, Hikiarni H, Nakagawa T, Kouta K, Shibahara N, Shimada Y, Terasawa K. Oren-gedoku-to and Keishi-bukuryo-gan- ryo inhibit the progression of atherosclerosis in diet-induced hypercholesterolemic rabbits. Biol Pharm Bull, 2005, 28:294-298. 被引量:1
  • 5Satoh K, Takano S, Kobayashi T. Keishikajutsubuto (Guizhi-shu-fu-tang) treatment for refractory accumulation of synovial fluid in a patient with pustulotic arthro-osteitis. Fukushima J Med Sci, 2007, 53:33-38. 被引量:1
  • 6马悦颖..桂枝汤苯丙烯类化合物解热构效关系及PGE<,2>释放与TRPV4相关性研究[D].中国中医科学院,2007:
  • 7Ma YY, Huo HR, Li CH, Zhao BS, Li LF, Sui F, Guo SY, Jiang TL. Effects of cinnamaldehyde on PGE(2) release and TRPV4 expression in mouse cerebral microvascular endothelial cells induced by interleukin-l beta. Biol Pharm Bull, 2008, 31:426-430. 被引量:1
  • 8Yang WZ, Ametaj BN, Benchaar C, He ML, Beauchemin KA. Cinnarnaldehyde in feedlot cattle diets: Intake, growth performance, carcass characteristics, and blood metabolites. JAnim Sci, 2010, 88:1082-1092. 被引量:1
  • 9Chao LK, Hua KF, Hsu HY, Cheng SS, Lin IF, Chen CJ, Chen ST, Chang ST. Cinnamaldehyde inhibits pro-inflammatory cytokines secretion from monocytes/macrophages through suppression of intracellular signaling. Food Chem Toxicol, 2008, 46:220-231. 被引量:1
  • 10Youn HS, Lee JK, Choi YJ, Saitoh SI, Miyake K, Hwang DH, Lee JY. Cinnamaldehyde suppresses toll-like receptor 4 activation mediated through the inhibition of receptor oligomerization. Biochem Pharmacol, 2008, 75:494-502. 被引量:1

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