Synthesis and antitussive evaluation of verticinone-cholic acid salt,a novel and potential cough therapeutic agent  被引量:2

Synthesis and antitussive evaluation of verticinone-cholic acid salt,a novel and potential cough therapeutic agent

在线阅读下载全文

作  者:Fang-zhou XU Chang CHEN Yong-hui ZHANG Han-li RUAN Hui-fang PI Pong ZHANG Ji-zhou WU 

机构地区:[1]Faculty of Pharmaceutical Sciences, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China [2]Dempartment of Pharmacy, Peking University Shenzhen Hospital, Shenzhen 518036, China

出  处:《Acta Pharmacologica Sinica》2007年第10期1591-1596,共6页中国药理学报(英文版)

基  金:the Fund of the Key Project of the Rducation Ministry, China, 2006;the Fund of the International Cooperation Project of Science and Techno-logy;the Ministry of Science and Techno-logy, China (China and Korea, № 2006DFA33210);The present study has been applied fnr patent in China (application № 200610019027.0).

摘  要:Aim: To seek a novel and potent antitussive drug based on Shedan-Chuanbei powder, a complex of traditional Chinese medicine preparation for cough therapy. Methods: Verticinone--cholic acid (Ver-CA) salt, a novel, salifying derivative of verticinone and cholic acid, both of which are the major bioactive components in Shedan-Chuanbei powder, was synthesized. We then evaluated the antitussive activity and the acute toxicity of the salt. Results: The new compound, with good solubility in water, has much more potent antitussive activity in comparison with the same dose of single verticinone and single cholic acid. The administration 3 mg/kg of Ver-CA could result in over 50% reduction of a citric acid-induced cough. Pretreatment with naloxone (0.8 mg/kg, ip) can only partially antagonize its antitussive effect. On the other hand, glybenclamide (3 mg/kg, ip), an ATP-sensitive K^+channel blocker, can also significantly reduce the antitussive effect of Ver-CA. A further acute toxicity study showed that the LD50 values of Ver-CA were 3 times that of verticinone. Conclusion: Based on the studies of pharmacology and acute toxicity, the salt has a synergic and attenuated toxicity compared with single verticinone and cholic acid. Moreover, the present study also suggests that VerCA, a potential novel antitussive agent, may exert its antitussive effect via both the peripheral (modulated by ATP-sensitive K^+ channels) and central mechanisms (modulated by the opioid receptor).Aim: To seek a novel and potent antitussive drug based on Shedan-Chuanbei powder, a complex of traditional Chinese medicine preparation for cough therapy. Methods: Verticinone--cholic acid (Ver-CA) salt, a novel, salifying derivative of verticinone and cholic acid, both of which are the major bioactive components in Shedan-Chuanbei powder, was synthesized. We then evaluated the antitussive activity and the acute toxicity of the salt. Results: The new compound, with good solubility in water, has much more potent antitussive activity in comparison with the same dose of single verticinone and single cholic acid. The administration 3 mg/kg of Ver-CA could result in over 50% reduction of a citric acid-induced cough. Pretreatment with naloxone (0.8 mg/kg, ip) can only partially antagonize its antitussive effect. On the other hand, glybenclamide (3 mg/kg, ip), an ATP-sensitive K^+channel blocker, can also significantly reduce the antitussive effect of Ver-CA. A further acute toxicity study showed that the LD50 values of Ver-CA were 3 times that of verticinone. Conclusion: Based on the studies of pharmacology and acute toxicity, the salt has a synergic and attenuated toxicity compared with single verticinone and cholic acid. Moreover, the present study also suggests that VerCA, a potential novel antitussive agent, may exert its antitussive effect via both the peripheral (modulated by ATP-sensitive K^+ channels) and central mechanisms (modulated by the opioid receptor).

关 键 词:verticinone-cholic acid salt Shedan-Chuan-bei powder  cholic acid verticinone antitussive effect ATP-sensitive K^+ channels 

分 类 号:R98[医药卫生—药品]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象