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Research Article

Inhibitory activities of baicalin against renin and angiotensin-converting enzyme

, , , &
Pages 401-406 | Received 04 Jun 2011, Accepted 22 Jul 2011, Published online: 02 Dec 2011
 

Abstract

Context: Baicalin has been characterized as the active compound and quality control marker in Scutellaria baicalensis Georgi, traditionally used as a hypotensive herb.

Objectives: To investigate the inhibitory activities of baicalin against renin and angiotensin-I converting enzyme (ACE) and their molecule mechanism of interactions.

Methods: The fluorescence method using renin substrate 1(R-2932) and the spectroscopy method by Cushman were used to determine renin and ACE activities, respectively. The fluorescence quench techniques were used to characterize their interactions.

Results: The results showed that baicalin inhibited renin activity with an IC50 value of 120.36 µM and inhibited ACE activity with an IC50 value of 2.24 mM in vitro. The fluorescence emission of both renin and ACE were efficiently quenched by baicalin and a complete quenching was achieved at a high concentration of baicalin. Furthermore, baicalin was more effective in quenching the fluorescence of renin (KSV = 60 × 103 M−1) than ACE (KSV = 17.1 × 103 M−1). The quenching of fluorescence of renin and ACE involved static interactions, which was characterized by the formation of quencher–enzyme complex. The baicalin–renin complex formed through three-sites binding including the active site with a binding constant of 796.15 × 1013 M−1, but there was only one binding site for the baicalin–ACE complex with a much smaller binding constant of 6.8 × 105 M−1.

Conclusion: The inhibition activity of baicalin against renin was a result of the formation of stable complex through multisites binding including the active site, which could explain the higher inhibitory efficiency.

Acknowledgments

This work was supported by the National Natural Science Foundation of China (20673084), the Natural Science Foundation Project of CQ CSTC (CSTC, 2007BB0345), and the Natural Sciences and Engineering Research Council of Canada (NSERC).

Declaration of interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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