|Year : 2013 | Volume
| Issue : 35 | Page : 196-201
Interaction of lobed kudzuvine root, rhizoma chuanxiong with both acetylcholinesterase and beta-amyloid (Aβ1-42)
Li Shuai1, Zhi Chen2, Ruixi Gao1, Tianming Yang1
1 College of Pharmacy, South-Central University for Nationalities, Minyuan Road 708, Hongshan District, Wuhan, Hubei, 430074, China
2 Center of Analysis, Guangdong Medical College, Dongguan, 523808, China
|Date of Submission||20-Jun-2012|
|Date of Acceptance||03-Oct-2012|
|Date of Web Publication||11-Jun-2013|
Pharmacy College of South-Central, University for Nationalities, Wuhan, Hubei Province 430074
Source of Support: The Special Fund for Basic Scientific Research of
Central Colleges, South-Central University for Nationalities (CZQ12020)., Conflict of Interest: None
| Abstract|| |
Background: Lobed kudzuvine root and rhizoma chuanxiong are effective drugs in traditional Chinese medicine. Objective: Extracts of the two medicines were investigated for their in vitro of beta-amyloid (Aβ1-42)-aggregation-and acetylcholinesterase (AChE)-inhibitory activities. Materials and Methods: The interaction of lobed kudzuvine root, rhizoma chuanxiong with both acetylcholinesterase and beta-amyloid (Aβ1-42) were studied by Michaelis-Menten equations, Thioflavin T (ThT) fluorescence analysis and transmission electron microscope (TEM). Results: Inhibition of acetylcholinesterase showed that 1-butanol fraction of the two medicines were noncompetitive inhibition, apparent inhibition constants were 9.947 and 7.1523. ThT fluorescence analysis and TEM results indicated that inhibition of the water fraction and 1-butanol fraction (both lobed kudzuvine root and rhizoma chuanxiong) was better. Conclusion: The result supported further research on chemical constituents and pharmacological mechanisms.
Keywords: Acetylcholinesterase, Beta-amyloid, lobed kudzuvine root, rhizoma chuanxiong
|How to cite this article:|
Shuai L, Chen Z, Gao R, Yang T. Interaction of lobed kudzuvine root, rhizoma chuanxiong with both acetylcholinesterase and beta-amyloid (Aβ1-42). Phcog Mag 2013;9:196-201
|How to cite this URL:|
Shuai L, Chen Z, Gao R, Yang T. Interaction of lobed kudzuvine root, rhizoma chuanxiong with both acetylcholinesterase and beta-amyloid (Aβ1-42). Phcog Mag [serial online] 2013 [cited 2019 Oct 21];9:196-201. Available from: http://www.phcog.com/text.asp?2013/9/35/196/113262
| Introduction|| |
Alzheimer's disease (AD) is a debilitating neurodegenerative disorder affecting millions of elderly individuals throughout the world. As the "baby boom" generation ages and medical advances enable people to live longer, the number of people afflicted by AD is expected to increase dramatically. Given these trends, there is a tremendous need to develop therapeutics that block or reverse this debilitating neurodegenerative disease.
Multiple factors for AD are thought to be the etiology of the disease, including oxidative stress, aluminum toxicity, cholinergic hypothesis,  amyloid cascade hypothesis.  In cholinergic hypothesis, function of acetylcholinesterase was damaged in AD, so some acetylcholinesterase inhibitors are developed as a drug. In Aβ hypothesis, the conclusion of increasing and depositing abnormal Aβ is to start the core of the event. 
Many kinds of active constituents such as alkaloids, flavonoids, saponins, coumarins, and lignanoids, etc., in Chinese materia medica aim directly at the pathogenesy of AD. And the alkaloids are usually contained in the water fraction. Flavonoids and coumarins are usually contained in 1-butanol fractions.
Rhizoma Chuanxiong is one of the most commonly used of the Chinese herbs; it has an excellent safety record and no evident toxicity. , The initial applications were based on traditional uses of the crude herb in decoctions and pills: for vitalizing blood circulation in the treatment of cardiovascular diseases and for treatment of headache and vertigo. , Lobed kudzuvine root was derived from Shen Nong Ben Cao Jing, which had a long history. Active ingredient is daidzein. It is commonly used for treatment of exogenous fever, head, and neck pain.
Therefore, in this work, we first prepared water, petroleum ether, ethyl acetate, and 1-butanol fractions (both lobed kudzuvine root and rhizoma chuanxiong). Then, the AChE-inhibitory activities of extracts of the two medicines were screened in detail. It was found that 1-butanol fraction showed typical noncompetitive inhibition of AChE. Finally, the interaction with Aβ1-42 was analyzed using Thioflavin T (ThT) and transmission electron microscope (TEM). The water fraction and 1-butanol fractions (both lobed kudzuvine root and rhizoma chuanxiong) were found to suppress the formation of amyloid fibrils.
| Materials and Methods|| |
Materials and reagent
The dried leaves of lobed kudzuvine root and rhizoma chuanxiong were authenticated by Dr. Wan Dingrong, Professor in Pharmacognosy at School of Pharmacy, South-central University for Nationalities. The dried leaves of lobed kudzuvine root and rhizoma chuanxiong were extracted with 70% aqueous ethyl alcohol for three times. It was refluxed for 2 h each time. The combined solution was filtered and concentrated under reduced pressure to afford the 70% ethanolic extract. The majority of the 70% ethanolic extract was suspended with water and successively extracted with petroleum ether, ethyl acetate, and 1-butanol.
AChE was obtained from Sigma(St Louis, MO, US), phosphate buffer (PBS) pH=8.0, 5,5′-dithiobis-2-nitrobenzoic acid (DTNB, 10 mM) and acetylthiocholine iodide (ATCI, 2 mM) were purchased from A Johnson Matthey Company and reconstituted in 50 mM aq. phosphate buffer (pH=8.0), ThT was obtained from Sigma-Aldrich, other reagents are analyzed pure. UV-Visible spectrophotometer (UV-1800PC) was supplied from Shanghai Mapada Instruments Co. Ltd.
Aβ 1-42 was purchased from Shanghai Apeptide Co. Ltd., purity was higher than 95% (weight). Aβ 1-42 was dissolved in 100% PBS and stored at -20°C. Fractions of Lobed kudzuvine root and rhizoma chuanxiong were dissolved in dimethylsulfoxide (DMSO) and diluted to 2.5 g/l in PBS.
Inhibition of AChE
All tests were conducted according to reported standard procedures. , The components were added in the following order: 1000 μL of DTNB (5 mM), different concentrations of ATCI 500 μL (0.25, 0.4, and 0.5 mM), testing samples (inhibitor) 20 μL (20 μl DMSO in control) were mixed and then adjusted to 2000 μl by addition of buffer. AChE solution (40 μL, 10 U/ml) was added to initiate the reaction at room temperature. Reaction kinetics were analyzed by UV-VIS spectrophotometry, following the absorbance of the thioate product at 412 nm (measuring time was 90 s). Kinetics data were then analyzed by double-reciprocal plots using standard Michaelis-Menten equations  for noncompetitive and competitive inhibition, respectively. The actual type of inhibition was determined by analyzing the graphs of double-reciprocal plots. Parameters Km and Vm were calculated in the absence of inhibitor (I), and apparent inhibition constants Ki were obtained from Km /Vm as a function of inhibitor concentration [I] at a given substrate concentration [S] [Figure 1].
ThT fluorescence assay
ThT dye was used to determine the presence of amyloid-like aggregates. The fluorescence emission of ThT is changed when ThT binds to β-sheet aggregate structures.  A solution of Ab1-42 (10 mM) with/without fractions of lobed kudzuvine root and rhizoma chuanxiong was incubated at 37°C for 48 h. To determine amyloid fibril formation, the solutions containing Aβ1-42 with/without fractions of lobed kudzuvine root and rhizoma chuanxiong were added to 50 mM glycine-NaOH buffer, pH 8.5, containing 25 mM ThT 180 μL, 50 mM PBS 200 μL to a final volume of 420 μL. Each assay was run in triplicate and fluorescence intensities were measured at 440 nm (excitation) and 490 nm (emission). 
To prepare specimens for TEM imaging, 10 mM Aβ1-42 and preformed Aβ1-42 were incubated in the presence or absence of fractions of lobed kudzuvine root and rhizoma chuanxiong for 48 h at 37°C, and then a 10 mL aliquot of each sample was spotted onto a glow-discharged, carbon-coated grid, and incubated for 20 min. The droplet then was displaced with an equal volume of 2.5% glutaraldehyde (v/v) and incubated for an additional 5 min. Finally, the grid was stained with 10 μL uranyl acetate twice, and the solution was wicked off and then the grid was air-dried. , Samples were examined using a JEOL JEM-2100 (HR) transmission electron microscope. All images were captured at voltage of 200 kV at instrumental magnification of 6000×.
| Results|| |
Inhibition of AChE
In [Figure 2]a and b, a plot of 1/V 0 vs. 1/[ATCI] is shown for 1-butanol fraction (rhizoma chuanxiong) together with a plot of Km /Vm as inhibitor concentration ([I]) 2 . The findings show that, at the drug concentrations tested (0.25, 0.4, and 0.5 mM), water saturated 1-butanol fraction showed typical noncompetitive inhibition of AChE, that is, the saturation parameter Vm was decreasing with increasing inhibitor concentration, while Km changed only slightly. [Figure 2]c and d present the kinetics analysis and double-reciprocal plot of 1-butanol fraction (lobed kudzuvine root). The 1-butanol fraction of both Rhizoma chuanxiong and lobed kudzuvine root showed typical noncompetitive inhibition of AChE [Figure 2].
|Figure 2: Kinetics analysis (a) and double-reciprocal plot (b) of acetylcholinesterase inhibition by 1-butanol fraction of rhizoma chuanxiong. Kinetics analysis (c) and double-reciprocal plot (d) of acetylcholinesterase inhibition by 1-butanol fraction of lobed kudzuvine root|
Click here to view
Analysis of Thioflavin T fluorescence intensity
[Figure 3] shows the ThT fluorescence spectra of Aβ (control) with/without fractions of lobed kudzuvine root [Figure 3]a and rhizoma chuanxiong [Figure 3]b, incubated for 48 h). [Figure 3]c and d displays the ThT fluorescence spectra of elderly Aβ with/without those fractions. The fluorescence intensity of untreated Aβ (control) was relatively strong. When fractions, especially the water fraction, 1-butanol fraction and ethyl acetate fraction (lobed kudzuvine root and rhizoma chuanxiong), were added into Aβ, the fluorescence intensity decreased. The inhibitory effect of 1-butanol fraction (rhizoma chuanxiong and lobed kudzuvine root) was much stronger than that of other fractions. The fluorescence intensity of the 1-butanol fraction (lobed kudzuvine root and rhizoma chuanxiong) is about 13% and 50% compared with the control, respectively. As seen in [Figure 3]c and d, four fractions (lobed kudzuvine root) and three fractions (rhizoma chuanxiong) inhibit the aggregated Aβ [Figure 3].
|Figure 3: ThT fluorescence emission spectra profiles in the presence of Aβ1-42 (control) with or without lobed kudzuvine root (a, c), rhizoma chuanxiong (b, d). Results of the elderly group were c and d|
Click here to view
[Figure 4]a shows the typical amyloid fibril formation form untreated aged (incubated for 48 h) Aβ 1-42.  The filaments are several microns in length. However, when Aβ 1-42 was coincubated with the water fraction and 1-butanol fraction (both lobed kudzuvine root and rhizoma chuanxiong), only less fibrils and a few short fibrils were observed [Figure 4]b-e.
|Figure 4: TEM of Aβ 1-42 aggregation with or without lobed kudzuvine root and rhizoma chuanxiong when incubated alone (a), or with rhizoma chuanxiong (water fraction, b, 1-butanol fraction, c) and lobed kudzuvine root (water fraction, d, 1-butanol fraction, e)|
Click here to view
| Discussion|| |
Acetylthiocholine iodide (ATCI) was used as substrate to screen two medicines' AChE activities. , From [Figure 2], we could calculate that the values of the apparent inhibition constants (Ki ) calculated for 1-butanol fraction (rhizoma chuanxiong and lobed kudzuvine root) were 9.947 and 7.1523, respectively.
ThT binds specifically to amyloid and this binding produces a shift in its emission spectrum and a fluorescent signal proportional to the amount of amyloid formed. The method is more specific than other methods, such as turbidity or sedimentation, for the semi-quantitative determination of amyloid-like aggregates. Both the water fraction and ethyl acetate fraction (lobed kudzuvine root and rhizoma chuanxiong) significantly inhibit the aggregation of Aβ/the aggregated Aβ.
TEM imaging results are consistent with above fluorescence results. It suggests that the water fraction and 1-butanol fraction (both lobed kudzuvine root and rhizoma chuanxiong) can inhibit formation of Aβ fibrils.
In the present study, the 70% ethanolic extract from lobed kudzuvine root (rhizoma chuanxiong) are separated into the four fractions of petroleum ether fraction, ethylacetate fraction, 1-butanol fraction, and water fraction by liquid-liquid extraction. The result indicates that extracts of lobed kudzuvine root and rhizoma chuanxiong can inhibit aggregation of Aβ1-42, especially the water fraction and 1-butanol fraction. The 1-butanol fraction (lobed kudzuvine root and rhizoma chuanxiong) shows the highest AChE-inhibition and Aβ-aggregation-inhibition activities. However, due to the nature of multiple chemical constituents involved in the natural plants as well as the multifactorial condition of AD, it is very important to further separate chemical constituents from the 1-butanol fraction and water fraction. Further research will be conducted on chemical constituents and pharmacological mechanisms in the future.
| Acknowledgement|| |
The authors gratefully acknowledge the Special Fund for Basic Scientific Research of Central Colleges, South-Central University for Nationalities (CZQ12020).
| References|| |
|1.||Kasa P, Rakonczay Z, Gulya K. The cholinergic system in Alzheimer's disease. Prog Neurobiol 1997;52: 511-35. |
|2.||Hardy JA, Higgins GA. Alzheimer's disease: The amyloid cascade hypothesis. Science 1992;256:184-5. |
|3.||Hardy J, Selkoe DJ. The Amyloid Hypothesis of Alzheimer's Disease: Progress and Problems on the Road to Therapeutics. Science 2002;297:353-6. |
|4.||Li W, Guo J, Tang Y, Wang H, Huang M, Qian D, et al. Pharmacokinetic comparison of ferulic acid in normal and blood deficiency rats after oral administration of angelica sinensis, ligusticum chuanxiong and their combination. Int J Mol Sci 2012;13:3583-97. |
|5.||Zhang WJ, Wang P, Yang MJ, Wang YG, Ju Y, Du RH. Analyze and compare activities of polysaccharide form rhizoma chuanxiong and radix paeoniae rubra. Chin Med Mat 2011;34:1569-74. |
|6.||Peng C, Xie X, Wang L, Guo L, Hu T. Pharmacodynamic action and mechanism of volatile oil from Rhizoma Ligustici Chuanxiong Hort. on treating headache. Phytomedicine 2009;16:25-34. |
|7.||Zhao PY. Clinical effect of ligustrazine in patients with benign paroxysmal positional vertigo. Chin J Int Tradit West Med 1991;11:719-20. |
|8.||Chou P, Fasman GD. Empirical predictions of protein conformation. Annu Rev Biochem 1978;47:251-76. |
|9.||Pastorin G, Marchesan S, Hoebeke J, Da Ros T, Ehret-Sabatier L,Briand JP, et al. Design and activity of cationic fullerene derivatives as inhibitors of acetylcholinesterase. Biomol Chem 2006;4:2556-62. |
|10.||Ellman GL, Courtney KD, Andres VJ, Feather-stone RM. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol 1961;7:88-95. |
|11.||Levine H. Thioflavine T interaction with synthetic Alzheimer's disease β-amyloid peptides: Detection of amyloid aggregation in solution. Protein Science 1993;2:404-10. |
|12.||Feng Y, Wang XP, Yang SG, Wang YJ, Zhang X, Du XT, et al. Resveratrol inhibits beta-amyloid oligomeric cytotoxicity but does not prevent oligomer formation. Neuro Toxicol 2009;30: 986-95. |
|13.||Tang CH, Wang CS. Formation and Characterization of Amyloid-like Fibrils from Soy β-Conglycinin and Glycinin. J Agric Food Chem 2010;58:11058-66. |
|14.||Hindo SS, Mancino AM, Braymer JJ, Liu Y, Vivekanandan S, Ramamoorthy A, et al. Small Molecule Modulators of Copper-Induced Aβ Aggregation. J Am Chem Soc 2009;131:16663-5. |
|15.||Kogan MJ, Bastus NG, Amigo R, Grillo-Bosch D, Araya E, Turiel A, et al. Nanoparticle-Mediated Local and Remote Manipulation of Protein Aggregation. Nano Lett 2006;6:110-5. |
|16.||White BJ, Harmon HJ. Interaction of monosulfonate tetraphenyl porphyrin, a competitive inhibitor, with acetylcholinesterase. Biosens Bioelectron 2002;17:463-9. |
|17.||Liu Q, Zhou PJ, Chen Y. Inhibition Effect of Chlorophenols on Acetylcholineterase and Its Kinetics. Wuhan Univ (Nat Sci Ed) 2010;56:542-6. |
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
|This article has been cited by|
||Study on Pharmacokinetics of Three Preparations from Levistolide A by LC–MS-MS
| ||Wen-Qing He,Wei-Sheng Lv,Yu Zhang,Zhao Qu,Ren-Rong Wei,Lei Zhang,Chang-Hui Liu,Xin-Xin Zhou,Wei-Rong Li,Xiao-Tao Huang,Qi Wang |
| ||Journal of Chromatographic Science. 2015; 53(8): 1265 |
|[Pubmed] | [DOI]|