The Screening of Anticholinergic Accumulation by Traditional Chinese Medicine

被引:6
作者
Zhang, Ming [1 ]
Vrolijk, Misha [1 ]
Haenen, Guido R. M. M. [1 ]
机构
[1] Maastricht Univ, Dept Pharmacol & Toxicol, NL-6200 MD Maastricht, Netherlands
关键词
Traditional Chinese Medicine; anticholinergic accumulation; Total Atropine Equivalents; ANTIOXIDANT CAPACITY; OLDER-PEOPLE; RISK SCALES; ASTHMA; DRUGS; POPULATION; RECEPTORS; EQUATION; OUTCOMES; BLOOD;
D O I
10.3390/ijms19010018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many Western drugs can give rise to serious side effects due to their ability to bind to acetylcholine receptors in the brain. This aggravates when they are combined, which is known as anticholinergic accumulation (AA). Some bioactives in Traditional Chinese Medicine (TCM) are known to block acetylcholine receptors and thus potentially cause AA. The AA of TCM was screened by quantifying the displacement of [H-3] pirenzepine on acetylcholine receptors in a rat brain homogenate. We used a new unit to express AA, namely the Total Atropine Equivalents (TOAT). The TOAT of various herbs used in TCM was very diverse and even negative for some herbs. This is indicative for the broadness of the pallet of ingredients used in TCM. Three TCM formulas were screened for AA: Ma Huang Decotion (MHD), Antiasthma Simplified Herbal Medicine intervention (ASHMI), and Yu Ping Feng San (YPFS). The TOAT of ASHMI was indicative for an additive effect of herbs used in it. Nevertheless, it can be calculated that one dose of ASHMI is probably too low to cause AA. The TOAT of YPFS was practically zero. This points to a protective interaction of AA. Remarkably, MHD gave a negative TOAT, indicating that the binding to the acetylcholine receptors was increased, which also circumvents AA. In conclusion, our results indicate that TCM is not prone to give AA and support that there is an intricate interaction between the various bioactives in TCM to cure diseases with minimal side effects.
引用
收藏
页数:12
相关论文
共 33 条
[1]   Anticholinergic effect on cognition (AEC) of drugs commonly used in older people [J].
Bishara, Delia ;
Harwood, Daniel ;
Sauer, Justin ;
Taylor, David M. .
INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY, 2017, 32 (06) :650-656
[2]  
Boustani M., 2008, Aging Health, V4, P311, DOI [10.2217/1745509XA3.311, DOI 10.2217/1745509X.4.3.311, 10.2217/1745509X.4.3.311]
[3]  
Campbell N, 2009, CLIN INTERV AGING, V4, P225
[4]  
CHAN TYK, 1995, VET HUM TOXICOL, V37, P156
[5]   The power issue:: determination of KB or Ki from IC50 -: A closer look at the Cheng-Prusoff equation, the Schild plot and related power equations [J].
Cheng, HC .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 2001, 46 (02) :61-71
[6]  
Cheng KL, 2013, HONG KONG MED J, V19, P38
[7]  
CHENG Y, 1973, BIOCHEM PHARMACOL, V22, P3099
[8]   A model of anticholinergic activity of atypical antipsychotic medications [J].
Chew, Marci L. ;
Mulsant, Benoit H. ;
Pollock, Bruce G. ;
Lehman, Mark E. ;
Greenspan, Andrew ;
Kirshner, Margaret A. ;
Bies, Robert R. ;
Kapur, Shitij ;
Gharabawi, Georges .
SCHIZOPHRENIA RESEARCH, 2006, 88 (1-3) :63-72
[9]   G-protein coupled receptors in lipid rafts and caveolae: how, when and why do they go there? [J].
Chini, B ;
Parenti, M .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2004, 32 (02) :325-338
[10]   Insights from modelling the 3D structure of the extracellular domain of α7 nicotinic acetylcholine receptor [J].
Chou, KC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 319 (02) :433-438