Metabolic characteristics of active parts of lipid-lowering flavonoid extract of Daidai in liver and intestinal microsomes of rats.
10.19540/j.cnki.cjcmm.20181129.007
- Author:
Hua-Ping ZENG
1
;
Hong CHEN
2
;
Dan CHEN
3
;
Guo-Ping MA
3
;
Xian-Mu ZHU
3
;
Xiu-Mian LIU
3
;
Li-Ting HONG
3
Author Information
1. Institute of Senile Disease,Fujian Provincial Hospital Cadre Special Clinic Fuzhou 350001,China Department of Pharmacy,Fujian University of Traditional Chinese Medicine Fuzhou 350122,China.
2. Institute of Senile Disease,Fujian Provincial Hospital Cadre Special Clinic Fuzhou 350001,China.
3. Department of Pharmacy,Fujian University of Traditional Chinese Medicine Fuzhou 350122,China.
- Publication Type:Journal Article
- Keywords:
Daidai lipid-lowering flavonoid extract;
intestinal microsomes;
liver microsomes;
narngin;
neohesperidin;
phase Ⅰmetabolism
- MeSH:
Animals;
Chromatography, Liquid;
Citrus sinensis;
Flavonoids;
Intestines;
Lipids;
Liver;
Microsomes, Liver;
Rats;
Rats, Sprague-Dawley;
Tandem Mass Spectrometry
- From:
China Journal of Chinese Materia Medica
2019;44(4):819-826
- CountryChina
- Language:Chinese
-
Abstract:
The paper studies and compares the metabolic difference of active ingredients of lipid-lowering flavonoid extract of Daidai in rat livers and intestinal microsomes,in order to explore the phase Ⅰ metabolism characteristics of active ingredients in livers and intestines. UPLC-MS/MS was used to establish a quantitative analysis method for active ingredients,neohesperidin and narngin,in a phase Ⅰ metabolism incubation system of liver and intestinal microsomes. Differential centrifugation was used to make liver and intestinal microsomes of rats. A phase Ⅰ metabolism incubation system was established,and the concentrations of the residual at different incubation time points were analyzed. Graphs were plotted to calculate the metabolic elimination half-life of the main active parts,with the natural logarithm residual percentage values ln( X) at different time points as the y axis,and time t as the x axis. The metabolism characteristics of the active ingredients were compared. The established UPLC-MS/MS quantitative analysis method has a good specialization,standard curve and linear range,accuracy and precision,with a satisfactory lower quantitative limit. The method allows quantitative detection of the active ingredients in a phase Ⅰ metabolism incubation system of liver and intestinal microsomes of rats. In the rats liver microsomes incubation system,the metabolic elimination half-life of neohesperidin and narngin were( 2. 20 ± 0. 28) h and( 1. 97±0. 28) h respectively. The elimination half-life of neohesperidin was larger than that of narngin,but with no statistically significant difference. In the rats intestinal microsomes incubation system,the metabolic elimination half-lives of neohesperidin and narngin were( 3. 68±0. 54) h and( 2. 26±0. 13) h respectively. The elimination half-life of neohesperidin was larger than that of narngin,with statistically significant differences( P<0. 05). The elimination half-lives of the active ingredients in liver microsomes were smaller than those in intestinal microsomes. The experiment results showed that the active ingredients of lipid-lowering flavonoid extract of Daidai had different elimination half-lives in phase Ⅰ rats liver and intestinal microsomes incubation system. This implied that they had different metabolic characteristics in rats liver and intestine,and liver may be the main metabolism site of the active ingredients. The phaseⅠ metabolism of narngin was stronger than that of neohesperidin. The differences between their metabolic characteristics may be related to the binding sites of B-ring hydroxyl in flavonoid glycosides and the number of methoxyl group. The results provided an important experimental basis for further development and clinical application of lipid-lowering flavonoid extract preparation of Daidai.
