The pharmacokinetics study of ginkgolide A, B and the effect of food on bioavailability after oral administration of ginkgolide extracts in beagle dogs

被引:10
作者
Aa, Lixiang [1 ]
Fei, Fei [1 ]
Tan, Zhaoyi [1 ]
Aa, Jiye [1 ]
Wang, Guangji [1 ]
Liu, Changxiao [2 ]
机构
[1] China Pharmaceut Univ, Jiangsu Prov Key Lab Drug Metab & Pharmacokinet, Jiangsu Key Lab Drug Design & Optim, State Key Lab Nat Med, Nanjing, Jiangsu, Peoples R China
[2] Tianjin Inst Pharmaceut Res, State Key Lab Drug Delivery Technol & Pharmacokin, Tianjin, Peoples R China
关键词
beagle dog; bioavailability; food; ginkgolides; LC-MS; MS; IONIZATION MASS-SPECTROMETRY; ACTIVATING-FACTOR PAF; BILOBA EXTRACT; TERPENE LACTONES; RAT MODEL; PLASMA; INHIBITION; LEAF; INFLAMMATION; ANTAGONIST;
D O I
10.1002/bmc.4212
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ginkgolides are the primarily active components in Ginkgo products that are popular worldwide. However, few studies have evaluated the bioavailability of ginkgolides and the effects of food on it after oral administration of ginkgolides. In this article, pharmacokinetics and absolute bioavailability of the primary components in ginkgolide extracts were evaluated in beagle dogs. For the first time, we showed that the fed dogs had significantly increased area under the concentration-time curve and peak concentration relative to the fasted dogs based on the data from both the prototype form and total lactones of ginkgolide A (GA) and ginkgolide B (GB). In terms of the free form of the prototype ginkgolides, the absolute bioavailabilities of GA and GB were 34.8 and 5.2% in the fasted dogs, respectively, which significantly increased to an average of 78.6 and 17.0%, respectively, in the fed dogs. In terms of acidified total lactones, the absolute bioavailabilities of GA and GB were 7.5 and 14.5% in the fed dogs, and the percentages declined to 4.1 and 3.7% in the fasted dogs, respectively. It was suggested that administration of ginkgolides after meals could promote the in vivo exposure and the bioavailability of GA and GB, and hence potentially enhance therapeutic outcomes.
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页数:8
相关论文
共 27 条
[1]   Neuroprotective effects of Ginkgo biloba extract [J].
Ahlemeyer, B ;
Krieglstein, J .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (09) :1779-1792
[2]   Neuroprotective effects of Ginkgo biloba extract in brain ischemia are mediated by inhibition of nitric oxide synthesis [J].
Calapai, G ;
Crupi, A ;
Firenzuoli, F ;
Marciano, MC ;
Squadrito, F ;
Inferrera, G ;
Parisi, A ;
Rizzo, A ;
Crisafulli, C ;
Fiore, A ;
Caputi, AP .
LIFE SCIENCES, 2000, 67 (22) :2673-2683
[3]  
Center for Drug Evaluation and Research Center for Biologics Evaluation and Research, 2020, AN PROC METH VAL DRU
[4]   Systemic and cerebral exposure to and pharmacokinetics of flavonols and terpene lactones after dosing standardized Ginkgo biloba leaf extracts to rats via different routes of administration [J].
Chen, Feng ;
Li, Li ;
Xu, Fang ;
Sun, Yan ;
Du, Feifei ;
Ma, Xutao ;
Zhong, Chenchun ;
Li, Xiuxue ;
Wang, Fengqing ;
Zhang, Nating ;
Li, Chuan .
BRITISH JOURNAL OF PHARMACOLOGY, 2013, 170 (02) :440-457
[5]   Pharmacokinetics and bioavailability of a Ginkgo biloba extract [J].
Drago, F ;
Floriddia, ML ;
Cro, M ;
Giuffrida, S .
JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS, 2002, 18 (02) :197-202
[6]   Cardioprotective effects of the calcineurin inhibitor FK506 and the PAF receptor antagonist and free radical scavenger, EGb 761, in isolated ischemic/reperfused rat hearts [J].
Haines, DD ;
Bak, I ;
Ferdinandy, P ;
Mahmoud, FF ;
Al-Harbi, SA ;
Blasig, IE ;
Tosaki, A .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2000, 35 (01) :37-44
[7]   Effects of food and gender on the pharmacokinetics of ginkgolides A, B, C and bilobalide in rats after oral dosing with ginkgo terpene lactones extract [J].
Huang, Ping ;
Zhang, Liang ;
Chai, Chuan ;
Qian, Xiao-Cui ;
Li, Wen ;
Li, Jun-Song ;
Di, Liu-Qing ;
Cai, Bao-Chang .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2014, 100 :138-144
[8]   The effects of Ginkgo biloba extract on lipopolysaccharide-induced inflammation in vitro and in vivo [J].
Ilieva, I ;
Ohgami, K ;
Shiratori, K ;
Koyama, Y ;
Yoshida, K ;
Kase, S ;
Kitamei, H ;
Takemoto, Y ;
Yazawa, K ;
Ohno, S .
EXPERIMENTAL EYE RESEARCH, 2004, 79 (02) :181-187
[9]   Neuroprotective effect of Ginkgo biloba L. extract in a rat model of Parkinson's disease [J].
Kim, MS ;
Lee, JI ;
Lee, WY ;
Kim, SE .
PHYTOTHERAPY RESEARCH, 2004, 18 (08) :663-666
[10]   INHIBITION OF PLATELET-ACTIVATING FACTOR (PAF)-INDUCED CHEMOTAXIS AND PAF BINDING TO HUMAN EOSINOPHILS AND NEUTROPHILS BY THE SPECIFIC GINKGOLIDE-DERIVED PAF ANTAGONIST, BN-52021 [J].
KURIHARA, K ;
WARDLAW, AJ ;
MOQBEL, R ;
KAY, AB .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1989, 83 (01) :83-90