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Potential accumulation of protopanaxadiol-type ginsenosides in six-months toxicokinetic study of SHENMAI injection in dogs.
Yu, Jian; Gu, Li-Qiang; Xin, Yan-Fei; Bai, Yun-Sheng; Zhang, Sheng; Gao, Hai-Yan; Xu, Pan-Sheng; Ma, Zhu-Feng; You, Zhen-Qiang; Wang, Zhi; Xuan, Yao-Xian.
Afiliação
  • Yu J; Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, China.
  • Gu LQ; Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, China.
  • Xin YF; Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, China. Electronic address: xinyanfei@gmail.com.
  • Bai YS; Beijing Space Odyssey Biotechnology Co., Ltd., Beijing, China.
  • Zhang S; Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, China.
  • Gao HY; Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, China.
  • Xu PS; Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, China.
  • Ma ZF; Chiatai QingChunbao Pharmaceutical Co., Ltd., Hangzhou, Zhejiang, China.
  • You ZQ; Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, China.
  • Wang Z; Chiatai QingChunbao Pharmaceutical Co., Ltd., Hangzhou, Zhejiang, China.
  • Xuan YX; Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, China.
Regul Toxicol Pharmacol ; 83: 5-12, 2017 Feb.
Article em En | MEDLINE | ID: mdl-27840091
ABSTRACT
SHENMAI injection (SMI), derived from famous Shen Mai San, is a herbal injection widely used in China. Ginsenosides are the major components of SMI. To monitor the exposure level of SMI during long-term treatment, a 6-month toxicokinetic experiment was performed. Twenty-four beagle dogs were dived into four groups (n = 6 in each group) a control group (0.9% NaCl solution) and three SMI groups (2, 6 or 3 mg/kg). The dogs were i.v. infused with vehicle or SMI daily for 180 d. Blood samples for analysis were collected at specific time points as follows pre-dose (0 h); at 10, 30, and 60 min during infusion; and at 10, 30, 60, 90, 120, 240, and 300 min post-administration. Concentrations of ginsenosides Rb1, Rb2, Rc, Rd, Re, Rf, and Rg1 in the plasma were determined simultaneously by liquid chromatography-tandem mass spectrometry. Non-compartmental parameters were further calculated and analyzed. Significant differences were found between the kinetic behavior of 20(S)-protopanaxadiol-type (PPD-type) and 20(S)-protopanaxatriol-type (PPT-type) ginsenosides. Increasing in the exposure level of PPD-type ginsenosides was observed in dogs during the experiment. Therefore, PPD-type ginsenosides are closely related to the immunity modulation effect of SMI. Increased PPD-type ginsenoside exposure level may present potential toxicity and induce drug-drug interaction risks during SMI administration. As such, PPD-type ginsenoside accumulation must be carefully monitored in future SMI research.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sapogeninas / Medicamentos de Ervas Chinesas / Ginsenosídeos / Toxicocinética Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sapogeninas / Medicamentos de Ervas Chinesas / Ginsenosídeos / Toxicocinética Idioma: En Ano de publicação: 2017 Tipo de documento: Article