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Cardiotonic Pills® protects from myocardial fibrosis caused by in stent restenosis in miniature pigs.
Yan, Lu-Lu; Wei, Xiao-Hong; Shi, Qiu-Ping; Pan, Chun-Shui; Li, Kai-Yin; Zhang, Bin; Wang, Xin-Gang; Zheng, Bo; Wang, Ming-Xia; Yan, Li; Huang, Ping; Liu, Jian; Fan, Jing-Yu; Li, Huan; Wang, Chuan-She; Chen, Ming; Han, Jing-Yan.
Afiliación
  • Yan LL; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
  • Wei XH; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
  • Shi QP; Beijing Laboratory of Integrative Microangiopathy, Haidian District, Beijing 100191, China; Department of Cardiology, Peking University First Hospital, XiCheng District, Beijing 100034, China.
  • Pan CS; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
  • Li KY; Beijing Laboratory of Integrative Microangiopathy, Haidian District, Beijing 100191, China; Department of Cardiology, Peking University First Hospital, XiCheng District, Beijing 100034, China.
  • Zhang B; Beijing Laboratory of Integrative Microangiopathy, Haidian District, Beijing 100191, China; Department of Cardiology, Peking University First Hospital, XiCheng District, Beijing 100034, China.
  • Wang XG; Beijing Laboratory of Integrative Microangiopathy, Haidian District, Beijing 100191, China; Department of Cardiology, Peking University First Hospital, XiCheng District, Beijing 100034, China.
  • Zheng B; Beijing Laboratory of Integrative Microangiopathy, Haidian District, Beijing 100191, China; Department of Cardiology, Peking University First Hospital, XiCheng District, Beijing 100034, China.
  • Wang MX; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
  • Yan L; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
  • Huang P; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
  • Liu J; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key Laboratory of Core Technology in Innovative Chinese Medicine, Haidian District, Beijing 100191, China; Beijing Laboratory of
  • Fan JY; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
  • Li H; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
  • Wang CS; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
  • Chen M; Beijing Laboratory of Integrative Microangiopathy, Haidian District, Beijing 100191, China; Department of Cardiology, Peking University First Hospital, XiCheng District, Beijing 100034, China. Electronic address: cm6141@sina.com.
  • Han JY; Tasly Microcirculation Research Center, Peking University Health Science Center, Haidian District, Beijing 100191, China; Key Laboratory of Stasis and Phlegm, State Administration of Traditional Chinese Medicine of the People's Republic of China, Haidian District, Beijing 100191, China; State Key La
Phytomedicine ; 106: 154405, 2022 Nov.
Article en En | MEDLINE | ID: mdl-36067659
ABSTRACT

BACKGROUND:

Stent implantation has been increasingly applied for the treatment of obstructive coronary artery disease, which, albeit effective, often harasses patients by in-stent restenosis (ISR).

PURPOSE:

The present study was to explore the role of compound Chinese medicine Cardiotonic Pills® (CP) in attenuating ISR-evoked myocardial injury and fibrosis. STUDY

DESIGN:

Chinese miniature pigs were used to establish ISR model by implanting obsolete degradable stents into coronary arteries. Quantitative coronary angiography (QCA) was performed to confirm the success of the model.

METHODS:

CP was given at 0.2 g/kg daily for 30 days after ISR. On day 30 and 60 after stent implantation, the myocardial infarct and myocardial blood flow (MBF) were assessed. Myocardial histology was evaluated by hematoxylin-eosin and Masson's trichrome staining. The content of ATP, MPO, and the activity of mitochondrial respiratory chain complex Ⅳ were determined by ELISA. Western blot was performed to assess the expression of ATP5D and related signaling proteins, and the mediators of myocardial fibrosis.

RESULTS:

Treatment with CP diminished myocardial infarct size, retained myocardium structure, attenuated myocardial fibrosis, and restored MBF. CP ameliorated energy metabolism disorder, attenuated TGFß1 up-regulation and reversed its downstream gene expression, such as Smad6 and Smad7, and inhibited the increased expression of MCP-1, PR S19, MMP-2 and MMP-9.

CONCLUSION:

CP effectively protects myocardial structure and function from ISR challenge, possibly by regulating energy metabolism via inactivation of RhoA/ROCK signaling pathway and inhibition of monocyte chemotaxis and TGF ß1/Smads signaling pathway.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Reestenosis Coronaria / Infarto del Miocardio Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals Idioma: En Revista: Phytomedicine Asunto de la revista: TERAPIAS COMPLEMENTARES Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Reestenosis Coronaria / Infarto del Miocardio Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals Idioma: En Revista: Phytomedicine Asunto de la revista: TERAPIAS COMPLEMENTARES Año: 2022 Tipo del documento: Article