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Dynamic Changes in Plasma Urotensin II and Its Correlation With Plaque Stability.
Yin, Chun-Lin; Liu, Xue; Wang, Hong-Xia; Yan, Ming-Cong; Guo, Li-Juan; Li, Guo-Nan; Xia, Jing-Gang; Yuan, Hui-Hui; Yin, Yan.
Afiliação
  • Yin CL; Department of Cardiology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China; and.
  • Liu X; Department of Cardiology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China; and.
  • Wang HX; Department of Physiology and Pathophysiology, Capital Medical University, Beijing, China.
  • Yan MC; Department of Cardiology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China; and.
  • Guo LJ; Department of Cardiology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China; and.
  • Li GN; Department of Cardiology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China; and.
  • Xia JG; Department of Cardiology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China; and.
  • Yuan HH; Department of Cardiology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China; and.
  • Yin Y; Department of Cardiology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China; and.
J Cardiovasc Pharmacol ; 78(1): e147-e155, 2021 07 01.
Article em En | MEDLINE | ID: mdl-34173803
ABSTRACT: Urotensin II (UII) is involved in the formation of atherosclerosis, but its role in the stability of atherosclerotic plaques is unknown. The purpose of this study was to observe the dynamic changes in plasma UII and analyze its relationship to the stability of atherosclerotic plaques. One hundred thirty-five consecutive patients with acute coronary syndrome (ACS) were enrolled. The plasma UII levels were measured immediately after admission and during three-month follow-up. A vulnerable plaque model was established using local transfection of a recombinant P53 adenovirus into plaques in rabbits fed with a high-cholesterol diet and subjected to balloon arterial injury. The levels of plasma UII were measured weekly. The changes in plasma UII during the formation of atherosclerotic plaques and before and after plaque transfection were observed. The morphology of the plaques and the expression, distribution, and quantitative expression of UII in the plaques also were observed. Our results showed that the levels of plasma UII in patients with ACS at admission were lower than levels observed at the three-month follow-up. UII dynamic changes and its correlation with plaque stabilities were further verified in rabbits with atherosclerotic vulnerable plaques. The UII levels in rabbits were significantly decreased immediately after the P53 gene transfection, which led to plaque instability and rupture. These results suggested that UII expression was down-regulated in ACS, which may be related to its ability to modulate mechanisms involved in plaque stability and instability.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças da Aorta / Urotensinas / Aterosclerose / Síndrome Coronariana Aguda / Placa Aterosclerótica Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças da Aorta / Urotensinas / Aterosclerose / Síndrome Coronariana Aguda / Placa Aterosclerótica Idioma: En Ano de publicação: 2021 Tipo de documento: Article