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Changes and significance of the fibrinolytic system following two pulmonary thromboembolisms in a rabbit model.
Liu, D-C; Duan, B; Zhao, M-N; Wu, L; Cao, Y-Z; Liu, N-B; Xue, Z; He, Z-H; Mi, J.
Afiliação
  • Liu DC; Department of Cardiology, Shijiazhuang People's Hospital, Shijiazhuang, China.
  • Duan B; Department of Cardiology, Shijiazhuang People's Hospital, Shijiazhuang, China.
  • Zhao MN; Department of Cardiology, Shijiazhuang People's Hospital, Shijiazhuang, China.
  • Wu L; Department of Cardiology, Shijiazhuang People's Hospital, Shijiazhuang, China.
  • Cao YZ; Department of Cardiology, Shijiazhuang People's Hospital, Shijiazhuang, China.
  • Liu NB; Department of Cardiology, Shijiazhuang People's Hospital, Shijiazhuang, China.
  • Xue Z; Department of Cardiology, Shijiazhuang People's Hospital, Shijiazhuang, China.
  • He ZH; Department of Emergency Medicine, Shijiazhuang People's Hospital, Shijiazhuang, China. hezhihonghezh@126.com.
  • Mi J; Department of Cardiology, Shijiazhuang People's Hospital, Shijiazhuang, China. jeremymijie@126.com.
J Physiol Pharmacol ; 75(2): 137-144, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38736261
ABSTRACT
In this study, we examined the changes in the fibrinolytic system in a rabbit model of two acute pulmonary thromboembolisms (PTE). Fourteen healthy adult New Zealand white rabbits were divided into three groups the single PTE group (five rabbits), the double PTE group (five rabbits), and the control group (four rabbits). A rabbit model of acute pulmonary embolism was established, and immunohistochemistry and polymerase chain reaction (PCR) were performed on tissue plasminogen activator (t-PA), plasminogen activator inhibitor-1 (PAI-1) in plasma, and pulmonary embolism tissue. Plasma

results:

1) t-PA levels one hour following the initial modeling, the levels of t-PA in the modeling groups were significantly lower than those in the control group (P<0.05). In addition, the t-PA levels in the double PTE group were found to be lower after the modeling, as compared to the pre-modeling period (P<0.05). One hour after the second modeling, the double PTE group had lower t-PA levels compared to the control group (P<0.05). However, t-PA rebounded two hours after modeling in the double PTE group. One week after the second modeling, the double PTE group had higher t-PA levels compared to the other two groups (P<0.05). 2) PAI-1

results:

one hour after the initial modeling, PAI-1 levels in the two modeling groups were lower compared to the pre-modeling period and control groups (P<0.05). Two hours following modeling, PAI-1 levels in both modeling groups were lower compared to the control group (P<0.05). PAI-1 levels were lower in the double PTE group one and two hours after the second modeling compared to the other two groups and pre-modeling period (P<0.05). 3) The immunohistochemistry

results:

the expression of PAI-1 decreased in the two modeling groups, while t-PA expression increased compared to the control group. 4) PCR

results:

t-PA mRNA expression did not differ among the three groups. The PAI-1 mRNA expression was lower in the two PTE groups compared to the control group. We conclude that in the early stages of PTE, the local fibrinolytic activity of the thrombus is increased, which is favorable for thrombolysis. However, as the thrombus persists, the activity of the fibrinolytic system is inhibited, contributing to the development of chronic thromboembolic pulmonary hypertension.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Embolia Pulmonar / Ativador de Plasminogênio Tecidual / Inibidor 1 de Ativador de Plasminogênio / Modelos Animais de Doenças / Fibrinólise Limite: Animals Idioma: En Revista: J Physiol Pharmacol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Embolia Pulmonar / Ativador de Plasminogênio Tecidual / Inibidor 1 de Ativador de Plasminogênio / Modelos Animais de Doenças / Fibrinólise Limite: Animals Idioma: En Revista: J Physiol Pharmacol Ano de publicação: 2024 Tipo de documento: Article