EXPERIMENTAL RESEARCH
Correlative study on the expression of adipokine CTRP9 in a rat model of right ventricular outflow tract obstruction
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1
Fujian Medical University, Fuzhou, Fujian, China
2
Department of Intensive Care Unit, Xiamen Cardiovascular Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian Province, China
3
Department of Cardiovascular Surgery, Union Hospital, Fujian Medical University, Fuzhou, Fujian, China
4
Fujian Key Laboratory of Cardio-Thoracic Surgery (Fujian Medical University), Fuzhou, Fujian, China
These authors had equal contribution to this work
Submission date: 2024-09-25
Final revision date: 2025-01-07
Acceptance date: 2025-01-08
Online publication date: 2025-04-03
Corresponding author
Dongshan Liao
Department of
Cardiovascular Surgery
Union Hospital
Fujian Medical University
Fuzhou, Fujian, China
Fujian Key Laboratory
of Cardio-Thoracic
Surgery
Fujian Medical
University, Fuzhou
Fujian, China
KEYWORDS
TOPICS
ABSTRACT
Introduction:
Right ventricular outflow tract obstruction (RVOTO) is linked to right ventricular hypertrophy and fibrosis, which can lead to significant cardiovascular complications. C1q-tumor necrosis factor-related protein-9 (CTRP9) may serve as a biomarker for cardiac remodeling. This study examined CTRP9 expression in a rat model of RVOTO and its association with hypertrophy and fibrosis.
Material and methods:
Thirty male Sprague Dawley rats were divided into three groups: operation, sham operation, and control (10 rats each). The operation group underwent pulmonary arterial constriction, while the sham group had thoracotomy without pulmonary arterial constriction. After 4 weeks, heart specimens were collected for plasma CTRP9 quantification with ELISA, myocardial thickness measurement, and collagen fiber volume assessment. CTRP9 expression was analyzed using immunohistochemistry and Western blot. Statistical evaluations included t-tests and Pearson correlation analysis.
Results:
The operation group showed a significantly (p < 0.001) higher collagen fiber volume ratio in right ventricular hypertrophy than the sham and control groups, indicating notable myocardial fibrosis. CTRP9 levels in plasma were significantly lower in the operation group (p < 0.001) as compared to the sham and control groups. Moreover, plasma CTRP9 showed a negative correlation with hypertrophy (r = –0.910, p = 0.029). Western blotting and immunohistochemical analysis confirmed significantly higher myocardial CTRP9 concentrations in the operation group compared to the sham (p = 0.032) and control (p = 0.029) groups, correlating strongly with hypertrophy (r = 0.948, p = 0.036) and fibrosis (r = 0.947, p = 0.027) respectively.
Conclusions:
In this RVOTO model, decreased circulating plasma CTRP9 levels were observed alongside increased myocardial expression, suggesting a vital role for CTRP9 in the pathological processes of right ventricular hypertrophy during the remodeling process.
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