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Published on: February 17, 2023
[Effect of long-term crotonaldehyde exposure on heart damage in male rats]
1School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Jinan, Shandong 250062, China.
Insights
Long-term exposure to crotonaldehyde caused significant heart damage in male rats by increasing cardiac inflammatory cytokines and disrupting the angiotensin-aldosterone-brain natriuretic peptide balance. This study reveals crotonaldehyde
Area of Science:
- Toxicology
- Cardiovascular Science
- Biochemistry
Background:
- Crotonaldehyde is an industrial chemical with potential toxic effects.
- Understanding its long-term impact on cardiac health is crucial for occupational safety and public health.
Purpose of the Study:
- To investigate the effects of chronic crotonaldehyde exposure on male rat hearts.
- To elucidate the underlying mechanisms of crotonaldehyde-induced cardiotoxicity.
Main Methods:
- Male Wistar rats were exposed to varying doses of crotonaldehyde (0-8.5 mg/kg) daily for 150 days.
- Cardiac organ coefficient, histopathology, serum enzyme activities (CK, LDH-L), and cardiac marker levels (cTnT, Ang II, BNP, ALD, ILs, TNF-α, IFN-γ) were assessed.
Main Results:
- Crotonaldehyde exposure led to decreased body weight gain, heart weight, and heart coefficient in a dose-dependent manner.
- Histopathological examination revealed lymphocyte infiltration, necrosis, and fibrosis in the heart tissue.
- Elevated serum CK and LDH-L, increased cardiac Ang II and ALD, decreased BNP, and upregulated inflammatory cytokines (IL-1β, IL-6, IL-8, TNF-α, IFN-γ) were observed.
Conclusions:
- Chronic crotonaldehyde exposure induces significant heart damage in male rats.
- The cardiotoxicity is mediated by the upregulation of cardiac inflammatory cytokines and disruption of the renin-angiotensin-aldosterone system and natriuretic peptide balance.
Abstract:
Objective: To observe the effect of long term crotonaldehyde exposure on heart damage in male rats, and to explore the possible mechanism of toxic action. Methods: 24 specific pathogen free healthy male wistar rats were randomly divided into 4 groups with 6 rats in each group. Rats were treated with with 8.5, 4.5, 2.5 and 0.0 mg/kg body weight crotonaldehyde by gavage, once a day for consecutive 150 days. After the last treatment, they were anesthetized and collected blood samples by cardiac puncture. The heart was rapidly separated after cervical dislocation. The cardiac organ coefficient was calculated and the histopathology changes in heart were observed by HE staining. At the same time, the activities of creatine kinase (CK) , lactate dehydrogenase-L (LDH-L) in serum were determined by automatic biochemical analyzer. Moreover, the levels of cardiac troponin (cTnT) , Angiotensin Ⅱ (Ang Ⅱ) , Brain natriuretic peptide (BNP) , Aldosterone (ALD) and interleukin (IL) -6, 8, 1β, interferon (IFN) -γ and tumor necrosis factor (TNF) -α in heart were determined by enzyme linked immunosorbent assay. Results: At the 90d, 120 d, and 150 d exposure, compared with the control group, the body weight gain in 4.5 and 8.5 mg/kg groups were decreased. Moreover, the heart weight in 4.5 and 8.5 mg/kg groups, and heart coefficient in 8.5 mg/kg group were decreased (P<0.05) . With the increasing dosage of crotonaldehyde, the degree of pathological changes in the heart of exposed rats were aggravated. The major pathological changes of heart in 4.5 and 8.5 mg/kg groups could be summarized as lymphocyte infiltration, abnormal cardiac muscle fiber arrangements, necrosis and fibrous connective tissue hyperplasia. Compared with the control group, the serum CK activity in 4.5 mg/kg group, CK and LDH-L activitivies in 8.5 mg/kg group were increased (P<0.05) ; Compared with the control group, the levels of ALD and ANGII in the heart of 4.5 and 8.5 mg/kg groups were increased, BNP level were decreased, and cTNT level in 8.5 mg/kg group were increased (P<0.05) . Compared with the control group, the levels of IL-1β、IL-6、IL-8 in 4.5 mg/kg group and IL-1β、IL-6、IL-8、TNF-α、IFN-γ in 8.5 mg/kg group were increased (P<0.05) . Conclusion: Crotonaldehyde could up-regulate cardiac inflammatory cytokines and alter the balance ofangiotensin-aldosterone-brain natriuretic peptide causing heart damage.
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