Key result
Amitriptyline administration in rats significantly prolonged the QRS complex (P<.0001) and QT interval (P=0.002) and increased cTnT and NT-proBNP levels.
Why the study?
Do cardiac troponin T and NT-proBNP serve as early indicators of amitriptyline-induced cardiotoxicity in a rat model?
RCT
randomly divided
Do cardiac troponin T and NT-proBNP serve as early indicators of amitriptyline-induced cardiotoxicity in a rat model?
p-value: p=<.0001
Rat-specific assays for cTnT and NT-proBNP can detect early myocardial damage in amitriptyline-induced cardiotoxicity in a preclinical model.
Should not change clinical practice; hypothesis-generating for cTnT and NT-proBNP as early markers in amitriptyline rat cardiotoxicity.
The main objective of this study was to investigate whether cardiac troponin (cTn) and N-terminal, protein B-type natriuretic peptide (NT-proBNP) can be useful as indicators for amitriptyline cardiotoxicity which is a known drug having sublethal toxic cardiac effects. At the same time, this study looked at detecting potential histopathological changes specific to irreversible cardiac injuries in a rat model of amitriptyline cardiotoxicity. Male Wistar rats were randomly divided into 2 groups, control (saline) group and amitriptyline group (100 mg/kg body weight intraperitoneally, equivalent for lethal dose at 50%). Blood was collected 30 minutes after the administration. The cTn was measured using 3 different methods (2 methods designed for human use and a sandwich enzyme immunoassay specific for rat cTnT). The brain natriuretic peptide was measured by 2 different methods (1 for human and 1 specific for rats). Electrocardiography showed that the QRS complex (P < .0001) and the QT interval (P = .002) were significantly prolonged for amitriptyline-treated animals. Troponin T and NT-proBNP had significantly increased levels in all the rats but showed positive results only when using rat-specific quantitative measurement. In certain rats, the histopathological examination identified a few small foci of acute myocardial necrosis. In conclusion, elevation of cTnT and NT-proBNP are early indicators of cardiotoxicity, yet the significance of irreversible myocardial damage in amitriptyline cardiotoxicity needs to be further understood.
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Șorodoc et al. (2013) conducted an RCT in Amitriptyline-induced cardiovascular toxicity. Amitriptyline vs. Saline was evaluated on QRS complex prolongation (p=<.0001). Amitriptyline administration in rats significantly prolonged the QRS complex (P<.0001) and QT interval (P=0.002) and increased cTnT and NT-proBNP levels.
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