Key result
Centruroides tecomanus venom triggers biphasic heart rate changes and conduction abnormalities without overt myocardial necrosis.
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Why the study?
The early cardiac effects of Centruroides tecomanus scorpion venom remain poorly characterized despite its medical relevance.
Does Centruroides tecomanus venom induce early cardiotoxicity in Wistar rats?
Does Centruroides tecomanus venom induce early cardiotoxicity in Wistar rats?
Centruroides tecomanus envenomation in a rat model induces acute rhythm and conduction abnormalities with mild structural myocardial changes, occurring prior to or without typical serum biomarker elevation.
May support early ECG monitoring in scorpion envenomation; hypothesis-generating and requires human validation before practice change.
Scorpion envenomation is a medical emergency that can produce severe cardiovascular complications . Centruroides tecomanus , an endemic scorpion species from western Mexico, is medically relevant, although its early cardiac effects remain poorly characterized. This study evaluated the initial cardiotoxic effects of C. tecomanus venom in Wistar rats using serial electrocardiographic recordings, algorithm-based ECG signal processing, histopathology, and serum biochemical markers. Fourteen rats were allocated to control and venom-treated groups (n = 7 per group). The experimental group received an intraperitoneal sublethal dose equivalent to one-third of the LD 50 . One-minute ECG recordings obtained at 5-min intervals during the first hour were analyzed using an enhanced computational algorithm for noise reduction, R-peak detection, R–R interval analysis, and characterization of cardiac conduction. Venom-treated animals showed a biphasic chronotropic response, with early tachycardia followed by progressive bradycardia, together with altered impulse generation, migratory atrial pacemaker activity, and atrioventricular conduction abnormalities. Histopathological analysis revealed increased inter-fiber separation and eosinophilic changes in the ventricular myocardium, without overt necrosis, whereas pulmonary architecture remained largely preserved. CK, CK-MB, and AST showed no significant changes at 8 h after envenomation, while LDH decreased significantly. These findings characterize the early temporal progression of C. tecomanus venom-associated cardiotoxicity, beginning with rhythm and atrioventricular conduction abnormalities and accompanied by mild myocardial inter-fiber separation, but without overt necrosis or a conventional serum enzyme pattern of myocardial injury.
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Romero-Murguia et al. (2026) studied Scorpion envenomation cardiotoxicity (n=14). Centruroides tecomanus venom vs. Control group was evaluated on Initial cardiotoxic effects (ECG changes, histopathology, and serum biochemical markers). Administration of C. tecomanus venom in rats induced early tachycardia followed by progressive bradycardia and conduction abnormalities, alongside mild myocardial changes without overt necrosis.
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