Key result
Exposure to methyl-2-tetradecylglycidate (MTG) in female rats led to massive changes in heart tissue energy reserves and significant increases in non-esterified fatty acid content.
Why the study?
The cardiotoxic effects and mechanisms of methyl-2-tetradecylglycidate (MTG) and its induced eccentric hypertrophy required further elucidation using ex vivo heart perfusion methods.
Recirculating, retrograde heart perfusion according to the Langendorff method was used in an attempt to further elucidate the cardiotoxicity of methyl-2-tetradecylglycidate (McNeil 3716, MTG) and the eccentric hypertrophy elicited by the compound. In subchronic experiments female rats were exposed to MTG 2 x 10 mg/kg and 2 x 25 mg/kg per day for 4 weeks. At various times hearts were perfused ex vivo for up to 2 hr with either 5 mmolar glucose or 0.5 mmolar palmitate as substrate. Substrate uptake (glucose or palmitate) and enzyme release (LDH-lactic dehydrogenase or CPK-creatine-phosphate kinase) were assessed during perfusion. Biochemical analysis (ATP, ADP, AMP, c-AMP, CP, creatine, pyruvate, lactate, glucose-6-phosphate, glycogen, phospholipids, triglycerides and non-esterified fatty acids) were done in hearts before (drug effect) and after perfusion (stress of perfusion). Besides changes in energy metabolism and high-energy phosphate production, as observed in previous experiments (Bachmann et al. 1984) massive changes were seen in energy reserves in heart tissue (ATP, CP, glycogen, phospholipids and triglycerides). As expected, MTG led to significant increases also in non-esterified fatty acids content in hearts.
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Bachmann et al. (1993) studied Cardiomyopathy (MTG-induced). Methyl-2-tetradecylglycidate (McNeil 3716, MTG) was evaluated on Changes in energy metabolism, energy reserves, and non-esterified fatty acids. Exposure to methyl-2-tetradecylglycidate (MTG) in female rats led to massive changes in heart tissue energy reserves and significant increases in non-esterified fatty acid content.
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