Bachmann E, Weber E
Institute of Toxicology, Swiss Federal Institute of Technology, Schwerzenbach, Schweiz.
Pharmacol Toxicol. 1993 Feb;72(2):98-106. doi: 10.1111/j.1600-0773.1993.tb00298.x.
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.
为了进一步阐明十四烷基缩水甘油酸甲酯(麦克尼尔3716,MTG)的心脏毒性以及该化合物引起的离心性肥大,采用了根据朗根多夫方法进行的循环逆行心脏灌注。在亚慢性实验中,雌性大鼠每天暴露于2×10毫克/千克和2×25毫克/千克的MTG中,持续4周。在不同时间,将心脏离体灌注长达2小时,分别以5毫摩尔葡萄糖或0.5毫摩尔棕榈酸酯作为底物。在灌注过程中评估底物摄取(葡萄糖或棕榈酸酯)和酶释放(乳酸脱氢酶或肌酸磷酸激酶)。在灌注前(药物作用)和灌注后(灌注应激)对心脏进行生化分析(ATP、ADP、AMP、环磷酸腺苷、磷酸肌酸、肌酸、丙酮酸、乳酸、6-磷酸葡萄糖、糖原、磷脂、甘油三酯和非酯化脂肪酸)。除了能量代谢和高能磷酸生成的变化,如先前实验(巴赫曼等人,1984年)中所观察到的,心脏组织中的能量储备(ATP、磷酸肌酸、糖原、磷脂和甘油三酯)也出现了大量变化。正如预期的那样,MTG还导致心脏中非酯化脂肪酸含量显著增加。