Brown Christopher E, Trauth Stanley E, Grippo Richard S, Gurley Bill J, Grippo Anne A
Department of Biological Sciences, Arkansas State University , State University, Arkansas.
Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences , College of Pharmacy, Little Rock, Arkansas.
J Caffeine Res. 2012 Sep;2(3):123-132. doi: 10.1089/jcr.2012.0021.
Cigarette smokers have an increased risk for coronary artery disease. Nicotine present in cigarettes can adversely affect the cardiovascular system via stimulation of both sympathetic and parasympathetic neurons. Caffeine, another cardiovascular and central nervous system (CNS) stimulant, is commonly found in and -free dietary supplements. These caffeine-containing supplements also have been linked to cardiovascular toxicities. Although no longer on the U.S market, -containing supplements are another source of cardiovascular and CNS stimulants, namely the ephedrine alkaloids. Together caffeine, nicotine, and ephedrine can individually stress the cardiovascular system, and an overlap of these agents is predicted in smokers and dieters. To understand the collective effects of these stimulants on the heart morphology and ultrastructure, rats were exposed to synthetic combinations of nicotine (0.2 mg/kg/day), ephedrine (0-30 mg/kg/day), and/or caffeine (0-24 mg/kg/day) as well as an extract from a caffeine-containing supplement (Metabolife 356). After exposure for 3 days, the hearts were removed and examined for hypersensitivity myocarditis and myocardial necrosis. None of the drugs tested alone affected heart tissue morphology, nor were atypical cardiac cells observed. However, in combination, significant interactions were found between caffeine and ephedrine; the interventricular septum was most susceptible, with a significant increase in atypical cardiac cells observed. Nicotine pretreatment caused greater susceptibility to cardiotoxicity associated with combinations of caffeine + ephedrine or Metabolife, particularly in the left ventricle wall. These results indicate that sympathomimetic combinations present in supplements may have produced cardiotoxicity reported in consumers of these products. Moreover, the presence of nicotine exacerbates these toxic effects.
吸烟者患冠状动脉疾病的风险增加。香烟中的尼古丁可通过刺激交感神经和副交感神经神经元对心血管系统产生不利影响。咖啡因是另一种心血管和中枢神经系统兴奋剂,常见于不含和含的膳食补充剂中。这些含咖啡因的补充剂也与心血管毒性有关。虽然含的补充剂不再在美国市场上,但它们是心血管和中枢神经系统兴奋剂的另一个来源,即麻黄碱生物碱。咖啡因、尼古丁和麻黄碱各自都可能给心血管系统带来压力,预计吸烟者和节食者中会出现这些物质的重叠摄入情况。为了了解这些兴奋剂对心脏形态和超微结构的综合影响,将大鼠暴露于尼古丁(0.2毫克/千克/天)、麻黄碱(0 - 30毫克/千克/天)和/或咖啡因(0 - 24毫克/千克/天)的合成组合以及一种含咖啡因的补充剂(Metabolife 356)的提取物中。暴露3天后,取出心脏并检查是否有过敏性心肌炎和心肌坏死。单独测试的任何一种药物都未影响心脏组织形态,也未观察到非典型心脏细胞。然而,联合使用时,发现咖啡因和麻黄碱之间存在显著相互作用;室间隔最敏感,观察到非典型心脏细胞显著增加。尼古丁预处理使大鼠对与咖啡因 + 麻黄碱组合或Metabolife相关的心脏毒性更敏感,特别是在左心室壁。这些结果表明,补充剂中存在的拟交感神经组合可能导致了这些产品消费者中报告的心脏毒性。此外,尼古丁的存在会加剧这些毒性作用。