Carr C J
Annu Rev Pharmacol Toxicol. 1982;22:19-29. doi: 10.1146/annurev.pa.22.040182.000315.
A significant contribution could be made to patient care if nutritional biochemists, basic and clinical toxicologists, and pharmacologists in the various fields were to mount the studies needed to understand the nature of food-drug interactions. If only a small fraction of the 120 billion dollars per year spent for food or the 10 billion dollars expended for drugs were allocated for research in this area, advances might be made for the health of the nation. Changes in man's diet produce marked effects on drug metabolism. We know that changing a customary diet to one high in protein and low in carbohydrate increases the rates of metabolism of antipyrine and theophylline, and shifting to an isocaloric diet of low protein-high carbohydrate slows the rates of metabolism of these drugs. Presumably, high-protein-low carbohydrate diets in man resemble the animal studies with high protein diets that show enhanced hepatic drug metabolism. However, numerous studies emphasize the considerable individual variability to changes in human diets; some people have dramatic changes, whereas others exhibit little or no response. Similar individuality has been found in the response to enzyme induction by smoking. Numerous foods and food ingredients affect drug metabolism in human beings and apparently follow the same patterns as found in experimental animal studies with changes in the levels of cytochrome P-450 dependent monooxygenases in the liver and intestine. These changes presumably exert some protective action against environmental carcinogens, cocarcinogens, or promoters. Dietary modifications are brought about by use of weight-reducing diets, vegetarian diets, hospitalization, or post-operative regimens. These diets are often continued for long periods of time and it is likely they result in changes in the metabolism by the body of subsequently administered drugs or exposure to environmental chemicals. Methods are needed to measure inter-individual and inter-group differences in metabolism of foreign compounds in order to accurately assess dietary influences on drug metabolism and vice versa. Epidemiologic studies of rigorously selected human populations, coupled with the newer sensitive chemical analytical methods, will provide the necessary data base for these investigations.
如果各个领域的营养生物化学家、基础和临床毒理学家以及药理学家开展所需研究,以了解食物与药物相互作用的本质,那么对患者护理将有重大贡献。如果每年用于食品的1200亿美元或用于药物的100亿美元中,只有一小部分用于该领域的研究,那么可能会为国民健康带来进步。人类饮食的变化对药物代谢有显著影响。我们知道,将习惯饮食改为高蛋白、低碳水化合物饮食会增加安替比林和茶碱的代谢率,而改为低蛋白、高碳水化合物的等热量饮食则会减缓这些药物的代谢率。据推测,人类的高蛋白、低碳水化合物饮食类似于动物研究中的高蛋白饮食,后者显示肝脏药物代谢增强。然而,大量研究强调了人类饮食变化存在相当大的个体差异;有些人有显著变化,而另一些人则几乎没有或没有反应。在对吸烟引起的酶诱导反应中也发现了类似的个体差异。许多食物和食物成分会影响人类的药物代谢,显然与实验动物研究中发现的模式相同,即肝脏和肠道中细胞色素P - 450依赖性单加氧酶水平发生变化。这些变化可能对环境致癌物、辅致癌物或促癌物起到某种保护作用。饮食调整是通过使用减肥饮食、素食饮食、住院治疗或术后养生法实现的。这些饮食通常会持续很长时间,很可能会导致身体对随后服用的药物或接触环境化学物质的代谢发生变化。需要有方法来测量个体间和群体间对外源化合物代谢的差异,以便准确评估饮食对药物代谢的影响,反之亦然。对经过严格挑选的人群进行流行病学研究,再结合更新的灵敏化学分析方法,将为这些调查提供必要的数据库。