Goldstein R S, Chism J P, Sherrill J M, Hamm T E
Toxicol Appl Pharmacol. 1984 Sep 30;75(3):547-53. doi: 10.1016/0041-008x(84)90191-1.
Intestinal microfloral metabolism of nitrobenzene is essential for the production of methemoglobin. Since dietary pectin alters intestinal microflora, these studies were designed to examine the effects of dietary pectin on nitrobenzene-induced methemoglobinemia. Male Fischer-344 rats were fed either AIN-76A (purified diet containing 5% cellulose), AIN-76A with 5% pectin replacing the cellulose, or NIH-07 (cereal-based diet containing 8.4% pectin) for 28 days. Following this period, nitrobenzene (200 mg/kg) was administered by gastric intubation, and methemoglobin concentrations were determined after 1, 2, 4, 8, and 24 hr. Nitrobenzene-induced methemoglobinemia was evident as early as 1 hr, peaked at 4 hr, and diminished thereafter in rats fed NIH-07 diet. In contrast, nitrobenzene-induced methemoglobinemia was not detectable in rats fed AIN-76A; however, inclusion of 5% pectin in this diet resulted in methemoglobinemia comparable to that of NIH-07-fed animals at 4, 8, and 24 hr. Administration of 400 or 600 mg/kg nitrobenzene resulted in significant diet-related differences in methemoglobinemia. Administration of 600 mg/kg nitrobenzene to animals fed NIH-07 resulted in the highest methemoglobin concentrations (64 +/- 1%); those fed AIN-76A had the lowest (20 +/- 5%), and those fed AIN-76A containing pectin had intermediate methemoglobin concentrations (44 +/- 6%). No diet-related differences in the microbial population of the stomach or small intestine were observed. However, the number of anaerobes present in the ceca of rats fed AIN-76A containing pectin was 2 to 2.5 times greater than that of rats fed AIN-76A. In vitro reductive metabolism of [14C]nitrobenzene was significantly greater in the cecal contents of rats fed NIH-07 than that in the cecal contents of either of the groups fed the AIN-76A-based diets. These studies indicate that intestinal microfloral metabolism and red blood cell toxicity of nitrobenzene is markedly different in animals fed cereal-based versus purified diets. Furthermore, since inclusion of pectin into the purified diet diminishes the magnitude of these effects, differences in dietary composition of fermentable carbohydrates in cereal-based and purified diets may mediate differences in metabolism and toxicity of nitrobenzene.
肠道微生物对硝基苯的代谢是高铁血红蛋白产生的关键环节。鉴于膳食果胶会改变肠道微生物群,本研究旨在探究膳食果胶对硝基苯诱导的高铁血红蛋白血症的影响。将雄性Fischer - 344大鼠分别喂食AIN - 76A(含5%纤维素的纯化饲料)、用5%果胶替代纤维素的AIN - 76A饲料或NIH - 07(含8.4%果胶的谷类饲料),持续28天。在此期间过后,通过胃插管给予硝基苯(200 mg/kg),并在1、2、4、8和24小时后测定高铁血红蛋白浓度。在喂食NIH - 07饲料的大鼠中,硝基苯诱导的高铁血红蛋白血症早在1小时就已明显出现,4小时达到峰值,之后逐渐下降。相比之下,在喂食AIN - 76A的大鼠中未检测到硝基苯诱导的高铁血红蛋白血症;然而,在此饲料中添加5%果胶后,在4、8和24小时时产生的高铁血红蛋白血症与喂食NIH - 07的动物相当。给予400或600 mg/kg硝基苯会导致高铁血红蛋白血症出现显著的饲料相关差异。给喂食NIH - 07的动物给予600 mg/kg硝基苯会导致高铁血红蛋白浓度最高(64±1%);喂食AIN - 76A的动物浓度最低(20±5%),而喂食含果胶的AIN - 76A的动物高铁血红蛋白浓度处于中间水平(44±6%)。未观察到胃或小肠微生物群存在饲料相关差异。然而,喂食含果胶的AIN - 76A的大鼠盲肠中的厌氧菌数量比喂食AIN - 76A的大鼠多2至2.5倍。喂食NIH - 07的大鼠盲肠内容物中[14C]硝基苯的体外还原代谢显著高于喂食基于AIN - 76A饲料的两组大鼠的盲肠内容物。这些研究表明,在喂食谷类饲料与纯化饲料的动物中,硝基苯的肠道微生物代谢和对红细胞的毒性存在显著差异。此外,由于在纯化饲料中添加果胶会减弱这些影响的程度,谷类饲料和纯化饲料中可发酵碳水化合物的膳食组成差异可能介导了硝基苯代谢和毒性的差异。