Til H P, Bär A
TNO-Nutrition and Food Research Institute, Zeist, 3700 AJ, The Netherlands.
Regul Toxicol Pharmacol. 1998 Apr;27(2):159-65. doi: 10.1006/rtph.1998.1220.
The oral toxicity of gamma-cyclodextrin (gamma-CD) was examined in a 13-week feeding study in which four groups of four male and four female Beagle dogs received gamma-CD in the diet at concentrations of 0 (control), 5, 10, or 20%. No treatment-related changes were noted in behavior or appearance of the dogs and no mortalities occurred. Transient diarrhea occurred in some dogs of the 5 and 10% dose groups and in all dogs of the 20% dose group. However, all dogs remained in good health and gained weight. During the last 6 weeks of the study, the males of the 20% dose group gained less weight, but body weights were not significantly reduced in comparison to controls. Food intakes and food efficiencies were comparable among all groups. No treatment-related differences were observed with respect to ophthalmoscopic examinations, hematological parameters, clinicochemical analyses of the plasma, and semiquantitative urine analyses. Only the urinary pH was slightly below control levels in males of the 20% dose group. No abnormalities were seen at necropsy that could be attributed to treatment. The organ weight data revealed some cecal enlargement in the 10 and 20% dose groups. Relative ovary weights were significantly increased in the 10 and 20% groups but this was probably a result of an unusually low ovary weight in the controls. An increase of relative liver weights in males of the 10 and 20% dose groups also was considered to lack toxicological relevance because it was not associated with changes in plasma liver enzyme levels or histopathological changes. On microscopic examination, no treatment-related effects were observed in any of the various organs and tissues. In conclusion, transient diarrhea, cecal enlargement, and a slightly increased acidity of the urine were the only treatment-related effects reported. These changes are well-known physiological responses to the presence of increased amounts of undigested, fermentable carbohydrates in the lower gut. At the high applied intakes an incomplete digestion of gamma-CD and/or a partial inhibition of pancreatic amylase by gamma-CD could account for these effects. It is concluded that daily gamma-CD consumption of up to 20% in the diet (approximately 7.7 g/kg body wt in male and 8.3 g/kg body wt in female dogs) was tolerated without any toxic effects.
在一项为期13周的喂养研究中,对γ-环糊精(γ-CD)的口服毒性进行了检测。该研究中,四组比格犬,每组四只雄性和四只雌性,在饮食中分别摄入浓度为0(对照)、5%、10%或20%的γ-CD。未观察到与治疗相关的犬行为或外观变化,也未发生死亡。5%和10%剂量组的部分犬以及20%剂量组的所有犬出现短暂腹泻。然而,所有犬均保持健康且体重增加。在研究的最后6周,20%剂量组的雄性犬体重增加较少,但与对照组相比,体重并未显著降低。所有组的食物摄入量和食物利用率相当。在眼科检查、血液学参数、血浆临床化学分析和半定量尿液分析方面,未观察到与治疗相关的差异。仅20%剂量组雄性犬的尿液pH略低于对照水平。尸检未发现可归因于治疗的异常情况。器官重量数据显示,10%和20%剂量组的盲肠有一定程度的肿大。10%和20%组的相对卵巢重量显著增加,但这可能是由于对照组卵巢重量异常低所致。10%和20%剂量组雄性犬的相对肝脏重量增加也被认为缺乏毒理学相关性,因为这与血浆肝酶水平变化或组织病理学变化无关。显微镜检查未在任何器官和组织中观察到与治疗相关的影响。总之,短暂腹泻、盲肠肿大和尿液酸度略有增加是唯一报告的与治疗相关的影响。这些变化是对下消化道中未消化、可发酵碳水化合物含量增加的常见生理反应。在高摄入量时,γ-CD的不完全消化和/或γ-CD对胰腺淀粉酶的部分抑制可能导致这些影响。得出的结论是,饮食中每日摄入高达20%的γ-CD(雄性犬约为7.7克/千克体重,雌性犬约为8.3克/千克体重)可耐受,且无任何毒性作用。