Yuasa H, Kawanishi K, Watanabe J
Faculty of Pharmaceutical Sciences, Nagoya City University, Japan.
J Pharm Pharmacol. 1995 Jul;47(7):576-80. doi: 10.1111/j.2042-7158.1995.tb06717.x.
The effects of ageing on the oral (gastrointestinal) absorption of D-xylose were investigated by analysing the gastrointestinal disposition after oral administration to young (9 weeks) and old (53 weeks) rats. A linear model assuming first-order gastric emptying followed by first-order intestinal absorption was fitted to remaining fraction vs time profiles for the stomach and small intestine to estimate the gastric emptying rate constant (kg) and the intestinal absorption rate constant (ka). In young and old rats, Kg values were 0.087 +/- 0.008 and 0.070 +/- 0.007 min-1, respectively, and ka values were 0.020 +/- 0.002 and 0.018 +/- 0.002 min-1, suggesting an insignificant effect on ageing on the rate of oral absorption. The average intestinal lumen volume (Vav) was unchanged with ageing, and so was the apparent intestinal membrane permeability clearance (CLapp) as the product of Ka and Vav. However, the small intestinal transit time (Tsi) was suggested to be twice that in older rats (171 min) than in young rats (78 min) by the analysis of gastrointestinal disposition of inulin, a non-absorbable marker. It was also shown that our preceding finding of an increase in the fraction absorbed of D-xylose with ageing can be solely ascribable to the delay in intestinal transit. Thus, among various determinants of oral absorption, only Tsi was found to be altered with ageing. The CLa,app and ka of passively absorbed drugs such as D-xylose may be generally unchanged, and the fraction absorbed may increase with ageing by the delay in intestinal transit.
通过分析给年轻(9周龄)和老年(53周龄)大鼠口服后胃肠道的处置情况,研究了衰老对D-木糖口服(胃肠道)吸收的影响。将假设一级胃排空随后一级肠道吸收的线性模型拟合到胃和小肠的剩余分数与时间曲线,以估计胃排空速率常数(kg)和肠道吸收速率常数(ka)。在年轻和老年大鼠中,kg值分别为0.087±0.008和0.070±0.007 min-1,ka值分别为0.020±0.002和0.018±0.002 min-1,表明衰老对口服吸收速率的影响不显著。平均肠腔容积(Vav)不随衰老而变化,作为Ka和Vav乘积的表观肠膜通透性清除率(CLapp)也是如此。然而,通过对不可吸收标记物菊粉的胃肠道处置分析,提示老年大鼠(171分钟)的小肠转运时间(Tsi)是年轻大鼠(78分钟)的两倍。还表明,我们之前发现的D-木糖吸收分数随衰老增加的现象可完全归因于肠道转运延迟。因此,在口服吸收的各种决定因素中,仅发现Tsi随衰老而改变。被动吸收药物如D-木糖的CLa,app和ka通常可能不变,吸收分数可能因肠道转运延迟而随衰老增加。