Xu G, Salen G, Tint G S, Batta A K, Shefer S
Gastroenterology Laboratory, Department of Veterans Affairs, New Jersey Health Care System, East Orange 07018-1095, USA.
Metabolism. 1999 Mar;48(3):363-8. doi: 10.1016/s0026-0495(99)90086-0.
Campestanol (24-methyl-5alpha-cholestan-3beta-ol) is a naturally occurring plant stanol, structurally similar to cholesterol (5-cholesten-3beta-ol) and widely distributed in vegetable oils consumed in human diets. We measured the absorption and turnover of campestanol by the plasma dual-isotope ratio method and mathematical analysis of specific activity versus time decay curves after simultaneous oral and intravenous pulse-labeling with [3alpha-3H]- and [23-14C]-labeled campestanol, respectively, in New Zealand White (NZW) rabbits: six fed chow and six fed chow with 125 mg/d campestanol and 175 mg/d sitostanol (24-ethyl-5alpha-cholestan-3beta-ol). Plasma concentrations increased insignificantly from 0.08+/-0.01 to 0.09+/-0.01 mg/dL with dietary stanols. The percent campestanol absorption measured by the plasma dual-isotope ratio method after the rabbits were fasted for 6 hours yielded the percent absorption in the absence of competing intestinal sterols and stanols and declined insignificantly from 11.6%+/-3.5% in controls to 8.1%+/-3.7% in the treated rabbit groups. In contrast, the turnover, which measured actual absorption averaged over 24 hours, increased from 0.12+/-0.05 to 0.37+/-0.05 mg/d (P < .05) with campestanol and sitostanol added to the diet. However, the actual percent absorption declined from 3% to 0.3% of dietary intake with the campestanol and sitostanol-enriched diet. Campestanol pool sizes, although remaining small, increased slightly from 1.1+/-0.4 to 2.5+/-1.5 mg. The removal constant (KA) from pool A (MA) did not change significantly with added dietary campestanol and sitostanol (KA= -0.040+/-0.005 v -0.037+/-0.007 d(-1)). The results demonstrate small campestanol plasma concentrations and body pools even when the rabbits consumed substantial amounts because (1) intestinal absorption was limited and (2) was further reduced by competing dietary sitostanol, and (3) campestanol was removed rapidly from the body. Thus, campestanol, which shares the same basic structure and intestinal absorption pathway with cholesterol, does not accumulate when fed, and may be incorporated into the diet to block cholesterol absorption.
菜油甾醇(24-甲基-5α-胆甾烷-3β-醇)是一种天然存在的植物甾烷醇,其结构与胆固醇(5-胆甾烯-3β-醇)相似,广泛分布于人类饮食中所摄入的植物油中。我们采用血浆双同位素比率法以及在新西兰白兔(NZW)中分别用[3α-³H]-和[23-¹⁴C]-标记的菜油甾醇进行口服和静脉脉冲标记后,通过对比放射性与时间衰减曲线进行数学分析,来测定菜油甾醇的吸收和周转率:六只喂普通饲料,六只喂添加了125mg/d菜油甾醇和175mg/d谷甾醇(24-乙基-5α-胆甾烷-3β-醇)的普通饲料。饮食中添加甾烷醇后,血浆浓度从0.08±0.01mg/dL略微升高至0.09±0.01mg/dL。在兔子禁食6小时后,采用血浆双同位素比率法测得的菜油甾醇吸收百分比得出了在不存在竞争性肠道甾醇和甾烷醇情况下的吸收百分比,其在对照组中从11.6%±3.5%略微下降至处理组兔子中的8.1%±3.7%。相比之下,周转率(测量的是24小时内的实际平均吸收量)在饮食中添加菜油甾醇和谷甾醇后从0.12±0.05mg/d增加至0.37±0.05mg/d(P<0.05)。然而,实际吸收百分比随着富含菜油甾醇和谷甾醇的饮食从饮食摄入量的3%下降至0.3%。菜油甾醇池大小虽然仍然较小,但从1.1±0.4mg略微增加至2.5±1.5mg。来自池A(MA)的清除常数(KA)在饮食中添加菜油甾醇和谷甾醇后没有显著变化(KA=-0.040±0.005对-0.037±0.007 d⁻¹)。结果表明,即使兔子摄入大量菜油甾醇,其血浆浓度和体内池也较小,原因在于:(1)肠道吸收受限;(2)竞争性饮食谷甾醇使其进一步降低;(3)菜油甾醇从体内迅速清除。因此,与胆固醇具有相同基本结构和肠道吸收途径的菜油甾醇在喂食时不会积累,并且可以添加到饮食中以阻断胆固醇吸收。