Institute for Clinical Chemistry and Clinical Pharmacology, University Clinics of Bonn, D-53127 Bonn, Germany.
Department of Radiology, University Clinics of Bonn, D-53127 Bonn, Germany.
Nutrients. 2018 Jan 11;10(1):72. doi: 10.3390/nu10010072.
Chitosan treatment results in significantly lower serum low density lipoprotein (LDL) cholesterol concentrations. To assess the working mechanisms of chitosan, we measured serum surrogate markers of cholesterol absorption (campesterol, sitosterol, cholestanol), synthesis (lathosterol, lanosterol, desmosterol), and degradation to bile acids (7α-hydroxy-cholesterol, 27-hydroxy-cholesterol), corrected for cholesterol concentration (R_sterols). Over 12 weeks, 116 obese subjects (Body Mass Index, BMI 31.7, range 28.1-38.9 kg/m²) were studied under chitosan ( = 61) and placebo treatments ( = 55). The participants were briefly educated regarding improvement of nutrition quality and energy expenditure. Daily chitosan intake was 3200 mg. Serum LDL cholesterol concentration decreased significantly more ( = 0.0252) under chitosan (-8.67 ± 18.18 mg/dL, 5.6%) than under placebo treatment (-1.00 ± 24.22 mg/dL, 0.9%). This reduction was not associated with the expected greater decreases in markers of cholesterol absorption under chitosan treatment. Also, increases in markers of cholesterol synthesis and bile acid synthesis under chitosan treatment were not any greater than under placebo treatment. In conclusion, a significant selective reduction of serum LDL cholesterol under chitosan treatment is neither associated with a reduction of serum surrogate markers of cholesterol absorption, nor with increases of markers for cholesterol and bile acid synthesis.
壳聚糖处理可显著降低血清低密度脂蛋白(LDL)胆固醇浓度。为了评估壳聚糖的作用机制,我们测量了血清胆固醇吸收(菜油固醇、豆固醇、胆甾烷醇)、合成(羊毛甾醇、菜油甾醇、去甲胆固醇)和降解为胆汁酸(7α-羟胆固醇、27-羟胆固醇)的替代标志物,同时对胆固醇浓度进行了校正(R-甾醇)。在 12 周的时间里,116 名肥胖受试者(体重指数,BMI 31.7,范围 28.1-38.9 kg/m²)接受了壳聚糖(=61)和安慰剂(=55)治疗。研究人员简要地向参与者介绍了改善营养质量和能量消耗的方法。受试者每日摄入壳聚糖 3200mg。与安慰剂组(-1.00 ± 24.22mg/dL,0.9%)相比,壳聚糖组(-8.67 ± 18.18mg/dL,5.6%)的血清 LDL 胆固醇浓度显著下降(=0.0252)。这一降低与预期的壳聚糖治疗下胆固醇吸收替代标志物的更大降低无关。此外,壳聚糖治疗下胆固醇和胆汁酸合成标志物的增加并不比安慰剂治疗组更大。总之,壳聚糖治疗下血清 LDL 胆固醇的显著选择性降低与血清胆固醇吸收替代标志物的降低无关,也与胆固醇和胆汁酸合成标志物的增加无关。