Tso P, Balint J A, Bishop M B, Rodgers J B
Am J Physiol. 1981 Dec;241(6):G487-97. doi: 10.1152/ajpgi.1981.241.6.G487.
Lymph fistula rats were used to determine the acute effects of the hydrophobic surfactant, Pluronic L-81, on lipid transport by the small bowel. Animals were infused intraduodenally with a lipid emulsion containing [3H]triolein and Pluronic L-81, and the rate of intestinal transport of absorbed lipid into lymph was studied using liquid scintillation spectrometry. With this technique, various dose levels of Pluronic L-81 were analyzed for a possible inhibitory effect on lipid transport. Also, the rate at which this agent produced inhibition of intestinal lipid transport was determined. Results were correlated with electron microscopic studies of jejunal enterocytes and lipoprotein particles recovered in intestinal lymph. Infusion of Pluronic L-81 at a rate of 0.25 mg/h had no effect, but infusion at 0.5 and 1 mg/h produced a dramatic reduction in lipid transport by the small bowel. The rate of inhibition of lymphatic lipid output was rapid, with a t1/2 of 69 min for the 0.5 mg/h dose and 35 min for the 1 mg/h dose. This inhibition of lipid transport was associated with marked mucosal accumulation of lipid as demonstrated by radiochemical and morphological data. By electron microscopic analysis, only very low-density lipoprotein-sized particles were transported into lymph by enterocytes exposed to an effective dose of Pluronic L-81. It is concluded that small amounts of Pluronic L-81 produce a striking inhibition in the intracellular transport of chylomicron-sized particles, thereby blocking secretion of chylomicrons by the enterocytes. Furthermore, this action is very rapidly produced by effective doses of this agent.
使用淋巴瘘大鼠来确定疏水性表面活性剂普朗尼克L - 81对小肠脂质转运的急性影响。通过十二指肠向动物输注含有[3H]甘油三油酸酯和普朗尼克L - 81的脂质乳剂,并使用液体闪烁光谱法研究吸收的脂质进入淋巴的肠道转运速率。利用该技术,分析了不同剂量水平的普朗尼克L - 81对脂质转运可能的抑制作用。此外,还确定了该药剂产生肠道脂质转运抑制的速率。结果与空肠肠细胞的电子显微镜研究以及在肠淋巴中回收的脂蛋白颗粒相关。以0.25毫克/小时的速率输注普朗尼克L - 81没有效果,但以0.5和1毫克/小时的速率输注会使小肠的脂质转运显著降低。淋巴脂质输出的抑制速率很快,0.5毫克/小时剂量的t1/2为69分钟,1毫克/小时剂量的t1/2为35分钟。如放射化学和形态学数据所示,这种脂质转运的抑制与脂质在黏膜中的大量积累有关。通过电子显微镜分析,暴露于有效剂量普朗尼克L - 81的肠细胞仅将极低密度脂蛋白大小的颗粒转运到淋巴中。得出的结论是,少量的普朗尼克L - 81对乳糜微粒大小颗粒的细胞内转运产生显著抑制,从而阻止肠细胞分泌乳糜微粒。此外,该药剂的有效剂量能非常迅速地产生这种作用。