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大鼠小肠的最大淋巴甘油三酯转运率。

Maximal lymphatic triglyceride transport rate from the rat small intestine.

作者信息

Tso P, Buch K L, Balint J A, Rodgers J B

出版信息

Am J Physiol. 1982 Apr;242(4):G408-15. doi: 10.1152/ajpgi.1982.242.4.G408.

Abstract

In previous studies, we demonstrated that the hydrophobic surfactant Pluronic L-81 blocks lymphatic triglyceride transport from the small intestine and leads to accumulation of triglyceride in the mucosa. The onset of action of Pluronic L-81 is rapid and quickly reversed once its administration is discontinued. We have taken advantage of these effects of Pluronic L-81 on intestinal lipid transport in order to determine the apparent maximal triglyceride transport capacity of the proximal half of the rat small bowel using lymph fistula rats infused intraduodenally with a phosphate-buffered, taurocholate-stabilized emulsion containing 40 mumol [3H]triolein and 0.5 mg Pluronic L-81 at 3 ml/h for 8 h to load the proximal small bowel with lipid. Studies were done in one group of rats in order to be certain that only the proximal half of the small bowel contained 3H-lipid after this period of infusion. In other rats treated similarly, the 8 h of lipid-Pluronic L-81 infusion were followed by infusion of 3 ml/h of 0.15 M salt solution for 5 h. Lymphatic transport of lipid was determined throughout the entire period of infusion. During lipid-Pluronic L-81 infusion, transport of 3H-triglyceride fatty acid into lymph was only 22-27 mumol/h but rose steadily after substitution of saline and reached a maximal transport rate of 109 +/- 6.2 mumol/h (means +/- SE) after 3.5 h. During this 3.5-h period, the amount of 3H-lipid in the proximal mucosa declined from 530 to 263 mumol. While Pluronic L-81 was infused, only very low-density-lipoprotein-sized particles were seen in lymph by electron microscopy, whereas, at the peak of triglyceride transport during saline infusion, chylomicrons of up to 6,000 A were observed in lymph.

摘要

在先前的研究中,我们证明疏水性表面活性剂普朗尼克L-81可阻断小肠淋巴甘油三酯的转运,并导致甘油三酯在黏膜中蓄积。普朗尼克L-81的起效迅速,一旦停药其作用很快逆转。我们利用普朗尼克L-81对肠道脂质转运的这些作用,通过向十二指肠内以3 ml/h的速度输注含40 μmol [3H]三油酸甘油酯和0.5 mg普朗尼克L-81的磷酸盐缓冲、牛磺胆酸盐稳定的乳剂8小时,使大鼠近端小肠负荷脂质,从而确定大鼠小肠近端一半的表观最大甘油三酯转运能力。对一组大鼠进行了研究,以确保在这段输注期后只有小肠近端一半含有3H标记的脂质。在其他同样处理的大鼠中,在8小时的脂质-普朗尼克L-81输注后,接着以3 ml/h的速度输注0.15 M盐溶液5小时。在整个输注期间测定脂质的淋巴转运。在脂质-普朗尼克L-81输注期间,3H-甘油三酯脂肪酸向淋巴中的转运仅为22 - 27 μmol/h,但在换用生理盐水后稳步上升,在3.5小时后达到最大转运速率109±6.2 μmol/h(平均值±标准误)。在这3.5小时期间,近端黏膜中3H标记脂质的量从530 μmol降至263 μmol。当输注普朗尼克L-81时,电子显微镜观察到淋巴中仅见极低密度脂蛋白大小的颗粒,而在生理盐水输注期间甘油三酯转运达到峰值时,在淋巴中观察到直径达6000 Å的乳糜微粒。

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