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运输阻断后小肠脂质动员的机制。

Mechanism of lipid mobilization by the small intestine after transport blockade.

作者信息

Halpern J, Tso P, Mansbach C M

机构信息

Department of Medicine, University of Tennessee, Memphis 38163.

出版信息

J Clin Invest. 1988 Jul;82(1):74-81. doi: 10.1172/JCI113604.

Abstract

The nonionic detergent, Pluronic L-81 (L-81) has been shown to block the transport of intestinal mucosal triacylglycerol (TG) in chylomicrons. This results in large lipid masses within the enterocyte that are greater in diameter than chylomicrons. On removal of L-81, mucosal TG is rapidly mobilized and appears in the lymph. We questioned whether the blocked TG requires partial or complete hydrolysis before its transport. Rats were infused intraduodenally with [3H]glyceryl, [14C]oleoyl trioleate (TO) and 0.5 mg L-81/h for 8 h, followed by 120 mumol/h linoleate for 18 h. Mesenteric lymph was collected and analyzed for TG content and radioactivity. An HPLC method was developed to separate TG on the basis of its acyl group species. The assumed acyl group composition was confirmed by gas liquid chromatography analysis. TG lymphatic output was low for the first 8 h but increased to 52 mumol/h at the 11th h of infusion (3 h after stopping L-81). 38% of the infused TO was retained in the mucosa after the 8-h infusion. 95% of mucosal TG was TO, 92% of the radioactivity was in TG, and 2.4% of the 14C disintegrations per minute was in fatty acid. HPLC analysis of lymph at 6, 10, 12, and 14.5 h of infusion showed a progressive rise in TG composed of one linoleate and two oleates, to 39%; and in TG composed of two linoleates and one oleate to 20% at 14.5 h of infusion. On a mass basis, however, 80% of the TG acyl groups were oleate. 3H/14C ratios in the various TG acyl group species reflected the decrease in oleate. We conclude that first, unlike liver, most mucosal TG is not hydrolyzed before transport. The mechanism of how the large lipid masses present in mucosal cells after L-81 infusion are converted to the much smaller chylomicrons is unknown. Second, the concomitant infusion of linoleate did not impair lymph TG delivery after L-81 blockade.

摘要

已证实非离子去污剂普朗尼克L-81(L-81)可阻断肠黏膜中三酰甘油(TG)以乳糜微粒形式的转运。这导致肠细胞内出现大量脂质团块,其直径大于乳糜微粒。去除L-81后,黏膜TG迅速动员并出现在淋巴中。我们质疑被阻断的TG在转运前是否需要部分或完全水解。给大鼠十二指肠内输注[3H]甘油、[14C]油酰三油酸甘油酯(TO)和0.5毫克L-81/小时,持续8小时,随后以120微摩尔/小时输注亚油酸,持续18小时。收集肠系膜淋巴并分析其TG含量和放射性。开发了一种高效液相色谱法,根据TG的酰基种类分离TG。通过气相色谱分析确认了假定的酰基组成。输注的前8小时TG淋巴输出量较低,但在输注第11小时(停止L-81后3小时)增加到52微摩尔/小时。8小时输注后,38%的输注TO保留在黏膜中。95%的黏膜TG是TO,92%的放射性存在于TG中,每分钟14C衰变的2.4%存在于脂肪酸中。输注6、10、12和14.5小时时淋巴的高效液相色谱分析显示,由一个亚油酸酯和两个油酸酯组成的TG逐渐增加,在输注14.5小时时达到39%;由两个亚油酸酯和一个油酸酯组成的TG在输注14.5小时时增加到20%。然而,以质量计,80%的TG酰基是油酸酯。各种TG酰基种类中的3H/14C比值反映了油酸酯的减少。我们得出结论,第一,与肝脏不同,大多数黏膜TG在转运前不被水解。L-81输注后黏膜细胞中存在的大量脂质团块如何转化为小得多的乳糜微粒的机制尚不清楚。第二,L-81阻断后同时输注亚油酸不会损害淋巴TG的输送。

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