Nishimura M, Seishima M, Ohashi H, Noma A
Department of Laboratory Medicine, Gifu University School of Medicine, Japan.
Am J Physiol. 1996 Aug;271(2 Pt 1):G322-9. doi: 10.1152/ajpgi.1996.271.2.G322.
We examined the mesenteric lymphatic and portal venous transport of triglyceride (TG), free fatty acids (FFA), apolipoproteins (apo)A-IV and B in response to a bolus duodenal infusion of a TG-free control solution, and long-chain (18:1) and medium-chain (8:0) TG (LCT and MCT, respectively) emulsions in the rat. Additionally, intestinal and hepatic apo A-IV and apo B mRNA levels were also measured. Lymph apo A-IV, apo B (B-48), FFA, and TG output increased after LCT infusion, whereas only apo A-IV and FFA outputs increased after MCT infusion. On the other hand, portal FFA and apo A-IV transports increased at 15 min after MCT infusion but not after LCT infusion. Portal TG and apo B transports were not altered by either MCT or LCT infusion. Jejunal apo A-IV mRNA was increased after both MCT and LCT infusions. Hepatic apo A-IV mRNA levels increased only after MCT infusion. Conversely, neither LCT nor MCT had any effect on apo B mRNA levels in intestine or liver. These results indicate that apo A-IV is regulated by MCT absorption and that fatty acid reesterification and lipoprotein assembly are not prerequisite for such regulation. Conversely, it is likely that apo B-48 participates only in the formation and/or transport of chylomicrons after LCT absorption.
我们研究了在大鼠中,十二指肠推注无甘油三酯(TG)的对照溶液、长链(18:1)和中链(8:0)TG(分别为LCT和MCT)乳剂后,肠系膜淋巴和门静脉对TG、游离脂肪酸(FFA)、载脂蛋白(apo)A-IV和B的转运情况。此外,还测量了肠道和肝脏中apo A-IV和apo B的mRNA水平。输注LCT后,淋巴apo A-IV、apo B(B-48)、FFA和TG输出增加,而输注MCT后仅apo A-IV和FFA输出增加。另一方面,输注MCT后15分钟门静脉FFA和apo A-IV转运增加,而输注LCT后未增加。门静脉TG和apo B转运不受MCT或LCT输注的影响。输注MCT和LCT后空肠apo A-IV mRNA均增加。仅输注MCT后肝脏apo A-IV mRNA水平增加。相反,LCT和MCT对肠道或肝脏中的apo B mRNA水平均无影响。这些结果表明,apo A-IV受MCT吸收调节,脂肪酸再酯化和脂蛋白组装并非这种调节的先决条件。相反,apo B-48可能仅参与LCT吸收后乳糜微粒的形成和/或转运。