Meal-contingent intestinal lymph sampling from awake, unrestrained rats

被引:17
作者
Arnold, Myrtha [1 ]
Dai, Yunting [1 ]
Tso, Patrick [2 ]
Langhans, Wolfgang [1 ]
机构
[1] Swiss Fed Inst Technol, Swiss Fed Inst Technol, Inst Food Nutr & Hlth, Physiol & Behav Lab, CH-8603 Schwerzenbach, Switzerland
[2] Univ Cincinnati, Dept Pathol, Cincinnati, OH USA
基金
瑞士国家科学基金会;
关键词
lymphatic system; gastrointestinal physiology; fat absorption; intestinal peptides; glucagon-like peptide-1; GLUCAGON-LIKE PEPTIDE-1; TRANSPORT; HORMONES; FAT;
D O I
10.1152/ajpregu.00497.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Arnold M, Dai Y, Tso P, Langhans W. Meal-contingent intestinal lymph sampling from awake, unrestrained rats. Am J Physiol Regul Integr Comp Physiol 302: R1365-R1371, 2012. First published April 18, 2012; doi:10.1152/ajpregu.00497.2011.-Standard procedures for intestinal lymph collection involve continuous, quantitative drainage of the lymph fluid in anesthetized or restrained animals that are often euthanized within 48 h. We here describe a novel technique for the nonocclusive cannulation of the major intestinal lymph duct in rats that allows for repetitive in vivo sampling of intestinal lymph from unrestrained, awake, and ad libitum-fed animals. The distinctive feature of this novel technique is that a 5- to 7-mm long piece of Vialon tubing (OD/ID: 0.8/0.7 mm) with a small hole in its wall is first implanted into the major intestinal lymph duct for stabilization. The tapered tip (OD: approximate to 0.1 mm) of the catheter is then inserted into the hole of the tubing and fixed in place with a polyamid suture and a drop of tissue glue. In our hands, catheters implanted this way remain patent for up to 6 wk after surgery. In an initial experiment we collected lymph from six adult rats before (0) and 15, 30, 45, 60, 75, 90, 120, and 180 min (120 mu l, each) after the onset of isocaloric (12.5 kcal) low-fat (LF) or high-fat (HF) test meals and measured active glucagon-like peptide-1 (GLP-1). Intestinal lymphatic GLP-1 concentration increased (P < 0.05) from approximate to 4 pmol/l (0 min) to a peak of 33 +/- 6 (means +/- SE) or 22 +/- 4 pmol/l at 15 (HF) or 30 min (LF) after meal onset and gradually returned to baseline levels by 180 min. With this new technique fewer animals are required to generate physiologically relevant data for various aspects of gastrointestinal physiology that involve the lymphatic system. Furthermore, the advantage of this system is that the animal can act as its own control when the effect of different experimental protocols is tested.
引用
收藏
页码:R1365 / R1371
页数:7
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