Iordache Claudiu, Drozdowski Laurie, Clandinin Tom, Wild Gary, Todd Zoe, Thomson Alan B R
Nutrition and Metabolism Group, University of Alberta, Edmonton, Alberta, Canada.
JPEN J Parenter Enteral Nutr. 2004 Sep-Oct;28(5):355-63. doi: 10.1177/0148607104028005355.
Glucagon-like peptide 2 (GLP-2) has a trophic effect on the intestine and enhances intestinal absorption in adult animals, but its effect in young rats is unknown. Glucocorticosteroids accelerate the ontogeny of the intestine, and in adult animals they increase the uptake of sugars and lipids. We hypothesized that GLP-2 and dexamethasone (DEX), when administrated to lactating rat dams, will enhance lipid uptake in the suckling and weanling offspring.
Eight nursing rats were treated during lactation, 19 to 21 days, with GLP-2 (0.1 microg/g/d subcutaneously [s.c.]), DEX (0.128 microg/g/d s.c.), GLP-2 + DEX (GLP-2 0.1 microg/g/d s.c. plus DEX 0.128 microg/g/d s.c.), or placebo. Half of the offspring ("sucklings") were killed at 19 to 21 days of age, and half were killed 4 weeks later ("weanlings"). The rate of intestinal uptake of fatty acids (12:0, lauric; 16:0, palmitic; 18:0, stearic; 18:1, oleic; 18:2, linoleic; and 18:3, linolenic) and cholesterol were assessed using an in vitro ring technique.
GLP-2 and DEX resulted in loss of body weight in sucklings, which was prevented by giving the combination GLP-2 + DEX. The jejunal atrophy in sucklings given DEX was prevented by giving GLP-2 + DEX, but GLP-2 + DEX did not prevent the decline in jejunal and ileal villous height and crypt depth observed in weanlings given DEX. GLP-2 had little effect on lipid uptake in sucklings, whereas DEX or GLP-2 + DEX increased the uptake of lipids. In contrast, in weanlings there was malabsorption of several lipids with GLP-2 or GLP-2 + DEX, but not with DEX. Lipid uptake was lower in weanlings than in sucklings, and this age-associated decline was not altered by GLP-2 or DEX.
The loss of body weight and the jejunal atrophy induced by DEX in sucklings is prevented by adding GLP-2. Giving DEX or GLP-2 + DEX to lactating mothers enhances lipid uptake in their suckling offspring. In marked contrast, a month after lactating dams were given GLP-2 or GLP-2 + DEX, there was reduced lipid absorption in the postweaning animals. Thus, giving GLP-2 + DEX during lactation may be useful to enhance lipid uptake in the suckling offspring, without adverse effects on body weight or intestinal characteristics. However, the late effects of this treatment on lipid absorption were of concern, and could be potentially deleterious to the nutritional well-being of the animal.
胰高血糖素样肽2(GLP - 2)对成年动物的肠道具有营养作用,并能增强肠道吸收,但它在幼鼠中的作用尚不清楚。糖皮质激素可加速肠道的个体发育,在成年动物中,它们会增加糖和脂质的摄取。我们推测,给哺乳期大鼠母鼠注射GLP - 2和地塞米松(DEX)会增强其哺乳和断奶后代的脂质摄取。
8只哺乳大鼠在哺乳期(第19至21天)接受治疗,分别注射GLP - 2(0.1微克/克/天皮下注射)、DEX(0.128微克/克/天皮下注射)、GLP - 2 + DEX(GLP - 2 0.1微克/克/天皮下注射加DEX 0.128微克/克/天皮下注射)或安慰剂。一半的后代(“哺乳幼崽”)在19至21日龄时处死,另一半在4周后(“断奶幼崽”)处死。使用体外环技术评估脂肪酸(12:0,月桂酸;16:0,棕榈酸;18:0,硬脂酸;18:1,油酸;18:2,亚油酸;18:3,亚麻酸)和胆固醇的肠道摄取率。
GLP - 2和DEX导致哺乳幼崽体重减轻,而给予GLP - 2 + DEX可预防这种情况。给予GLP - 2 + DEX可预防给予DEX的哺乳幼崽的空肠萎缩,但GLP - 2 + DEX不能预防给予DEX的断奶幼崽空肠和回肠绒毛高度及隐窝深度的下降。GLP - 2对哺乳幼崽的脂质摄取影响很小,而DEX或GLP - 2 + DEX可增加脂质摄取。相反,在断奶幼崽中,GLP - 2或GLP - 2 + DEX会导致几种脂质吸收不良,而DEX则不会。断奶幼崽的脂质摄取低于哺乳幼崽,并且这种与年龄相关的下降不受GLP - 2或DEX的影响。
添加GLP - 2可预防DEX诱导的哺乳幼崽体重减轻和空肠萎缩。给哺乳期母亲注射DEX或GLP - 2 + DEX可增强其哺乳后代的脂质摄取。与之形成鲜明对比的是,在给哺乳期母鼠注射GLP - 2或GLP - 2 + DEX一个月后,断奶后动物的脂质吸收减少。因此,在哺乳期给予GLP - 2 + DEX可能有助于增强哺乳后代的脂质摄取,而对体重或肠道特征无不良影响。然而,这种治疗对脂质吸收的后期影响令人担忧,可能对动物的营养健康产生潜在危害。