Lee S H E, Hossner K L
Department of Animal Sciences, Colorado State University, Fort Collins 80523, USA.
J Anim Sci. 2002 Nov;80(11):2840-9. doi: 10.2527/2002.80112840x.
The current study examined the acute effects of intravenous propionate infusion on plasma hormones and metabolites and the expression of adipose tissue lipogenic genes. Four yearling rams were assigned to one oftwo groups (saline or propionate infusion) in a crossover design. All sheep were cannulated in both jugular veins and infused with 1.2 M propionate at a rate of 64 micromol x mix(-1) x kg BW(-1) for 30 min. Blood samples were collected at -10, 0, 5, 10, 20, 30, 60, and 120 min after initiation of infusion. Subcutaneous adipose tissue biopsies were obtained from the tailhead at 0 and 2 h after propionate infusion and analyzed for gene expressions of lipoprotein lipase, acetyl CoA carboxylase, fatty acid synthase, peroxisome proliferator-activated receptor gamma, leptin, and uncoupling protein-2 using a nonisotopic ribonuclease protection assay. The partial cDNA of the enoyl reductase region of ovine fatty acid synthase was cloned and sequenced from s.c. adipose tissue of sheep. The deduced amino acid sequence (210 amino acids) was 86% identical to human, 88% identical to rat, 88% identical to mouse, and 72% identical to chicken. Plasma glucose and insulin concentrations abruptly increased 5 min after beginning propionate infusion and further increased up until 30 min but were unaffected in saline-infused sheep (P < 0.05). Plasma concentration of NEFA decreased (P < 0.05) during propionate infusion, whereas IGF-I levels were unaltered. The amounts of lipoprotein lipase, acetyl CoA carboxylase, fatty acid synthase, peroxisome proliferator-activated receptor gamma, and leptin mRNA increased (P < 0.05) in s.c. adipose tissue of propionate-infused sheep compared with those of saline-infused sheep. However, uncoupling protein-2 mRNA decreased (P < 0.05) in propionate-infused sheep. This study demonstrates that an acute nutrient challenge, in the form of i.v. propionate, can stimulate or inhibit the expression of various adipose tissue genes involved with lipogenesis and adipose tissue metabolism.
本研究检测了静脉输注丙酸盐对血浆激素、代谢物以及脂肪组织脂肪生成基因表达的急性影响。采用交叉设计,将4只一岁公羊分配到两组之一(生理盐水组或丙酸盐输注组)。所有绵羊的双侧颈静脉均插管,并以64微摩尔×分钟⁻¹×千克体重⁻¹的速率输注1.2 M丙酸盐,持续30分钟。在输注开始后的-10、0、5、10、20、30、60和120分钟采集血样。在丙酸盐输注后0小时和2小时从尾根处获取皮下脂肪组织活检样本,使用非同位素核糖核酸酶保护分析法分析脂蛋白脂肪酶、乙酰辅酶A羧化酶、脂肪酸合酶、过氧化物酶体增殖物激活受体γ、瘦素和解偶联蛋白-2的基因表达。从绵羊的皮下脂肪组织中克隆并测序了绵羊脂肪酸合酶烯酰还原酶区域的部分cDNA。推导的氨基酸序列(210个氨基酸)与人类的同源性为86%,与大鼠的同源性为88%,与小鼠的同源性为88%,与鸡的同源性为72%。丙酸盐输注开始5分钟后,血浆葡萄糖和胰岛素浓度突然升高,并持续升高至30分钟,但在输注生理盐水的绵羊中未受影响(P < 0.05)。丙酸盐输注期间,血浆非酯化脂肪酸浓度降低(P < 0.05),而胰岛素样生长因子-I水平未改变。与输注生理盐水的绵羊相比,输注丙酸盐的绵羊皮下脂肪组织中脂蛋白脂肪酶、乙酰辅酶A羧化酶、脂肪酸合酶、过氧化物酶体增殖物激活受体γ和瘦素mRNA的量增加(P < 0.05)。然而,输注丙酸盐的绵羊中解偶联蛋白-2 mRNA减少(P < 0.05)。本研究表明,以静脉注射丙酸盐形式的急性营养刺激可刺激或抑制参与脂肪生成和脂肪组织代谢的各种脂肪组织基因的表达。