Bauchart-Thevret Caroline, Stoll Barbara, Chacko Shaji, Burrin Douglas G
US Department of Agriculture/Agricultural Research Service Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030, USA.
Am J Physiol Endocrinol Metab. 2009 Jun;296(6):E1239-50. doi: 10.1152/ajpendo.91021.2008. Epub 2009 Mar 17.
We recently showed that the developing gut is a significant site of methionine transmethylation to homocysteine and transsulfuration to cysteine. We hypothesized that sulfur amino acid (SAA) deficiency would preferentially reduce mucosal growth and antioxidant function in neonatal pigs. Neonatal pigs were enterally fed a control or an SAA-free diet for 7 days, and then whole body methionine and cysteine kinetics were measured using an intravenous infusion of [1-(13)C;methyl-(2)H(3)]methionine and [(15)N]cysteine. Body weight gain and plasma methionine, cysteine, homocysteine, and taurine and total erythrocyte glutathione concentrations were markedly decreased (-46% to -85%) in SAA-free compared with control pigs. Whole body methionine and cysteine fluxes were reduced, yet methionine utilization for protein synthesis and methionine remethylation were relatively preserved at the expense of methionine transsulfuration, in response to SAA deficiency. Intestinal tissue concentrations of methionine and cysteine were markedly reduced and hepatic levels were maintained in SAA-free compared with control pigs. SAA deficiency increased the activity of methionine metabolic enzymes, i.e., methionine adenosyltransferase, methionine synthase, and cystathionine beta-synthase, and S-adenosylmethionine concentration in the jejunum, whereas methionine synthase activity increased and S-adenosylmethionine level decreased in the liver. Small intestine weight and protein and DNA mass were lower, whereas liver weight and DNA mass were unchanged, in SAA-free compared with control pigs. Dietary SAA deficiency induced small intestinal villus atrophy, lower goblet cell numbers, and Ki-67-positive proliferative crypt cells in association with lower tissue glutathione, especially in the jejunum. We conclude that SAA deficiency upregulates intestinal methionine cycle activity and suppresses epithelial growth in neonatal pigs.
我们最近发现,发育中的肠道是蛋氨酸转甲基生成同型半胱氨酸以及转硫生成半胱氨酸的重要场所。我们推测,硫氨基酸(SAA)缺乏会优先降低新生仔猪的黏膜生长和抗氧化功能。将新生仔猪经肠道饲喂对照日粮或无SAA日粮7天,然后通过静脉输注[1-(13)C;甲基-(2)H(3)]蛋氨酸和[(15)N]半胱氨酸来测定全身蛋氨酸和半胱氨酸的动力学。与对照仔猪相比,无SAA仔猪的体重增加以及血浆蛋氨酸、半胱氨酸、同型半胱氨酸、牛磺酸和总红细胞谷胱甘肽浓度显著降低(-46%至-85%)。全身蛋氨酸和半胱氨酸通量降低,但为应对SAA缺乏,用于蛋白质合成的蛋氨酸利用率和蛋氨酸再甲基化相对得以保留,代价是蛋氨酸转硫作用。与对照仔猪相比,无SAA仔猪的肠道组织蛋氨酸和半胱氨酸浓度显著降低,而肝脏水平保持不变。无SAA仔猪的小肠重量、蛋白质和DNA质量较低,而肝脏重量和DNA质量未变。日粮SAA缺乏导致小肠绒毛萎缩、杯状细胞数量减少以及Ki-67阳性增殖性隐窝细胞减少,同时组织谷胱甘肽水平降低,尤其是在空肠。我们得出结论,SAA缺乏会上调新生仔猪肠道蛋氨酸循环活性并抑制上皮生长。