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结肠腔氨和门脉血 L-谷氨酰胺和 L-精氨酸浓度:结肠黏膜与肝脏尿素生成之间的可能联系。

Colonic luminal ammonia and portal blood L-glutamine and L-arginine concentrations: a possible link between colon mucosa and liver ureagenesis.

机构信息

INRA, CNRH-IdF, AgroParisTech, UMR 914 Nutrition Physiology and Ingestive Behavior, 16 rue Claude Bernard, 75005, Paris, France.

出版信息

Amino Acids. 2009 Oct;37(4):751-60. doi: 10.1007/s00726-008-0218-3. Epub 2008 Dec 11.

Abstract

The highest ammonia concentration in the body is found in the colon lumen and although there is evidence that this metabolite can be absorbed through the colonic epithelium, there is little information on the capacity of the colonic mucosa to transfer and metabolize this compound. In the present study, we used a model of conscious pig with a canula implanted into the proximal colon to inject endoluminally increasing amounts of ammonium chloride and to measure during 5 h the kinetics of ammonia and amino acid concentration changes in the portal and arterial blood. By injecting as a single dose from 1 to 5 g ammonia into the colonic lumen, a dose-related increase in ammonia concentration in the portal blood was recorded. Ammonia concentration remained unchanged in the arterial blood except for the highest dose tested, i.e. 5 g which thus apparently exceeds the hepatic ureagenesis capacity. By calculating the apparent net ammonia absorption, it was determined that the pig colonic epithelium has the capacity to absorb 4 g ammonia. Ammonia absorption through the colonic epithelium was concomitant with increase of L-glutamine and L-arginine concentrations in the portal blood. This coincided with the expression of both glutamate dehydrogenase and glutamine synthetase in isolated colonic epithelial cells. Since L-glutamine and L-arginine are known to represent activators for liver ureagenesis, we propose that increased portal concentrations of these amino acids following increased ammonia colonic luminal concentration represent a metabolic link between colon mucosa and liver urea biosynthesis.

摘要

体内氨浓度最高的部位是结肠腔,尽管有证据表明这种代谢物可以通过结肠上皮吸收,但关于结肠黏膜转运和代谢这种化合物的能力的信息却很少。在本研究中,我们使用了一种在近端结肠内置入导管的清醒猪模型,向肠腔内注入递增剂量的氯化铵,并在 5 小时内测量门静脉和动脉血中氨和氨基酸浓度变化的动力学。通过向结肠腔内单次注入 1 至 5 克氨,记录到门静脉中氨浓度呈剂量相关性增加。除了最高测试剂量 5 克外,动脉血中的氨浓度保持不变,这显然超过了肝脏尿素生成能力。通过计算表观净氨吸收量,确定猪结肠上皮具有吸收 4 克氨的能力。氨通过结肠上皮的吸收伴随着门静脉中 L-谷氨酰胺和 L-精氨酸浓度的增加。这与分离的结肠上皮细胞中谷氨酸脱氢酶和谷氨酰胺合成酶的表达相一致。由于 L-谷氨酰胺和 L-精氨酸已知是肝脏尿素生成的激活剂,我们提出,在结肠腔中氨浓度增加后,门静脉中这些氨基酸浓度的增加代表了结肠黏膜和肝脏尿素合成之间的代谢联系。

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