Murray Margaret, Barlow Christopher K, Blundell Scott, Buecking Mark, Gibbon Anne, Goeckener Bernd, Kaminskas Lisa M, Leitner Patricia, Selby-Pham Sophie, Sinclair Andrew, Waktola Habtewold D, Williamson Gary, Bennett Louise E
School of Chemistry, Monash University, Clayton, VIC, Australia.
Department of Nutrition, Dietetics and Food, Monash University, Notting Hill, VIC, Australia.
Front Nutr. 2023 Mar 9;10:1127729. doi: 10.3389/fnut.2023.1127729. eCollection 2023.
There is a need to better understand the relationship between the diet, the gut microbiota and mental health. Metabolites produced when the human gut microbiota metabolize amino acids may enter the bloodstream and have systemic effects. We hypothesize that fermentation of amino acids by a resistant protein-primed gut microbiota could yield potentially toxic metabolites and disturb the availability of neurotransmitter precursors to the brain. However, these mechanisms are challenging to investigate typical and clinical methods.
We developed a novel workflow using C radiolabeling to investigate complex nutrient-disease relationships. The first three steps of the workflow are reported here. α-Linolenic acid (ALA) was used as a model nutrient to confirm the efficacy of the workflow, and tyrosine (Tyr) was the test nutrient. C-Tyr was administered to male weanling pigs fed a high resistant protein diet, which primed the gut microbiota for fermenting protein. The hypotheses were; (1) that expected biodistribution of C-ALA would be observed, and (2) that radioactivity from C-Tyr, representing Tyr and other amino acids released from resistant protein following gut microbial fermentation, would be bioavailable to the brain.
Radioactivity from the C-ALA was detected in tissues reflecting normal utilization of this essential fatty acid. Radioactivity from the C-Tyr was detected in the brain (0.15% of original dose).
Metabolites of gut-fermented protein and specifically amino acid precursors to neurotransmitters such as tyrosine, are potentially able to affect brain function. By extension, resistant proteins in the diet reaching the gut microbiota, also have potential to release metabolites that can potentially affect brain function. The high specificity of detection of C radioactivity demonstrates that the proposed workflow can similarly be applied to understand other key diet and health paradigms.
有必要更好地理解饮食、肠道微生物群与心理健康之间的关系。人类肠道微生物群代谢氨基酸时产生的代谢产物可能进入血液并产生全身效应。我们假设,由抗性蛋白引发的肠道微生物群对氨基酸的发酵可能产生潜在有毒的代谢产物,并干扰大脑中神经递质前体的供应。然而,用典型和临床方法研究这些机制具有挑战性。
我们开发了一种使用碳放射性标记来研究复杂营养-疾病关系的新流程。本文报告了该流程的前三个步骤。α-亚麻酸(ALA)用作模型营养素以确认该流程的有效性,酪氨酸(Tyr)为测试营养素。将碳-酪氨酸给予喂食高抗性蛋白饮食的雄性断奶仔猪,这种饮食会引发肠道微生物群对蛋白质的发酵。假设为:(1)将观察到碳-ALA的预期生物分布,以及((2)代表肠道微生物发酵后从抗性蛋白释放的酪氨酸和其他氨基酸的碳-酪氨酸的放射性将可被大脑利用。
在反映这种必需脂肪酸正常利用的组织中检测到了碳-ALA的放射性。在大脑中检测到了碳-酪氨酸的放射性(占原始剂量的0.15%)。
肠道发酵蛋白的代谢产物,特别是神经递质的氨基酸前体,如酪氨酸,有可能影响脑功能。由此推断,到达肠道微生物群的饮食中的抗性蛋白也有可能释放出可能影响脑功能的代谢产物。碳放射性检测的高特异性表明,所提出的流程同样可用于理解其他关键的饮食与健康模式。