Institute of Veterinary Physiology, Freie Universität Berlin, Königsweg 56, 14163 Berlin, Germany.
American Institute for Goat Research, Langston University, Langston, OK 73050, USA.
Nutrients. 2024 Oct 9;16(19):3418. doi: 10.3390/nu16193418.
Methionine (Met) is a popular nutritional supplement in humans and animals. It is routinely supplemented to pigs as L-Met, DL-Met, or DL-2-hydroxy-4-(methylthio) butanoic acid (DL-HMTBA). We investigated the effect of these Met supplements on jejunal amino acid (AA) transport in male castrated Piétrain × Danbred pigs, also including a non-supplemented group. The mucosal-to-serosal flux of ten [C]-labeled AAs (L-glutamine, glycine, L-leucine, L-lysine, L-Met, L-serine, L-threonine, L-tryptophan, L-tyrosine and L-valine) was investigated at two concentrations (50 µM and 5 mM). Inhibition of apical uptake by mucosal L-Met was also measured for these AAs. The intestinal expression of apical AA transporters, angiotensin-converting enzyme II and inflammation-related genes were compared with those of a previous study. Except for tryptophan and lysine at 5 mM, all AA fluxes were Na-dependent ( ≤ 0.05), and the uptake of most AAs, except glycine and lysine, was inhibited by L-Met ( < 0.001). A correlation network existed between Na-dependent fluxes of most AAs (except tryptophan and partly glycine). We observed the upregulation of BAT1 () ( < 0.001), the downregulation of ATB () ( < 0.001) and a lower expression of , , , and in the present vs. the previous study ( < 0.001). The correlating AAs likely share the same Na-dependent transporter(s). A varying effect of the Met supplement type on AA transport in the two studies might be related to a different level of supplementation or a different inflammatory status of the small intestine.
蛋氨酸(Met)是人类和动物常用的营养补充剂。它通常以 L-Met、DL-Met 或 DL-2-羟基-4-(甲硫基)丁酸(DL-HMTBA)的形式补充给猪。我们研究了这些 Met 补充剂对去势皮特兰×丹布罗猪空肠氨基酸(AA)转运的影响,也包括未补充组。在两种浓度(50 μM 和 5 mM)下,研究了十个 [C]标记 AA(L-谷氨酰胺、甘氨酸、L-亮氨酸、L-赖氨酸、L-Met、L-丝氨酸、L-苏氨酸、L-色氨酸、L-酪氨酸和 L-缬氨酸)的黏膜到浆膜通量。还测量了这些 AA 对黏膜 L-Met 摄取的抑制作用。与之前的研究相比,比较了肠腔 AA 转运体、血管紧张素转换酶 II 和炎症相关基因的表达。除了 5 mM 时的色氨酸和赖氨酸外,所有 AA 通量均依赖 Na(≤0.05),并且大多数 AA 的摄取(除甘氨酸和赖氨酸外)被 L-Met 抑制(<0.001)。大多数 AA(除色氨酸和部分甘氨酸外)的 Na 依赖性通量之间存在关联网络。我们观察到 BAT1()的上调(<0.001),ATB()的下调(<0.001),以及在本研究中与之前研究相比 、 、 、 和 的表达降低(<0.001)。相关的 AA 可能共享相同的 Na 依赖性转运体。两种研究中 Met 补充类型对 AA 转运的不同影响可能与补充水平不同或小肠炎症状态不同有关。