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细胞外因子对大鼠肾氨生成的调节。I. 酸中毒与生理燃料的联合作用。

The regulations of renal ammoniagenesis in the rat by extracellular factors. I. The combined effects of acidosis and physiologic fuels.

作者信息

Preuss H G, Eastman S T, Vavatsi-Manos O, Baird K, Roxe D M

出版信息

Metabolism. 1978 Nov;27(11):1626-38. doi: 10.1016/0026-0495(78)90285-8.

Abstract

Substrate oxidation by rat kidney slices regulates renal ammoniagenesis from glutamine. At concentrations close to those expected in plasma, lactate alone, or combined with other renal fuels, inhibits ammoniagenesis markedly; glucose and citrate decrease ammoniagenesis slightly. However, lactate, citrate, and glucose inhibit ammoniagenesis of kidney slices from acidotic rats less than ammoniagenesis of kidney slices from control rats. Lesser inhibition of ammoniagenesis is seen also when acidotic slices rather than control slices are incubated in the presence of all the tested substrates combined in the same medium. In addition to decreasing the ammoniagenesis of renal slices from control rats, the presence of lactate causes an augmented accumulation of glutamate. In contrast, adding lactate to acidotic slices does not increase glutamate accumulation nearly as much. When glutamate is substituted for glutamine in the medium, lactate still decreases ammonia production, but to a lesser extent with acidotic slices. Changes in medium pH from 7.0 to 7.8 have no, or only small, overall effects on net renal slice ammonia production from glutamine under any of the circumstances tested. We conclude that lactate alone and combined with other substrates decreases ammoniagenesis primarily at the glutamate dehydrogenase step and that slices from acidotic rats are relatively resistant to substrate mediated inhibition.

摘要

大鼠肾切片的底物氧化调节谷氨酰胺的肾氨生成。在接近血浆预期浓度时,单独的乳酸盐或与其他肾内燃料联合使用时,会显著抑制氨生成;葡萄糖和柠檬酸盐会轻微降低氨生成。然而,乳酸盐、柠檬酸盐和葡萄糖对酸中毒大鼠肾切片氨生成的抑制作用比对对照大鼠肾切片氨生成的抑制作用小。当在相同培养基中联合存在所有测试底物的情况下孵育酸中毒切片而非对照切片时,也可见到对氨生成的抑制作用较小。除了降低对照大鼠肾切片的氨生成外,乳酸盐的存在还会导致谷氨酸积累增加。相比之下,向酸中毒切片中添加乳酸盐几乎不会增加谷氨酸积累。当培养基中的谷氨酰胺被谷氨酸替代时,乳酸盐仍会降低氨的产生,但对酸中毒切片的影响程度较小。在任何测试情况下,将培养基pH从7.0变为7.8对谷氨酰胺净肾切片氨生成没有或只有很小的总体影响。我们得出结论,单独的乳酸盐以及与其他底物联合使用时,主要在谷氨酸脱氢酶步骤降低氨生成,并且酸中毒大鼠的切片对底物介导的抑制相对具有抗性。

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