Alleyne G A, Barnswell J, McFarlane-Anderson N, Alexander J E
Am J Physiol. 1981 Aug;241(2):F112-6. doi: 10.1152/ajprenal.1981.241.2.F112.
The acute metabolic responses to metabolic acidosis in the rat include an increase in ammoniagenesis and gluconeogenesis before enzyme adaptations have taken place. In the present studies rats were made acidotic with NH4Cl or HCl. Preincubation of renal cortical slices from normal rats in plasma from acidotic rats produced an increase in ammoniagenic capacity. However, when slices were incubated directly in diluted plasma from acidotic rats, there was also an increase in ammoniagenesis and gluconeogenesis from glutamine. The ammoniagenic factor was detectable within 0.5 h of induction of acidosis, was not detectable in chronic acidosis, was not of adrenal origin, was not a protein, was dialyzable, and acted by an alpha-adrenergic-like mechanism in that its action was blocked by phentolamine but not by propranolol. Phentolamine injected into rats depressed the ammoniagenic response to acidosis. The plasma factor did not show its ammoniagenic effect in a low-sodium buffer and there was no absolute requirement for calcium. The acute response to acidosis is thus mediated by a humoral substance with the above characteristics.
大鼠对代谢性酸中毒的急性代谢反应包括在酶适应性变化发生之前氨生成和糖异生增加。在本研究中,用氯化铵或盐酸使大鼠发生酸中毒。将正常大鼠的肾皮质切片在酸中毒大鼠的血浆中预孵育,会使氨生成能力增加。然而,当切片直接在酸中毒大鼠的稀释血浆中孵育时,谷氨酰胺的氨生成和糖异生也会增加。氨生成因子在酸中毒诱导后0.5小时内即可检测到,在慢性酸中毒中检测不到,不是肾上腺来源,不是蛋白质,可透析,并且通过类似α-肾上腺素能的机制起作用,因为其作用可被酚妥拉明阻断,但不能被普萘洛尔阻断。给大鼠注射酚妥拉明会抑制对酸中毒的氨生成反应。血浆因子在低钠缓冲液中未显示其氨生成作用,并且对钙没有绝对需求。因此,对酸中毒的急性反应是由具有上述特征的体液物质介导的。