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胰岛素对肝脏蛋白水解的抑制作用。激素诱导的细胞钾离子平衡改变的作用。

Inhibition of hepatic proteolysis by insulin. Role of hormone-induced alterations of the cellular K+ balance.

作者信息

Hallbrucker C, vom Dahl S, Lang F, Gerok W, Häussinger D

机构信息

Medizinische Universitätsklinik, Freiburg, Federal Republic of Germany.

出版信息

Eur J Biochem. 1991 Jul 15;199(2):467-74. doi: 10.1111/j.1432-1033.1991.tb16145.x.

Abstract
  1. Proteolysis was measured as [3H]leucine release from isolated perfused livers from rats, which had been labeled in vivo by an intraperitoneal injection of [3H]leucine about 16 h prior to the perfusion experiment. In livers from fed rats, insulin (35 nM) inhibited [3H]leucine release by 24.5 +/- 1.3% (n = 15) and led to an amiloride-sensitive, bumetanide-sensitive and furosemide-sensitive net K+ uptake of 5.53 +/- 0.31 mumol.g-1 (n = 15). Both the insulin effects on net K+ uptake and on [3H]leucine release were diminished by about 65% or 55% in presence of furosemide (0.1 mM) or bumetanide (5 microM), respectively. The insulin-induced net K+ uptake was virtually abolished in the presence of amiloride (1 mM) plus furosemide (0.1 mM). 2. In perfused livers from 24-h-starved rats, both the insulin-stimulated net K+ uptake and the insulin-induced inhibition of [3H]leucine release were about 80% lower than observed in experiments with livers from fed rats. The insulin effects on K+ balance and [3H]leucine release were not significantly influenced in the presence of glycine (2 mM), although glycine itself inhibited [3H]leucine release by 30.3 +/- 0.3% (n = 4) and 13.8 +/- 1.2% (n = 5) in livers from starved and fed rats, respectively. When livers from fed rats were preswollen by hypoosmotic perfusion (225 mOsmol.l-1), both the insulin-induced net K+ uptake and the inhibition of [3H]leucine release were diminished by 50-60%. 3. During inhibition of [3H]leucine release by insulin, further addition of glucagon (100 nM) led to a marked net K+ release from the liver (3.82 +/- 0.24 mumol.g-1), which was accompanied by stimulation of [3H]leucine release by 16.4 +/- 4.6% (n = 4). 4. Ba2+ (1 mM) infusion led to a net K+ uptake by the liver of 3.2 +/- 0.2 mumol.g-1 (n = 4) and simultaneously inhibited [3H]leucine release by 12.4 +/- 1.7% (n = 4). 5. There was a close relationship between the Ba2+ or insulin-induced net K+ uptake and the degree of inhibition of [3H]leucine release, even when the K+ response to insulin was modulated by bumetanide, furosemide, glucagon, hypotonic or glycine-induced cell swelling or the nutritional state. 6. The data suggest that the insulin-induced net K+ uptake involves activation of both NaCl/KCl cotransport and Na+/H+ exchange.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 蛋白水解作用通过测量大鼠离体灌注肝脏中[³H]亮氨酸的释放来测定,这些大鼠在灌注实验前约16小时通过腹腔注射[³H]亮氨酸在体内进行了标记。在喂食大鼠的肝脏中,胰岛素(35 nM)抑制[³H]亮氨酸释放24.5±1.3%(n = 15),并导致氨氯地平敏感、布美他尼敏感和呋塞米敏感的净钾摄取量为5.53±0.31 μmol·g⁻¹(n = 15)。在存在呋塞米(0.1 mM)或布美他尼(5 μM)的情况下,胰岛素对净钾摄取和[³H]亮氨酸释放的作用分别降低约65%或55%。在存在氨氯地平(1 mM)加呋塞米(0.1 mM)的情况下,胰岛素诱导的净钾摄取几乎完全被消除。2. 在24小时饥饿大鼠的灌注肝脏中,胰岛素刺激的净钾摄取和胰岛素诱导的[³H]亮氨酸释放抑制均比喂食大鼠肝脏实验中观察到的低约80%。在存在甘氨酸(2 mM)的情况下,胰岛素对钾平衡和[³H]亮氨酸释放的作用没有显著影响,尽管甘氨酸本身在饥饿和喂食大鼠的肝脏中分别抑制[³H]亮氨酸释放30.3±0.3%(n = 4)和13.8±1.2%(n = 5)。当喂食大鼠的肝脏通过低渗灌注(225 mOsmol·L⁻¹)预先肿胀时,胰岛素诱导的净钾摄取和[³H]亮氨酸释放抑制均降低5 ⁃ 60%。3. 在胰岛素抑制[³H]亮氨酸释放期间,进一步添加胰高血糖素(100 nM)导致肝脏显著净钾释放(3.82±0.24 μmol·g⁻¹),同时[³H]亮氨酸释放增加16.4±4.6%(n = 4)。4. 注入Ba²⁺(1 mM)导致肝脏净钾摄取量为3.2±0.2 μmol·g⁻¹(n = 4),同时抑制[³H]亮氨酸释放12.4±1.7%(n = 4)。5. 即使钾对胰岛素的反应受到布美他尼、呋塞米、胰高血糖素、低渗或甘氨酸诱导的细胞肿胀或营养状态的调节,Ba²⁺或胰岛素诱导的净钾摄取与[³H]亮氨酸释放的抑制程度之间仍存在密切关系。6. 数据表明,胰岛素诱导的净钾摄取涉及NaCl/KCl共转运和Na⁺/H⁺交换的激活。(摘要截短至400字)

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