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Diabetes and insulin-induced stimulation of L-arginine transport and nitric oxide synthesis in rabbit isolated gastric glands.

机译:糖尿病和胰岛素诱导的兔离体胃腺中L-精氨酸转运和一氧化氮合成的刺激。

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摘要

1. The properties of L-arginine transport have been characterized and correlated with cGMP production (index of nitric oxide (NO)) in whole gastric glands isolated from non-diabetic and alloxan-diabetic rabbits. 2. In non-diabetic and diabetic glands, transport of L-arginine was stereoselective, Na+ and pH independent and inhibited by other cationic amino acids. L-Arginine transport was slightly inhibited by L-leucine and L-phenylalanine, but unaffected by other neutral amino acids. 3. Diabetes enhanced the Vmax for saturable L-arginine transport from 10.7 +/- 1.0 to 17.7 +/- 0.5 pmol (mg protein)-1 s-1, with negligible changes in K(m). 4. Accumulation of the membrane potential-sensitive probe tetra[3H]phenylphosphonium (TPP+) was increased 2-fold in diabetic compared with non-diabetic gastric glands, suggesting a membrane hyperpolarization. 5. Basal intracellular cGMP levels were elevated 2-fold in diabetic gastric glands, and in non-diabetic glands histamine, vasoactive intestinal peptide, and bradykinin increased cGMP levels. The NO synthase inhibitor NG-nitro-L-arginine methyl ester (100 microM) abolished basal cGMP accumulation. 6. Addition of extracellular L-arginine induced a concentration-dependent increase in cGMP levels in gastric glands isolated from non-diabetic rabbits, but had no effect on elevated cGMP levels in diabetic glands. 7. Insulin induced a rapid (5 min) concentration-dependent increase in cGMP levels in non-diabetic gastric glands, but reduced elevated cGMP levels in diabetic gastric glands. 8. The present study has identified a specific transport system for L-arginine in gastric glands which resembles the classical system y+. Our findings also provide the first direct evidence that diabetes increases the basal activity of system y+ and NO synthase in gastric glands. The differential modulation of L-arginine transport by insulin and L-arginine identified in non-diabetic and diabetic glands, may be of importance in protecting the gastric mucosa from injuries associated with diabetes.
机译:1.从非糖尿病和四氧嘧啶糖尿病兔体内分离出的整个胃腺中,L-精氨酸的转运特性已被表征并与cGMP产生(一氧化氮(NO)指数)相关。 2.在非糖尿病和糖尿病腺体中,L-精氨酸的转运是立体选择性的,Na +和pH无关的,并受到其他阳离子氨基酸的抑制。 L-精氨酸的转运受到L-亮氨酸和L-苯丙氨酸的抑制,但不受其他中性氨基酸的影响。 3.糖尿病使可饱和L-精氨酸转运的Vmax从10.7 +/- 1.0增至17.7 +/- 0.5 pmol(毫克蛋白)-1 s-1,K(m)的变化可忽略不计。 4.与非糖尿病胃腺相比,糖尿病患者中膜电位敏感探针四[3H]苯基phosph(TPP +)的积累增加了2倍,提示膜超极化。 5.在糖尿病性胃腺中,基础细胞内cGMP水平升高了2倍,在非糖尿病性腺中,组胺,血管活性肠肽和缓激肽使cGMP水平升高。 NO合酶抑制剂NG-硝基-L-精氨酸甲酯(100 microM)消除了基础cGMP的积累。 6.细胞外L-精氨酸的添加引起非糖尿病兔胃腺中cGMP水平的浓度依赖性增加,但对糖尿病腺中cGMP水平升高没有影响。 7.胰岛素在非糖尿病胃腺中引起cGMP水平快速(5分钟)浓度依赖性升高,但在糖尿病胃腺中降低了cGMP水平升高。 8.本研究已确定了类似于传统系统y +的胃腺中L-精氨酸的特定转运系统。我们的发现还提供了第一个直接证据,表明糖尿病会增加胃腺中y +和NO合酶的基础活性。在非糖尿病和糖尿病腺体中,胰岛素和L-精氨酸对L-精氨酸转运的差异调节可能对保护胃粘膜免受糖尿病相关损伤很重要。

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