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糖尿病与胰岛素对兔离体胃腺中L-精氨酸转运及一氧化氮合成的刺激作用。

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

作者信息

Contreras R, Fuentes O, Mann G E, Sobrevia L

机构信息

Department of Physiology, Faculty of Biological Sciences, University of Concepción, Chile.

出版信息

J Physiol. 1997 Feb 1;498 ( Pt 3)(Pt 3):787-96. doi: 10.1113/jphysiol.1997.sp021902.

Abstract
  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.
摘要
  1. 已对从非糖尿病和四氧嘧啶糖尿病兔分离出的全胃腺中L-精氨酸转运的特性进行了表征,并将其与环鸟苷酸(一氧化氮(NO)的指标)的产生相关联。2. 在非糖尿病和糖尿病胃腺中,L-精氨酸的转运具有立体选择性,不依赖于Na⁺和pH,并受到其他阳离子氨基酸的抑制。L-精氨酸转运受到L-亮氨酸和L-苯丙氨酸的轻微抑制,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增加到17.7±0.5 pmol(mg蛋白)⁻¹ s⁻¹,而K(m)的变化可忽略不计。4. 与非糖尿病胃腺相比,糖尿病胃腺中膜电位敏感探针四[³H]苯基鏻(TPP⁺)的积累增加了2倍,表明膜超极化。5. 糖尿病胃腺中的基础细胞内环鸟苷酸水平升高了2倍,在非糖尿病胃腺中,组胺、血管活性肠肽和缓激肽可增加环鸟苷酸水平。一氧化氮合酶抑制剂NG-硝基-L-精氨酸甲酯(100 microM)消除了基础环鸟苷酸的积累。6. 添加细胞外L-精氨酸可使从非糖尿病兔分离出的胃腺中环鸟苷酸水平呈浓度依赖性增加,但对糖尿病胃腺中升高的环鸟苷酸水平无影响。7. 胰岛素可使非糖尿病胃腺中环鸟苷酸水平迅速(5分钟)呈浓度依赖性增加,但可降低糖尿病胃腺中升高的环鸟苷酸水平。8. 本研究确定了胃腺中L-精氨酸的一种特定转运系统,其类似于经典的系统y⁺。我们的研究结果还提供了首个直接证据,即糖尿病会增加胃腺中系统y⁺和一氧化氮合酶的基础活性。在非糖尿病和糖尿病胃腺中发现的胰岛素和L-精氨酸对L-精氨酸转运的差异调节,可能对保护胃黏膜免受与糖尿病相关的损伤具有重要意义。

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