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Characterization of aldose reductase from the thick ascending limb of Henle's loop of rabbit kidney.

机译:兔肾Henle环粗大上升肢中醛糖还原酶的特征。

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BACKGROUND: The organic osmolyte sorbitol plays an important role in the osmoregulation of immortalized epithelial cells of the thick ascending limb of Henle's loop (TALH) of rabbit. The intracellular sorbitol content seems to depend strongly on the extracellular osmolarity. To investigate the nature of the osmotic regulation we characterized the aldose reductase. METHODS: We determined aldose reductase activity enzymatically and the content of organic osmolytes by HPLC. RESULTS: The aldose reductase activity correlates with the extracellular tonicity. Elevating the osmolarity of the medium from 300 to 600 mosm/l by addition of NaCl or sucrose resulted in a significant increase of maximal velocity (V(max)) of the adapted cells from 8 +/- 1 micromol/g x min (300 mosm/l) to 322 +/- 28 micromol/g x min (600 mosm/l, NaCl) or 54 +/- 9 micromol/g x min (600 mosm/l, sucrose), respectively, while affinity (K(m)) remained unchanged. But we found no rise of aldose reductase activity when extracellular urea concentration was elevated. Similar alterations in V(max) were observed when the activity of the highly enriched enzyme was determined with glucose as substrate. Elevation of the extracellular osmolarity by NaCl and sucrose strongly induced the expression of aldose reductase protein with an apparent molecular weight of 39 kD. The affinity of glucose is characteristically low with a K(m) above 300 mmol/l. Aldose reductase utilizes both NADPH and with lower affinity NADH as coenzymes. In vitro sulfate ions (0.4 mol/l) results in a two-fold activation of the aldose reductase activity whereas sodium (200-400 mmol/l) decreased the activity significantly (22-33%). Potassium and chloride up to 400 mmol/l did not alter the aldose reductase activity in vitro. CONCLUSIONS: These results indicate that the aldose reductase of TALH cells of the outer medulla is osmotically regulated and has many similarities with aldose reductase in renal inner medulla. Therefore, intracellular sorbitol synthesis seems to be of similar importance in the osmoregulation of TALH cells as in the inner medulla.
机译:背景:有机渗透性山梨糖醇在兔Henle's Loop(TALH)厚上升肢的永生化上皮细胞的渗透调节中起着重要作用。细胞内山梨糖醇含量似乎强烈依赖于细胞外渗透压。为了研究渗透调节的性质,我们表征了醛糖还原酶。方法:我们通过酶法测定了醛糖还原酶的活性,并通过HPLC测定了有机渗透压的含量。结果:醛糖还原酶活性与细胞外张力有关。通过添加NaCl或蔗糖将介质的渗透压从300 mosm / l提高到300 mosm / l,导致适应细胞的最大速度(V(max))从8 +/- 1 micromol / gx min(300 mosm)显着增加/ l)至322 +/- 28 micromol / gx min(600 mosm / l,NaCl)或54 +/- 9 micromol / gx min(600 mosm / l,蔗糖),亲和力(K(m))保持不变。但是,当细胞外尿素浓度升高时,我们发现醛糖还原酶活性没有增加。当以葡萄糖为底物测定高度富集的酶的活性时,观察到V(max)的类似变化。 NaCl和蔗糖引起的细胞外渗透压升高,强烈诱导了表观分子量为39 kD的醛糖还原酶蛋白的表达。葡萄糖的亲和力通常较低,K(m)高于300 mmol / l。醛糖还原酶利用NADPH和较低亲和力的NADH作为辅酶。体外硫酸根离子(0.4 mol / l)导致醛糖还原酶活性的两倍活化,而钠(200-400 mmol / l)则显着降低活性(22-33%)。钾和氯化物高达400 mmol / l不会改变体外醛糖还原酶的活性。结论:这些结果表明外延髓的TALH细胞的醛糖还原酶是渗透调节的,并且与肾内延髓的醛糖还原酶有很多相似之处。因此,细胞内山梨糖醇的合成似乎在渗透性调节TALH细胞方面与在内部髓质中具有相似的重要性。

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