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Increased Urinary Excretion of Pyridinium Crosslinks in Streptozotocin-induced Diabetic Rats

机译:链脲佐菌素诱导的糖尿病大鼠中吡啶鎓交联的尿排泄增加

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摘要

We assessed the changes in the urinary excretions of bone breakdown markers, i.e. two pyridinium crosslinks, pyridinoline (Pyr) and deoxyphridinoline (D-Pyr), and two hydroxylysine glycosides, glucosylgalactosylhydroxylysine (GGH) and galactosylhydroxylysine (GH), in streptozotocin (STZ)-induced diabetic rats. The 24-h urinary excretions of the crosslinks in diabetic rats increased in a biphasic manner after STZ-injecion. The first peak appeared during the day after the STZ-injection, i.e., 53% higher that control for Pyr and 62% higher for D-Pyr and the second peak appeared during the second week after the STZ-injection, being 56% higher for Pyr and 81% for D-Pyr. The urinary excretions of glycosides, however, were almost the same level as those of the control throughout the experimental period (6 weeks). In normal rats, the ratio of the crosslinks to the glycosides in urine was found to be lower than that in serum. This suggests that the selective reabsorption of the closslinks occurs in the rat kidney. The apparent increased urinary excretion of pyridinolines in diabetic rats might be ascribed to the disorder of the renal reabsorption.
机译:我们在链脲佐菌素(ST)中评估了骨分解标志物,即两个吡啶鎓交联吡啶和(Pyr)吡啶和脱氧肾上腺素(D-Pyr)以及两个羟基赖氨酸糖苷,葡萄糖基半乳糖基羟基赖氨酸(GGH)和半乳糖基羟基赖氨酸(GH)的尿排泄变化。诱导的糖尿病大鼠。 STZ注射后,糖尿病大鼠交联的24小时尿排泄呈双相增加。第一个高峰出现在注射STZ后的第二天,即比对照高53%,D-Pyr高出62%,第二个高峰出现在STZ注射后的第二周,高出56%。 Pyr,D-Pyr为81%。然而,在整个实验期间(6周),糖苷的尿排泄量几乎与对照组的排泄量相同。在正常大鼠中,发现尿液中交联与糖苷的比率低于血清中的比率。这表明在大鼠肾脏中发生了Closslinks的选择性重吸收。吡啶类吡啶类药物尿排泄明显增加可能归因于肾脏重吸收异常。

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