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Human parathyroid hormone (1-34) increases urinary excretion of lysosomal enzymes in rats

机译:人甲状旁腺激素(1-34)增加大鼠溶酶体酶的尿排泄

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The kidney is the major target of parathyroid hormone (PTH), and PTH influences the urinary excretion of calcium, phosphate and hydrogen ions. It was previously reported that the urinary excretion of N-acetyl-#beta#-D-glucosaminidase (NAG), a lysosomal enzyme, transiently increases after human PTH (hPTH) (1-34) infusion in normal subjects and idiopathic hypoparathyroidism patients, but not in pseudohypoparathyroidism type I patients. Here we report that intravenous infusion of hPTH(1-34) to rats transiently increased the urinary excretion of various lysosomal enzymes, such as #beta#-glucuronidase and acid phosphatase as well as NAG. However, it did not affect the urinary excretion of tubular brush border membrane enzymes, i. e. alkaline phosphatase, leucine aminopeptidase and #gamma#-glutamyl transpeptidase. Human PTH(1-34) dose-dependently increased the urinary excretion of NAG in rats with a peak at 30 min, which returned to a baseline within 60 min. The increase in the urinary NAG excretion caused by hPTH(1-34) positively correlated with the increase in the urinary cAMP excretion (r = 0.844, p < 0.01), and infusion of dibutyryl cAMP at a dose of 20 mg/kg similarly increased the urinary excretion of NAG. These results suggested that the increase in the urinary excretion of lysosomal enzymes caused by hPTH(1-34) may be a functional response to hPTH(1-34) occurring in the renal tubules via PTH signaling pathway.
机译:肾脏是甲状旁腺激素(PTH)的主要靶标,PTH影响尿液中钙,磷酸根和氢离子的排泄。先前有报道称,正常人和特发性甲状旁腺功能低下患者输注人PTH(hPTH)(1-34)后,溶酶体酶N-乙酰基-#β#-D-氨基葡萄糖苷酶(NAG)的尿排泄瞬时增加,但不适用于I型假性甲状旁腺功能减退症患者。在这里我们报告静脉注射hPTH(1-34)给大鼠瞬时增加了各种溶酶体酶,如#beta#-葡萄糖醛酸苷酶和酸性磷酸酶以及NAG的尿排泄。然而,它不影响管状刷状缘膜酶的尿排泄,即。 e。碱性磷酸酶,亮氨酸氨肽酶和#γ#-谷氨酰转肽酶。人PTH(1-34)剂量依赖性地增加了大鼠NAG的尿排泄量,该排泄在30分钟达到峰值,并在60分钟内恢复到基线。 hPTH(1-34)引起的尿中NAG排泄的增加与尿中cAMP排泄的增加呈正相关(r = 0.844,p <0.01),并且以20 mg / kg的剂量输注二丁酰cAMP同样增加NAG的尿排泄。这些结果表明,由hPTH(1-34)引起的溶酶体酶尿排泄的增加可能是对通过PTH信号通路在肾小管中发生的hPTH(1-34)的功能性反应。

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