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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Effects of volume depletion and NaHCO3 loading on the expression of Na+/H+ exchanger isoform 3, Na+: HCO3- cotransporter type 1 and nitric oxide synthase in rat kidney.
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Effects of volume depletion and NaHCO3 loading on the expression of Na+/H+ exchanger isoform 3, Na+: HCO3- cotransporter type 1 and nitric oxide synthase in rat kidney.

机译:体积耗尽和NaHCO3加载对大鼠肾脏Na + / H +交换剂同种型3,Na +:HCO3- COTORANSPORTER型1和一氧化氮合成酶表达的影响。

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1. The effects of volume depletion and NaHCO(3) loading on the expression of Na(+)/H(+) exchanger isoform 3 (NHE3), Na(+) : HCO(3)(-) cotransporter type 1 (NBC1) and neuronal (n) and inducible (i) isoforms of nitric oxide synthase (NOS) were determined in rat kidney. 2. Adult male Sprague-Dawley rats were used. Rats were divided into four groups: (i) euvolaemic (EC); (ii) hypovolaemic (HC); (iii) euvolaemia with NaHCO(3) loading (EB); and (iv) hypovolaemia with NaHCO(3) loading (HB). The expression of NHE3, NBC1, nNOS and iNOS proteins was determined in the cortex of the kidney by immunoblotting and immunohistochemistry. Tissue content of nitric oxide (NO) metabolites (NO(x)) were also determined in the cortex using a colourimetric assay. 3. Compared with the EC group, the expression of NHE3 and NBC1 was increased in the HC group and decreased in the EB group. Comparing the EB and HB groups, the expression of NHE3 and NBC1 was higher in the latter group. The expression of NHE3 was decreased and that ofNBC1 was increased in the HB group compared with the HC group. The NO(x) content and nNOS expression were decreased in the hypovolaemic (HC) and NaHCO(3)-loaded (EB and HB) rats. Moreover, the expression of iNOS was decreased in the HB group compared with the other groups. 4. An altered volume status and NaHCO(3) loading may affect the regulation of NHE3 and NBC1 in the kidney and the endogenous NO system may play a role in the observed effects.
机译:1.体积耗尽和NaHCO(3)加载对Na(+)/ h(+)交换剂同种型3(NHE3),Na(+):HCO(3)( - )Cotroangerporter 1型(NBC1)表达的影响(NBC1 )在大鼠肾脏中测定一氧化氮合酶(NOS)的神经元(n)和诱导型(I)同种型。 2.使用成人雄性Sprague-Dawley大鼠。大鼠分为四组:(i)Euvolaem(EC); (ii)缓解(HC); (iii)与Nahco(3)装载(EB)的Euvolaemia; (IV)具有NaHCO(3)载荷(HB)的低血症。通过免疫印迹和免疫组织化学在肾的皮质中测定NHE3,NBC1,NNOS和InOS蛋白的表达。使用Colourecetric测定,在皮质中也测定一氧化氮(NO)代谢物(NO(x))的组织含量。 3.与EC组相比,HC组中NHE3和NBC1的表达增加,EB组在eB组下降。比较EB和HB组,后一组NHE3和NBC1的表达较高。降低NHE3的表达,与HB组与HC组相比,在HB组中增加了NBC1。在低温(HC)和NaHCO(3) - 加载(EB和HB)大鼠中,NO(X)含量和NNO表达减少。此外,与其他基团相比,Hb组中InOS的表达减少。 4.体积状态和NaHCO(3)加载可能影响肾脏中NHE3和NBC1的调节,内源性没有系统可能在观察到的效果中发挥作用。

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