Literature DB >> 16488623

Tumor necrosis factor alpha down-regulates the Na+-K+ ATPase and the Na+-K+2Cl- cotransporter in the kidney cortex and medulla.

Sawsan Ibrahim Kreydiyyeh1, Sarine Markossian.   

Abstract

The effect of TNF-alpha on the renal Na+-K+ pump and the Na+-K+2Cl- cotransporter was investigated in the rat. Animals were injected with the cytokine, and 4h later, a homogenate from the cortical and medullary tissues was prepared and used to assay the activity of the Na+-K+ ATPase and the protein expression of the pump and symporter. TNF-alpha reduced the activity and expression of the pump in both cortex and medulla, and its effect disappeared when animals were pre-treated with indomethacin, suggesting that TNF-alpha acts via PGE2. Higher levels of PGE2 were detected by enzyme immunoassay, in kidney tissues isolated from rats treated with PGE2, thus confirming this hypothesis. The cytokine also down-regulated the Na+-K+2Cl- cotransporter but this effect was not abrogated by indomethacin. PGE2, injected into animals, exerted a dose-dependent effect. Low doses did not have any effect on the two transporters in the cortex while high doses inhibited and down-regulated the pump and up-regulated the cotransporter. In the medulla low doses increased the activity and expression of the pump but down-regulated the cotransporter while high doses exerted an exactly opposite effect on the two transporters. It was concluded that the effect of TNF-alpha on the pump is mediated via PGE2 which is released at relatively high doses. The effect of the cytokine on the cotransporter is, however, independent of PGE2.

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Year:  2006        PMID: 16488623     DOI: 10.1016/j.cyto.2005.12.007

Source DB:  PubMed          Journal:  Cytokine        ISSN: 1043-4666            Impact factor:   3.861


  9 in total

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2.  Renal-Specific Silencing of TNF (Tumor Necrosis Factor) Unmasks Salt-Dependent Increases in Blood Pressure via an NKCC2A (Na+-K+-2Cl- Cotransporter Isoform A)-Dependent Mechanism.

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Review 4.  Salt-Sensitive Hypertension: Perspectives on Intrarenal Mechanisms.

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5.  Tumor necrosis factor-α receptor type 1, not type 2, mediates its acute responses in the kidney.

Authors:  Alexander Castillo; M Toriqul Islam; Minolfa C Prieto; Dewan S A Majid
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6.  Involvement of tumor necrosis factor-alpha in natriuretic response to systemic infusion of nitric oxide synthase inhibitor in anesthetized mice.

Authors:  Mohd Shahid; Joseph Francis; Khalid Matrougui; Dewan S A Majid
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7.  Tumor necrosis factor-alpha induces renal vasoconstriction as well as natriuresis in mice.

Authors:  Mohd Shahid; Joseph Francis; Dewan S A Majid
Journal:  Am J Physiol Renal Physiol       Date:  2008-10-15

8.  Exacerbation of celecoxib-induced renal injury by concomitant administration of misoprostol in rats.

Authors:  Dustin L Cooper; Derek E Murrell; Christopher M Conder; Victoria E Palau; Grace E Campbell; Shaun P Lynch; James W Denham; Angela V Hanley; Kenny W Bullins; Peter C Panus; Krishna Singh; Sam Harirforoosh
Journal:  PLoS One       Date:  2014-02-21       Impact factor: 3.240

Review 9.  Proinflammatory Cytokines and Potassium Channels in the Kidney.

Authors:  Kazuyoshi Nakamura; Hikaru Hayashi; Manabu Kubokawa
Journal:  Mediators Inflamm       Date:  2015-10-05       Impact factor: 4.711

  9 in total

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