Down regulation of kidney neutral endopeptidase mRNA, protein and activity during acute renal failure: Possible mechanism for ischemia-induced acute renal failure in rats?

Ponnal Nambi, Mark Pullen, Hsiao Ling Wu, Uma Prabhakar, Louis Hersh, Mikios Gellai

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Neutral endopeptidase (NEP, 24.11) is an ectoenzyme involved in the degradation of peptide hormones such as endothelin (ET), atrial natriuretic factor and enkephalins. The current study was designed to assess the involvement of NEP in ischemia-induced acute renal failure (ARF). In unilaterally nephrectomized Sprague-Dawley rats, the left renal artery was occluded for 30 min under pentobarbital anesthesia (40 mg/kg, i.p.) at 37°C. In addition to plasma creatinine levels, NEP activity was determined in renal cortical membranes at 0, 2, 5, and 24 h following reperfusion. Plasma creatinine levels significantly increased at 2, 5 and 24 h. There was a significant decrease in NEP activity as early as 2 h following reperfusion that was maintained up to 24 h (57.9 ± 4%) with a concomitant loss of enzyme protein shown by Western analysis. Northern analysis of kidney cortical RNA, probed with an NEP cDNA, showed a 45% decrease in NEP mRNA level by the end of the ischemic period and decreased further during reperfusion. Thus, decrease in NEP mRNA levels preceded the changes in protein level, enzyme activity and plasma creatinine levels. These data, along with the reported increase in the tissue level of ET in kidney cortex, and the beneficial effect of ET antibody as well as ET receptor antagonist in ARE suggest that down regulation of NEP, one of the mechanisms leading to increased tissue level of ET, may be a contributing factor to ARF.

Original languageEnglish
Pages (from-to)53-59
Number of pages7
JournalMolecular and Cellular Biochemistry
Volume197
Issue number1-2
DOIs
StatePublished - 1999

Bibliographical note

Funding Information:
We would like to thank Sue Tirri for her expert secretarial assistance. This work was supported in part by NIH DA 02243 to Louis B. Hersh.

Funding

We would like to thank Sue Tirri for her expert secretarial assistance. This work was supported in part by NIH DA 02243 to Louis B. Hersh.

FundersFunder number
National Institutes of Health (NIH)
National Institute on Drug AbuseR01DA002243

    Keywords

    • Acute renal failure
    • Endothelin
    • Neutral endopeptidase

    ASJC Scopus subject areas

    • Molecular Biology
    • Clinical Biochemistry
    • Cell Biology

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