Immunoreactive endothelin in the human kidney: Comparison with natriuretic peptides

Kazuhiro Takahashi, Masahiko Sone, Kazuhito Totsune, Fumitoshi Satoh, Osamu Murakami, Makoto Ohneda, Toraichi Mouri

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6 Citations (Scopus)

Abstract

The presence of immunoreactive endothelin (IR-ET) was studied by radioimmunoassay in human kidney with and without clinical renal failure, and the levels were compared with those of three natriuretic peptides: Atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), and C-type natriuretic peptide (CNP). Kidney tissues were obtained at autopsy from three subjects with renal disorders (diabetic nephropathy, renal tubular necrosis, and end-stage kidney disease). Normal renal tissue was obtained at surgery from two patients with renal cell carcinoma. IR-ET was detected in three diseased kidneys obtained at autopsy (0.101 ± 0.043 pmol/g wet weight, mean ± SD) but not in tissues of two normal kidneys obtained at surgery (<0.015 pmol/g wet weight). Reverse-phase HPLC showed that most of the IR-ET in the kidney (>90%) was eluted in the position of ET-1. IR-ANP(0.23 ± 0.06 pmol/g wet weight), IR-BNP (1.15 ± 0.94 pmol/g wet weight), and IR-CNP (0.44 ± 0.16 pmol/g wet weight) were detected in all samples examined. Higher concentrations of IR-BNP were found in three diseased kidneys obtained at autopsy (1.70 ± 0.83 pmol/g wet weight vs. mean in two normal kidney tissues, 0.32 pmol/g wet weight). Such increases were not observed in IR-ANP or IR-CNP. These findings indicate that IR-ET is present in the human diseased kidney even in end-stage disease, with high concentrations comparable to those ol natriuretic peptides. This raises the possibility that the production of ET-1 and BNP is increased in kidneys of patients with renal disorders.

Original languageEnglish
Pages (from-to)S510-S512
JournalJournal of Cardiovascular Pharmacology
Volume26
Publication statusPublished - 1995 Jan 1

Keywords

  • Endothelin
  • Kidney-Renal failure
  • Natriuretic peptide
  • Radioimmunoassay

ASJC Scopus subject areas

  • Pharmacology
  • Cardiology and Cardiovascular Medicine

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