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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1997-11-13
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pubmed:abstractText |
A 20-amino acid peptide, KYEIKEGDCPVQSGKTWQDC (PU-D1), released by pepsin hydrolysis of LMW kininogen domain 1 was tested for its ability to antagonize the diuretic and natriuretic effect of ANP(103-125) in anesthetized rats. A single dose of 10.8 or 21.6 pmol (25 or 50 ng) PU-D1 given intravenously or into the duodenal lumen suppressed the diuresis-natriuresis induced by 209 pmol (500 ng) ANP by 43% to 59% and 69% to 96%, respectively. None of the doses tested (2.16 to 432 pmol, 5 ng to 1 microg) modified systemic blood pressure. Strikingly, a single IV dose of 10.8 pmol PU-D1 blocked the action of ANP for more than 3 hours. ANP blockade by PU-D1 was annulled completely by the bradykinin (BK) B2 receptor inhibitor Hoe 140. On a molar basis, PU-D1 is more effective than BK and kinins of 15, 16, and 18 amino acids for blocking the ANP-mediated diuresis-natriuresis. As with BK and other kinins, the inhibitory effect of Pu-D1 on ANP is obtained only within a small range of picomol doses. A single dose of 2.16 or 4.32 pmol PU-D1 or 47 pmol (50 ng) BK is ineffective against ANP if injected alone. However, when both substances are administered concomitantly at these subthreshold doses, they totally suppress ANP-induced diuresis-natriuresis. These results raise the question of whether PU-D1, released from kininogen domain 1, either alone or associated with BK, may interact with ANP in the regulation of urinary water and electrolyte excretion in physiological and pathological conditions.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Atrial Natriuretic Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Bradykinin,
http://linkedlifedata.com/resource/pubmed/chemical/Kininogens,
http://linkedlifedata.com/resource/pubmed/chemical/Pepsin A,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/icatibant
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0194-911X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
897-904
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9336390-Amino Acid Sequence,
pubmed-meshheading:9336390-Animals,
pubmed-meshheading:9336390-Atrial Natriuretic Factor,
pubmed-meshheading:9336390-Bradykinin,
pubmed-meshheading:9336390-Diuresis,
pubmed-meshheading:9336390-Dose-Response Relationship, Drug,
pubmed-meshheading:9336390-Duodenum,
pubmed-meshheading:9336390-Female,
pubmed-meshheading:9336390-Injections,
pubmed-meshheading:9336390-Injections, Intravenous,
pubmed-meshheading:9336390-Kidney,
pubmed-meshheading:9336390-Kininogens,
pubmed-meshheading:9336390-Molecular Sequence Data,
pubmed-meshheading:9336390-Natriuresis,
pubmed-meshheading:9336390-Pepsin A,
pubmed-meshheading:9336390-Peptide Fragments,
pubmed-meshheading:9336390-Rats
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pubmed:year |
1997
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pubmed:articleTitle |
A peptide released by pepsin from kininogen domain 1 is a potent blocker of ANP-mediated diuresis-natriuresis in the rat.
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pubmed:affiliation |
Departamento de Ciencias Fisiológicas, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago. mboric@genes.bio.puc.cl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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