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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

L-Arginine Transport and Nitric Oxide Production in Kinin Receptor B-1(-/-) Endothelial Cells

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Author(s):
Tudela, Renato C. [1] ; Loiola, Rodrigo A. [1] ; Torres, Tathiany C. [1] ; Gil, Noemi L. [1] ; Assuncao, Nilson A. [1] ; de Noronha, Samuel M. R. [2] ; Correa-Noronha, Silvana A. [2] ; Landgraf, Richardt G. [1] ; Fernandes, Liliam [1]
Total Authors: 9
Affiliation:
[1] Univ Fed Sao Paulo, Inst Environm Chem & Pharmaceut Sci, Diadema, SP - Brazil
[2] Univ Fed Sao Paulo, Dept Surg, Escola Paulista Med, Sao Paulo, SP - Brazil
Total Affiliations: 2
Document type: Journal article
Source: PROTEIN AND PEPTIDE LETTERS; v. 22, n. 12, p. 1111-1116, 2015.
Web of Science Citations: 0
Abstract

Kinins are important vasoactive peptides, but the role of the B-1 receptor subtype in the vascular control is poorly understood. This study analyzed the nitric oxide (NO) release, L-arginine (L-Arg) uptake and the expression of the cationic amino acid transporter (CAT) -1 in endothelial cells obtained from B-1 receptor knockout (B-1(-/-)) and wild type (WT) mice. NO production was assessed through a fluorescent dye in living cells stimulated with acetylcholine. L-Arg uptake was determined indirectly in the culture medium by HPLC, in the presence or absence of the CAT-1 blocker N-ethylmaleimide (NEM). CAT-1 mRNA levels and protein expression were determined by qPCR and western blot, respectively. NO release was significantly reduced in B-1(-/-) when compared to WT cells. This result was accompanied by a decreased rate in the L-Arg uptake by B-1(-/-) cells. Incubation with NEM impaired the L-Arg uptake in WT, but had no effect in B-1(-/-) cells. Protein expression and mRNA levels for CAT-1 were reduced in B-1(-/-) in comparison to WT cells. These findings suggest an important role of the endothelial B-1 receptor in the vascular control by interfering with CAT-1 expression, L-Arg uptake and NO release. (AU)

FAPESP's process: 10/01404-0 - In vivo and in vitro studies of the leptin role in different models of lung inflammation: inflammatory mediators and signaling airways participation
Grantee:Richardt Gama Landgraf
Support Opportunities: Research Grants - Young Investigators Grants
FAPESP's process: 14/18760-4 - Venous endothelial factors: influence of angiotensin II and endothelin-1
Grantee:Liliam Fernandes
Support Opportunities: Regular Research Grants