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C‐peptide inhibits leukocyte‐endothelium interaction in the microcirculation during acute endothelial dysfunction
Author(s) -
Scalia Rosario,
Coyle Kathleen M.,
Levine Brian J.,
Booth Gregory,
Lefer Allan M.
Publication year - 2000
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.00-0183com
Subject(s) - endothelium , enos , peptide , nitric oxide , nitric oxide synthase , endothelial stem cell , cell adhesion , intravital microscopy , cell adhesion molecule , chemistry , vasodilation , microbiology and biotechnology , biology , medicine , biochemistry , endocrinology , microcirculation , in vitro , cell
C‐peptide is a cleavage product that comes from processing proinsulin to insulin that induces nitric oxide (NO) ‐mediated vasodilation. NO modulates leukocyte‐endothelium interaction. We hypothesized that C‐peptide might inhibit leukocyte‐endothelium interaction via increased release of endothelial NO. Using intravital microscopy of the rat mesentery, we measured leukocyte‐ endothelium interactions after administration of C‐peptide to the rat. Superfusion of the rat mesentery with either thrombin or L‐NAME consistently and significantly increased the number of rolling, adhering, and transmigrated leukocytes. C‐peptide significantly attenuated either thrombin‐ or L‐NAME‐induced leukocyte‐endothelium interactions in rat mesenteric venules. A control scrambled sequence of C‐peptide characterized by the same amino acid composition in a randomized sequence failed to inhibit leukocyte‐endothelium interactions. These effects of C‐peptide were associated with decreased surface expression of the cell adhesion molecules P‐selectin and ICAM‐1 on the microvascular endothelium. Endothelial nitric oxide synthase (eNOS) mRNA levels were increased in rats injected with C‐peptide. This enhanced eNOS expression was associated with a marked increase in basal NO release from the aorta of C‐peptide‐treated rats. We conclude that C‐peptide is a potent inhibitor of leukocyte‐endothelium interaction and that this effect is specifically related to inhibition of endothelial cell adhesion molecules via maintenance of NO release from the vascular endothelium.—Scalia, R., Coyle, K. M., Levine, B. J., Booth, G., Lefer, A. M. C‐peptide inhibits leukocyte‐endothelium interaction in the microcirculation during acute endothelial dysfunction. FASEB J. 14, 2357‐2364 (2000)