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Vascular endothelial growth factor and nitric oxide in rat liver regeneration

Authors
Journal
Life Sciences
0024-3205
Publisher
Elsevier
Publication Date
Volume
81
Issue
9
Identifiers
DOI: 10.1016/j.lfs.2007.07.009
Keywords
  • Liver Regeneration
  • Nitric Oxide
  • Vascular Endothelial Growth Factor
  • Partial Hepatectomy
Disciplines
  • Biology
  • Medicine

Abstract

Abstract In this work we investigated the role of nitric oxide (NO) in the angiogenesis mediated by vascular endothelial growth factor (VEGF) during rat liver regeneration after two-thirds partial hepatectomy. Sham operated (Sh) and partially hepatectomized (PH) male Wistar rats were randomized in three experimental groups: control (treated with vehicle); pre-treated with sodium nitroprusside (SNP: 0.25 mg/kg body weight, i.v. at a rate of 1 ml/h) and pre-treated with the preferential iNOS inhibitor, aminoguanidine (AG, 100 mg/kg body weight, i.p.). Animals were killed at 5, 24 and 72 h after surgery. At 5 h post-surgery, NO production was estimated by EPR (Sh-Control: 37.65 ± 10.70; PH-Control: 88.13 ± 1.60 ⁎; Sh-SNP: 90.35 ± 3.11 ⁎; PH-SNP: 119.5 ± 12.10 ⁎ #; Sh-AG: 33.27 ± 5.23, PH-AG: 36.80 ± 3.40 #) ( p < 0.05 vs Sh-Control; # p < 0.05 vs PH-Control). At 24 h after PH, VEGF levels showed no difference between PH-Control and PH-SNP animals. However, after 72 h, VEGF protein levels in PH-SNP animals were found to be increased (above 300%) with respect to PH-Control. On the other hand, aminoguanidine (AG) pre-treatment blocked the rise of inhibition of NO generation and decreased VEGF expression. Our results demonstrated that NO plays a role in modulating VEGF protein expression after hepatectomy in rats.

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