Acute VEGF Effect on Solute Permeability of Mammalian Microvessels in Vivo

Document Type

Article

Publication Date

7-2004

Publication Title

Microvascular Research

Volume

68

Issue

1

First page number:

51

Last page number:

62

Abstract

To investigate the effect of vascular endothelial growth factor (VEGF) on solute permeability of mammalian microvessels, we measured the apparent permeability (P) of various-sized solutes on the postcapillary venules of rat mesentery in vivo. Exposure to 1 nM VEGF transiently increased P from a mean of 1.4 (±0.11 SE, n = 17) to a peak of 2.8 (±0.28 SE) × 10−5 cm/s, a 2.4-fold increase for small solute sodium fluorescein (Stokes radius 0.45 nm), from a mean of 0.44 (±0.05 SE, n = 16) to a peak of 1.5 (±0.19 SE) × 105 cm/s, a 3.6-fold increase for intermediate-sized solute α-lactalbumin (Stokes radius 2.01 nm), from a mean of 0.049 (±0.0032 SE, n = 16) to a peak of 0.36 (±0.032 SE) × 10−5 cm/s, a 7.9-fold increase for large solute bovine serum albumin (Stokes radius 3.55 nm), within 30 s. In approximately 2 min, all increased P returned to the baseline values. The response pattern of P to VEGF and the ratios of the peak to control values for rat mesenteric microvessels are similar to those of frog mesenteric microvessels [Am. J. Physiol.: Heart Circ. Physiol. 284 (2003) H2124]. Instead of considerable heterogeneity in the frog mesenteric microvessels, the acute response to 1 nM VEGF is homogeneous in the rat mesenteric microvessels.

Keywords

Mesentery; Microvessel permeability of various-sized solutes; Paired measurement; Rat mesenteric microvessels; Rats; Tissues – Permeability; Vascular endothelial growth factors; VEGF effect

Disciplines

Biomechanics and Biotransport | Biomedical Engineering and Bioengineering | Molecular, Cellular, and Tissue Engineering

Language

English

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