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Maternal Therapy with Ad.VEGF-A 165 Increases Fetal Weight at Term in a Guinea-Pig Model of Fetal Growth Restriction.

Authors :
Swanson AM
Rossi CA
Ofir K
Mehta V
Boyd M
Barker H
Ledwozyw A
Vaughan O
Martin J
Zachary I
Sebire N
Peebles DM
David AL
Source :
Human gene therapy [Hum Gene Ther] 2016 Dec; Vol. 27 (12), pp. 997-1007. Date of Electronic Publication: 2016 Aug 16.
Publication Year :
2016

Abstract

In a model of growth-restricted sheep pregnancy, it was previously demonstrated that transient uterine artery VEGF overexpression can improve fetal growth. This approach was tested in guinea-pig pregnancies, where placental physiology is more similar to humans. Fetal growth restriction (FGR) was attained through peri-conceptual nutrient restriction in virgin guinea pigs. Ad.VEGF-A <subscript>165</subscript> or Ad.LacZ (1 × 10 <superscript>10</superscript> vp) was applied at mid-gestation via laparotomy, delivered externally to the uterine circulation with thermosensitive gel. At short-term (3-8 days post surgery) or at term gestation, pups were weighed, and tissues were sampled for vector spread analysis, VEGF expression, and its downstream effects. Fetal weight at term was increased (88.01 ± 13.36 g; n = 26) in Ad.VEGF-A <subscript>165</subscript> -treated animals compared with Ad.LacZ-treated animals (85.52 ± 13.00 g; n = 19; p = 0.028). The brain, liver, and lung weight and crown rump length were significantly larger in short-term analyses, as well as VEGF expression in transduced tissues. At term, molecular analyses confirmed the presence of VEGF transgene in target tissues but not in fetal samples. Tissue histology analysis and blood biochemistry/hematological examination were comparable with controls. Uterine artery relaxation in Ad.VEGF-A <subscript>165</subscript> -treated dams was higher compared with Ad.LacZ-treated dams. Maternal uterine artery Ad.VEGF-A <subscript>165</subscript> increases fetal growth velocity and term fetal weight in growth-restricted guinea-pig pregnancy.

Details

Language :
English
ISSN :
1557-7422
Volume :
27
Issue :
12
Database :
MEDLINE
Journal :
Human gene therapy
Publication Type :
Academic Journal
Accession number :
27530140
Full Text :
https://doi.org/10.1089/hum.2016.046