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Updated: Aug 7, 2026

Vein Interposition Model: A Suitable Model to Study Bypass Graft Patency
Published on: January 15, 2017
Inducible nitric oxide synthase expression in human vein grafts
J B Dattilo1, M P Dattilo, J A Spratt
1Department of Surgery, Medical College of Virginia/Virginia Commonwealth University, Richmond 23298-0108, USA.
Inducible nitric oxide synthase (iNOS) gene expression is elevated in human aortocoronary vein grafts compared to infrainguinal grafts. This finding may lead to new therapies for preventing intimal hyperplasia in vascular reconstructive procedures.
Area of Science:
- Vascular Biology
- Molecular Biology
- Surgical Research
Background:
- Intimal hyperplasia (IH) limits vascular reconstructive procedure patency.
- Nitric oxide (NO) may inhibit IH development.
- Inducible nitric oxide synthase (iNOS) produces NO, but its role in human vein grafts is unclear.
Purpose of the Study:
- To investigate iNOS gene expression in human aortocoronary vein grafts (ACVG) and infrainguinal vein grafts (IVG).
Main Methods:
- Quantitative reverse transcription-polymerase chain reaction (RT-PCR) was used to measure iNOS gene expression.
- Samples from ACVG (n=5), IVG (n=5), and control saphenous vein (SV; n=4) were analyzed.
- Glyceraldehyde-3-phosphate-dehydrogenase (GAPDH) served as the internal control.
Main Results:
- iNOS gene expression was significantly higher in ACVG (0.049) compared to IVG (0.019) and normal SV (0.011) (P < 0.05).
- No significant difference in iNOS expression was observed between normal SV and IVG.
- Sequencing confirmed 84% homology of the amplified gene product with the human sequence.
Conclusions:
- iNOS is expressed in human vein bypass grafts.
- ACVGs exhibit significantly elevated iNOS expression compared to IVGs and normal SV.
- Targeting iNOS expression could offer therapeutic strategies against IH in vein grafts.
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