Abstract | BACKGROUND: METHODS AND RESULTS: In DDAH1 transgenic (TG) and wild-type mice (each n=42), the role of DDAH overexpression on angiogenesis was studied by use of the disk angiogenesis system and a murine model of hindlimb ischemia (each n=21). After surgery, animals were treated with either PBS or the NOS inhibitors ADMA or N(omega)-nitro-L-arginine methyl ester ( L-NAME; each 250 micromol x kg(-1) x d(-1)) by use of osmotic minipumps (each n=7). L-NAME was chosen to study an inhibitor that is not degraded by DDAH. Neovascularization in the disk angiogenesis system was impaired by both NOS inhibitors; however, TG animals were resistant to the effects of ADMA on neovascularization. Similarly, TG mice were more resistant to the inhibitory effect of ADMA on angioadaptation (angiogenesis and arteriogenesis) after hindlimb ischemia, as assessed by fluorescent microsphere studies and postmortem microangiograms. Enhanced neovascularization and limb perfusion in TG mice were associated with reduced plasma and tissue ADMA levels and enhanced tissue NOS enzyme activity. CONCLUSIONS: We describe a novel mechanism by which DDAH regulates postnatal neovascularization. Therapeutic manipulation of DDAH expression or activity may represent a novel approach to restore tissue perfusion.
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Authors | Johannes Jacobi, Karsten Sydow, Georges von Degenfeld, Ying Zhang, Hayan Dayoub, Bingyin Wang, Andrew J Patterson, Masumi Kimoto, Helen M Blau, John P Cooke |
Journal | Circulation
(Circulation)
Vol. 111
Issue 11
Pg. 1431-8
(Mar 22 2005)
ISSN: 1524-4539 [Electronic] United States |
PMID | 15781754
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Nitrates
- Nitrites
- Recombinant Fusion Proteins
- Nitric Oxide
- N,N-dimethylarginine
- Arginine
- Nitric Oxide Synthase
- Amidohydrolases
- dimethylargininase
- NG-Nitroarginine Methyl Ester
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Topics |
- Amidohydrolases
(genetics, physiology)
- Animals
- Arginine
(analogs & derivatives, blood, pharmacokinetics, pharmacology)
- Enzyme Induction
- Female
- Hindlimb
(blood supply)
- Humans
- Ischemia
(physiopathology)
- Laser-Doppler Flowmetry
- Mice
- Mice, Transgenic
- Microspheres
- Muscle, Skeletal
(blood supply)
- NG-Nitroarginine Methyl Ester
(pharmacology)
- Neovascularization, Physiologic
(physiology)
- Nitrates
(blood)
- Nitric Oxide
(physiology)
- Nitric Oxide Synthase
(antagonists & inhibitors)
- Nitrites
(blood)
- Prostheses and Implants
- Recombinant Fusion Proteins
(physiology)
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