Donate Help Contact The AHA Sign In Home
American Heart Association
Arteriosclerosis, Thrombosis, and Vascular Biology
Search: search_blue_button Advanced Search
Published Online
on March 26, 2009

Arteriosclerosis, Thrombosis, and Vascular Biology. 2009
Published online before print March 26, 2009, doi: 10.1161/ATVBAHA.108.182584
A more recent version of this article appeared on June 1, 2009
This Article
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow All Versions of this Article:
29/6/796    most recent
ATVBAHA.108.182584v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kubo, M.
Right arrow Articles by Sunagawa, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kubo, M.
Right arrow Articles by Sunagawa, K.
Related Collections
Right arrow Angiogenesis
Right arrow Endothelium/vascular type/nitric oxide

Submitted on December 9, 2008
Accepted on March 16, 2009

Therapeutic Neovascularization by Nanotechnology-Mediated Cell-Selective Delivery of Pitavastatin Into the Vascular Endothelium

Mitsuki Kubo ; Kensuke Egashira *; Takahiro Inoue ; Jun-ichiro Koga ; Shinichiro Oda ; Ling Chen ; Kaku Nakano ; Tetsuya Matoba ; Yoshiaki Kawashima ; Kaori Hara ; Hiroyuki Tsujimoto ; Katsuo Sueishi ; Ryuji Tominaga ; and Kenji Sunagawa

From the Department of Cardiovascular Medicine (M.K., K.E., T.I., J.K., L.C., K.N., T.K., K. Sunagawa), Surgery (S.O., R.T.), and Pathology (K. Sueishi), Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; the School of Pharmaceutical Science (Y.K.), Aichi Gakuin University, Aichi, Japan; and Hosokawa Powder Technology Research Institute (K.H., H.T.), Osaka, Japan.

* To whom correspondence should be addressed. E-mail: egashira{at}cardiol.med.kyushu-u.ac.jp.

Objective—Recent clinical studies of therapeutic neovascularization using angiogenic growth factors demonstrated smaller therapeutic effects than those reported in animal experiments. We hypothesized that nanoparticle (NP)-mediated cell-selective delivery of statins to vascular endothelium would more effectively and integratively induce therapeutic neovascularization.

Methods and Results—In a murine hindlimb ischemia model, intramuscular injection of biodegradable polymeric NP resulted in cell-selective delivery of NP into the capillary and arteriolar endothelium of ischemic muscles for up to 2 weeks postinjection. NP-mediated statin delivery significantly enhanced recovery of blood perfusion to the ischemic limb, increased angiogenesis and arteriogenesis, and promoted expression of the protein kinase Akt, endothelial nitric oxide synthase (eNOS), and angiogenic growth factors. These effects were blocked in mice administered a nitric oxide synthase inhibitor, or in eNOS-deficient mice.

Conclusions—NP-mediated cell-selective statin delivery may be a more effective and integrative strategy for therapeutic neovascularization in patients with severe organ ischemia.


Key words: nanotechnology • drug delivery system • statin • therapeutic neovascularization