Literature DB >> 12233810

Nitric oxide synthase gene therapy for cardiovascular disease.

Alex F Chen1, Jun Ren, Chao-Yu Miao.   

Abstract

Gene therapy refers to the transfer of specific genes to the host tissue to intervene in a disease process, with resultant alleviation of the symptoms of a particular disease. Cardiovascular gene transfer is not only a powerful technique for studying the function of specific genes in cardiovascular biology and pathobiology, but also a novel and promising strategy for treating cardiovascular diseases. Since the mid-1990s, nitric oxide synthase (NOS), the enzyme that catalyzes the formation of nitric oxide (NO) from L-arginine, has received considerable attention as a potential candidate for cardiovascular gene therapy, because NO exerts critical and diverse functions in the cardiovascular system, and abnormalities in NO biology are apparent in a number of cardiovascular disease processes including cerebral vasospasm, atherosclerosis, postangioplasty restenosis, transplant vasculopathy, hypertension, diabetes mellitus, impotence and delayed wound healing. There are three NOS isoforms, i.e., endothelial (eNOS), neuronal (nNOS) and inducible (iNOS). All three NOS isoforms have been used in cardiovascular gene transfer studies with encouraging results. This review will discuss the rationale of NOS gene therapy in different cardiovascular disease settings and summarize the results of experimental NOS gene therapy from various animal models of cardiovascular disease to date.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12233810     DOI: 10.1254/jjp.89.327

Source DB:  PubMed          Journal:  Jpn J Pharmacol        ISSN: 0021-5198


  8 in total

1.  Thromboresistant/anti-biofilm catheters via electrochemically modulated nitric oxide release.

Authors:  Hang Ren; Alessandro Colletta; Dipankar Koley; Jianfeng Wu; Chuanwu Xi; Terry C Major; Robert H Bartlett; Mark E Meyerhoff
Journal:  Bioelectrochemistry       Date:  2014-12-18       Impact factor: 5.373

2.  MRI assessment of coronary microvascular endothelial nitric oxide synthase function using myocardial T1 mapping.

Authors:  Sophia X Cui; Frederick H Epstein
Journal:  Magn Reson Med       Date:  2017-08-07       Impact factor: 4.668

Review 3.  Nitric oxide synthases: regulation and function.

Authors:  Ulrich Förstermann; William C Sessa
Journal:  Eur Heart J       Date:  2011-09-01       Impact factor: 29.983

Review 4.  Opportunities for Nitric Oxide in Potentiating Cancer Immunotherapy.

Authors:  Jihoon Kim; Susan N Thomas
Journal:  Pharmacol Rev       Date:  2022-10       Impact factor: 18.923

5.  Non-viral eNOS gene delivery and transfection with stents for the treatment of restenosis.

Authors:  Luis A Brito; Saradha Chandrasekhar; Steven R Little; Mansoor M Amiji
Journal:  Biomed Eng Online       Date:  2010-09-27       Impact factor: 2.819

6.  Local delivery of gene vectors from bare-metal stents by use of a biodegradable synthetic complex inhibits in-stent restenosis in rat carotid arteries.

Authors:  Ilia Fishbein; Ivan Alferiev; Marina Bakay; Stanley J Stachelek; Peter Sobolewski; Meizan Lai; Hoon Choi; I-W Chen; Robert J Levy
Journal:  Circulation       Date:  2008-04-14       Impact factor: 29.690

Review 7.  Physical Exercise and Selective Autophagy: Benefit and Risk on Cardiovascular Health.

Authors:  Ne N Wu; Haili Tian; Peijie Chen; Dan Wang; Jun Ren; Yingmei Zhang
Journal:  Cells       Date:  2019-11-14       Impact factor: 6.600

8.  Potassium concentration on admission is an independent risk factor for target lesion revascularization in acute myocardial infarction.

Authors:  Tsuyoshi Honda; Kazuteru Fujimoto; Yuji Miyao; Hidenobu Koga; Masanobu Ishii
Journal:  ScientificWorldJournal       Date:  2014-01-12
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.