Abstract |
Renal ischaemia-reperfusion (I/R) injury is a clinically significant problem and an invariable consequence of renal transplantation. The problem begins at the onset of acute tubular necrosis (ATN), when the transplantation takes a long ischaemic interval by using the cardiac arrest donor's kidney. In addition, the longer the ischaemic interval, the higher the incidence rate of ATN. It is clinically important that renal I/R injury is reduced. The antisense oligodeoxynucleotide (AS-ODN), developed as a therapy for intractable diseases at the gene level, has recently been established as an important method in examining specific gene functions. The authors have previously demonstrated that AS-ODN/ tissue factor (TF) prevents renal I/R injury. This review discusses the efficacy of AS-ODN/TF and AS-ODN/ intercellular adhesion molecule-1 as existing targets, and the potential of AS-ODN/ nuclear factor-kappaB, AS-ODN/ cyclooxygenase and AS-ODN/ 5-lipoxygenase as prospective targets.
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Authors | Masahide Matsuyama, Rikio Yoshimura |
Journal | Expert opinion on biological therapy
(Expert Opin Biol Ther)
Vol. 4
Issue 12
Pg. 1931-7
(Dec 2004)
ISSN: 1744-7682 [Electronic] England |
PMID | 15571455
(Publication Type: Journal Article, Review)
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Chemical References |
- Oligonucleotides, Antisense
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Topics |
- Animals
- Gene Targeting
(methods)
- Humans
- Kidney
(blood supply, drug effects, metabolism)
- Kidney Diseases
(drug therapy, genetics, metabolism)
- Oligonucleotides, Antisense
(administration & dosage, therapeutic use)
- Reperfusion Injury
(drug therapy, genetics, metabolism)
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