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Non-viral Systemic Delivery of SiRNA or Antisense Oligonucleotides Targeted to Jun N-terminal Kinase 1 Prevents Cellular Hypoxic Damage

Overview
Publisher Springer
Specialty Pharmacology
Date 2011 Apr 5
PMID 21461383
Citations 8
Authors
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Abstract

Many pathological conditions and environmental impacts lead to the development of severe tissue hypoxia that aggravates the primary disorder, provokes cell death, and limits the patient's recovery. We hypothesized that suppression of Jun N-terminal kinase 1 (JNK1) will limit tissue damage induced by severe hypoxia. To test the hypothesis, antisense oligonucleotides (ASO) or small interfering RNA (siRNA) targeted to JNK1 mRNA were incorporated or complexed with neutral or cationic liposomes, respectively, and administered systemically to mice prior to hypoxia exposure. The animals were placed in a special chamber ventilated with room air (normoxia) or a gas mixture containing 6% O(2) and 94% N(2) (hypoxia). Liposomes, ASO, and siRNA were found to accumulate in the lungs, kidney, spleen, and heart. Only trace amounts of liposomes and their payloads (ASO and siRNA) were found in the brain. The down regulation of JNK1 protein limited activation of cell death signal, apoptotic, and necrotic tissue damage under hypoxic conditions. Consequently, we were able to verify our hypothesis and provide proof of concept of a unique approach to the prevention of cellular hypoxic damage by the suppression of JNK1 signaling pathways after the efficient delivery of ASO or siRNA.

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References
1.
Soni V, Kohli D, Jain S . Transferrin-conjugated liposomal system for improved delivery of 5-fluorouracil to brain. J Drug Target. 2008; 16(1):73-8. DOI: 10.1080/10611860701725381. View

2.
Carlsson Y, Leverin A, Hedtjarn M, Wang X, Mallard C, Hagberg H . Role of mixed lineage kinase inhibition in neonatal hypoxia-ischemia. Dev Neurosci. 2009; 31(5):420-6. DOI: 10.1159/000232560. View

3.
Chihab R, Ferry C, Koziel V, Monin P, Daval J . Sequential activation of activator protein-1-related transcription factors and JNK protein kinases may contribute to apoptotic death induced by transient hypoxia in developing brain neurons. Brain Res Mol Brain Res. 1998; 63(1):105-20. DOI: 10.1016/s0169-328x(98)00266-6. View

4.
Dharap S, Wang Y, Chandna P, Khandare J, Qiu B, Gunaseelan S . Tumor-specific targeting of an anticancer drug delivery system by LHRH peptide. Proc Natl Acad Sci U S A. 2005; 102(36):12962-7. PMC: 1200279. DOI: 10.1073/pnas.0504274102. View

5.
Hossain M . Hypoxic-ischemic injury in neonatal brain: involvement of a novel neuronal molecule in neuronal cell death and potential target for neuroprotection. Int J Dev Neurosci. 2007; 26(1):93-101. PMC: 2350216. DOI: 10.1016/j.ijdevneu.2007.08.013. View