Antisense prevention of neuronal damages following head injury in mice

E. Shohami, D. Kaufer, Y. Chen, S. Seidman, O. Cohen, D. Ginzberg, N. Melamed-Book, R. Yirmiya, H. Soreq*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

56 Scopus citations


Closed head injury (CHI) is an important cause of death among young adults and a prominent risk factor for nonfamilial Alzheimer's disease. Emergency intervention following CHI should therefore strive to improve survival, promote recovery, and prevent delayed neuropathologies. We employed high-resolution nonradioactive in situ hybridization to determine whether a single intracerebro-ventricular injection of 500 ng 2'-O-methyl RNA-capped antisense oligonucleotide (AS-ODN) against acetylcholinesterase (AChE) mRNA blocks overexpression of the stress-related readthrough AChE (AChE-R) mRNA splicing variant in head-injured mice. Silver-based Golgi staining revealed pronounced dendrite outgrowth in somatosensory cortex of traumatized mice 14 days postinjury that was associated with sites of AChE-R mRNA overexpression and suppressed by anti-AChE AS-ODNs. Furthermore, antisense treatment reduced the number of dead CA3 hippocampal neurons in injured mice, and facilitated neurological recovery as determined by performance in tests of neuromotor coordination. In trauma-sensitive transgenic mice overproducing AChE, antisense treatment reduced mortality from 50% to 20%, similar to that displayed by head-injured control mice. These findings demonstrate the potential of antisense therapeutics in treating acute injury, and suggest antisense prevention of AChE-R overproduction to mitigate the detrimental consequences of various traumatic brain insults.

Original languageAmerican English
Pages (from-to)228-236
Number of pages9
JournalJournal of Molecular Medicine
Issue number4
StatePublished - 2000

Bibliographical note

Funding Information:
Acknowledgements The authors are indebted to Dr. Aharon S. Cohen (Boston) for fruitful discussions. This work was supported by grants to H.S. from the United States Army Medical Research and Development Command (DAMD17-99-1-9547), The Israel Science Foundation (590/97), the United States–Israel Binational Science Foundation (96-00110), and Ester Neurosciences, Ltd. E.S. is affiliated with the David R. Bloom Center for Pharmacy, the Hebrew University, Jerusalem.


  • Acetylcholinesterase
  • Antisense
  • Emergency medicine
  • Head injury
  • Oligonucleotides


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