Evidence map›Paper›PMID 19428218›Full record

ReviewEpilepsy research2009

Adenosine augmentation therapies (AATs) for epilepsy: prospect of cell and gene therapies.

Detlev Boison

Abstract readReview
In one paragraph

Review in Epilepsy research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 91 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Adenosine Kinase: An Epigenetic Modulator and Drug Target.Journal of inherited metabolic disease · 2025
    Review
  6. Review
  7. The role of adenosine in epilepsy.Brain research bulletin · 2019
    Review
  8. Review
  9. Adenosinergic signaling in epilepsy.Neuropharmacology · 2016
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Adenosine-associated delivery systems.Journal of drug targeting · 2015
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Detlev BoisonRobert Stone Dow Neurobiology Laboratories, Legacy Research, 1225 NE 2nd Ave, Portland, OR 97232, USA. dboison@downeurobiology.org
Legacy Health · US

Funding

Adenosine-releasing brain implants for epilepsy therapyR01NS058780 · NINDS · LEGACY EMANUEL HOSPITAL AND HEALTH CENTER · PI BOISON, DETLEV · 2008 to 2011
$1.2M
Adenosine kinase as novel therapeutic target to prevent acquired epilepsyR21NS057475 · NINDS · LEGACY EMANUEL HOSPITAL AND HEALTH CENTER · PI BOISON, DETLEV · 2008 to 2009
$379k
Adenosine kinase as therapeutic target to induce and maintain ischemic toleranceR21NS057538 · NINDS · LEGACY EMANUEL HOSPITAL AND HEALTH CENTER · PI BOISON, DETLEV · 2008 to 2009
$379k
NINDS NIH HHS R01 NS058780NINDS NIH HHS R01NS058780-01NINDS NIH HHS R21 NS057475NINDS NIH HHS R21NS057475-01NINDS NIH HHS R21 NS057538NINDS NIH HHS R21NS057538-01
6 · The paper itself

Abstract

Deficiencies in the brain's own adenosine-based seizure control system contribute to seizure generation. Consequently, reconstitution of adenosinergic neuromodulation constitutes a rational approach for seizure control. This review will critically discuss focal adenosine augmentation strategies and their potential for antiepileptic and disease modifying therapy. Due to systemic side effects of adenosine focal adenosine augmentation--ideally targeted to an epileptic focus--becomes a therapeutic necessity. This has experimentally been achieved in kindled seizure models as well as in post-status epilepticus models of spontaneous recurrent seizures using three different therapeutic strategies that will be discussed here: (i) polymer-based brain implants that were loaded with adenosine; (ii) brain implants comprised of cells engineered to release adenosine and embedded in a cell-encapsulation device; (iii) direct transplantation of stem cells engineered to release adenosine. To meet the therapeutic goal of focal adenosine augmentation, genetic disruption of the adenosine metabolizing enzyme adenosine kinase (ADK) in rodent and human cells was used as a molecular strategy to induce adenosine release from cellular brain implants, which demonstrated antiepileptic and neuroprotective properties. New developments and therapeutic challenges in using AATs for epilepsy therapy will critically be evaluated.

Indexed as

AdenosineAnimalsAnticonvulsantsCell- and Tissue-Based TherapyDrug Delivery SystemsEpilepsyGenetic TherapyHumansMiceStem Cell TransplantationAdenosineAnticonvulsants

Identifiers

PMID19428218
PMCPMC2713801
OpenAlexW2059898784

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.