Abstract | BACKGROUND: METHODS: Twenty rabbits survived a thoracic spinal cord impact of 30 g-cm. One group received 0.06 microg/kg/min ATL-146e for the first 3 hours after impact (A2A group), whereas a second group received saline carrier (T/C group). Neurologic outcome was measured using the Tarlov scale (0-5). Histologic sections from the A2A and T/C groups were compared for neuronal viability. RESULTS: There was significant improvement in Tarlov scores of A2A animals compared with T/C animals at 12 hours (p = 0.007), with a trend toward improvement at 36 (p = 0.08) and 48 (p = 0.09) hours after injury. There was decreased neuronal attrition in A2A animals (p = 0.06). CONCLUSION: Systemic ATL-146e given after spinal cord trauma results in improved neurologic outcome. Adenosine A2A agonists may hold promise as a rapidly acting alternative to steroids in the early treatment of the spinal cord injured patient.
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Authors | David C Cassada, Curtis G Tribble, Jeffrey S Young, James J Gangemi, A Reza Gohari, Paris D Butler, Jayson M Rieger, Irving L Kron, Joel Linden, John A Kern |
Journal | The Journal of trauma
(J Trauma)
Vol. 53
Issue 2
Pg. 225-9; discussion 229-31
(Aug 2002)
ISSN: 0022-5282 [Print] United States |
PMID | 12169926
(Publication Type: Evaluation Study, Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- ATL 146e
- Cyclohexanecarboxylic Acids
- Neuroprotective Agents
- Purinergic P1 Receptor Agonists
- Purines
- Receptor, Adenosine A2A
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Topics |
- Animals
- Cyclohexanecarboxylic Acids
(therapeutic use)
- Hemodynamics
(drug effects)
- Neuroprotective Agents
(therapeutic use)
- Paralysis
(prevention & control)
- Purinergic P1 Receptor Agonists
- Purines
(therapeutic use)
- Rabbits
- Receptor, Adenosine A2A
- Spinal Cord Injuries
(drug therapy, pathology, surgery)
- Statistics, Nonparametric
- Wounds, Nonpenetrating
(drug therapy)
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