TY - JOUR
T1 - κ-Selective Opiate Antagonist Nor-Binaltorphimine Improves Outcome After Traumatic Spinal Cord Injury in Rats
AU - Faden, Alan I.
AU - Takemori, A. E.
AU - Portoghese, P. S.
PY - 1987
Y1 - 1987
N2 - Nor-binaltorphimine (nor-BNI) is a recently developed opiate antagonist that has a high degree of selectivity for κ-opiate receptors. Because of the proposed role of κ-opiate receptors in mediating secondary damage after spinal trauma, the effect of nor-BNI was studied in a well-characterized model of traumatic spinal cord injury in rats. Nor-BNI, at a dose of 10 mg/kg administered intravenously at 15 min following impact trauma to T-9, significantly improved neurological recovery, measured both in terms of Tarlov motor scores and ability to maintain position on an inclined plane. Given intrathecally, at doses that were ineffective systemically (0.1 mg/kg), nor-BNI also significantly improved neurological recovery after trauma. These data are consistent with the hypothesis that endogenous opioids, through actions at κ-opiate receptors within the spinal cord, contribute to the pathophysiological changes after spinal trauma that lead to irreversible tissue damage, and indicate that κ-receptor antagonists may be beneficial for the treatment of acute spinal cord injury.
AB - Nor-binaltorphimine (nor-BNI) is a recently developed opiate antagonist that has a high degree of selectivity for κ-opiate receptors. Because of the proposed role of κ-opiate receptors in mediating secondary damage after spinal trauma, the effect of nor-BNI was studied in a well-characterized model of traumatic spinal cord injury in rats. Nor-BNI, at a dose of 10 mg/kg administered intravenously at 15 min following impact trauma to T-9, significantly improved neurological recovery, measured both in terms of Tarlov motor scores and ability to maintain position on an inclined plane. Given intrathecally, at doses that were ineffective systemically (0.1 mg/kg), nor-BNI also significantly improved neurological recovery after trauma. These data are consistent with the hypothesis that endogenous opioids, through actions at κ-opiate receptors within the spinal cord, contribute to the pathophysiological changes after spinal trauma that lead to irreversible tissue damage, and indicate that κ-receptor antagonists may be beneficial for the treatment of acute spinal cord injury.
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U2 - 10.1089/cns.1987.4.227
DO - 10.1089/cns.1987.4.227
M3 - Article
C2 - 3446373
AN - SCOPUS:0023597416
SN - 0737-5999
VL - 4
SP - 227
EP - 234
JO - Central Nervous System Trauma
JF - Central Nervous System Trauma
IS - 4
ER -