Progesterone facilitates the acquisition of avoidance learning and protects against subcortical neuronal death following prefrontal cortex ablation in the rat
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作者:
Asbury, ET
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Texas Christian Univ, Dept Psychol, Ft Worth, TX 76129 USATexas Christian Univ, Dept Psychol, Ft Worth, TX 76129 USA
Asbury, ET
[1
]
Fritts, ME
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机构:Texas Christian Univ, Dept Psychol, Ft Worth, TX 76129 USA
Fritts, ME
Horton, JE
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机构:Texas Christian Univ, Dept Psychol, Ft Worth, TX 76129 USA
Horton, JE
Isaac, WL
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机构:Texas Christian Univ, Dept Psychol, Ft Worth, TX 76129 USA
Isaac, WL
机构:
[1] Texas Christian Univ, Dept Psychol, Ft Worth, TX 76129 USA
[2] E Tennessee State Univ, Dept Psychol, Johnson City, TN 37614 USA
Following a cortical injury, neurons in areas near and connected to the site of injury begin to degenerate. The observed neuronal death may contribute to the severity of the observed behavioral impairments. The purpose of the present study was to examine if progesterone, a hormone known for its effectiveness at reducing cerebral edema, could protect against secondary neuronal death and facilitate the acquisition of an avoidance learning task in an ablation model of cortical injury. Rats served as sham controls or received bilateral ablation of the medial prefrontal cortex followed by a 10-day regimen of progesterone (4 mg/kg) or oil vehicle (1 ml/kg) beginning 1 h after cortical lesions. Progesterone-treated lesion rats showed a significant facilitation of avoidance learning compared to oil-treated lesion controls. In addition, progesterone-treated lesion animals did not differ from either progesterone- or oil-treated sham controls in avoidance learning. Anatomical analysis revealed that progesterone treatment decreased the amount of neuronal death seen in the striatum and the mediodorsal nucleus of the thalamus. The findings are consistent with the notion that progesterone is an effective neuroprotective agent and suggest that the hormone can reduce the behavioral impairments associated with frontal cortical ablation injury. (C) 1998 Elsevier Science B.V. All rights reserved.