Effects of the suppression of 5-HT1A receptors in the left, right, or bilateral basolateral amygdala on memory consolidation in chronic stress in male rats
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Valipour, Habib
[1
,2
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Jahromi, Gila Pirzad
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Mohammadi, Alireza
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Baqiyatallah Univ Med Sci, Neurosci Res Ctr, Tehran, IranBaqiyatallah Univ Med Sci, Neurosci Res Ctr, Tehran, Iran
Mohammadi, Alireza
[1
]
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Meftahi, Gholam Hossein
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[1] Baqiyatallah Univ Med Sci, Neurosci Res Ctr, Tehran, Iran
[2] Baqiyatallah Univ Med Sci, Student Res Comm, Tehran, Iran
The serotonin-1A receptors (5-HT1A) in the two cerebral hemispheres are differentially involved in memory. The distribution of 5-HT1A receptors in the left and right amygdala is different. Furthermore, evidence shows that the 5-HT1A receptors in the left and right amygdala work differently in memory function. The basolateral amygdala (BLA) also regulates hippocampal long-term potentiation (LTP) during stress. However, which BLA structure in each hemisphere underlies such lateralized function is unclear. The present research investigated the possible involvement of 5-HT1A lateralization in the BLA on stress-induced memory impairment. 5-HT1A receptor antagonist (Way-100-635) was injected into the left, right, or bilateral BLA twenty minutes before chronic restraint stress (CRS) for 14 consecutive days. Results indicated that suppression of 5HT(1A)-receptors in the BLA plays an essential role in reducing the acquisition of passive avoidance in the shuttle box test and spatial memory in the Barnes maze test in the stress animals. This decrease was significant in the CRS animals with left and bilateral suppressed 5HT(1A)-receptors in the BLA. Field potential recording results showed that the left, right, and bilateral injection of Way-100-635 into the BLA significantly reduced the slope and amplitude of fEPSP in the CA1 area of the hippocampus in stressed rats. No significant difference was observed in neuronal arborization in the CA1 area of the hippocampus. In conclusion, the 5-HT1A receptor in the left and right sides of BLA nuclei play a different role in memory consolidation in the hippocampus under stress.
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Duquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Duquesne Univ, Chron Pain Res Consortium, Pittsburgh, PA 15282 USADuquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Allen, Heather N.
Bobnar, Harley J.
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Duquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Duquesne Univ, Chron Pain Res Consortium, Pittsburgh, PA 15282 USADuquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Bobnar, Harley J.
Kolber, Benedict J.
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Duquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Duquesne Univ, Chron Pain Res Consortium, Pittsburgh, PA 15282 USA
Univ Texas Dallas, Dept Neurosci, 800 Campbell Rd, Richardson, TX 75080 USA
Univ Texas Dallas, Ctr Adv Pain Studies, Richardson, TX 75080 USADuquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
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Univ Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England
Bocchio, Marco
McHugh, Stephen B.
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Univ Oxford, Dept Expt Psychol, S Parks Rd, Oxford OX1 3UD, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England
McHugh, Stephen B.
Bannerman, David M.
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Univ Oxford, Dept Expt Psychol, S Parks Rd, Oxford OX1 3UD, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England
Bannerman, David M.
Sharp, Trevor
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Univ Oxford, Dept Pharmacol, S Parks Rd, Oxford OX1 3QT, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England
Sharp, Trevor
Capogna, Marco
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Univ Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England
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Duquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Duquesne Univ, Chron Pain Res Consortium, Pittsburgh, PA 15282 USADuquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Allen, Heather N.
Bobnar, Harley J.
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Duquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Duquesne Univ, Chron Pain Res Consortium, Pittsburgh, PA 15282 USADuquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Bobnar, Harley J.
Kolber, Benedict J.
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Duquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
Duquesne Univ, Chron Pain Res Consortium, Pittsburgh, PA 15282 USA
Univ Texas Dallas, Dept Neurosci, 800 Campbell Rd, Richardson, TX 75080 USA
Univ Texas Dallas, Ctr Adv Pain Studies, Richardson, TX 75080 USADuquesne Univ, Dept Biol Sci, Pittsburgh, PA 15282 USA
机构:
Univ Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England
Bocchio, Marco
McHugh, Stephen B.
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Univ Oxford, Dept Expt Psychol, S Parks Rd, Oxford OX1 3UD, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England
McHugh, Stephen B.
Bannerman, David M.
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Univ Oxford, Dept Expt Psychol, S Parks Rd, Oxford OX1 3UD, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England
Bannerman, David M.
Sharp, Trevor
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Univ Oxford, Dept Pharmacol, S Parks Rd, Oxford OX1 3QT, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England
Sharp, Trevor
Capogna, Marco
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Univ Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, EnglandUniv Oxford, Dept Pharmacol, MRS Brain Network Dynam Unit, S Parks Rd, Oxford OX1 3QT, England