Effects of GABAB, 5-HT1A, and 5-HT2 receptor stimulation on activation and inhibition of the rat lateral amygdala following medial geniculate nucleus stimulation in vivo
dThe input from the medial geniculate nucleus of the thalamus (MGN) to the lateral amygdala is known to be important in the regulation of fear and anxiety. Modulation of this pathway may be useful for the treatment of anxiety disorders. We set out to determine whether simple extracellular electrophysiological techniques could be used to study pharmacological modulation of this pathway in vivo. We studied the effects of GABA(B), 5-HT1, and 5-HT2 receptor agonists on activity in the lateral amygdala following stimulation of the MGN in isoflurane-anaesthetised rats. Electrical stimulation of the MGN evoked a characteristic biphasic field potential in the lateral amygdala. Baclofen (10 mg kg(-1), iv) inhibited the evoked potential with an effect that was most marked on the positive-going component (80 +/- 9% inhibition; P < 0.05). Baclofen also significantly reduced paired-pulse inhibition of the negative-going component at short interpulse intervals (<200 ms). The 5-HT1A receptor ligands, 8-OH-DPAT (60 mug kg(-1), iv) and WAY-100635 (0.5 mg kg(-1), iv) were without effect on evoked responses or paired-pulse relationship. In contrast, the 5-HT2 receptor agonist, DOI, caused a rapid inhibition of the field potential (to 59.33 +/- 11.41% of the baseline response; P < 0.05). This effect was blocked by ketanserin, either following systemic (0.5 mg kg(-1), iv) or intra-amygdala administration. These results show that GABAB and 5-HT2 receptor agonists can modulate activation of the lateral amygdala following MGN stimulation; furthermore, GABA(B) receptor agonists appear to have a profound effect on local circuit inhibition within the lateral amygdala. The results support the use of in vivo field potential recording within the MGN-lateral amygdala pathway to evaluate this as a possible site of action for novel anxiolytic drugs. (C) 2004 Elsevier B.V. All rights reserved.
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Hamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, IranHamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Iran
Shahidi, Siamak
Hashemi-Firouzi, Nasrin
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Hamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, IranHamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Iran
Hashemi-Firouzi, Nasrin
Afshar, Simin
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Hamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Iran
Islamic Azad Univ, Dept Biol, Sci & Res Branch, Tehran, IranHamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Iran
Afshar, Simin
Asl, Sara Soleimani
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Hamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Iran
Hamadan Univ Med Sci, Sch Med, Anat Dept, Hamadan, IranHamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Iran
Asl, Sara Soleimani
Komaki, Alireza
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Hamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, IranHamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Iran
Komaki, Alireza
MALAYSIAN JOURNAL OF MEDICAL SCIENCES,
2019,
26
(02):
: 40
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51
机构:
Univ Sao Paulo, Psychobiol Grad Program, Ribeirao Preto Dent Sch, Dept Morphol Physiol & Basic Pathol, BR-14040901 Ribeirao Preto, SP, BrazilUniv Sao Paulo, Psychobiol Grad Program, Ribeirao Preto Dent Sch, Dept Morphol Physiol & Basic Pathol, BR-14040901 Ribeirao Preto, SP, Brazil
de Paula, Bruna Balbino
Andrade Leite-Panissi, Christie Ramos
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Univ Sao Paulo, Psychobiol Grad Program, Ribeirao Preto Dent Sch, Dept Morphol Physiol & Basic Pathol, BR-14040901 Ribeirao Preto, SP, Brazil
Univ Sao Paulo, Dept Morphol Physiol & Basic Pathol, Dent Sch Ribeirao Preto, BR-14040904 Ribeirao Preto, SP, BrazilUniv Sao Paulo, Psychobiol Grad Program, Ribeirao Preto Dent Sch, Dept Morphol Physiol & Basic Pathol, BR-14040901 Ribeirao Preto, SP, Brazil