Hippocampal a5-GABAA Receptors Modulate Dopamine Neuron Activity in the Rat Ventral Tegmental Area

被引:9
|
作者
Perez, Stephanie M. [1 ,2 ,3 ]
McCoy, Alexandra M. [1 ,2 ,3 ]
Prevot, Thomas D. [4 ,5 ]
Mian, Md Yeunus [7 ]
Carreno, Flavia R. [1 ,2 ]
Frazer, Alan [1 ,2 ,3 ]
Cook, James M. [7 ]
Sibille, Etienne [4 ,5 ,6 ]
Lodge, Daniel J. [1 ,2 ,3 ]
机构
[1] UT Hlth San Antonio, Dept Pharmacol, San Antonio, TX 78229 USA
[2] UT Hlth San Antonio, Ctr Biomed Neurosci, San Antonio, TX 78229 USA
[3] South Texas Vet Hlth Care Syst, Audie L Murphy Mem Vet Hosp, San Antonio, TX 78229 USA
[4] Ctr Addict & Mental Hlth, Campbell Family Mental Hlth Res Inst, Toronto, ON, Canada
[5] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[6] Univ Toronto, Dept Pharmacol & Toxicol, Toronto, ON, Canada
[7] Univ Wisconsin Milwaukee, Dept Chem & Biochem, Milwaukee, WI USA
来源
基金
美国国家卫生研究院;
关键词
CONTAINING GABA(A) RECEPTORS; INVERSE AGONIST; SYSTEM FUNCTION; RODENT MODEL; METHYLAZOXYMETHANOL ACETATE; TRANSPORTER BINDING; ANIMAL-MODEL; BRAIN; DYSREGULATION; SCHIZOPHRENIA;
D O I
10.1016/j.bpsgos.2021.12.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BACKGROUND: Aberrant dopamine neuron activity is attributable to hyperactivity in hippocampal subfields driving a pathological increase in dopamine neuron activity, which is positively correlated with psychosis in humans. Evidence indicates that hippocampal hyperactivity is due to loss of intrinsic GABAergic (gamma-aminobutyric acidergic) in-hibition. We have previously demonstrated that hippocampal GABAergic neurotransmission can be modulated by targeting a5-GABAA receptors, which are preferentially expressed in hippocampal regions. Positive and negative allosteric modulators of a5-GABAA receptors (a5-PAMs and a5-NAMs) elicit effects on hippocampal-dependent behaviors. We posited that the selective manipulation of hippocampal inhibition, using a5-PAMs or a5-NAMs, would modulate dopamine activity in control rats. Further, a5-PAMs would reverse aberrant dopamine neuron activity in a rodent model with schizophrenia-related pathophysiologies (methylazoxymethanol acetate [MAM] model). METHODS: We performed in vivo extracellular recordings of ventral tegmental area dopamine neurons in anes-thetized rats to compare the effects of two novel, selective a5-PAMs (GL-II-73, MP-III-022), a nonselective a-PAM (midazolam), and two selective a5-NAMs (L-655,708, TB 21007) in control and MAM-treated male Sprague Dawley rats (n = 5-9). RESULTS: Systemic or intracranial administration of selective a5-GABAA receptor modulators regulated dopamine activity. Specifically, both a5-NAMs increased dopamine neuron activity in control rats, whereas GL-II-73, MP-III-022, and L-655,708 attenuated aberrant dopamine neuron activity in MAM-treated rats, an effect mediated by the ventral hippocampus. CONCLUSIONS: This study demonstrated that a5-GABAA receptor modulation can regulate dopamine neuron activity under control or abnormal activity, providing additional evidence that a5-PAMs and a5-NAMs may have therapeutic applications in psychosis and other psychiatric diseases where aberrant hippocampal activity is present.
引用
收藏
页码:78 / 86
页数:9
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