Activation of Lateral Parabrachial Nucleus (LPBn) PACAP-Expressing Projection Neurons to the Bed Nucleus of the Stria Terminalis (BNST) Enhances Anxiety-like Behavior

被引:17
作者
Boucher, Melissa N. [1 ,2 ]
Aktar, Mahafuza [1 ,2 ]
Braas, Karen M. [1 ,2 ]
May, Victor [1 ,2 ]
Hammack, Sayamwong E. [1 ,2 ]
机构
[1] Univ Vermont, Dept Psychol Sci, 2 Colchester Ave, Burlington, VT 05405 USA
[2] Univ Vermont, Coll Med, Dept Neurol Sci, 149 Beaumont Ave, Burlington, VT 05405 USA
基金
美国国家卫生研究院;
关键词
Anxiety; Stress; PAC1; receptor; DREADD; Extended amygdala; Post-traumatic stress disorder; POLYPEPTIDE PACAP; WEIGHT-LOSS; STRESS; AMYGDALA; RECEPTORS; BRAIN; DISORDERS; ANOREXIA; CIRCUIT; PEPTIDE;
D O I
10.1007/s12031-021-01946-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Anxiety disorders are among the most common psychiatric disorders, and understanding the underlying neurocircuitry of anxiety- and stress-related behaviors may be important for treatment. The bed nucleus of the stria terminalis (BNST) has been studied for its role in many stress-related pathologies, such as anxiety, pain, depression, and addiction. Our prior work has demonstrated that pituitary adenylate cyclase-activating polypeptide (PACAP) receptor activation in the BNST mediates many of the behavioral consequences of chronic stress. While the BNST contains local PACAP-expressing neurons, a major source of afferent PACAP is the lateral parabrachial nucleus (LPBn), and excitotoxic lesions of the LPBn substantially decreasess PACAP immunostaining in the BNST. Here, we first assessed Cre-dependent reporter expression by injecting AAV2-hSyn-DIO-mCherry into the LPBn of PACAP-IRES-Cre mice for circuit mapping studies and identified PACAP projections to the BNST, lateral capsular central nucleus of the amygdala (CeLC), and ventromedial hypothalamus (VMH). In a second study, we assessed the effects of chemogenetically activating LPBn PACAP afferents in the BNST by injecting AAV2-hSyn-DIO-hM3D(Gq)-mCherry into the LPBn of PACAP-IRES-Cre mice for Cre-dependent expression of excitatory designer receptors exclusively activated by designer drugs (DREADDs). Before behavioral testing, clozapine-N-oxide (CNO), the selective agonist of our DREADD, was infused directly into the BNST. We found that after specific activation of LPBn PACAP afferents in the BNST, mice had increased anxiety-like behavior compared with controls, while total locomotor activity was unaffected. These results indicate that activation of PACAPergic LPBn projections to the BNST may play an important role in producing anxiety-like behavior.
引用
收藏
页码:451 / 458
页数:8
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