Stimulation of lateral parabrachial (LPB) to central amygdala (CeA) pituitary adenylate cyclase-activating polypeptide (PACAP) neurons induces anxiety-like behavior and mechanical allodynia

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES Pharmacology Biochemistry and Behavior Pub Date : 2023-09-01 DOI:10.1016/j.pbb.2023.173605
Mariel P. Seiglie , Lauren Lepeak , Sophia Miracle, Pietro Cottone, Valentina Sabino
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Abstract

Background

Anxiety disorders are the most prevalent psychiatric disorders, and they are highly comorbid with chronic pain conditions. The central nucleus of the amygdala (CeA) is known not only for its role in the regulation of anxiety but also as an important site for the negative affective dimension of pain. Pituitary adenylate cyclase activating polypeptide (PACAP), a neuropeptide whose terminals are abundant in the CeA, is strongly implicated in the stress response as well as in pain processing. Here, using Cre-dependent viral vectors, we explored in greater detail the role of the PACAP projection to the CeA that originates in the lateral parabrachial nucleus (LPB).

Methods

We first performed a circuit mapping experiment by injecting an anterograde Cre-dependent virus expressing a fluorescent reporter in the LPB of PACAP-Cre mice and observing their projections. Then, we used a chemogenetic approach (a Cre-dependent Designer Receptors Activated by Designer Drugs, DREADDs) to assess the effects of the direct stimulation of the PACAP LPB to CeA projection on general locomotor activity, anxiety-like behavior (using a defensive withdrawal test), and mechanical pain sensitivity (using the von Frey test).

Results

We found that the CeA, together with other areas, is one of the major downstream projection targets of PACAP neurons originating in the lateral parabrachial nucleus (LPB). In the DREADD experiment, we then found that the selective activation of this neuronal pathway is sufficient to increase both anxiety-like behavior and mechanical pain sensitivity in mice, without affecting general locomotor activity.

Conclusion

In conclusion, our data suggest that the dysregulation of this circuit may contribute to a variety of anxiety disorders and chronic pain states, and that PACAP may represent an important therapeutic target for the treatment of these conditions.

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臂旁外侧(LPB)对中央杏仁核(CeA)、垂体腺苷酸环化酶激活多肽(PACAP)神经元的刺激可诱导焦虑样行为和机械性异常性疼痛。
背景:焦虑症是最常见的精神疾病,与慢性疼痛有高度的共病性。杏仁核中央核(CeA)不仅因其在焦虑调节中的作用而闻名,而且也是疼痛负面情感维度的重要部位。垂体腺苷酸环化酶激活多肽(PACAP)是一种末端在CeA中丰富的神经肽,与应激反应和疼痛处理密切相关。在这里,使用Cre依赖性病毒载体,我们更详细地探索了PACAP向源自臂旁外侧核(LPB)的CeA的投射的作用。然后,我们使用化学遗传学方法(一种由设计药物激活的Cre依赖性设计受体,DREADDs)来评估PACAP LPB对CeA投射的直接刺激对一般运动活动、焦虑样行为(使用防御性戒断测试)和机械疼痛敏感性(使用von Frey测试)的影响。结果:我们发现,其与其他区域一起是起源于臂旁外侧核(LPB)的PACAP神经元的主要下游投射靶点之一。在DREADD实验中,我们发现这种神经元通路的选择性激活足以增加小鼠的焦虑样行为和机械疼痛敏感性,而不会影响一般的运动活动。结论:总之,我们的数据表明,该回路的失调可能导致各种焦虑症和慢性疼痛状态,PACAP可能是治疗这些疾病的重要治疗靶点。
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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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