Region-specific activation in the accumbens nucleus by itch with modified scratch efficacy in mice - a model-free multivariate analysis.

IF 3.3 3区 医学 Q2 NEUROSCIENCES Molecular Brain Pub Date : 2024-05-23 DOI:10.1186/s13041-024-01101-w
Sanae Inokuchi-Sakata, Ryo Narita, Yukari Takahashi, Yozo Ishiuji, Akihiko Asahina, Fusao Kato
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Abstract

Itch is a protective/defensive function with divalent motivational drives. Itch itself elicits an unpleasant experience, which triggers the urge to scratch, relieving the itchiness. Still, it can also result in dissatisfaction when the scratch is too intense and painful or unsatisfactory due to insufficient scratch effect. Therefore, it is likely that the balance between the unpleasantness/pleasure and satisfaction/unsatisfaction associated with itch sensation and scratching behavior is determined by complex brain mechanisms. The physiological/pathological mechanisms underlying this balance remain largely elusive. To address this issue, we targeted the "reward center" of the brain, the nucleus accumbens (NAc), in which itch-responsive neurons have been found in rodents. We examined how neurons in the NAc are activated or suppressed during histamine-induced scratching behaviors in mice. The mice received an intradermal injection of histamine or saline at the neck, and the scratching number was analyzed by recording the movement of the bilateral hind limbs for about 45 min after injection. To experimentally manipulate the scratch efficacy in these histamine models, we compared histamine's behavioral and neuronal effects between mice with intact and clipped nails on the hind paws. As expected, the clipping of the hind limb nail increased the number of scratches after the histamine injection. In the brains of mice exhibiting scratching behaviors, we analyzed the expression of the c-fos gene (Fos) as a readout of an immediate activation of neurons during itch/scratch and dopamine receptors (Drd1 and Drd2) using multiplex single-molecule fluorescence in situ hybridization (RNAscope) in the NAc and surrounding structures. We performed a model-free analysis of gene expression in geometrically divided NAc subregions without assuming the conventional core-shell divisions. The results indicated that even within the NAc, multiple subregions responded differentially to various itch/scratch conditions. We also found different clusters with neurons showing similar or opposite changes in Fos expression and the correlation between scratch number and Fos expression in different itch/scratch conditions. These regional differences and clusters would provide a basis for the complex role of the NAc and surrounding structures in encoding the outcomes of scratching behavior and itchy sensations.

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小鼠因痒而激活的凹凸核区域特异性改变--一种无模型多变量分析。
痒是一种具有二重动机驱动的保护/防御功能。痒本身会引起不愉快的体验,从而引发抓挠的冲动,缓解痒感。然而,当抓挠过于剧烈和痛苦,或因抓挠效果不够理想时,也会导致不满。因此,与痒感和搔抓行为相关的不快感/快感和满足感/不满足感之间的平衡很可能是由复杂的大脑机制决定的。这种平衡的生理/病理机制在很大程度上仍然难以捉摸。为了解决这个问题,我们以大脑的 "奖赏中心"--啮齿类动物的痒反应神经元所在的阿肯伯氏核(NAc)为研究对象。我们研究了在组胺诱导的小鼠抓挠行为中,NAc 中的神经元是如何被激活或抑制的。小鼠颈部皮内注射组胺或生理盐水,注射后约45分钟记录双侧后肢的运动,分析抓挠次数。为了在实验中操纵这些组胺模型的抓挠效果,我们比较了组胺对后爪指甲完整和指甲被剪的小鼠的行为和神经元影响。不出所料,在注射组胺后,剪掉后肢指甲会增加抓痕的数量。在有抓挠行为的小鼠大脑中,我们使用多重单分子荧光原位杂交技术(RNAscope)分析了NAc和周围结构中c-fos基因(Fos)和多巴胺受体(Drd1和Drd2)的表达情况,前者是痒/抓挠过程中神经元立即激活的读数。我们对按几何形状划分的 NAc 亚区的基因表达进行了无模型分析,而没有假设传统的核心-外壳划分。结果表明,即使在 NAc 中,多个亚区也会对各种痒/抓痕条件做出不同的反应。我们还发现,在不同的痒/抓条件下,神经元集群的Fos表达和抓痕数量与Fos表达之间的相关性变化相似或相反。这些区域差异和集群将为 NAc 及其周围结构在编码抓挠行为和痒感结果中的复杂作用提供依据。
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来源期刊
Molecular Brain
Molecular Brain NEUROSCIENCES-
CiteScore
7.30
自引率
0.00%
发文量
97
审稿时长
>12 weeks
期刊介绍: Molecular Brain is an open access, peer-reviewed journal that considers manuscripts on all aspects of studies on the nervous system at the molecular, cellular, and systems level providing a forum for scientists to communicate their findings. Molecular brain research is a rapidly expanding research field in which integrative approaches at the genetic, molecular, cellular and synaptic levels yield key information about the physiological and pathological brain. These studies involve the use of a wide range of modern techniques in molecular biology, genomics, proteomics, imaging and electrophysiology.
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