纹状体多巴胺组胺调节中的性别差异。

Sex differences in histamine regulation of striatal dopamine.

作者信息

Van Zandt Meghan, Pittenger Christopher

机构信息

Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA, 06519.

Yale Child Study Center, Yale University School of Medicine, New Haven, CT, USA, 06519.

出版信息

J Neurosci. 2025 May 12. doi: 10.1523/JNEUROSCI.2182-24.2025.

Abstract

Dopamine modulation of the basal ganglia differs in males and females and is implicated in numerous neuropsychiatric conditions, including some, like Tourette Syndrome (TS) and attention deficit hyperactivity disorder (ADHD), that have marked sex differences in prevalence. Genetic studies in TS and subsequent work in animals suggest that a loss of histamine may contribute to dysregulation of dopamine. Motivated by this, we characterized the modulation of striatal dopamine by histamine, using microdialysis, targeted pharmacology, and shRNA knockdown of histamine receptors. Intracerebroventricular (ICV) histamine reduced striatal dopamine in male mice, replicating previous work. In contrast, and unexpectedly, ICV histamine increased striatal dopamine in females. ICV or targeted infusion of agonists revealed that the effect in males depends on H2R receptors in the substantia nigra pars compacta (SNc). Knockdown of H2R in SNc GABAergic neurons abrogated the effect, identifying these cells as a key locus of histamine's regulation of dopamine in males. In females, however, H2R had no discernible role; instead, H3R agonists in the striatum increased striatal dopamine. Strikingly, the effect of histamine on dopamine in females was modulated by the estrous cycle, appearing only in estrus/proestrus, when estrogen levels are high. These findings confirm the regulation of striatal dopamine by histamine but identify marked sexual differences in and estrous modulation of this effect. These findings may shed light on the mechanistic underpinnings of sex differences in the striatal circuitry, and in several neuropsychiatric conditions. Dysregulation of the basal ganglia contributes to the pathophysiology of numerous neuropsychiatric diseases, including several, such as Tourette syndrome (TS), that are characterized by sex differences. Previous genetic studies in humans identified histamine dysregulation as a potential to the development of TS; follow-up work in mice highlighted the role of histamine in regulating striatal dopamine tone. Striatal dopamine dysregulation has been implicated in numerous neuropsychiatric disorders, including TS, schizophrenia, and attention deficit-hyperactivity disorder. Here, we uncover novel and significant sex differences in histamine regulation of dopaminergic modulation of the striatum. A better understanding of these differences may provide insight into the mechanisms underlying sex-dependent outcomes in neuropsychiatric disease.

摘要

多巴胺对基底神经节的调节在雄性和雌性中存在差异,并且与多种神经精神疾病有关,包括一些如妥瑞氏症(TS)和注意力缺陷多动障碍(ADHD)等在患病率上有明显性别差异的疾病。对TS的遗传学研究以及随后在动物身上开展的工作表明,组胺的缺失可能导致多巴胺调节失调。受此启发,我们利用微透析、靶向药理学以及组胺受体的短发夹RNA敲低技术,对组胺对纹状体多巴胺的调节作用进行了表征。脑室内(ICV)注射组胺可降低雄性小鼠纹状体中的多巴胺水平,这与之前的研究结果一致。然而,出乎意料的是,ICV注射组胺却增加了雌性小鼠纹状体中的多巴胺水平。ICV注射或靶向注射激动剂表明,雄性小鼠中的这种作用取决于黑质致密部(SNc)中的H2R受体。敲低SNc中GABA能神经元的H2R可消除这种作用,表明这些细胞是组胺在雄性中调节多巴胺的关键位点。然而,在雌性小鼠中,H2R没有明显作用;相反,纹状体中的H3R激动剂可增加纹状体多巴胺水平。引人注目的是,组胺对雌性小鼠多巴胺的作用受发情周期调节,仅在雌激素水平较高的发情期/发情前期出现。这些发现证实了组胺对纹状体多巴胺的调节作用,但也确定了这种作用在性别上的显著差异以及发情周期的调节作用。这些发现可能有助于揭示纹状体神经回路以及几种神经精神疾病中性别差异的机制基础。基底神经节的调节失调会导致多种神经精神疾病的病理生理过程,包括一些如妥瑞氏症(TS)等具有性别差异特征的疾病。先前在人类中的遗传学研究确定组胺调节失调是TS发病的一个潜在因素;后续在小鼠中的研究突出了组胺在调节纹状体多巴胺张力中的作用。纹状体多巴胺调节失调与多种神经精神疾病有关,包括TS、精神分裂症和注意力缺陷多动障碍。在这里,我们发现了组胺对纹状体多巴胺能调节的新颖且显著的性别差异。更好地理解这些差异可能有助于深入了解神经精神疾病中性别依赖性结果的潜在机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索