Activation of 5-HT7 receptors in the mouse dentate gyrus does not affect theta-burst-induced plasticity at the perforant path synapse.

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacological Reports Pub Date : 2024-12-01 Epub Date: 2024-11-02 DOI:10.1007/s43440-024-00674-6
Marcin Siwiec, Bartosz Bobula, Michal Kielbinski, Nikola Multan, Grzegorz Hess, Krzysztof Tokarski
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Abstract

Background: The study examined the effects of 5-HT7 receptor activation on GABAergic transmission within the dentate gyrus and plasticity at the glutamatergic perforant path input.

Methods: Immunofluorescence imaging was performed using transverse hippocampal slices from transgenic mice expressing green fluorescent protein (GFP) under the Htr7 promoter. This was followed by whole-cell patch clamp electrophysiological recordings assessing the effects of pharmacologically activating 5-HT7 receptors on spontaneous inhibitory postsynaptic currents recorded from dentate granule cells and hilar mossy cells-two glutamatergic neuron types present in the dentate gyrus. Extracellular recordings of field excitatory postsynaptic potentials were then performed to assess whether 5-HT7 receptor activation influenced theta-burst stimulation-evoked plasticity of the perforant path synaptic input.

Results: It was found that parvalbumin and somatostatin interneurons in the dentate gyrus expressed GFP, which suggests they express 5-HT7 receptors. However, activation of 5-HT7 receptors had no effect on GABAergic transmission targeting mossy cells or granule cells. There was also no effect of 5-HT7 receptor activation on perforant path plasticity either with intact or blocked GABAA receptor signaling.

Conclusion: The presence of 5-HT7 receptors in a subset of parvalbumin and somatostatin interneurons in the mouse dentate gyrus could mean that they are involved in the inhibitory control of dentate gyrus activity. However, this potential effect was not evident in slice recordings of inhibitory transmission targeting principal cells and did not affect perforant path plasticity. Further experiments are needed to fully elucidate the functional role of these receptors in the dentate gyrus.

激活小鼠齿状回中的5-HT7受体不会影响θ-脉冲诱导的穿孔路径突触可塑性。
背景:该研究考察了5-HT7受体激活对齿状回内GABA能传导和谷氨酸能穿孔路径输入可塑性的影响:本研究探讨了 5-HT7 受体激活对齿状回内 GABA 能传导和谷氨酸能穿孔路径输入可塑性的影响:方法:使用在Htr7启动子下表达绿色荧光蛋白(GFP)的转基因小鼠的横向海马切片进行免疫荧光成像。随后进行了全细胞膜片钳电生理记录,评估药理激活 5-HT7 受体对自发抑制性突触后电流的影响。然后进行了场兴奋突触后电位的细胞外记录,以评估 5-HT7 受体的激活是否会影响θ-脉冲刺激诱发的穿孔路径突触输入的可塑性:结果:研究发现,齿状回中的parvalbumin和somatostatin中间神经元表达GFP,这表明它们表达5-HT7受体。然而,激活 5-HT7 受体对以苔藓细胞或颗粒细胞为目标的 GABA 能传导没有影响。5-HT7受体激活对穿孔路径的可塑性也没有影响,无论是在GABAA受体信号完整还是受阻的情况下:结论:5-HT7 受体存在于小鼠齿状回的副发光体和体视蛋白中间神经元亚群中,这可能意味着它们参与了对齿状回活动的抑制性控制。然而,这种潜在的影响在以主细胞为目标的抑制性传导的切片记录中并不明显,也不影响穿孔路径的可塑性。要全面阐明这些受体在齿状回中的功能作用,还需要进一步的实验。
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来源期刊
Pharmacological Reports
Pharmacological Reports 医学-药学
CiteScore
8.40
自引率
0.00%
发文量
91
审稿时长
6 months
期刊介绍: Pharmacological Reports publishes articles concerning all aspects of pharmacology, dealing with the action of drugs at a cellular and molecular level, and papers on the relationship between molecular structure and biological activity as well as reports on compounds with well-defined chemical structures. Pharmacological Reports is an open forum to disseminate recent developments in: pharmacology, behavioural brain research, evidence-based complementary biochemical pharmacology, medicinal chemistry and biochemistry, drug discovery, neuro-psychopharmacology and biological psychiatry, neuroscience and neuropharmacology, cellular and molecular neuroscience, molecular biology, cell biology, toxicology. Studies of plant extracts are not suitable for Pharmacological Reports.
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