Immunohistochemical determination of the excitatory and inhibitory axonal endings contacting NUCB2/nesfatin-1 neurons

IF 2.5 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM Neuropeptides Pub Date : 2023-12-25 DOI:10.1016/j.npep.2023.102401
Aynura Aghayeva, Duygu Gok Yurtseven, Nursel Hasanoglu Akbulut, Ozhan Eyigor
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Abstract

Nesfatin-1 is an anorexigenic peptide suppressing food intake and is synthesized and secreted by neurons located in the hypothalamus. Our study was aimed to demonstrate the effect of excitatory and inhibitory neurotransmitters on NUCB2/nesfatin-1 neurons. In this context, dual peroxidase immunohistochemistry staining was performed using NUCB2/nesfatin-1 primary antibody with each of the primary antibodies of vesicular transporter proteins applied as markers for neurons using glutamate, acetylcholine, and GABA as neurotransmitters. In double labeling applied on floating sections, the NUCB2/nesfatin-1 reaction was determined in brown color with diaminobenzidine, while vesicular carrier proteins were marked in black. Slides were analyzed to determine the ratio of nesfatin-1 neurons in the three hypothalamic nucleus in contact with a relevant vesicular carrier protein. The ratios of NUCB2/nesfatin-1 neurons with the innervation were compared among neurotransmitters. In addition, possible gender differences between males and females were examined. The difference in the number of VGLUT2-contacting NUCB2/nesfatin-1 neurons was significantly higher in males when compared to females. When both genders were compared in different nuclei, it was seen that there was no statistical significance in terms of the percentage of NUCB2/nesfatin-1 neuron apposition with VGLUT3. The statistical evaluation showed that number of NUCB2/nesfatin-1 neurons receiving GABAergic innervation is higher in males when compared to females (*p ≤ 0.05; p = 0.045). When the axonal contact of vesicular neurotransmitter transporter proteins was compared between the neurotransmitters, it was determined that the most prominent innervation is GABAergic. In the supraoptic region, no contacts of VAChT-containing axons were found on NUCB2/nesfatin-1 neurons in both female and male subjects. In conclusion, it is understood that both excitatory and inhibitory neurons can innervate the NUCB2/nesfatin-1 neurons and the glutamatergic system is effective in the excitatory innervation while the GABAergic system plays a role in the inhibitory mechanism.

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免疫组化法测定与 NUCB2/nesfatin-1 神经元接触的兴奋性和抑制性轴突末梢
Nesfatin-1 是一种抑制食物摄入的厌食肽,由位于下丘脑的神经元合成和分泌。我们的研究旨在证明兴奋性和抑制性神经递质对内司蛋白-1神经元的影响。在这种情况下,我们使用nesfatin-1一抗与囊泡转运蛋白一抗进行了双过氧化物酶免疫组化染色,将谷氨酸、乙酰胆碱和GABA作为神经递质标记神经元。在对浮动切片进行双重标记时,用二氨基联苯胺将内司法亭-1反应标记为棕色,而将囊泡载体蛋白标记为黑色。对切片进行分析,以确定与相关囊泡载体蛋白接触的三个下丘脑核中内司法亭-1神经元的比例。比较了神经递质与神经支配的nesfatin-1神经元比例。此外,还研究了男性和女性之间可能存在的性别差异。与VGLUT2-接触的nesfatin-1神经元数量男性明显高于女性。在比较不同细胞核中的男女性别时,发现nesfatin-1神经元与VGLUT3贴附的百分比没有统计学意义。统计评估表明,男性接受 GABA 能支配的 nesfatin-1 神经元数量高于女性(*p ≤ 0.05; p = 0.045)。当比较不同神经递质的囊泡神经递质转运蛋白的轴突接触时,发现最主要的神经递质是 GABA 能。在视交叉上区,男女受试者均未发现含有 VAChT 的轴突与 nesfatin-1 神经元接触。总之,兴奋性和抑制性神经元均可支配 nesfatin-1 神经元,谷氨酸能系统对兴奋性神经元的支配有效,而 GABA 能系统则在抑制机制中发挥作用。
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来源期刊
Neuropeptides
Neuropeptides 医学-内分泌学与代谢
CiteScore
5.40
自引率
6.90%
发文量
55
审稿时长
>12 weeks
期刊介绍: The aim of Neuropeptides is the rapid publication of original research and review articles, dealing with the structure, distribution, actions and functions of peptides in the central and peripheral nervous systems. The explosion of research activity in this field has led to the identification of numerous naturally occurring endogenous peptides which act as neurotransmitters, neuromodulators, or trophic factors, to mediate nervous system functions. Increasing numbers of non-peptide ligands of neuropeptide receptors have been developed, which act as agonists or antagonists in peptidergic systems. The journal provides a unique opportunity of integrating the many disciplines involved in all neuropeptide research. The journal publishes articles on all aspects of the neuropeptide field, with particular emphasis on gene regulation of peptide expression, peptide receptor subtypes, transgenic and knockout mice with mutations in genes for neuropeptides and peptide receptors, neuroanatomy, physiology, behaviour, neurotrophic factors, preclinical drug evaluation, clinical studies, and clinical trials.
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