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肥大细胞脱粒化合物 48/80 直接激活神经元。

The mast cell degranulator compound 48/80 directly activates neurons.

机构信息

Human Biology, Technische Universität München, Freising, Germany.

出版信息

PLoS One. 2012;7(12):e52104. doi: 10.1371/journal.pone.0052104. Epub 2012 Dec 18.

Abstract

BACKGROUND

Compound 48/80 is widely used in animal and tissue models as a "selective" mast cell activator. With this study we demonstrate that compound 48/80 also directly activates enteric neurons and visceral afferents.

METHODOLOGY/PRINCIPAL FINDINGS: We used in vivo recordings from extrinsic intestinal afferents together with Ca(++) imaging from primary cultures of DRG and nodose neurons. Enteric neuronal activation was examined by Ca(++) and voltage sensitive dye imaging in isolated gut preparations and primary cultures of enteric neurons. Intraluminal application of compound 48/80 evoked marked afferent firing which desensitized on subsequent administration. In egg albumen-sensitized animals, intraluminal antigen evoked a similar pattern of afferent activation which also desensitized on subsequent exposure to antigen. In cross-desensitization experiments prior administration of compound 48/80 failed to influence the mast cell mediated response. Application of 1 and 10 µg/ml compound 48/80 evoked spike discharge and Ca(++) transients in enteric neurons. The same nerve activating effect was observed in primary cultures of DRG and nodose ganglion cells. Enteric neuron cultures were devoid of mast cells confirmed by negative staining for c-kit or toluidine blue. In addition, in cultured enteric neurons the excitatory action of compound 48/80 was preserved in the presence of histamine H(1) and H(2) antagonists. The mast cell stabilizer cromolyn attenuated compound 48/80 and nicotine evoked Ca(++) transients in mast cell-free enteric neuron cultures.

CONCLUSIONS/SIGNIFICANCE: The results showed direct excitatory action of compound 48/80 on enteric neurons and visceral afferents. Therefore, functional changes measured in tissue or animal models may involve a mast cell independent effect of compound 48/80 and cromolyn.

摘要

背景

化合物 48/80 广泛应用于动物和组织模型中,作为一种“选择性”肥大细胞激活剂。通过这项研究,我们证明化合物 48/80 也可以直接激活肠神经元和内脏传入纤维。

方法/主要发现:我们使用来自外在肠传入纤维的体内记录,以及来自 DRG 和结状神经节神经元原代培养的 Ca(++)成像。通过在分离的肠道制剂和肠神经元原代培养物中的 Ca(++)和电压敏感染料成像来检查肠神经元的激活。腔内给予化合物 48/80 可诱发明显的传入纤维放电,随后给予可使其脱敏。在卵白蛋白致敏动物中,腔内抗原引起类似的传入纤维激活模式,随后再次暴露于抗原也可使其脱敏。在交叉脱敏实验中,预先给予化合物 48/80 并不能影响肥大细胞介导的反应。给予 1 和 10 µg/ml 的化合物 48/80 可诱发肠神经元的锋电位放电和 Ca(++)瞬变。在 DRG 和结状神经节神经元的原代培养中观察到相同的神经激活作用。肠神经元培养物中缺乏肥大细胞,通过 c-kit 或甲苯胺蓝的阴性染色证实。此外,在培养的肠神经元中,化合物 48/80 的兴奋作用在组胺 H(1)和 H(2)拮抗剂存在的情况下得以保留。肥大细胞稳定剂色甘酸钠可减弱化合物 48/80 和烟碱诱发的无肥大细胞的肠神经元培养物中的 Ca(++)瞬变。

结论/意义:结果表明化合物 48/80 对肠神经元和内脏传入纤维有直接的兴奋作用。因此,在组织或动物模型中测量的功能变化可能涉及化合物 48/80 和色甘酸钠的肥大细胞独立作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/338b/3525567/81f29284c37f/pone.0052104.g001.jpg

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