大鼠离体输精管 6-氰基多巴胺的基础释放及其对组织收缩力的作用

IF 2.9 4区 医学 Q2 PHYSIOLOGY
Caroline Fernanda Sanches Dal Pozzo, Jose Eduardo Maldonado Junior, José Britto-Júnior, João Felipe Agostini Badin, Valéria Barbosa de Souza, André Almeida Schenka, Larryn W Peterson, Adriano Fregonesi, Edson Antunes, Gilberto De Nucci
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引用次数: 0

摘要

6-氰基多巴胺是从兔离体心脏中释放出的一种新型儿茶酚胺。然而,这种儿茶酚胺是否具有生物活性尚不清楚。在此,研究人员对大鼠输精管是否释放 6-氰基多巴胺(6-CYD)及其对该组织收缩力的影响进行了评估。通过 LC-MS/MS,对输精管中 6-CYD、6-硝基多巴胺(6-ND)、6-溴多巴胺、6-硝基多巴和 6-硝基肾上腺素的基础释放量进行了量化。在 6-CYD 和/或 6-ND 不存在和存在的情况下,对大鼠离体附睾输精管(RIEVD)进行了电场刺激(EFS)并绘制了去甲肾上腺素、肾上腺素和多巴胺的浓度反应曲线。酪氨酸羟化酶的表达通过免疫组化进行评估。大鼠离体输精管释放了大量 6-CYD 和 6-ND。电压门控钠离子通道阻断剂河豚毒素对 6-CYD 的释放没有影响,但几乎消除了 6-ND 的释放。单独使用 6-CYD 时,其 RIEVD 收缩活性可忽略不计;但在 10 nM 时,6-CYD 可显著增强去甲肾上腺素和 EFS 诱导的 RIEVD 收缩,而在 10 nM 和 100 nM 时,它还可显著增强肾上腺素和多巴胺诱导的收缩。河豚毒素不会影响 6-CYD 对去甲肾上腺素和肾上腺素诱导的收缩的增效作用。将 6-CYD(100 pM)与 6-ND(10 pM)共孵育会引起明显的左移,并增加对去甲肾上腺素的最大收缩反应,即使在河豚毒素存在的情况下也是如此。免疫组化显示,RIEVD 的粘膜上皮细胞胞浆和神经纤维中都存在酪氨酸羟化酶。上皮源性 6-CYD 的鉴定及其与儿茶酚胺的显著协同作用表明,上皮细胞可能调节输精管平滑肌的收缩力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Basal release of 6-cyanodopamine from rat isolated vas deferens and its role on the tissue contractility.

Basal release of 6-cyanodopamine from rat isolated vas deferens and its role on the tissue contractility.

6-Cyanodopamine is a novel catecholamine released from rabbit isolated heart. However, it is not known whether this catecholamine presents any biological activity. Here, it was evaluated whether 6-cyanodopamine (6-CYD) is released from rat vas deferens and its effect on this tissue contractility. Basal release of 6-CYD, 6-nitrodopamine (6-ND), 6-bromodopamine, 6-nitrodopa, and 6-nitroadrenaline from vas deferens were quantified by LC-MS/MS. Electric-field stimulation (EFS) and concentration-response curves to noradrenaline, adrenaline, and dopamine of the rat isolated epididymal vas deferens (RIEVD) were performed in the absence and presence of 6-CYD and /or 6-ND. Expression of tyrosine hydroxylase was assessed by immunohistochemistry. The rat isolated vas deferens released significant amounts of both 6-CYD and 6-ND. The voltage-gated sodium channel blocker tetrodotoxin had no effect on the release of 6-CYD, but it virtually abolished 6-ND release. 6-CYD alone exhibited a negligible RIEVD contractile activity; however, at 10 nM, 6-CYD significantly potentiated the noradrenaline- and EFS-induced RIEVD contractions, whereas at 10 and 100 nM, it also significantly potentiated the adrenaline- and dopamine-induced contractions. The potentiation of noradrenaline- and adrenaline-induced contractions by 6-CYD was unaffected by tetrodotoxin. Co-incubation of 6-CYD (100 pM) with 6-ND (10 pM) caused a significant leftward shift and increased the maximal contractile responses to noradrenaline, even in the presence of tetrodotoxin. Immunohistochemistry revealed the presence of tyrosine hydroxylase in both epithelial cell cytoplasm of the mucosae and nerve fibers of RIEVD. The identification of epithelium-derived 6-CYD and its remarkable synergism with catecholamines indicate that epithelial cells may regulate vas deferens smooth muscle contractility.

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来源期刊
CiteScore
8.80
自引率
2.20%
发文量
121
审稿时长
4-8 weeks
期刊介绍: Pflügers Archiv European Journal of Physiology publishes those results of original research that are seen as advancing the physiological sciences, especially those providing mechanistic insights into physiological functions at the molecular and cellular level, and clearly conveying a physiological message. Submissions are encouraged that deal with the evaluation of molecular and cellular mechanisms of disease, ideally resulting in translational research. Purely descriptive papers covering applied physiology or clinical papers will be excluded. Papers on methodological topics will be considered if they contribute to the development of novel tools for further investigation of (patho)physiological mechanisms.
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