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大鼠离体输精管中 6-氰基多巴胺的基础释放及其对组织收缩性的作用。

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

机构信息

Department of Pharmacology, Faculty of Medical Sciences, State University of Campinas (UNICAMP), Campinas, Brazil.

Department of Surgery, Faculty of Medicine of Jundiaí, Jundiaí, Brazil.

出版信息

Pflugers Arch. 2024 Aug;476(8):1263-1277. doi: 10.1007/s00424-024-02985-2. Epub 2024 Jul 4.

Abstract

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.

摘要

6- 氰基多巴胺是一种从兔离体心脏释放的新型儿茶酚胺。然而,目前尚不清楚这种儿茶酚胺是否具有任何生物学活性。在这里,评估了 6- 氰基多巴胺(6-CYD)是否从大鼠输精管中释放出来及其对该组织收缩性的影响。通过 LC-MS/MS 定量测定了输精管中 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。在不存在和存在 6-CYD 和/或 6-ND 的情况下,对大鼠离体附睾输精管(RIEVD)进行了去甲肾上腺素、肾上腺素和多巴胺的电场刺激(EFS)和浓度反应曲线。通过免疫组织化学评估酪氨酸羟化酶的表达。大鼠离体输精管释放大量的 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,但实际上完全阻断了 6-ND 的释放。6-CYD 本身表现出微不足道的 RIEVD 收缩活性;然而,在 10 nM 时,6-CYD 显著增强了去甲肾上腺素和 EFS 诱导的 RIEVD 收缩,而在 10 和 100 nM 时,它还显著增强了肾上腺素和多巴胺诱导的收缩。6-CYD 对去甲肾上腺素和肾上腺素诱导的收缩的增强作用不受河豚毒素的影响。6-CYD(100 pM)与 6-ND(10 pM)共孵育导致去甲肾上腺素的显著左移,并增加了最大收缩反应,即使在存在河豚毒素的情况下也是如此。免疫组织化学显示,RIEVD 的黏膜上皮细胞细胞质和神经纤维中均存在酪氨酸羟化酶。上皮细胞衍生的 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性。

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