de Queiroz D B, Sastre E, Caracuel L, Callejo M, Xavier F E, Blanco-Rivero J, Balfagón G
Departamento de Fisiologia e Farmacologia, Universidade Federal de Pernambuco, Recife, Brazil.
Departamento de Fisiología, Facultad de Medicina, Universidad Autónoma de Madrid, Madrid, Spain.
Br J Pharmacol. 2015 Oct;172(19):4699-713. doi: 10.1111/bph.13244. Epub 2015 Aug 14.
We have reported that exposure to a diabetic intrauterine environment during pregnancy increases blood pressure in adult offspring, but the mechanisms involved are not completely understood. This study was designed to analyse a possible role of perivascular sympathetic and nitrergic innervation in the superior mesenteric artery (SMA) in this effect.
Diabetes was induced in pregnant Wistar rats by a single injection of streptozotocin. Endothelium-denuded vascular rings from the offspring of control (O-CR) and diabetic rats (O-DR) were used. Vasomotor responses to electrical field stimulation (EFS), NA and the NO donor DEA-NO were studied. The expressions of neuronal NOS (nNOS) and phospho-nNOS (P-nNOS) and release of NA, ATP and NO were determined. Sympathetic and nitrergic nerve densities were analysed by immunofluorescence.
Blood pressure was higher in O-DR animals. EFS-induced vasoconstriction was greater in O-DR animals. This response was decreased by phentolamine more in O-DR animals than their controls. L-NAME increased EFS-induced vasoconstriction more strongly in O-DR than in O-CR segments. Vasomotor responses to NA or DEA-NO were not modified. NA, ATP and NO release was increased in segments from O-DR. nNOS expression was not modified, whereas P-nNOS expression was increased in O-DR. Sympathetic and nitrergic nerve densities were similar in both experimental groups.
The activity of sympathetic and nitrergic innervation is increased in SMA from O-DR animals. The net effect is an increase in EFS-induced contractions in these animals. These effects may contribute to the increased blood pressure observed in the offspring of diabetic rats.
我们曾报道,孕期暴露于糖尿病子宫内环境会使成年子代血压升高,但其涉及的机制尚未完全明确。本研究旨在分析肠系膜上动脉(SMA)周围血管交感神经和一氧化氮能神经支配在此效应中可能发挥的作用。
通过单次注射链脲佐菌素诱导怀孕的Wistar大鼠患糖尿病。使用来自对照大鼠子代(O-CR)和糖尿病大鼠子代(O-DR)的去内皮血管环。研究了血管对电场刺激(EFS)、去甲肾上腺素(NA)和一氧化氮供体DEA-NO的血管舒缩反应。测定了神经元型一氧化氮合酶(nNOS)和磷酸化nNOS(P-nNOS)的表达以及NA、三磷酸腺苷(ATP)和一氧化氮(NO)的释放。通过免疫荧光分析交感神经和一氧化氮能神经密度。
O-DR动物的血压更高。O-DR动物中EFS诱导的血管收缩更强。酚妥拉明对这种反应的抑制在O-DR动物中比其对照组更明显。L- NAME在O-DR中比在O-CR节段更强烈地增强了EFS诱导的血管收缩。对NA或DEA-NO的血管舒缩反应未改变。O-DR节段中NA、ATP和NO的释放增加。nNOS表达未改变,而O-DR中P-nNOS表达增加。两个实验组的交感神经和一氧化氮能神经密度相似。
O-DR动物的SMA中交感神经和一氧化氮能神经支配的活性增加。其净效应是这些动物中EFS诱导的收缩增加。这些效应可能导致糖尿病大鼠子代血压升高。