Laboratory of Pharmacology, Marília Medical School, Av. Monte Carmelo, 800, Fragata, Marília, São Paulo 17 519-030, Brazil.
Laboratory of Human Embryology, Marília Medical School, Av. Monte Carmelo, 800, Fragata, Marília, São Paulo 17 519-030, Brazil.
J Smooth Muscle Res. 2022;58(0):63-77. doi: 10.1540/jsmr.58.63.
This study aimed to verify whether Adjuvant-Induced Arthritis (AIA) and/or Orchiectomy (ORX) modify the expression of the Nox1, Nox2 and Nox4 isoforms, the endothelial function or the structure of rat aortas.
Sixty-three Wistar rats were distributed into four groups: 1) Control; 2) ORX; 3) AIA; 4) Orchiectomy plus to Arthritis-induction (ORX/AIA). Thus, 21 days after the onset of AIA (by intradermal injection of Mycobacterium tuberculosis), the presence of Nox1, Nox2 and Nox4, the acetylcholine (ACh)-induced relaxation and the media layer thickness were assessed in the aorta taken from these animals.
The Nox1, Nox2 and Nox4 were immunostained in intima, media and adventitia layers of aortas taken from all studied groups and AIA apparently increased this immunostaining. These modifications of Nox1, Nox2 or Nox4 expression, however, were not confirmed by Western blotting. In addition, neither AIA nor ORX changed the endothelial function, but ORX increased the media layer thickness in the studied aortas.
The present study showed weak clues of increased expression of Nox1, Nox2 and Nox4 as a result of AIA, as well as of Nox1 reduction caused by ORX. In addition, the endothelial function was not modified in the aortas of these animals by both AIA and/or ORX. On the other hand, ORX increased significantly the aorta media layer thickness in the studied animals, which was apparently mitigated by AIA.
本研究旨在验证佐剂诱导关节炎(AIA)和/或睾丸切除术(ORX)是否改变 Nox1、Nox2 和 Nox4 同工型的表达、内皮功能或大鼠主动脉的结构。
63 只 Wistar 大鼠分为 4 组:1)对照组;2)ORX 组;3)AIA 组;4)关节炎诱导加去势(ORX/AIA)组。因此,在 AIA 发病 21 天后(通过皮内注射结核分枝杆菌),评估这些动物主动脉中 Nox1、Nox2 和 Nox4 的存在、乙酰胆碱(ACh)诱导的松弛和中膜层厚度。
Nox1、Nox2 和 Nox4 在所有研究组的主动脉内膜、中膜和外膜层均有免疫染色,AIA 明显增加了这种免疫染色。然而,Western blot 并未证实 Nox1、Nox2 或 Nox4 表达的这些改变。此外,AIA 或 ORX 均未改变内皮功能,但 ORX 增加了研究主动脉的中膜层厚度。
本研究显示,AIA 导致 Nox1、Nox2 和 Nox4 表达增加的微弱迹象,以及 ORX 导致 Nox1 减少的微弱迹象。此外,AIA 和/或 ORX 均未改变这些动物主动脉的内皮功能。另一方面,ORX 显著增加了研究动物主动脉的中膜层厚度,而 AIA 明显减轻了这种情况。