Department of Human and Animal Physiology, Faculty of Biology, M.V. Lomonosov Moscow State University, 119234 Moscow, Russia.
Department of Physiology, Russian National Research Medical University, 117513 Moscow, Russia.
Int J Mol Sci. 2021 Jun 3;22(11):6037. doi: 10.3390/ijms22116037.
Previously, the abundance of p42/44 and p38 MAPK proteins had been shown to be higher in arteries of 1- to 2-week-old compared to 2- to 3-month-old rats. However, the role of MAPKs in vascular tone regulation in early ontogenesis remains largely unexplored. We tested the hypothesis that the contribution of p42/44 and p38 MAPKs to the contraction of peripheral arteries is higher in the early postnatal period compared to adulthood. Saphenous arteries of 1- to 2-week-old and 2- to 3-month-old rats were studied using wire myography and western blotting. The α-adrenoceptor agonist methoxamine did not increase the phosphorylation level of p38 MAPK in either 1- to 2-week-old or 2- to 3-month-old rats. Accordingly, inhibition of p38 MAPK did not affect arterial contraction to methoxamine in either age group. Methoxamine increased the phosphorylation level of p42/44 MAPKs in arteries of 2- to 3-month-old and of p44 MAPK in 1- to 2-week-old rats. Inhibition of p42/44 MAPKs reduced methoxamine-induced contractions in arteries of 2- to 3-month-old, but not 1- to 2-week-old rats. Thus, despite a high abundance in arterial tissue, p38 and p42/44 MAPKs do not regulate contraction of the saphenous artery in the early postnatal period. However, p42/44 MAPK activity contributes to arterial contractions in adult rats.
先前的研究表明,1 至 2 周龄大鼠的动脉中 p42/44 和 p38 MAPK 蛋白的丰度高于 2 至 3 月龄大鼠。然而,MAPK 在早期胚胎发生过程中对血管张力调节的作用在很大程度上仍未得到探索。我们假设 p42/44 和 p38 MAPK 对周围动脉收缩的贡献在出生后早期比成年期更高。使用线描记法和 Western blot 研究了 1 至 2 周龄和 2 至 3 月龄大鼠的隐静脉。α-肾上腺素能受体激动剂甲氧胺均未增加 1 至 2 周龄或 2 至 3 月龄大鼠中 p38 MAPK 的磷酸化水平。因此,p38 MAPK 的抑制作用均不影响两个年龄组对甲氧胺的动脉收缩。甲氧胺增加了 2 至 3 月龄大鼠的 p42/44 MAPKs 和 1 至 2 周龄大鼠的 p44 MAPK 的磷酸化水平。p42/44 MAPK 的抑制作用降低了 2 至 3 月龄大鼠中甲氧胺诱导的收缩,但对 1 至 2 周龄大鼠没有影响。因此,尽管动脉组织中 p38 和 p42/44 MAPK 的丰度很高,但它们不调节出生后早期隐动脉的收缩。然而,p42/44 MAPK 活性有助于成年大鼠的动脉收缩。