Department of Orthopaedics and Traumatology, Faculty of Medicine, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, 85-090 Bydgoszcz, Poland.
Department of Pharmacology and Therapeutics, Faculty of Medicine, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, 85-090 Bydgoszcz, Poland.
Int J Mol Sci. 2023 Jun 19;24(12):10355. doi: 10.3390/ijms241210355.
The phenomena of ischemia and reperfusion are associated with the pathological background of cardiovascular diseases. Ischemia is initiated by ischemia reperfusion injury (IRI), which involves disruption of intracellular signaling pathways and causes cell death. The aim of this study was to assess the reactivity of vascular smooth muscle cells in the conditions of induced ischemia and reperfusion, and to determine the mechanisms leading to contractility disorders. This study was conducted using classical pharmacometric methods on an isolated model of the rat caudal artery. The experiment consisted of the analysis of the final and initial perfusate pressure measurements after induction of arterial contraction with phenylephrine in the presence of forskolin and A7 hydrochloride, two ligands modifying the contractility of vascular smooth muscle cells (VSMC). The pharmacometric analysis showed that in simulated reperfusion, cyclic nucleotides have a vasoconstrictive effect, and calmodulin has a vasodilating effect. The responsiveness of vascular smooth muscle cells to the vasopressor effects of α1-adrenomimetics during reperfusion may change uncontrollably, and the effects of secondary messengers may be counter physiological. Further studies are needed to evaluate the function of other second messengers on VSMCs in the process of ischemia and reperfusion.
缺血再灌注现象与心血管疾病的病理背景有关。缺血由缺血再灌注损伤(IRI)引发,涉及细胞内信号通路的破坏,并导致细胞死亡。本研究旨在评估在诱导缺血和再灌注条件下血管平滑肌细胞的反应性,并确定导致收缩功能障碍的机制。本研究使用经典的药效计量学方法在大鼠尾动脉的离体模型上进行。实验包括在 forskolin 和 A7 盐酸盐存在下,用苯肾上腺素诱导动脉收缩后,对终末和初始灌流压测量值进行分析,这两种配体可调节血管平滑肌细胞(VSMC)的收缩性。药效计量学分析表明,在模拟再灌注中,环核苷酸具有血管收缩作用,钙调蛋白具有血管舒张作用。在再灌注期间,血管平滑肌细胞对α1-肾上腺素能激动剂的升压作用的反应性可能会失控,第二信使的作用可能与生理相反。需要进一步研究来评估在缺血和再灌注过程中其他第二信使对 VSMC 的功能。