Aksoy M O, Stewart G J, Harakal C
Biochem Biophys Res Commun. 1986 Mar 28;135(3):735-41. doi: 10.1016/0006-291x(86)90990-3.
The role of 20000 dalton myosin light chain phosphorylation in mediating venous smooth muscle contraction was studied in isolated preparations of canine jugular and femoral vein. One min 10(-5) M norepinephrine-induced contraction was accompanied by significant increases in phosphorylation (jugular - 21 to 46%; femoral - 19 to 54%) which were reversed within 10 min after agonist washout. During 40 min stimulation, phosphorylation and isometric force redevelopment rates declined to near basal levels while force was maintained. These findings implicate light chain phosphorylation as a prerequisite for initial tension development by crossbridge cycling in venous smooth muscle. However, long term tension can be maintained through a process similar to the latchbridge state in tracheal and arterial smooth muscle.
在犬颈静脉和股静脉的离体标本中研究了20000道尔顿肌球蛋白轻链磷酸化在介导静脉平滑肌收缩中的作用。1分钟10⁻⁵M去甲肾上腺素诱导的收缩伴随着磷酸化的显著增加(颈静脉 - 21%至46%;股静脉 - 19%至54%),在激动剂洗脱后10分钟内恢复。在40分钟的刺激过程中,磷酸化和等长力重建率下降至接近基础水平,而张力得以维持。这些发现表明轻链磷酸化是静脉平滑肌通过横桥循环产生初始张力的先决条件。然而,长期张力可以通过类似于气管和动脉平滑肌中的闩锁桥状态的过程来维持。