Chen L E, Seaber A V, Otto-Hagen P, Urbaniak J
Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710.
J Reconstr Microsurg. 1993 Jan;9(1):49-54. doi: 10.1055/s-2007-1006638.
The vascular endothelium plays an important role in the regulation of vascular tone, by producing both vasodilating and vasoconstricting mediators. Using intravital videomicroscopy, this study examined the in vivo responses of the rat cremaster muscle microcirculation to topical application of endothelin-1 (ET-1), as well as the effect of verapamil pretreatment on these responses. ET-1 produced a potent and persistent vasoconstriction in arteries and veins which lasted for 150 min. The contractile response to ET-1 was significantly more prolonged in arterioles (11 to 30 microns) than in small arteries (40 to 70 microns). Pretreatment of the muscle with verapamil did not inhibit the initial vasoconstrictive action of ET-1, but produced a significant (p < 0.0001) reduction in the recovery time required for vessel relaxation in both small arteries and arterioles. The results suggest that Ca2+ channels contribute to the prolonged vasoconstriction induced in microvessels by ET-1. Because this prolonged vasoconstriction may be responsible for the "no-reflow" phenomenon which occurs in microsurgical procedures, therapy with a calcium antagonist may be useful in attenuating its duration.
血管内皮通过产生血管舒张和血管收缩介质,在调节血管张力方面发挥重要作用。本研究采用活体视频显微镜技术,观察了大鼠提睾肌微循环对局部应用内皮素-1(ET-1)的体内反应,以及维拉帕米预处理对这些反应的影响。ET-1可在动脉和静脉中产生强烈且持久的血管收缩,持续150分钟。小动脉(11至30微米)对ET-1的收缩反应明显比小动脉(40至70微米)更持久。用维拉帕米预处理肌肉并未抑制ET-1的初始血管收缩作用,但显著(p<0.0001)缩短了小动脉和小动脉血管舒张所需的恢复时间。结果表明,Ca2+通道参与了ET-1诱导的微血管长时间血管收缩。由于这种长时间的血管收缩可能是微血管手术中“无复流”现象的原因,钙拮抗剂治疗可能有助于缩短其持续时间。