Department of Kinesiology, Kansas State University, Manhattan, Kansas, USA.
Am J Physiol Regul Integr Comp Physiol. 2010 Feb;298(2):R478-85. doi: 10.1152/ajpregu.00631.2009. Epub 2009 Dec 9.
The control of vascular tone during exercise is highly complex and integrated. Specifically, in regards to the contribution of nitric oxide (NO), the observed magnitude and muscle fiber-type dependency of the NO contribution to exercise hyperemia may differ depending on the timing of NO synthase (NOS) inhibition with respect to the exercise bout (i.e., administration prior to vs. during exercise). We tested the hypothesis that, in the presence of prior cyclooxygenase inhibition (indomethacin, 5 mg/kg(-1)), NOS inhibition (N(G)-nitro-L-arginine methyl ester, L-NAME; 10 mg/kg) administered during submaximal treadmill exercise would blunt blood flow and vascular conductance (VC) in the hindlimb muscle(s) of the rat with the greatest reductions in blood flow and VC occurring in the predominantly oxidative muscles. Adult female Wistar rats (n = 10, age: 3-4 mo) ran on a motor-driven treadmill (20 m/min, 10% grade). Total and regional hindlimb muscle blood flow and VC were determined via radiolabeled microspheres before (control) and after L-NAME administration during exercise. L-NAME reduced (P < 0.05) total hindlimb muscle blood flow (control: 123 + or - 10, L-NAME: 103 + or - 7 ml x min(-1) x 100g(-1)) and VC (control: 0.95 + or - 0.09, L-NAME: 0.63 + or - 0.05 ml x min(-1) x 100g(-1) x mmHg(-1)). There was a significant correlation (r = 0.51, P < 0.05) between the absolute reductions in VC after L-NAME and the percent sum of type I and IIa fibers in the individual muscles and muscle parts; however, there was no correlation (P = 0.62) when expressed as blood flow. Surprisingly, the highly oxidative muscles demonstrated a marked ability to maintain oxygen delivery, which differs substantially from previous reports of L-NAME infusion prior to exercise in these muscles. The demonstration that NO is an important regulator of blood flow and VC in the rat hindlimb during treadmill exercise, but that the fiber-type dependency of NO is altered markedly when NOS inhibition is performed during, vs. prior to, exercise, lends important insights into the integrated nature of vascular control during exercise.
运动期间血管张力的控制非常复杂和综合。具体来说,就一氧化氮(NO)的贡献而言,NO 对运动性充血的贡献的幅度和肌纤维类型依赖性可能因 NO 合酶(NOS)抑制与运动回合的时间关系而异(即在运动前给予与运动期间给予)。我们检验了这样一个假设,即在预先给予环氧化酶抑制(吲哚美辛,5mg/kg(-1))的情况下,NOS 抑制(N(G)-硝基-L-精氨酸甲酯,L-NAME;10mg/kg)在亚最大速度跑步机运动期间给药会使大鼠后肢肌肉的血流和血管传导(VC)变钝,血流和 VC 的最大减少发生在主要氧化的肌肉中。成年雌性 Wistar 大鼠(n=10,年龄:3-4 个月)在电动跑步机上跑步(20m/min,10%坡度)。通过放射性标记微球在运动前(对照)和运动期间给予 L-NAME 后确定总后肢肌肉血流和 VC。L-NAME 降低(P<0.05)总后肢肌肉血流(对照:123±10,L-NAME:103±7ml x min(-1) x 100g(-1))和 VC(对照:0.95±0.09,L-NAME:0.63±0.05ml x min(-1) x 100g(-1) x mmHg(-1))。L-NAME 后 VC 的绝对减少与个体肌肉和肌肉部位中 I 型和 IIa 型纤维的总和百分比之间存在显著相关性(r=0.51,P<0.05);然而,当以血流表示时,没有相关性(P=0.62)。令人惊讶的是,高度氧化的肌肉表现出维持氧输送的显著能力,这与之前在这些肌肉中进行运动前 L-NAME 输注的报告有很大不同。证明在跑步机运动期间,NO 是大鼠后肢血流和 VC 的重要调节剂,但当在运动期间而不是运动前进行 NOS 抑制时,NO 的纤维类型依赖性发生明显改变,这为运动期间血管控制的综合性质提供了重要的见解。