Masuki Shizue, Takeoka Michiko, Taniguchi Shun'ichiro, Yokoyama Minesuke, Nose Hiroshi
Department of Sports Medical Sciences, Institute on Aging and Adaptation, Shinshu University Graduate School of Medicine, Matsumoto, Japan.
J Physiol. 2003 Nov 15;553(Pt 1):203-12. doi: 10.1113/jphysiol.2003.047803. Epub 2003 Sep 8.
Calponin is known to be an actin binding protein in smooth muscle, inhibiting actomyosin ATPase activity in vitro. We previously reported that alpha-adrenergic vasoconstriction in calponin knockout (KO) mice was reduced compared with that in wild-type C57BL/6J (WT) mice and, as a compensation, arterial baroreflex sensitivity in KO mice was enhanced at rest. In the present study, we assessed arterial pressure regulation in WT and KO mice during graded treadmill exercise at 5, 10, and 15 m min-1. Mean arterial pressure (MAP) in KO mice fluctuated more than that in WT mice at every speed of exercise with two-fold higher variances (P < 0.001). The baroreflex sensitivity (Delta HR/Delta MAP) in WT mice (n = 6), determined from the heart rate response (Delta HR) to spontaneous change in MAP (Delta MAP), was -5.1 +/- 0.6 beats min-1 mmHg-1 (mean +/- S.E.M.) at rest and remained unchanged at -5.0 +/- 0.9 beats min-1 mmHg-1 during exercise (P < 0.01), while that in KO mice (n = 6) was -9.9 +/- 1.7 beats min-1 mmHg-1 at rest, significantly higher than that in WT mice (P < 0.001), and was reduced to -4.7 +/- 0.4 beats min-1 mmHg-1 during exercise (P < 0.01), not significantly different from that in WT mice. In another experiment, we measured muscle blood flow (MBF) in the thigh by laser-Doppler flowmetry, electromyogram (EMG), and MAP during voluntary locomotion in KO (n = 7) and WT (n = 7) mice. Muscle vascular conductance, MBF/MAP, started to increase immediately after locomotion, judged from EMG, and reached 50% of the maximum after the time of 2.3 +/- 0.2 s in KO mice, shorter than 5.8 +/- 0.6 s in WT mice (P < 0.001). Prior administration of alpha-adrenergic blockade (phentolamine) shortened the time in WT mice to that in KO mice (P < 0.001), but did not shorten the time in KO mice. Thus, impaired MAP regulation in KO mice during exercise was caused by a blunted muscle vascular alpha-adrenergic contractile response and by the attenuated HR response to spontaneous change in MAP due to reduced baroreflex sensitivity.
钙调蛋白是一种已知的平滑肌肌动蛋白结合蛋白,在体外可抑制肌动球蛋白ATP酶活性。我们之前报道过,与野生型C57BL/6J(WT)小鼠相比,钙调蛋白基因敲除(KO)小鼠的α-肾上腺素能血管收缩作用减弱,作为一种代偿,KO小鼠在静息时动脉压力反射敏感性增强。在本研究中,我们评估了WT和KO小鼠在5、10和15米/分钟的分级跑步机运动过程中的动脉血压调节情况。在每个运动速度下,KO小鼠的平均动脉压(MAP)波动均比WT小鼠更大,方差高出两倍(P<0.001)。根据心率反应(ΔHR)对MAP自发变化(ΔMAP)测定的WT小鼠(n = 6)的压力反射敏感性,在静息时为-5.1±0.6次/分钟·毫米汞柱-1(平均值±标准误),运动期间保持不变,为-5.0±0.9次/分钟·毫米汞柱-1(P<0.01),而KO小鼠(n = 6)在静息时为-9.9±1.7次/分钟·毫米汞柱-1,显著高于WT小鼠(P<0.001),运动期间降至-4.7±0.4次/分钟·毫米汞柱-1(P<0.01),与WT小鼠无显著差异。在另一项实验中,我们在KO(n = 7)和WT(n = 7)小鼠自主运动期间,通过激光多普勒血流仪、肌电图(EMG)和MAP测量了大腿肌肉血流量(MBF)。根据EMG判断,肌肉血管传导率(MBF/MAP)在运动开始后立即开始增加,KO小鼠在2.3±0.2秒时达到最大值的50%,短于WT小鼠的5.8±0.6秒(P<0.001)。预先给予α-肾上腺素能阻滞剂(酚妥拉明)可使WT小鼠的时间缩短至与KO小鼠相同(P<0.001),但不能缩短KO小鼠的时间。因此,KO小鼠在运动期间MAP调节受损是由于肌肉血管α-肾上腺素能收缩反应减弱以及压力反射敏感性降低导致的对MAP自发变化的心率反应减弱所致。