Moffitt Julia A, Grippo Angela J, Beltz Terry G, Johnson Alan Kim
Department of Psychology, The University of Iowa, Iowa City, IA 52242-1407, USA.
J Appl Physiol (1985). 2008 Oct;105(4):1049-59. doi: 10.1152/japplphysiol.90535.2008. Epub 2008 Jul 17.
The hindlimb-unloaded (HU) rat model elicits cardiovascular deconditioning and simulates the physiological adaptations to microgravity or prolonged bed rest in humans. Although psychological deficits have been documented following bed rest and spaceflight in humans, few studies have explored the psychological effects of cardiovascular deconditioning in animal models. Given the bidirectional link established between cardiac autonomic imbalance and psychological depression in both humans and in animal models, we hypothesized that hindlimb unloading would elicit an alteration in sympathovagal tone and behavioral indexes of psychological depression. Male, Sprague-Dawley rats confined to 14 days of HU displayed anhedonia (a core feature of human depression) compared with casted control (CC) animals evidenced by reduced sucrose preference (CC: 81 +/- 2.9% baseline vs. HU: 58 +/- 4.5% baseline) and reduced (rightward shift) operant responding for rewarding electrical brain stimulation (CC: 4.4 +/- 0.3 muA vs. 7.3 +/- 1.0 muA). Cardiac autonomic blockade revealed elevated sympathetic [CC: -54 +/- 14.1 change in (Delta) beats/min vs. HU: -118 +/- 7.6 Delta beats/min] and reduced parasympathetic (CC: 45 +/- 11.8 Delta beats/min vs. HU: 8 +/- 7.3 Delta beats/min) cardiac tone in HU rats. Heart rate variability was reduced (CC: 10 +/- 1.4 ms vs. HU: 7 +/- 0.7 ms), and spectral analysis of blood pressure indicated loss of total, low-, and high-frequency power, consistent with attenuated baroreflex function. These data indicate that cardiovascular deconditioning results in sympathovagal imbalance and behavioral signs consistent with psychological depression. These findings further elucidate the pathophysiological link between cardiovascular diseases and affective disorders.
后肢去负荷(HU)大鼠模型会引发心血管失健,并模拟人类对微重力或长期卧床休息的生理适应。尽管已有文献记载人类在卧床休息和太空飞行后会出现心理缺陷,但很少有研究探讨动物模型中心血管失健的心理影响。鉴于在人类和动物模型中均已建立起心脏自主神经失衡与心理抑郁之间的双向联系,我们推测后肢去负荷会引起交感迷走神经张力改变以及心理抑郁的行为指标变化。与假手术对照组(CC)动物相比,限制后肢去负荷14天的雄性Sprague-Dawley大鼠表现出快感缺失(人类抑郁症的核心特征),蔗糖偏好降低(CC组:81±2.9%基线水平,HU组:58±4.5%基线水平)以及对奖励性脑电刺激的操作性反应减少(右移)(CC组:4.4±0.3 μA,HU组:7.3±1.0 μA)可证明这一点。心脏自主神经阻滞显示,HU大鼠的交感神经活动增强(CC组:每分钟心跳变化量为-54±14.1次,HU组:-118±7.6次),副交感神经张力降低(CC组:每分钟心跳变化量为45±11.8次,HU组:8±7.3次)。心率变异性降低(CC组:10±1.4毫秒,HU组:7±0.7毫秒),血压频谱分析表明总功率、低频功率和高频功率均降低,这与压力反射功能减弱一致。这些数据表明,心血管失健会导致交感迷走神经失衡以及与心理抑郁相符的行为体征。这些发现进一步阐明了心血管疾病与情感障碍之间的病理生理联系。