Marina Feeley, Tomoki Watada, Go Ito, Ai Shimada, Toru Sawai, Hideomi Nakata, Shingo Otsuki, Tadayoshi Miyamoto
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During LBNP exposure, thoracic admittance, an indicator of CBV reduction, decreased by 13.4% (p < 0.001), indicating significant CBV reduction. Following rigorous statistical correction for multiple comparisons, time-course analysis revealed that mean blood pressure decreased temporarily during the initial phase (0-30 s), whereas heart rate increased progressively (16.4%, p < 0.001). End-tidal <math> <semantics><msub><mi>P</mi> <mrow><mi>C</mi> <msub><mi>O</mi> <mn>2</mn></msub> </mrow> </msub> <annotation>${P_{{\\mathrm{C}}{{\\mathrm{O}}_2}}}$</annotation></semantics> </math> showed a consistent reduction (5.9%, p < 0.001), whereas minute ventilation and middle cerebral artery mean blood velocity showed no significant changes after statistical correction (-9.3% and -5.0%, respectively, p > 0.05). Exploratory correlation analysis revealed a significant negative correlation between mean blood pressure and tidal volume during the initial phase only (r = -0.78, p = 0.004). 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引用次数: 0
摘要
中枢血容量(CBV)减少挑战循环和呼吸稳态,特别是在初始代偿阶段(0-2分钟),当快速生理适应发生时。在这项研究中,我们检测了11名健康年轻男性使用下体负压(LBNP)降低CBV时的动态心肺反应。参与者在-45 mmHg下完成了三个标准化的2分钟LBNP试验,通过流量测量和呼吸气体分析评估呼吸变量,同时使用ECG、血压和经颅多普勒超声监测心血管参数和脑血流量。在LBNP暴露期间,CBV降低指标胸腔导纳下降13.4% (p p C O 2 ${P_{\ mathm {C}}{{\ mathm {O}}_2}}}$显示一致降低(5.9%,p 0.05)。探索性相关分析显示,平均血压与潮气量仅在初始阶段呈显著负相关(r = -0.78, p = 0.004)。交叉相关分析显示呼吸和脑血管反应的时间模式,呼吸变化先于脑血管调整10-20秒。这些发现以及个体差异表明,在直立压力下心肺和脑血管的快速相互作用,展示了具有不同时间模式的动态心血管和呼吸反应,为在重力压力下维持体内平衡的生理机制提供了见解。
Time-course analysis of cerebral circulation and cardiorespiratory responses to acute central blood volume reduction in healthy young males.
Central blood volume (CBV) reduction challenges circulatory and respiratory homeostasis, particularly during the initial compensatory phase (0-2 min), when rapid physiological adaptations occur. In this study, we examined dynamic cardiorespiratory responses to CBV reduction using lower-body negative pressure (LBNP) in 11 healthy young males. Participants completed three standardized 2 min LBNP trials at -45 mmHg, with respiratory variables assessed via flow measurement and breath-by-breath gas analysis, while cardiovascular parameters and cerebral blood flow were monitored using ECG, blood pressure and transcranial Doppler ultrasonography. During LBNP exposure, thoracic admittance, an indicator of CBV reduction, decreased by 13.4% (p < 0.001), indicating significant CBV reduction. Following rigorous statistical correction for multiple comparisons, time-course analysis revealed that mean blood pressure decreased temporarily during the initial phase (0-30 s), whereas heart rate increased progressively (16.4%, p < 0.001). End-tidal showed a consistent reduction (5.9%, p < 0.001), whereas minute ventilation and middle cerebral artery mean blood velocity showed no significant changes after statistical correction (-9.3% and -5.0%, respectively, p > 0.05). Exploratory correlation analysis revealed a significant negative correlation between mean blood pressure and tidal volume during the initial phase only (r = -0.78, p = 0.004). Cross-correlation analysis suggested temporal patterns between respiratory and cerebrovascular responses, with respiratory changes preceding cerebrovascular adjustments by 10-20 s. These findings, along with individual variability, suggest rapid cardiorespiratory and cerebrovascular interactions during orthostatic stress, demonstrating dynamic cardiovascular and respiratory responses with distinct temporal patterns that provide insights into physiological mechanisms maintaining homeostasis during gravitational stress.
期刊介绍:
Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged.
Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.