Noradrenergic regulation of skeletal muscle oxygen pressures: Impact of heart failure with preserved ejection fraction and heat therapy.

IF 2.8 4区 医学 Q2 PHYSIOLOGY
Edward T N Calvo, Jacob M Pontorno, Benjamin Zeidler, Taciane M M Pejon, Michael D Belbis, Scott K Ferguson, Craig J Goergen, Timothy P Gavin, Bruno T Roseguini, Igor A Fernandes, Daniel M Hirai
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引用次数: 0

Abstract

Attenuation of sympathetic vasoconstriction during exercise (functional sympatholysis) contributes to skeletal muscle oxygen delivery-utilization matching. However, the extent to which muscle contractions impact noradrenergic regulation of interstitial oxygen pressures ( P O 2 is ${P_{{{\mathrm{O}}_2}}}_{{\mathrm{is}}}$ ; the driving force for blood-myocyte oxygen flux) is unknown. We tested the hypotheses that (1) muscle contractions would attenuate the noradrenaline-induced reduction in muscle P O 2 is ${P_{{{\mathrm{O}}_2}}}_{{\mathrm{is}}}$ compared to rest (thus indicating functional sympatholysis) in healthy rats, and (2) functional sympatholysis would be impaired in rats with heart failure with preserved ejection fraction (HFpEF) but ameliorated with heat therapy. Skeletal muscle P O 2 is ${P_{{{\mathrm{O}}_2}}}_{{\mathrm{is}}}$ was determined via phosphorescence quenching in anaesthetized healthy (Sprague-Dawley, n = 14) and HFpEF rats (obese ZSF1, n = 20) at rest and during contractions following noradrenaline superfusion (5 × 10-4  M). HFpEF rats underwent 8 weeks of heat therapy (HEAT, n = 10) or control treatment (CON; n = 10). Functional sympatholysis was evaluated based on the noradrenaline-induced changes in P O 2 is ${P_{{{\mathrm{O}}_2}}}_{{\mathrm{is}}}$ at rest and during contractions normalized to mean arterial pressure (Δ P O 2 is ${P_{{{\mathrm{O}}_2}}}_{{\mathrm{is}}}$ /MAP; %/mmHg). Consistent with our hypothesis, muscle contractions attenuated the noradrenaline-evoked P O 2 is ${P_{{{\mathrm{O}}_2}}}_{{\mathrm{is}}}$ reductions in healthy rats (rest: -0.50 ± 0.23, contractions: -0.25 ± 0.16; P < 0.05). Compared to healthy rats, the noradrenergic response at rest was exacerbated in HFpEF-CON (-0.85 ± 0.13; P < 0.05) but restored in HFpEF-HEAT (-0.61 ± 0.25; P > 0.05). During contractions, the noradrenergic response was not different between HFpEF-CON and HFpEF-HEAT (-0.94 ± 0.07 and -0.86 ± 0.09, respectively; P > 0.05). Moreover, the magnitude of sympatholysis was lower in both HFpEF-CON and HFpEF-HEAT compared to healthy. Taken together, these results indicate that heat therapy failed to improve functional sympatholysis in HFpEF rats but restored the noradrenergic response in resting skeletal muscle.

骨骼肌氧压的去甲肾上腺素能调节:保留射血分数和热疗法对心力衰竭的影响。
运动过程中交感血管收缩的减弱(功能性交感解)有助于骨骼肌氧输送-利用匹配。然而,肌肉收缩对间质氧压去肾上腺素能调节的影响程度(P o2为${P_{{\ mathm {O}}_2}} {{\ mathm{为}}}$;血液-肌细胞氧通量的驱动力是未知的。我们检验了以下假设:(1)与休息相比,健康大鼠肌肉收缩会减弱去甲肾上腺素诱导的肌肉P O 2的减少(P_{{\mathrm{O}}_2}}} {{\mathrm{is}}}$)(从而表明功能性交感神经溶解);(2)心力衰竭大鼠的功能性交感神经溶解会受到损害,并保留射血分数(HFpEF),但通过热疗法得到改善。在去甲肾上腺素灌注(5 × 10-4 M)后,麻醉健康大鼠(Sprague-Dawley, n = 14)和肥胖大鼠(肥胖ZSF1, n = 20)静息和收缩时,采用磷光猝灭法测定骨骼肌p2值${P_{{{\mathrm{O}}_2}} _{{\mathrm{s}}}}$。HFpEF大鼠接受8周的热治疗(heat, n = 10)或对照治疗(CON;n = 10)。根据去甲肾上腺素诱导的血压变化来评估功能性交感神经功能,在休息时和收缩时,P = ${P_{{\ mathm {O}}_2}} {{\ mathm {is}}}$ (Δ P = ${P_{{\ mathm {O}}_2}} {{\ mathm {is}}}$ /MAP;% /毫米汞柱)。与我们的假设一致,健康大鼠肌肉收缩对去甲肾上腺素诱发的p2的减弱为${P_{{\ mathm {O}}_2}} {{\ mathm {is}}}$(休息:-0.50±0.23,收缩:-0.25±0.16;P 0.05)。在收缩期间,HFpEF-CON和HFpEF-HEAT的去甲肾上腺素能反应无显著差异(分别为-0.94±0.07和-0.86±0.09);p > 0.05)。此外,HFpEF-CON和HFpEF-HEAT组的交感神经解解程度均低于健康组。综上所述,这些结果表明热疗法不能改善HFpEF大鼠的功能性交感神经溶解,但可以恢复静息骨骼肌的去甲肾上腺素能反应。
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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
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.
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