Penn State Hershey Heart and Vascular Institute, Pennsylvania State University College of Medicine, Milton S. Hershey Medical Center, Hershey, Pennsylvania.
J Appl Physiol (1985). 2013 Oct 15;115(8):1183-90. doi: 10.1152/japplphysiol.00100.2013. Epub 2013 Aug 22.
Muscle mechanoreflex activation decreases the sensitivity of carotid baroreflex (CBR)-heart rate (HR) control during local metabolite accumulation in humans. However, the contribution of thromboxane A2 (TXA2) toward this response is unknown. Therefore, the effect of inhibiting TXA2 production via low-dose aspirin on CBR-HR sensitivity during muscle mechanoreflex and metaboreflex activation in humans was examined. Twelve young subjects performed two trials during two visits, preceded by 7 days' low-dose aspirin (81 mg) or placebo. One trial involved 3-min passive calf stretch (mechanoreflex) during 7.5-min limb circulatory occlusion (CO). In another trial, CO was preceded by 1.5 min of 70% maximal voluntary contraction isometric calf exercise to accumulate metabolites during CO and stretch (mechanoreflex and metaboreflex). HR (ECG) and mean arterial pressure (Finometer) were recorded. CBR function was assessed using rapid neck pressures ranging from +40 to -80 mmHg. Aspirin significantly decreased baseline thromboxane B2 production by 84 ± 4% (P < 0.05) but did not affect 6-keto prostaglandin F1α. Following aspirin, stretch with metabolite accumulation significantly augmented maximal gain (GMAX) and operating point gain (GOP) of CBR-HR (GMAX; -0.71 ± 0.14 vs. -0.37 ± 0.08 and GOP; -0.69 ± 0.13 vs. -0.35 ± 0.12 beats·min(-1)·mmHg(-1) for aspirin and placebo, respectively; P < 0.05). CBR-HR function curves were reset similarly with aspirin and placebo during stretch with metabolite accumulation. In conclusion, these findings suggest that low-dose aspirin augments CBR-HR sensitivity during concurrent muscle mechanoreflex and metaboreflex activation in humans. This increased sensitivity appears linked to reduced TXA2 production, which likely plays a role in metabolite sensitization of muscle mechanoreceptors.
肌肉机械感受器反射激活会降低人类局部代谢物积累时颈动脉压力反射(CBR)-心率(HR)控制的敏感性。然而,血栓素 A2(TXA2)对此反应的贡献尚不清楚。因此,本研究旨在检查通过低剂量阿司匹林抑制 TXA2 产生对人类肌肉机械感受器反射和代谢感受器激活时 CBR-HR 敏感性的影响。12 名年轻受试者在两次就诊期间进行了两次试验,每次试验前 7 天服用低剂量阿司匹林(81mg)或安慰剂。一项试验涉及在肢体循环闭塞(CO)期间进行 3 分钟的被动小腿伸展(机械感受器反射),同时进行 7.5 分钟的 CO。在另一项试验中,CO 前进行 1.5 分钟 70%最大自主收缩等长小腿运动,以在 CO 和伸展期间积累代谢物(机械感受器反射和代谢感受器反射)。记录心率(ECG)和平均动脉压(Finometer)。使用从+40 到-80mmHg 的快速颈部压力评估 CBR 功能。阿司匹林可显著降低基础 TXB2 产生 84±4%(P<0.05),但不影响 6-酮前列腺素 F1α。服用阿司匹林后,代谢物积累时的伸展显著增加 CBR-HR 的最大增益(GMAX)和工作点增益(GOP)(GMAX:-0.71±0.14 与-0.37±0.08,GOP:-0.69±0.13 与-0.35±0.12 beats·min(-1)·mmHg(-1),分别为阿司匹林和安慰剂;P<0.05)。在代谢物积累时的伸展中,阿司匹林和安慰剂同样重置了 CBR-HR 功能曲线。结论:这些发现表明,低剂量阿司匹林可增强人类同时发生的肌肉机械感受器反射和代谢感受器激活时 CBR-HR 的敏感性。这种敏感性增加似乎与 TXA2 产生减少有关,这可能在肌肉机械感受器对代谢物的敏感性中起作用。