AbstractWe investigated second‐messenger signalling components linked to the stimulation of Gq protein‐coupled receptors (e.g. thromboxane A2 and bradykinin B2 receptors) on the sensory endings of thin fibre muscle afferents in the chronic mechanoreflex sensitization in rats with myocardial infarction‐induced heart failure with reduced ejection fraction (HF‐rEF). We hypothesized that injection of either the inositol 1,4,5‐trisphosphate (IP3) receptor antagonist xestospongin C (5 µg) or the PKCε translocation inhibitor PKCe141 (45 µg) into the arterial supply of the hindlimb would reduce the increase in renal sympathetic nerve activity (RSNA) and mean arterial pressure (MAP) evoked during 30 s of 1 Hz dynamic hindlimb muscle stretch in decerebrate, unanaesthetized HF‐rEF rats but not sham‐operated controls (SHAM). Ejection fraction was significantly reduced in HF‐rEF (45 (19)%) compared to SHAM (80 (9)%; P < 0.001) rats. In HF‐rEF rats (n = 3M/2F), IP3 receptor blockade had no effect on the peak ΔRSNA (pre: 99 (74)%; post: 133 (79)%; P = 0.974) or peak ΔMAP response to stretch (peak ΔMAP: pre: 32 (14) mmHg; post: 36 (21) mmHg; P = 0.719). Conversely, in another group of HF‐rEF rats (n = 4M/3F), the PKCε translocation inhibitor reduced the peak ΔRSNA (pre: 110 (77)%; post: 62 (58)%; P = 0.029) and peak ΔMAP response to stretch (pre: 30 (20) mmHg; post: 17 (16) mmHg; P = 0.048). In SHAM counterparts, neither drug affected the mechanoreflex responses. Our findings highlight PKCε, but not IP3 receptors, as a significant second‐messenger in the chronic mechanoreflex sensitization in HF‐rEF which may play a crucial role in the exaggerated sympathetic response to exercise in this patient population.
imageKey pointsSkeletal muscle contraction results in an exaggerated reflex increase in sympathetic nerve activity in heart failure patients with reduced ejection fraction (HF‐rEF) compared to healthy individuals, contributing to increased cardiovascular risk and impaired tolerance for mild exercise.The exaggerated reflex sympathetic responses in HF‐rEF may be attributed to a chronic sensitization of mechanically sensitive thin fibre muscle afferents mediated, at least in part, by stimulation of Gq protein‐coupled thromboxane A2 and bradykinin B2 receptors on muscle afferent sensory endings.The specific Gq protein‐linked signalling mechanisms that produce the chronic mechanoreflex sensitization in HF‐rEF have not been investigated but may involve inositol 1,4,5‐trisphosphate (IP3) receptors and/or protein kinase C epsilon (PKCε).Here we demonstrate that PKCε, but not IP3 receptors, within the sensory endings of thin fibre muscle afferents plays a role in the sensitization of mechanically sensitive thin fibre muscle afferents in rats with HF‐rEF.
