Vagal tone dominates autonomic control of mouse heart rate at thermoneutrality

• Published in: American journal of physiology. Heart and circulatory physiology Vol. 294; no. 4; p. H1581
• Main Authors: Swoap, S J, Li, C, Wess, J, Parsons, A D, Williams, T D, Overton, J M
• Format: Journal Article
• Language: English
• Published: United States 01-04-2008
• Subjects: Animals; Autonomic Nervous System - metabolism; Blood Pressure; Body Temperature; Bradycardia - etiology; Bradycardia - metabolism; Bradycardia - physiopathology; Caloric Restriction - adverse effects; Cold Temperature; Heart - innervation; Heart Rate; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Receptor, Muscarinic M2 - deficiency; Receptor, Muscarinic M2 - genetics; Receptor, Muscarinic M2 - metabolism; Receptors, Adrenergic, beta - deficiency; Receptors, Adrenergic, beta - genetics; Receptors, Adrenergic, beta - metabolism; Vagus Nerve - metabolism
• ISSN: 0363-6135
• DOI: 10.1152/ajpheart.01000.2007

It is generally accepted that cardiac sympathetic tone dominates the control of heart rate (HR) in mice. However, we have recently challenged this notion given that HR in the mouse is responsive to ambient temperature (T(a)) and that the housing T(a) is typically 21-23 degrees C, well below the thermoneutral zone ( approximately 30 degrees C) of this species. To specifically test the hypothesis that cardiac sympathetic tone is the primary mediator of HR control in the mouse, we first examined the metabolic and cardiovascular responses to rapid changes in T(a) to demonstrate the sensitivity of the mouse cardiovascular system to T(a). We then determined HR in 1) mice deficient in cardiac sympathetic tone ("beta-less" mice), 2) mice deficient in cardiac vagal tone [muscarinic M(2) receptor (M(2)R(-/-)) mice], and 3) littermate controls. At a T(a) of 30 degrees C, the HR of beta-less mice was identical to that of wild-type mice (351 +/- 11 and 363 +/- 10 beats/min, respectively). However, the HR of M(2)R(-/-) mice was significantly greater (416 +/- 7 beats/min), demonstrating that vagal tone predominates over HR control at this T(a). When these mice were calorically restricted to 70% of normal intake, HR fell equally in wild-type, beta-less, and M(2)R(-/-) mice (DeltaHR = 73 +/- 9, 76 +/- 3, and 73 +/- 7 beats/min, respectively), suggesting that the fall in intrinsic HR governs bradycardia of calorically restricted mice. Only when the T(a) was relatively cool, at 23 degrees C, did beta-less mice exhibit a HR (442 +/- 14 beats/min) that was different from that of littermate controls (604 +/- 10 beats/min) and M(2)R(-/-) mice (602 +/- 5 beats/min). These experiments conclusively demonstrate that in the absence of cold stress, regulation of vagal tone and modulation of intrinsic rate are important determinants of HR control in the mouse.