Effects of Rat Sinoaortic Denervation on the Vagal Responsiveness and Expression of Muscarinic Acetylcholine Receptors

• Published in: Journal of cardiovascular pharmacology Vol. 47; no. 3; pp. 331 - 336
• Main Authors: da Silva Soares, Pedro Paulo, Porto, Catarina Segreti, Francis Abdalla, Fernando Maurício, De La Fuente, Raquel Nitrosi, Moreira, Edson Dias, Krieger, Eduardo Moacyr, Irigoyen, Maria Claudia
• Format: Journal Article
• Language: English
• Published: United States Lippincott Williams & Wilkins, Inc 01-03-2006
• Subjects: Animals; Baroreflex - physiology; Blood Pressure; Denervation; Electric Stimulation; Heart Rate; Male; N-Methylscopolamine - metabolism; Rats; Rats, Wistar; Receptors, Muscarinic - analysis; Vagus Nerve - physiology
• ISSN: 0160-2446
• DOI: 10.1097/01.fjc.0000205982.67653.26

We studied heart rate (HR) responses to vagal electrical stimulation (VES) and the expression of muscarinic acetylcholine receptors (mAChRs) in the rat atria 1 day (SADa) and 20 days (SADc) after sinoaortic denervation (SAD). Arterial blood pressure (BP) was recorded in conscious, unrestrained rats and during vagal electrical stimulation of the vagus nerve. In the acute phase, SADa rats had hypertension, tachycardia, and increased blood pressure lability. In the chronic phase, heart rate and blood pressure in SADc rats returned to normal whereas blood pressure lability remained increased. VES produced a frequency-dependent bradycardia that was higher in SADa and SADc groups. Binding experiments with [
3
H] N-methylscopolamine showed that in the chronic phase of SAD mAChRs density (SADc=412.2±28.64, SADa=273.38±48.37 and CTR=241.5±25.35 fmol/mg of protein,
P
<0.05) and affinity increased in SADc rats (reduced dissociation constantSADc=0.45±0.05, SADa=1.01±0.26, and CTR=0.98±0.12 mM,
P
<0.05). Our study provides evidence that vagal hyperresponsiveness coexists with increased sympathetic activity in SADa rats without a concomitant increase in mAChRs density or affinity, suggesting that complex mechanisms might modulate the “accentuated antagonism” observed in the acute SAD phase. However, SADc rats had increased bradycardia to VES, increased affinity, and upregulation of mAChRs in the atria. Our results show that, 20 days after SAD in the rat, functional and cellular adaptations occur in the cardiac parasympathetic efferent pathway that may contribute to other regulatory mechanisms to compensate for cardiovascular changes provoked by baroreceptor arch disruption.