Abstract
The vasovagal reflex, underlying vasovagal syncope (VVS), is likely to be an effective defence mechanism both in animals and humans. Within the vasovagal reflex, the vaso-inhibitory component plays a major role accounting for the limited efficacy of pacemaker implant in preventing VVS relapse, even if asystole has been previously documented by internal loop recordings. An effective neural sympathetic control of arterial vasculature upon standing is obtained in humans by both a proper increase of the sympathetic bursts activity and a baroreceptor mediated sympathetic neural discharge rhythmicity at 0.1 Hz. Adenosine and B-type natriuretic peptides are promising markers to be used in typifying clinical forms of VVS, their aetiology and prognosis. Although vagal activity is usually thought to be protective for the heart and brain, an excessive vagal activity resulting from the combination of diving and emotional VV reflexes or from a prolonged and forced head-up position may be harmful for humans.
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References
Mosqueda-Garcia R, Furlan R, Tank J et al (2000) The elusive pathophysiology of neurally mediated syncope. Circulation 102:2898–2906
Oberg B, Thoren P (1972) Increased activity in left ventricular receptors during hemorrhage or occlusion of caval veins in the cat: a possible cause of the vaso-vagal reaction. Acta Physiol Scand 85:164–173
Gabrielsen GW, Smith EN (1985) Physiological responses associated with feigned death in the American opossum. Acta Physiol Scand 123:393–398
Bracha HS, Bracha AS, Williams AE et al (2005) The human fear-circuitry and fear-induced fainting in healthy individuals: the paleolithic-threat hypothesis. Clin Auton Res 15:238–241
Diehl RR (2005) Vasovagal syncope and Darwinian fitness. Clin Auton Res 15:126–129
Levi M (2005) Vasovagal fainting as an evolutionary remnant of the fight against hemorrhage. Clin Auton Res 15:69–70
Darwin C (1900) A posthumous essay on instinct. In: Romanes GJ (ed) Mental evolution in animals. Appleton, New York
Hoagland H (1928) On the mechanism of tonic immobility (“animal hypnosis”). J Gen Physiol 1:426–427
EL Sergeant AB (1975) Death feigning by ducks in response to predation by red foxes (Vulpes fulva). Am Midl Nat 94:108–119
Alboni P, Alboni M, Bertorelle G (2008) The origin of vasovagal syncope: to protect the heart or to escape predation? Clin Auton Res 18:170–178
Lewis T (1932) Vasovagal syncope and the carotid sinus mechanism with comments on Gowers’ and Nothnagel’s syndrome. Br Med J I:873–876
Brignole M, Menozzi C, Moya A et al (2012) Pacemaker therapy in patients with neurally mediated syncope and documented asystole: Third International Study on Syncope of Uncertain Etiology (ISSUE-3): a randomized trial. Circulation 125:2566–2571
Fucà G, Dinelli M, Suzzani P et al (2006) The venous system is the main determinant of hypotension in patients with vasovagal syncope. Europace 8:839–845
Verheyden BLJ, van Dijk N, Westerhof BE et al (2008) Steep fall in cardiac output is main determinant of hypotension during drug-free and nitroglycerine-induced orthostatic vasovagal syncope. Heart Rhythm 12:1695–1702
Mosqueda-Garcia R, Furlan R, Fernandez-Violante R et al (1997) Sympathetic and baroreceptor reflex function in neurally mediated syncope evoked by tilt. J Clin Invest 99:2736–2744
Jardine DL (2013) Vasovagal syncope new physiologic insights. In: Sheldon R (ed) Syncope. Elsevier, Philadelphia, pp 75–87
Vaddadi G, Esler MD, Dawood T et al (2010) Persistence of muscle sympathetic nerve activity during vasovagal syncope. Eur Heart J 31:2027–2033
Furlan R, Porta A, Costa F et al (2000) Oscillatory patterns in sympathetic neural discharge and cardiovascular variables during orthostatic stimulus. Circulation 101:886–892
Rowell LB, Seals DR (1990) Sympathetic activity during graded central hypovolemia in hypoxemic humans. Am J Physiol 259:H1197–H1206
Calkins H, Kadish A, Sousa J et al (1991) Comparison of responses to isoproterenol and epinephrine during head-up tilt in suspected vasodepressor syncope. Am J Cardiol 67:207–209
Ludbrook J, Rutter PC (1988) Effect of naloxone on haemodynamic responses to acute blood loss in unanaesthetized rabbits. J Physiol 400:1–14
Smith ML, CMaTM (1993) Naloxone does not prevent vasovagal syncope during simulated orthostasis in humans. J Auton Nerv Syst 45:1–9
Saadjian AY, Levy S, Franceschi F et al (2002) Role of endogenous adenosine as a modulator of syncope induced during tilt testing. Circulation 106:569–574
Shryock JC, Belardinelli L (1997) Adenosine and adenosine receptors in the cardiovascular system: biochemistry, physiology, and pharmacology. Am J Cardiol 79:2–10
Lerman BB, Belardinelli L (1991) Cardiac electrophysiology of adenosine. Basic and clinical concepts. Circulation 83:1499–1509
Koeppen M, Eckle T, Eltzschig HK (2009) Selective deletion of the A1 adenosine receptor abolishes heart-rate slowing effects of intravascular adenosine in vivo. PLoS One 4:e6784
Brignole M, Deharo JC, De Roy L et al (2011) Syncope due to idiopathic paroxysmal atrioventricular block: long-term follow-up of a distinct form of atrioventricular block. J Am Coll Cardiol 58:167–173
Maisel AS, Krishnaswamy P, Nowak RM et al (2002) Rapid measurement of B-type natriuretic peptide in the emergency diagnosis of heart failure. N Engl J Med 347:161–167
Lega JC, Lacasse Y, Lakhal L et al (2009) Natriuretic peptides and troponins in pulmonary embolism: a meta-analysis. Thorax 64:869–875
Wozakowska-Kapton B (2004) Effects of sinus rhythm restoration on plasma brain natriuretic peptide in patients with atrial fibrillation. Am J Cardiol 93:155–158
Sutuvosky I, Katoh T, Ohno T et al (2004) Relationship between brain natriuretic peptide, myocardial wall stress, and ventricular arrhythmia severity. Jpn Heart J 45:771–777
Pfister R, Hagemeister J, Esser S et al (2012) NT-pro-BNP for diagnostic and prognostic evaluation in patients hospitalized for syncope. Int J Cardiol 155:268–272
Reed MJ, Newby DE, Coull AJ et al (2010) The ROSE (risk stratification of syncope in the emergency department) study. J Am Coll Cardiol 55:713–721
Costantino G, Solbiati M, Sagone A et al (2011) Time course of B-type natriuretic peptides changes after ventricular fibrillation: relationships with cardiac syncope. Int J Cardiol 153:333–335
Costantino G, Solbiati M, Casazza G et al (2014) Usefulness of N-terminal pro-B-type natriuretic Peptide increase as a marker for cardiac arrhythmia in patients with syncope. Am J Cardiol 113:98–102
Soteriades ES, Evans JC, Larson MG et al (2002) Incidence and prognosis of syncope. N Engl J Med 347:878–885
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Furlan, R., Alboni, P., Mosqueda-Garcia, R. (2015). Pathophysiology of Vasovagal Syncope: Conclusive Remarks. In: Alboni, P., Furlan, R. (eds) Vasovagal Syncope. Springer, Cham. https://doi.org/10.1007/978-3-319-09102-0_9
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DOI: https://doi.org/10.1007/978-3-319-09102-0_9
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