Frasch MG, Mü ller T, Hoyer D, Weiss C, Schubert H, Schwab M. Nonlinear properties of vagal and sympathetic modulations of heart rate variability in ovine fetus near term. Am J Physiol Regul Integr Comp Physiol 296: R702-R707, 2009. First published December 17, 2008; doi:10.1152/ajpregu.90474.2008.-Fetal heart rate (FHR) monitoring is commonly used although clinical studies questioned its diagnostic value. Sophisticated FHR variability (fHRV) measures such as fHRV complexity may improve the sensitivity and specificity of FHR monitoring. A more detailed understanding of the physiology underlying fHRV complexity is essential to harness its use for monitoring fetal health. To examine the specific effects of vagal and sympathetic modulations on fHRV complexity, we blocked vagal activity with atropine and sympathetic activity with propranolol in near-term fetal sheep (n ϭ 7, 0.85 gestation). Under these conditions, we analyzed the linear and nonlinear parts of fHRV complexity from autonomic information flow. Overall fHRV complexity decreased with both drugs compared with nonrapid eye movement sleep baseline (P Ͻ 0.05). With atropine, this was because of a decrease of the linear part of fHRV complexity on the long-term time scale (P Ͻ 0.05), suggesting that vagal modulation of fHRV is adequately described by linear fHRV measures. With propranolol, the nonlinear part of fHRV complexity decreased on the short-term time scale (P Ͻ 0.05), suggesting that sympathetic influences on fHRV can be detected by the nonlinear part of fHRV complexity. Thus the complex interplay of vagal and sympathetic modulations of fHRV is reflected differently and specifically in the linear and nonlinear properties of fHRV complexity, and on different time scales. Analysis of linear and nonlinear properties of fHRV may improve sensitivity and specificity of FHR monitoring. fetal sheep; autonomic nervous system; autonomic information flow; complexity FETAL HEART RATE (FHR) monitoring is used to monitor fetal well-being noninvasively in utero. Some studies questioned its diagnostic value (24). Recent studies in human fetuses suggested potential of FHR variability (fHRV) complexity estimation to improve clinical monitoring of fetal health (18,31). This requires a deeper understanding of the physiological meaning of fHRV complexity, including how its linear and nonlinear properties are modulated by sympathetic and vagal activity of the autonomic nervous system (ANS). Understanding fHRV dynamics during physiological (e.g., sleep states dependent changes) and pathophysiological (e.g., asphyxia) conditions has evolved over the past two decades, propelled by analyses of the linear aspects of fHRV in human and ovine fetuses (4,11,16,20,29,32). However, characterization of the linear fHRV properties is fundamentally limited in its power to describe the nonlinear structure of the underlying sympathovagal interactions (12,14).The origin of the nonlinearity of sympathovagal interactions lies in their intrinsic complexity. This complexity emerges from intera...