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This Article Full Text Full Text (PDF) All Versions of this Article: 296/3/R702    most recent 90474.2008v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Frasch, M. G. Articles by Schwab, M. Search for Related Content PubMed PubMed Citation Articles by Frasch, M. G. Articles by Schwab, M.

DEVELOPMENTAL PHYSIOLOGY AND PREGNANCY

Nonlinear properties of vagal and sympathetic modulations of heart rate variability in ovine fetus near term

¹Department of Obstetrics and Gynecology, Lawson Health Research Institute, The University of Western Ontario, London, Ontario, Canada; ²Department of Neurology, ³Institute of Laboratory Animal Science, ⁴Biomagnetic Center, Department of Neurology, Friedrich Schiller University, Jena, Germany

Submitted 4 June 2008 ; accepted in final form 16 December 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 = 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 < 0.05). With atropine, this was because of a decrease of the linear part of fHRV complexity on the long-term time scale (P < 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 < 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