In the circulatory system, a change in blood pressure operates through the baroreflex to alter sympathetic efferent nerve activity, which in turn affects blood pressure. Existence of this closed feedback loop makes it difficult to identify the baroreflex open-loop transfer characteristics by means of conventional frequency domain approaches. Although several investigators have demonstrated the advantages of the time domain approach using parametric models such as the autoregressive moving average model, specification of the model structure critically affects their results. Thus we investigated the applicability of a nonparametric closed-loop identification technique to the carotid sinus baroreflex system by using an exogenous perturbation according to a binary white-noise sequence. To validate the identification method, we compared the transfer functions estimated by the closed-loop identification with those estimated by open-loop identification. The transfer functions determined by the two identification methods did not differ statistically in their fitted parameters. We conclude that exogenous perturbation to the baroreflex system enables us to estimate the open-loop baroreflex transfer characteristics under closed-loop conditions.
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http://dx.doi.org/10.1152/ajpheart.1997.273.2.H1024 | DOI Listing |
Background: Simulation offers an opportunity to practice neonatal resuscitation and test clinical systems to improve safety. The authors used simulation-based clinical systems testing (SbCST) with a Healthcare Failure Mode and Effect Analysis (HFMEA) rubric to categorize and quantify latent safety threats (LSTs) during in situ training in eight rural delivery hospitals. The research team hypothesized that most LSTs would be common across hospitals.
View Article and Find Full Text PDFCrit Rev Oncol Hematol
January 2025
Institute of Human Genetics, Jena University Hospital, Jena, Germany; Urology and Nephrology Research Center, Research Institute for Urology and Nephrology, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address:
Circular RNAs (circRNAs) have emerged as critical regulators in cancer biology, contributing to various cancer hallmarks, including cell proliferation, apoptosis, metastasis, and drug resistance. Defined by their covalently closed loop structure, circRNAs possess unique characteristics like high stability, abundance, and tissue-specific expression. These non-coding RNAs function through mechanisms such as miRNA sponging, interactions with RNA-binding proteins (RBPs), and modulating transcription and splicing.
View Article and Find Full Text PDFISA Trans
December 2024
Department of Automation, Xiamen University, Xiamen City 361000, China. Electronic address:
In general, auto-tuning implementation of PID controllers relies on dual controllers, exciting/identification experiments or some prior knowledge on the process and hence the considerable cost on auto-tuning implementation occurs. To deal with such a problem, a new auto-tuning scheme of the FPID controller is developed for minimum variance tasks under routine operating conditions in which the closed-loop system is running without any external excitation other than natural disturbances. This paper reveals that the stochastic disturbance model can be uniquely determined from the first several terms of the impulse response coefficients of the closed-loop system when the precondition on the time delay and the order of the disturbance model is satisfied.
View Article and Find Full Text PDFPlant Genome
March 2025
Department of Plant and Microbial Biology, North Carolina State University, Raleigh, North Carolina, USA.
Circular RNAs (circRNAs) are closed-loop RNAs forming a covalent bond between their 3' and 5' ends, the back splice junction (BSJ), rendering them resistant to exonucleases and thus more stable compared to linear RNAs. Identification of circRNAs and distinction from their cognate linear RNA is only possible by sequencing the BSJ that is unique to the circRNA. CircRNAs are involved in the regulation of their cognate RNAs by increasing transcription rates, RNA stability, and alternative splicing.
View Article and Find Full Text PDFSci Adv
December 2024
Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
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