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In the generalized framework of circulatory equilibrium, the cardiac output (CO), right (RAP) and left (LAP) atrial pressures at equilibrium are predicted from the intersection between the CO curve and venous return (VR) surface. The VR surface is represented by the following equation: VR=V/W-G∙RAP-G∙LAP, where V is stressed blood volume, and W, G, and G are parameters. For future clinical application of this framework, we examined whether the VR surface is valid, whether the parameters are allometrically scalable based on Kleiber's law, and whether the VR surface with allometrically scaled parameters accurately predicts hemodynamic variables across different animal species and a diverse range of body weights (BW). Anesthetized dogs (n=18) and pigs (n=8) with BW ranging from 9 to 50 kg were used. In 20 animals, we characterized the VR surface under total heart bypass and examined allometric scalability of the parameters. In 19 animals, we assessed whether the allometrically scaled VR surface allows accurate predictions of CO, LAP, and RAP. VR correlated significantly with RAP and LAP as per the equation, with a median coefficient of determination (r) of 0.95. G and G were allometrically scalable with BW, but W was not. However, if population-representative W was combined with allometrically scaled G and G, predicted CO, RAP, and LAP correlated strongly with those measured (r=0.99, 0.98, and 0.94, respectively). In conclusion, the VR surface is valid across species and body sizes, and the allometrically scaled VR surface allows accurate hemodynamic prediction, supporting the clinical application potential of this framework.
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http://dx.doi.org/10.1152/ajpheart.00413.2025 | DOI Listing |
Pharm Res
September 2025
Axcelead Tokyo West Partners, Inc. Translational Science, Discovery DMPK, Hino-Shi, Tokyo, 191-0065, Japan.
Purpose: Accurate prediction of human clearance (CL) is essential in early drug development. Single Species Scaling (SSS) using rat pharmacokinetic (PK) data, particularly with unbound plasma fraction (f), is widely used. However, its accuracy declines for compounds with extremely low f, and no systematic method has addressed this limitation.
View Article and Find Full Text PDFTarget Oncol
September 2025
Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
Background: Population pharmacokinetic models can potentially provide suggestions for an initial dose and the magnitude of dose adjustment during therapeutic drug monitoring procedures of imatinib. Several population pharmacokinetic models for imatinib have been developed over the last two decades. However, their predictive performance is still unknown when extrapolated to different populations, especially children.
View Article and Find Full Text PDFJ Control Release
September 2025
Department of Bioengineering, Rice University, Houston, TX, USA. Electronic address:
The development of continuous-release devices or injectables for the long-term delivery of biologics is of great interest, especially monoclonal antibodies (mAbs) that require frequent, high-dose injections. Preclinical testing of these technologies in murine models is necessary for clinical translation; however, xenogeneic responses to the mAb and foreign body responses to the implants or injectables can confound results. Immune system knockout (KO) models that affect immune cells are often used in these experiments, but the effects of KO models on mAb pharmacokinetics (PK) are not well characterized.
View Article and Find Full Text PDFJ Clin Pharmacol
September 2025
Division of Systems Pharmacology and Pharmacy, Leiden Academic Centre for Drug Research, Leiden University, Leiden, The Netherlands.
A preterm and term neonate to adult (PTNA) maturation equation was introduced recently to describe the glomerular filtration rate maturation from birth to adulthood for neonates of varying gestational age. This study aims to evaluate the newly developed PTNA equation against common maturation approaches like allometric scaling (AS0.75), the AS0.
View Article and Find Full Text PDFSpecies and sex-specific differences in organ size are fundamental features of animal biology, yet the mechanisms that drive these differences remain debated. Adult female are larger than males. While most organs are present across both sexes, the underlying mechanisms driving sex-specific organ and body size scaling of remain unclear.
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