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      Validating Excised Rodent Lungs for Functional Hyperpolarized Xenon-129 MRI

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          Abstract

          Ex vivo rodent lung models are explored for physiological measurements of respiratory function with hyperpolarized (hp) 129Xe MRI. It is shown that excised lung models allow for simplification of the technical challenges involved and provide valuable physiological insights that are not feasible using in vivo MRI protocols. A custom designed breathing apparatus enables MR images of gas distribution on increasing ventilation volumes of actively inhaled hp 129Xe. Straightforward hp 129Xe MRI protocols provide residual lung volume ( RV) data and permit for spatially resolved tracking of small hp 129Xe probe volumes during the inhalation cycle. Hp 129Xe MRI of lung function in the excised organ demonstrates the persistence of post mortem airway responsiveness to intravenous methacholine challenges. The presented methodology enables physiology of lung function in health and disease without additional regulatory approval requirements and reduces the technical and logistical challenges with hp gas MRI experiments. The post mortem lung functional data can augment histological measurements and should be of interest for drug development studies.

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          Most cited references53

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          Nuclear magnetic resonance of laser-polarized noble gases in molecules, materials, and organisms.

          The sensitivity of conventional nuclear magnetic resonance (NMR) techniques is fundamentally limited by the ordinarily low spin polarization achievable in even the strongest NMR magnets. However, by transferring angular momentum from laser light to electronic and nuclear spins, optical pumping methods can increase the nuclear spin polarization of noble gases by several orders of magnitude, thereby greatly enhancing their NMR sensitivity. This review describes the principles and magnetic resonance applications of laser-polarized noble gases. The enormous sensitivity enhancement afforded by optical pumping can be exploited to permit a variety of novel NMR experiments across numerous disciplines. Many such experiments are reviewed, including the void-space imaging of organisms and materials, NMR and MRI of living tissues, probing structure and dynamics of molecules in solution and on surfaces, NMR sensitivity enhancement via polarization transfer, and low-field NMR and MRI. (c) 2002 Elsevier Science (USA).
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            The anesthetic properties of xenon in animals and human beings, with additional observations on krypton.

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              Characterisation of guinea pig precision-cut lung slices: comparison with human tissues.

              Precision-cut lung slices (PCLS) allow comparison of the airway responses of different species under identical experimental conditions. The aim of this study was to establish and characterise PCLS from guinea pigs (GPs) and to compare them with human PCLS. GP PCLS were prepared according to previously published procedures with the exception that the agarose solution and the initial incubation medium contained isoproterenol to avoid post mortem airway contraction. The median effective concentrations (EC50, expressed as nM) for agonist-induced bronchoconstriction in GP and human PCLS, respectively, were: leukotriene D4 (1.8, 5.0); thromboxane (16, 1.3); serotonin (69, unresponsive); histamine (217, 2,170); and methacholine (231, 234). Allergen-induced bronchoconstriction of passively sensitised PCLS was attenuated by histamine or thromboxane-prostanoid receptor antagonists and was almost completely prevented by their combination with leukotriene receptor antagonists. Airways pre-contracted with methacholine were relaxed by the beta-agonist salbutamol or the phosphodiesterase inhibitor 3-isobutyl-1-methylxanthine. Simultaneous studies of airways and vessels are possible with, for example, EC50 values for endothelin-1 of 37 nM (pulmonary arteries), 10 nM (pulmonary veins) and 9.6 nM (airway). When compared with previous findings in rat and mouse, these data show that guinea pig lungs are a more appropriate model for human airway pharmacology than lungs from rats or mice.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2013
                30 August 2013
                : 8
                : 8
                : e73468
                Affiliations
                [1 ]Sir Peter Mansfield Magnetic Resonance Centre, School of Clinical Sciences, University of Nottingham, Nottingham, United Kingdom
                [2 ]Nottingham Respiratory Research Unit, Nottingham City Hospital, Nottingham, United Kingdom
                Bascom Palmer Eye Institute, University of Miami School of Medicine; United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: DMLL GEP TM. Performed the experiments: DMLL THR JS KFS GEP TM. Analyzed the data: DMLL DES TM. Contributed reagents/materials/analysis tools: GEP. Wrote the paper: DMLL DES TM.

                [¤]

                Current address: Division of Magnetics, National Institute of Standards and Technology, Boulder, Colorado, United States of America

                Article
                PONE-D-13-24331
                10.1371/journal.pone.0073468
                3758272
                24023683
                3ea3dc50-176e-4f8c-9abc-c2a90c671e98
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 11 June 2013
                : 21 July 2013
                Page count
                Pages: 13
                Funding
                This study was supported by the Medical Research Council of the United Kingdom under Grant No. G0900785 and by the Royal Society through the Paul Instrument Fund. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Anatomy and Physiology
                Respiratory System
                Respiratory Physiology
                Histology
                Model Organisms
                Animal Models
                Medicine
                Anatomy and Physiology
                Respiratory System
                Respiratory Physiology
                Pulmonology
                Radiology
                Diagnostic Radiology
                Magnetic Resonance Imaging
                Physics
                Interdisciplinary Physics
                Medical Physics

                Uncategorized
                Uncategorized

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