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      Direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography

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          Abstract

          We describe the development and application of intravital confocal micro-videography to visualize entrance, distribution, and clearance of drugs within various tissues and organs. We use a Nikon A1R confocal laser scanning microscope system attached to an upright ECLIPSE FN1. The Nikon A1R allows simultaneous four channel acquisition and speed of 30 frames per second while maintaining high resolution of 512 × 512 scanned points. The key techniques of our intravital imaging are (1) to present a flat and perpendicular surface to the objective lens, and (2) to expose the subject with little or no bleeding to facilitate optical access to multiple tissues and organs, and (3) to isolate the subject from the body movement without compressing the blood vessels, and (4) to insert a tail vein catheter for timed injection without moving the subject. Ear lobe dermis tissue was accessible without surgery. Liver, kidney, and subcutaneous tumor were accessed following exteriorization through skin incision. In order to image initial extravasations of compounds into tissue following intravenous injection, movie acquisition was initialized prior to drug administration. Our technique can serve as a powerful tool for investigating biological mechanisms and functions of intravenously injected drugs, with both spatial and temporal resolution.

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          Most cited references12

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          High levels of foreign gene expression in hepatocytes after tail vein injections of naked plasmid DNA.

          We have previously shown that the intramuscular injection of naked plasmid DNA enables foreign gene expression in muscle. Further studies showed that the intravascular delivery of naked plasmid DNA enables high levels of expression not only in muscle but also in hepatocytes. For the liver, this technique required injection directly into the liver vessels (portal vein, hepatic vein, or bile duct) and occlusion of outflow. The present study now demonstrates that high levels of plasmid DNA expression in hepatocytes can be easily obtained by tail vein injections. The highest levels of expression are achieved by rapidly injecting the plasmid DNA in large volumes, approximately 2.5 ml. This technique has great potential for a wide variety of laboratory studies.
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            Hydroporation as the mechanism of hydrodynamic delivery.

            We have reported that a rapid tail vein injection of a large volume of plasmid DNA solution into a mouse results in high level of transgene expression in the liver. Gene transfer efficiency of this hydrodynamics-based procedure is determined by the combined effect of a large volume and high injection speed. Here, we show that the hydrodynamic injection induces a transient irregularity of heart function, a sharp increase in venous pressure, an enlargement of liver fenestrae, and enhancement of membrane permeability of the hepatocytes. At the cellular level, our results suggest that hepatic delivery by the hydrodynamic injection is accomplished by the generation of membrane pores in the hepatocytes.
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              Progress and prospects: naked DNA gene transfer and therapy.

              Increases in efficiency have made naked DNA gene transfer a viable method for gene therapy. Intravascular delivery results in effective gene delivery to liver and muscle, and provides in vivo transfection methods for basic and applied gene therapy and antisense strategies with oligonucleotides and small interfering RNA (siRNA). Delivery via the tail vein in rodents provides an especially simple and effective means for in vivo gene transfer. Electroporation methods significantly enhance direct injection of naked DNA for genetic immunization. The availability of plasmid DNA expression vectors that enable sustained high level expression, allows for the development of gene therapies based on the delivery of naked plasmid DNA.
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                Author and article information

                Journal
                Biomed Opt Express
                BOE
                Biomedical Optics Express
                Optical Society of America
                2156-7085
                01 November 2010
                21 October 2010
                21 October 2010
                : 1
                : 4
                : 1209-1216
                Affiliations
                [1 ]Division of Clinical Biotechnology, Center for Disease Biology and Integrative Medicine, 
Graduate School of Medicine, The University of Tokyo, Japan
                [2 ]Department of Otorhinolaryngology and Head and Neck Surgery,
Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Japan
                [3 ]Department of Otorhinolaryngology and Head and Neck Surgery, Mitsui Memorial Hospital, Japan
                [4 ]Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, Japan
                [5 ]Department of Obstetrics and Gynecology, Graduate School of Medicine and Faculty of Medicine, 
The University of Tokyo, Japan
                [6 ]Division of Nephrology and Endocrinology, Department of Internal Medicine, 
Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Japan
                [7 ]Department of Internal Medicine, Teikyo University School of Medicine, Japan
                [8 ]Department of Materials Engineering, Graduate School of Engineering, The University of Tokyo, Japan
                [9 ]Department of Vascular Regeneration, Division of Tissue Engineering, The University of Tokyo Hospital, Japan
                [10 ]Nikon Instech Co., Ltd., Japan
                Author notes
                Article
                135496
                10.1364/BOE.1.001209
                3018094
                21258542
                5d31cb04-b1f8-498a-91e0-c70b3660c9cb
                ©2010 Optical Society of America

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.

                History
                : 27 September 2010
                : 16 October 2010
                : 17 October 2010
                Funding
                Funded by: Core Research Program for Evolutional Science and Technology
                Funded by: Japan Science and Technology Corporation
                Funded by: World-Leading Innovative R&D on Science and Technology
                Funded by: Japan Society for the Promotion of Science
                Funded by: Japanese Ministry of Education, Culture, Sports, Science and Technology of Japan
                Award ID: 21890051
                Categories
                Microscopy
                Custom metadata
                True
                12

                Vision sciences
                (170.1790) confocal microscopy,(170.2655) functional monitoring and imaging

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