Literature DB >> 17994673

Murine neonatal intravascular injections: modeling newborn disease.

Kirsten A Kienstra1, Drifa Freysdottir, Naomi M Gonzales, Karen K Hirschi.   

Abstract

The ability to perform murine neonatal intravascular injections likely will prove useful in studying many newborn-specific disease states that are modeled in mice. Unfortunately, effective intravascular injection in the neonatal mouse has been limited by developmental immaturity and small size. To establish a mouse model of neonatal intravascular injection, C57Bl/6 pups between birth and 6 d of age were injected with a buffered solution containing cells or vehicle alone. For both external jugular and superficial temporal vein injections, a 2-member team was used to position the pup, insert the needle, and perfuse the injectate. For superficial temporal vein injections, the vascular anatomy was visualized by using transillumination. After injection into the jugular or superficial temporal vein, the survival rate to adulthood was 100% (n = 30 pups per group), with no long-term complications. Occasional extravasation of injectate was well tolerated, allowing for serial injections (n = 40 pups). Intravascular access was confirmed by using fluorescent dye perfusion studies and cellular engraftment analysis. The 2 techniques are safe and reproducible methods of obtaining intravascular access via the external jugular and superficial temporal veins in newborn mice. These methods provide a mechanism for delivering a wide variety of substances, ranging from aqueous solutions to suspensions.

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Year:  2007        PMID: 17994673

Source DB:  PubMed          Journal:  J Am Assoc Lab Anim Sci        ISSN: 1559-6109            Impact factor:   1.232


  14 in total

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7.  Intravenous injections in neonatal mice.

Authors:  Sara E Gombash Lampe; Brian K Kaspar; Kevin D Foust
Journal:  J Vis Exp       Date:  2014-11-11       Impact factor: 1.355

8.  Repression of miR-142 by p300 and MAPK is required for survival signalling via gp130 during adaptive hypertrophy.

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Journal:  EMBO Mol Med       Date:  2012-04-24       Impact factor: 12.137

9.  A neonatal model of intravenous Staphylococcus epidermidis infection in mice <24 h old enables characterization of early innate immune responses.

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Journal:  PLoS One       Date:  2012-09-06       Impact factor: 3.240

10.  Characterization of Kupffer cells in livers of developing mice.

Authors:  Bryan G Lopez; Monica S Tsai; Janie L Baratta; Kenneth J Longmuir; Richard T Robertson
Journal:  Comp Hepatol       Date:  2011-07-12
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