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Acute and subacute toxicity of 7.5% hypertonic saline/6% dextran-70 (hsd) in dogs 1. serum immunoglobulin and complement responses

✍ Scribed by James J. Summary; Michael A. Dubick; Gary M. Zaucha; Ahmed F. Kilani; Don W. Korte Jr; Charles E. Wade


Book ID
102871362
Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
637 KB
Volume
12
Category
Article
ISSN
0260-437X

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✦ Synopsis


Abstract

Clinical use of modern dextran solutions has been limited by concerns of anaphylactoid reactions. To assess the short‐term antigenic response to 7.5% hypertonic saline in 6% Dextran‐70 (HSD), sera were obtained from dogs involved in the acute and subacute toxicology testing of HSD and its individual components, and analyzed for IgG, IgM and C3 complement. In separate studies, beagles were infused i.v. with a single dose of HSD or its components at 20 ml kg^−1^ (the maximum tolerated dose; MTD), or the MTD daily for 14 days, and serum was obtained prior to and at various times after infusion up to 14 days. In both studies, despite serum dextran concentrations exceeding 2000 mg dl^−1^, no induction of IgG, IgM or C3 complement concentrations were observed. In addition, serum IgG immunoelectrophoretic patterns were of normal curvature, position and intensity; the immunoprecipitin bands were not displaced, bowed, inhibited or thicker than the normal preinfusion immunoelectrophoretograms.

The data suggest that single or multiple HSD i.v. injections, as much as five times the proposed therapeutic level for the treatment of hypovolemia, evoked no increase in antibody titers in dogs. Therefore, therapeutic use of HSD in the treatment of hemorrhagic shock should not be associated with widespread concomitant allergic complications.


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Acute and subacute toxicity of 7.5% hype
✍ Michael A. Dubick; Gary M. Zaucha; Don W. Korte Jr.; Charles E. Wade 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 724 KB

7.5% Hypertonic saline4% Dextran-70 (HSD) is currently being evaluated in our laboratory as a resuscitation solution for the treatment of hypovolemia at a dose of 4 ml kg-' body weight. A few reports of dextran toxicity, particularly of the kidney, have been cited in the literature, so the present s