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J Appl Physiol 97: 29-38, 2004. First published February 20, 2004; doi:10.1152/japplphysiol.01304.2003
8750-7587/04 $5.00
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Hypergravity-induced immunomodulation in a rodent model: hematological and lymphocyte function analyses

Michael J. Pecaut,1 Glen M. Miller,2 Gregory A. Nelson,1 and Daila S. Gridley1,2

1Department of Radiation Medicine, Radiobiology Program, and 2Department of Microbiology and Molecular Genetics, Loma Linda University School of Medicine and Medical Center, Loma Linda, California 92354

Submitted 5 December 2003 ; accepted in final form 9 February 2004

The major purpose of this study was to quantify hypergravity-induced changes in erythrocyte and thrombocyte characteristics, spontaneous and mitogen-induced lymphoblastogenesis, and capacity of splenocytes to secrete immunoregulatory cytokines. C57BL/6 mice were subjected to chronic 1, 2, and 3 G; subsets were euthanized after 1, 4, 7, 10, and 21 days of centrifugation. Erythrocyte counts, hematocrit, and hemoglobin were significantly reduced by day 21 in both centrifuged groups. Hemoglobin concentration and volume per red blood cell were generally low, but an early, transient spike above normal was noted in thrombocyte counts in the 3-G group. Fluctuations above and below normal in blood and spleen cell spontaneous blastogenesis were dependent on the length of centrifugation time and not on the level of gravity. Depression in splenocyte responses to phytohemagglutinin and lipopolysaccharide due to gravity were noted when the data were expressed as stimulation indexes. Cytokine production by spleen cells was primarily affected during the first week of centrifugation: IL-2, IL-4, and tumor necrosis factor-{alpha} increased, whereas interferon-{gamma} decreased. These findings, although not identical to those reported for spaceflight, indicate that altered gravity can influence both hematological and functional variables that may translate into serious health consequences during extended missions.

centrifugation; immune; cytokine; erythrocyte



Address for reprint requests and other correspondence: M. J. Pecaut, Chan Shun Pavilion, Rm. A-1010, 11175 Campus St., Loma Linda Univ. School of Medicine, Loma Linda, CA 92354 (E-mail: mpecaut{at}dominion.llumc.edu).







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