Abstract
Granulocyte colony-stimulating factor (G-CSF) at 250 μg kg−1 per day stimulates white blood cell (WBC) proliferation in mice with significant increases from 72–120 h. Lipopolysaccharide (LPS) treatment as a single dose (5 mg kg−1) at 72 h abolishes the induced WBC proliferation of G-CSF from 72–120 h. Pentoxifylline at 50 mg kg−1 per day does not interfere with the proliferation effect of G-CSF on white blood cells; the drug did not protect against the effects of LPS in abolishing WBC proliferation. LPS alone or with G-CSF treatment at 250 μg kg−1 per day in-vivo significantly elevated tumour necrosis factor-α (TNF-α) levels after 90 min. These levels were significantly reduced by pentoxifylline at 50 or 100 mg kg−1 per day after 72 h, but not when administered 30 min before LPS treatment. Factors other than TNF-α levels appear to be involved in the regulation of haematopoiesis by G-CSF.
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