When chondroitin sulfate (CS) or dextran sulfate (DxS) was administere
d intravenously in rats the levels of circulating hyaluronan (HA) rapi
dly increased, 70 min after injection the levels were found to be abou
t 10-20 times the initial values. Saline injections were without effec
t on HA levels, CS given intraperitoneally was found to give prolonged
blocking of liver uptake of labeled HA and increased endogenous serum
HA to about 10 times the initial level at 180 min, HA excretion in ur
ine was dramatically increased by CS given intravenously, intraperiton
eally as well as subcutaneously, Size-exclusion chromatography showed
a mean MW of the circulating HA of around 50 kDa while urinary HA had
a mean MW of about 10 kDa. Circulating HA has previously been shown to
be very effectively cleared via receptor mediated endocytosis by reti
culoendothelial cells, primarily liver endothelial cells. As CS and Dx
S bind to the same receptors and inhibits HA clearance, the effects of
sulfated polysaccharides on inflammatory conditions and angiogenesis
might be via HA, previously shown to affect these processes. Such a me
chanism could also explain increased HA levels as a secondary event to
increased CS and other sulfated biological polysaccharides in some ph
ysiological and pathological conditions.