Hh. Donaubauer et al., SUBCHRONIC INTRAVENOUS TOXICITY STUDIES WITH GAMMA-CYCLODEXTRIN IN RATS, Regulatory toxicology and pharmacology, 27(2), 1998, pp. 189-198
The toxicity of gamma-cyclodextrin (gamma-CD), a cyclic polymer of 8 a
lpha-1,4-linked glucopyranosyl units with potential applications in fo
od and pharmaceutical preparations, was examined in two toxicity studi
es in rats with intravenous administration of gamma-CD for 1 and 3 mon
ths, respectively. Each study comprised four groups of 15 rats/sex eac
h. In the 1-month study, gamma-CD was administered to the four groups
at daily doses of 0 (controls), 200, 630, or 2000 mg/kg body wt, respe
ctively. In the 3-month study, dose levels of 0, 60, 120, and 600 mg/k
g body wt were tested. gamma-CD was administered by injection of an aq
ueous solution in the tail vein. At the end of the treatment period, 1
0 rats/sex/ group were killed. The remaining 5 rats continued the stud
y without treatment (recovery period) for 4 weeks (1-month study) or 5
weeks (3-month study). The treatment was generally well tolerated and
there were no mortalities in either study. Mean body weights tended t
o be slightly reduced during the first and second week in the groups r
eceiving gamma-CD at doses of greater than or equal to 600 mg/kg body
wt. Thereafter, body weights did not differ between treated groups and
controls. Examination of standard hematological parameters at the end
of the treatment period revealed decreased erythrocyte counts, hemogl
obin, hematocrit values, and thrombocyte counts in both studies at gam
ma-CD doses of greater than or equal to 600 mg/ kg body wt. Concomitan
tly, the relative weight of the spleen was increased. In the high-dose
group of the 1-month study, hemoglobin was detected in the urine. It
is likely that a direct interaction of the injected gamma-CD with bloo
d cells accounts for these effects. Examination of standard clinicoche
mical parameters at the end of the treatment period did not reveal any
changes that mould point to the liver as a target organ for gamma-CD
toxicity. This was confirmed by the absence of histopathological chang
es in the liver. The only noteworthy observation was an increase of se
rum urea in the high-dose group (either sex) of the 1-month study and
in males of the high-dose group of the 3-month study, suggesting a sli
ght impairment of the renal function. On histopathological examination
, reabsorptive vacuolation was seen in the renal tubular epithelium of
some rats receiving gamma-CD at doses of 630 or 600 mg/kg body wt in
the 1- and 3-month study, respectively. In the high-dose group of the
1-month study, all animals exhibited this morphological effect. Howeve
r, degenerative changes were not observed in the kidneys, and the vacu
olation was fully reversible on cessation of the treatment. The occurr
ence of absorptive vacuolation was attributed to the presence of gamma
-CD in urine (parenterally administered gamma-CD is excreted unchanged
in the urine). Simple or focal hyperplasia of the urinary bladder epi
thelium was observed in some animals of the high-dose group of the S-m
onth study. This hyperplasia was not seen at the end of the recovery p
eriod and, therefore, was considered to be a reactive response to the
treatment. The most prominent morphological effect was an accumulation
of phagocytosing alveolar macrophages (histiocytosis) in the lungs of
rats receiving gamma-CD at a dose of 600 mg/kg body wt. This effect w
as associated with an increase of relative lung weights. However, dege
nerative changes (fibrosis) were not seen, and at the end of the recov
ery period only some small residual changes were noted in the lungs of
a few animals. In conclusion, daily intravenous gamma-CD doses of 120
-200 mg/kg body wt were tolerated without adverse effects. The changes
observed at higher dose levels (greater than or equal to-600-630 mg/k
g body wt) were reversible on cessation of the treatment and are consi
dered to be biochemical responses, without toxicological relevance, to
the presence of transiently high concentrations of gamma-CD in the ci
rculating blood. (C) 1998 Academic Press.