Fermented soybean-derived Touchi-extract with anti-diabetic effect via alpha-glucosidase inhibitory action in a long-term administration study with KKA(y) mice
H. Fujita et T. Yamagami, Fermented soybean-derived Touchi-extract with anti-diabetic effect via alpha-glucosidase inhibitory action in a long-term administration study with KKA(y) mice, LIFE SCI, 70(2), 2001, pp. 219-227
A water-soluble Touchi-extract (TE) exerts a potent inhibitory activity aga
inst rat intestinal alpha -glucosidase in foodstuffs, and elicited anti-gly
cemic effects in rats and humans with single-bolus oral administration. In
the present study, genetically modified diabetic model KKA(y) mice were use
d to examine the long-term effects of TE. Eight-week-old male KKA(y) mice w
ere fed with CE-2 chow containing 0.08 and 0.4% of TE for 60 days. In the l
atter group, fasting blood glucose levels decreased (6.68 +/- 0.41 mmol/L)
significantly (p<0.05) after a 60-day ingestion period compared with contro
ls (8.75 +/- 0.54 mmol/L). Moreover, postprandial blood glucose levels were
also significantly reduced (16.79 +/- 2.28 mmol/L; p<0.01) after ingesting
TE for only 30 days compared with controls (28.49 +/- 0.59 mmol/L). On ora
l TE treatment for 60 days, postprandial increases in the blood glucose lev
el after oral loading of sucrose (2 g/kg) at 30 (p<0.05) and 60 (p<0.01) mi
n were significantly depressed compared with controls. Indexes for serum li
pids; viz., total cholesterol (p<0.05) and triglyceride (p<0.01) levels sig
nificantly decreased after TE ingestion. Indexes for hepatic functions, suc
h as glutamic-oxaloacetic transaminase (p<0.01), glutamic-pyruvic transamin
ase and gama-glutamyl transpeptide levels, were similarly suppressed. Organ
weights of the heart, kidney, jejunum, liver and spleen increased in contr
ol KKA(y) mice due to hyperinsulinemia. Interestingly, the respective organ
weights decreased (p<0.05, 0.01) and the jejunum length was reduced (p<0.0
5) significantly in the TE-treated groups. All in all, TE demonstrated an a
nti-hyperglycemic effect and may have potential use in the management of no
n-insulin-dependent diabetic mellitus. ((C) 2001 Elsevier Science Inc. All
rights reserved.