Abstract
Though supplementation of chromium has been found to improve deranged carbohydrate
and lipid metabolism associated with suboptimal chromium intake in patients, its usefulness
in the treatment of diabetes mellitus of variable etiology remains questionable. In
the present investigation, the effect of 6 wk oral administration of chromium chloride
(CC) on the glucose and lipid metabolism was studied in streptozotocin (STZ) diabetic
and neonatal-STZ (nSTZ) diabetic rats. Further, its cellular mechanism was studied
using 3T3-L1 adipocyte and C2C12 myoblast cell lines. Treatment with CC significantly
improved the impaired glucose tolerance and insulin sensitivity of both STZ diabetic
and nSTZ diabetic rats without any change in basal or glucose stimulated insulin response
indicating insulin-sensitizing action of chromium. CC treatment also significantly
improved deranged lipid metabolism. CC per se did not produce any effect in vitro,
however, significantly increased insulin stimulated glucose uptake in C2C12 myoblasts
and differentiation of 3T3-L1 preadipocytes into mature adipocytes supporting the
in vivo insulin-sensitizing action of chromium. This study shows that CC exhibited
significant anti-diabetic potential in chemically-induced diabetes in rats, the mechanism
of which appears to be potentiation of insulin actions at the target tissues leading
to improved peripheral insulin sensitivity.
Key words
Chromium chloride - insulin resistance - 3T3-L1 adipocytes - C2C12 myoblasts
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Dr. Ramesh K. Goyal
Department of Pharmacology
L.M. College of Pharmacy
P.O. Box 4011, Navrangpura
Ahmedabad 380 009
India
Telefon: 91-79-6302746
Fax: 91-79-6 30 48 65
eMail: goyalrk@rediffmail.com