Brassica oleracea var. acephala (kale) CHCl3 fraction induces adipocyte differentiation and reduces plasma glucose concentration in animal models of type 2 diabetes
We recently discovered that MeOH extract from Brassica oleracea var. acephala (kale) (BO) promotes adipocyte differentiation in vitro. Furthermore, we discovered that the CHCl 3 fraction, in particular, promotes adipocyte differentiation in vitro and acts as an insulin sensitizer in vivo. BO is wide...
Saved in:
Published in | Journal of Traditional Medicines Vol. 24; no. 6; pp. 187 - 192 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English Japanese |
Published |
Medical and Pharmaceutical Society for WAKAN-YAKU
2007
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | We recently discovered that MeOH extract from Brassica oleracea var. acephala (kale) (BO) promotes adipocyte differentiation in vitro. Furthermore, we discovered that the CHCl 3 fraction, in particular, promotes adipocyte differentiation in vitro and acts as an insulin sensitizer in vivo. BO is widely taken as juice in Japan because of its vitamins and functional compounds that are beneficial to health and wellness. However, there are no studies evaluating the antihyperglycemic activity of BO in the literature. We examined the effect of the CHCl 3 fraction on plasma glucose concentrations in obese hyperglycemic db/db mice. The CHCl 3 fraction reduced hyperglycemia in mouse models of type 2 diabetes and acted as an insulin sensitizer, as indicated by the lowered plasma glucose concentration after chronic oral administration of the CHCl 3 fraction. This fraction and thiazoridinedione antidiabetic agents, such as ciglitazone, share many biological activities: induction of adipocyte differentiation in vitro, and reduction of hyperglycemia in animal models of type 2 diabetes. This finding demonstrates that BO may contain insulin-sensitizing constituents and could lead to the discovery of novel candidates for a new type of insulin-sensitizing drug. |
---|---|
ISSN: | 1880-1447 1881-3747 |
DOI: | 10.11339/jtm.24.187 |