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Description
Some preclinical data suggest additional anti-inflammatory or Kupffer-cellmediated effects, but the dominant, best-supported mechanism is metabolic: less substrate delivered to a less insulin-resistant liver
Tetrahydropyrroloquinolinone type dual inhibitors of aromatase/aldosterone synthase as a novel strategy for breast cancer patients with elevated cardiovascular risks
Materials and methods There were 10 experimental groups (n = 68 rats/group)
Cell scratch experiment L929 cells were seeded in 6-well plates (8 10 5 cells per well) and cultured for 24 h to form a cell monolayer
American Journal of Clinical Nutrition 1994;60(1):211
