Close
  Indian J Med Microbiol
 

Figure 1: Rat aorta angiogenesis assay. (a) negative control (1% dimethyl sulfoxide), suramin (b) 12.5 μg/mL zerumbone (c), 6.25 μg/mL zerumbone (d), 3.125 μg/mL zerumbone (e), and (f) 1.56 μg/mL zerumbone. The antiangiogenesis activity was quantified by measuring the cell sprouting area around the aorta. Arrows indicate the sprouting of microvessel from the rat aorta, magnification (×4)

Figure 1: Rat aorta angiogenesis assay. (a) negative control (1% dimethyl sulfoxide), suramin (b) 12.5 μg/mL zerumbone (c), 6.25 μg/mL zerumbone (d), 3.125 μg/mL zerumbone (e), and (f) 1.56 μg/mL zerumbone. The antiangiogenesis activity was quantified by measuring the cell sprouting area around the aorta. Arrows indicate the sprouting of microvessel from the rat aorta, magnification (×4)