Figures & data
Figure 2. Vasorelaxation effects of CTAD and CTAE in endothelium-denude (E−) aortic rings that were pre-contracted with KCl (60 mM, A) or PE (1 µΜ, B). **p < 0.01, *p < 0.05 with the control group. CTAD and CTAE: 50% and 70% ethanol eluates of ethanol extracts from C. tinctoria with AB-8 resin, respectively. Values are means ± SD (n = 10), expressed as the percentage of the vascular tension induced by KCl (60 mM) or PE (1 µΜ).
![Figure 2. Vasorelaxation effects of CTAD and CTAE in endothelium-denude (E−) aortic rings that were pre-contracted with KCl (60 mM, A) or PE (1 µΜ, B). **p < 0.01, *p < 0.05 with the control group. CTAD and CTAE: 50% and 70% ethanol eluates of ethanol extracts from C. tinctoria with AB-8 resin, respectively. Values are means ± SD (n = 10), expressed as the percentage of the vascular tension induced by KCl (60 mM) or PE (1 µΜ).](/cms/asset/bb6c33fb-ea1c-45ec-b8d7-4eafb7f81325/iphb_a_782320_f0002_b.jpg)
Table 1. Vasorelaxant effects of extracts from C. tinctoria against high K+-induced contractions in rat aortic rings.
Figure 3. Concentration-dependent effects of flavanomarein, querceagetin 7-O-β-d-glucoside, marein, okanin, luteolin, quercetin and dihydromelanoxetin on intact rat aorta rings precontracted with KCl (μM). **p < 0.01, *p < 0.05 with the control group. Values are means ± SD (n = 10 rings).
![Figure 3. Concentration-dependent effects of flavanomarein, querceagetin 7-O-β-d-glucoside, marein, okanin, luteolin, quercetin and dihydromelanoxetin on intact rat aorta rings precontracted with KCl (μM). **p < 0.01, *p < 0.05 with the control group. Values are means ± SD (n = 10 rings).](/cms/asset/81f65f3d-799a-4673-aa57-abf955a6cb0f/iphb_a_782320_f0003_b.jpg)
Figure 4. Concentration-dependent effects of quercetin, luteolin and propranolol on intact rat aorta rings precontracted with PE 1 μM. **p < 0.01, *p < 0.05 with control group. Values are means ± SD (n = 10 rings).
![Figure 4. Concentration-dependent effects of quercetin, luteolin and propranolol on intact rat aorta rings precontracted with PE 1 μM. **p < 0.01, *p < 0.05 with control group. Values are means ± SD (n = 10 rings).](/cms/asset/202d996e-e684-4386-aa74-1e1354eefe0f/iphb_a_782320_f0004_b.jpg)
Figure 5. Effects of CTAD and CTAE (3 g/L) on the dose–response curve of the percentage contraction in high K+–Ca2+-free depolarizing solution and cumulative concentration of CaCl2 (0.25 mM–5.00 mM). **p < 0.01, *p < 0.05 with the control group. CTAD and CTAE: 50% and 70% ethanol eluates of ethanol extracts from C. tinctoria with AB-8 resin, respectively. *p < 0.05 compared with control group (n = 10 rings).
![Figure 5. Effects of CTAD and CTAE (3 g/L) on the dose–response curve of the percentage contraction in high K+–Ca2+-free depolarizing solution and cumulative concentration of CaCl2 (0.25 mM–5.00 mM). **p < 0.01, *p < 0.05 with the control group. CTAD and CTAE: 50% and 70% ethanol eluates of ethanol extracts from C. tinctoria with AB-8 resin, respectively. *p < 0.05 compared with control group (n = 10 rings).](/cms/asset/1a1d8448-47fe-4bd3-a928-fd8fb69da8e6/iphb_a_782320_f0005_b.jpg)
Figure 6. Effects of CTA, CTAD and CTAE on PE-induced transient contractions in Ca2+-free solution. **p < 0.01, *p < 0.05 with the control group. CTA: ethanol extracts from C. tinctoria, CTAD and CTAE were 50% and 70% ethanol eluates of CTA with AB-8 resin, respectively. Values represent mean ± SD of 10 determinations.
![Figure 6. Effects of CTA, CTAD and CTAE on PE-induced transient contractions in Ca2+-free solution. **p < 0.01, *p < 0.05 with the control group. CTA: ethanol extracts from C. tinctoria, CTAD and CTAE were 50% and 70% ethanol eluates of CTA with AB-8 resin, respectively. Values represent mean ± SD of 10 determinations.](/cms/asset/d0ee28d9-102e-4e78-9de1-998477fb9750/iphb_a_782320_f0006_b.jpg)