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Research Article

Gastrointestinal effect of methanol extract of Radix Aucklandiae and selected active substances on the transit activity of rat isolated intestinal strips

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Pages 1141-1149 | Received 06 Oct 2013, Accepted 12 Dec 2013, Published online: 20 Mar 2014

Figures & data

Figure 1. Chemical structures of costunolide and dehydrocostuslactone.

Figure 1. Chemical structures of costunolide and dehydrocostuslactone.

Table 1. Effects of different doses of RA ext on gastrointestinal transit in normal mice (n = 8).

Table 2. Effects of different doses of RA ext on gastrointestinal transit in neostigmine mice (n = 8).

Figure 2. Effects of different concentrations of RA ext on smooth muscle contraction of rat-isolated jejunum.

Figure 2. Effects of different concentrations of RA ext on smooth muscle contraction of rat-isolated jejunum.

Figure 3. Effects of different concentrations of RA ext on Ach (A), 5-HT (B), KCl (C)-induced contraction of rat-isolated jejunum. The contractions induced by Ach, 5-HT and KCl in the absence of the extract acted as control. Results are mean ± SEM, n = 5. Significantly different from control ***p < 0.001.

Figure 3. Effects of different concentrations of RA ext on Ach (A), 5-HT (B), KCl (C)-induced contraction of rat-isolated jejunum. The contractions induced by Ach, 5-HT and KCl in the absence of the extract acted as control. Results are mean ± SEM, n = 5. Significantly different from control ***p < 0.001.

Figure 4. Dose–effect curves of CaCl2 on rabbit-isolated ileum in the absence (♦) and in the presence of RA ext (▴ 0.1 mg/mL; × 0.2 mg/mL; --- 0.3 mg/mL; • 0.4 mg/mL) and verapamil (▪ 0.025 mM). Results are mean ± SEM, n = 5.

Figure 4. Dose–effect curves of CaCl2 on rabbit-isolated ileum in the absence (♦) and in the presence of RA ext (▴ 0.1 mg/mL; × 0.2 mg/mL; --- 0.3 mg/mL; • 0.4 mg/mL) and verapamil (▪ 0.025 mM). Results are mean ± SEM, n = 5.

Figure 5. Dose–effect curves of CaCl2 on rabbit-isolated ileum in the absence (♦) and in the presence of RA ext, costunolide, and dehydrocostuslactone. (A) RA ext (▴ 0.2 mg/mL), costunolide (× 0.54 μg/mL), dehydrocostuslactone (--- 0.46 μg/mL), costunolide–dehydrocostuslactone (• 0.54–0.46 μg/mL), and verapamil (▪ 0.01 mM). (B) RA ext (▴ 0.3 mg/mL), costunolide (× 0.81 μg/mL), dehydrocostuslactone (--- 0.69 μg/mL), costunolide–dehydrocostuslactone (• 0.81–0.69 μg/mL), and verapamil (▪ 0.01 mM). (C) RA ext (▴ 0.4 mg/mL), costunolide (× 1.08 μg/mL), dehydrocostuslactone (--- 0.92 μg/mL), costunolide–dehydrocostuslactone (• 1.08–0.92 μg/mL), and verapamil (▪ 0.01 mM). Results are mean ± SEM, n = 5.

Figure 5. Dose–effect curves of CaCl2 on rabbit-isolated ileum in the absence (♦) and in the presence of RA ext, costunolide, and dehydrocostuslactone. (A) RA ext (▴ 0.2 mg/mL), costunolide (× 0.54 μg/mL), dehydrocostuslactone (--- 0.46 μg/mL), costunolide–dehydrocostuslactone (• 0.54–0.46 μg/mL), and verapamil (▪ 0.01 mM). (B) RA ext (▴ 0.3 mg/mL), costunolide (× 0.81 μg/mL), dehydrocostuslactone (--- 0.69 μg/mL), costunolide–dehydrocostuslactone (• 0.81–0.69 μg/mL), and verapamil (▪ 0.01 mM). (C) RA ext (▴ 0.4 mg/mL), costunolide (× 1.08 μg/mL), dehydrocostuslactone (--- 0.92 μg/mL), costunolide–dehydrocostuslactone (• 1.08–0.92 μg/mL), and verapamil (▪ 0.01 mM). Results are mean ± SEM, n = 5.

Figure 6. Dose–effect curves of CaCl2 on rabbit-isolated ileum in the absence (♦) and in the presence of costunolide and dehydrocostuslactone.

Figure 6. Dose–effect curves of CaCl2 on rabbit-isolated ileum in the absence (♦) and in the presence of costunolide and dehydrocostuslactone.

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