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. 2022 Nov 10;14(22):4752. doi: 10.3390/nu14224752

Table 4.

Comparison of pharmacokinetic parameters of resveratrol and its main metabolites administered alone and combined with alcohol.

Parameters (Unit) Resveratrol R3G R3S
Alone Combination Alone Combination Alone Combination
AUC(0–12h) (nmol.h/mL) 7779.5 ± 1103.0 1036.0 ± 181.4 ***↓ 52,550.5 ± 11,692.2 26,734.7 ± 3102.9 *↓ 2716.0 ± 455.0 1195.0 ± 193.7 *↓
AUC(0-∞) (nmol.h/mL) 10,302.1 ± 2484.6 2215.5 ± 908.7 *↓ 56,446.3 ± 11,852.6 31,948.1 ± 1964.0 2358.4 ± 390.4 1764.8 ± 363.9
Cmax (nmol/mL) 4986.0 ± 865.0 453.6 ± 134.5 ***↓ 11,211.7 ± 2441.7 6012.0 ± 259.0 801.8 ± 160.6 333.8 ± 57.2 *↓
Tmax (h) 0.7 ±0.1 0.3 ± 0.1 ***↓ 0.8 ± 0.1 0.3± 0.0 ***↓ 0.7 ± 0.1 0.3 ± 0.0 *↓
t1/2 (h) 1.7 ± 0.2 4.2 ± 0.8 *↑ 2.1 ± 0.5 5.2 ± 1.1 *↑ 2.4 ± 0.3 6.5 ± 1.4 ***↑

AUC(0–12h), area under the plasma concentration-time curve from 0 to 12 h; AUC(0–∞), area under the plasma concentration-time curve from 0 to infinity hours; Cmax, maximal concentration; Tmax, time to peak concentration; t1/2, eliminate half-life. R3G, trans-resveratrol-3-o-β-glucuronide; R3S, trans-resveratrol-3-sulfate salt. Data are expressed as the mean ± SEM. * p < 0.05; *** p < 0.001. : significantly increased; : significantly decreased.