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Published in: BMC Complementary Medicine and Therapies 1/2019

Open Access 01-12-2019 | Pharmacokinetics | Research article

Comparative pharmacokinetics of oxyresveratrol alone and in combination with piperine as a bioenhancer in rats

Authors: Dhirarin Junsaeng, Tosapol Anukunwithaya, Phanit Songvut, Boonchoo Sritularak, Kittisak Likhitwitayawuid, Phisit Khemawoot

Published in: BMC Complementary Medicine and Therapies | Issue 1/2019

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Abstract

Background

Oxyresveratrol is a major bioactive component derived from the heartwood of Artocarpus lacucha. This compound exerts several biological activities, including neuroprotective effects in vitro and in vivo. However, there is limited pharmacokinetic information on this compound, especially its distribution in neuronal tissue and its route of excretion. The aim of this study was to investigate the pharmacokinetic profiles of oxyresveratrol alone and in combination with piperine as a bioenhancer in rats.

Methods

Male Wistar rats were administered with oxyresveratrol 10 mg/kg, oxyresveratrol 10 mg/kg plus piperine 1 mg/kg via intravenous or oxyresveratrol 100 mg/kg, oxyresveratrol 100 mg/kg plus piperine 10 mg/kg via oral gavage. Plasma, internal organs, urine, and feces were collected. Determination of the oxyresveratrol concentration in biological samples was performed by liquid chromatography tandem mass spectrometry.

Results

The combination with piperine had shown a significantly higher maximum concentration in plasma approximately 1500 μg/L within 1–2 h after oral dosing, and could increase oral bioavailability of oxyresveratrol approximately 2–fold. Oxyresveratrol could widely distributed most of the internal organs with a tissue to plasma ratio of 10–100 fold within 5 min after dosing. Urinary excretion of oxyresveratrol glucuronide was the major route of excretion after administration of oxyresveratrol alone and in combination with piperine.

Conclusion

The addition of piperine could enhance some of the pharmacokinetic properties of oxyresveratrol via both intravenous and oral administration. This pharmacokinetic information will be useful for appropriate strategies to develop oxyresveratrol as a phytopharmaceutical product.
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Literature
1.
go back to reference Sritularak B, De-Eknamkul W, Likhitwitayawuid K. Tyrosinase inhibitors from Artocarpus lakoocha. Thai J Pharm Sci. 1998;22:149–55. Sritularak B, De-Eknamkul W, Likhitwitayawuid K. Tyrosinase inhibitors from Artocarpus lakoocha. Thai J Pharm Sci. 1998;22:149–55.
2.
go back to reference Likhitwitayawuid K, Sornsute A, Sritularak B, Ploypradith P. Chemical transformations of oxyresveratrol (trans–2,4,3′,5′–tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent. Bioorg Med Chem Lett. 2006;16:5650–3.CrossRef Likhitwitayawuid K, Sornsute A, Sritularak B, Ploypradith P. Chemical transformations of oxyresveratrol (trans–2,4,3′,5′–tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent. Bioorg Med Chem Lett. 2006;16:5650–3.CrossRef
3.
go back to reference Tengamnuay P, Pengrungruangwong K, Pheansri I, Likhitwitayawuid K. Artocarpus lakoocha heartwood extract as a novel cosmetic ingredient: evaluation of the in vitro anti–tyrosinase and in vivo skin whitening activities. Int J Cosmet Sci. 2006;28:269–76.CrossRef Tengamnuay P, Pengrungruangwong K, Pheansri I, Likhitwitayawuid K. Artocarpus lakoocha heartwood extract as a novel cosmetic ingredient: evaluation of the in vitro anti–tyrosinase and in vivo skin whitening activities. Int J Cosmet Sci. 2006;28:269–76.CrossRef
4.
go back to reference Aftab N, Likhitwitayawuid K, Vieira A. Comparative antioxidant activities and synergism of resveratrol and oxyresveratrol. Nat Prod Res. 2010;24:1726–33.CrossRef Aftab N, Likhitwitayawuid K, Vieira A. Comparative antioxidant activities and synergism of resveratrol and oxyresveratrol. Nat Prod Res. 2010;24:1726–33.CrossRef
5.
go back to reference Ashraf MI, Shahzad M, Shabbir A. Oxyresveratrol ameliorates allergic airway inflammation via attenuation of IL–4, IL–5, and IL–13 expression levels. Cytokine. 2010;76:375–81.CrossRef Ashraf MI, Shahzad M, Shabbir A. Oxyresveratrol ameliorates allergic airway inflammation via attenuation of IL–4, IL–5, and IL–13 expression levels. Cytokine. 2010;76:375–81.CrossRef
6.
go back to reference Chung KO, Kim BY, Lee MH, Kim YR, Chung HY, Park JH, Moon JO. In–vitro and in–vivo anti–inflammatory effect of oxyresveratrol from Morus alba L. J Pharm Pharmacol. 2003;55:1695–700.CrossRef Chung KO, Kim BY, Lee MH, Kim YR, Chung HY, Park JH, Moon JO. In–vitro and in–vivo anti–inflammatory effect of oxyresveratrol from Morus alba L. J Pharm Pharmacol. 2003;55:1695–700.CrossRef
7.
go back to reference Galindo I, Hernáez B, Berná J, Fenoll J, Cenis JL, Escribano JM, Alonso C. Comparative inhibitory activity of the stilbenes resveratrol and oxyresveratrol on African swine fever virus replication. Antivir Res. 2011;91:57–63.CrossRef Galindo I, Hernáez B, Berná J, Fenoll J, Cenis JL, Escribano JM, Alonso C. Comparative inhibitory activity of the stilbenes resveratrol and oxyresveratrol on African swine fever virus replication. Antivir Res. 2011;91:57–63.CrossRef
8.
go back to reference Lipipun V, Sasivimolphan P, Yoshida Y, Daikoku T, Sritularak B, Ritthidej G, Likhitwitayawuid K, Pramyothin P, Hattori M, Shiraki K. Topical cream–based oxyresveratrol in the treatment of cutaneous HSV–1 infection in mice. Antivir Res. 2011;91:154–60.CrossRef Lipipun V, Sasivimolphan P, Yoshida Y, Daikoku T, Sritularak B, Ritthidej G, Likhitwitayawuid K, Pramyothin P, Hattori M, Shiraki K. Topical cream–based oxyresveratrol in the treatment of cutaneous HSV–1 infection in mice. Antivir Res. 2011;91:154–60.CrossRef
9.
go back to reference Weber JT, Lamont M, Chibrikova L, Fekkes D, Vlug AS, Lorenz P, Kreutzmann P, Slemmer JE. Potential neuroprotective effects of oxyresveratrol against traumatic injury. Eur J Pharmacol. 2012;680:55–62.CrossRef Weber JT, Lamont M, Chibrikova L, Fekkes D, Vlug AS, Lorenz P, Kreutzmann P, Slemmer JE. Potential neuroprotective effects of oxyresveratrol against traumatic injury. Eur J Pharmacol. 2012;680:55–62.CrossRef
10.
go back to reference Suwannalert P, Povichit N, Puchadapirom P, Junking M. Anti–aging activity and non–toxic dose of phytooxyresveratrol from Artocarpus lakoocha Roxb. Trop J Pharm Res. 2012;11:69–74.CrossRef Suwannalert P, Povichit N, Puchadapirom P, Junking M. Anti–aging activity and non–toxic dose of phytooxyresveratrol from Artocarpus lakoocha Roxb. Trop J Pharm Res. 2012;11:69–74.CrossRef
11.
go back to reference Chen W, Yeo SCM, Elhennawy MGAA, Lin HS. Oxyresveratrol: a bioavailable dietary polyphenol. J Funct Foods. 2016;22:122–31.CrossRef Chen W, Yeo SCM, Elhennawy MGAA, Lin HS. Oxyresveratrol: a bioavailable dietary polyphenol. J Funct Foods. 2016;22:122–31.CrossRef
12.
go back to reference Breuer C, Wolf G, Andrabi SA, Lorenz P, Horn TFW. Blood–brain barrier permeability to the neuroprotectant oxyresveratrol. Neurosci Lett. 2006;393:113–8.CrossRef Breuer C, Wolf G, Andrabi SA, Lorenz P, Horn TFW. Blood–brain barrier permeability to the neuroprotectant oxyresveratrol. Neurosci Lett. 2006;393:113–8.CrossRef
13.
go back to reference Huang HL, Zhang JQ, Chena GT, Lu ZQ, Sha N, Guo DA. Simultaneous determination of oxyresveratrol and resveratrol in rat bile and urine by HPLC after oral administration of Smilax China extract. Nat Prod Commun. 2009;4:825–30.PubMed Huang HL, Zhang JQ, Chena GT, Lu ZQ, Sha N, Guo DA. Simultaneous determination of oxyresveratrol and resveratrol in rat bile and urine by HPLC after oral administration of Smilax China extract. Nat Prod Commun. 2009;4:825–30.PubMed
14.
go back to reference Mei M, Ruan JQ, Wu WJ, Zhou RN, Lei JP, Zhao HY, Yan R, Wang YT. In vitro pharmacokinetic characterization of mulberroside a, the main polyhydroxylated stilbene in mulberry (Morus alba L.), and its bacterial metabolite oxyresveratrol in traditional oral use. J Agric Food Chem. 2012;60:2299–308.CrossRef Mei M, Ruan JQ, Wu WJ, Zhou RN, Lei JP, Zhao HY, Yan R, Wang YT. In vitro pharmacokinetic characterization of mulberroside a, the main polyhydroxylated stilbene in mulberry (Morus alba L.), and its bacterial metabolite oxyresveratrol in traditional oral use. J Agric Food Chem. 2012;60:2299–308.CrossRef
15.
go back to reference Sangsen Y, Sooksawate T, Likhitwitayawuid K, Sritularak B, Wiwattanapatapee R. A self-microemulsifying formulation of oxyresveratrol prevents amyloid beta protein-induced neurodegeneration in mice. Planta Med. 2018;84:830–28. Sangsen Y, Sooksawate T, Likhitwitayawuid K, Sritularak B, Wiwattanapatapee R. A self-microemulsifying formulation of oxyresveratrol prevents amyloid beta protein-induced neurodegeneration in mice. Planta Med. 2018;84:830–28.
16.
go back to reference Johnson JJ, Nihal M, Siddiqui CO, Bailey HH, Mukhtar H, Ahmad N. Enhancing the bioavailability of resveratrol by combining it with piperine. Mol Nutr Food Res. 2011;55:1169–76.CrossRef Johnson JJ, Nihal M, Siddiqui CO, Bailey HH, Mukhtar H, Ahmad N. Enhancing the bioavailability of resveratrol by combining it with piperine. Mol Nutr Food Res. 2011;55:1169–76.CrossRef
17.
go back to reference Sun Y, Xia ZY, Zheng JK, Qiu PJ, Zhang LJ, McClements DJ, Xiao H. Nanoemulsion-based delivery systems for nutraceuticals: influence of carrier oil type on bioavailability of pterostilbene. J Funct Foods. 2015;13:61–70.CrossRef Sun Y, Xia ZY, Zheng JK, Qiu PJ, Zhang LJ, McClements DJ, Xiao H. Nanoemulsion-based delivery systems for nutraceuticals: influence of carrier oil type on bioavailability of pterostilbene. J Funct Foods. 2015;13:61–70.CrossRef
18.
go back to reference Suresh D, Srinivasan K. Influence of curcumin, capsaicin, and piperine on the rat liver drug–metabolizing enzyme system in vivo and in vitro. Can J Physiol Pharmacol. 2006;84:1259–65.CrossRef Suresh D, Srinivasan K. Influence of curcumin, capsaicin, and piperine on the rat liver drug–metabolizing enzyme system in vivo and in vitro. Can J Physiol Pharmacol. 2006;84:1259–65.CrossRef
19.
go back to reference Atal CK, Dubey RK, Singh J. Biochemical basis of enhanced drug bioavailability by piperine: evidence that piperine is a potent inhibitor of drug metabolism. J Pharmacol Exp Ther. 1985;232:258–62.PubMed Atal CK, Dubey RK, Singh J. Biochemical basis of enhanced drug bioavailability by piperine: evidence that piperine is a potent inhibitor of drug metabolism. J Pharmacol Exp Ther. 1985;232:258–62.PubMed
20.
go back to reference Bhardwaj RK, Glaeser H, Becquemont L, Klotz U, Gupta SK, Fromm MF. Piperine, a major constituent of black pepper, inhibits human P–glycoprotein and CYP3A4. J Pharmacol Exp Ther. 2002;302:645–50.CrossRef Bhardwaj RK, Glaeser H, Becquemont L, Klotz U, Gupta SK, Fromm MF. Piperine, a major constituent of black pepper, inhibits human P–glycoprotein and CYP3A4. J Pharmacol Exp Ther. 2002;302:645–50.CrossRef
21.
go back to reference Charan J, Kantharia ND. How to calculate sample size in animal studies? J Pharmacol Pharmacother. 2013;4:303–6.CrossRef Charan J, Kantharia ND. How to calculate sample size in animal studies? J Pharmacol Pharmacother. 2013;4:303–6.CrossRef
22.
go back to reference Huang H, Chen G, Lu Z, Zhang J, Guo DA. Identification of seven metabolites of oxyresveratrol in rat urine and bile using liquid chromatography/tandem mass spectrometry. Biomed Chromatogr. 2010;24:426–32.CrossRef Huang H, Chen G, Lu Z, Zhang J, Guo DA. Identification of seven metabolites of oxyresveratrol in rat urine and bile using liquid chromatography/tandem mass spectrometry. Biomed Chromatogr. 2010;24:426–32.CrossRef
23.
go back to reference Basu S, Patel VB, Jana S, Patel H. Liquid chromatography tandem mass spectrometry method (LC–MS/MS) for simultaneous determination of piperine, cinnamic acid and gallic acid in rat plasma using a polarity switch technique. Anal Methods. 2013;5:967–76.CrossRef Basu S, Patel VB, Jana S, Patel H. Liquid chromatography tandem mass spectrometry method (LC–MS/MS) for simultaneous determination of piperine, cinnamic acid and gallic acid in rat plasma using a polarity switch technique. Anal Methods. 2013;5:967–76.CrossRef
24.
go back to reference Hu N, Mei M, Ruan J, Wu W, Wang Y, Yan R. Regioselective glucuronidation of oxyresveratrol, a natural hydroxystilbene, by human liver and intestinal microsomes and recombinant UGTs. Drug Metab Pharmacokinet. 2014;29:229–36.CrossRef Hu N, Mei M, Ruan J, Wu W, Wang Y, Yan R. Regioselective glucuronidation of oxyresveratrol, a natural hydroxystilbene, by human liver and intestinal microsomes and recombinant UGTs. Drug Metab Pharmacokinet. 2014;29:229–36.CrossRef
25.
go back to reference Abdulla MA, Ali HM, Ahmed KAA, Noor SM, Ismail S. Evaluation of the anti–ulcer activities of Morus albaextracts in experimentally–induced gastric ulcer in rats. Biomed Res. 2009;20:35–9. Abdulla MA, Ali HM, Ahmed KAA, Noor SM, Ismail S. Evaluation of the anti–ulcer activities of Morus albaextracts in experimentally–induced gastric ulcer in rats. Biomed Res. 2009;20:35–9.
26.
go back to reference Andrabi SA, Spina MG, Lorenz P, Ebmeyer U, Wolf G, Horn TF. Oxyresveratrol (trans–2,3′,4,5′–tetrahydroxystilbene) is neuroprotective and inhibits the apoptotic cell death in transient cerebral ischemia. Brain Res Rev. 2004;1017:98–107.CrossRef Andrabi SA, Spina MG, Lorenz P, Ebmeyer U, Wolf G, Horn TF. Oxyresveratrol (trans–2,3′,4,5′–tetrahydroxystilbene) is neuroprotective and inhibits the apoptotic cell death in transient cerebral ischemia. Brain Res Rev. 2004;1017:98–107.CrossRef
27.
go back to reference Baur JA, Sinclair DA. Therapeutic potential of resveratrol: the in vivo evidence. Nat Rev Drug Discov. 2006;5:493–506.CrossRef Baur JA, Sinclair DA. Therapeutic potential of resveratrol: the in vivo evidence. Nat Rev Drug Discov. 2006;5:493–506.CrossRef
28.
go back to reference Das S, Lin HS, Ho PC, Ng KY. The impact of aqueous solubility and dose on the pharmacokinetic profiles of resveratrol. Pharm Res. 2008;25:2593–600.CrossRef Das S, Lin HS, Ho PC, Ng KY. The impact of aqueous solubility and dose on the pharmacokinetic profiles of resveratrol. Pharm Res. 2008;25:2593–600.CrossRef
29.
go back to reference Marier JF, Vachon P, Gritsas A, Zhang J, Moreau JP, Ducharme MP. Metabolism and disposition of resveratrol in rats: extent of absorption, glucuronidation, andenterohepatic recirculation evidenced by a linked-rat model. J Pharmacol Exp Ther. 2002;302:369–73.CrossRef Marier JF, Vachon P, Gritsas A, Zhang J, Moreau JP, Ducharme MP. Metabolism and disposition of resveratrol in rats: extent of absorption, glucuronidation, andenterohepatic recirculation evidenced by a linked-rat model. J Pharmacol Exp Ther. 2002;302:369–73.CrossRef
30.
go back to reference Ndiaye M, Kumar R, Ahmad N. Resveratrol in cancer management: where are we and where we go from here? Ann N Y Acad Sci. 2011;1215:144–9.CrossRef Ndiaye M, Kumar R, Ahmad N. Resveratrol in cancer management: where are we and where we go from here? Ann N Y Acad Sci. 2011;1215:144–9.CrossRef
31.
go back to reference Shoba G, Joy D, Joseph T, Majeed M, Rajendran R, Srinivas PS. Influence of piperine on the pharmacokinetics of curcumin in animals and human volunteers. Planta Med. 1998;64:353–6.CrossRef Shoba G, Joy D, Joseph T, Majeed M, Rajendran R, Srinivas PS. Influence of piperine on the pharmacokinetics of curcumin in animals and human volunteers. Planta Med. 1998;64:353–6.CrossRef
32.
go back to reference Lambert JD, Hong J, Kim DH, Mishin VM, Yang CS. Piperine enhances the bioavailability of the tea polyphenol [−]–epigallocatechin-3-gallate in mice. J Nutr. 2004;134:1948–52.CrossRef Lambert JD, Hong J, Kim DH, Mishin VM, Yang CS. Piperine enhances the bioavailability of the tea polyphenol [−]–epigallocatechin-3-gallate in mice. J Nutr. 2004;134:1948–52.CrossRef
33.
go back to reference Reen RK, Jamwal DS, Taneja SC, Koul JL, Dubey RK, Wiebel FJ, Singh J. Impairment of UDP–glucose dehydrogenase and glucuronidation activities in liver and small intestine of rat and Guinea pig in vitro by piperine. Biochem Pharmacol. 1993;46:229–38.CrossRef Reen RK, Jamwal DS, Taneja SC, Koul JL, Dubey RK, Wiebel FJ, Singh J. Impairment of UDP–glucose dehydrogenase and glucuronidation activities in liver and small intestine of rat and Guinea pig in vitro by piperine. Biochem Pharmacol. 1993;46:229–38.CrossRef
Metadata
Title
Comparative pharmacokinetics of oxyresveratrol alone and in combination with piperine as a bioenhancer in rats
Authors
Dhirarin Junsaeng
Tosapol Anukunwithaya
Phanit Songvut
Boonchoo Sritularak
Kittisak Likhitwitayawuid
Phisit Khemawoot
Publication date
01-12-2019
Publisher
BioMed Central
Published in
BMC Complementary Medicine and Therapies / Issue 1/2019
Electronic ISSN: 2662-7671
DOI
https://doi.org/10.1186/s12906-019-2653-y

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