Evidence map›Paper›PMID 38904001›Full record

ArticleFrontiers in pharmacology2024

Unraveling the interconversion pharmacokinetics and oral bioavailability of the major ginger constituents: [6]-gingerol, [6]-shogaol, and zingerone after single-dose administration in rats.

Phanit Songvut, Watanyoo Nakareangrit, Wanida Cholpraipimolrat, Jackapun Kwangjai, Luksamee Worasuttayangkurn, Piyajit Watcharasit, Jutamaad Satayavivad

Abstract read
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Article in Frontiers in pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Phanit Songvut *Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.
Watanyoo Nakareangrit *Translational Research Unit, Chulabhorn Research Institute, Bangkok, Thailand.
Wanida CholpraipimolratLaboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.
Jackapun KwangjaiFood and Drug Quality Unit, Chulabhorn Research Institute, Bangkok, Thailand.
Luksamee WorasuttayangkurnLaboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.
Piyajit WatcharasitLaboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.
Jutamaad SatayavivadLaboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The available Purpose: This study presents the first comprehensive Methods: The pharmacokinetics was investigated through single intravenous (3 mg/kg) or oral (30 mg/kg) administration of [6]-gingerol, [6]-shogaol, or zingerone, followed by the determination of their tissue distribution after oral dosing (30 mg/kg). Intravenous pharmacokinetics was leveraged to evaluate the interconversion, circumventing potential confounders associated with the oral route. Results: All rats tolerated these compounds throughout the pharmacokinetic study. The parent compounds exhibited rapid but partial absorption, and extensive organ distribution with substantial biotransformation, thereby limiting the oral bioavailability of each compound to below 2% when administered as pure compounds. Conversion of [6]-gingerol to [6]-shogaol after intravenous administration, demonstrated a significantly larger clearance compared to the reverse conversion ([6]-shogaol to [6]-gingerol). The irreversible metabolic clearance for both compounds was significantly greater than their reversible bioconversions. Furthermore, [6]-gingerol underwent biotransformation to zingerone. Conjugated glucuronides were eliminated partly through renal excretion, with minimal fecal excretion. Conclusion: This

Indexed as

[6]-gingerol[6]-shogaolbioavailabilityinterconversionpharmacokineticszingerone

Identifiers

PMID38904001
PMCPMC11187260

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.