Evidence map›Paper›PMID 39144552›Full record

ArticleACS pharmacology & translational science2024

Multiple-Dose Pharmacokinetics and Safety of Mitragynine, the Major Alkaloid of Kratom, in Rats.

Yi-Hua Chiang, Erin C Berthold, Michelle A Kuntz, Siva Rama Raju Kanumuri, Alexandria S Senetra, Sushobhan Mukhopadhyay, Aidan J Hampson, Christopher R McCurdy, Abhisheak Sharma

Abstract read
In one paragraph

Article in ACS pharmacology & translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 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

9 authors.

Yi-Hua ChiangDepartment of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, Florida 32610, United States.
Erin C BertholdDepartment of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, Florida 32610, United States.ORCID https://orcid.org/0000-0003-2868-8073
Michelle A KuntzDepartment of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, Florida 32610, United States.
Siva Rama Raju KanumuriDepartment of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, Florida 32610, United States.
Alexandria S SenetraDepartment of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, Florida 32610, United States.
Sushobhan MukhopadhyayDepartment of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, Florida 32610, United States.
Aidan J HampsonDivision of Therapeutics and Medical Consequences, National Institute on Drug Abuse, National Institutes of Health, Bethesda, Maryland 20892, United States.
Christopher R McCurdyTranslational Drug Development Core, Clinical and Translational Science Institute, University of Florida, Gainesville, Florida 32610, United States.ORCID https://orcid.org/0000-0001-8695-2915
Abhisheak SharmaDepartment of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, Florida 32610, United States.ORCID https://orcid.org/0000-0003-0553-4039

Funding

Opioid use disorders: UF Pharmacy medications discovery and developmentUH3DA048353 · NIDA · UNIVERSITY OF FLORIDA · PI MCCURDY, CHRISTOPHER R, MCMAHON, LANCE R. · 2021 to 2023
$4.5M
Opioid use disorders: UF Pharmacy medications discovery and developmentUG3DA048353 · NIDA · UNIVERSITY OF FLORIDA · PI MCCURDY, CHRISTOPHER R, MCMAHON, LANCE R. · 2019 to 2020
$3.6M
Kratom alkaloids: in vitro and in vivo pharmacological mechanismsR01DA047855 · NIDA · UNIVERSITY OF FLORIDA · PI MCCURDY, CHRISTOPHER R, MCMAHON, LANCE R. · 2019 to 2023
$3.6M
Kratom alkaloid exposure during pregnancyR21DA055908 · NIDA · UNIVERSITY OF FLORIDA · PI SHARMA, ABHISHEAK, WILKERSON, JENNY · 2023 to 2024
$424k
NIDA NIH HHS R01 DA047855NIDA NIH HHS R21 DA055908NIDA NIH HHS UG3 DA048353NIDA NIH HHS UH3 DA048353
6 · The paper itself

Abstract

This study reports the steady-state pharmacokinetic parameters for mitragynine and characterizes its elimination in male and female rats. Four male and female rats were dosed q12h with 40 mg/kg, and orally administered mitragynine for 5 and 6 days, respectively. Using a validated ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method, the plasma concentrations of mitragynine, its metabolites (7-hydroxymitragynine, 9-hydroxycorynantheidine, and mitragynine acid), and a non-CYP oxidation product (3-dehydromitragynine) were determined at various time points. Sex differences in pharmacokinetics were observed, with females demonstrating significantly higher systemic exposure of mitragynine than males. The mitragynine area under the curve normalized by the dose interval (AUC/τ) was 6741.6 ± 869.5 h*ng/mL in female rats and 1808.9 ± 191.3 h*ng/mL in males (

Identifiers

PMID39144552
PMCPMC11320740

What Socratic holds

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Registered trials

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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 Socratic graph.